ALDOA - aldolase, fructose-bisphosphate A Gene

Also Known as ALDA; GSD12; HEL-S-87p

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 226

About ALDOA

Cytogenetic location: 16p11.2 Genomic coordinates (GRCh38): 16:30,064,279-30,070,420 (from NCBI)

This gene has 19 transcripts (splice variants), 266 orthologues, 2 paralogues and is associated with 3 phenotypes. Ubiquitous expression in heart (RPKM 290.3), esophagus (RPKM 221.3) and 25 other tissues.

Summary

This gene encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10. [provided by RefSeq, Sep 2017]

ALDOA Products (4)

mRNA Protein Name
NM_001127617.2 NP_001121089.1 fructose-bisphosphate aldolase A isoform 1
NM_001243177.4 NP_001230106.1 fructose-bisphosphate aldolase A isoform 2
NM_184041.5 NP_908930.1 fructose-bisphosphate aldolase A isoform 1
NM_184043.2 NP_908932.1 fructose-bisphosphate aldolase A isoform 1
Molecular Function GO Annotation Evidence Verweise Source
enables cytoskeletal protein binding IDA
IDA: Inferred from direct assay
9244396 GOA
enables fructose binding IDA
IDA: Inferred from direct assay
10048322 GOA
enables fructose-bisphosphate aldolase activity IDA
IDA: Inferred from direct assay
9244396 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
10944123 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
20849852 GOA
Biological Process GO Annotation Evidence Verweise Source
involved in ATP biosynthetic process IMP
IMP: Inferred from mutant phenotype
14615364 GOA
involved in binding of sperm to zona pellucida IMP
IMP: Inferred from mutant phenotype
23355646 GOA
involved in fructose 1,6-bisphosphate metabolic process IDA
IDA: Inferred from direct assay
9244396 GOA
involved in fructose metabolic process IMP
IMP: Inferred from mutant phenotype
14615364 GOA
involved in glycolytic process IMP
IMP: Inferred from mutant phenotype
14615364 GOA
involved in muscle cell cellular homeostasis IMP
IMP: Inferred from mutant phenotype
14615364 GOA
involved in regulation of cell shape IDA
IDA: Inferred from direct assay
9244396 GOA
involved in striated muscle contraction IMP
IMP: Inferred from mutant phenotype
14615364 GOA
Cellular Component GO Annotation Evidence Verweise Source
located in actin cytoskeleton IDA
IDA: Inferred from direct assay
9244396 GOA
located in extracellular exosome IDA
IDA: Inferred from direct assay
17641064 GOA
located in sperm head IDA
IDA: Inferred from direct assay
23355646 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ALDOA Protein Structure

Glycolytic

Glycolytic: Fructose-bisphosphate aldolase class-I (15 - 364)

  • 0
  • 100
  • 200
  • 300
  • 364 a.a.
Protein Preferred Names Protein Names

fructose-bisphosphate aldolase A

  • aldolase A, fructose-bisphosphate

ALDOA Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
ALDOA P04075 ALDOB Homo sapiens P05062 33961781
Intra
ALDOA P04075 CARM1 Homo sapiens Q86X55 33961781
Intra
ALDOA P04075 ALDOC Homo sapiens P09972 31515488
Intra
ALDOA P04075 ALDOC Homo sapiens P09972 26496610
Intra
ALDOA P04075 ALDOC Homo sapiens P09972 33961781
Intra
ALDOA P04075 PCNA Homo sapiens P12004 20849852
Intra
ALDOA P04075 ALDOA Homo sapiens P04075 10944123
Intra
ALDOA P04075 ALDOA Homo sapiens P04075
Y2H
21988832
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ALDOA Proteins

Art. -Nr. Produktname Accession Reinheit
HY-P7877 Fructose-bisphosphate aldolase A/ALDOA Protein, Human (His, solution) P04075 (P2-Y364) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P700265 Fructose-bisphosphate aldolase A/ALDOA Protein, Human (His) P04075 (P2-Y364) ≥ 90%, as determined by reducing SDS-PAGE.

ALDOA Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P82292 ALDOA Antibody (YA2037) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat
HY-P82292A ALDOA Antibody (YA2037)(PBS only) WB, IHC-F, IHC-P, ICC/IF Human, Mouse, Rat
HY-P83934 ALDOA Antibody (YA3631) WB, IHC-P, FC, ELISA Human, Mouse
HY-P83934A ALDOA Antibody (YA3631)(PBS only) WB, IHC-P, FC, ELISA Human, Mouse

