| 731668 | Caly | calcyon neuron-specific vesicular protein | Predicted to enable clathrin light chain binding activity. Involved in postsynaptic neurotransmitter receptor internalization. Is active in glutamatergic synapse. Is expressed in central nervous system; sensory organ; and skeleton. Human ortholog(s) of this gene implicated in attention deficit hyper activity disorder. Orthologous to human CALY (calcyon neuron specific vesicular protein). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 139649793 | 139662485 | Mouse | 109 | symbol , PhenoGen , description | gene, protein-coding, VALIDATED [RefSeq] |
| 1618841 | Aak1 | AP2 associated kinase 1 | Predicted to enable AP-2 adaptor complex binding activity; Notch binding activity; and protein serine/threonine kinase activity. Involved in presynaptic endocytosis. Predicted to be located in several cellular components, including clathrin-coated pit; clathrin-coated vesicle; and terminal bouton. P redicted to be part of clathrin complex. Predicted to be active in calyx of Held. Is expressed in cranial ganglion; dorsal root ganglion; retina nuclear layer; and telencephalon. Orthologous to human AAK1 (AP2 associated kinase 1). [provided by Alliance of Genome Resources, Jul 2025] | 6 | 86826252 | 86980209 | Mouse | 182 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1550394 | Abhd14b | abhydrolase domain containing 14b | Predicted to enable hydrolase activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to be located in cytosol; nucleolus; and nucleoplasm. Predicted to be active in cytoplasm. Is expressed in epidermis; nose; and renal caly '>calyx. Orthologous to human ABHD14B (abhydrolase domain containing 14B). [provided by Alliance of Genome Resources, Jul 2025] | 9 | 106324936 | 106330122 | Mouse | 117 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1557933 | C1s1 | complement component 1, s subcomponent 1 | Predicted to enable identical protein binding activity and serine-type endopeptidase activity. Predicted to be involved in complement activation, classical pathway; innate immune response; and proteolysis. Predicted to be located in extracellular region. Predicted to be active in extracellular space . Is expressed in chondrocranium; liver lobe; renal calyx; and urogenital ridge. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome periodontal type 2. Orthologous to human C1S (complement C1s). [provided by Alliance of Genome Resources, Apr 2025] | 6 | 124507303 | 124519340 | Mouse | 280 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 10258 | C4bp | complement component 4 binding protein | Predicted to be involved in several processes, including negative regulation of complement activation, classical pathway; regulation of opsonization; and response to symbiotic bacterium. Predicted to be located in extracellular region. Predicted to be active in extracellular space and plasma membran e. Is expressed in foregut-midgut junction; midgut; midgut loop; renal calyx; and renal pelvis. Human ortholog(s) of this gene implicated in COVID-19. Orthologous to human C4BPA (complement component 4 binding protein alpha). [provided by Alliance of Genome Resources, Jul 2025] | 1 | 130562510 | 130589365 | Mouse | 70 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 10278 | Calm2 | calmodulin 2 | Enables calcium-dependent protein binding activity. Involved in negative regulation of calcium ion export across plasma membrane; negative regulation of calcium ion transmembrane transporter activity; and presynaptic endocytosis. Acts upstream of or within G2/M transition of mitotic cell cycle and r egulation of calcium-mediated signaling. Located in membrane; myelin sheath; and vesicle. Part of voltage-gated potassium channel complex. Is active in calyx of Held and presynaptic cytosol. Is expressed in several structures, including alimentary system; brain; heart; metanephros; and sensory organ. Human ortholog(s) of this gene implicated in long QT syndrome 15. Orthologous to human CALM2 (calmodulin 2). [provided by Alliance of Genome Resources, Apr 2025] | 17 | 87740829 | 87754363 | Mouse | 328 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 10282 | Calm3 | calmodulin 3 | Predicted to enable several functions, including enzyme activator activity; enzyme binding activity; and titin binding activity. Involved in presynaptic endocytosis. Acts upstream of or within G2/M transition of mitotic cell cycle. Located in myelin sheath. Part of voltage-gated potassium channel co mplex. Is active in calyx of Held. Is expressed in several structures, including alimentary system; cardiovascular system; nervous system; respiratory system; and sensory organ. Human ortholog(s) of this gene implicated in familial hypertrophic cardiomyopathy and long QT syndrome 16. Orthologous to human CALM3 (calmodulin 3). