| 1343189 | NDP | norrin cystine knot growth factor NDP | This gene encodes a secreted protein with a cystein-knot motif that activates the Wnt/beta-catenin pathway. The protein forms disulfide-linked oligomers in the extracellular matrix. Mutations in this gene result in Norrie disease and X-linked exudative vitreoretinopathy. [provided by RefSeq, Feb 200 9] | X | 43948776 | 43973390 | Human | 316 | symbol , old_gene_name , COSMIC , name , Human Proteome Map | gene, protein-coding, REVIEWED [RefSeq] |
| 1558298 | Ndp | Norrie disease (pseudoglioma) (human) | This gene encodes a secreted protein that acts a ligand for multiple different receptors and participates in both Wnt and Wnt-independant signalling. Its activity is important in vascular development of the eye and inner ear. Mutation of the related gene in humans causes Norrie syndrome. [provided b y RefSeq, May 2015] | X | 16751760 | 16778013 | Mouse | 210 | symbol , PhenoGen , old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1563968 | Ndp | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (ortholog); frizzled binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN decidualization; action potential (ortholog); angiogenesis (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitr eoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (ortholog); extracellular space (ortholog); INTERACTS WITH acrylamide; bisphenol A; vinclozolin | X | 8379569 | 8404019 | Rat | 170 | symbol , old_gene_name , PhenoGen , name , old_gene_symbol | gene, protein-coding, PROVISIONAL [RefSeq] |
| 8961118 | Ndp | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (ortholog); frizzled binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (ortholog); extracellular space (ortholog) | NW_004955516 | 4218703 | 4244774 | Chinchilla | 92 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 11670174 | NDP | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (inferred); frizzled binding (inferred); protein homodimerization activity (inferred); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (inferred); extracellular region (inferred); extracellular space (inferred) | X | 36399868 | 36424953 | Bonobo | 100 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 12246377 | NDP | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (ortholog); frizzled binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (ortholog); extracellular space (ortholog) | X | 37949560 | 37975573 | Dog | 92 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 12477793 | Ndp | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (inferred); frizzled binding (inferred); protein homodimerization activity (inferred); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (inferred); extracellular region (inferred); extracellular space (inferred) | NW_004936502 | 10080169 | 10105155 | Squirrel | 100 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 13845440 | NDP | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (inferred); frizzled binding (inferred); protein homodimerization activity (inferred); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (inferred); extracellular region (inferred); extracellular space (inferred) | | | | Pig | 100 | symbol , old_gene_name , name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 18468222 | NDP | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (inferred); frizzled binding (inferred); protein homodimerization activity (inferred); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (inferred); extracellular region (inferred); extracellular space (inferred) | | | | Green Monkey | 100 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 18923007 | Ndp | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (inferred); frizzled binding (inferred); protein homodimerization activity (inferred); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (inferred); extracellular region (inferred); extracellular space (inferred) | | | | Naked Mole-Rat | 100 | symbol , old_gene_name , name | gene, protein-coding, MODEL [RefSeq] |
| 284664818 | ndp | | | | | | Tropical Clawed Frog | | symbol | gene, null |
