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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-2220-5p (MIMAT0011461)
Filtering By: Base pair min value: 12 | Folding energy max value (Kcal/mol): -21 | Min miRNA targets: 1


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Gene IDTranscript IDCommon Gene Name# of miRNA targets
for specified miRNAs
ChromosomeStrand DirectionTranscript Link to view miRNA target predictionsGene LinkDescription
B0395.1B0395.1nhx-1123 XForwardView as cDNA map |
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Ensembl
nhx-1 encodes a sodium/proton exchanger expressed intracellularly within hypodermal and muscle cells. NHX-1 is required for embryonic viability, and is thought to prevent intracellular acidification by catalysing the electroneutral exchange of vesicular sodium for an intracellular proton. [Source: WormBase]
B0395.2B0395.2mboa-1123 XForwardView as cDNA map |
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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]
B0416.3B0416.3B0416.3123 XForwardView as cDNA map |
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Ensembl
C02B4.1C02B4.1adt-1123 XForwardView as cDNA map |
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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 |
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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]
C02F12.7C02F12.7tag-278123 XReverseView as cDNA map |
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Ensembl
C04E7.4C04E7.4C04E7.4123 XReverseView as cDNA map |
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Ensembl
C04F6.7C04F6.7C04F6.7123 XReverseView as cDNA map |
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Ensembl
C06E2.3C06E2.3ubc-21123 XForwardView as cDNA map |
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Ensembl
C07A12.3C07A12.3anhr-35123 XForwardView as cDNA map |
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Ensembl
C09B8.7C09B8.7a.1pak-1123 XReverseView as cDNA map |
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Ensembl
pak-1 encodes, by alternative splicing, at least five isoforms of a putative p21-activated kinase orthologous to human PAK1, PAK2 (OMIM:?), and PAK3 (OMIM:300142, mutated in nonsyndromic mental retardation). PAK-1 is required (redundantly with its paralog, MAX-2) for normal axonal guidance of motoneurons, P cell migration, and locomotion, with max-2(cy2).pak-1(ok448) double mutants phenotypically resembling unc-73 or ced-10.mig-2 mutants. pak-1 is expressed in pharyngeal muscles, CAN neurons, ventral cord motoneurons, migrating distal tip cells, developing uterus, B, Y, and T cells in the male tail, and vulval muscle cells. by itself, the null pak-1(ok448) mutation has no known phenotype. [Source: WormBase]
C09B8.7C09B8.7a.2pak-1123 XReverseView as cDNA map |
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Ensembl
pak-1 encodes, by alternative splicing, at least five isoforms of a putative p21-activated kinase orthologous to human PAK1, PAK2 (OMIM:?), and PAK3 (OMIM:300142, mutated in nonsyndromic mental retardation). PAK-1 is required (redundantly with its paralog, MAX-2) for normal axonal guidance of motoneurons, P cell migration, and locomotion, with max-2(cy2).pak-1(ok448) double mutants phenotypically resembling unc-73 or ced-10.mig-2 mutants. pak-1 is expressed in pharyngeal muscles, CAN neurons, ventral cord motoneurons, migrating distal tip cells, developing uterus, B, Y, and T cells in the male tail, and vulval muscle cells. by itself, the null pak-1(ok448) mutation has no known phenotype. [Source: WormBase]
C11H1.4C11H1.4aprx-1123 XForwardView as cDNA map |
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prx-1 encodes a predicted peroxin, a subfamily 2 member of the AAA (ATPases Associated with diverse cellular Activities) family that affects growth in one large-scale RNAi screen. expressed in intestinal cells throughout development. [Source: WormBase]
C14F11.7C14F11.7C14F11.7123 XReverseView as cDNA map |
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C14F5.5C14F5.5sem-5123 XReverseView as cDNA map |
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Ensembl
sem-5 encodes a Src homology (SH) domain 2 and 3-containing protein, orthologous to human GRB2 (OMIM:108355) and Drosophila Drk. sem-5 functions in multiple signaling pathways during development including those regulating sex myoblast migration, muscle membrane extension, vulval induction, fluid balance, viability, and formation of the male tail. SEM-5 acts downstream of the LET-23 epidermal growth factor receptor to negatively regulate RAS-, MAP-, and IP-3-, mediated signal transduction. a sem-5::yfp promoter fusion is expressed in many cells throughout development, including the hypodermis, intestine, neurons, body wall muscles, and vulval precursor cells. [Source: WormBase]
C16B8.4C16B8.4C16B8.4123 XReverseView as cDNA map |
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Ensembl
C18B12.4C18B12.4C18B12.4123 XReverseView as cDNA map |
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C23H4.4C23H4.4aC23H4.4123 XForwardView as cDNA map |
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C23H4.4C23H4.4bC23H4.4123 XForwardView as cDNA map |
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C24A3.6C24A3.6.1twk-18123 XForwardView as cDNA map |
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Ensembl
twk-18 encodes one of 44 C. elegans TWK (two-P domain K+) potassium channel subunits that contain two pore-forming domains and four transmembrane domains. TWK-18 was originally defined by gain-of-function mutations that result in embryonic lethality at the two-fold stage, locomotion defects, longer than normal body length, abnormal egg-laying, and temperature-sensitive paralysis. as loss of TWK-18 function via reversion or RNA-mediated interference does not result in any abnormalities, TWK-18 likely functions redundantly with other TWK channels. TWK-18 can function as an outwardly rectifying K+ channel, and is activated by temperature increases, thus making it a temperature-gated channel. TWK-18 is expressed in body wall muscle. [Source: WormBase]
C24A3.6C24A3.6.2twk-18123 XForwardView as cDNA map |
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Ensembl
twk-18 encodes one of 44 C. elegans TWK (two-P domain K+) potassium channel subunits that contain two pore-forming domains and four transmembrane domains. TWK-18 was originally defined by gain-of-function mutations that result in embryonic lethality at the two-fold stage, locomotion defects, longer than normal body length, abnormal egg-laying, and temperature-sensitive paralysis. as loss of TWK-18 function via reversion or RNA-mediated interference does not result in any abnormalities, TWK-18 likely functions redundantly with other TWK channels. TWK-18 can function as an outwardly rectifying K+ channel, and is activated by temperature increases, thus making it a temperature-gated channel. TWK-18 is expressed in body wall muscle. [Source: WormBase]
C24A3.6C24A3.6.3twk-18123 XForwardView as cDNA map |
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Ensembl
twk-18 encodes one of 44 C. elegans TWK (two-P domain K+) potassium channel subunits that contain two pore-forming domains and four transmembrane domains. TWK-18 was originally defined by gain-of-function mutations that result in embryonic lethality at the two-fold stage, locomotion defects, longer than normal body length, abnormal egg-laying, and temperature-sensitive paralysis. as loss of TWK-18 function via reversion or RNA-mediated interference does not result in any abnormalities, TWK-18 likely functions redundantly with other TWK channels. TWK-18 can function as an outwardly rectifying K+ channel, and is activated by temperature increases, thus making it a temperature-gated channel. TWK-18 is expressed in body wall muscle. [Source: WormBase]
C24H10.4C24H10.4C24H10.4223 XReverseView as cDNA map |
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C25F6.7C25F6.7aC25F6.7123 XForwardView as cDNA map |
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Ensembl
C25G6.2C25G6.2tsp-9123 XForwardView as cDNA map |
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C27C12.3C27C12.3C27C12.3123 XReverseView as cDNA map |
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C27C12.3 encodes a novel protein that is conserved in C. elegans. three other genes related to C27C12.3 are present in tandem on the X chromosome. in situ hybridization studies indicate that C27C12.3 mRNA is expressed in the proximal germline. [Source: WormBase]
C27C12.7C27C12.7dpf-2123 XForwardView as cDNA map |
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C30E1.6C30E1.6C30E1.6123 XForwardView as cDNA map |
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C31H2.1C31H2.1atbc-7223 XForwardView as cDNA map |
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C31H2.1C31H2.1btbc-7123 XForwardView as cDNA map |
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C33D3.5C33D3.5C33D3.5123 XForwardView as cDNA map |
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C33E10.5C33E10.5C33E10.5123 XForwardView as cDNA map |
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C33G3.5C33G3.5C33G3.5123 XReverseView as cDNA map |
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C34F6.11C34F6.11C34F6.11123 XReverseView as cDNA map |
