Back to main page

Genome: Caenorhabditis Elegans | mRNA | miRBase 18 (Nov. 2011), ENSEMBL 65 (Dec. 2011) and RNA22v1.0
Description: List of transcripts that are targeted by all of the below miRNA identifiers simultaneously
miRNA's: cel-miR-4814-5p (MIMAT0020002)
Filtering By: Base pair min value: 12 | Folding energy max value (Kcal/mol): -21 | Min miRNA targets: 1


Please hold, your search is in progress...
TIP! If you show ALL results, you'll be able to dynamically sort by one or multiple columns (hold shift)
TIP! You can save this HTML file locally by going to File->Save As if you want to access it quickly later on


Gene IDTranscript IDCommon Gene Name# of miRNA targets
for specified miRNAs
ChromosomeStrand DirectionTranscript Link to view miRNA target predictionsGene LinkDescription
AC8.10AC8.10AC8.10123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
AC8.11AC8.11AC8.11123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
AC8.3AC8.3AC8.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
AC8.4AC8.4AC8.4123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0198.2B0198.2aB0198.2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0198.2B0198.2bB0198.2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0198.3B0198.3aB0198.3223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0272.1B0272.1tbb-4123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0272.2B0272.2memb-1123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0272.3B0272.3.1B0272.3123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0272.3 encodes a 3-hydroxyacyl-CoA dehydrogenase. by homology, the product of B0272.3 is predicted to function in mitochondrial fatty acid metabolism by catalyzing the NAD+-dependent oxidation of short-chain hydroxyacyl CoAs. large-scale expression studies indicate that B0272.3 is widely expressed. [Source: WormBase]
B0272.3B0272.3.2B0272.3123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0272.3 encodes a 3-hydroxyacyl-CoA dehydrogenase. by homology, the product of B0272.3 is predicted to function in mitochondrial fatty acid metabolism by catalyzing the NAD+-dependent oxidation of short-chain hydroxyacyl CoAs. large-scale expression studies indicate that B0272.3 is widely expressed. [Source: WormBase]
B0272.4B0272.4B0272.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0310.3B0310.3B0310.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0310.5B0310.5ugt-46123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0403.4B0403.4tag-320123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0403.5B0403.5B0403.5123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0410.3B0410.3B0410.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
B0416.1B0416.1B0416.1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0416.3B0416.3B0416.3123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
B0416.6B0416.6gly-13223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
gly-13 encodes an experimentally verified UDP-N-acetylglucosamine alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GnT I), that is the primary GnT I enzyme in vivo, and that can act on unusual substrates. gly-13 is expressed throughout development in many cell types. gly-13 has no obvious function in vivo, since a deletion allele of gly-13 is phenotypically normal even as a double or triple mutant with gly-12 and gly-14. [Source: WormBase]
C01C10.1C01C10.1clc-2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
clc-2 encodes a claudin homolog, closely similar to CLC-1, that is required for normal cohesion of apical junctions in epithelia. claudins are integral membrane proteins with four transmembrane sequences that are found in mammalian tight junctions (TJs), induce TJs when transgenically expressed in cells normally lacking them, and can mediate the specific conductance of of specific ions (e.g., magnesium or calcium) through TJs while blocking the flow of water. CLC-2 maintains the impermeability ('barrier function') of epithelia, since clc-1(RNAi) animals have abnormal permeability of the hypodermis to dyes. clc-2 is expressed in hypodermal seam cells, with two diffuse lines of CLC-2 protein. [Source: WormBase]
C01C10.2C01C10.2aC01C10.2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C01C10.2C01C10.2bC01C10.2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C01C10.3C01C10.3.1acl-12223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C01C10.3C01C10.3.2acl-12223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C02B4.1C02B4.1adt-1523 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
The adt-1 gene encodes a metalloproteinase with disintegrin-like and metalloproteinase with thrombospondin type I motifs (ADAMTS) that is required for male tail morphogenesis. [Source: WormBase]
