RLN1 (relaxin 1)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 6013 |
| Gene name | Relaxin 1 |
| Gene symbol | RLN1 |
| Synonyms (NCBI Gene) |
H1H1RLXRLXH1bA12D24.3.1bA12D24.3.2
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| Chromosome | 9 |
| Chromosome location | 9p24.1 |
| Summary | Relaxins are known endocrine and autocrine/paracrine hormones, belonging to the insulin gene superfamily. In humans there are three non-allelic relaxin genes, RLN1, RLN2 and RLN3, where RLN1 and RLN2 share high sequence homology. The protein encoded by th |
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miRNA
miRNA information provided by mirtarbase database.
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Transcription factors
Transcription factors information provided by TRRUST V2 database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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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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P04808 | ||||||||||
| Protein name | Prorelaxin H1 [Cleaved into: Relaxin B chain; Relaxin A chain] | ||||||||||
| Protein function | Relaxin is an ovarian hormone that acts with estrogen to produce dilatation of the birth canal in many mammals. May be involved in remodeling of connective tissues during pregnancy, promoting growth of pubic ligaments and ripening of the cervix. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Prostate. Not expressed in placenta, decidua or ovary. {ECO:0000269|PubMed:8735594}. | ||||||||||
| Sequence | |||||||||||
| Sequence length | 185 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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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)
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Related Genes
Genes most often co-reported with RLN1 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to RLN1 (see Related Genes above), that are NOT already directly curated for RLN1 itself -- a lead worth checking, not a confirmed association.
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