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Protein Coding Gene : Aldh4a1 aldehyde dehydrogenase 4 family, member A1
Primary Identifier  MGI:2443883 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  212647
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables 1-pyrroline-5-carboxylate dehydrogenase activity. Predicted to be involved in proline catabolic process to glutamate. Predicted to act upstream of or within proline metabolic process. Located in mitochondrion. Is expressed in several structures, including alimentary system; brain; integumental system; metanephros; and respiratory system. Human ortholog(s) of this gene implicated in hyperprolinemia type 2. Orthologous to human ALDH4A1 (aldehyde dehydrogenase 4 family member A1).
  • synonyms:
  • MGD-MRK-1205,
  • RIKEN cDNA A930035F14 gene,
  • MGD-MRK-16330,
  • Aldh4a1,
  • A930035F14Rik,
  • ALDH4,
  • MGI:1353453,
  • MGI:99552,
  • aldehyde dehydrogenase-1, mitochondrial,
  • MGD-MRK-1212,
  • succinic semialdehyde dehydrogenase,
  • Ssdh1,
  • P5CDH,
  • Ahd1,
  • aldehyde dehydrogenase 4 family, member A1,
  • Ahd-1
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Features --> Cross References

Genome

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0 Canonical

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0 Exons

0 Genomic Clusters

3 Involved In Mutations

Trail: ProteinCodingGene

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0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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