| 625964329 | Ndp | norrin cystine knot growth factor NDP | ENCODES a protein that exhibits cytokine activity (ortholog); frizzled binding (ortholog); protein homodimerization activity (ortholog); INVOLVED IN action potential (ortholog); angiogenesis (ortholog); blood vessel remodeling (ortholog); PARTICIPATES IN Wnt signaling, canonical pathway; ASSOCIATED WITH exudative vitreoretinopathy (ortholog); Hereditary Eye Diseases (ortholog); macular retinal edema (ortholog); FOUND IN cell surface (ortholog); extracellular space (ortholog) | | | | Black Rat | 92 | symbol , name | gene, protein-coding, MODEL [RefSeq] |
| 284665340 | ndp.L | | | | | | African Clawed Frog | | symbol | gene, null |
| 288083495 | ndp.S | | | | | | African Clawed Frog | | symbol | gene, null |
| 6481394 | NDP-AS1 | NDP antisense RNA 1 | | X | 43949732 | 43971552 | Human | | symbol , COSMIC , name , Human Proteome Map | gene, ncrna, VALIDATED [RefSeq] |
| 1623116 | Calcoco2 | calcium binding and coiled-coil domain 2 | Predicted to enable protein homodimerization activity. Predicted to be involved in positive regulation of autophagosome maturation; response to type II interferon; and xenophagy. Predicted to be located in cytosol; intracellular membrane-bounded organelle; and perinuclear region of cytoplasm. Predic ted to be active in PML body and autophagosome. Orthologous to human CALCOCO2 (calcium binding and coiled-coil domain 2). [provided by Alliance of Genome Resources, Apr 2025] | 11 | 95990195 | 96015362 | Mouse | 85 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 735394 | Nme1 | NME/NM23 nucleoside diphosphate kinase 1 | Predicted to enable several functions, including DNA binding activity; nuclease activity; and purine ribonucleoside triphosphate binding activity. Acts upstream of or within lactation. Located in mitochondrion and myelin sheath. Is expressed in several structures, including alimentary system; brain; genitourinary system; integumental system; and sensory organ. Human ortholog(s) of this gene implicated in neuroblastoma; ovary epithelial cancer; and teratoma. Orthologous to human NME1 (NME/NM23 nucleoside diphosphate kinase 1). [provided by Alliance of Genome Resources, Apr 2025] | 11 | 93849751 | 93859341 | Mouse | 406 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 70497 | Nme1 | NME/NM23 nucleoside diphosphate kinase 1 | ENCODES a protein that exhibits enzyme binding; farnesyl diphosphate kinase activity; gamma-tubulin binding; INVOLVED IN cellular response to fatty acid; cellular response to glucose stimulus; cellular response to xenobiotic stimulus; PARTICIPATES IN adefovir pharmacokinetics pathway; de novo pyrimi dine biosynthetic pathway; E-cadherin signaling pathway; ASSOCIATED WITH Cardiomegaly; breast cancer (ortholog); breast carcinoma (ortholog); FOUND IN centrosome; intermediate filament; mitochondrial outer membrane; INTERACTS WITH 1,2,4-trimethylbenzene; 17alpha-ethynylestradiol; 17beta-estradiol | 10 | 79403939 | 79426620 | Rat | 351 | old_gene_name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 735393 | NME1 | NME/NM23 nucleoside diphosphate kinase 1 | This gene (NME1) was identified because of its reduced mRNA transcript levels in highly metastatic cells. Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by this gene) and 'B' (encoded by NME2) isoforms. Mutations in this gene have been identified in aggressive neuro blastomas. Two transcript variants encoding different isoforms have been found for this gene. Co-transcription of this gene and the neighboring downstream gene (NME2) generates naturally-occurring transcripts (NME1-NME2), which encodes a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Jul 2008] | 17 | 51153559 | 51162168 | Human | 356 | old_gene_name , old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 12394063 | NME1 | non-metastatic cells 1, protein (NM23A) expressed in | ENCODES a protein that exhibits 3'-5'-DNA exonuclease activity (ortholog); acetyl-CoA binding (ortholog); ADP binding (ortholog); INVOLVED IN acetyl-CoA catabolic process (ortholog); apoptotic DNA fragmentation (ortholog); cellular response to fatty acid (ortholog); PARTICIPATES IN adefovir pharmaco kinetics pathway; de novo pyrimidine biosynthetic pathway; E-cadherin signaling pathway; ASSOCIATED WITH breast cancer (ortholog); breast carcinoma (ortholog); Cardiomegaly (ortholog); FOUND IN centrosome (ortholog); cytoplasm (ortholog); cytosol (ortholog) | 9 | 26990336 | 26998895 | Dog | 134 | old_gene_name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1642401 | NME1-NME2 | NME1-NME2 readthrough | This locus represents naturally occurring read-through transcription between the neighboring NME1 and NME2 genes. The significance of this read-through transcription and the function of the resulting protein product have not yet been determined. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2010] | 17 | 51153559 | 51171744 | Human | 35 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 619877 | Nme2 | NME/NM23 nucleoside diphosphate kinase 2 | ENCODES a protein that exhibits enzyme binding; fatty acid binding; heterocyclic compound binding; INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway; cellular response to fatty acid; cellular response to glucose stimulus; PARTICIPATES IN adefovir pharmacokinetics pathway; de novo pyrimidine biosynthetic pathway; Glut1 deficiency syndrome pathway; ASSOCIATED WITH decreased metastatic potential; ASSOCIATED WITH Neoplasm Metastasis; arteriosclerosis (ortholog); Chemical and Drug Induced Liver Injury (ortholog); FOUND IN intermediate filament; mitochondrial membrane; perinuclear region of cytoplasm; INTERACTS WITH 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine; 4,4'-sulfonyldiphenol | 10 | 79394999 | 79400418 | Rat | 259 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1346564 | NME2 | NME/NM23 nucleoside diphosphate kinase 2 | Nucleoside diphosphate kinase (NDK) exists as a hexamer composed of 'A' (encoded by NME1) and 'B' (encoded by this gene) isoforms. Multiple alternatively spliced transcript variants have been found for this gene. Read-through transcription from the neighboring upstream gene (NME1) generates naturall y-occurring transcripts (NME1-NME2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product. [provided by RefSeq, Nov 2010] | 17 | 51165536 | 51171744 | Human | 254 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1552274 | Nme2 | NME/NM23 nucleoside diphosphate kinase 2 | Predicted to enable several functions, including anion binding activity; kinase activity; and transcription coactivator activity. Predicted to be involved in several processes, including integrin-mediated signaling pathway; negative regulation of myeloid leukocyte differentiation; and ribonucleoside triphosphate biosynthetic process. Located in mitochondrion and myelin sheath. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; integumental system; and sensory organ. Human ortholog(s) of this gene implicated in teratoma. Orthologous to several human genes including NME2 (NME/NM23 nucleoside diphosphate kinase 2). [provided by Alliance of Genome Resources, Apr 2025] | 11 | 93840640 | 93847082 | Mouse | 285 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 12238112 | NME2 | non-metastatic cells 2, protein (NM23B) expressed in | ENCODES a protein that exhibits coenzyme A binding (ortholog); DNA binding (ortholog); DNA-binding transcription activator activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); cellular response to fatty acid (ortholog); cellular respo nse to glucose stimulus (ortholog); PARTICIPATES IN adefovir pharmacokinetics pathway; de novo pyrimidine biosynthetic pathway; Glut1 deficiency syndrome pathway; ASSOCIATED WITH arteriosclerosis (ortholog); Chemical and Drug Induced Liver Injury (ortholog); Colorectal Neoplasms (ortholog); FOUND IN cell periphery (ortholog); cytoplasm (ortholog); cytosol (ortholog) | 9 | 27002114 | 27005740 | Dog | 108 | old_gene_name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 14067043 | NME2 | NME/NM23 nucleoside diphosphate kinase 2 | ENCODES a protein that exhibits coenzyme A binding (ortholog); DNA binding (ortholog); DNA-binding transcription activator activity (ortholog); INVOLVED IN adenylate cyclase-activating G protein-coupled receptor signaling pathway (ortholog); cellular response to fatty acid (ortholog); cellular respo nse to glucose stimulus (ortholog); PARTICIPATES IN adefovir pharmacokinetics pathway; de novo pyrimidine biosynthetic pathway; Glut1 deficiency syndrome pathway; ASSOCIATED WITH arteriosclerosis (ortholog); Chemical and Drug Induced Liver Injury (ortholog); Colorectal Neoplasms (ortholog); FOUND IN cell periphery (ortholog); cytoplasm (ortholog); cytosol (ortholog) | | | | Pig | 108 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 733554 | NME3 | NME/NM23 nucleoside diphosphate kinase 3 | Enables nucleoside diphosphate kinase activity. Involved in DNA repair; mitochondrial fusion; and nucleoside triphosphate biosynthetic process. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Jul 2025] | 16 | 1770320 | 1771543 | Human | 148 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1551685 | Nme3 | NME/NM23 nucleoside diphosphate kinase 3 | Enables nucleoside diphosphate kinase activity. Predicted to be involved in DNA repair; mitochondrial fusion; and nucleoside triphosphate biosynthetic process. Located in ciliary basal body. Is expressed in several structures, including gut; hemolymphoid system gland; nervous system; respiratory sys tem; and sensory organ. Orthologous to human NME3 (NME/NM23 nucleoside diphosphate kinase 3). [provided by Alliance of Genome Resources, Apr 2025] | 17 | 25115474 | 25116505 | Mouse | 170 | old_gene_name , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 1318408 | NME4 | NME/NM23 nucleoside diphosphate kinase 4 | The nucleoside diphosphate (NDP) kinases (EC 2.7.4.6) are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates. The enzymes are products of the nm23 gene family, which includes NME4 (Milon et al., 1997 [PubMed 9099850]).[supplied by OMIM, May 2008] | 16 | 396729 | 400754 | Human | 150 | old_gene_name , description , old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 61896 | Nme6 | NME/NM23 nucleoside diphosphate kinase 6 | ENCODES a protein that exhibits nucleoside diphosphate kinase activity (ortholog); INVOLVED IN negative regulation of cell growth (ortholog); negative regulation of mitotic nuclear division (ortholog); nucleotide metabolic process (ortholog); PARTICIPATES IN adenine phoshoribosyltransferase deficien cy pathway; adenosine monophosphate deaminase deficiency pathway; adenylosuccinate lyase deficiency pathway; FOUND IN mitochondrial inner membrane (ortholog); mitochondrial matrix (ortholog); mitochondrion (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; 4-amino-2,6-dinitrotoluene | 8 | 118708092 | 118717756 | Rat | 112 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 62189 | Nme6 | NME/NM23 nucleoside diphosphate kinase 6 | Predicted to enable nucleoside diphosphate kinase activity. Predicted to be involved in negative regulation of cell growth and negative regulation of mitotic nuclear division. Located in mitochondrion. Is expressed in several structures, including alimentary system; genitourinary system; hemolymphoi d system; nervous system; and sensory organ. Orthologous to human NME6 (NME/NM23 nucleoside diphosphate kinase 6). [provided by Alliance of Genome Resources, Apr 2025] | 9 | 109661830 | 109672042 | Mouse | 121 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1604057 | NME6 | NME/NM23 nucleoside diphosphate kinase 6 | Nucleoside diphosphate (NDP) kinases (EC 2.7.4.6), such as NME6, are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates (Mehus et al., 1999 [PubMed 1045 3732]).[supplied by OMIM, Jul 2010] | 3 | 48287640 | 48301367 | Human | 113 | old_gene_name , description | gene, protein-coding, VALIDATED [RefSeq] |
| 619880 | Nme7 | NME/NM23 family member 7 | ENCODES a protein that exhibits 3'-5'-DNA exonuclease activity (ortholog); nucleoside diphosphate kinase activity (ortholog); protein kinase activity (ortholog); INVOLVED IN brain development (ortholog); cellular response to leukemia inhibitory factor (ortholog); cilium assembly (ortholog); PARTICIP ATES IN purine metabolic pathway; pyrimidine metabolic pathway; ASSOCIATED WITH COVID-19 (ortholog); gastrointestinal stromal tumor (ortholog); hydrocephalus (ortholog); FOUND IN axonemal A tubule inner sheath (ortholog); axonemal microtubule (ortholog); centrosome (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; 2,4-dinitrotoluene; 2,6-dinitrotoluene | 13 | 79190462 | 79319890 | Rat | 191 | old_gene_name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 733959 | NME7 | NME/NM23 family member 7 | This gene encodes a member of the non-metastatic expressed family of nucleoside diphosphate kinases. Members of this family are enzymes that catalyzes phosphate transfer from nucleoside triphosphates to nucleoside diphosphates. This protein contains two kinase domains, one of which is involved in au tophosphorylation and the other may be inactive. This protein localizes to the centrosome and functions as a component of the gamma-tubulin ring complex which plays a role in microtubule organization. Mutations in this gene may be associated with venous thromboembolism. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016] | 1 | 169132531 | 169367797 | Human | 157 | old_gene_name | gene, protein-coding, REVIEWED [RefSeq] |
| 733960 | Nme7 | NME/NM23 family member 7 | Predicted to enable 3'-5' exonuclease activity and protein kinase activity. Involved in flagellated sperm motility. Acts upstream of or within several processes, including cellular response to leukemia inhibitory factor; epithelial cilium movement involved in extracellular fluid movement; and intrac iliary transport. Located in axonemal microtubule; centrosome; and ciliary basal body. Is active in axonemal A tubule inner sheath and sperm flagellum. Is expressed in several structures, including alimentary system; genitourinary system; nervous system; respiratory system; and sensory organ. Used to study hydrocephalus. Orthologous to human NME7 (NME/NM23 family member 7). [provided by Alliance of Genome Resources, Apr 2025] | 1 | 164135091 | 164264870 | Mouse | 176 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1343010 | NME5 | NME/NM23 family member 5 | Enables 3'-5' exonuclease activity. Involved in spermatid development. Predicted to be located in 9+2 motile cilium. Predicted to be part of radial spoke. Predicted to be active in cilium. Implicated in primary ciliary dyskinesia. [provided by Alliance of Genome Resources, Jul 2025] | 5 | 138115175 | 138139428 | Human | 148 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1623132 | Nme5 | NME/NM23 family member 5 | Predicted to enable 3'-5' exonuclease activity. Involved in spermatid development. Acts upstream of or within several processes, including epithelial cilium movement involved in extracellular fluid movement; negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway; and v entricular system development. Located in sperm flagellum. Part of radial spoke. Is expressed in lung epithelium; nasal cavity respiratory epithelium; and nasopharynx epithelium. Used to study hydrocephalus. Human ortholog(s) of this gene implicated in primary ciliary dyskinesia. Orthologous to human NME5 (NME/NM23 family member 5). [provided by Alliance of Genome Resources, Apr 2025] | 18 | 34695687 | 34712168 | Mouse | 112 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1318409 | Nme4 | NME/NM23 nucleoside diphosphate kinase 4 | Predicted to enable cardiolipin binding activity and nucleoside diphosphate kinase activity. Predicted to be involved in lipid transport. Located in mitochondrion. Is expressed in several structures, including brain; genitourinary system; gut; immune system; and trigeminal ganglion. Orthologous to h uman NME4 (NME/NM23 nucleoside diphosphate kinase 4). [provided by Alliance of Genome Resources, Apr 2025] | 17 | 26310708 | 26314650 | Mouse | 163 | old_gene_name , old_gene_symbol | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1594734 | Nme2-ps1 | NME/NM23 nucleoside diphosphate kinase 2, pseudogene 1 | INTERACTS WITH ammonium chloride | 20 | 11178950 | 11179551 | Rat | 1 | old_gene_name | gene, pseudo, INFERRED [RefSeq] |
| 1595422 | Nme2-ps7 | NME/NM23 nucleoside diphosphate kinase 2, pseudogene 7 | | 2 | 35204942 | 35207505 | Rat | | old_gene_name | gene, pseudo, MODEL [RefSeq] |
| 1565403 | Nme2-ps8 | NME/NM23 nucleoside diphosphate kinase 2, pseudogene 8 | INTERACTS WITH methoxychlor | 8 | 108002561 | 108003149 | Rat | 1 | old_gene_name | gene, pseudo, MODEL [RefSeq] |
| 1583004 | Nme5 | NME/NM23 family member 5 | ENCODES a protein that exhibits 3'-5'-DNA exonuclease activity (ortholog); nucleoside diphosphate kinase activity (ortholog); INVOLVED IN cilium assembly (ortholog); DNA catabolic process (ortholog); epithelial cilium movement involved in extracellular fluid movement (ortholog); ASSOCIATED WITH Here ditary Neoplastic Syndromes (ortholog); hydrocephalus (ortholog); Primary Ciliary Dyskinesia 48 (ortholog); FOUND IN 9+2 motile cilium (ortholog); radial spoke (ortholog); sperm flagellum (ortholog); INTERACTS WITH 2,3,7,8-tetrachlorodibenzodioxine; bisphenol A; cadmium dichloride | 18 | 26437705 | 26454828 | Rat | 77 | old_gene_name | gene, protein-coding, VALIDATED [RefSeq] |
