Gene Symbol:
WFS1
HGNC:12762
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
4p16.1
Filters:

Definitive classifications

Wolfram-like syndrome
Submitted as: OMIM:614296
AD
10/21/2022
Evaluated
08/19/2023
Submitted
Wolfram syndrome 1
Submitted as: OMIM:222300
AR
07/16/2020
Evaluated
09/11/2023
Submitted
Wolfram-like syndrome
Submitted as: OMIM:614296
AD
07/16/2020
Evaluated
09/11/2023
Submitted
AR
04/17/2018
Evaluated
10/18/2023
Submitted
Wolfram-like syndrome
AD
04/17/2018
Evaluated
10/18/2023
Submitted

Strong classifications

Wolfram syndrome 1
Submitted as: OMIM:222300
AR
10/09/2020
Evaluated
11/09/2020
Submitted
Wolfram syndrome 1
Submitted as: OMIM:222300
AR
09/28/2023
Evaluated
11/30/2023
Submitted
autosomal dominant nonsyndromic hearing loss 6
Submitted as: OMIM:600965
AD
04/12/2023
Evaluated
11/30/2023
Submitted
AD
03/29/2023
Evaluated
11/30/2023
Submitted
Wolfram-like syndrome
Submitted as: OMIM:614296
AD
06/22/2023
Evaluated
11/30/2023
Submitted
Wolfram-like syndrome
Submitted as: OMIM:614296
AD
10/09/2020
Evaluated
11/09/2020
Submitted
Wolfram syndrome 1
Submitted as: OMIM:222300
AR
01/29/2021
Evaluated
03/31/2021
Submitted
Wolfram-like syndrome
Submitted as: OMIM:614296
AD
01/29/2021
Evaluated
03/31/2021
Submitted

Supportive classifications

early-onset nuclear cataract
Submitted as: Orphanet:98991
AD
09/14/2021
Evaluated
09/14/2021
Submitted
autosomal dominant nonsyndromic hearing loss
Submitted as: Orphanet:90635
AD
09/14/2021
Evaluated
09/14/2021
Submitted
Wolfram syndrome
Submitted as: Orphanet:3463
AR
09/14/2021
Evaluated
09/14/2021
Submitted
Wolfram-like syndrome
Submitted as: Orphanet:411590
AD
09/14/2021
Evaluated
09/14/2021
Submitted

Limited classifications

AD
08/30/2017
Evaluated
09/11/2023
Submitted
type 2 diabetes mellitus
Submitted as: OMIM:125853
Unknown
02/02/2022
Evaluated
11/30/2023
Submitted

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