TMEM232 (transmembrane protein 232)

Gene Gene information from NCBI Gene database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID 642987
Gene name Transmembrane protein 232
Gene symbol TMEM232
Synonyms (NCBI Gene)
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Chromosome 5
Chromosome location 5q22.1
miRNA miRNA information provided by mirtarbase database.
4
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (4)
miRTarBase ID miRNA Experiments Reference
MIRT2130653 hsa-miR-200b CLIP-seq
MIRT2130654 hsa-miR-200c CLIP-seq
MIRT2130655 hsa-miR-338-5p CLIP-seq
MIRT2130656 hsa-miR-429 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide all (12)
GO ID Ontology Definition Evidence Reference
GO:0001520 Component Outer dense fiber IBA
GO:0001520 Component Outer dense fiber IEA
GO:0007283 Process Spermatogenesis IEA
GO:0007283 Process Spermatogenesis ISS
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
620143 37270 ENSG00000186952
Protein Protein information from UniProt database.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
C9JQI7
Protein name Transmembrane protein 232
Protein function Plays a critical role for male fertility and sperm motility by regulating sperm cytoplasm removal and maintaining axoneme integrity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15877 TMEM232 42 → 485 Transmembrane protein family 232 Family
Sequence
Sequence length 657
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (1)
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autism Uncertain significance rs1786159030 RCV003328507
Show/Hide Text Mining Associations (4)
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Asthma Associate 22545103
Dermatitis Atopic Associate 22545103, 28351738, 34750414, 39596646
Drug Hypersensitivity Associate 39596646
Multiple Sclerosis Associate 31064978