| 1591334 | Nme4 | NME/NM23 nucleoside diphosphate kinase 4 | ENCODES a protein that exhibits GTPase binding; protein-containing complex binding; cardiolipin binding (ortholog); INVOLVED IN intermembrane phospholipid transfer (ortholog); lipid transport (ortholog); protein hexamerization (ortholog); PARTICIPATES IN cardiolipin metabolic pathway; de novo pyrimi dine biosynthetic pathway; purine metabolic pathway; FOUND IN mitochondrial inner membrane (ortholog); mitochondrial intermembrane space (ortholog); mitochondrial matrix (ortholog); INTERACTS WITH 1-naphthyl isothiocyanate; 17alpha-ethynylestradiol; 2,3,7,8-tetrachlorodibenzodioxine | 10 | 15619106 | 15622961 | Rat | 144 | old_gene_name | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1351599 | CARD8 | caspase recruitment domain family member 8 | The protein encoded by this gene belongs to the caspase recruitment domain (CARD)-containing family of proteins, which are involved in pathways leading to activation of caspases or nuclear factor kappa-B (NFKB). This protein may be a component of the inflammasome, a protein complex that plays a role in the activation of proinflammatory caspases. It is thought that this protein acts as an adaptor molecule that negatively regulates NFKB activation, CASP1-dependent IL1B secretion, and apoptosis. Polymorphisms in this gene may be associated with a susceptibility to rheumatoid arthritis. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010] | 19 | 48203148 | 48255946 | Human | 112 | old_gene_name , old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1601886 | CALCOCO2 | calcium binding and coiled-coil domain 2 | This gene encodes a coiled-coil domain-containing protein. The encoded protein functions as a receptor for ubiquitin-coated bacteria and plays an important role in innate immunity by mediating macroautophagy. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012] | 17 | 48831035 | 48865245 | Human | 87 | old_gene_name , old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1316988 | ENAH | ENAH actin regulator | This gene encodes a member of the enabled/ vasodilator-stimulated phosphoprotein. Members of this gene family are involved in actin-based motility. This protein is involved in regulating the assembly of actin filaments and modulates cell adhesion and motility. Alternate splice variants of this gene have been correlated with tumor invasiveness in certain tissues and these variants may serve as prognostic markers. A pseudogene of this gene is found on chromosome 3. [provided by RefSeq, Sep 2016] | 1 | 225486829 | 225653878 | Human | 144 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1332566 | Enah | ENAH actin regulator | Enables SH3 domain binding activity and profilin binding activity. Involved in actin filament organization and actin polymerization-dependent cell motility. Acts upstream of or within actin polymerization or depolymerization; cellular response to leukemia inhibitory factor; and nervous system develo pment. Located in several cellular components, including focal adhesion; lamellipodium; and stress fiber. Is expressed in several structures, including brain; early embryo; embryo ectoderm; gonad; and limb bud. Human ortholog(s) of this gene implicated in stomach cancer. Orthologous to human ENAH (ENAH actin regulator). [provided by Alliance of Genome Resources, Jul 2025] | 1 | 181723949 | 181848132 | Mouse | 182 | old_gene_symbol | gene, protein-coding, VALIDATED [RefSeq] |
| 731754 | GABBR2 | gamma-aminobutyric acid type B receptor subunit 2 | The multi-pass membrane protein encoded by this gene belongs to the G-protein coupled receptor 3 family and GABA-B receptor subfamily. The GABA-B receptors inhibit neuronal activity through G protein-coupled second-messenger systems, which regulate the release of neurotransmitters, and the activity of ion channels and adenylyl cyclase. This receptor subunit forms an active heterodimeric complex with GABA-B receptor subunit 1, neither of which is effective on its own. Allelic variants of this gene have been associated with nicotine dependence.[provided by RefSeq, Jan 2010] | 9 | 98288109 | 98708935 | Human | 1189 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |
| 1352693 | SLC9A6 | solute carrier family 9 member A6 | This gene encodes a sodium-hydrogen exchanger that is amember of the solute carrier family 9. The encoded protein localizes to early and recycling endosomes and may be involved in regulating endosomal pH and volume. Defects in this gene are associated with X-linked syndromic cognitive disability, Ch ristianson type. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Apr 2010] | X | 135973837 | 136047269 | Human | 300 | old_gene_symbol | gene, protein-coding, REVIEWED [RefSeq] |