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C35B8.3C35B8.3bC35B8.3123 XForwardView as cDNA map |
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C35C5.8C35C5.8aC35C5.8123 XForwardView as cDNA map |
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C35C5.8C35C5.8bC35C5.8123 XForwardView as cDNA map |
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C39B10.7C39B10.7C39B10.7123 XForwardView as cDNA map |
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C41A3.1C41A3.1C41A3.1123 XForwardView as cDNA map |
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C42D8.2C42D8.2avit-2123 XForwardView as cDNA map |
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The vit-2 gene encodes the vitellogenin homolog YP170. [Source: WormBase]
C42D8.2C42D8.2bvit-2123 XForwardView as cDNA map |
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The vit-2 gene encodes the vitellogenin homolog YP170. [Source: WormBase]
C52B9.4C52B9.4C52B9.4123 XForwardView as cDNA map |
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C54D1.4C54D1.4alh-10123 XReverseView as cDNA map |
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Ensembl
C54D1.5C54D1.5.1lam-2123 XReverseView as cDNA map |
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lam-2 encodes a laminin gamma subunit. lam-2 activity is required for embryonic development and for regulation of muscle arm extension. loss of lam-2 function via large-scale RNAi screens results in embryonic, larval, and adult lethality, sterility, body morphology defects, and abnormal locomotion. [Source: WormBase]
C54D1.5C54D1.5.2lam-2123 XReverseView as cDNA map |
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Ensembl
lam-2 encodes a laminin gamma subunit. lam-2 activity is required for embryonic development and for regulation of muscle arm extension. loss of lam-2 function via large-scale RNAi screens results in embryonic, larval, and adult lethality, sterility, body morphology defects, and abnormal locomotion. [Source: WormBase]
C54D2.5C54D2.5acca-1123 XReverseView as cDNA map |
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Ensembl
cca-1 encodes a calcium channel alpha subunit that is homologous to vertebrate T-type calcium channel alpha 1 subunits. CCA-1 is required for regulation of pharyngeal pumping, specifically for the efficient initiation of action potentials in the pharynx in response to excitatory inputs. a CCA-1::GFP fusion protein is expressed strongly in pharyngeal muscle as well as in many neurons, including particular subsets of neurons in the head, pharynx, ventral nerve cord, and anal ganglia. [Source: WormBase]
C54D2.5C54D2.5ccca-1123 XReverseView as cDNA map |
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Ensembl
cca-1 encodes a calcium channel alpha subunit that is homologous to vertebrate T-type calcium channel alpha 1 subunits. CCA-1 is required for regulation of pharyngeal pumping, specifically for the efficient initiation of action potentials in the pharynx in response to excitatory inputs. a CCA-1::GFP fusion protein is expressed strongly in pharyngeal muscle as well as in many neurons, including particular subsets of neurons in the head, pharynx, ventral nerve cord, and anal ganglia. [Source: WormBase]
C54D2.5C54D2.5dcca-1123 XReverseView as cDNA map |
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Ensembl
cca-1 encodes a calcium channel alpha subunit that is homologous to vertebrate T-type calcium channel alpha 1 subunits. CCA-1 is required for regulation of pharyngeal pumping, specifically for the efficient initiation of action potentials in the pharynx in response to excitatory inputs. a CCA-1::GFP fusion protein is expressed strongly in pharyngeal muscle as well as in many neurons, including particular subsets of neurons in the head, pharynx, ventral nerve cord, and anal ganglia. [Source: WormBase]
C54D2.5C54D2.5ecca-1123 XReverseView as cDNA map |
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Ensembl
cca-1 encodes a calcium channel alpha subunit that is homologous to vertebrate T-type calcium channel alpha 1 subunits. CCA-1 is required for regulation of pharyngeal pumping, specifically for the efficient initiation of action potentials in the pharynx in response to excitatory inputs. a CCA-1::GFP fusion protein is expressed strongly in pharyngeal muscle as well as in many neurons, including particular subsets of neurons in the head, pharynx, ventral nerve cord, and anal ganglia. [Source: WormBase]
C54D2.5C54D2.5fcca-1123 XReverseView as cDNA map |
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Ensembl
