CAPRIN2 (original) (raw)

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Protein-coding gene in humans

CAPRIN2
Available structuresPDBOrtholog search: PDBe RCSB List of PDB id codes4OUL, 4OUM
Identifiers
Aliases CAPRIN2, C1QDC1, EEG-1, EEG1, RNG140, caprin family member 2
External IDs OMIM: 610375; MGI: 2448541; HomoloGene: 11393; GeneCards: CAPRIN2; OMA:CAPRIN2 - orthologs
Gene location (Human)Chromosome 12 (human)Chr.Chromosome 12 (human)[1]Chromosome 12 (human)Genomic location for CAPRIN2Genomic location for CAPRIN2Band12p11.21Start30,709,552 bp[1]End30,754,951 bp[1]
Gene location (Mouse)Chromosome 6 (mouse)Chr.Chromosome 6 (mouse)[2]Chromosome 6 (mouse)Genomic location for CAPRIN2Genomic location for CAPRIN2Band6|6 G3Start148,743,990 bp[2]End148,797,735 bp[2]
RNA expression patternBgeeHuman Mouse (ortholog)Top expressed inspinal gangliacerebellar vermisright hemisphere of cerebellumtrigeminal gangliontesticlesural nervelateral nuclear group of thalamuspars compactapars reticulataexternal globus pallidusTop expressed inlensepithelium of lenszygoteprimary oocytesecondary oocytetail of embryoneural layer of retinalumbar spinal ganglionsupraoptic nucleusparaventricular nucleus of hypothalamusMore reference expression dataBioGPSn/a
Gene ontologyMolecular function signaling receptor binding protein binding RNA binding metal ion binding Cellular component centrosome receptor complex nucleus mitochondrion cytoplasm cytosol plasma membrane membrane Biological process positive regulation of canonical Wnt signaling pathway regulation of growth cell differentiation negative regulation of translation positive regulation of protein binding negative regulation of cell growth positive regulation of peptidyl-serine phosphorylation positive regulation of transcription by RNA polymerase II positive regulation of dendrite morphogenesis positive regulation of dendritic spine morphogenesis Sources:Amigo / QuickGO
OrthologsSpeciesHuman MouseEntrez65981232560EnsemblENSG00000110888ENSMUSG00000030309UniProtQ6IMN6Q05A80RefSeq (mRNA)NM_001002259NM_001206856NM_023925NM_032156NM_001319842NM_001319843NM_001319844NM_001319845NM_001319846NM_001301351NM_181541RefSeq (protein)NP_001002259NP_001193785NP_001306771NP_001306772NP_001306773NP_001306774NP_001306775NP_076414NP_115532NP_001288280NP_853519Location (UCSC)Chr 12: 30.71 – 30.75 MbChr 6: 148.74 – 148.8 MbPubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

caprin family member 2, also known as CAPRIN2, is a human gene.[5]

The protein encoded by this gene may be involved in the transitioning of erythroblasts from a highly proliferative state to a terminal phase of differentiation. High level expression of the encoded protein can lead to apoptosis. Several transcript variants encoding different isoforms have been found for this gene.[5]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000110888Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030309Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: caprin family member 2". Retrieved 2011-08-30.