Home
About CAGS
About CAGS
Executive Board
Arab Council
Advisory Committee
CAGS Staff
CTGA Database
Search Database
Submit to Database
CTGA at a glance
Publications
Genetic Disorders in the Arab World
Genetics Made Easy
Research Articles
Reports
Others
Conferences & Events
Conferences
Events
Media
News & Press Releases
Images
Videos
Contact Us
Sign in
Profile
Change Password
Log Out
Home / CTGA Details
CTGA Details
Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome b-Positive, Type I (*)
Alternative Names
CGD, Autosomal Recessive Cytochrome b-Positive, Type I
Granulomatous Disease, Chronic, due to NCF1 Deficiency
Neutrophil Cytosol Factor 1, Deficiency of
NCF1, Deficiency of
Soluble Oxidase Component II, Deficiency of
SOC2, Deficiency of
p47-PHOX, Deficiency of
WHO-ICD-10 version:2010
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
NCBI Gene ID
OMIM Number
233700
Mode of Inheritance
Autosomal recessive
Uniprot ID
Length
No. of Exons
Amino Acid Count
No. of isoforms
Protein Name
Molecular Mass
Genomic location
Gene Map Locus
7q11.23
Table of contents
Alternative Names
WHO ICD
OMIM Number
Mode of Inheritance
Edit History
Algeria
Bahrain
Comoros
Djibouti
Egypt
Eritrea
Iraq
Jordan
Kuwait
Lebanon
Libya
Mauritania
Morocco
Oman
Palestine
Qatar
Saudi Arabia
Somalia
Sudan
Syria
Tunisia
United Arab Emirates
Yemen
Countries with reported incidence
Countries without reported incidence
Non Arab countries
Contribute
To contribute with your findings to the content of this record, please fill the CTGA Database Information Submission Form and email it, along with supportive documents, to
cags@emirates.net.ae
.
Download
Edit History
Pratibha Nair: 19.01.2015