FAM136A

Protein FAM136A is a protein that in humans is encoded by the FAM136A gene.^[5][6]

FAM136A
Identifiers
Aliases	FAM136A, family with sequence similarity 136 member A
External IDs	OMIM: 616275; MGI: 1913738; HomoloGene: 135942; GeneCards: FAM136A; OMA:FAM136A - orthologs
Gene location (Human) Chr. Chromosome 2 (human)[1] Band 2p13.3 Start 70,295,975 bp[1] End 70,302,090 bp[1]
Gene location (Mouse) Chr. Chromosome 6 (mouse)[2] Band 6|6 D1 Start 86,342,628 bp[2] End 86,347,040 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in parotid gland body of pancreas gingival epithelium rectum mucosa of transverse colon epithelium of nasopharynx hair follicle duodenum right lobe of liver pancreatic epithelial cell Top expressed in primitive streak embryo abdominal wall epiblast embryo endocardial cushion yolk sac somite migratory enteric neural crest cell cumulus cell More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 84908 66488 Ensembl ENSG00000035141 ENSMUSG00000057497 UniProt Q96C01 Q9CR98 RefSeq (mRNA) NM_001329752 NM_001329753 NM_001329755 NM_001329757 NM_001329758 NM_032822 NM_025591 NM_001368363 RefSeq (protein) NP_001316681 NP_001316682 NP_001316684 NP_001316686 NP_001316687 NP_116211 NP_079867 NP_001355292 Location (UCSC) Chr 2: 70.3 – 70.3 Mb Chr 6: 86.34 – 86.35 Mb PubMed search [3] [4]
Wikidata
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Clinical significance

Mutations in FAM136A are associated to Ménière's disease.^[7][8]