C02B8.5C02B8.5C02B8.5123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C02B8.5 encodes a homolog of the functionally active Fmrf Receptor (FR. CG2114) of D. melanogaster. it is thus possible that C02B8.5 is a receptor for one of the FMRF-like neurotransmitters in C. elegans (e.g., FLP-1 through FLP-12). [Source: WormBase]
C02C6.1C02C6.1adyn-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
dyn-1 encodes the C. elegans ortholog of the dynamin GTPase. dyn-1 activity is required for endocytosis, synaptic vesicle recycling, cytokinesis, and the CED-1 pathway that regulates engulfment and degradation of apoptotic cells. mutations in dyn-1 affect locomotion, egg-laying, defecation, and embryonic development, indicating that dyn-1's endocytic function is required for a number of diverse processes. dyn-1 reporter fusion constructs are expressed in motor neurons, intestinal cells, and pharyngeal muscle. [Source: WormBase]
C02C6.1C02C6.1bdyn-1323 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
dyn-1 encodes the C. elegans ortholog of the dynamin GTPase. dyn-1 activity is required for endocytosis, synaptic vesicle recycling, cytokinesis, and the CED-1 pathway that regulates engulfment and degradation of apoptotic cells. mutations in dyn-1 affect locomotion, egg-laying, defecation, and embryonic development, indicating that dyn-1's endocytic function is required for a number of diverse processes. dyn-1 reporter fusion constructs are expressed in motor neurons, intestinal cells, and pharyngeal muscle. [Source: WormBase]
C02C6.2C02C6.2aolrn-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
olrn-1 encodes, by alternative splicing, two isoforms of a transmembrane protein required for differentiation of the AWC[ON] neuron, expression of str-2 in AWC[ON], adaptation to benzaldehyde, chemotaxis to butanone, and enhancement of chemotaxis to butanone by the presence of food. OLRN-1 is orthologous to Drosophila melanogaster RAW and Schistosoma japonicum SJCHGC05616. while OLRN-1 has orthologs in nematodes, trematodes, and arthropods, its has no obvious chordate homologs. OLRN-6 is expressed in many pharyngeal neurons and some head neurons, but is required solely in the AWC[ON] neuron for butanone enhancement. OLRN-6's function in butanone enhancement is both serotonin- and dopamine-independent, and appears to also act in chemotactic enhancement of 2,3-pentanedione and isoamyl alcohol. by orthology with RAW, OLRN-6 is predicted to inhibit JNK-1 signalling, which may in turn allow the asymmetrical AWC[ON] fate to emerge. [Source: WormBase]
C02C6.2C02C6.2bolrn-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
olrn-1 encodes, by alternative splicing, two isoforms of a transmembrane protein required for differentiation of the AWC[ON] neuron, expression of str-2 in AWC[ON], adaptation to benzaldehyde, chemotaxis to butanone, and enhancement of chemotaxis to butanone by the presence of food. OLRN-1 is orthologous to Drosophila melanogaster RAW and Schistosoma japonicum SJCHGC05616. while OLRN-1 has orthologs in nematodes, trematodes, and arthropods, its has no obvious chordate homologs. OLRN-6 is expressed in many pharyngeal neurons and some head neurons, but is required solely in the AWC[ON] neuron for butanone enhancement. OLRN-6's function in butanone enhancement is both serotonin- and dopamine-independent, and appears to also act in chemotactic enhancement of 2,3-pentanedione and isoamyl alcohol. by orthology with RAW, OLRN-6 is predicted to inhibit JNK-1 signalling, which may in turn allow the asymmetrical AWC[ON] fate to emerge. [Source: WormBase]
C02D4.1C02D4.1jud-4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
jud-4 encodes an unfamiliar protein, putatively secreted, that is required both for normal sensitivity to ethanol and for survival after freezing and thawing. JUD-4 is expressed in hypodermis and vulval muscles. JUD-4 is orthologous to Brugia malayi Bm1_40315, but lacks obvious orthologies to non-nematode proteins. JUD-4's C-terminal domain has possible similarity to F40E10.5, and to proteins such as human HOMER1. jud-4(ys18) mutants show delayed sensitivity to ethanol levels that rapidly paralyze normal worms, but do not survive freezing and rethawing as does wild-type. JUD-4 has no obvious function in mass RNAi assays. [Source: WormBase]
C02D4.2C02D4.2aser-2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
ser-2 encodes at least four tyramine 7-transmembrane domain receptors (GPCRs), by alternative splicing from three different promoters, that have distinct but partially overlapping expression patterns. ser-2 has at least three alternative promoters that drive SER-2 expression in a set of sensory, inter- and motor neurons (e.g., AIY, AIZ, and RIA) adding up to ~10% of all neurons in the nervous system, as well as pharyngeal cells and head muscles. the deletion ser-2(pk1397) has no obvious mutant phenotype. LIM-4 is required for SER-2 expression, and MAB-23 is required for SER-2 expression at normally high levels. [Source: WormBase]
