Gene Symbol:
MET
HGNC:7029
Locus Group:
protein-coding gene
Locus Type:
gene with protein product
Location:
7q31.2
Filters:

Definitive classifications

hereditary papillary renal cell carcinoma
Submitted as: OMIM:605074
AD
05/09/2023
Evaluated
08/19/2023
Submitted
hereditary papillary renal cell carcinoma
Submitted as: OMIM:605074
AD
11/29/2016
Evaluated
09/11/2023
Submitted
papillary renal cell carcinoma
AD
10/11/2018
Evaluated
04/21/2024
Submitted

Strong classifications

papillary renal cell carcinoma
Submitted as: OMIM:605074
AD
03/04/2020
Evaluated
03/31/2021
Submitted
autosomal recessive nonsyndromic hearing loss 97
Submitted as: OMIM:616705
AR
12/15/2018
Evaluated
11/30/2023
Submitted
hereditary papillary renal cell carcinoma
Submitted as: OMIM:605074
AD
03/05/2023
Evaluated
11/30/2023
Submitted

Supportive classifications

papillary renal cell carcinoma
Submitted as: Orphanet:47044
AD
09/14/2021
Evaluated
09/14/2021
Submitted
hearing loss, autosomal recessive
Submitted as: Orphanet:90636
AR
09/14/2021
Evaluated
09/14/2021
Submitted
osteofibrous dysplasia
Submitted as: Orphanet:488265
AD
09/14/2021
Evaluated
09/14/2021
Submitted

Limited classifications

autosomal recessive nonsyndromic hearing loss 97
Submitted as: OMIM:616705
AR
10/09/2020
Evaluated
11/09/2020
Submitted
osteofibrous dysplasia
Submitted as: OMIM:607278
AD
06/12/2023
Evaluated
08/19/2023
Submitted
autosomal recessive nonsyndromic hearing loss 97
Submitted as: OMIM:616705
AR
05/10/2023
Evaluated
08/19/2023
Submitted
arthrogryposis, distal, IIa 11
Submitted as: OMIM:620019
AD
05/10/2023
Evaluated
08/19/2023
Submitted
arthrogryposis, distal, IIa 11
Submitted as: OMIM:620019
Unknown
09/29/2022
Evaluated
11/30/2023
Submitted
nonsyndromic genetic hearing loss
AR
03/26/2021
Evaluated
04/21/2024
Submitted

Disputed Evidence classifications

complex neurodevelopmental disorder
AD
01/19/2021
Evaluated
04/21/2024
Submitted

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