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Pathways
Genes search result for Rattus norvegicus
(View Results for all Objects and Ontologies)


16 records found for search term shr
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
2592Fabp6fatty acid binding protein 6ENCODES a protein that exhibits fatty acid binding; INVOLVED IN steroid metabolic process; PARTICIPATES IN eicosanoid signaling pathway via peroxisome proliferator-activated receptor gamma; FOUND IN cytoplasm (inferred); membrane (inferred); INTERACTS WITH 1,1,1-trichloro-2,2-bis(4-hydroxyphenyl)eth102856505428569727Rat94old_gene_namegene, protein-coding, PROVISIONAL [RefSeq]
1308066Shroom1shroom family member 1ENCODES a protein that exhibits actin filament binding (ortholog); myosin II binding (ortholog); INVOLVED IN actin filament bundle assembly (ortholog); cell morphogenesis (ortholog); ASSOCIATED WITH COVID-19 (ortholog); FOUND IN cytoskeleton (inferred); microtubule (inferred); INTERACTS WITH 17beta-103812197138134832Rat85symbol , PhenoGen , namegene, protein-coding, MODEL [RefSeq]
1565163Shroom2shroom family member 2ENCODES a protein that exhibits actin binding (ortholog); actin filament binding (ortholog); beta-catenin binding (ortholog); INVOLVED IN actin filament bundle assembly (ortholog); cell migration (ortholog); cell morphogenesis (ortholog); ASSOCIATED WITH Meniere's disease (ortholog); FOUND IN adhereX2530816325480194Rat127symbol , PhenoGen , namegene, protein-coding, VALIDATED [RefSeq]
1310470Shroom3shroom family member 3ENCODES a protein that exhibits actin binding (ortholog); INVOLVED IN actin cytoskeleton organization (ortholog); columnar/cuboidal epithelial cell development (ortholog); neural tube closure (ortholog); ASSOCIATED WITH tetralogy of Fallot (ortholog); FOUND IN adherens junction (ortholog); apical ju141538376915681158Rat117symbol , old_gene_name , PhenoGen , name , old_gene_symbolgene, protein-coding, PROVISIONAL [RefSeq]
1563434Shroom4shroom family member 4ENCODES a protein that exhibits actin filament binding (ortholog); myosin II binding (ortholog); INVOLVED IN regulation of postsynaptic membrane neurotransmitter receptor levels; actin filament organization (ortholog); brain development (ortholog); ASSOCIATED WITH intellectual disability (ortholog);X1853737118748665Rat93symbol , PhenoGen , namegene, protein-coding, PROVISIONAL [RefSeq]
14394503Klrb1aem1Mcwikiller cell lectin-like receptor subfamily B, member 1A; CRISPR/Cas9 induced mutant 1, McwiCRISPR/Cas9 system was used to introduce a 5-bp deletion in exon 2 in SHR/NCrl embryos.Ratdescriptiongene, allele
14394505Klrb1aem2Mcwikiller cell lectin-like receptor subfamily B, member 1A; CRISPR/Cas9 induced mutant 2, McwiCRISPR/Cas9 system was used to introduce a 102-bp deletion in exon 2 in SHR/NCrl embryos.Ratdescriptiongene, allele
149735372C3em1Kyocomplement C3; ZFN induced mutant 1, KyoZFN constructs specific for the rat C3 gene were designed to target bases 1803-1841 (NCBI reference sequence: NM_016994) of C3 (target sequence: cagggggcccgagtgggctagtggctgtggacaagggg) by Sigma-Aldrich (Tokyo, Japan). The ZFN systems were injected into the pronucleus of SHRRatdescriptiongene, allele
19259465Camk2n1em1Tjacalcium/calmodulin-dependent protein kinase II inhibitor 1; ZFN induced mutant 1, TjaINVOLVED IN positive regulation of insulin secretion involved in cellular response to glucose stimulus; positive regulation of systemic arterial blood pressure; ASSOCIATED WITH decreased brown adipose tissue mass; decreased epididymal fat pad weight; decreased heart left ventricle weightRat9descriptiongene, allele
127285405Cfbem1Tjacomplement factor B, ZFN induced mutant 1, TjaASSOCIATED WITH decreased brown adipose tissue amount; decreased circulating aldosterone level; decreased circulating cholesterol levelRat13descriptiongene, allele
12791992Gja8m1Cubgap junction protein, alpha 8; mutant 1 CubASSOCIATED WITH abnormal lens capsule morphology; abnormal lens development; abnormal lens epithelium morphology; ASSOCIATED WITH cataract; cataract 1 multiple types; microphthalmiaRat34descriptiongene, allele
10002755Sbf1m1IpcvSET binding factor 1; mutation 1, Institute of Physiology, Czechoslovac Academy of SciencesASSOCIATED WITH arrest of spermiogenesis; azoospermia; decreased testis weightRat4descriptiongene, allele
150340624Zbtb16em1Ipcvzinc finger and BTB domain containing 16; TALEN induced mutant 1, IpcvASSOCIATED WITH cardiac interstitial fibrosis; decreased body weight; decreased circulating cholesterol levelRat10descriptiongene, allele
12910834Zbtb16Lxzinc finger and BTB domain containing 16, Lx mutantASSOCIATED WITH preaxial polydactyly; ASSOCIATED WITH polydactylyRat2descriptiongene, allele
1590138Ajap1adherens junctions associated protein 1ENCODES a protein that exhibits beta-catenin binding (ortholog); protein domain specific binding (ortholog); protein-containing complex binding (ortholog); INVOLVED IN negative regulation of cell-matrix adhesion (ortholog); negative regulation of wound healing (ortholog); regulation of polarized epi5169190477169302938Rat89old_gene_namegene, protein-coding, PROVISIONAL [RefSeq]
13792814Spp1em2Mcwisecreted phosphoprotein 1; CRISPR/Cas9 induced mutant 2, McwiCRISPR/Cas9 system was used to introduce a mutation in the Spp1 gene of SHRSP/A3NCrl rat embryos. The resulting mutation is a 11-bp deletion in Exon 3 of the Spp1 gene.Ratdescriptiongene, allele