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MAB21L2

From Wikipedia, the free encyclopedia
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
View/Edit HumanView/Edit Mouse

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

Function

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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

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000181541Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000057777Ensembl, 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. ^ "Entrez Gene: Mab-21-like 2 (C. elegans)".

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.