1. Gene
  2. SLC25A24 - solute carrier family 25 member 24 Gene

SLC25A24 - solute carrier family 25 member 24 Gene

Homo sapiens

Also known as APC1; SCAMC1; SCAMC-1

Gene ID: 29957 | Gene type: protein coding

About SLC25A24

Cytogenetic location: 1p13.3 Genomic coordinates (GRCh38): 1:108,134,043-108,200,343 (from NCBI)

This gene has 5 transcripts (splice variants), 1 gene allele, 189 orthologues, 49 paralogues and is associated with 4 phenotypes. Ubiquitous expression in small intestine (RPKM 21.4), colon (RPKM 20.9) and 25 other tissues.

Summary

This gene encodes a carrier protein that transports ATP-Mg exchanging it for phosphate. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

SLC25A24 Products(2)

mRNA Protein Name
NM_013386.5 NP_037518.3 calcium-binding mitochondrial carrier protein SCaMC-1 isoform 1
NM_213651.3 NP_998816.1 calcium-binding mitochondrial carrier protein SCaMC-1 isoform 2

SLC25A24 Protein Structure

EF-hand_7

EF-hand_7: EF-hand domain pair (24 - 83)

EF-hand_7

EF-hand_7: EF-hand domain pair (92 - 150)

Mito_carr

Mito_carr: Mitochondrial carrier protein (192 - 281)

Mito_carr

Mito_carr: Mitochondrial carrier protein (285 - 374)

Mito_carr

Mito_carr: Mitochondrial carrier protein (384 - 472)

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  • 477 a.a.
Protein Preferred Names Protein Names

calcium-binding mitochondrial carrier protein SCaMC-1

ATP-Mg/P(i) co-transporter 1

Related Diseases

Diseases Alias
Fontaine Progeroid Syndrome

Gorlin-Chaudhry-Moss Syndrome

Gcms

Craniofacial Dysostosis, Hypertrichosis, Hypoplasia Of Labia Majora, Dental And Eye Anomalies, Patent Ductus Arteriosus, And Normal Intelligence

Gorlin Chaudhry Moss Syndrome

Gcm Syndrome

FPS

Progeroid Syndrome, Congenital, Petty Type

Progeroid Syndrome Petty Type

Craniofacial Dysostosis, Patent Ductus Arteriosus, Hypertrichosis, Hypoplasia Of Labia Majora, Dental And Eye Anomalies

Petty Laxova Wiedemann Syndrome

Progeroid Syndrome Congenital Petty Type

Craniofacial Dysostosis-Genital, Dental, Cardiac Anomalies Syndrome

Cranofacial Dysostosis-Hypertrichosis-Hypoplasia Of Labia Majora Syndrome

Dental And Eye Anomalies-Patent Ductus Arteriosus-Normal Intelligence Syndrome

Progeroid Syndrome, Petty Type

Petty Syndrome

Petty-Laxova-Wiedemann Syndrome

Progeroid Syndrome
Dementia

Dementias

Presenile Dementia

Alzheimer Type Dementia

Alzheimer Sclerosis

Alzheimer Disease Dementia

Alzheimer Dementia

Primary Degenerative Alzheimer Type Dementia

End Stage Alzheimer'S Dementia

Alzheimer'S Type Atypical Dementia

Alzheimer Type Presenile Dementia

Early Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 2

Dementia In Alzheimer Disease With Early Onset

Early Onset Alzheimer Type Dementia, Uncomplicated

Primary Degenerative Alzheimer Type Dementia, Early Onset

Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

Alzheimer Disease Dementia With Early Onset

Presenile Sclerosis

Presenile Brain Sclerosis

Presenile Alzheimer Brain Sclerosis

Late Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 1

Dementia In Alzheimer Disease With Late Onset

Primary Degenerative Alzheimer Type Dementia, Late Onset

Sdat - [Senile Dementia, Alzheimer Type]

Alzheimer Disease Dementia With Late Onset

Late Onset Alzheimer Brain Sclerosis

Senile Alzheimer Brain Disease

Senile Alzheimer Brain Sclerosis

Senile Primary Degenerative Alzheimer Type Dementia

Senile Dementia Of The Alzheimer Type

Arteriosclerotic Dementia

Strategic-Infarct Dementia

Post Stroke Dementia

Vascular Cognitive Impairment

Vascular Dementia

Dementia Of The Lewy Body Type

Dementia With Lewy Bodies

Sdlt - [Senile Dementia Of The Lewy Body Type]

Senile Dementia Of The Lewy Body Type

Alcohol-Related Dementia

Alcoholic Dementia Nos

Alcohol-Induced Dementia

Alcoholic Brain Syndrome

Chronic Alcoholic Brain Syndrome

Alcohol Dementia

Late Onset Alcoholic Psychosis

Residual And Late-Onset Alcohol-Induced Psychotic Disorder

Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

Late-Onset Psychoactive Substance-Induced Psychotic Disorder

Inhalant Dementia

Volatile Solvents Dementia

Dementia In Paralysis Agitans

Pdd - [Parkinson Disease Dementia]

Dementia Syndrome Of Parkinson Disease

Dementia In Parkinson Disease

Parkinson Related Dementia

Dementia In Huntington Chorea

Hiv - [Human Immunodeficiency Virus] Dementia

Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

Aids Related Dementia

Dementia Due To Niacin Deficiency

Craniosynostosis

Premature Closure Of Cranial Sutures

Craniostenosis

Craniosynostosis Syndrome

Cso

Craniosynostoses

Congenital Ossification Of Cranial Sutures

Congenital Ossification Of Sutures Of Skull

Craniostosis

Imperfect Fusion Of Skull

Congenital Imperfect Closure Skull

Imperfect Closure Skull

Premature Closure Cranium Sutures

Deficiency Of Craniofacial Axis

Hypertrichosis
Conduct Disorder
Cecum Adenocarcinoma

Cecal Adenocarcinoma

Adenocarcinoma Of Cecum

Colon Mucinous Adenocarcinoma

Colonic Mucinous Adenocarcinoma

Mucinous Adenocarcinoma Of The Colon

Body Dysmorphic Disorder

Dysmorphophobia

Body Dysmorphia

Dysmorphic Syndrome

Body Dysmorphic Disorders

Umbilical Hernia

Hernia, Umbilical

Sengers Syndrome

Mitochondrial Dna Depletion Syndrome 10

Cardiomyopathy And Cataract

Cataract And Cardiomyopathy

MTDPS10

Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome

Cardiomyopathic Mitochondrial Dna Depletion Syndrome 10

Senger Syndrome

Myoclonic Epilepsy Associated With Ragged-Red Fibers

Merrf Syndrome

MERRF

Fukuhara Syndrome

Myoclonic Epilepsy Associated With Ragged Red Fibers

Myoencephalopathy Ragged-Red Fiber Disease

Myoclonic Epilepsy - Ragged Red Fibers

Myoclonus Epilepsy And Ragged Red Fibers

Myoclonus With Epilepsy And With Ragged Red Fibers

Myoclonic Epilepsy With Ragged Red Fibers

Myoclonic Epilepsy With Ragged-Red Fibers

Fukuhara Disease

Myoclonus Epilepsy Associated With Ragged-Red Fibres

Myoclonus With Epilepsy With Ragged Red Fibers

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SLC25A24 VGNC VGNC:54068
Mus musculus SLC25A24 MGD MGI:1917160
Macaca mulatta SLC25A24 VGNC VGNC:100140
Felis catus SLC25A24 VGNC VGNC:65265
Bos taurus SLC25A24 VGNC VGNC:55682
Rattus norvegicus SLC25A24 RGD RGD:1311982