Identity
HGNC
LOCATION
1p13.3
LOCUSID
ALIAS
APC1,SCAMC-1,SCAMC1
FUSION GENES
Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 29957
MIM: 608744
HGNC: 20662
Ensembl: ENSG00000085491
Variants:
dbSNP: 29957
ClinVar: 29957
TCGA: ENSG00000085491
COSMIC: SLC25A24
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35241150 | 2022 | Tumor bud-derived CCL5 recruits fibroblasts and promotes colorectal cancer progression via CCR5-SLC25A24 signaling. | 12 |
| 35241150 | 2022 | Tumor bud-derived CCL5 recruits fibroblasts and promotes colorectal cancer progression via CCR5-SLC25A24 signaling. | 12 |
| 34561420 | 2021 | SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study. | 2 |
| 34561420 | 2021 | SLC25A24 gene methylation and gray matter volume in females with and without conduct disorder: an exploratory epigenetic neuroimaging study. | 2 |
| 31686588 | 2019 | Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients. | 4 |
| 31686588 | 2019 | Genes identified through genome-wide association studies of osteonecrosis in childhood acute lymphoblastic leukemia patients. | 4 |
| 29100093 | 2017 | De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. | 32 |
| 29100094 | 2017 | De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise. | 32 |
| 29100093 | 2017 | De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. | 32 |
| 29100094 | 2017 | De Novo Mutations in SLC25A24 Cause a Disorder Characterized by Early Aging, Bone Dysplasia, Characteristic Face, and Early Demise. | 32 |
| 25599384 | 2015 | SLC25A24 as a novel susceptibility gene for low fat mass in humans and mice. | 10 |
| 25599384 | 2015 | SLC25A24 as a novel susceptibility gene for low fat mass in humans and mice. | 10 |
| 24332718 | 2014 | A self-sequestered calmodulin-like Ca²⁺ sensor of mitochondrial SCaMC carrier and its implication to Ca²⁺-dependent ATP-Mg/P(i) transport. | 14 |
| 24332718 | 2014 | A self-sequestered calmodulin-like Ca²⁺ sensor of mitochondrial SCaMC carrier and its implication to Ca²⁺-dependent ATP-Mg/P(i) transport. | 14 |
| 23266187 | 2013 | The 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)
