OMIM Links for Protein (Select 291045302) - OMIM - NCBI

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Links from Protein

Items: 20

Select item 6191471.

#619147 - LEUKOENCEPHALOPATHY, PROGRESSIVE, INFANTILE-ONSET, WITH OR WITHOUT DEAFNESS; LEPID

Cytogenetic locations: Spondyloepimetaphyseal

OMIM:: 619147

Gene summaries Genetic tests Medical literature

Select item 6189522.

#618952 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46; COXPD46

Cytogenetic locations: 17q21.2

OMIM:: 618952

Gene summaries Genetic tests Medical literature

Select item 6188353.

#618835 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40; COXPD40

Cytogenetic locations: 26741492

OMIM:: 618835

Gene summaries Genetic tests Medical literature

Select item 6182434.

#618243 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22; MC1DN22

Cytogenetic locations: 605991

OMIM:: 618243

Gene summaries Genetic tests Medical literature

Select item 6182395.

#618239 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17; MC1DN17

Cytogenetic locations: 18614015

OMIM:: 618239

Gene summaries Genetic tests Medical literature

Select item 6172096.

*617209 - GLUTAMINYL-tRNA AMIDOTRANSFERASE SUBUNIT QRSL1; QRSL1

Cytogenetic locations: 19805282

OMIM:: 617209

Gene summaries Genetic tests Medical literature

Select item 6154577.

#615457 - BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 18; BMIQ18

Cytogenetic locations: 19390624

OMIM:: 615457

Gene summaries Genetic tests Medical literature

Select item 6154108.

*615410 - MELANOCORTIN 2 RECEPTOR ACCESSORY PROTEIN 2; MRAP2

Cytogenetic locations: 23869017

OMIM:: 615410

Gene summaries Genetic tests Medical literature

Select item 6123929.

*612392 - NADH DEHYDROGENASE (UBIQUINONE) COMPLEX I, ASSEMBLY FACTOR 6; NDUFAF6

Cytogenetic locations: 18614015

OMIM:: 612392

Gene summaries Genetic tests Medical literature

Select item 61198510.

*611985 - MITOCHONDRIAL RIBOSOMAL PROTEIN S23; MRPS23

Cytogenetic locations: 17q21.2

OMIM:: 611985

Gene summaries Genetic tests Medical literature

Select item 61067811.

#610678 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 4; COXPD4

Cytogenetic locations: 17160893

OMIM:: 610678

Gene summaries Genetic tests Medical literature

Select item 60956712.

*609567 - PATATIN-LIKE PHOSPHOLIPASE DOMAIN-CONTAINING PROTEIN 3; PNPLA3

Cytogenetic locations: 15181042

OMIM:: 609567

Gene summaries Genetic tests Medical literature

Select item 60905913.

*609059 - PATATIN-LIKE PHOSPHOLIPASE DOMAIN-CONTAINING PROTEIN 2; PNPLA2

Cytogenetic locations: 15550674

OMIM:: 609059

Gene summaries Genetic tests Medical literature

Select item 60383514.

*603835 - NADH-UBIQUINONE OXIDOREDUCTASE SUBUNIT A10; NDUFA10

Cytogenetic locations: 605991

OMIM:: 603835

Gene summaries Genetic tests Medical literature

Select item 60238915.

*602389 - Tu TRANSLATION ELONGATION FACTOR, MITOCHONDRIAL; TUFM

Cytogenetic locations: 21051640

OMIM:: 602389

Gene summaries Genetic tests Medical literature

Select item 60142116.

*601421 - LYSYL-tRNA SYNTHETASE 1; KARS1

Cytogenetic locations: Spondyloepimetaphyseal

OMIM:: 601421

Gene summaries Genetic tests Medical literature

Select item 30102117.

#301021 - MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30; MC1DN30

Cytogenetic locations: 26741492

OMIM:: 301021

Gene summaries Genetic tests Medical literature

Select item 30095218.

#300952 - LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 3; LSDMCA3

Cytogenetic locations: 25772934

OMIM:: 300952

Gene summaries Genetic tests Medical literature

Select item 30040319.

*300403 - NADH-UBIQUINONE OXIDOREDUCTASE 1 BETA SUBCOMPLEX, 11; NDUFB11

Cytogenetic locations: 25772934

OMIM:: 300403

Gene summaries Genetic tests Medical literature

Select item 30010220.

*300102 - PATATIN-LIKE PHOSPHOLIPASE DOMAIN-CONTAINING PROTEIN 4; PNPLA4

Cytogenetic locations: 604702

OMIM:: 300102

Gene summaries Genetic tests Medical literature

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