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Gene: SLC25A19 (solute carrier family 25 member 19) Homo sapiens
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Symbol: SLC25A19
Name: solute carrier family 25 member 19
Description: Predicted to have thiamine transmembrane transporter activity. Predicted to be involved in thiamine pyrophosphate transmembrane transport. Localizes to the nucleus. Implicated in inherited metabolic disorder and microcephaly.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: DNC; MCPHA; microcephaly, Amish; mitochondrial thiamine pyrophosphate carrier; mitochondrial uncoupling protein 1; MUP1; solute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19; solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19; THMD3; THMD4; TPC
Orthologs:
Mus musculus (house mouse) : Slc25a19 (solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19)  MGI  Alliance
Rattus norvegicus (Norway rat) : Slc25a19 (solute carrier family 25 member 19)  Alliance
Chinchilla lanigera (long-tailed chinchilla) : Slc25a19 (solute carrier family 25 member 19)
Pan paniscus (bonobo/pygmy chimpanzee) : SLC25A19 (solute carrier family 25 member 19)
Canis lupus familiaris (dog) : SLC25A19 (solute carrier family 25 member 19)
Ictidomys tridecemlineatus (thirteen-lined ground squirrel) : Slc25a19 (solute carrier family 25 member 19)
Sus scrofa (pig) : SLC25A19 (solute carrier family 25 member 19)
Chlorocebus sabaeus (African green monkey) : SLC25A19 (solute carrier family 25 member 19)
Heterocephalus glaber (naked mole-rat) : Slc25a19 (solute carrier family 25 member 19)
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1775,272,981 - 75,289,510 (-)Ensembl
GRCh381775,272,980 - 75,289,958 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371773,269,061 - 73,285,530 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361770,780,669 - 70,797,109 (-)NCBINCBI36hg18NCBI36
Build 341770,780,668 - 70,797,109NCBI
Celera1769,861,413 - 69,877,887 (-)NCBI
Cytogenetic Map17q25.1NCBI
HuRef1768,679,265 - 68,696,066 (-)NCBIHuRef
CHM1_11773,333,658 - 73,350,100 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
Phenotype Annotations
References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SLC25A19
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1343771
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.