| 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 |
|---|---|---|---|---|---|---|---|---|
| B0310.1 | B0310.1b | B0310.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | B0310.1 encodes a nematode-specific transmembrane protein. loss of B0310.1 activity via RNAi results in reduced fat content in wild-type and tub-1 mutant animals, suggesting that B0301.1 plays a role in lipid metabolism. [Source: WormBase] |
| B0310.3 | B0310.3 | B0310.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| B0395.3 | B0395.3.1 | B0395.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | B0395.3 is orthologous to the human gene CHOLINE ACETYLTRANSFERASE ISOFORM R (CHAT. OMIM:118490), which when mutated leads to disease. [Source: WormBase] |
| B0395.3 | B0395.3.2 | B0395.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | B0395.3 is orthologous to the human gene CHOLINE ACETYLTRANSFERASE ISOFORM R (CHAT. OMIM:118490), which when mutated leads to disease. [Source: WormBase] |
| B0416.4 | B0416.4 | B0416.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| B0563.4 | B0563.4.1 | tmbi-4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| B0563.4 | B0563.4.2 | tmbi-4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C02B4.1 | C02B4.1 | adt-1 | 3 | 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] |
| C02C6.1 | C02C6.1a | dyn-1 | 1 | 23 X | Forward | View 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] |
| C02C6.1 | C02C6.1b | dyn-1 | 1 | 23 X | Forward | View 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] |
| C02F12.7 | C02F12.7 | tag-278 | 3 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C02H7.1 | C02H7.1 | dyf-11 | 3 | 23 X | Forward | View 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] |
| C03B1.7 | C03B1.7 | C03B1.7 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C03F11.2 | C03F11.2 | C03F11.2 | 1 | 23 X | Reverse | 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] |
| C04B4.3 | C04B4.3 | lips-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C04E7.3 | C04E7.3 | C04E7.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C04F6.1 | C04F6.1 | vit-5 | 1 | 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] |
| 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 | |
| C05D9.9 | C05D9.9a | C05D9.9 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C05D9.9 | C05D9.9b | C05D9.9 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C05E11.4 | C05E11.4 | amt-1 | 1 | 23 X | Forward | View 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] |
| C05E7.3 | C05E7.3 | C05E7.3 | 1 | 23 X | Reverse | 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 | |
| C06E2.3 | C06E2.3 | ubc-21 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C06G1.5 | C06G1.5 | C06G1.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C07A12.3 | C07A12.3a | nhr-35 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C07A12.5 | C07A12.5a | spr-3 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C09G1.2 | C09G1.2 | C09G1.2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C09G1.4 | C09G1.4 | C09G1.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C10A4.8 | C10A4.8 | mnm-2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C10E2.2 | C10E2.2.1 | C10E2.2 | 1 | 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] |
| C11G10.2 | C11G10.2 | C11G10.2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C11G6.3 | C11G6.3 | C11G6.3 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | C11G6.3 encodes a plant homeodomain-containing protein that is related to the ING (Inhibitor of Growth) family of proteins that function in regulation of gene expression and are candidate tumor suppressors. [Source: WormBase] |
| C11H1.2 | C11H1.2 | C11H1.2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14A11.3 | C14A11.3b | cgef-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C14A11.5 | C14A11.5 | C14A11.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14A11.7 | C14A11.7 | ssr-2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14F11.4 | C14F11.4a | C14F11.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14F11.4 | C14F11.4b | C14F11.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14H10.3 | C14H10.3a | C14H10.3 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14H10.3 | C14H10.3b.1 | C14H10.3 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14H10.3 | C14H10.3b.2 | C14H10.3 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C14H10.4 | C14H10.4 | str-74 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C15B12.6 | C15B12.6 | C15B12.6 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| 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] |