Related Diseases

Diseases Alias
Glycogen Storage Disease Xii
  • Aldolase A Deficiency

  • Red Cell Aldolase Deficiency

  • GSD12

  • Aldoa Deficiency

  • Gsd Xii

  • Glycogen Storage Disease Type 12

  • Glycogen Storage Disease 12

  • Aldolase Deficiency, Red Cell

  • Aldolase Deficiency Red Cell

  • Glycogen Storage Disease Due To Aldolase A Deficiency

  • Gsd Due To Aldolase A Deficiency

  • Gsd Type 12

  • Gsd Type Xii

  • Glycogen Storage Disease Type Xii

  • Glycogenosis Due To Aldolase A Deficiency

  • Glycogenosis Type 12

  • Glycogenosis Type Xii

  • Storage Disease, Glycogen, Type Xii

Hemolytic Anemia
  • Anemia, Hemolytic

  • Anemia Hemolytic

  • Anaemia Due To Other Disorders Of Glutathione Metabolism

  • Chronic Non Spherocytic Anaemia

  • G6pd - [Glucose-6-Phosphate Dehydrogenase Deficiency] Anaemia

  • Anaemia Due To Glucose-6-Phosphate Dehydrogenase Deficiency

  • Glucose-6-Phosphate Dehydrogenase Deficiency With Anaemia

  • Glucose-6-Phosphate Dehydrogenase Deficiency Anaemia

  • Favism Anaemia

  • Haemolytic Anaemia Due Tog6pd Deficiency

  • Favism

  • Pentose Phosphate Pathway Disorder Anaemia

  • Anaemia Due To Pentose Phosphate Pathway Defect

Glycogen Storage Disease
  • Glycogenosis

  • Glycogenoses

  • Gsd

  • Storage Disease, Glycogen

  • Gsd - [Glycogen Storage Disease]

  • Glycogen Thesaurismosis

  • Diffuse Glycogenosis

  • Generalised Glycogen Storage Disease

  • Generalised Glycogenosis

  • Generalised Glycogen Storage Disease Of Infants

  • Glycogen Synthase Deficiency

Myopathy
  • Muscular Diseases

  • Myopathies

Lung Cancer
  • Lung Carcinoma

  • Non-Small Cell Lung Carcinoma

  • Lung Cancer, Susceptibility To

  • Lung Cancer, Protection Against

  • Adenocarcinoma Of Lung, Somatic

  • Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer

  • Lung Neoplasm

  • Carcinoma Of Lung

  • Lung Non-Small Cell Carcinoma

  • Non-Small Cell Lung Cancer

  • Nsclc

  • Lung Neoplasms

  • Malignant Neoplasm Of Lung

  • Alveolar Cell Carcinoma

  • Nonsmall Cell Lung Cancer, Somatic

  • Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

  • Nonsmall Cell Lung Cancer, Susceptibility To

  • Lung Cancer, Somatic

  • Lung Cancer, Resistance To

  • Cancer Of Lung

  • Cancer Of Bronchus

  • Cancer Of The Lung

  • Lung Malignancies

  • Lung Malignant Tumors

  • Malignant Lung Tumor

  • Malignant Tumor Of Lung

  • Pulmonary Cancer

  • Pulmonary Carcinoma

  • Pulmonary Neoplasms

  • Respiratory Carcinoma

  • LNCR

  • Adenocarcinoma Of Lung

  • Neoplasm Of Lung

  • Cancer Lung

  • Carcinoma Non-Small Cell Lung

  • Carcinoma, Non-Small-Cell Lung

  • Lung Cancers

  • Lung Carcinomas

  • Cancer, Lung

  • Cancer, Lung, Non-Small Cell

  • Primary Malignant Neoplasm Of Lung

  • Bronchioloalveolar Adenocarcinoma

Urinary System Disease
  • Abnormality Of The Urinary System

  • Non-Neoplastic Urinary Tract Disease

  • Urinary Tract Disease

  • Urinary Tract Diseases

  • Urinary Tract Anomaly

  • Urologic Diseases

  • Non-Neoplastic Urinary System Disorder

  • Congenital Malformation Of The Urinary System

Renal Cell Carcinoma, Nonpapillary
  • Renal Cell Carcinoma

  • RCC

  • Nonpapillary Renal Cell Carcinoma

  • Clear Cell Renal Cell Carcinoma

  • Hypernephroma

  • Adenocarcinoma Of Kidney

  • Renal Carcinoma, Chromophobe, Somatic

  • Clear Cell Carcinoma Of Kidney

  • Clear-Cell Metastatic Renal Cell Carcinoma

  • Clear Cell Renal Carcinoma

  • Renal Cell Carcinoma, Somatic

  • Conventional Renal Cell Carcinoma

  • Conventional Renal Cell Carcinoma

  • Renal Clear Cell Carcinoma

  • Ccrcc

  • Hereditary Clear Cell Renal Cell Carcinoma

  • Carcinoma, Renal Cell

  • Renal Cell Carcinoma, Clear Cell, Somatic

  • Renal Cell Carcinoma, Clear Cell

  • Clear Cell Kidney Carcinoma

  • Clear Cell Rcc

  • Cystic-Multilocular Variant

  • Clear Cell Renal Cell Adenocarcinoma

  • Hereditary Clear Cell Renal Cell Adenocarcinoma

  • Common Renal Cell Carcinoma

  • Crcc

  • Renal Cell Carcinoma Non-Papillary

  • Carcinoma Renal Cell

  • Renal Cell Cancer

  • Carcinoma, Renal Cell, Nonpapillary

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus ALDOA VGNC VGNC:107737
Macaca mulatta ALDOA VGNC VGNC:103785
Bos taurus ALDOA VGNC VGNC:25821
Rattus norvegicus ALDOA RGD RGD:2089
Mus musculus ALDOA MGD MGI:87994
Others ALDOA NCBI