Gene ID | Transcript ID | Common Gene Name | # of miRNA targets for specified miRNAs | Chromosome | Strand Direction | Transcript Link to view miRNA target predictions | Gene Link | Description |
---|---|---|---|---|---|---|---|---|
AC8.10 | AC8.10 | AC8.10 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
AC8.3 | AC8.3 | AC8.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
B0198.1 | B0198.1 | tsp-20 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
B0198.2 | B0198.2a | B0198.2 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
B0198.2 | B0198.2b | B0198.2 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
B0198.3 | B0198.3a | B0198.3 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
B0272.1 | B0272.1 | tbb-4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
B0272.3 | B0272.3.1 | B0272.3 | 1 | 23 X | Forward | View 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] |
B0272.3 | B0272.3.2 | B0272.3 | 1 | 23 X | Forward | View 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] |
B0344.2 | B0344.2 | wrt-9 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | wrt-9 encodes a hedgehog-like protein, with an N-terminal signal sequence, a Wart domain, and a C-terminal region of proline-rich, low-complexity sequence. the Wart domain is predicted to form a cysteine-crosslinked protein involved in intercellular signalling, and it has subtle similarity to the N-terminal Hedge domain of HEDGEHOG proteins. WRT-9 has no obvious function in RNAi assays. [Source: WormBase] |
B0395.2 | B0395.2 | mboa-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | mboa-1 encodes a putative acyl-Coenzyme A:cholesterol ('sterol') O-acyltransferase, orthologous to human SOAT1 (OMIM:102642). MBOA-1 is required for normal locomotion and normally long lifespan in mass RNAi assays. mboa-1 is expressed in the seam cells and nervous systems of larvae and adults, and in the adult reproductive system. [Source: WormBase] |
B0403.2 | B0403.2 | ubc-17 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
B0410.2 | B0410.2a | vang-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | vang-1 encodes an ortholog of Drosophila VAN GOGH (also known as STRABISMUS). VANG-1 enables Wnt-directed planar cell polarity. VANG-1 is required for the fully asymmetrical division of B.a versus B.p cells, though this requirement is quantitatively weak. [Source: WormBase] |
B0410.2 | B0410.2b | vang-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | vang-1 encodes an ortholog of Drosophila VAN GOGH (also known as STRABISMUS). VANG-1 enables Wnt-directed planar cell polarity. VANG-1 is required for the fully asymmetrical division of B.a versus B.p cells, though this requirement is quantitatively weak. [Source: WormBase] |
B0416.1 | B0416.1 | B0416.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
B0563.2 | B0563.2 | tsp-11 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
B0563.7 | B0563.7 | B0563.7 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C02B4.1 | C02B4.1 | adt-1 | 1 | 23 X | Forward | View 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] |
C02B8.4 | C02B8.4 | hlh-8 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | The hlh-8 gene encodes a helix-loop-helix protein required for normal muscle development, and hence for normal defecation and egg-laying. [Source: WormBase] |
C02F12.1 | C02F12.1a | tsp-17 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C02F12.1 | C02F12.1b | tsp-17 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C02F12.7 | C02F12.7 | tag-278 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C02H7.3 | C02H7.3a | aex-3 | 3 | 23 X | Reverse | View 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] |
C03A3.3 | C03A3.3 | C03A3.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C03B1.2 | C03B1.2 | C03B1.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C03B1.7 | C03B1.7 | C03B1.7 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C04A11.2 | C04A11.2 | C04A11.2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C04A11.3 | C04A11.3 | gck-4 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C04A11.4 | C04A11.4 | adm-2 | 1 | 23 X | Forward | View 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] |
C04A11.5 | C04A11.5.1 | C04A11.5 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C04A11.5 | C04A11.5.2 | C04A11.5 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C04B4.5 | C04B4.5 | C04B4.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | C04B4.5 encodes a novel protein. [Source: WormBase] |
C04F6.1 | C04F6.1 | vit-5 | 2 | 23 X | Forward | View 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] |
C04F6.4 | C04F6.4a | unc-78 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | The unc-78 gene encodes a homolog of actin-interacting protein 1 (AIP1) that regulates the ordered assembly of actin and cofilin in myofibrils. [Source: WormBase] |
C04F6.7 | C04F6.7 | C04F6.7 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C05A9.1 | C05A9.1a | pgp-5 | 1 | 23 X | Reverse | View 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] |
C05A9.1 | C05A9.1b | pgp-5 | 1 | 23 X | Reverse | View 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] |