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 16649304 | 16657957 | Mouse | 314 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 736979 | Capn10 | calpain 10 | Predicted to enable SNARE binding activity; calcium-dependent cysteine-type endopeptidase activity; and cytoskeletal protein binding activity. Involved in several processes, including cellular response to insulin stimulus; positive regulation of transport; and type B pancreatic cell apoptotic proces s. Acts upstream of or within positive regulation of type B pancreatic cell apoptotic process. Predicted to be located in several cellular components, including cytoskeleton; cytosol; and mitochondrion. Predicted to be active in cytoplasm. Is expressed in dorsal root ganglion and renal calyx. Human ortholog(s) of this gene implicated in obesity; pancreatic cancer; polycystic ovary syndrome; and type 2 diabetes mellitus. Orthologous to human CAPN10 (calpain 10). [provided by Alliance of Genome Resources, Apr 2025] | 1 | 92862130 | 92875670 | Mouse | 164 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1314006 | Casp8ap2 | caspase 8 associated protein 2 | Enables cysteine-type endopeptidase activator activity involved in apoptotic process; identical protein binding activity; and protease binding activity. Acts upstream of or within extrinsic apoptotic signaling pathway via death domain receptors. Predicted to be located in cytoplasm and nucleus. Pred icted to be active in PML body and mitochondrion. Is expressed in several structures, including brain ventricular layer; incisor; inner cell mass; renal calyx; and submandibular gland primordium. Orthologous to human CASP8AP2 (caspase 8 associated protein 2). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 32615462 | 32653271 | Mouse | 138 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1617144 | Ccin | calicin | Predicted to enable ubiquitin-like ligase-substrate adaptor activity. Involved in spermatogenesis. Located in cytoskeletal calyx. Human ortholog(s) of this gene implicated in spermatogenic failure 91. Orthologous to human CCIN (calicin). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 43983504 | 43985533 | Mouse | 44 | description | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1312900 | Cdkl1 | cyclin dependent kinase like 1 | Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in regulation of cilium assembly. Predicted to be located in ciliary transition zone and nucleoplasm. Predicted to be active in nucleus. Is expressed in renal calyx and rest o f cerebellum mantle layer. Orthologous to human CDKL1 (cyclin dependent kinase like 1). [provided by Alliance of Genome Resources, Jul 2025] | 12 | 69791944 | 69838057 | Mouse | 85 | description | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1558033 | Chchd10 | coiled-coil-helix-coiled-coil-helix domain containing 10 | Predicted to be involved in several processes, including mitochondrial nucleoid organization; oxidative phosphorylation; and regulation of mitochondrion organization. Located in mitochondrion. Is expressed in several structures, including brain ventricle and choroid plexus; early embryo; hypothalamu s mantle layer; renal calyx; and ventral grey horn. Used to study isolated mitochondrial myopathy. Human ortholog(s) of this gene implicated in frontotemporal dementia and/or amyotrophic lateral sclerosis 2; isolated mitochondrial myopathy; and spinal muscular atrophy, Jokela type. Orthologous to human CHCHD10 (coiled-coil-helix-coiled-coil-helix domain containing 10). [provided by Alliance of Genome Resources, Apr 2025] | 10 | 75768964 | 75773584 | Mouse | 187 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 733328 | Cplx1 | complexin 1 | Enables lipid binding activity. Involved in regulation of vesicle-mediated transport and signal release. Part of SNARE complex. Is active in several cellular components, including Schaffer collateral - CA1 synapse; calyx of Held; and glutamatergic synapse. Is ex pressed in nervous system; retina; and tongue. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 63. Orthologous to human CPLX1 (complexin 1). [provided by Alliance of Genome Resources, Jul 2025] | 5 | 108666420 | 108697893 | Mouse | 165 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 732284 | Cplx2 | complexin 2 | Predicted to enable calcium-dependent protein binding activity and syntaxin-1 binding activity. Involved in positive regulation of synaptic plasticity and regulation of synaptic vesicle fusion to presynaptic active zone membrane. Is active in calyx of Held and g lutamatergic synapse. Is expressed in nervous system; retina layer; and skeletal muscle. Used to study schizophrenia. Orthologous to human CPLX2 (complexin 2). [provided by Alliance of Genome Resources, Jul 2025] | 13 | 54455447 | 54531736 | Mouse | 187 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1618148 | Eva1a | eva-1 homolog A, regulator of programmed cell death | Acts upstream of or within several processes, including TOR signaling; cardiac left ventricle morphogenesis; and connective tissue replacement. Predicted to be located in intracellular membrane-bounded organelle and plasma membrane. Is expressed in foot; hand; left lung; renal caly ht:700;'>calyx; and right lung. Orthologous to human EVA1A (eva-1 homolog A, regulator of programmed cell death). [provided by Alliance of Genome Resources, Apr 2025] | 6 | 82018058 | 82070079 | Mouse | 140 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 62100 | Faah | fatty acid amide hydrolase | Enables monoacylglycerol lipase activity. Involved in regulation of trans-synaptic signaling by endocannabinoid, modulating synaptic transmission. Is active in glutamatergic synapse. Is expressed in several structures, including brain; ganglia; gut; olfactory epithelium; and renal caly weight:700;'>calyx. Human ortholog(s) of this gene implicated in obesity and substance-related disorder. Orthologous to human FAAH (fatty acid amide hydrolase). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 115853866 | 115876034 | Mouse | 288 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1315506 | Fam149a | family with sequence similarity 149, member A | Is expressed in renal calyx. Orthologous to human FAM149A (family with sequence similarity 149 member A). [provided by Alliance of Genome Resources, Jul 2025] | 8 | 45789752 | 45835328 | Mouse | 104 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 737425 | Git1 | GIT ArfGAP 1 | Predicted to enable several functions, including GTPase activator activity; enzyme binding activity; and gamma-tubulin binding activity. Predicted to be a structural constituent of postsynaptic specialization. Involved in several processes, including modulation of chemical synaptic transmission; neg ative regulation of metabolic process; and nervous system development. Acts upstream of or within ephrin receptor signaling pathway. Located in postsynapse. Is active in calyx of Held. Is expressed in embryo. Used to study attention deficit hyperactivity disorder. Human ortholog(s) of this gene implicated in attention deficit hyperactivity disorder. Orthologous to human GIT1 (GIT ArfGAP 1). [provided by Alliance of Genome Resources, Jul 2025] | 11 | 77384114 | 77398600 | Mouse | 242 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1550927 | Git2 | GIT ArfGAP 2 | Predicted to enable GTPase activator activity and small GTPase binding activity. Involved in presynaptic modulation of chemical synaptic transmission and regulation of synaptic vesicle exocytosis. Acts upstream of or within behavioral response to pain. Is active in caly yx of Held. Is expressed in genitourinary system. Orthologous to human GIT2 (GIT ArfGAP 2). [provided by Alliance of Genome Resources, Jul 2025] | 5 | 114865469 | 114912647 | Mouse | 121 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1623058 | Gpn2 | GPN-loop GTPase 2 | Predicted to enable GTPase activity. Is expressed in collecting duct; liver; renal calyx; and ureter. Orthologous to human GPN2 (GPN-loop GTPase 2). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 133311684 | 133319046 | Mouse | 58 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 10791 | Il1rap | interleukin 1 receptor accessory protein | Enables interleukin-1 receptor activity and interleukin-33 receptor activity. Involved in several processes, including interleukin-33-mediated signaling pathway; positive regulation of cytokine production; and regulation of synapse assembly. Acts upstream of or within cytokine-mediated signaling pat hway. Is active in glutamatergic synapse. Is expressed in several structures, including aorta-gonad-mesonephros; brain ventricle and choroid plexus; forebrain; renal calyx; and ventral grey horn. Orthologous to human IL1RAP (interleukin 1 receptor accessory protein). [provided by Alliance of Genome Resources, Jul 2025] | 16 | 26400259 | 26548878 | Mouse | 229 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1332367 | Itsn1 | intersectin 1 (SH3 domain protein 1A) | Enables kinase activator activity. Involved in synaptic vesicle endocytosis. Acts upstream of or within several processes, including negative regulation of neuron apoptotic process; positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction; and small GTPase-mediated s ignal transduction. Located in clathrin-coated pit; endocytic vesicle; and lamellipodium. Is active in calyx of Held; cytosol; and presynaptic endocytic zone. Is expressed in several structures, including alimentary system; central nervous system; genitourinary system; sensory organ; and skeleton. Orthologous to human ITSN1 (intersectin 1). [provided by Alliance of Genome Resources, Jul 2025] | 16 | 91526198 | 91717479 | Mouse | 247 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 733064 | Kcnc3 | potassium voltage gated channel, Shaw-related subfamily, member 3 | Enables voltage-gated potassium channel activity. Involved in regulation of synaptic vesicle endocytosis. Acts upstream of or within regulation of neurotransmitter secretion. Located in several cellular components, including neuromuscular junction; neuron projection membrane; and neuronal cell body membrane. Is active in calyx of Held. Is expressed in aorta; aortic valve; and brain. Human ortholog(s) of this gene implicated in spinocerebellar ataxia type 13. Orthologous to human KCNC3 (potassium voltage-gated channel subfamily C member 3). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 44236405 | 44254175 | Mouse | 168 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1550963 | Kcnq5 | potassium voltage-gated channel, subfamily Q, member 5 | Enables voltage-gated potassium channel activity. Acts upstream of or within potassium ion transport. Predicted to be located in plasma membrane. Predicted to be part of clathrin coat and voltage-gated potassium channel complex. Predicted to be active in calyx o f Held and presynaptic membrane. Is expressed in heart. Human ortholog(s) of this gene implicated in autosomal dominant intellectual developmental disorder 46. Orthologous to human KCNQ5 (potassium voltage-gated channel subfamily Q member 5). [provided by Alliance of Genome Resources, Jul 2025] | 1 | 21468623 | 22032874 | Mouse | 123 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1623931 | Krt80 | keratin 80 | Predicted to be a structural constituent of skin epidermis. Predicted to be involved in intermediate filament organization and keratinization. Predicted to be located in cytoplasm and intermediate filament. Predicted to be active in keratin filament. Is expressed in molar; naris; renal caly font-weight:700;'>calyx; submandibular gland primordium; and vibrissa. Orthologous to human KRT80 (keratin 80). [provided by Alliance of Genome Resources, Jul 2025] | 15 | 101246196 | 101268043 | Mouse | 115 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1623807 | Ly6g2 | lymphocyte antigen 6 family member G2 | Predicted to enable acetylcholine receptor binding activity and acetylcholine receptor inhibitor activity. Predicted to be involved in acetylcholine receptor signaling pathway. Predicted to be active in plasma membrane. Is expressed in midgut; renal calyx; and r enal pelvis. [provided by Alliance of Genome Resources, Jul 2025] | 15 | 75088227 | 75094510 | Mouse | 12 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1552593 | Marveld3 | MARVEL (membrane-associating) domain containing 3 | Predicted to enable mitogen-activated protein kinase kinase kinase binding activity. Acts upstream of or within cell-cell junction organization; negative regulation of epithelial cell migration; and negative regulation of epithelial cell proliferation. Located in bicellular tight junction. Is expres sed in brain ventricle and choroid plexus; foregut; renal calyx; retina; and trachea. Orthologous to human MARVELD3 (MARVEL domain containing 3). [provided by Alliance of Genome Resources, Jul 2025] | 8 | 110674541 | 110688837 | Mouse | 119 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1319560 | Nacc2 | nucleus accumbens associated 2, BEN and BTB (POZ) domain containing | Predicted to enable several functions, including DNA-binding transcription repressor activity, RNA polymerase II-specific; histone deacetylase binding activity; and protein homodimerization activity. Predicted to be involved in several processes, including negative regulation of transcription by RNA polymerase II; positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage; and