Gene Gene information from NCBI Gene database.
Entrez ID 9020
Gene name Mitogen-activated protein kinase kinase kinase 14
Gene symbol MAP3K14
Synonyms (NCBI Gene)
FTDCR1BHSHSNIKIMD112NIK
Chromosome 17
Chromosome location 17q21.31
Summary This gene encodes mitogen-activated protein kinase kinase kinase 14, which is a serine/threonine protein-kinase. This kinase binds to TRAF2 and stimulates NF-kappaB activity. It shares sequence similarity with several other MAPKK kinases. It participates
miRNA miRNA information provided by mirtarbase database.
203
miRTarBase ID miRNA Experiments Reference
MIRT020850 hsa-miR-155-5p Reporter assay 20584899
MIRT052929 hsa-miR-520e 5.0 22105365
MIRT052929 hsa-miR-520e 5.0 22105365
MIRT440287 hsa-miR-106b-5p HITS-CLIP 22473208
MIRT020850 hsa-miR-155-5p HITS-CLIP 22473208
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
HSF1 Unknown 19381566
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade IBA
GO:0000166 Function Nucleotide binding IEA
GO:0001650 Component Fibrillar center IDA
GO:0004672 Function Protein kinase activity IDA 15001576
GO:0004672 Function Protein kinase activity IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604655 6853 ENSG00000006062
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q99558
Protein name Mitogen-activated protein kinase kinase kinase 14 (EC 2.7.11.25) (NF-kappa-beta-inducing kinase) (HsNIK) (Serine/threonine-protein kinase NIK)
Protein function Lymphotoxin beta-activated kinase which seems to be exclusively involved in the activation of NF-kappa-B and its transcriptional activity. Phosphorylates CHUK/IKKA, thereby promoting proteolytic processing of NFKB2/P100, which leads to NF-kappa-
PDB 4DN5 , 4G3D , 4IDT , 4IDV , 6WPP , 6Z1Q , 6Z1T , 8YHW
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 401 649 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Weakly expressed in testis, small intestine, spleen, thymus, peripheral blood leukocytes, prostate, ovary and colon. {ECO:0000269|PubMed:9020361}.
Sequence
MAVMEMACPGAPGSAVGQQKELPKAKEKTPPLGKKQSSVYKLEAVEKSPVFCGKWEILND
VITKGTAKEGSEAGPAAISIIAQAECENSQEFSPTFSERIFIAGSKQYSQSESLDQIPNN
VAHATEGKMARVCWKGKRRSKARKKRKKKSSKSLAHAGVALAKPLPRTPEQESCTIPVQE
DESPLGAPYVRNTPQFTKPLKEPGLGQLCFKQLGEGLRPALPRSELHKLISPLQCLNHVW
KLHHPQDGGPLPLPTHPFPYSRLPHPFPFHPLQPWKPHPLESFLGKLACVDSQKPLPDPH
LSKLACVDSPKPLPGPHLEPSCLSRGAHEKFSVEEYLVHALQGSVSSGQAHSLTSLAKTW
AARGSRSREPSPKTEDNEGVLLTEKLKPVDYEYREEVHWATHQLRLGRGSFGEVHRMEDK
QTGFQCAVKKVRLEVFRAEELMACAGLTSPRIVPLYGAVREGPWVNIFMELLEGGSLGQL
VKEQGCLPEDRALYYLGQALEGLEYLHSRRILHGDVKADNVLLSSDGSHAALCDFGHAVC
LQPDGLGKSLLTGDYIPGTETHMAPEVVLGRSCDAKVDVWSSCCMMLHMLNGCHPWTQFF
RGPLCLKIASEPPPVREIPPSCAPLTAQAIQEGLRKEPIHRVSAAELGG
KVNRALQQVGG
LKSPWRGEYKEPRHPPPNQANYHQTLHAQPRELSPRAPGPRPAEETTGRAPKLQPPLPPE
PPEPNKSPPLTLSKEESGMWEPLPLSSLEPAPARNPSSPERKATVPEQELQQLEIELFLN
SLSQPFSLEEQEQILSCLSIDSLSLSDDSEKNPSKASQSSRDTLSSGVHSWSSQAEARSS
SWNMVLARGRPTDTPSYFNGVKVQIQSLNGEHLHIREFHRVKVGDIATGISSQIPAAAFS
LVTKDGQPVRYDMEVPDSGIDLQCTLAPDGSFAWSWRVKHGQLENRP
Sequence length 947
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
445
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Immunodeficiency 112 Pathogenic rs773929665 RCV004525819
NIK deficiency Likely pathogenic rs2143820144 RCV001978448
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs17846855 RCV005914279
Hepatocellular carcinoma Benign rs17846855 RCV005914280
Malignant lymphoma, large B-cell, diffuse Benign rs17846855 RCV005914282
MAP3K14-related disorder Benign; Likely benign rs17846855, rs2509021695, rs1323408203, rs151296471, rs2508980027, rs2509019273, rs2044155646, rs184263319 RCV003980528
RCV003898567
RCV003944133
RCV003941468
RCV003944436
RCV003969350
RCV003983716
RCV003938004
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Agammaglobulinemia Associate 25406581
Anti Neutrophil Cytoplasmic Antibody Associated Vasculitis Associate 37931331
Arthritis Rheumatoid Associate 25963989
Atherosclerosis Associate 29407886
Autoimmune Diseases Associate 37931331, 39766197
Breast Neoplasms Associate 19538528, 20735436, 26823811
Carcinogenesis Associate 32000390
Carcinoma Hepatocellular Associate 17711513
Carcinoma Non Small Cell Lung Associate 30195659, 31586084
Carcinoma Pancreatic Ductal Associate 23301098, 33525943