| C16B8.1 | C16B8.1.1 | lin-18 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | lin-18 encodes a predicted receptor tyrosine kinase that is a member of the Ryk/Derailed family of tyrosine kinase-related receptors (OMIM:600524, mutations in humans are associated with cleft palate). in C. elegans, LIN-18 is required for establishing the polarity of the secondary vulval cell lineage produced by the P7.p vulval precursor cell. LIN-18 may be a receptor for Wnt-like signaling molecules, and in vulval development appears to function independently of, but in parallel with, LIN-17, a Frizzled-like Wnt receptor, also required for proper orientation of the P7.p lineage. a lin-18 reporter gene is expressed in body wall muscle, neurons, and the developing vulva. in the vulva, expression is detected in P5.p, P6.p, and P7.p and all of their descendants during the L3 and L4 larval stages. [Source: WormBase] |
| C16B8.1 | C16B8.1.2 | lin-18 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | lin-18 encodes a predicted receptor tyrosine kinase that is a member of the Ryk/Derailed family of tyrosine kinase-related receptors (OMIM:600524, mutations in humans are associated with cleft palate). in C. elegans, LIN-18 is required for establishing the polarity of the secondary vulval cell lineage produced by the P7.p vulval precursor cell. LIN-18 may be a receptor for Wnt-like signaling molecules, and in vulval development appears to function independently of, but in parallel with, LIN-17, a Frizzled-like Wnt receptor, also required for proper orientation of the P7.p lineage. a lin-18 reporter gene is expressed in body wall muscle, neurons, and the developing vulva. in the vulva, expression is detected in P5.p, P6.p, and P7.p and all of their descendants during the L3 and L4 larval stages. [Source: WormBase] |
| C16E9.1 | C16E9.1 | C16E9.1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C16H3.3 | C16H3.3a | C16H3.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C16H3.3 | C16H3.3b | C16H3.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C17G1.2 | C17G1.2 | C17G1.2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C17G1.3 | C17G1.3a | ugt-23 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C17G1.3 | C17G1.3b.1 | ugt-23 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C17G1.3 | C17G1.3b.2 | ugt-23 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C17G1.7 | C17G1.7.1 | C17G1.7 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C18B12.3 | C18B12.3 | dsc-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C18B12.6 | C18B12.6 | C18B12.6 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C23F12.1 | C23F12.1a | fln-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C23F12.1 | C23F12.1b | fln-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C23H4.1 | C23H4.1.1 | cab-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | Novel protein which has a C-terminal motif weakly homologous to mouse NPDC-1 and is involved in synaptic regulation. it is expressed in various neurons including ventral cord and tail ganglion neurons. it physically interacts with AEX-3, which is a guanine nucleotide exchange factor for the Rab3 GTPase. [Source: WormBase] |
| C23H4.1 | C23H4.1.2 | cab-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | Novel protein which has a C-terminal motif weakly homologous to mouse NPDC-1 and is involved in synaptic regulation. it is expressed in various neurons including ventral cord and tail ganglion neurons. it physically interacts with AEX-3, which is a guanine nucleotide exchange factor for the Rab3 GTPase. [Source: WormBase] |
| C23H4.1 | C23H4.1.3 | cab-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | Novel protein which has a C-terminal motif weakly homologous to mouse NPDC-1 and is involved in synaptic regulation. it is expressed in various neurons including ventral cord and tail ganglion neurons. it physically interacts with AEX-3, which is a guanine nucleotide exchange factor for the Rab3 GTPase. [Source: WormBase] |
| C23H4.1 | C23H4.1.4 | cab-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | Novel protein which has a C-terminal motif weakly homologous to mouse NPDC-1 and is involved in synaptic regulation. it is expressed in various neurons including ventral cord and tail ganglion neurons. it physically interacts with AEX-3, which is a guanine nucleotide exchange factor for the Rab3 GTPase. [Source: WormBase] |
| C23H4.1 | C23H4.1.5 | cab-1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | Novel protein which has a C-terminal motif weakly homologous to mouse NPDC-1 and is involved in synaptic regulation. it is expressed in various neurons including ventral cord and tail ganglion neurons. it physically interacts with AEX-3, which is a guanine nucleotide exchange factor for the Rab3 GTPase. [Source: WormBase] |
