Gene Gene information from NCBI Gene database.
Entrez ID 346673
Gene name Stimulated by retinoic acid 8
Gene symbol STRA8
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7q33
Summary This gene encodes a retinoic acid-responsive protein. A homologous protein in mouse has been shown to be involved in the regulation of meiotic initiation in both spermatogenesis and oogenesis, though feature differences between the mouse and human protein
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
24
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IDA 22899867
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus ISS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
609987 30653 ENSG00000146857
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7Z7C7
Protein name Stimulated by retinoic acid gene 8 protein homolog
Protein function Meiosis-inducer required for the transition into meiosis for both female and male germ cells. In female germ cells, acts downstream of ZGLP1 as a key effector of the meiotic program: required for premeiotic DNA replication and subsequent events
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed specifically in testis and fetal ovaries. {ECO:0000269|PubMed:12489526, ECO:0000269|PubMed:26742488}.
Sequence
MGKIDVDKILFFNQEIRLWQLIMATPEENSNPHDRATPQLPAQLQELEHRVARRRLSQAR
HRATLAALFNNLRKTVYSQSDLIASKWQVLNKAKSHIPELEQTLDNLLKLKASFNLEDGH
ASSLEEVKKEYASMYSGNDSFPQNGSSPWYLNFYKQTMDLLTGSGIITPQEAALPIVSAA
ISHLWQNLSEERKASLRQAWAQKHRGPATLAEACREPACAEGSVKDSGVDSQGASCSLVS
TPEEILFEDAFDVASFLDKSEVPSTSSSSSVLASCNPENPEEKFQLYMQIINFFKGLSCA
NTQVKQEASFPVDEEMIMLQCTETFDDEDL
Sequence length 330
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Arrest of spermatogenesis Associate 37867192
★☆☆☆☆
Found in Text Mining only
Azoospermia Associate 23320086
★☆☆☆☆
Found in Text Mining only
Infertility Associate 37867192
★☆☆☆☆
Found in Text Mining only
Male Infertility with Large Headed Multiflagellar Polyploid Spermatozoa Associate 24803180
★☆☆☆☆
Found in Text Mining only
Oligospermia Associate 23320086
★☆☆☆☆
Found in Text Mining only
Primary Ovarian Insufficiency Associate 36732629
★☆☆☆☆
Found in Text Mining only
Spermatogenic Failure Nonobstructive Y Linked Associate 23320086
★☆☆☆☆
Found in Text Mining only