Mus musculus Gene: Pank2
Summary
InnateDB Gene IDBG-207069.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Pank2
Gene Name pantothenate kinase 2
Synonyms 4933409I19Rik; AI642621
Species Mus musculus
Ensembl Gene ENSMUSG00000037514
Encoded Proteins
pantothenate kinase 2
pantothenate kinase 2
pantothenate kinase 2
pantothenate kinase 2
pantothenate kinase 2
pantothenate kinase 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000125779:
This gene encodes a protein belonging to the pantothenate kinase family and is the only member of that family to be expressed in mitochondria. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by acyl CoA species. Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. Alternative splicing, involving the use of alternate first exons, results in multiple transcripts encoding different isoforms. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:131262495-131299188
Strand Forward strand
Band F1
Transcripts
ENSMUST00000131779
ENSMUST00000150843 ENSMUSP00000119606
ENSMUST00000145904 ENSMUSP00000115034
ENSMUST00000138509
ENSMUST00000184105 ENSMUSP00000138992
ENSMUST00000184932 ENSMUSP00000139259
ENSMUST00000183388 ENSMUSP00000139197
ENSMUST00000183349 ENSMUSP00000139203
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 9 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 9 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004594 pantothenate kinase activity
GO:0005524 ATP binding
Biological Process
GO:0007286 spermatid development
GO:0009060 aerobic respiration
GO:0015937 coenzyme A biosynthetic process
GO:0016310 phosphorylation
GO:0051881 regulation of mitochondrial membrane potential
GO:0070584 mitochondrion morphogenesis
Cellular Component
GO:0005739 mitochondrion
GO:0005829 cytosol
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Pantothenate and CoA biosynthesis pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Coenzyme A biosynthesis pathway
Vitamin B5 (pantothenate) metabolism pathway
Defective HLCS causes multiple carboxylase deficiency pathway
Defective MUT causes methylmalonic aciduria mut type pathway
Defective MMAA causes methylmalonic aciduria type cblA pathway
Defective TCN2 causes hereditary megaloblastic anemia pathway
Metabolism of water-soluble vitamins and cofactors pathway
Defective AMN causes hereditary megaloblastic anemia 1 pathway
Defective MTR causes methylmalonic aciduria and homocystinuria type cblG pathway
Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF pathway
Defective CD320 causes methylmalonic aciduria pathway
Defects in cobalamin (B12) metabolism pathway
Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC pathway
Defects in biotin (Btn) metabolism pathway
Defective BTD causes biotidinase deficiency pathway
Defective GIF causes intrinsic factor deficiency pathway
Defects in vitamin and cofactor metabolism pathway
Defective CUBN causes hereditary megaloblastic anemia 1 pathway
Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD pathway
Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE pathway
Metabolism pathway
Defective MMAB causes methylmalonic aciduria type cblB pathway
Disease pathway
Metabolism of vitamins and cofactors pathway
KEGG
Pantothenate and CoA biosynthesis pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL V9GXP9
UniProt Splice Variant
Entrez Gene 74450
UniGene
RefSeq NM_153501 XM_006500297 XM_006500298 XM_006500299
OMIM
CCDS CCDS16761
HPRD
IMGT
MGI ID MGI:1921700
MGI Symbol Pank2
EMBL AL808128
GenPept
RNA Seq Atlas 74450