KREMEN1

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

Kremen protein 1 is a protein that in humans is encoded by the KREMEN1 gene.[5][6] Kremen1 is conserved in chordates including amphioxus[7] and most vertebrate species.[8] The protein is a type I transmembrane receptor of ligands Dickkopf1,[9] Dickkopf2, Dickkopf3, Dickkopf4, EpCAM[10] and Rspondin1.

PDBOrtholog search: PDBe RCSB
AliasesKREMEN1, KREMEN, KRM1, kringle containing transmembrane protein 1, ECTD13
Quick facts Available structures, PDB ...
KREMEN1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKREMEN1, KREMEN, KRM1, kringle containing transmembrane protein 1, ECTD13
External IDsOMIM: 609898; MGI: 1933988; HomoloGene: 12935; GeneCards: KREMEN1; OMA:KREMEN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001039570
NM_032045
NM_153379

NM_032396

RefSeq (protein)

NP_001034659
NP_114434

NP_115772

Location (UCSC)Chr 22: 29.07 – 29.17 MbChr 11: 5.14 – 5.21 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes a high-affinity dickkopf homolog 1 (DKK1) transmembrane receptor that functionally cooperates with DKK1 to block wingless (WNT)/beta-catenin signaling. The encoded protein is a component of a membrane complex that modulates canonical WNT signaling through lipoprotein receptor-related protein 6 (LRP6). It contains extracellular Kringle, WSC, and CUB domains. Alternatively spliced transcript variants encoding distinct isoforms have been observed for this gene.[6]

Kremen1 also has a function in the induction of cell death by apoptosis.[8] This proapoptotic activity is conditional and depends on the absence of ligand Dickkopf1.[8] These observations led to the classification of this protein as a Dependence Receptor.

A mouse knock out of Kremen1 and its paralog Kremen2 is viable and fertile.[11]

References

Further reading

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