Details for: TECR
Associated with
Other Information
Genular Protein ID: 1740968351
Symbol: TECR_HUMAN
Name: Synaptic glycoprotein SC2
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9653160
Title: Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning.
PubMed ID: 9653160
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: 12482854
Title: Identification of two mammalian reductases involved in the two-carbon fatty acyl elongation cascade.
PubMed ID: 12482854
PubMed ID: 19608861
Title: Lysine acetylation targets protein complexes and co-regulates major cellular functions.
PubMed ID: 19608861
PubMed ID: 20937905
Title: ELOVL1 production of C24 acyl-CoAs is linked to C24 sphingolipid synthesis.
PubMed ID: 20937905
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 25049234
Title: Dual functions of the trans-2-enoyl-CoA reductase TER in the sphingosine 1-phosphate metabolic pathway and in fatty acid elongation.
PubMed ID: 25049234
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 21212097
Title: Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
PubMed ID: 21212097
DOI: 10.1093/hmg/ddq569
PubMed ID: 24220030
Title: Mutation for nonsyndromic mental retardation in the trans-2-enoyl-CoA reductase TER gene involved in fatty acid elongation impairs the enzyme activity and stability, leading to change in sphingolipid profile.
PubMed ID: 24220030
Sequence Information:
- Length: 308
- Mass: 36034
- Checksum: 120AD0883820784D
- Sequence:
MKHYEVEILD AKTREKLCFL DKVEPHATIA EIKNLFTKTH PQWYPARQSL RLDPKGKSLK DEDVLQKLPV GTTATLYFRD LGAQISWVTV FLTEYAGPLF IYLLFYFRVP FIYGHKYDFT SSRHTVVHLA CICHSFHYIK RLLETLFVHR FSHGTMPLRN IFKNCTYYWG FAAWMAYYIN HPLYTPPTYG AQQVKLALAI FVICQLGNFS IHMALRDLRP AGSKTRKIPY PTKNPFTWLF LLVSCPNYTY EVGSWIGFAI MTQCLPVALF SLVGFTQMTI WAKGKHRSYL KEFRDYPPLR MPIIPFLL
Genular Protein ID: 431162064
Symbol: B3KSQ1_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
Sequence Information:
- Length: 323
- Mass: 37467
- Checksum: 1E1861954C204D9F
- Sequence:
MILQETKAAC GIPAIPHCSR VEILDAKTRE KLCFLDKVEP HATIAEIKNL FTKTHPQWYP ARQSLRLDPK GKSLKDEDVL QKLPVGTTAT LYFRDLGAQI SWVTVFLTEY AGPLFIYLLF YFRVPFIYGH KYDFTSSRHT VVHLACICHS FHYIKRLLET LFVHRFSHGT MPLRNIFKNC TYYWGFAAWM AYYINHPLYT PPTYGAQQVK LALAIFVICQ LGNFSIHMAL RDLRPAGSKT RKIPYPTKNP FTWLFLLVSC PNYTYEVGSW IGFAIMTQCL PVALFSLVGF TQMTIWAKGK HRSYLKEFRD YPPLRMPIIP FLL
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.