ALDH1L1 - aldehyde dehydrogenase 1 family member L1 Gene

Also Known as FDH; FTHFD; 10-fTHF; 10-FTHFDH

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10840

About ALDH1L1

Cytogenetic location: 3q21.3 Genomic coordinates (GRCh38): 3:126,103,570-126,197,945 (from NCBI)

This gene has 18 transcripts (splice variants), 176 orthologues and 17 paralogues. Biased expression in liver (RPKM 99.3), kidney (RPKM 65.2) and 8 other tissues.

Summary

The protein encoded by this gene catalyzes the conversion of 10-formyltetrahydrofolate, nicotinamide adenine dinucleotide phosphate (NADP+), and water to tetrahydrofolate, NADPH, and carbon dioxide. The encoded protein belongs to the aldehyde dehydrogenase family. Loss of function or expression of this gene is associated with decreased Apoptosis, increased cell motility, and Cancer progression. There is an antisense transcript that overlaps on the opposite strand with this gene locus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jun 2012]

ALDH1L1 Products (3)

mRNA Protein Name
NM_001270364.2 NP_001257293.1 cytosolic 10-formyltetrahydrofolate dehydrogenase isoform 1
NM_001270365.2 NP_001257294.1 cytosolic 10-formyltetrahydrofolate dehydrogenase isoform 3
NM_012190.4 NP_036322.2 cytosolic 10-formyltetrahydrofolate dehydrogenase isoform 2
Molecular Function GO Annotation Evidence References Source
enables formyltetrahydrofolate dehydrogenase activity IDA
IDA: Inferred from direct assay
19933275 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
28514442 GOA
Biological Process GO Annotation Evidence References Source
involved in 10-formyltetrahydrofolate catabolic process IDA
IDA: Inferred from direct assay
19933275 GOA
involved in NADPH regeneration IDA
IDA: Inferred from direct assay
19933275 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

ALDH1L1 Protein Structure

Formyl_trans_N

Formyl_trans_N: Formyl transferase (1 - 180)

Formyl_trans_C

Formyl_trans_C: Formyl transferase, C-terminal domain (205 - 309)

PP-binding

PP-binding: Phosphopantetheine attachment site (326 - 391)

Aldedh

Aldedh: Aldehyde dehydrogenase family (430 - 898)

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  • 800
  • 902 a.a.
Protein Preferred Names Protein Names

cytosolic 10-formyltetrahydrofolate dehydrogenase

  • 10-formyltetrahydrofolate dehydrogenase

ALDH1L1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ALDH1L1 O75891 ALDH1L2 Homo sapiens Q3SY69 33961781
Intra
ALDH1L1 O75891 ALDH1L2 Homo sapiens Q3SY69 28514442
Cross: Cross-species interaction Intra: Intraspecies interaction

ALDH1L1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82286 ALDH1L1 Antibody (YA2031) WB Mouse, Rat
HY-P82286A ALDH1L1 Antibody (YA2031)(PBS only) WB Mouse, Rat
HY-P83869 ALDH1L1 Antibody (YA3566) WB, IHC-P, FC, ELISA Human, Mouse, Rat
HY-P83869A ALDH1L1 Antibody (YA3566)(PBS only) WB, IHC-P, FC, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
Megalencephalic Leukoencephalopathy With Subcortical Cysts 1
  • Van Der Knaap Disease

  • Leukoencephalopathy With Swelling And Cysts

  • MLC1

  • Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts

  • Lvm

  • Vl

  • Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, 1

  • Leukoencephalopathy, Megalencephalic, With Subcortical Cysts, Type 1

  • Megalencephalic Leukoencephalopathy With Subcortical Cysts

Neural Tube Defects
  • Spina Bifida

  • Neural Tube Defect

  • NTD

  • Neural Tube Defects, Susceptibility To

  • Spinal Dysraphism

  • Spina Bifida, Susceptibility To

  • Rachischisis

  • Cleft Spine

  • Open Spine

  • Hydrocele Spinalis

  • Neural Tube Defect Nos

  • Sb - [Spina Bifida]

  • Spinal Hernia Nos

  • Spinal Fissure Nos

Focal Dermal Hypoplasia
  • Goltz Syndrome

  • Goltz-Gorlin Syndrome

  • FDH

  • FODH

  • Dhof

  • Goltz Gorlin Syndrome

  • Hypoplasia, Dermal, Focal

Megalencephalic Leukoencephalopathy With Subcortical Cysts
  • Vacuolating Megalencephalic Leukoencephalopathy With Subcortical Cysts

  • Mlc

  • Van Der Knaap Disease

  • Lvm

  • Leukoencephalopathy With Swelling And Cysts

  • Megalencephaly-Cystic Leukodystrophy

  • Megalencephalic Leukodystrophy Megalencephaly-Cystic Leukodystorphy Syndrome

  • Infantile Leukoencephalopathy And Megalencephaly

  • Leukoencephalopathy With Swelling And A Discrepantly Mild Course

  • Vacuolating Leukoencephalopathy

  • Megalencephalic Leukodystrophy

  • Megalencephaly-Cystic Leukodystrophy Syndrome

  • Van Der Knaap Syndrome

  • Leukoencephalopathy, Megalencephalic, With Subcortical Cysts

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

Pilomyxoid Astrocytoma
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
Rattus norvegicus ALDH1L1 RGD RGD:621294
Macaca mulatta ALDH1L1 VGNC VGNC:81355
Mus musculus ALDH1L1 MGD MGI:1340024
Bos taurus ALDH1L1 VGNC VGNC:25811
Others ALDH1L1 NCBI