SLC25A24 (solute carrier family 25 member 24)

2014-08-01  

Identity

HGNC
LOCATION
1p13.3
LOCUSID
ALIAS
APC1,SCAMC-1,SCAMC1
FUSION GENES

Other Information

Locus ID:

NCBI: 29957
MIM: 608744
HGNC: 20662
Ensembl: ENSG00000085491

Variants:

dbSNP: 29957
ClinVar: 29957
TCGA: ENSG00000085491
COSMIC: SLC25A24

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000085491ENST00000264128J3KN42
ENSG00000085491ENST00000370041Q6NUK1
ENSG00000085491ENST00000565488Q6NUK1
ENSG00000085491ENST00000569674H3BMI3
ENSG00000085491ENST00000648874A0A3B3IU96

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
352411502022Tumor bud-derived CCL5 recruits fibroblasts and promotes colorectal cancer progression via CCR5-SLC25A24 signaling.12
352411502022Tumor bud-derived CCL5 recruits fibroblasts and promotes colorectal cancer progression via CCR5-SLC25A24 signaling.12
345614202021SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study.2
345614202021SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study.2
316865882019Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients.4
316865882019Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients.4
291000932017De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.32
291000942017De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.32
291000932017De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.32
291000942017De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise.32
255993842015SLC25A24 as a novel susceptibility gene for low fat mass in humans and mice.10
255993842015SLC25A24 as a novel susceptibility gene for low fat mass in humans and mice.10
243327182014A self-sequestered calmodulin-like Ca²⁺ sensor of mitochondrial SCaMC carrier and its implication to Ca²⁺-dependent ATP-Mg/P(i) transport.14
243327182014A self-sequestered calmodulin-like Ca²⁺ sensor of mitochondrial SCaMC carrier and its implication to Ca²⁺-dependent ATP-Mg/P(i) transport.14
232661872013The mitochondrial transporter family SLC25: identification, properties and physiopathology.0

Citation

Dessen P

SLC25A24 (solute carrier family 25 member 24)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54627/slc25a24-(solute-carrier-family-25-member-24)