Details for: CRLF1
Associated with
Other Information
Genular Protein ID: 2021736150
Symbol: CRLF1_HUMAN
Name: Cytokine receptor-like factor 1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9686600
Title: Cytokine-like factor-1, a novel soluble protein, shares homology with members of the cytokine type I receptor family.
PubMed ID: 9686600
PubMed ID: 12975309
Title: The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.
PubMed ID: 12975309
DOI: 10.1101/gr.1293003
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: 15340161
Title: Signal peptide prediction based on analysis of experimentally verified cleavage sites.
PubMed ID: 15340161
DOI: 10.1110/ps.04682504
PubMed ID: 10966616
Title: CLF associates with CLC to form a functional heteromeric ligand for the CNTF receptor complex.
PubMed ID: 10966616
DOI: 10.1038/78765
PubMed ID: 26858303
Title: Cytokine-like factor 1, an essential facilitator of cardiotrophin-like cytokine:ciliary neurotrophic factor receptor alpha signaling and sorLA-mediated turnover.
PubMed ID: 26858303
DOI: 10.1128/mcb.00917-15
PubMed ID: 12509788
Title: Cold-induced sweating syndrome is caused by mutations in the CRLF1 gene.
PubMed ID: 12509788
DOI: 10.1086/346120
PubMed ID: 16952376
Title: Cold-induced sweating syndrome: a report of two cases and demonstration of genetic heterogeneity.
PubMed ID: 16952376
PubMed ID: 17436251
Title: Mutations in cytokine receptor-like factor 1 (CRLF1) account for both Crisponi and cold-induced sweating syndromes.
PubMed ID: 17436251
DOI: 10.1086/513608
PubMed ID: 17436252
Title: Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1.
PubMed ID: 17436252
DOI: 10.1086/516843
PubMed ID: 21326283
Title: Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders.
PubMed ID: 21326283
PubMed ID: 23026229
Title: Multiple small hyperintense lesions in the subcortical white matter on cranial MR images in two Turkish brothers with cold-induced sweating syndrome caused by a novel missense mutation in the CRLF1 gene.
PubMed ID: 23026229
PubMed ID: 24488861
Title: Expanding the mutational spectrum of CRLF1 in Crisponi/CISS1 syndrome.
PubMed ID: 24488861
DOI: 10.1002/humu.22522
Sequence Information:
- Length: 422
- Mass: 46302
- Checksum: AD9DEFCB01B84228
- Sequence:
MPAGRRGPAA QSARRPPPLL PLLLLLCVLG APRAGSGAHT AVISPQDPTL LIGSSLLATC SVHGDPPGAT AEGLYWTLNG RRLPPELSRV LNASTLALAL ANLNGSRQRS GDNLVCHARD GSILAGSCLY VGLPPEKPVN ISCWSKNMKD LTCRWTPGAH GETFLHTNYS LKYKLRWYGQ DNTCEEYHTV GPHSCHIPKD LALFTPYEIW VEATNRLGSA RSDVLTLDIL DVVTTDPPPD VHVSRVGGLE DQLSVRWVSP PALKDFLFQA KYQIRYRVED SVDWKVVDDV SNQTSCRLAG LKPGTVYFVQ VRCNPFGIYG SKKAGIWSEW SHPTAASTPR SERPGPGGGA CEPRGGEPSS GPVRRELKQF LGWLKKHAYC SNLSFRLYDQ WRAWMQKSHK TRNQDEGILP SGRRGTARGP AR
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.