Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79663
Gene name Gene Name - the full gene name approved by the HGNC.
HSPB1 associated protein 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HSPBAP1
Synonyms (NCBI Gene) Gene synonyms aliases
PASS1
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3q21.1
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a protein that binds to one of the small heat shock proteins, specifically hsp27. Hsp27 is involved with cell growth and differentiation. This encoded protein was found to be abnormally expressed in patients with intractable epilepsy, al
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT024673 hsa-miR-215-5p Microarray 19074876
MIRT026793 hsa-miR-192-5p Microarray 19074876
MIRT1056599 hsa-miR-1 CLIP-seq
MIRT1056600 hsa-miR-1276 CLIP-seq
MIRT1056601 hsa-miR-206 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 24981860, 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0016706 Function 2-oxoglutarate-dependent dioxygenase activity IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
608263 16389 ENSG00000169087
Protein
UniProt ID Q96EW2
Protein name HSPB1-associated protein 1 (27 kDa heat shock protein-associated protein 1) (Protein associated with small stress protein 1)
Protein function May play a role in cellular stress response.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13621 Cupin_8 30 279 Cupin-like domain Domain
Tissue specificity TISSUE SPECIFICITY: Widely expressed. {ECO:0000269|PubMed:11978969}.
Sequence
MAAGSEATTPVIVAAGAGGEEGEHVKPFKPEKAKEIIMSLQQPAIFCNMVFDWPARHWNA
KYLSQVLHGKQIRFRMGMKSMSTVPQFETTCNYVEATLEEFLTWNCDQSSISGPFRDYDH
SKFWAYADYKYFVSLFEDKTDLFQDVKWSDFGFPGRNGQESTLWIGSLGAHTPCHLDSYG
CNLVFQVQGRKRWHLFPPEDTPFLYPTRIPYEESSVFSKINVVNPDLKRFPQFRKAQRHA
VTLSPGQVLFVPRHWWHYVESIDPVTVSINSWIELEEDH
LARVEEAITRMLVCALKTAEN
PQNTRAWLNPTEVEETSHAVNCCYLNAAVSAFFDRCRTSEVVEIQALRTDGEHMKKEELN
VCNHMEVGQTGSQNLTTGTDKPEAASPFGPDLVPVAQRSEEPPSERGGIFGSDGKDFVDK
DGEHFGKLHCAKRQQIMSNSENAIEEQIASNTTTTPQTFISTDDLLDCLVNPQVTRIVAQ
LLIQGRSL
Sequence length 488
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Hereditary renal carcinoma Hereditary clear cell renal cell carcinoma 12939738 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Hepatocellular Associate 25798051
Neoplasms Associate 25798051
pediatric multisystem inflammatory disease COVID 19 related Associate 37255317