C02D4.2C02D4.2bser-2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
ser-2 encodes at least four tyramine 7-transmembrane domain receptors (GPCRs), by alternative splicing from three different promoters, that have distinct but partially overlapping expression patterns. ser-2 has at least three alternative promoters that drive SER-2 expression in a set of sensory, inter- and motor neurons (e.g., AIY, AIZ, and RIA) adding up to ~10% of all neurons in the nervous system, as well as pharyngeal cells and head muscles. the deletion ser-2(pk1397) has no obvious mutant phenotype. LIM-4 is required for SER-2 expression, and MAB-23 is required for SER-2 expression at normally high levels. [Source: WormBase]
C02D4.2C02D4.2eser-2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
ser-2 encodes at least four tyramine 7-transmembrane domain receptors (GPCRs), by alternative splicing from three different promoters, that have distinct but partially overlapping expression patterns. ser-2 has at least three alternative promoters that drive SER-2 expression in a set of sensory, inter- and motor neurons (e.g., AIY, AIZ, and RIA) adding up to ~10% of all neurons in the nervous system, as well as pharyngeal cells and head muscles. the deletion ser-2(pk1397) has no obvious mutant phenotype. LIM-4 is required for SER-2 expression, and MAB-23 is required for SER-2 expression at normally high levels. [Source: WormBase]
C02D4.2C02D4.2fser-2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
ser-2 encodes at least four tyramine 7-transmembrane domain receptors (GPCRs), by alternative splicing from three different promoters, that have distinct but partially overlapping expression patterns. ser-2 has at least three alternative promoters that drive SER-2 expression in a set of sensory, inter- and motor neurons (e.g., AIY, AIZ, and RIA) adding up to ~10% of all neurons in the nervous system, as well as pharyngeal cells and head muscles. the deletion ser-2(pk1397) has no obvious mutant phenotype. LIM-4 is required for SER-2 expression, and MAB-23 is required for SER-2 expression at normally high levels. [Source: WormBase]
C02F12.1C02F12.1atsp-17123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C02F12.1C02F12.1btsp-17123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C02F12.3C02F12.3.1C02F12.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C02F12.7C02F12.7tag-278223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C02H7.1C02H7.1dyf-11123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
dyf-11 encodes a conserved protein orthologous to the human microtubule-binding protein MIP-T3 and that contains a lysine-rich region and a C-terminal coiled-coil domain present in a number of intraflagellar transport (IFT) complex B proteins. DYF-11 activity is required continuously in sensory neurons for formation of medial and distal ciliary segments and thus, for normal sensory cilium morphology and function and chemotaxis. a dyf-11::gfp promoter fusion is expressed in all ciliated sensory neurons as well as in the AQR, PQR, ADE, and PDR neurons. a DYF-11::GFP protein fusion is detected throughout the cilium and appears to localize to IFT-B particles in a manner consistent with an early role in IFT-B particle assembly. dyf-11 expression in ciliated neurons is dependent upon the presence of the DAF-19 RFX transcription factor. [Source: WormBase]
C02H7.3C02H7.3aaex-3323 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
aex-3 encodes a guanine nucleotide exchange factor for the rab-3 GTPase that is orthologous to human MAP kinase activating protein containing death domain (MADD, OMIM:603584). AEX-3 is required for intracellular vesicle trafficking as well as synaptic vesicle release and interacts with CAB-1 and RAB-3 to regulate separate pathways for neural activities such as defecation and male mating, respectively. AEX-3 is also required for egg laying and locomotion. AEX-3 is expressed in nearly all neurons. [Source: WormBase]
C03A3.1C03A3.1aC03A3.1123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C03A3.1C03A3.1bC03A3.1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C03A3.3C03A3.3C03A3.3223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C03B1.12C03B1.12.1lmp-1123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
lmp-1 encodes a protein with similarity to vertebrate lysosome-associated membrane proteins CD68, and appears to be the only protein in C. elegans that has a GYXX (phi) vertebrate lysosomal targeting sequence at its carboxy terminus. localized to the periphery of a large population of membrane bound organelles (granules) seen throughout the early embryos and restricted to the cells of the intestine during later stages. [Source: WormBase]
