ZNF761

zinc finger protein 761, the group of Zinc fingers C2H2-type

Basic information

Region (hg38): 19:53431984-53461862

Links

ENSG00000160336NCBI:388561HGNC:23179Uniprot:Q86XN6AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the ZNF761 gene.

  • not_specified (21 variants)

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the ZNF761 gene is commonly pathogenic or not. These statistics are base on transcript: NM_001289951.2. Only rare variants are included in the table.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
19
clinvar
2
clinvar
21
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total 0 0 19 2 0
Loading clinvar variants...

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP

Function
FUNCTION: May be involved in transcriptional regulation. {ECO:0000250}.;
Pathway
Gene expression (Transcription);Generic Transcription Pathway;RNA Polymerase II Transcription (Consensus)

Haploinsufficiency Scores

pHI
0.0433
hipred
hipred_score
ghis

Mouse Genome Informatics

Gene name
Zfp51
Phenotype

Gene ontology

Biological process
regulation of transcription, DNA-templated
Cellular component
nucleus
Molecular function
DNA binding;metal ion binding