Details for: ALDH3A2
Associated with
Other Information
Genular Protein ID: 2017178677
Symbol: AL3A2_HUMAN
Name: Aldehyde dehydrogenase family 3 member A2
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 8528251
Title: Sjogren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene.
PubMed ID: 8528251
DOI: 10.1038/ng0196-52
PubMed ID: 9027499
Title: Genomic organization and expression of the human fatty aldehyde dehydrogenase gene (FALDH).
PubMed ID: 9027499
PubMed ID: 9070922
Title: Human fatty aldehyde dehydrogenase gene (ALDH10): organization and tissue-dependent expression.
PubMed ID: 9070922
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
PubMed ID: 15489334
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
PubMed ID: 15489334
DOI: 10.1101/gr.2596504
PubMed ID: 9133646
Title: Human liver fatty aldehyde dehydrogenase: microsomal localization, purification, and biochemical characterization.
PubMed ID: 9133646
PubMed ID: 9662422
Title: Involvement of microsomal fatty aldehyde dehydrogenase in the alpha-oxidation of phytanic acid.
PubMed ID: 9662422
PubMed ID: 18035827
Title: Characterisation of recombinant human fatty aldehyde dehydrogenase: implications for Sjoegren-Larsson syndrome.
PubMed ID: 18035827
PubMed ID: 18182499
Title: Characterization of the human omega-oxidation pathway for omega-hydroxy-very-long-chain fatty acids.
PubMed ID: 18182499
DOI: 10.1096/fj.07-099150
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 22633490
Title: The Sjogren-Larsson syndrome gene encodes a hexadecenal dehydrogenase of the sphingosine 1-phosphate degradation pathway.
PubMed ID: 22633490
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 25047030
Title: A gatekeeper helix determines the substrate specificity of Sjogren-Larsson Syndrome enzyme fatty aldehyde dehydrogenase.
PubMed ID: 25047030
DOI: 10.1038/ncomms5439
PubMed ID: 9254849
Title: A missense mutation in the FALDH gene identified in Sjogren-Larsson syndrome patients originating from the northern part of Sweden.
PubMed ID: 9254849
PubMed ID: 9829906
Title: Spectrum of mutations and sequence variants in the FALDH gene in patients with Sjoegren-Larsson syndrome.
PubMed ID: 9829906
DOI: 10.1002/(sici)1098-1004(1998)12:6<377::aid-humu3>3.0.co;2-i
PubMed ID: 10577908
Title: The molecular basis of Sjoegren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase gene.
PubMed ID: 10577908
DOI: 10.1086/302681
PubMed ID: 10792573
Title: A novel point mutation of the FALDH gene in a Japanese family with Sjoegren-Larsson syndrome.
PubMed ID: 10792573
Sequence Information:
- Length: 485
- Mass: 54848
- Checksum: 209601CB5803C7E3
- Sequence:
MELEVRRVRQ AFLSGRSRPL RFRLQQLEAL RRMVQEREKD ILTAIAADLC KSEFNVYSQE VITVLGEIDF MLENLPEWVT AKPVKKNVLT MLDEAYIQPQ PLGVVLIIGA WNYPFVLTIQ PLIGAIAAGN AVIIKPSELS ENTAKILAKL LPQYLDQDLY IVINGGVEET TELLKQRFDH IFYTGNTAVG KIVMEAAAKH LTPVTLELGG KSPCYIDKDC DLDIVCRRIT WGKYMNCGQT CIAPDYILCE ASLQNQIVWK IKETVKEFYG ENIKESPDYE RIINLRHFKR ILSLLEGQKI AFGGETDEAT RYIAPTVLTD VDPKTKVMQE EIFGPILPIV PVKNVDEAIN FINEREKPLA LYVFSHNHKL IKRMIDETSS GGVTGNDVIM HFTLNSFPFG GVGSSGMGAY HGKHSFDTFS HQRPCLLKSL KREGANKLRY PPNSQSKVDW GKFFLLKRFN KEKLGLLLLT FLGIVAAVLV KAEYY
Database document:
This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.