OMIM Links for Protein (Select 186928858) - OMIM - NCBI

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Links from Protein

Items: 3

Select item 6137101.

#613710 - THIAMINE METABOLISM DYSFUNCTION SYNDROME 4 (BILATERAL STRIATAL DEGENERATION AND PROGRESSIVE POLYNEUROPATHY TYPE); THMD4

Cytogenetic locations: mutation

OMIM:: 613710

Gene summaries Genetic tests Medical literature

Select item 6071962.

#607196 - MICROCEPHALY, AMISH TYPE; MCPHA

Cytogenetic locations: mutation

OMIM:: 607196

Gene summaries Genetic tests Medical literature

Select item 6065213.

*606521 - SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL THIAMINE PYROPHOSPHATE CARRIER), MEMBER 19; SLC25A19

Cytogenetic locations: mutation

OMIM:: 606521

Gene summaries Genetic tests Medical literature

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OMIM Links for Protein (Select 186928858) (3)
OMIM
terminal nucleotidyltransferase 4A isoform 2 [Homo sapiens]
terminal nucleotidyltransferase 4A isoform 2 [Homo sapiens]
gi|1393643648|ref|NP_001165276.2|

Protein
Mus musculus F-box protein 43 (Fbxo43), transcript variant 1, mRNA
Mus musculus F-box protein 43 (Fbxo43), transcript variant 1, mRNA
gi|1573307356|ref|NM_001368658.1|

Nucleotide

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