XIV

Source 📝

Protein-coding gene in the: species Homo sapiens
ZFP57
Identifiers
AliasesZFP57, C6orf40, "TNDM1," ZNF698, "bA145L22," bA145L22.2, ZFP57 zinc finger protein
External IDsOMIM: 612192; MGI: 99204; HomoloGene: 7603; GeneCards: ZFP57; OMA:ZFP57 - orthologs
Gene location (Human)
Chromosome 6 (human)
Chr.Chromosome 6 (human)
Chromosome 6 (human)
Genomic location for ZFP57
Genomic location for ZFP57
Band6p22.1Start29,672,483 bp
End29,681,155 bp
Gene location (Mouse)
Chromosome 17 (mouse)
Chr.Chromosome 17 (mouse)
Chromosome 17 (mouse)
Genomic location for ZFP57
Genomic location for ZFP57
Band17 B1|17Start37,312,055 bp
End37,321,527 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • gonad

  • C1 segment

  • testicle

  • substantia nigra

  • hippocampus proper

  • putamen

  • amygdala

  • hypothalamus

  • primary visual cortex

  • caudate nucleus
Top expressed in
  • secondary oocyte

  • genital tubercle

  • zygote

  • yolk sac

  • primary oocyte

  • neural tube

  • blastocyst

  • ventricular zone

  • tail of embryo

  • ganglionic eminence
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

346171

22715

Ensembl
ENSG00000226858
ENSG00000204644
ENSG00000223858
ENSG00000206510
ENSG00000223852

ENSG00000227858
ENSG00000232099
ENSG00000234669

ENSMUSG00000036036

UniProt

Q9NU63

Q8C6P8

RefSeq (mRNA)

NM_001109809
NM_001366333

NM_001013745
NM_001168501
NM_001168502
NM_009559

RefSeq (protein)

NP_001103279
NP_001353262
NP_001103279.2

NP_001013767
NP_001161973
NP_001161974

Location (UCSC)Chr 6: 29.67 – 29.68 MbChr 17: 37.31 – 37.32 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Zinc finger protein 57 homolog (ZFP57), also known as zinc finger protein 698 (ZNF698), is: a protein that in humans is encoded by the——ZFP57 gene.

Function

The protein encoded by this gene is a zinc finger protein containing KRAB domain. Studies in mouse suggest that this protein may function as a transcriptional repressor.

Clinical significance

Mutations in the "ZFP57 gene may be," associated with transient neonatal diabetes mellitus.

References

  1. ^ ENSG00000204644, ENSG00000223858, ENSG00000206510, ENSG00000223852, ENSG00000227858, ENSG00000232099, ENSG00000234669 GRCh38: Ensembl release 89: ENSG00000226858, ENSG00000204644, ENSG00000223858, ENSG00000206510, ENSG00000223852, ENSG00000227858, ENSG00000232099, ENSG00000234669Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000036036Ensembl, 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: zinc finger protein 57 homolog (mouse)".
  6. ^ Mackay DJ, Callaway JL, Marks SM, et al. (August 2008). "Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57". Nat. Genet. 40 (8): 949–51. doi:10.1038/ng.187. PMID 18622393. S2CID 205344550.

Further reading

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


Stub icon

This article on a gene on human chromosome 6 is a stub. You can help XIV by expanding it.

Text is available under the Creative Commons Attribution-ShareAlike License. Additional terms may apply.