ALDH3B1 - aldehyde dehydrogenase 3 family member B1 Gene

Also Known as ALDH4; ALDH7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 221

About ALDH3B1

Cytogenetic location: 11q13.2 Genomic coordinates (GRCh38): 11:68,008,547-68,029,276 (from NCBI)

This gene has 9 transcripts (splice variants), 355 orthologues and 17 paralogues. Broad expression in lung (RPKM 26.2), bone marrow (RPKM 14.3) and 17 other tissues.

Summary

This gene encodes a member of the aldehyde dehydrogenase protein family. Aldehyde dehydrogenases are a family of isozymes that may play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. The encoded protein is able to oxidize long-chain fatty aldehydes in vitro, and may play a role in protection from oxidative stress. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

ALDH3B1 Products (5)

mRNA Protein Name
NM_000694.4 NP_000685.1 aldehyde dehydrogenase family 3 member B1 isoform a
NM_001030010.3 NP_001025181.1 aldehyde dehydrogenase family 3 member B1 isoform b
NM_001161473.3 NP_001154945.1 aldehyde dehydrogenase family 3 member B1 isoform a
NM_001290058.2 NP_001276987.1 aldehyde dehydrogenase family 3 member B1 isoform c
NM_001290059.2 NP_001276988.1 aldehyde dehydrogenase family 3 member B1 isoform d
Molecular Function GO Annotation Evidence References Source
enables aldehyde dehydrogenase [NAD(P)+] activity IDA
IDA: Inferred from direct assay
20699116 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within aldehyde catabolic process IDA
IDA: Inferred from direct assay
20699116 GOA
acts upstream of or within cellular response to oxidative stress IDA
IDA: Inferred from direct assay
20699116 GOA
acts upstream of or within response to oxidative stress IDA
IDA: Inferred from direct assay
20699116 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
20699116 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

ALDH3B1 Protein Structure

Aldedh

Aldedh: Aldehyde dehydrogenase family (52 - 386)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 429 a.a.
Protein Preferred Names Protein Names

aldehyde dehydrogenase family 3 member B1

  • aldehyde dehydrogenase 3B1

ALDH3B1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ALDH3B1 P43353 KRT40 Homo sapiens Q6A162 25416956
Intra
ALDH3B1 P43353 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ALDH3B1 P43353 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ALDH3B1 P43353 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ALDH3B1 P43353 KRTAP10-8 Homo sapiens P60410 25416956
Intra
ALDH3B1 P43353 KRTAP10-9 Homo sapiens P60411 25416956
Intra
ALDH3B1 P43353 KRTAP10-5 Homo sapiens P60370 25416956
Intra
ALDH3B1 P43353 KRTAP10-5 Homo sapiens P60370 25416956
Intra
ALDH3B1 P43353 KRTAP10-5 Homo sapiens P60370 25416956
Intra
ALDH3B1 P43353 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ALDH3B1 P43353 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ALDH3B1 P43353 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ALDH3B1 P43353 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ALDH3B1 P43353 KRT34 Homo sapiens O76011 32296183
Intra
ALDH3B1 P43353 KRT34 Homo sapiens O76011 32296183
Intra
ALDH3B1 P43353 KRTAP1-3 Homo sapiens Q8IUG1 32296183
Intra
ALDH3B1 P43353 KRTAP1-3 Homo sapiens Q8IUG1 32296183
Intra
ALDH3B1 P43353 KRTAP12-3 Homo sapiens P60328 32296183
Intra
ALDH3B1 P43353 KRTAP12-3 Homo sapiens P60328 32296183
Intra
ALDH3B1 P43353 KRTAP12-3 Homo sapiens P60328 32296183
Intra
ALDH3B1 P43353 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ALDH3B1 P43353 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ALDH3B1 P43353 KRTAP1-1 Homo sapiens Q07627 32296183
Intra
ALDH3B1 P43353 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ALDH3B1 P43353 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
ALDH3B1 P43353 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
ALDH3B1 P43353 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
ALDH3B1 P43353 KRTAP3-3 Homo sapiens Q9BYR6 32296183
Intra
ALDH3B1 P43353 KRTAP5-9 Homo sapiens P26371 32296183
Intra
ALDH3B1 P43353 KRTAP5-9 Homo sapiens P26371 32296183
Intra
ALDH3B1 P43353 NOTCH2NLA Homo sapiens Q7Z3S9 25416956
Intra
ALDH3B1 P43353 KRT31 Homo sapiens Q15323 25416956
Intra
ALDH3B1 P43353 KRT31 Homo sapiens Q15323 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Paranoid Schizophrenia
  • Chronic Paranoid Schizophrenia

  • Paranoid Type Schizophrenia

  • Paranoid Type Schizophrenia Subchronic State

  • Paraphrenia - Late

  • Paraphrenic Schizophrenia

  • Schizophrenia, Paranoid

Sjogren-Larsson Syndrome
  • Sjögren-Larsson Syndrome

  • SLS

  • Faldh Deficiency

  • Fatty Aldehyde Dehydrogenase Deficiency

  • Fatty Acid Alcohol Oxidoreductase Deficiency

  • Ichthyosis, Spastic Neurologic Disorder, And Oligophrenia

  • Sjogren Larsson Syndrome

  • Fatty Alcohol:Nad+ Oxidoreductase Deficiency

  • Sjogren-Larsson'S Syndrome

  • Fadh Deficiency

  • Fao Deficiency

  • Congenital Icthyosis Mental Retardation Spasticity Syndrome

  • Ichthyosis Oligophrenia Syndrome

  • Sjoegren-Larsson Syndrome

Paraneoplastic Polyneuropathy
Epilepsy, Pyridoxine-Dependent
  • Pyridoxine-Dependent Epilepsy

  • PDE

  • Pyridoxine Dependency With Seizures

  • Vitamin B6-Dependent Seizures

  • EPD

  • Aasa Dehydrogenase Deficiency

  • Antiquitin Deficiency

  • Pyridoxine Dependency

  • Glutamate Decarboxylase Deficiency

  • Pyridoxine-Dependent Seizures

  • Deficiency Of Glutamate Decarboxylase

Hyperprolinemia
  • Proline Oxidase Deficiency

  • Hyperprolinemia Type 1

  • Proline Hydrogenase Deficiency

  • Prolinemia

  • Pyrroline Carboxylate Dehydrogenase Deficiency

  • Pyrroline-5-Carboxylate Dehydrogenase Deficiency

  • Proline Dehydrogenase Deficiency

  • Hyperprolinemia Type 2

Succinic Semialdehyde Dehydrogenase Deficiency
  • 4-Hydroxybutyric Aciduria

  • Ssadh Deficiency

  • Gamma-Hydroxybutyric Aciduria

  • Gaba Metabolic Defect

  • SSADHD

  • Ssadh

  • Succinate-Semialdehyde Dehydrogenase Deficiency

  • Gamma-Hydroxybutyricaciduria

  • 4-Hydroxybutyricaciduria

  • Gamma-Hydroxybutyric Acidemia

  • Succinate Semialdehyde Dehydrogenase Deficiency

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
Bos taurus ALDH3B1 VGNC VGNC:56255
Macaca mulatta ALDH3B1 VGNC VGNC:69789
Mus musculus ALDH3B1 MGD MGI:1914939
Rattus norvegicus ALDH3B1 RGD RGD:1359546
Canis familiaris ALDH3B1 VGNC VGNC:51840
Others ALDH3B1 NCBI