cca-1 encodes a calcium channel alpha subunit that is homologous to vertebrate T-type calcium channel alpha 1 subunits. CCA-1 is required for regulation of pharyngeal pumping, specifically for the efficient initiation of action potentials in the pharynx in response to excitatory inputs. a CCA-1::GFP fusion protein is expressed strongly in pharyngeal muscle as well as in many neurons, including particular subsets of neurons in the head, pharynx, ventral nerve cord, and anal ganglia. [Source: WormBase]
D1025.4D1025.4nspc-20123 XReverseView as cDNA map |
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D1025.6D1025.6nspc-16123 XForwardView as cDNA map |
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D1025.7D1025.7nspc-18123 XReverseView as cDNA map |
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D1025.8D1025.8nspc-17123 XReverseView as cDNA map |
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D1025.9D1025.9nspc-19123 XForwardView as cDNA map |
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E03G2.2E03G2.2mrp-3123 XReverseView as cDNA map |
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F01E11.3F01E11.3F01E11.3123 XForwardView as cDNA map |
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F01E11.5F01E11.5ctyra-2123 XReverseView as cDNA map |
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F02C12.1F02C12.1F02C12.1123 XForwardView as cDNA map |
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F02D10.5F02D10.5flr-1123 XReverseView as cDNA map |
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flr-1 encodes an ion channel that belongs to the DEG/ENaC sodium channel superfamily. flr-1 activity is essential for normal defecation rhythm, growth rates, expulsion, and dauer larvae formation. a rescuing FLR-1::GFP reporter is expressed in the intestine from embryonic to adult stages where it localizes to the membranes facing the inner lumen as well as to part of the lateral membrane between intestinal cells. [Source: WormBase]
F02E8.4F02E8.4F02E8.4123 XForwardView as cDNA map |
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F02E8.6F02E8.6ncr-1123 XReverseView as cDNA map |
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ncr-1 encodes a large transmembrane glycoprotein with a patched-like domain that is orthologous to human NPC1 (OMIM:257220, mutated in Niemann-Pick type C disease). NCR-1 and NPC1 are eukaryotic members of the resistance-nodulation-division (RND) family of membrane permeases, and have a putative sterol-sensing domain. by homology, NCR-1 is predicted to function in intracellular cholesterol and glycolipid trafficking. in C. elegans, NCR-1 is required for growth and survival in the absence of cholesterol, newly hatched ncr-1 mutant larvae grow poorly on cholesterol-free medium and die at the L1 or L2 stage. NCR-1 is also involved in negative regulation of dauer formation, being required redundantly with NCR-2, a second C. elegans NPC1-like protein, for preventing constitutive dauer formation. dauer formation in ncr-1. ncr-2 double mutants is suppressed by mutations in daf-12, which encodes a steroid hormone receptor, and by overexpression of daf-9, which encodes a cytochrome P450, suggesting that NCR-1 and NCR-2 may function to transport a sterol precursor that is metabolized by DAF-9 to then serve as the DAF-12 ligand. [Source: WormBase]
F07G6.1F07G6.1dgn-3123 XForwardView as cDNA map |
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F08C6.6F08C6.6apy-1123 XReverseView as cDNA map |
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apy-1 encodes a membrane-bound UDP/GDPase (endo-apyrase) required for repression of the unfolded protein response of stressed endoplasmic reticulum (ER), for normally organized pharynx and thin muscle fibers in adults, and for normally high fertility, rapid growth, and long lifespan. APY-1 is orthologous to human CANT1 and paralogous to ZK563.7. apy-1 is transcriptionally activated by tunicamycin, 6% EtOH, or excess heat (25 deg. C.), each of which stresses the ER, and this activation requires both ATF-6 and IRE-1. APY-1 can hydrolyze either UDP or GDP, but has more activity with UDP. [Source: WormBase]
F08C6.7F08C6.7unc-98123 XReverseView as cDNA map |
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unc-98 encodes a protein with four C2H2 zinc fingers and several possible nuclear localization and export sequences. UNC-98 is required for normal mobility, M-line, and dense body (Z-disk analog) structures. UNC-98 binds the C-terminal portion of myosin heavy chain, as well as a number of proteins that localize to the base of dense bodies and M lines, including UNC-97/PINCH, suggesting that in vivo UNC-98 functions to link myosin thick filaments to an integrin-associated protein complex at the muscle cell membrane. UNC-98 also interacts with UNC-96, UNC-15/paramyosin, the unconventional myosin HUM-6 and the zinc-finger protein MEP-1. UNC-98 localizes to M-lines, muscle cell nuclei, and perhaps also to dense bodies. [Source: WormBase]
