HSP90AA5P (heat shock protein 90 alpha family class A member 5, pseudogene)

Gene
Gene Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
730211
Gene name Gene Name - the full gene name approved by the HGNC.
Heat shock protein 90 alpha family class A member 5, pseudogene
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HSP90AA5P
Synonyms (NCBI Gene) Gene synonyms aliases
HSP90Ae
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q27.1
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide all(4)
GO ID Ontology Definition Evidence Reference
GO:0005524 Function ATP binding IEA
GO:0005737 Component Cytoplasm IEA
GO:0006457 Process Protein folding IEA
GO:0051082 Function Unfolded protein binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
HGNC 32535 N/A
Protein
Gene Gene ontology Other IDs Protein Associated diseases
UniProt ID Q58FG0
Protein name Putative heat shock protein HSP 90-alpha A5 (Heat shock protein 90-alpha E) (Heat shock protein 90Ae)
Protein function Putative molecular chaperone that may promote the maturation, structural maintenance and proper regulation of specific target proteins.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00183 HSP90 26 → 164 Hsp90 protein Family
PF00183 HSP90 159 → 280 Hsp90 protein Family
Sequence 
MGFHHVGQAGLELLTSGHPALERRPEYLEERRIKEIVKKHSQFIGYPITLFVEKKRNKQV
SDAEAEKKEDKRKKKKESNDKPEIEDVGSDEEEEKKDADKKKKKSKEKYIDQELNKTKPI
WTRNPDAITNEEYGEFHQSLTNNWEDHLAVKHFSVEGQLEELKDSRRVMKANQKHIYYIT
GETKDQVANSAFVECLQKHGLEVIYMIELIDKYCVQQLKELESKTVVSVAKEGLELPEDE
EEKKKQEEKKTKFENLCKIMKDMLEKKVKKVVVSNCMEDPQRHTNKIYRMIKLGLGVDEY
DPTANDINAAITKEMPPLRGGDDTSRMEEVGGSG
Sequence length 334
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene Gene ontology Other IDs Protein Associated diseases
Show/Hide Causal Diseases (1)
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959