C03B1.12C03B1.12.2lmp-1123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
lmp-1 encodes a protein with similarity to vertebrate lysosome-associated membrane proteins CD68, and appears to be the only protein in C. elegans that has a GYXX (phi) vertebrate lysosomal targeting sequence at its carboxy terminus. localized to the periphery of a large population of membrane bound organelles (granules) seen throughout the early embryos and restricted to the cells of the intestine during later stages. [Source: WormBase]
C03B1.7C03B1.7C03B1.7223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C03G5.1C03G5.1.1sdha-1123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
sdha-1 is orthologous to the human gene SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN (SDHA. OMIM:600857), which when mutated leads to complex II mitochondrial respiratory chain deficiency presenting as Leigh syndrome. [Source: WormBase]
C03G5.1C03G5.1.2sdha-1123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
sdha-1 is orthologous to the human gene SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN (SDHA. OMIM:600857), which when mutated leads to complex II mitochondrial respiratory chain deficiency presenting as Leigh syndrome. [Source: WormBase]
C03H12.1C03H12.1C03H12.1123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C04A11.2C04A11.2C04A11.2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C04A11.3C04A11.3gck-4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C04A11.4C04A11.4adm-2223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
adm-2 encodes a protein containing a snake venom disintegrin-domain and a metalloprotease-like domain (i.e., a protein of the ADAM family). like ADM-1, ADM-2 is homologous to a mammalian sperm glycoprotein (PH-30/fertilin) implicated in sperm-egg fusion, and ADM-2 might thus be a fusogenic protein mediating the merging of plasma membranes during development. [Source: WormBase]
C04C11.2C04C11.2.1arrd-25423 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C04C11.2C04C11.2.2arrd-25423 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C04E7.1C04E7.1C04E7.1123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C04E7.2C04E7.2sor-3123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
sor-3 encodes a novel protein that contains an MBT (malignant brain tumor) domain related to the MBT domains found in the Sex comb on midleg (SCM) and Sfmbt Polycomb group proteins. during development, SOR-3 activity is required to specify the correct number of dopaminergic and serotonergic neurons in males, as well as for proper ray neuron axon guidance, distal tip cell migration, and normal body size. SOR-3 activity is necessary for maintaining repression of Hox gene expression, notably that of egl-5 in many head neurons. in regulating neurotransmitter phenotype, sor-3 functions together with sop-2, which also encodes a Polycomb group protein, and members of the TGF-beta signaling pathway. sor-3 and sop-2 also function together to regulate progression through larval development. a SOR-3::GFP reporter fusion is expressed ubiquitously throughout the life cycle and localizes to both the cytoplasm and the nucleus. [Source: WormBase]
C04E7.3C04E7.3C04E7.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C04E7.4C04E7.4C04E7.4123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C04F6.1C04F6.1vit-5223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
vit-5 encodes a vitellogenin, a lipid-binding protein precursor related to vertebrate vitellogenins and mammalian ApoB-100, a core LDL particle constituent. by homology, VIT-5 is predicted to function as a lipid transport protein. loss of vit-5 activity via large-scale RNA-mediated interference (RNAi) screens indicates that VIT-5 is required for embryogenesis and normal rates of postembryonic growth. VIT-5 is a major yolk component and is expressed exclusively in the adult hermaphrodite intestine from which it is secreted into the pseudocoelomic space and taken up by oocytes. [Source: WormBase]
C05A9.1C05A9.1apgp-5323 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
pgp-5 encodes a transmembrane protein that is a member of the P-glycoprotein subclass of the ATP-binding cassette (ABC) transporter superfamily. by homology, PGP-5 is predicted to function as an ATP-dependent efflux pump that protects C. elegans by exporting exogenous toxins. however, as loss of pgp-5 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of PGP-5 in C. elegans development and/or behavior is not yet known. [Source: WormBase]
C05A9.1C05A9.1bpgp-5323 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
