SLC25A44 (solute carrier family 25 member 44)

2014-11-01  

Identity

HGNC
LOCATION
1q22
LOCUSID
ALIAS
-
FUSION GENES

Other Information

Locus ID:

NCBI: 9673
MIM: 610824
HGNC: 29036
Ensembl: ENSG00000160785

Variants:

dbSNP: 9673
ClinVar: 9673
TCGA: ENSG00000160785
COSMIC: SLC25A44

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000160785ENST00000359511Q96H78
ENSG00000160785ENST00000423538E9PGQ0

Expression (GTEx)

0
5
10
15
20
25

References

Pubmed IDYearTitleCitations
337621342021The GBA-370Rec Parkinson's disease risk haplotype harbors a potentially pathogenic variant in the mitochondrial gene SLC25A44.1
340735122021Genome Evolutionary Dynamics Meets Functional Genomics: A Case Story on the Identification of SLC25A44.2
337621342021The GBA-370Rec Parkinson's disease risk haplotype harbors a potentially pathogenic variant in the mitochondrial gene SLC25A44.1
340735122021Genome Evolutionary Dynamics Meets Functional Genomics: A Case Story on the Identification of SLC25A44.2
232661872013The mitochondrial transporter family SLC25: identification, properties and physiopathology.0
232661872013The mitochondrial transporter family SLC25: identification, properties and physiopathology.0
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20
208776242010Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression.20

Citation

Dessen P

SLC25A44 (solute carrier family 25 member 44)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73363/case-report-explorer/js/lib/jquery-3.5.1.min.js