F09A5.1F09A5.1F09A5.1123 XForwardView as cDNA map |
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F10D7.2F10D7.2.1F10D7.2123 XReverseView as cDNA map |
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F10D7.2F10D7.2.2F10D7.2123 XReverseView as cDNA map |
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F11C1.3F11C1.3scav-4123 XForwardView as cDNA map |
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F11C1.6F11C1.6a.1nhr-25123 XForwardView as cDNA map |
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nhr-25 encodes a nuclear hormone receptor orthologous to Drosophila Ftz-F1. NHR-25 is required for embryogenesis, molting, vulval and gonadal development, and hypodermal expression of acn-1. nhr-25 is expressed in gonads and loaded into embryos as a maternal transcript. nhr-25 is zygotically expressed in progeny of the E cell, and then in hypodermis and gut. the role of NHR-25 in molting may be evolutionarily conserved between nematodes and arthopods. [Source: WormBase]
F11C7.6F11C7.6aF11C7.6123 XForwardView as cDNA map |
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F11C7.6F11C7.6bF11C7.6123 XForwardView as cDNA map |
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F13E6.3F13E6.3F13E6.3123 XForwardView as cDNA map |
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F13E6.6F13E6.6rhgf-1123 XReverseView as cDNA map |
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rhgf-1 encodes an RGS RhoGEF (Regulator of G-protein Signaling Rho Guanine Nucleotide Exchange Factor). RHGF-1 functions within cholingergic motor neurons in one of four G-protein-mediated signaling pathways that control locomotion via regulation of acetylcholine (ACh) release at neuromuscular junctions. in regulating ACh release, RHGF-1 functions downstream of the C. elegans Galpha12 ortholog, GPA-12, and upstream of the Rho GTPase ortholog, RHO-1. additionally, rhgf-1 activity is required for normal mechanosensory behavior, egg laying, and embryonic development. an rhgf-1 reporter fusion is expressed in ventral cord motor neurons as well as several head neurons. [Source: WormBase]
F16B12.2F16B12.2dsl-4123 XForwardView as cDNA map |
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dsl-4 encodes a putative secreted protein with a single DSL domain and three EGF domains in series, somewhat like Delta/LAG-2. unlike the nematode-specific family of Delta/LAG-2-like proteins (including DSL-1, -2, -3, -5, -6, and -7), DSL-4 is evolutionarily divergent, with perhaps a distant affinity to APX-1, ARG-1, and LAG-2. [Source: WormBase]
F16H11.3F16H11.3F16H11.3123 XReverseView as cDNA map |
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F17A2.8F17A2.8srd-44123 XForwardView as cDNA map |
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F18E9.5F18E9.5a.1tag-279123 XForwardView as cDNA map |
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F18E9.5 encodes, by alternative splicing, two isoforms of a histone H3 trimethyllysine-27 (H3K27me3) demethylase that is required for normal gonad migration and organization. F18E9.5 protein demethylates H3K27me3 in vitro. F18E9.5 contains an N-terminal TonB domain and a C-terminal JmjC domain, and is homologous to human JMJD3, UTX (OMIM:300128), and UTY (OMIM:400009). null F18E9.5(gk384) and F18E9.5(gk387) mutants have aberrant gonad migration and disordered diakinesis-phase oocytes, phenotypes enhanced at 25 deg. C.. F18E9.5 is expected to antagonize transcriptional repression by polycomb repressor complexes, which mark stem cells (and presumably germline) by H3K27me3-mediated repression of somatic genes. [Source: WormBase]
F18E9.5F18E9.5a.2tag-279123 XForwardView as cDNA map |
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F18E9.5 encodes, by alternative splicing, two isoforms of a histone H3 trimethyllysine-27 (H3K27me3) demethylase that is required for normal gonad migration and organization. F18E9.5 protein demethylates H3K27me3 in vitro. F18E9.5 contains an N-terminal TonB domain and a C-terminal JmjC domain, and is homologous to human JMJD3, UTX (OMIM:300128), and UTY (OMIM:400009). null F18E9.5(gk384) and F18E9.5(gk387) mutants have aberrant gonad migration and disordered diakinesis-phase oocytes, phenotypes enhanced at 25 deg. C.. F18E9.5 is expected to antagonize transcriptional repression by polycomb repressor complexes, which mark stem cells (and presumably germline) by H3K27me3-mediated repression of somatic genes. [Source: WormBase]
F18E9.5F18E9.5b.1tag-279123 XForwardView as cDNA map |
