MYT1

Source: Wikipedia, the free encyclopedia.

MYT1
Available structures
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Ensembl
UniProt
RefSeq (mRNA)

NM_004535

NM_001171615
NM_001171616
NM_001171680
NM_008665

RefSeq (protein)

NP_004526

NP_001165086
NP_001165087
NP_001165151
NP_032691

Location (UCSC)Chr 20: 64.1 – 64.24 MbChr 2: 181.76 – 181.83 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Myelin transcription factor 1 is a protein that in humans is encoded by the MYT1 gene.[5][6][7]

Function

The protein encoded by this gene is a member of a family of neural specific, zinc finger-containing DNA-binding proteins. The protein binds to the promoter regions of proteolipid proteins of the central nervous system and plays a role in the developing nervous system.[7]

Interactive pathway map

Click on genes, proteins and metabolites below to visit related articles. [§ 1]

[[File:
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MECP2_and_Associated_Rett_Syndrome_WP3584Go to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to WikiPathwaysGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to miRBaseGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to Entrez GeneGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to articleGo to article
|alt=MECP2 and associated Rett Syndrome edit]]
MECP2 and associated Rett Syndrome edit
  1. ^ The interactive pathway map can be edited at WikiPathways: "WP3584".

Interactions

MYT1 has been shown to

interact with PIN1.[8]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000196132Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000010505Ensembl, 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. PMID 1280325
    .
  6. .
  7. ^ a b "Entrez Gene: MYT1 myelin transcription factor 1".
  8. PMID 10504341
    .

Further reading

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


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