Slc25a32 solute carrier family 25 member 32 [Rattus norvegicus (Norway rat)] - Gene

Summary

Official Symbol: Slc25a32provided by RGD
Official Full Name: solute carrier family 25 member 32provided by RGD
Primary source: RGD:1565789
See related: EnsemblRapid:ENSRNOG00000004403 AllianceGenome:RGD:1565789
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Rattus norvegicus
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Muridae; Murinae; Rattus
Also known as: RGD1565789
Summary: Predicted to enable FAD transmembrane transporter activity and folic acid transmembrane transporter activity. Predicted to be involved in folate import into mitochondrion and mitochondrial FAD transmembrane transport. Predicted to be located in membrane. Predicted to be active in mitochondrion. Orthologous to human SLC25A32 (solute carrier family 25 member 32). [provided by Alliance of Genome Resources, Dec 2024]
Expression: Biased expression in Liver (RPKM 77.0), Adrenal (RPKM 62.4) and 9 other tissues See more
Orthologs: human mouse all
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Genomic context

Location:: 7q31

Exon count:: 8

Annotation release	Status	Assembly	Chr	Location
RS_2024_02	current	GRCr8 (GCF_036323735.1)	7	NC_086025.1 (72024535..72045692, complement)
RS_2023_06	previous assembly	mRatBN7.2 (GCF_015227675.2)	7	NC_051342.1 (70142958..70160726, complement)
106	previous assembly	Rnor_6.0 (GCF_000001895.5)	7	NC_005106.4 (77983885..78005058, complement)

Chromosome 7 - NC_086025.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

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Expression

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See details

Project title: A rat RNA-Seq transcriptomic BodyMap across 11 organs and 4 developmental stages
Description: 320 RNA samples isolated from 11 organs (adrenal gland, brain, heart, kidney, liver, lung, muscle, spleen, thymus, and testes or uterus) from both sexes of Fischer 344 rats across four developmental stages (2-, 6-, 21-, and 104-weeks-old)
BioProject: PRJNA238328
Publication: PMID 24510058
Analysis date: Mon Jun 6 17:44:12 2016

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

RH142696 (e-PCR)
- UniSTS:231943

AW529678 (e-PCR)
- UniSTS:261191

D7Rat23 (e-PCR), detects polymorphism
- UniSTS:228178

Gene Ontology Provided by RGD

Function	Evidence Code	Pubs
enables FAD transmembrane transporter activity	IBA Inferred from Biological aspect of Ancestor more info
enables FAD transmembrane transporter activity	ISO Inferred from Sequence Orthology more info
enables folic acid transmembrane transporter activity	IBA Inferred from Biological aspect of Ancestor more info

Process	Evidence Code	Pubs
involved_in biological_process	ND No biological Data available more info
involved_in folate import into mitochondrion	IBA Inferred from Biological aspect of Ancestor more info
involved_in folate import into mitochondrion	ISO Inferred from Sequence Orthology more info
involved_in mitochondrial FAD transmembrane transport	ISO Inferred from Sequence Orthology more info

Component	Evidence Code	Pubs
located_in membrane	IEA Inferred from Electronic Annotation more info
located_in mitochondrial inner membrane	IEA Inferred from Electronic Annotation more info
located_in mitochondrial inner membrane	ISO Inferred from Sequence Orthology more info
is_active_in mitochondrion	IBA Inferred from Biological aspect of Ancestor more info
located_in mitochondrion	ISO Inferred from Sequence Orthology more info

General protein information

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Preferred Names: solute carrier family 25 member 32

Names: mitochondrial folate transporter/carrier; solute carrier family 25 (mitochondrial folate carrier) , member 32

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.