Details for: SLC44A1
Associated with
Other Information
Genular Protein ID: 1102346502
Symbol: CTL1_HUMAN
Name: CDw92
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 10677542
Title: An electric lobe suppressor for a yeast choline transport mutation belongs to a new family of transporter-like proteins.
PubMed ID: 10677542
PubMed ID: 11698453
Title: Characterization of CDw92 as a member of the choline transporter-like protein family regulated specifically on dendritic cells.
PubMed ID: 11698453
PubMed ID: 15715662
Title: Molecular characterization of the family of choline transporter-like proteins and their splice variants.
PubMed ID: 15715662
PubMed ID: 15164053
Title: DNA sequence and analysis of human chromosome 9.
PubMed ID: 15164053
DOI: 10.1038/nature02465
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: 18669648
Title: A quantitative atlas of mitotic phosphorylation.
PubMed ID: 18669648
PubMed ID: 19357133
Title: The solute carrier 44A1 is a mitochondrial protein and mediates choline transport.
PubMed ID: 19357133
DOI: 10.1096/fj.08-121491
PubMed ID: 22223895
Title: Comparative large-scale characterisation of plant vs. mammal proteins reveals similar and idiosyncratic N-alpha acetylation features.
PubMed ID: 22223895
PubMed ID: 23651124
Title: Choline transporter-like protein 4 (CTL4) links to non-neuronal acetylcholine synthesis.
PubMed ID: 23651124
DOI: 10.1111/jnc.12298
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 25944712
Title: N-terminome analysis of the human mitochondrial proteome.
PubMed ID: 25944712
PubMed ID: 33789160
Title: Choline transporter-like proteins 1 and 2 are newly identified plasma membrane and mitochondrial ethanolamine transporters.
PubMed ID: 33789160
PubMed ID: 31855247
Title: Choline transporter-like 1 deficiency causes a new type of childhood-onset neurodegeneration.
PubMed ID: 31855247
DOI: 10.1093/brain/awz376
Sequence Information:
- Length: 657
- Mass: 73302
- Checksum: 10D70CAB8E33E3AC
- Sequence:
MGCCSSASSA AQSSKREWKP LEDRSCTDIP WLLLFILFCI GMGFICGFSI ATGAAARLVS GYDSYGNICG QKNTKLEAIP NSGMDHTQRK YVFFLDPCNL DLINRKIKSV ALCVAACPRQ ELKTLSDVQK FAEINGSALC SYNLKPSEYT TSPKSSVLCP KLPVPASAPI PFFHRCAPVN ISCYAKFAEA LITFVSDNSV LHRLISGVMT SKEIILGLCL LSLVLSMILM VIIRYISRVL VWILTILVIL GSLGGTGVLW WLYAKQRRSP KETVTPEQLQ IAEDNLRALL IYAISATVFT VILFLIMLVM RKRVALTIAL FHVAGKVFIH LPLLVFQPFW TFFALVLFWV YWIMTLLFLG TTGSPVQNEQ GFVEFKISGP LQYMWWYHVV GLIWISEFIL ACQQMTVAGA VVTYYFTRDK RNLPFTPILA SVNRLIRYHL GTVAKGSFII TLVKIPRMIL MYIHSQLKGK ENACARCVLK SCICCLWCLE KCLNYLNQNA YTATAINSTN FCTSAKDAFV ILVENALRVA TINTVGDFML FLGKVLIVCS TGLAGIMLLN YQQDYTVWVL PLIIVCLFAF LVAHCFLSIY EMVVDVLFLC FAIDTKYNDG SPGREFYMDK VLMEFVENSR KAMKEAGKGG VADSRELKPM ASGASSA
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.