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Mendeliome

Gene: TIMM44

Red List (low evidence)

TIMM44 (translocase of inner mitochondrial membrane 44)
EnsemblGeneIds (GRCh38): ENSG00000104980
EnsemblGeneIds (GRCh37): ENSG00000104980
OMIM: 605058, Gene2Phenotype
TIMM44 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence for association with Mendelian disease.
Created: 31 Mar 2022, 7:39 a.m. | Last Modified: 31 Mar 2022, 7:39 a.m.
Panel Version: 0.12352

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
605058
Clinvar variants
Variants in TIMM44
Penetrance
None
Panels with this gene

History Filter Activity

31 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: timm44 has been classified as Red List (Low Evidence).

31 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: timm44 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: TIMM44 was added gene: TIMM44 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: TIMM44 was set to Unknown