C05C9.2 | C05C9.2 | C05C9.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C05D9.1 | C05D9.1.1 | snx-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C05D9.1 | C05D9.1.2 | snx-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C05D9.1 | C05D9.1.3 | snx-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C05D9.2 | C05D9.2.1 | lmp-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | lmp-2 encodes a transmembrane protein that is one of two C. elegans LAMP (lysosomal associated membrane glycoprotein) homologs. [Source: WormBase] |
C05D9.2 | C05D9.2.2 | lmp-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | lmp-2 encodes a transmembrane protein that is one of two C. elegans LAMP (lysosomal associated membrane glycoprotein) homologs. [Source: WormBase] |
C05D9.2 | C05D9.2.3 | lmp-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | lmp-2 encodes a transmembrane protein that is one of two C. elegans LAMP (lysosomal associated membrane glycoprotein) homologs. [Source: WormBase] |
C05G5.2 | C05G5.2 | C05G5.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C05G5.5 | C05G5.5 | C05G5.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C06E2.1 | C06E2.1 | C06E2.1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C06G1.1 | C06G1.1a | C06G1.1 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C06G1.1 | C06G1.1b | C06G1.1 | 3 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C06G1.4 | C06G1.4.1 | ain-1 | 2 | 23 X | Forward | View 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] |
C06G1.4 | C06G1.4.2 | ain-1 | 1 | 23 X | Forward | View 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] |
C06G1.6 | C06G1.6 | C06G1.6 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C07A12.1 | C07A12.1a | ham-2 | 1 | 23 X | Forward | View 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] |
C07A12.1 | C07A12.1b | ham-2 | 1 | 23 X | Forward | View 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] |
C07A12.1 | C07A12.1c | ham-2 | 1 | 23 X | Forward | View 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] |
C07A12.4 | C07A12.4a.1 | pdi-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07A12.4 | C07A12.4a.2 | pdi-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07A12.4 | C07A12.4b | pdi-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07A12.4 | C07A12.4c | pdi-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07A12.5 | C07A12.5a | spr-3 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07B5.4 | C07B5.4a.1 | C07B5.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07B5.4 | C07B5.4a.2 | C07B5.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07B5.4 | C07B5.4b.1 | C07B5.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07B5.4 | C07B5.4b.2 | C07B5.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C07B5.5 | C07B5.5 | nuc-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | The nuc-1 gene encodes a DNase II homolog similar to mammalian and Drosophila DNaseII enzymes and is required for DNA degradation during apoptosis as well as for degradation of dietary DNA during normal feeding. during apoptosis, NUC-1 functions in apoptotic cells at an intermediate stage of DNA degradation, after the killing step, but prior to cell-corpse engulfment. [Source: WormBase] |
C07B5.8 | C07B5.8 | C07B5.8 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C08A9.9 | C08A9.9.1 | C08A9.9 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C08A9.9 | C08A9.9.2 | C08A9.9 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C09B8.6 | C09B8.6c.1 | hsp-25 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | hsp-25 encodes a member of the small heat shock family of proteins. HSP-25 is expressed throughout development and in vitro, exhibits chaperone activity. HSP-25 localizes to: 1) dense bodies and M lines in body wall muscle, 2) the lining of the pharynx, and 3) to cell-cell junctions in the spermathecal wall. consistent with a role in myofibril organization, HSP-25 binds vinculin and alpha-actinin in vitro. [Source: WormBase] |
C09B8.6 | C09B8.6c.2 | hsp-25 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | hsp-25 encodes a member of the small heat shock family of proteins. HSP-25 is expressed throughout development and in vitro, exhibits chaperone activity. HSP-25 localizes to: 1) dense bodies and M lines in body wall muscle, 2) the lining of the pharynx, and 3) to cell-cell junctions in the spermathecal wall. consistent with a role in myofibril organization, HSP-25 binds vinculin and alpha-actinin in vitro. [Source: WormBase] |
C09G1.4 | C09G1.4 | C09G1.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C10A4.9 | C10A4.9 | C10A4.9 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C10E2.2 | C10E2.2.1 | C10E2.2 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | This gene encodes a protein containing an F-box, a motif predicted to mediate protein-protein interactions either with homologs of yeast Skp-1p or with other proteins. [Source: WormBase] |
C11E4.2 | C11E4.2 | C11E4.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C11E4.6 | C11E4.6.1 | C11E4.6 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C11E4.6 | C11E4.6.2 | C11E4.6 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C11G6.1 | C11G6.1 | taf-3 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | taf-3 encodes the C. elegans ortholog of mammalian TAF3(TAFII140), a component of the RNA polymerase II TFIID transcription complex. TAF-3 contains a histone fold-like domain in its N-terminus and by homology, is predicted to function in transcriptional regulation. however, as loss of taf-3 activity via large-scale RNAi screens does not result in any obvious abnormalities, the precise role of taf-3 in C. elegans development and/or behavior is not yet known. [Source: WormBase] |
