Details for: NLRC4

Gene ID: 58484

Symbol: NLRC4

Ensembl ID: ENSG00000091106

Description: NLR family CARD domain containing 4

Associated with

Other Information

Genular Protein ID: 4059991602

Symbol: NLRC4_HUMAN

Name: NLR family CARD domain-containing protein 4

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11374873

Title: Human CARD12 is a novel CED4/Apaf-1 family member that induces apoptosis.

PubMed ID: 11374873

DOI: 10.1006/bbrc.2001.4928

PubMed ID: 11472070

Title: CLAN, a novel human CED-4-like gene.

PubMed ID: 11472070

DOI: 10.1006/geno.2001.6579

PubMed ID: 11390368

Title: Identification of Ipaf, a human caspase-1-activating protein related to Apaf-1.

PubMed ID: 11390368

DOI: 10.1074/jbc.c100250200

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: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15815621

Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

PubMed ID: 15815621

DOI: 10.1038/nature03466

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: 15107016

Title: Heterotypic interactions among NACHT domains: implications for regulation of innate immune responses.

PubMed ID: 15107016

DOI: 10.1042/bj20031506

PubMed ID: 22801494

Title: Novel role of PKR in inflammasome activation and HMGB1 release.

PubMed ID: 22801494

DOI: 10.1038/nature11290

PubMed ID: 33420028

Title: Structural basis for distinct inflammasome complex assembly by human NLRP1 and CARD8.

PubMed ID: 33420028

DOI: 10.1038/s41467-020-20319-5

PubMed ID: 25385754

Title: An inherited mutation in NLRC4 causes autoinflammation in human and mice.

PubMed ID: 25385754

DOI: 10.1084/jem.20141091

PubMed ID: 25217960

Title: Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation.

PubMed ID: 25217960

DOI: 10.1038/ng.3066

PubMed ID: 25217959

Title: An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome.

PubMed ID: 25217959

DOI: 10.1038/ng.3089

Sequence Information:

  • Length: 1024
  • Mass: 116159
  • Checksum: 49378DBB54938E0F
  • Sequence:
  • MNFIKDNSRA LIQRMGMTVI KQITDDLFVW NVLNREEVNI ICCEKVEQDA ARGIIHMILK 
    KGSESCNLFL KSLKEWNYPL FQDLNGQSLF HQTSEGDLDD LAQDLKDLYH TPSFLNFYPL 
    GEDIDIIFNL KSTFTEPVLW RKDQHHHRVE QLTLNGLLQA LQSPCIIEGE SGKGKSTLLQ 
    RIAMLWGSGK CKALTKFKFV FFLRLSRAQG GLFETLCDQL LDIPGTIRKQ TFMAMLLKLR 
    QRVLFLLDGY NEFKPQNCPE IEALIKENHR FKNMVIVTTT TECLRHIRQF GALTAEVGDM 
    TEDSAQALIR EVLIKELAEG LLLQIQKSRC LRNLMKTPLF VVITCAIQMG ESEFHSHTQT 
    TLFHTFYDLL IQKNKHKHKG VAASDFIRSL DHCGDLALEG VFSHKFDFEL QDVSSVNEDV 
    LLTTGLLCKY TAQRFKPKYK FFHKSFQEYT AGRRLSSLLT SHEPEEVTKG NGYLQKMVSI 
    SDITSTYSSL LRYTCGSSVE ATRAVMKHLA AVYQHGCLLG LSIAKRPLWR QESLQSVKNT 
    TEQEILKAIN INSFVECGIH LYQESTSKSA LSQEFEAFFQ GKSLYINSGN IPDYLFDFFE 
    HLPNCASALD FIKLDFYGGA MASWEKAAED TGGIHMEEAP ETYIPSRAVS LFFNWKQEFR 
    TLEVTLRDFS KLNKQDIRYL GKIFSSATSL RLQIKRCAGV AGSLSLVLST CKNIYSLMVE 
    ASPLTIEDER HITSVTNLKT LSIHDLQNQR LPGGLTDSLG NLKNLTKLIM DNIKMNEEDA 
    IKLAEGLKNL KKMCLFHLTH LSDIGEGMDY IVKSLSSEPC DLEEIQLVSC CLSANAVKIL 
    AQNLHNLVKL SILDLSENYL EKDGNEALHE LIDRMNVLEQ LTALMLPWGC DVQGSLSSLL 
    KHLEEVPQLV KLGLKNWRLT DTEIRILGAF FGKNPLKNFQ QLNLAGNRVS SDGWLAFMGV 
    FENLKQLVFF DFSTKEFLPD PALVRKLSQV LSKLTFLQEA RLVGWQFDDD DLSVITGAFK 
    LVTA

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.