protein homooligomerization. Predicted to be located in chromatin; mitochondrion; and nucleolus. Is expressed in several structures, including brain; limb; renal calyx; submandibular gland primordium; and tooth. Orthologous to human NACC2 (NACC family member 2). [provided by Alliance of Genome Resources, Jul 2025] | 2 | 25945547 | 26012823 | Mouse | 150 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 10991 | Nos1 | nitric oxide synthase 1, neuronal | Enables nitric-oxide synthase activity. Involved in several processes, including nitric oxide biosynthetic process; positive regulation of adenylate cyclase-activating G protein-coupled receptor signaling pathway; and positive regulation of the force of heart contraction. Acts upstream of or within several processes, including peptidyl-cysteine S-nitrosylation; positive regulation of transcription by RNA polymerase II; and regulation of metal ion transport. Located in several cellular components, including T-tubule; Z disc; and sarcoplasmic reticulum membrane. Is active in calyx of Held. Colocalizes with caveola. Is expressed in several structures, including alimentary system; genitourinary system; integumental system; nervous system; and sensory organ. Used to study achalasia and hypertrophic pyloric stenosis. Human ortholog(s) of this gene implicated in Alzheimer's disease; Parkinson's disease; asthma; and cystic fibrosis. Orthologous to human NOS1 (nitric oxide synthase 1). [provided by Alliance of Genome Resources, Jul 2025] | 5 | 118004904 | 118096905 | Mouse | 902 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1615897 | Pbld2 | phenazine biosynthesis-like protein domain containing 2 | Predicted to enable identical protein binding activity and isomerase activity. Predicted to be involved in maintenance of gastrointestinal epithelium. Predicted to act upstream of or within with a positive effect on negative regulation of transforming growth factor beta receptor signaling pathway. P redicted to be active in cytoplasm. Is expressed in pancreas epithelium and renal calyx. Orthologous to human PBLD (phenazine biosynthesis like protein domain containing). [provided by Alliance of Genome Resources, Jul 2025] | 10 | 62858319 | 62894592 | Mouse | 40 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 731879 | Plscr1 | phospholipid scramblase 1 | Predicted to enable several functions, including DNA-binding transcription activator activity, RNA polymerase II-specific; metal ion binding activity; and signaling receptor binding activity. Involved in several processes, including cellular response to lipopolysaccharide; negative regulation of vir al genome replication; and phosphatidylserine biosynthetic process. Acts upstream of or within myeloid cell differentiation; phosphatidylserine exposure on apoptotic cell surface; and positive regulation of intrinsic apoptotic signaling pathway in response to DNA damage. Located in cytosol; nucleus; and plasma membrane. Is expressed in hindgut; midgut; renal calyx; and renal pelvis. Orthologous to human PLSCR1 (phospholipid scramblase 1). [provided by Alliance of Genome Resources, Jul 2025] | 9 | 92132265 | 92154034 | Mouse | 280 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 737063 | Prkca | protein kinase C, alpha | Enables calcium,diacylglycerol-dependent serine/threonine kinase activity; integrin binding activity; and lipid binding activity. Involved in several processes, including modulation of chemical synaptic transmission; negative regulation of cytokine production involved in inflammatory response; and p ositive regulation of bone resorption. Acts upstream of or within several processes, including induction of positive chemotaxis; negative regulation of signal transduction; and regulation of protein phosphorylation. Located in several cellular components, including cone photoreceptor outer segment; intercalated disc; and ooplasm. Part of alphav-beta3 integrin-PKCalpha complex. Is active in calyx of Held and presynaptic cytosol. Is expressed in several structures, including alimentary system; brain; early embryo; genitourinary system; and sensory organ. Human ortholog(s) of this gene implicated in dilated cardiomyopathy; high grade glioma (multiple); large cell carcinoma; and reproductive organ cancer (multiple). Orthologous to human PRKCA (protein kinase C alpha). [provided by Alliance of Genome Resources, Apr 2025] | 11 | 107824213 | 108237360 | Mouse | 696 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1550017 | Prkcb | protein kinase C, beta | Enables calcium channel