Gene Gene information from NCBI Gene database.
Entrez ID 339168
Gene name Transmembrane protein 95
Gene symbol TMEM95
Synonyms (NCBI Gene)
UNQ9390
Chromosome 17
Chromosome location 17p13.1
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT2131649 hsa-miR-298 CLIP-seq
MIRT2131650 hsa-miR-3154 CLIP-seq
MIRT2131651 hsa-miR-3179 CLIP-seq
MIRT2131652 hsa-miR-578 CLIP-seq
MIRT2352982 hsa-miR-1229 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0002080 Component Acrosomal membrane IBA
GO:0002080 Component Acrosomal membrane IEA
GO:0002080 Component Acrosomal membrane ISS
GO:0005515 Function Protein binding IPI 32296183, 32814053
GO:0007338 Process Single fertilization IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617814 27898 ENSG00000182896
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q3KNT9
Protein name Sperm-egg fusion protein TMEM95 (Transmembrane protein 95)
Protein function Sperm protein required for fusion of sperm with the egg membrane during fertilization.
PDB 7UX0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15203 TMEM95 17 167 TMEM95 family Family
Tissue specificity TISSUE SPECIFICITY: Spermatozoa (at protein level). {ECO:0000269|PubMed:36161911}.
Sequence
Sequence length 176
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
UTERINE FIBROID GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations