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SLC25A44 - solute carrier family 25 member 44 Gene

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 9673

About SLC25A44

Cytogenetic location: 1q22 Genomic coordinates (GRCh38): 1:156,194,104-156,212,796 (from NCBI)

This gene has 6 transcripts (splice variants), 264 orthologues and 49 paralogues. Ubiquitous expression in brain (RPKM 13.3), kidney (RPKM 10.2) and 25 other tissues.

Summary

SLC25A44 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]).[supplied by OMIM, Mar 2008]

SLC25A44 Products (8)

mRNA	Protein	Name
NM_001286184.2	NP_001273113.1	solute carrier family 25 member 44 isoform 1
NM_001377385.1	NP_001364314.1	solute carrier family 25 member 44 isoform 1
NM_001377386.1	NP_001364315.1	solute carrier family 25 member 44 isoform 2
NM_001377387.1	NP_001364316.1	solute carrier family 25 member 44 isoform 2
NM_001377388.1	NP_001364317.1	solute carrier family 25 member 44 isoform 2
NM_001377389.1	NP_001364318.1	solute carrier family 25 member 44 isoform 3
NM_001377390.1	NP_001364319.1	solute carrier family 25 member 44 isoform 3
NM_014655.4	NP_055470.1	solute carrier family 25 member 44 isoform 2

Gene Ontology

Biological Process

Biological Process GO Annotation	Evidence	References	Source
involved in branched-chain amino acid catabolic process	IMP IMP: Inferred from mutant phenotype	31435015	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC25A44 Protein Structure

Mito_carr

0
100
200
300
314 a.a.

Protein Preferred Names	Protein Names
solute carrier family 25 member 44

Related Diseases

Diseases	Alias
Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, Type 1	Cadasil Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Casil Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Familial Vascular Leukoencephalopathy CADASIL1 Cadasil 1 Hereditary Multi-Infarct Dementia Cadasil Syndrome Dementia, Hereditary Multiinfarct Type Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy 1 Autosomal Dominant Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy Type 1 Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts Leukoencephalopathy Dementia, Hereditary Multi-Infarct Type Hereditary Dementia, Multi-Infarct Type Cerebral Autosomal Dominant Arteriopathy-Subcortical Infarcts-Leukoencephalopathy Cerebral Arteriopathy, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy, 1 Cerebral Arteriopathy With Subcortical Infarcts And Leukoencephalopathy, Autosomal Dominant Dementia Hereditary Multiinfarct Type Dementia Hereditary Multi-Infarct Type Arteriopathy, Cerebral, Autosomal Dominant, With Subcortical Infarcts And Leukoencephalopathy
Brain Small Vessel Disease

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

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13126	SLC25A44 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLC25A44	RGD	RGD:1307244
Felis catus	SLC25A44	VGNC	VGNC:65278
Bos taurus	SLC25A44	VGNC	VGNC:34769
Canis familiaris	SLC25A44	VGNC	VGNC:46315
Mus musculus	SLC25A44	MGD	MGI:2444391
Others	SLC25A44	NCBI