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Gene : TMEM38B Homo sapiens

Name  ? transmembrane protein 38B Cytological Location  9q31.2
Brief Description  transmembrane protein 38B
description  This gene encodes an intracellular monovalent cation channel that functions in maintenance of intracellular calcium release. Mutations in this gene may be associated with autosomal recessive osteogenesis. [provided by RefSeq, Oct 2012]
  • synonyms:
  • NM_018112,
  • HGNC:25535,
  • TRIC-B,
  • TRICB,
  • BC031938,
  • OTTHUMG00000020429,
  • bA219P18.1,
  • TMEM38B,
  • OI14,
  • C9orf87,
  • C9orf87,
  • FLJ10493,
  • uc004bcu.3,
  • chromosome 9 open reading frame 87,
  • D4Ertd89e,
  • bA219P18.1,
  • TRIC-B,
  • D4Ertd89e
  • identifiers:
  • 55151,
  • ENSG00000095209,
  • TMEM38B

Genome feature

Region: gene ? Length: 82087  
Location: 9:105694525-105776611 Cyto location: 9q31.2


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Function

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0 Pathways

Gene --> GO terms.

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

2011 SN Ps

5 Cross References

18 Data Sets

8 Homologues

0 Located Features

90 Rna Seq Results