Amnionless

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Amnionless is a protein that in humans is encoded by the AMN gene.[5][6]

AliasesAMN, PRO1028, amnionless, Amnionless, amnion associated transmembrane protein, IGS2
End102,933,596 bp[1]
Quick facts AMN, Identifiers ...
AMN
Identifiers
AliasesAMN, PRO1028, amnionless, Amnionless, amnion associated transmembrane protein, IGS2
External IDsOMIM: 605799; MGI: 1934943; HomoloGene: 12804; GeneCards: AMN; OMA:AMN - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_030943

NM_033603

RefSeq (protein)

NP_112205

NP_291081

Location (UCSC)Chr 14: 102.92 – 102.93 MbChr 12: 111.24 – 111.24 Mb
PubMed search[3][4]
Wikidata
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Function

A complex of amnionless and cubilin forms the cubam receptor.

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.[6]

Clinical significance

Mutations of the AMN gene may cause Imerslund–Gräsbeck syndrome.

References

Further reading

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