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Gene : BTN2A3P Homo sapiens

Name  ? butyrophilin subfamily 2 member A3, pseudogene Cytological Location  6p22.2
description  The butyrophilin (BTN) genes are a group of major histocompatibility complex (MHC)-associated genes that encode type I membrane proteins with 2 extracellular immunoglobulin (Ig) domains and an intracellular B30.2 (PRYSPRY) domain. Three subfamilies of human BTN genes are located in the MHC class I region: the single-copy BTN1A1 gene (MIM 601610) and the BTN2 (e.g., BTN2A3) and BTN3 (e.g., BNT3A1; MIM 613593) genes, which have undergone tandem duplication, resulting in 3 copies of each (summary by Smith et al., 2010 [PubMed 20208008]).[supplied by OMIM, Nov 2010]
  • synonyms:
  • AL021917,
  • butyrophilin, subfamily 2, member A3,
  • HGNC:13229,
  • BTN2.3,
  • butyrophilin, subfamily 2, member A3, pseudogene,
  • BTN2A3,
  • NR_027795,
  • BTN2A3,
  • OTTHUMG00000014453,
  • BTN2.3
  • identifiers:
  • 54718,
  • ENSG00000124549,
  • BTN2A3P

Genome feature

Region: gene ?
Location: No location information in HumanMine Cyto location: 6p22.2


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

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

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]

Homology

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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

4 Cross References

8 Data Sets

22 Homologues

0 Located Features

53 Rna Seq Results