Gene Gene information from NCBI Gene database.
Entrez ID 86614
Gene name Heat shock transcription factor Y-linked 1
Gene symbol HSFY1
Synonyms (NCBI Gene)
HSF2LHSFY
Chromosome Y
Chromosome location Yq11.222
Summary This gene encodes a member of the heat shock factor (HSF) family of transcriptional activators for heat shock proteins. This gene is a candidate gene for azoospermia, since it localizes to a region of chromosome Y that is sometimes deleted in infertile ma
miRNA miRNA information provided by mirtarbase database.
10
miRTarBase ID miRNA Experiments Reference
MIRT1055745 hsa-miR-3942-3p CLIP-seq
MIRT1055746 hsa-miR-578 CLIP-seq
MIRT2548066 hsa-miR-129-5p CLIP-seq
MIRT2548067 hsa-miR-2909 CLIP-seq
MIRT2548068 hsa-miR-296-3p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0003677 Function DNA binding IEA
GO:0003700 Function DNA-binding transcription factor activity IEA
GO:0005515 Function Protein binding IPI 24722188, 25416956, 25910212, 26871637, 29892012, 31515488, 32296183, 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
400029 18568 ENSG00000172468
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SPERMATOGENIC FAILURE, Y-LINKED, 2 ClinVar, HPO
ClinVar, HPO
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Azoospermia Azoospermia BEFREE 15044259
★☆☆☆☆
Found in Text Mining only
Azoospermia Azoospermia Pubtator 22820855 Stimulate
★☆☆☆☆
Found in Text Mining only
Azoospermia Azoospermia HPO_DG
★☆☆☆☆
Found in Text Mining only
Azoospermia Nonobstructive Nonobstructive azoospermia Pubtator 21676392, 22820855 Associate
★☆☆☆☆
Found in Text Mining only
Azoospermia, Nonobstructive Azoospermia BEFREE 22820855
★☆☆☆☆
Found in Text Mining only
Obstructive azoospermia Obstructive azoospermia BEFREE 22820855
★☆☆☆☆
Found in Text Mining only
Oligospermia Oligospermia BEFREE 15044259
★☆☆☆☆
Found in Text Mining only
Spermatogenic Failure, Nonobstructive, Y-Linked Nonobstructive Spermatogenic Failure, Y-Linked CTD_human_DG
★★☆☆☆
Found in Text Mining + Unknown/Other Associations