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Lactate dehydrogenase b

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LDHB
Available structures
PDBOrtholog search: PDBe RCSB
List of PDB id codes

1I0Z, 1T2F

Identifiers
AliasesLDHB, HEL-S-281, LDH-B, LDH-H, LDHBD, TRG-5, lactate dehydrogenase B
External IDsOMIM: 150100; MGI: 96763; HomoloGene: 55647; GeneCards: LDHB; OMA:LDHB - orthologs
Gene location (Human)
Chromosome 12 (human)
Chr.Chromosome 12 (human)
Chromosome 12 (human)Genomic location for LDHBGenomic location for LDHB
Band12p12.1Start21,635,342 bp
End21,757,857 bp
Gene location (Mouse)
Chromosome 6 (mouse)
Chr.Chromosome 6 (mouse)
Chromosome 6 (mouse)Genomic location for LDHBGenomic location for LDHB
Band6 G2|6 74.17 cMStart142,435,975 bp
End142,453,683 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • renal medulla

  • right ventricle

  • external globus pallidus

  • endothelial cell

  • lateral nuclear group of thalamus

  • myocardium of left ventricle

  • pars compacta

  • pars reticulata

  • kidney tubule

  • middle temporal gyrus
Top expressed in
  • primary oocyte

  • secondary oocyte

  • zygote

  • right kidney

  • right ventricle

  • primary visual cortex

  • superior frontal gyrus

  • vestibular membrane of cochlear duct

  • anterior horn of spinal cord

  • proximal tubule
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

3945

16832

Ensembl

ENSG00000111716

ENSMUSG00000030246

UniProt

P07195

P16125

RefSeq (mRNA)

NM_001174097
NM_002300
NM_001315537

NM_008492
NM_001302765
NM_001316322

RefSeq (protein)

NP_001167568
NP_001302466
NP_002291

NP_001289694
NP_001303251
NP_032518

Location (UCSC)Chr 12: 21.64 – 21.76 MbChr 6: 142.44 – 142.45 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Lactate dehydrogenase B is a protein that in humans is encoded by the LDHB gene.

Function

This gene encodes the B subunit of lactate dehydrogenase enzyme, which catalyzes the interconversion of pyruvate and lactate with concomitant interconversion of NADH and NAD+ in a post-glycolysis process. Alternatively spliced transcript variants have been found for this gene. Recent studies have shown that a C-terminally extended isoform is produced by use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism, and that this isoform is localized in the peroxisomes. Mutations in this gene are associated with lactate dehydrogenase B deficiency. Pseudogenes have been identified on chromosomes X, 5 and 13.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000111716Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000030246Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Lactate dehydrogenase B". Retrieved 2017-10-01.

Further reading


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