LDHAL6B
L-lactate dehydrogenase A-like 6B
Also known as: LDH6B, LDH6B_HUMAN, LDHAL6, LDHL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BYZ2
- Gene
- LDHAL6B
- Ensembl
- ENSG00000171989
- Chromosome
- 15
- Canonical length
- 381 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Cytosol
OverviewNCBI Gene
Predicted to enable L-lactate dehydrogenase activity. Involved in lactate metabolic process. Located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
381 residues, UniProt reviewed canonical sequence.
>Q9BYZ2|LDHAL6B
1 MSWTVPVVRA SQRVSSVGAN FLCLGMALCP RQATRIPLNG TWLFTPVSKM ATVKSELIER
61 FTSEKPVHHS KVSIIGTGSV GMACAISILL KGLSDELALV DLDEDKLKGE TMDLQHGSPF
121 TKMPNIVCSK DYFVTANSNL VIITAGARQE KGETRLNLVQ RNVAIFKLMI SSIVQYSPHC
181 KLIIVSNPVD ILTYVAWKLS AFPKNRIIGS GCNLDTARFR FLIGQKLGIH SESCHGWILG
241 EHGDSSVPVW SGVNIAGVPL KDLNSDIGTD KDPEQWKNVH KEVTATAYEI IKMKGYTSWA
301 IGLSVADLTE SILKNLRRIH PVSTIIKGLY GIDEEVFLSI PCILGENGIT NLIKIKLTPE
361 EEAHLKKSAK TLWEIQNKLK LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LDHAL6B can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- testis: 38 nTPM
- adipose tissue: 0.3 nTPM
- blood vessel: 0.3 nTPM
- liver: 0.3 nTPM
- small intestine: 0.3 nTPM
- breast: 0.2 nTPM
Single-cell type
- late primary spermatocytes: 197 nCPM
- early primary spermatocytes: 60 nCPM
- late spermatids: 6.3 nCPM
- early spermatids: 4.3 nCPM
- peritubular myoid cells: 1.2 nCPM
- sertoli cells: 1.1 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- choroid plexus: 5.8 nTPM
- white matter: 4.7 nTPM
- medulla oblongata: 3.5 nTPM
- thalamus: 3.2 nTPM
- pons: 3.1 nTPM
- basal ganglia: 2.8 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.46
- gnomAD pLI
- 0.07
- gnomAD missense Z
- -1.09
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Lactate/malate dehydrogenase, N-terminal
- L-lactate/malate dehydrogenase
- L-lactate dehydrogenase
- Lactate dehydrogenase/glycoside hydrolase, family 4, C-terminal
- L-lactate dehydrogenase, active site
- Lactate/malate dehydrogenase, C-terminal
- NAD(P)-binding domain superfamily
- lactate/malate dehydrogenase, NAD binding domain
- lactate/malate dehydrogenase, alpha/beta C-terminal domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LDHAL6B as an antibody target. Whether an autoantibody or antibody against LDHAL6B could matter depends on whether native LDHAL6B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LDHAL6B is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label LDHAL6B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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