Metazoan complexes |
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Emili & Marcotte labs |
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Details of FGF3 gene in Homo sapiens
IDs | |||||||||
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Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| FGF3 | INT2 | P11487 | FGF3_HUMAN | 2248 | ENSG00000186895 ENSG00000261155 | Fibroblast growth factor 3 | SPROT |
Disease | |||||||||
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Disease | OMIM id | ||||||||
Deafness with labyrinthine aplasia, microtia and microdontia (LAMM) [MIM:610706]: Unique autosomal recessive syndrome characterized by type I microtia, microdontia, and profound congenital deafness associated with a complete absence of inner ear structures (Michel aplasia). Note=The disease is caused by mutations affecting the gene represented in this entry. | 610706 |
Orthologs in other species | |||||||||
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M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
ENSMUSG00000031074 | --- | --- | Sp-Fgf9/16/20 |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
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