regulator activity and calcium,diacylglycerol-dependent serine/threonine kinase activity. Involved in several processes, including modulation of chemical synaptic transmission; phospholipase C-activating G protein-coupled acetylcholine receptor signaling pathway; and positive regulation of cell communication. Acts upstream of or within several processes, including cellular response to carbohydrate stimulus; intracellular calcium ion homeostasis; and protein phosphorylation. Located in cytoplasm and nucleus. Part of spectrin. Is active in calyx of Held; plasma membrane; and presynaptic cytosol. Is expressed in several structures, including central nervous system; exocrine system; genitourinary system; heart ventricle; and retina. Human ortholog(s) of this gene implicated in dilated cardiomyopathy and lung non-small cell carcinoma. Orthologous to human PRKCB (protein kinase C beta). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 121888327 | 122233625 | Mouse | 521 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 11147 | Prkcg | protein kinase C, gamma | Enables calcium,diacylglycerol-dependent serine/threonine kinase activity. Involved in several processes, including modulation of chemical synaptic transmission; negative regulation of protein metabolic process; and response to morphine. Acts upstream of or within chemosensory behavior; regulation o f phagocytosis; and synaptic signaling via neuropeptide. Located in several cellular components, including dendrite; postsynaptic density; and synaptic membrane. Is active in calyx of Held and presynaptic cytosol. Is expressed in several structures, including alimentary system; brain; early embryo; genitourinary system; and hemolymphoid system gland. Used to study spinocerebellar ataxia type 14. Human ortholog(s) of this gene implicated in spinocerebellar ataxia type 14. Orthologous to human PRKCG (protein kinase C gamma). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 3352038 | 3379615 | Mouse | 261 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 736434 | Ptprj | protein tyrosine phosphatase receptor type J | Enables protein tyrosine phosphatase activity. Involved in several processes, including peptidyl-tyrosine dephosphorylation involved in inactivation of protein kinase activity; regulation of cell migration; and regulation of signal transduction. Acts upstream of or within heart development; oligoden drocyte differentiation; and vasculogenesis. Located in immunological synapse and ruffle membrane. Is expressed in midbrain; renal calyx; renal pelvis; and superior colliculus. Human ortholog(s) of this gene implicated in colorectal cancer; lung adenocarcinoma; lung squamous cell carcinoma; and thrombocytopenia. Orthologous to human PTPRJ (protein tyrosine phosphatase receptor type J). [provided by Alliance of Genome Resources, Jul 2025] | 2 | 90260100 | 90411102 | Mouse | 308 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1552784 | Rhcg | Rhesus blood group-associated C glycoprotein | Enables ammonium channel activity. Involved in ammonium transmembrane transport and regulation of pH. Located in apical plasma membrane. Is expressed in medulla oblongata basal plate ventricular layer; renal calyx; spinal cord ventricular layer; and telencephalo n. Orthologous to human RHCG (Rh family C glycoprotein). [provided by Alliance of Genome Resources, Jul 2025] | 7 | 79243111 | 79267405 | Mouse | 129 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1319813 | Rigi | RNA sensor RIG-I | Enables double-stranded DNA binding activity; double-stranded RNA binding activity; and single-stranded RNA binding activity. Involved in several processes, including innate immune response; positive regulation of cytokine production; and response to virus. Acts upstream of or within response to exo genous dsRNA. Predicted to be located in actin cytoskeleton; bicellular tight junction; and ruffle membrane. Predicted to be part of ribonucleoprotein complex. Predicted to be active in cytoplasm. Is expressed in several structures, including foregut; olfactory epithelium; ovary; renal calyx; and submandibular gland primordium. Orthologous to human RIGI (RNA sensor RIG-I). