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Protein-coding gene in the species Homo sapiens
Formin-binding protein 4 is a protein that in humans is encoded by the FNBP4 gene .[ 5] [ 6]
Mutations in this gene have been found associated to cases similar to microphthalmia with limb anomalies (doi: 10.1002/ajmg.a.35983).
^ a b c ENSG00000285182 GRCh38: Ensembl release 89: ENSG00000109920, ENSG00000285182 – Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000008200 – Ensembl , May 2017^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Jul 1999). "Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro" . DNA Res . 6 (1): 63–70. doi :10.1093/dnares/6.1.63 PMID 10231032 . ^ "Entrez Gene: FNBP4 formin binding protein 4" .
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