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
View/Edit HumanView/Edit Mouse

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

Function

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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

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

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000166126Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000021278Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Kalantry S, Manning S, Haub O, Tomihara-Newberger C, Lee HG, Fangman J, Disteche CM, Manova K, Lacy E (Mar 2001). "The amnionless gene, essential for mouse gastrulation, encodes a visceral-endoderm-specific protein with an extracellular cysteine-rich domain". Nat Genet. 27 (4): 412–6. doi:10.1038/86912. PMID 11279523. S2CID 12758039.
  6. ^ a b "Entrez Gene: AMN amnionless homolog (mouse)".
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Further reading

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📚 Artikel Terkait di Wikipedia

Cubam

of amnionless (AMN), and cubilin. Cubilin is essential as a cell receptor recognizing the "vitamin B12-intrinsic factor" complex, whereas amnionless is

Imerslund–Gräsbeck syndrome

located in the terminal ileum. This receptor is composed of two proteins, amnionless (AMN), and cubilin. A defect in either of these protein components can

Cubilin

complexes by means of amnionless (AMN). Cubilinis essentially only present in the small intestine and kidneys. A complex of amnionless and cubilin forms the

Vitamin B12

the stomach. IF delivers the vitamin to receptor proteins cubilin and amnionless, which together form the cubam receptor in the distal ileum. The receptor

AMN

neuron (α-MNs), large lower motor neurons of the brainstem and spinal cord Amnionless, a gene for a protein necessary for efficient absorption of vitamin B12

CLCN5

formation/function of the endocytic complex that also involves megalin and cubilin/amnionless receptors, the sodium-hydrogen antiporter 3 (NHE3), and the V-ATPase.

LRP2

transcytosis. LRP2/megalin can also form complexes with CUBAM, the cubilin and amnionless complex. Those complexes are able to reabsorb several molecules and can

Lymphotoxin beta receptor

Wang X, Bornslaeger EA, Haub O, et al. (1996). "A candidate gene for the amnionless gastrulation stage mouse mutation encodes a TRAF-related protein". Dev