Results for the protein: Q86XK2

Results for the Protein: Q86XK2

124012093

80204

FBXO11

NCBI, UniProt

FBX11_HUMAN RecName: Full=F-box only protein 11; AltName: Full=Protein arginine N-methyltransferase 9; AltName: Full=Vitiligo-associated protein 1; Short=VIT-1

			0 7 0 2 5

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Default View: F-box - pfam00646 FBOX - smart00256 CASH - smart00722 ZnF_UBR1 - smart00396 zf-UBR - pfam02207	Swiss-Prot Protein: Q86XK2 Identical to: NP_001177203 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
zf-UBR	pfam02207	2.7e-15	838	903
FBOX	smart00256	7.8e-10	159	199
CASH	smart00722	1.8e-08	418	554
CASH	smart00722	3e-10	708	837
ZnF_UBR1	smart00396	1.5e-08	838	903

Table of Mutations found on the Protein

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
Swiss-Prot	VAR_070075	Polymorphism	p.GLY684GLU	N/A
Swiss-Prot	VAR_070076	Polymorphism	p.LYS715ASN	N/A
Swiss-Prot	VAR_070077	Polymorphism	p.LYS715GLN	N/A
dbSNP	rs61742810	Polymorphism	p.THR325ALA	N/A
dbSNP	rs17036993	Polymorphism	p.THR126SER	N/A
Swiss-Prot	VAR_070073	Polymorphism	p.TYR206CYS	N/A
Swiss-Prot	VAR_070074	Polymorphism	p.TYR644CYS	N/A

Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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