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ALAD (aminolevulinate dehydratase)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
210
Gene nameGene Name - the full gene name approved by the HGNC.
Aminolevulinate dehydratase
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
ALAD
SynonymsGene synonyms aliases
ALADH, PBGS
ChromosomeChromosome number
9
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
9q32
SummarySummary of gene provided in NCBI Entrez Gene.
The ALAD enzyme is composed of 8 identical subunits and catalyzes the condensation of 2 molecules of delta-aminolevulinate to form porphobilinogen (a precursor of heme, cytochromes and other hemoproteins). ALAD catalyzes the second step in the porphyrin a
SNPsSNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs1800435 C>G Pathogenic, likely-benign Missense variant, coding sequence variant, non coding transcript variant
rs121912980 C>T Pathogenic Coding sequence variant, non coding transcript variant, missense variant
rs121912981 C>T Pathogenic Coding sequence variant, missense variant, genic downstream transcript variant
rs121912982 G>A Pathogenic, uncertain-significance Downstream transcript variant, coding sequence variant, missense variant, genic downstream transcript variant
rs121912983 C>T Pathogenic Coding sequence variant, missense variant, genic downstream transcript variant
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021588 hsa-miR-142-3p Microarray 17612493
MIRT050633 hsa-miR-19b-3p CLASH 23622248
MIRT527170 hsa-miR-6504-3p PAR-CLIP 22012620
MIRT527169 hsa-miR-4272 PAR-CLIP 22012620
MIRT372415 hsa-miR-8063 PAR-CLIP 22012620
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001666 Process Response to hypoxia IEA
GO:0003824 Function Catalytic activity TAS 2063868
GO:0004655 Function Porphobilinogen synthase activity IBA 21873635
GO:0004655 Function Porphobilinogen synthase activity IDA 8175643, 11032836
GO:0005576 Component Extracellular region TAS
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID P13716
Protein name Delta-aminolevulinic acid dehydratase (ALADH) (EC 4.2.1.24) (Porphobilinogen synthase)
Protein function Catalyzes an early step in the biosynthesis of tetrapyrroles. Binds two molecules of 5-aminolevulinate per subunit, each at a distinct site, and catalyzes their condensation to form porphobilinogen. {ECO:0000269|PubMed:11032836, ECO:0000269|PubM
PDB 1E51 , 1PV8 , 5HMS , 5HNR
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00490 ALAD
5 326
Delta-aminolevulinic acid dehydratase
Domain
Sequence
Sequence length 330
Interactions View interactions
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
 
KEGG
 
Reactome
  Porphyrin metabolism
Metabolic pathways
Biosynthesis of cofactors
  Heme biosynthesis
Neutrophil degranulation
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Anemia Anemia, Hemolytic rs118204044, rs118204045, rs118204046, rs121918330, rs869320719, rs869312029, rs121918332, rs869320724, rs767094129, rs786205058, rs786205059, rs137853119, rs137853120, rs137853121, rs1384933966, rs137853122, rs137853123, rs786205060, rs267607121, rs121908584, rs80338697, rs80338699, rs120074166, rs120074167, rs1050828, rs74575103, rs137852314, rs5030868, rs137852316, rs137852317, rs137852318, rs137852319, rs137852320, rs137852321, rs137852322, rs137852323, rs137852324, rs72554665, rs387906468, rs5030872, rs137852326, rs137852333, rs137852327, rs137852328, rs137852329, rs137852330, rs137852331, rs137852332, rs137852334, rs137852335, rs137852336, rs137852339, rs76645461, rs137852340, rs137852341, rs78478128, rs137852343, rs137852344, rs137852345, rs587776730, rs137852346, rs137852347, rs137852349, rs2070404412, rs2070350038, rs2070350009, rs137852303, rs137852304, rs33946267, rs34378160, rs33933298, rs11549407, rs35724775, rs34598529, rs41469945, rs267607201, rs80338694, rs80338696, rs387907018, rs398123546, rs78365220, rs587777100, rs587777101, rs483352840, rs869312752, rs765487627, rs1557229599, rs1557230040, rs1555524842, rs782090947, rs1358275550, rs1557229736, rs1557230573, rs1556323334, rs1233124208, rs1293528130, rs146864395, rs1595503440, rs1603411214, rs137852325, rs1575247302, rs1603411177, rs1336651679, rs782322505
Hypertension Hypertensive disease rs13306026, rs13333226 20123609
Kidney disease Kidney Diseases rs74315342, rs749740335, rs757649673, rs112417755, rs35138315 24631795, 23792432
Meningioma Meningioma, Meningiomas, Multiple, Clear Cell Meningioma rs587776563, rs121434259, rs387906857, rs397509405, rs397509406, rs397509407, rs397509408, rs797045990, rs876659443, rs878854603, rs1057518166, rs1060501395, rs1554897280, rs1554898242, rs1555605347, rs587782187, rs1555605750, rs878853937, rs1589596143, rs2037146593, rs2037146907 16140629
Unknown
Disease name Disease term dbSNP ID References
Angioblastic meningioma Angioblastic Meningioma 16140629
Angiomatous meningioma Angiomatous Meningioma 16140629
Benign meningioma Benign Meningioma 16140629
Cerebral convexity meningioma Cerebral Convexity Meningioma 16140629

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