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Gene : FAM136A Homo sapiens

Name  ? family with sequence similarity 136 member A Cytological Location  2p13.3
Brief Description  family with sequence similarity 136 member A
Description  This gene encodes a mitochondrially localized protein that is highly conserved across species. The gene is expressed in a variety of tissues including human lymphoblast cells and rat neurosensorial epithelium of the cristaampullaris. A mutation in this gene has been associated with familial Meniere's disease, a chronic disorder of the inner ear. Several pseudogenes of this gene are found on other chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2016]
  • synonyms:
  • HGNC:25911,
  • family with sequence similarity 136, member A,
  • BC014975,
  • FAM136A,
  • hypothetical protein FLJ14668,
  • OTTHUMG00000129668,
  • FLJ14668,
  • uc002sgq.5,
  • NM_032822
  • identifiers:
  • 84908,
  • ENSG00000035141,
  • FAM136A

Genome feature

Region: gene ? Length: 6092  
Location: 2:70295976-70302067 reverse strand Cyto location: 2p13.3

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



0 Pathways

3753 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results