MAB21L2

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

Mab-21-like 2 (C. elegans) is a protein that in humans is encoded by the MAB21L2 gene.[5]

AliasesMAB21L2, MCOPS14, Mab-21-like 2 (C. elegans), mab-21 like 2, MCSKS14
End150,584,693 bp[1]
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MAB21L2
Identifiers
AliasesMAB21L2, MCOPS14, Mab-21-like 2 (C. elegans), mab-21 like 2, MCSKS14
External IDsOMIM: 604357; MGI: 1346022; HomoloGene: 7824; GeneCards: MAB21L2; OMA:MAB21L2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_006439

NM_011839

RefSeq (protein)

NP_006430

NP_035969

Location (UCSC)Chr 4: 150.58 – 150.58 MbChr 3: 86.45 – 86.46 Mb
PubMed search[3][4]
Wikidata
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Function

This gene is similar to the C. elegans MAB-21 cell fate-determining gene, a downstream target of transforming growth factor-beta signaling. It is thought that this gene may be involved in neural development. The protein encoded by this gene is primarily nuclear, although some cytoplasmic localization has been observed. [provided by RefSeq, Jul 2008].

References

Further reading

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