pgp-5 encodes a transmembrane protein that is a member of the P-glycoprotein subclass of the ATP-binding cassette (ABC) transporter superfamily. by homology, PGP-5 is predicted to function as an ATP-dependent efflux pump that protects C. elegans by exporting exogenous toxins. however, as loss of pgp-5 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of PGP-5 in C. elegans development and/or behavior is not yet known. [Source: WormBase]
C05C9.1C05C9.1C05C9.1123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C05C9.3C05C9.3C05C9.3323 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
The protein product of this gene is predicted to contain a glutamine/asparagine (Q/N)-rich ('prion') domain, by the algorithm of Michelitsch and Weissman (as of the WS77 release of WormBase, i.e., in wormpep77). [Source: WormBase]
C05D9.1C05D9.1.1snx-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C05D9.1C05D9.1.2snx-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C05D9.1C05D9.1.3snx-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C05D9.5C05D9.5ife-4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
The ife-4 gene encodes a member of the Initiation Factor 4E (eIF4E) family. [Source: WormBase]
C05E11.1C05E11.1.1lnp-1223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
lnp-1 encodes a highly conserved protein of unknown function, orthologous to human LUNAPARK/KIAA1715 (OMIM:610236), that is required for normally short body length, normal locomotion, fat content, acetylcholine neurotransmission, localization of RAB-3 and SNB-1, and sensitivity to aldicarb. LNP-1 is expressed in muscles, hypodermal cells, and neurons. within neurons, LNP-1 is localized to cell bodies, neuritic processes and commissures, and requiring UNC-104 for localization outside of cell bodies. LNP-1 is likely to act presynaptically. LNP-1 contains two N-terminal predicted transmembrane sequences, and an atypical zinc finger domain (C2HC2). [Source: WormBase]
C05E11.4C05E11.4amt-1123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
amt-1 encodes a transmembrane transporter that by homology, is predicted to transport ammonium ions across the plasma membrane. as loss of amt-1 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of AMT-1 in C. elegans development and/or behavior is not yet known. [Source: WormBase]
C05E11.7C05E11.7C05E11.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C05E11.8C05E11.8bflp-12123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
flp-12 encodes a predicted FMRFamide-like peptide neurotransmitter that affects locomotion when injected into A. suum. expressed in the ASE and PVM sensory neurons. [Source: WormBase]
C05E7.2C05E7.2C05E7.2123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C05E7.3C05E7.3C05E7.3123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C05G5.1C05G5.1C05G5.1223 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C05G5.2C05G5.2C05G5.2223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C05G5.4C05G5.4.2C05G5.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C06E2.9C06E2.9C06E2.9123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C06G1.4C06G1.4.1ain-1323 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
ain-1 encodes an unfamiliar protein synergistically required, with LIN-31, for the normal timing of vulval differentiation, independently of LET-60/RAS, and parallel to or downstream of LIN-14/LIN-28/HBL-1. AIN-1 is expressed in cytoplasmic foci (that are probably P bodies) in several tissues, including vulval precursor cells and neurons. AIN-1 coimmunoprecipitates with DCR-1 and ALG-1, also binds ALG-1 in vitro, and does not require DNA or RNA for its binding. in vivo, AIN-1 targets ALG-1 to cytoplasmic foci, in which it colocalizes with DCAP-2. AIN-1 is likely to be a RISC component, since anti-AIN-1 antibodies precipitate 29 different miRNAs, including mir-2, mir-52, mir-58, mir-71, mir-77, and mir-239a. ain-1(ku322) mutants are essentially wild-type, except for sporadically gapped alae and excess seam cell nuclei arising from retarded seam cell fusion. more prominently, ain-1(ku322) suppresses the multivulva phenotype of lin-31(n1053) mutations, while strongly enhancing lin-31(n1053)'s egg-laying defect. the cellular basis of lin-31(n1053).ain-1(ku322) phenotypes is a delay in vulval development in L4 larvae not seen with either mutation alone. ain-1(ku322) has no effect on let-60(n1046) or lin-3(e1275) mutations. ain-1(ku322) suppresses the precocious vulval development of lin-14(RNAi), lin-28 mutants, and hbl-1(RNAi). alg-1 or alg-1 ain-1 mutant alae resemble ain-1 alae, indicating that ALG-1 and AIN-1 act in a common genetic pathway. AIN-1 is homologous to Brugia malayi 14748.m00068, 14052.m00191, and 14963.m01790, and paralogous to C. elegans B0041.2. AIN-1 and its nematode homologs have weak similarity to human TNRC6A (GW182. OMIM:610739) and Drosophila GAWKY. [Source: WormBase]
C06G1.4C06G1.4.2ain-1323 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
