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Gene : AFM Homo sapiens

Name  ? afamin Cytological Location  4q13.3
Brief Description  afamin
description  This gene is a member of the albumin gene family, which is comprised of four genes that localize to chromosome 4 in a tandem arrangement. These four genes encode structurally-related serum transport proteins that are known to be evolutionarily related. The protein encoded by this gene is regulated developmentally, expressed in the liver and secreted into the bloodstream. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc003hhb.4,
  • OTTHUMG00000130004,
  • ALB2,
  • L32140,
  • HGNC:316,
  • AFM,
  • NM_001133,
  • ALBA,
  • ALF,
  • ALB2,
  • ALBA
  • identifiers:
  • 173,
  • ENSG00000079557,
  • AFM

Genome feature

Region: gene ? Length: 22257  
Location: 4:73481745-73504001 Cyto location: 4q13.3


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Gene Expression Atlas Tissues Displayer

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Publication Counts Displayer

Curated Proteins Displayer

Function

Gene Ontology Displayer

0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

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

Homologue Displayer

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

0 SN Ps

5 Cross References

15 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results