HSP90AB3P

heat shock protein 90 alpha family class B member 3, pseudogene

Basic information

Previous symbols: [ "HSPCP1" ]

Links

ENSG00000183199NCBI:3327HGNC:5259Uniprot:Q58FF7AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the HSP90AB3P gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the HSP90AB3P gene is commonly pathogenic or not.

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.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
0
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 0 0 0

GnomAD

Source: gnomAD

dbNSFP

Source: dbNSFP

Function
FUNCTION: Putative molecular chaperone that may promote the maturation, structural maintenance and proper regulation of specific target proteins. {ECO:0000250}.;

Haploinsufficiency Scores

pHI
0.133
hipred
hipred_score
ghis

Gene ontology

Biological process
protein folding;biological_process;negative regulation of proteasomal protein catabolic process;regulation of cellular protein localization
Cellular component
cytoplasm;cytosol;extracellular exosome
Molecular function
molecular_function;protein binding;ATP binding;protein kinase binding;unfolded protein binding