| C23H4.7 | C23H4.7 | C23H4.7 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C23H4.8 | C23H4.8 | C23H4.8 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C24A8.4 | C24A8.4 | cst-2 | 2 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C25F6.2 | C25F6.2b.1 | dlg-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | dlg-1 encodes a MAGUK protein, orthologous to Drosophila disks large, that is physically located to adherens junctions in all epithelia and that is genetically required for organization of the embryonic gut epithelium into an coherent tube. [Source: WormBase] |
| C25G6.3 | C25G6.3 | C25G6.3 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C26B9.6 | C26B9.6 | C26B9.6 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C26G2.1 | C26G2.1 | syg-2 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | syg-2 encodes a transmembrane protein that is a member of the immunoglobulin superfamily of proteins. during larval development, SYG-2 activity is required in vulval epithelial cells for proper synaptic specificity of the HSNL neuron. in regulating synapse formation, SYG-2 acts as a guidepost protein for the SYG-1 receptor that interacts with SYG-2 and acts within HSNL to regulate synaptic specificity. a SYG-2::GFP fusion protein is expressed in the primary vulval cell lineages beginning at the L3 larval stage, with expression increasing during the L4 stage and finally disappearing by adulthood. in embryos, SYG-2::GFP expression is detected in some head neurons and body wall muscles, the latter of which also express the reporter during the L1 and L2 larval stages. [Source: WormBase] |
| C29F7.5 | C29F7.5 | fkh-4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | fkh-4 encodes a member of the forkhead domain transcription factor family. [Source: WormBase] |
| C30F2.2 | C30F2.2 | C30F2.2 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C30G4.7 | C30G4.7 | C30G4.7 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C31E10.5 | C31E10.5 | C31E10.5 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C31E10.8 | C31E10.8 | tbc-19 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C31H2.2 | C31H2.2 | dpy-8 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | dpy-8 encodes a collagen with a nematode-specific N-terminal domain that is required for normal body morphology and (perhaps) for a normal embryonic cell division rate. dpy-8 interacts genetically with emb-5 and glp-1. [Source: WormBase] |
| C31H2.4 | C31H2.4 | C31H2.4 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | C31H2.4 encodes a possible 4-hydroxyphenylpyruvate dioxygenase, orthologous to human HPDL/GLOXD1, and paralogous to HPD-1 and human HPD (OMIM:609695, mutated in tyrosinemia type III). C31H2.4 has no obvious function in mass RNAi experiments. [Source: WormBase] |
| C33D12.3 | C33D12.3 | twk-26 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C33D3.4 | C33D3.4 | C33D3.4 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C33E10.5 | C33E10.5 | C33E10.5 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C33E10.8 | C33E10.8 | C33E10.8 | 1 | 23 X | Reverse | 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] |
| C33G3.1 | C33G3.1b.1 | dyc-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | dyc-1 encodes a homolog of murine CAPON, a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95. DYC-1 is expressed in muscle, and is required for a dystrophin-related function in muscle. [Source: WormBase] |
| C33G3.1 | C33G3.1b.2 | dyc-1 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | dyc-1 encodes a homolog of murine CAPON, a protein associated with neuronal nitric oxide synthase that regulates its interactions with PSD95. DYC-1 is expressed in muscle, and is required for a dystrophin-related function in muscle. [Source: WormBase] |
| C34E11.3 | C34E11.3a | tag-241 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34E11.3 | C34E11.3b | tag-241 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34E11.3 | C34E11.3c | tag-241 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34E11.3 | C34E11.3d | tag-241 | 2 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.10 | C34F6.10 | C34F6.10 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.1 | C34F6.1 | C34F6.1 | 1 | 23 X | Reverse | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.2 | C34F6.2 | col-178 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.3 | C34F6.3 | col-179 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.8 | C34F6.8.1 | idh-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.8 | C34F6.8.2 | idh-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C34F6.8 | C34F6.8.3 | idh-2 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl | |
| C35B8.3 | C35B8.3b | C35B8.3 | 1 | 23 X | Forward | View as cDNA map | View as Table | Internal | Ensembl |