OMIM Links for Gene (Select 291) - OMIM - NCBI

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Links from Gene

Items: 4

Select item 6171841.

#617184 - MITOCHONDRIAL DNA DEPLETION SYNDROME 12A (CARDIOMYOPATHIC TYPE), AUTOSOMAL DOMINANT; MTDPS12A

Cytogenetic locations: 606877

OMIM:: 617184

Gene summaries Genetic tests Medical literature

Select item 6154182.

#615418 - MITOCHONDRIAL DNA DEPLETION SYNDROME 12B (CARDIOMYOPATHIC TYPE), AUTOSOMAL RECESSIVE; MTDPS12B

Cytogenetic locations: 606877

OMIM:: 615418

Gene summaries Genetic tests Medical literature

Select item 6092833.

#609283 - PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL DOMINANT 2; PEOA2

Cytogenetic locations: 606877

OMIM:: 609283

Gene summaries Genetic tests Medical literature

Select item 1032204.

*103220 - SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, ADENINE NUCLEOTIDE TRANSLOCATOR), MEMBER 4; SLC25A4

Cytogenetic locations: 28103757

OMIM:: 103220

Gene summaries Genetic tests Medical literature

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OMIM Links for Gene (Select 291) (4)
OMIM
Homo sapiens stomatin like 1 (STOML1), transcript variant 7, mRNA
Homo sapiens stomatin like 1 (STOML1), transcript variant 7, mRNA
gi|375493510|ref|NM_001256677.1|

Nucleotide

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