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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
lactate dehydrogenase D
Summary
- Gene Symbol
-
- LDHD
- Organism
- Homo sapiens (human)
External Links
- NCBI Gene
- 197257
- HGNC
- 19708
- KEGG Gene ID
- hsa:197257
- PubChem
- 197257
- Alliance of Genome Resources
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Disease variant
- FAD
- Mitochondrion
- Oxidoreductase
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| Q86WU2 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| lactate catabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial inner membrane |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| D-lactate dehydrogenase (cytochrome) activity | ||
| flavin adenine dinucleotide binding | ||
| protein binding | ||
| D-lactate dehydrogenase activity | ||
| FAD binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000023 | Inguinal hernia |
| HP:0000252 | Microcephaly |
| HP:0000494 | Downslanted palpebral fissures |
| HP:0000526 | Aniridia |
| HP:0001249 | Intellectual disability |
| HP:0003648 | Lacticaciduria |
| Disease ID | Disease Name |
|---|---|
| OMIM:245450 |
|
PubChem Disease
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 713589 | MACMU26023 | ||
| 105491279 | MACNE07597 | ||
| 105537236 | MANLE05539 | ||
| 101129877 | GORGO12202 | ||
| 100978240 | PANPA15661 | ||
| 454245 | PANTR12851 | ||
| 100432706 | PONAB10863 | ||
| 610390 | CANLF15952 | ||
| 112915669 | VULVU07786 | ||
| 123791308 | URSAM02207 |
