FNBP4

Formin-binding protein 4 is a protein that in humans is encoded by the FNBP4 gene.^[5][6]

FNBP4
Identifiers
Aliases	FNBP4, FBP30, formin binding protein 4
External IDs	OMIM: 615265; MGI: 1860513; HomoloGene: 9087; GeneCards: FNBP4; OMA:FNBP4 - orthologs
Gene location (Human) Chr. Chromosome 11 (human)[1] Band 11p11.2 Start 47,716,494 bp[1] End 47,767,443 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 E1 Start 90,745,370 bp[2] End 90,781,021 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in sural nerve gastric mucosa Achilles tendon left ovary body of uterus right ovary canal of the cervix body of pancreas right uterine tube left lobe of thyroid gland Top expressed in tail of embryo neural layer of retina genital tubercle spermatocyte ventricular zone zygote granulocyte cerebellar cortex thymus neural tube More reference expression data BioGPS More reference expression data
Orthologs Species Human Mouse Entrez 23360 55935 Ensembl ENSG00000109920 ENSG00000285182 ENSMUSG00000008200 UniProt Q8N3X1 Q6ZQ03 RefSeq (mRNA) NM_015308 NM_001318339 NM_018828 RefSeq (protein) NP_001305268 NP_056123 NP_061298 Location (UCSC) Chr 11: 47.72 – 47.77 Mb Chr 2: 90.75 – 90.78 Mb PubMed search [3] [4]
Wikidata
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Mutations in this gene have been found associated to cases similar to microphthalmia with limb anomalies (doi: 10.1002/ajmg.a.35983).