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

FNBP4
Identifiers
AliasesFNBP4, FBP30, formin binding protein 4
External IDsOMIM: 615265; MGI: 1860513; HomoloGene: 9087; GeneCards: FNBP4; OMA:FNBP4 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_015308
NM_001318339

NM_018828

RefSeq (protein)

NP_001305268
NP_056123

NP_061298

Location (UCSC)Chr 11: 47.72 – 47.77 MbChr 2: 90.75 – 90.78 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Mutations in this gene have been found associated to cases similar to microphthalmia with limb anomalies (doi: 10.1002/ajmg.a.35983).


References

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  1. ^ a b c ENSG00000285182 GRCh38: Ensembl release 89: ENSG00000109920, ENSG00000285182Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000008200Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ 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.
  6. ^ "Entrez Gene: FNBP4 formin binding protein 4".

Further reading

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