WBSCR27 Products

Antibodies
WBSCR27 Antibody
WBSCR27 Antibody
NBP1-86008
Species: Hu
Applications: WB, ICC/IF, IHC, IHC-P
Host: Rabbit Polyclonal
Lysates
WBSCR27 Overexpression Lysate ...
WBSCR27 Overexpression Lysate (Nat...
NBL1-17786
Applications: WB
Proteins
WBSCR27 Recombinant Protein
WBSCR27 Recombinant Protein
H00155368-P01
Species: Hu
Applications: WB, ELISA, PA
WBSCR27 Recombinant Protein A ...
WBSCR27 Recombinant Protein Antigen
NBP1-86008PEP
Species: Hu
Applications: AC

Description

WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq]

Bioinformatics

Entrez Human
Uniprot Human
Human
Human
Product By Gene ID 155368
Alternate Names
  • Williams-Beuren syndrome chromosomal region 27 protein
  • MGC40131
  • Williams Beuren syndrome chromosome region 27

Diseases related to WBSCR27

Discover more about diseases related to WBSCR27.

Mutation, Out-of-frame

Bioinformatics Tool for WBSCR27

Discover related pathways, diseases and genes to WBSCR27. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
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