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F18E9.5 encodes, by alternative splicing, two isoforms of a histone H3 trimethyllysine-27 (H3K27me3) demethylase that is required for normal gonad migration and organization. F18E9.5 protein demethylates H3K27me3 in vitro. F18E9.5 contains an N-terminal TonB domain and a C-terminal JmjC domain, and is homologous to human JMJD3, UTX (OMIM:300128), and UTY (OMIM:400009). null F18E9.5(gk384) and F18E9.5(gk387) mutants have aberrant gonad migration and disordered diakinesis-phase oocytes, phenotypes enhanced at 25 deg. C.. F18E9.5 is expected to antagonize transcriptional repression by polycomb repressor complexes, which mark stem cells (and presumably germline) by H3K27me3-mediated repression of somatic genes. [Source: WormBase]
F18E9.5F18E9.5b.2tag-279123 XForwardView as cDNA map |
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F18E9.5 encodes, by alternative splicing, two isoforms of a histone H3 trimethyllysine-27 (H3K27me3) demethylase that is required for normal gonad migration and organization. F18E9.5 protein demethylates H3K27me3 in vitro. F18E9.5 contains an N-terminal TonB domain and a C-terminal JmjC domain, and is homologous to human JMJD3, UTX (OMIM:300128), and UTY (OMIM:400009). null F18E9.5(gk384) and F18E9.5(gk387) mutants have aberrant gonad migration and disordered diakinesis-phase oocytes, phenotypes enhanced at 25 deg. C.. F18E9.5 is expected to antagonize transcriptional repression by polycomb repressor complexes, which mark stem cells (and presumably germline) by H3K27me3-mediated repression of somatic genes. [Source: WormBase]
F18G5.3F18G5.3gpa-12123 XForwardView as cDNA map |
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gpa-12 encodes a member of the G protein alpha subunit family of heterotrimeric GTPases. it is expressed in the pharynx and in the hypodermis. [Source: WormBase]
F22F4.3F22F4.3aklp-13123 XForwardView as cDNA map |
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klp-13 encodes an atypical kinesin-like motor protein similar to Saccharomyces cerevisiae Kip3, which has been implicated in nuclear migration. as loss of KLP-13 function via RNA-mediated interference (RNAi) does not result in any abnormalities, the precise role of KLP-13 in C. elegans development and/or behavior is not yet known. [Source: WormBase]
F22H10.1F22H10.1F22H10.1123 XForwardView as cDNA map |
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F23D12.6F23D12.6fipr-3123 XForwardView as cDNA map |
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F27D9.7F27D9.7F27D9.7123 XReverseView as cDNA map |
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F29G6.1F29G6.1F29G6.1123 XForwardView as cDNA map |
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F29G6.3F29G6.3aF29G6.3123 XReverseView as cDNA map |
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F29G6.3F29G6.3b.1F29G6.3123 XReverseView as cDNA map |
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F29G6.3F29G6.3b.2F29G6.3123 XReverseView as cDNA map |
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F29G6.3F29G6.3c.1F29G6.3123 XReverseView as cDNA map |
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Ensembl
F29G6.3F29G6.3c.2F29G6.3123 XReverseView as cDNA map |
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F31F6.6F31F6.6nac-1123 XForwardView as cDNA map |
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nac-1 encodes a low-affinity sodium-coupled dicarboxylate transporter homologous to INDY in D. melanogaster and to mammalian NaDC1 and NaDC3. nac-1 has no obvious function in either mass or individual RNAi assays. nac-1 is expressed in the intestine, in larvae and adults. [Source: WormBase]
F34H10.4F34H10.4F34H10.4123 XForwardView as cDNA map |
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F35C8.1F35C8.1F35C8.1123 XForwardView as cDNA map |
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F35C8.3F35C8.3jkk-1123 XForwardView as cDNA map |
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jkk-1 encodes a member of the MAP kinase kinase superfamily that affects synaptic vesicle localization and is required in type-D motor neurons for normal locomotion. can function in the Hog1 MAP kinase pathway I in yeast as an activator of JNK and is expressed in most neurons [Source: WormBase]
F38E9.1F38E9.1F38E9.1123 XForwardView as cDNA map |
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F41C6.4F41C6.4aF41C6.4123 XReverseView as cDNA map |
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F41C6.4F41C6.4bF41C6.4123 XReverseView as cDNA map |
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Ensembl
F41D9.1F41D9.1tbc-18123 XForwardView as cDNA map |
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Ensembl
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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