Ferm domain containing 4b

FERM domain containing 4B is a protein that in humans is encoded by the FRMD4B gene. [5]

FRMD4B
Identifiers
Aliases	FRMD4B, 6030440G05Rik, GRSP1, FERM domain containing 4B
External IDs	OMIM: 617467 MGI: 2141794 HomoloGene: 14916 GeneCards: FRMD4B
Gene location (Human) Chr. Chromosome 3 (human)[1] Band 3p14.1 Start 69,168,782 bp[1] End 69,542,583 bp[1]
Gene location (Mouse) Chr. Chromosome 6 (mouse)[2] Band 6|6 D3 Start 97,286,867 bp[2] End 97,617,541 bp[2]
Orthologs
Species	Human	Mouse
Entrez	23150	232288
Ensembl	ENSG00000114541	ENSMUSG00000030064
UniProt	Q9Y2L6	Q920B0
RefSeq (mRNA)	NM_015123	NM_145148 NM_001346637 NM_001346639
RefSeq (protein)	NP_055938	NP_001333566 NP_001333568 NP_660130
Location (UCSC)	Chr 3: 69.17 – 69.54 Mb	Chr 6: 97.29 – 97.62 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Function

This gene encodes a GRP1-binding protein which contains a FERM protein interaction domain as well as two coiled coil domains. This protein may play a role as a scaffolding protein.

References

1. GRCh38: Ensembl release 89: ENSG00000114541 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000030064 - Ensembl, 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. "Entrez Gene: FERM domain containing 4B". Retrieved 2017-05-16.

Further reading

• Talmud PJ, Drenos F, Shah S, Shah T, Palmen J, Verzilli C, Gaunt TR, Pallas J, Lovering R, Li K, Casas JP, Sofat R, Kumari M, Rodriguez S, Johnson T, Newhouse SJ, Dominiczak A, Samani NJ, Caulfield M, Sever P, Stanton A, Shields DC, Padmanabhan S, Melander O, Hastie C, Delles C, Ebrahim S, Marmot MG, Smith GD, Lawlor DA, Munroe PB, Day IN, Kivimaki M, Whittaker J, Humphries SE, Hingorani AD (2009). "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip". Am. J. Hum. Genet. 85 (5): 628–42. doi:10.1016/j.ajhg.2009.10.014. PMC 2775832. PMID 19913121.
• Cappola TP, Li M, He J, Ky B, Gilmore J, Qu L, Keating B, Reilly M, Kim CE, Glessner J, Frackelton E, Hakonarson H, Syed F, Hindes A, Matkovich SJ, Cresci S, Dorn GW (2010). "Common variants in HSPB7 and FRMD4B associated with advanced heart failure". Circ Cardiovasc Genet. 3 (2): 147–54. doi:10.1161/CIRCGENETICS.109.898395. PMC 2957840. PMID 20124441.
• Rose JE, Behm FM, Drgon T, Johnson C, Uhl GR (2010). "Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score". Mol. Med. 16 (7–8): 247–53. doi:10.2119/molmed.2009.00159. PMC 2896464. PMID 20379614.
• Bailey SD, Xie C, Do R, Montpetit A, Diaz R, Mohan V, Keavney B, Yusuf S, Gerstein HC, Engert JC, Anand S (2010). "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study". Diabetes Care. 33 (10): 2250–3. doi:10.2337/dc10-0452. PMC 2945168. PMID 20628086.
• Matkovich SJ, Van Booven DJ, Cappola TP, Dorn GW (2010). "Association of an intronic, but not any exonic, FRMD4B sequence variant and heart failure". Clin Transl Sci. 3 (4): 134–9. doi:10.1111/j.1752-8062.2010.00220.x. PMC 2925316. PMID 20718813.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.