TMEM232 (transmembrane protein 232)

Gene
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
642987
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 232
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM232
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q22.1
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene miRNA Gene ontology Other IDs Protein Associated diseases
MIM HGNC e!Ensembl
620143 37270 ENSG00000186952
Protein
Gene miRNA Gene ontology Other IDs Protein Associated diseases
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Gene miRNA Gene ontology Other IDs Protein Associated diseases
Show/Hide Unknown Diseases (2)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Asthma Asthma (childhood onset), Atopic asthma N/A N/A GWAS
Astrocytoma Pilocytic astrocytoma N/A N/A GWAS
Show/Hide Text Mining Associations (4)
Associations from Text Mining Disease 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