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 40203775 | 40239843 | Mouse | 331 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 733346 | Rimbp2 | RIMS binding protein 2 | Enables voltage-gated calcium channel activity involved in regulation of presynaptic cytosolic calcium levels and voltage-gated monoatomic ion channel activity involved in regulation of presynaptic membrane potential. A structural constituent of presynaptic active zone. Involved in regulation of cal cium-dependent activation of synaptic vesicle fusion and regulation of presynaptic membrane potential. Is active in calyx of Held; glutamatergic synapse; and presynaptic active zone cytoplasmic component. Orthologous to human RIMBP2 (RIMS binding protein 2). [provided by Alliance of Genome Resources, Jul 2025] | 5 | 128834852 | 129030636 | Mouse | 101 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1316538 | Rprd1a | regulation of nuclear pre-mRNA domain containing 1A | Predicted to enable RNA polymerase II complex binding activity and identical protein binding activity. Predicted to be involved in RNA polymerase II promoter clearance and mRNA 3'-end processing. Predicted to be located in nucleus. Predicted to be part of transcription preinitiation complex. Is expr essed in dorsal root ganglion; renal calyx; and submandibular gland primordium. Orthologous to human RPRD1A (regulation of nuclear pre-mRNA domain containing 1A). [provided by Alliance of Genome Resources, Jul 2025] | 18 | 24618017 | 24663306 | Mouse | 89 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1550240 | Septin5 | septin 5 | Predicted to enable several functions, including GTPase activity; guanyl ribonucleotide binding activity; and protein homodimerization activity. Involved in adult behavior; regulation of synaptic vesicle docking; and social behavior. Located in cell cortex; synaptic vesicle; and terminal bouton. Par t of septin complex. Is active in calyx of Held. Is expressed in several structures, including alimentary system; cardiovascular system; central nervous system; genitourinary system; and sensory organ. Orthologous to human SEPTIN5 (septin 5). [provided by Alliance of Genome Resources, Apr 2025] | 16 | 18440561 | 18448688 | Mouse | 143 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1614439 | Serpina1a | serine (or cysteine) peptidase inhibitor, clade A, member 1A | Predicted to enable identical protein binding activity; protease binding activity; and serine-type endopeptidase inhibitor activity. Acts upstream of or within protein N-linked glycosylation; response to cytokine; and response to peptide hormone. Located in extracellular region. Is expressed in gut; liver lobe; and renal calyx. Human ortholog(s) of this gene implicated in several diseases, including alpha 1-antitrypsin deficiency; artery disease (multiple); chronic obstructive pulmonary disease (multiple); inflammatory bowel disease (multiple); and liver disease (multiple). Orthologous to human SERPINA1 (serpin family A member 1). [provided by Alliance of Genome Resources, Jul 2025] | 12 | 103819554 | 103829878 | Mouse | 88 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1614438 | Serpina1b | serine (or cysteine) preptidase inhibitor, clade A, member 1B | Enables serine-type endopeptidase inhibitor activity. Acts upstream of or within several processes, including in utero embryonic development; protein N-linked glycosylation; and response to peptide hormone. Located in extracellular region. Is expressed in gut; liver lobe; nucleus pulposus; and renal calyx. Human ortholog(s) of this gene implicated in several diseases, including alpha 1-antitrypsin deficiency; artery disease (multiple); chronic obstructive pulmonary disease (multiple); inflammatory bowel disease (multiple); and liver disease (multiple). Orthologous to human SERPINA1 (serpin family A member 1). [provided by Alliance of Genome Resources, Jul 2025] | 12 | 103694415 | 103704448 | Mouse | 72 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1615771 | Tbc1d10a | TBC1 domain family, member 10a | Predicted to enable GTPase activator activity and PDZ domain binding activity. Predicted to be involved in positive regulation of proteolysis and retrograde transport, endosome to Golgi. Predicted to be located in plasma membrane. Is expressed in renal calyx and vibrissa. Orthologous to human TBC1D10A (TBC1 domain family member 10A). [provided by Alliance of Genome Resources, Jul 2025] | 11 | 4136852 | 4167407 | Mouse | 96 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1319322 | Thnsl2 | threonine synthase-like 2 (bacterial) | Enables pyridoxal phosphate binding activity and serine binding activity. Involved in 2-oxobutyrate biosynthetic process; dephosphorylation; and serine family amino acid catabolic process. Is expressed in renal calyx. Orthologous to human THNSL2 (threonine synth ase like 2). [provided by Alliance of Genome Resources, Apr 2025] | 6 | 71105150 | 71121364 | Mouse | 110 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1614939 | Tmem252 | transmembrane protein 252 | Predicted to be located in membrane. Is expressed in brain; renal calyx; and spinal cord. Orthologous to human TMEM252 (transmembrane protein 252). [provided by Alliance of Genome Resources, Jul 2025] | 19 | 24651372 | 24657025 | Mouse | 73 | description | gene, protein-coding, PROVISIONAL [RefSeq] |
