SLC25A44 - solute carrier family 25 member 44 Gene

Homo sapiens

Gene ID: 9673 | Gene type: protein coding

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

SLC25A44 Protein Structure

Mito_carr

0
100
200
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

Bioactive Molecules (1)

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

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