Entity Details
Primary name |
CTSR2_HUMAN |
Entity type |
UniProt |
Source |
Source Link |
Details
Accession | Q96P56 |
EntryName | CTSR2_HUMAN |
FullName | Cation channel sperm-associated protein 2 |
TaxID | 9606 |
Evidence | evidence at protein level |
Length | 530 |
SequenceStatus | complete |
DateCreated | 2007-07-24 |
DateModified | 2021-06-02 |
Subcellular Location
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Subcellular Location |
Cell projection |
Domains
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Domain | Name | Category | Type |
IPR005821 | Ion transport domain | Domain | Domain |
IPR027359 | Voltage-dependent channel domain superfamily | Family | Homologous superfamily |
IPR028747 | Cation channel sperm-associated protein 2 | Family | Family |
Diseases
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Disease ID | Source | Name | Description |
611102 | OMIM | Deafness-infertility syndrome (DIS) | Characterized by deafness and infertility and is caused by large contiguous gene deletions at 15q15.3 that removes both STRC and CATSPER2 genes. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
1 interaction