C11H1.5 | C11H1.5 | C11H1.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C12D12.1 | C12D12.1a | C12D12.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C12D12.1 | C12D12.1b | C12D12.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C12D12.1 | C12D12.1c | C12D12.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C12D12.2 | C12D12.2a.1 | glt-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | glt-1 encodes a predicted plasma membrane glutamate transporter that is functional when expressed in Xenopus oocytes. expressed in the M3 pharyngeal neuron, the male tail, some anterior hypodermal cells, and in cells in the terminal bulb of the pharynx. [Source: WormBase] |
C12D12.2 | C12D12.2a.2 | glt-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | glt-1 encodes a predicted plasma membrane glutamate transporter that is functional when expressed in Xenopus oocytes. expressed in the M3 pharyngeal neuron, the male tail, some anterior hypodermal cells, and in cells in the terminal bulb of the pharynx. [Source: WormBase] |
C14A11.9 | C14A11.9 | C14A11.9 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C14E2.4 | C14E2.4 | C14E2.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C14E2.7 | C14E2.7 | C14E2.7 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C14F5.1 | C14F5.1a | dct-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | dct-1 encodes a protein with similarity to the mammalian BNIP3 proteins that interact with Bcl-2 and the Adenovirus E1B 19kDa protein and that have been shown to have pro-apoptotic activity. loss of dct-1 activity via RNAi in daf-2 mutants and in gld-1. daf-2 doubly mutant animals indicates that dct-1 can function to regulate both lifespan and tumor cell proliferation. when expressed in mammalian cells, DCT-1 can: 1) induce delayed apoptosis and increase apoptosis when coexpressed with CED-3 (perhaps by increasing proteolyic processing of CED-3), 2) physically interact with CED-9 or the CED-3 prodomain when coexpressed, and 3) physically interact with both CED-9 and CED-3 when all three are coexpressed. chromatin immunoprecipitation experiments have demonstrated that the dct-1 promoter is bound in vivo by the forkhead transcription factor DAF-16. expression of DCT-1 in mammalian cells suggests that, like its mammalian orthologs, DCT-1 localizes to mitochondria via a predicted C-terminal transmembrane domain. [Source: WormBase] |
C14F5.3 | C14F5.3b | tnt-3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | tnt-3 is orthologous to the human gene TROPONIN T (TNNT2. OMIM:191045), which when mutated leads to disease. [Source: WormBase] |
C14F5.3 | C14F5.3d | tnt-3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | tnt-3 is orthologous to the human gene TROPONIN T (TNNT2. OMIM:191045), which when mutated leads to disease. [Source: WormBase] |
C15B12.1 | C15B12.1 | C15B12.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C15B12.2 | C15B12.2.1 | C15B12.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C15B12.2 | C15B12.2.2 | C15B12.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
C15B12.4 | C15B12.4 | C15B12.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C15B12.5 | C15B12.5b | gar-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | gar-1 encodes a G-protein-linked acetylcholine receptor. though gar-1 is most closely related to muscarinic acetylcholine receptors (mAChR), it is pharmacologically distinct from them in its response to certain ligands. gar-1 gene transcripts are expressed at all developmental stages. the GAR-1-GFP fusion protein is expressed in some head neurons and in the PVM neuron. electrophysiological studies indicate that gar-1 couples to the inhibitory subunit of G proteins and not to Gs or to Go/Gq. [Source: WormBase] |
C15B12.6 | C15B12.6 | C15B12.6 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
C15B12.7 | C15B12.7b | cdf-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | a cation diffusion facilitator protein, affects vulva development, genetically interacts with let-60/ras signaling pathway. and is expressed in the vulval muscles, the intestinal cells, and in the vulval precursor cells. [Source: WormBase] |
C15C7.2 | C15C7.2.1 | klp-8 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | klp-8 encodes an atypical kinesin-like motor protein with the motor domain in the N-terminus. the motor domain of KLP-8 exhibits poor homology to the globular motor domain of the kinesin heavy chain. [Source: WormBase] |
C15C7.2 | C15C7.2.2 | klp-8 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | klp-8 encodes an atypical kinesin-like motor protein with the motor domain in the N-terminus. the motor domain of KLP-8 exhibits poor homology to the globular motor domain of the kinesin heavy chain. [Source: WormBase] |
C15H9.1 | C15H9.1 | nnt-1 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | nnt-1 encodes a proton-pumping nicotinamide nucleotide transhydrogenase predicted to be mitochondrial. [Source: WormBase] |
C15H9.3 | C15H9.3 | C15H9.3 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl |