MOSPD3 (motile sperm domain containing 3)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 64598 |
| Gene name | Motile sperm domain containing 3 |
| Gene symbol | MOSPD3 |
| Synonyms (NCBI Gene) |
CDS3NET30
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| Chromosome | 7 |
| Chromosome location | 7q22.1 |
| Summary | This gene encodes a multi-pass membrane protein with a major sperm protein (MSP) domain. The deletion of a similar mouse gene is associated with defective cardiac development and neonatal lethality. Alternate transcriptional splice variants, encoding diff |
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miRNA
miRNA information provided by mirtarbase database.
2
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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O75425 | ||||||||||
| Protein name | Motile sperm domain-containing protein 3 | ||||||||||
| Family and domains |
Pfam
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| Sequence |
MRRGAPQDQELVGPGPPGRGSRGAPPPLGPVVPVLVFPPDLVFRADQRSGPRQLLTLYNP |
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| Sequence length | 235 | ||||||||||
| Interactions | View interactions | ||||||||||
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Related Genes
Genes most often co-reported with MOSPD3 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to MOSPD3 (see Related Genes above), that are NOT already directly curated for MOSPD3 itself -- a lead worth checking, not a confirmed association.
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