| 1332420 | Tspoap1 | TSPO associated protein 1 | Enables voltage-gated calcium channel activity involved in regulation of presynaptic cytosolic calcium levels. Predicted to be involved in regulation of neurotransmitter secretion. Is active in calyx of Held and glutamatergic synapse. Is expressed in lung. Human ortholog(s) of this gene implicated in dystonia 22, adult-onset and dystonia 22, juvenile-onset. Orthologous to human TSPOAP1 (TSPO associated protein 1). [provided by Alliance of Genome Resources, Jul 2025] | 11 | 87649022 | 87676754 | Mouse | 113 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1620603 | Ttc22 | tetratricopeptide repeat domain 22 | Is expressed in anal canal; bladder; epidermis; external naris epithelium; and renal calyx. Orthologous to human TTC22 (tetratricopeptide repeat domain 22). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 106479646 | 106497393 | Mouse | 47 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1620684 | Ugt2b38 | UDP glucuronosyltransferase 2 family, polypeptide B38 | Predicted to enable glucuronosyltransferase activity. Predicted to be involved in steroid metabolic process. Predicted to be located in endoplasmic reticulum and nuclear outer membrane. Is expressed in renal calyx. Orthologous to several human genes including UG T2B10 (UDP glucuronosyltransferase family 2 member B10); UGT2B11 (UDP glucuronosyltransferase family 2 member B11); and UGT2B15 (UDP glucuronosyltransferase family 2 member B15). [provided by Alliance of Genome Resources, Apr 2025] | 5 | 87557798 | 87572062 | Mouse | 47 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1614780 | Unc13a | unc-13 homolog A | Enables calmodulin binding activity and diacylglycerol binding activity. Involved in several processes, including positive regulation of glutamate receptor signaling pathway; positive regulation of synaptic plasticity; and regulated exocytosis. Acts upstream of or within several processes, including chemical synaptic transmission; modulation of chemical synaptic transmission; and synaptic vesicle maturation. Located in axon; neuromuscular junction; and presynapse. Is active in calyx of Held; glutamatergic synapse; and presynaptic active zone. Is expressed in nervous system and neural retina. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis. Orthologous to human UNC13A (unc-13 homolog A). [provided by Alliance of Genome Resources, Jul 2025] | 8 | 72079356 | 72124418 | Mouse | 214 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 1551198 | Unc13b | unc-13 homolog B | Predicted to enable GTP-dependent protein binding activity; calmodulin binding activity; and syntaxin-1 binding activity. Involved in several processes, including positive regulation of defense response to bacterium; regulated exocytosis; and regulation of synaptic plasticity. Acts upstream of or wi thin chemical synaptic transmission; innervation; and neuromuscular junction development. Located in several cellular components, including early phagosome; presynaptic active zone; and ribbon synapse. Is active in calyx of Held; glutamatergic synapse; and hippocampal mossy fiber to CA3 synapse. Is expressed in several structures, including alimentary system; central nervous system; eye; genitourinary system; and respiratory system. Orthologous to human UNC13B (unc-13 homolog B). [provided by Alliance of Genome Resources, Jul 2025] | 4 | 43046193 | 43264873 | Mouse | 197 | description | gene, protein-coding, VALIDATED [RefSeq] |
| 735420 | Unc13c | unc-13 homolog C | Predicted to enable calmodulin binding activity and syntaxin-1 binding activity. Involved in negative regulation of synaptic plasticity and synaptic vesicle exocytosis. Acts upstream of or within chemical synaptic transmission. Is active in calyx of Held and par allel fiber to Purkinje cell synapse. Is expressed in several structures, including brain; limb interdigital region; molar; olfactory epithelium; and spinal cord mantle layer. Orthologous to human UNC13C (unc-13 homolog C). [provided by Alliance of Genome Resources, Jul 2025] | 9 | 73386704 | 73915421 | Mouse | 114 | description | gene, protein-coding, VALIDATED [RefSeq] |