Selected-GenAtlas references | SOURCE | GeneCards | NCBI Gene | Swiss-Prot | Orphanet | Ensembl |
HGNC | UniGene | Nucleotide | OMIM | UCSC |
Home Page |
FLASH GENE |
Symbol | FOXI1 | contributors: - updated : 23-05-2007 |
HGNC name | forkhead box I1 |
HGNC id | 3815 |
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ANIMAL & CELL MODELS |
mice with a targetted disruption of Frhl10 have a gross structural malformation of the cochlea and vestibulum replaced by a single irregular cavity |