Gene Symbol:
TCIRG1
HGNC:11647
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
11q13.2
Filters:

Definitive classifications

autosomal recessive osteopetrosis 1
AR
09/28/2023
Evaluated
10/18/2023
Submitted
autosomal recessive osteopetrosis
AR
08/06/2018
Evaluated
10/13/2020
Submitted

Strong classifications

autosomal recessive osteopetrosis 1
Submitted as: OMIM:259700
AR
09/21/2020
Evaluated
03/31/2021
Submitted
autosomal recessive osteopetrosis 1
Submitted as: OMIM:259700
AR
05/04/2023
Evaluated
11/30/2023
Submitted

Supportive classifications

autosomal dominant severe congenital neutropenia
Submitted as: Orphanet:486
AD
09/14/2021
Evaluated
09/14/2021
Submitted
dysosteosclerosis
Submitted as: Orphanet:1782
AR
09/14/2021
Evaluated
09/14/2021
Submitted
autosomal recessive osteopetrosis
Submitted as: Orphanet:667
AR
09/14/2021
Evaluated
09/14/2021
Submitted
autosomal recessive osteopetrosis 6
Submitted as: Orphanet:210110
AR
09/14/2021
Evaluated
09/14/2021
Submitted

The GenCC data are available free of restriction under a CC0 1.0 Universal (CC0 1.0) Public Domain Dedication. The GenCC requests that you give attribution to GenCC and the contributing sources whenever possible and appropriate. The accepted Flagship manuscript is now available from Genetics in Medicine (https://www.gimjournal.org/article/S1098-3600(22)00746-8/fulltext).

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. The GenCC does not independently verify the submitted information. Though the information is obtained from sources believed to be reliable, no warranty, expressed or implied, is made regarding accuracy, adequacy, completeness, reliability or usefulness of any information. This disclaimer applies to both isolated and aggregate uses of the information. The information is provided on an "as is" basis, collected through periodic submission and therefore may not represent the most up-to-date information from the submitters. If you have questions about the medical relevance of information contained on this website, please see a healthcare professional; if you have questions about specific gene-disease claims, please contact the relevant sources; and if you have questions about the representation of the data on this website, please contact gencc@thegencc.org.