Results for the protein: P0C862

Results for the Protein: P0C862

205686199

338872

C1QTNF9

NCBI, UniProt

C1T9A_HUMAN RecName: Full=Complement C1q and tumor necrosis factor-related protein 9A; AltName: Full=Complement C1q and tumor necrosis factor-related protein 9; Flags: Precursor

			0 6 0 6 0

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Default View: Collagen - pfam01391 C1Q - smart00110 C1q - pfam00386	Swiss-Prot Protein: P0C862 Identical to: NP_848635 Default View:

Domains found on the Protein

Domain ↕	CD Accession ↕	E-Value ↕	Start ↕	End ↕
Collagen	pfam01391	6.2e-09	84	133
Collagen	pfam01391	2.5e-12	134	193
C1q	pfam00386	5.5e-64	203	329
C1Q	smart00110	7.8e-56	195	332

Table of Mutations found on the Protein

Source ↕	Mut_ID ↕	Class ↕	HGVS ↕	Disease ↕
dbSNP	rs202198487	Polymorphism	p.ARG178GLN	N/A
dbSNP	rs78083136	Polymorphism	p.CYS243SER	N/A
dbSNP	rs1974332	Polymorphism	p.LEU6PHE	N/A
dbSNP	rs3751357	Polymorphism	p.MET219VAL	N/A
dbSNP	rs77554188	Polymorphism	p.MET281VAL	N/A
dbSNP	rs4589405	Polymorphism	p.VAL301MET	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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