ain-1 encodes an unfamiliar protein synergistically required, with LIN-31, for the normal timing of vulval differentiation, independently of LET-60/RAS, and parallel to or downstream of LIN-14/LIN-28/HBL-1. AIN-1 is expressed in cytoplasmic foci (that are probably P bodies) in several tissues, including vulval precursor cells and neurons. AIN-1 coimmunoprecipitates with DCR-1 and ALG-1, also binds ALG-1 in vitro, and does not require DNA or RNA for its binding. in vivo, AIN-1 targets ALG-1 to cytoplasmic foci, in which it colocalizes with DCAP-2. AIN-1 is likely to be a RISC component, since anti-AIN-1 antibodies precipitate 29 different miRNAs, including mir-2, mir-52, mir-58, mir-71, mir-77, and mir-239a. ain-1(ku322) mutants are essentially wild-type, except for sporadically gapped alae and excess seam cell nuclei arising from retarded seam cell fusion. more prominently, ain-1(ku322) suppresses the multivulva phenotype of lin-31(n1053) mutations, while strongly enhancing lin-31(n1053)'s egg-laying defect. the cellular basis of lin-31(n1053).ain-1(ku322) phenotypes is a delay in vulval development in L4 larvae not seen with either mutation alone. ain-1(ku322) has no effect on let-60(n1046) or lin-3(e1275) mutations. ain-1(ku322) suppresses the precocious vulval development of lin-14(RNAi), lin-28 mutants, and hbl-1(RNAi). alg-1 or alg-1 ain-1 mutant alae resemble ain-1 alae, indicating that ALG-1 and AIN-1 act in a common genetic pathway. AIN-1 is homologous to Brugia malayi 14748.m00068, 14052.m00191, and 14963.m01790, and paralogous to C. elegans B0041.2. AIN-1 and its nematode homologs have weak similarity to human TNRC6A (GW182. OMIM:610739) and Drosophila GAWKY. [Source: WormBase]
C06G1.5C06G1.5C06G1.5123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C06G1.6C06G1.6C06G1.6123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.1C07A12.1aham-2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
The ham-2 gene encodes a C2H2 zinc finger-containing protein required for proper migration of the hermaphrodite-specific neurons (HSNs) and proper attachment of the pharynx to the nose. HAM-2 is expressed in the nuclei of the HSNs during migration, and acts downstream of EGL-5, a posterior group Hox protein, in HSN specification. HAM-2 acts redundantly with UNC-86 to downregulate UNC-43 expression in the HSNs after migration is complete. [Source: WormBase]
C07A12.1C07A12.1bham-2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
The ham-2 gene encodes a C2H2 zinc finger-containing protein required for proper migration of the hermaphrodite-specific neurons (HSNs) and proper attachment of the pharynx to the nose. HAM-2 is expressed in the nuclei of the HSNs during migration, and acts downstream of EGL-5, a posterior group Hox protein, in HSN specification. HAM-2 acts redundantly with UNC-86 to downregulate UNC-43 expression in the HSNs after migration is complete. [Source: WormBase]
C07A12.1C07A12.1cham-2123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
The ham-2 gene encodes a C2H2 zinc finger-containing protein required for proper migration of the hermaphrodite-specific neurons (HSNs) and proper attachment of the pharynx to the nose. HAM-2 is expressed in the nuclei of the HSNs during migration, and acts downstream of EGL-5, a posterior group Hox protein, in HSN specification. HAM-2 acts redundantly with UNC-86 to downregulate UNC-43 expression in the HSNs after migration is complete. [Source: WormBase]
C07A12.3C07A12.3anhr-35123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.5C07A12.5aspr-3223 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.7C07A12.7a.1C07A12.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.7C07A12.7a.2C07A12.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.7C07A12.7bC07A12.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.7C07A12.7c.1C07A12.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A12.7C07A12.7c.2C07A12.7123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C07A4.1C07A4.1tiar-3323 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07B5.4C07B5.4a.1C07B5.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07B5.4C07B5.4a.2C07B5.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07B5.4C07B5.4b.1C07B5.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07B5.4C07B5.4b.2C07B5.4123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
C07B5.8C07B5.8C07B5.8123 XReverseView as cDNA map |
View as Table
Internal |
Ensembl
C08A9.10C08A9.10C08A9.10123 XForwardView as cDNA map |
View as Table
Internal |
Ensembl
Please email us for questions and/or suggestions
GUI created by the Computational Medicine Center at the Sidney Kimmel Medical College of Thomas Jefferson University
We gratefully acknowledge support of this work by the William M. Keck Foundation