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Gene : AMN Homo sapiens

Name  ? amnion associated transmembrane protein Cytological Location  14q32.32
Brief Description  amnion associated transmembrane protein
description  The protein encoded by this gene is a type I transmembrane protein. It is thought to modulate bone morphogenetic protein (BMP) receptor function by serving as an accessory or coreceptor, and thus facilitates or hinders BMP binding. It is known that the mouse AMN gene is expressed in the extraembryonic visceral endoderm layer during gastrulation, but it is found to be mutated in amnionless mouse. The encoded protein has sequence similarity to short gastrulation (Sog) and procollagen IIA proteins in Drosophila. [provided by RefSeq, Jul 2008]
  • synonyms:
  • amnionless,
  • amnionless,
  • HGNC:14604,
  • uc001ymg.5,
  • NM_030943,
  • PRO1028,
  • OTTHUMG00000171897,
  • AF328788,
  • AMN,
  • amnionless homolog (mouse)
  • identifiers:
  • 81693,
  • ENSG00000166126,
  • AMN

Genome feature

Region: gene ? Length: 11168  
Location: 14:102922430-102933597 Cyto location: 14q32.32


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Function

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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

1 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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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

205 SN Ps

5 Cross References

18 Data Sets

5 Homologues

0 Located Features

90 Rna Seq Results