1. Gene
  2. MAP3K14 - mitogen-activated protein kinase kinase kinase 14 Gene

MAP3K14 - mitogen-activated protein kinase kinase kinase 14 Gene

Homo sapiens

Also known as HS; NIK; HSNIK; FTDCR1B

Gene ID: 9020 | Gene type: protein coding

About MAP3K14

Cytogenetic location: 17q21.31 Genomic coordinates (GRCh38): 17:45,263,119-45,317,020 (from NCBI)

This gene has 6 transcripts (splice variants), 1 gene allele, 241 orthologues, 35 paralogues and is associated with 1 phenotype. Ubiquitous expression in lymph node (RPKM 11.1), spleen (RPKM 8.5) and 25 other tissues.

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 in an NF-kappaB-inducing signalling cascade common to receptors of the tumour-necrosis/nerve-growth factor (TNF/NGF) family and to the interleukin-1 type-I receptor. [provided by RefSeq, Jul 2008]

MAP3K14 Products(1)

mRNA Protein Name
NM_003954.5 NP_003945.2 mitogen-activated protein kinase kinase kinase 14
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
9020361 GOA
enables protein kinase activity IDA
IDA: Inferred from direct assay
15001576 GOA
enables protein serine/threonine kinase activity EXP
EXP: Inferred from Experiment
9520446 GOA
Biological Process GO Annotation Evidence Reference Source
involved in cellular response to mechanical stimulus IEP
IEP: Inferred from expression pattern
19593445 GOA
involved in defense response to virus IDA
IDA: Inferred from direct assay
21478870 GOA
involved in non-canonical NF-kappaB signal transduction IMP
IMP: Inferred from mutant phenotype
10094049 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

mitogen-activated protein kinase kinase kinase 14

NF-kappa-beta-inducing kinase

MAP3K14 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
MAP3K14 Q99558 RPS11 Homo sapiens P62280 31980649
Intra
MAP3K14 Q99558 KPNB1 Homo sapiens Q14974 30833792
Intra
MAP3K14 Q99558 CDC37 Homo sapiens Q16543 25036637
Intra
MAP3K14 Q99558 CDC37 Homo sapiens Q16543 30833792
Intra
MAP3K14 Q99558 CDC37 Homo sapiens Q16543 31980649
Intra
MAP3K14 Q99558 CDC37 Homo sapiens Q16543 32707033
Intra
MAP3K14 Q99558 HSP90AA1 Homo sapiens P07900 31980649
Intra
MAP3K14 Q99558 HSP90AA1 Homo sapiens P07900 30833792
Intra
MAP3K14 Q99558 HSP90AA1 Homo sapiens P07900 32707033
Intra
MAP3K14 Q99558 RPL4 Homo sapiens P36578 31980649
Intra
MAP3K14 Q99558 HRAS Homo sapiens P01112 32814053
Intra
MAP3K14 Q99558 HRAS Homo sapiens P01112 32814053
Intra
MAP3K14 Q99558 HRAS Homo sapiens P01112 32814053
Intra
MAP3K14 Q99558 RPS13 Homo sapiens P62277 31980649
Intra
MAP3K14 Q99558 HSP90AB1 Homo sapiens P08238 32707033
Intra
MAP3K14 Q99558 HSP90AB1 Homo sapiens P08238 22939624
Intra
MAP3K14 Q99558 HSP90AB1 Homo sapiens P08238 31980649
Intra
MAP3K14 Q99558 TRAF2 Homo sapiens Q12933 31980649
Intra
MAP3K14 Q99558 TRAF2 Homo sapiens Q12933
Y2H
9020361
Intra
MAP3K14 Q99558 TRAF2 Homo sapiens Q12933 25416956
Intra
MAP3K14 Q99558 TRAF2 Homo sapiens Q12933 25416956
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 32296183
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 31980649
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 32296183
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 33961781
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 28514442
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 32707033
Intra
MAP3K14 Q99558 TRAF3 Homo sapiens Q13114 30833792
Intra
MAP3K14 Q99558 RPL6 Homo sapiens Q02878 31980649
Intra
MAP3K14 Q99558 RPL8 Homo sapiens P62917 31980649
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 30833792
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 32707033
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 9520446
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 16498412
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 33961781
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 28514442
Intra
MAP3K14 Q99558 CHUK Homo sapiens O15111 31980649
Intra
MAP3K14 Q99558 IKBKB Homo sapiens O14920 33961781
Intra
MAP3K14 Q99558 IKBKB Homo sapiens O14920 30833792
Intra
MAP3K14 Q99558 IKBKB Homo sapiens O14920 28514442
Intra
MAP3K14 Q99558 IKBKB Homo sapiens O14920 32707033
Intra
MAP3K14 Q99558 IKBKB Homo sapiens O14920 9520446
Intra
MAP3K14 Q99558 IKBKG Homo sapiens Q9Y6K9 31980649
Intra
MAP3K14 Q99558 IKBKG Homo sapiens Q9Y6K9 33961781
Intra
MAP3K14 Q99558 IKBKG Homo sapiens Q9Y6K9 32707033
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Nik Deficiency

Primary Immunodeficiency With Multifaceted Aberrant Lymphoid Immunity

Pancreatic Ductal Adenocarcinoma

Ductal Adenocarcinoma Of The Pancreas

Immunodeficiency 50

Combined Immunodeficiency Due To Moesin Deficiency

IMD50

Immunodeficiency 50, X-Linked Recessive

Cid Due To Moesin Deficiency

Msn-Related Combined Immunodeficiency

X-Linked Moesin-Associated Immunodeficiency

Immunodeficiency 50 X Linked Recessive

Pancreatic Adenosquamous Carcinoma

Adenosquamous Carcinoma Of Pancreas

Adenosquamous Carcinoma Of The Pancreas

T-Cell Acute Lymphoblastic Leukemia

T-Cell Leukemia

Acute T Cell Leukemia

Precursor T Lymphoblastic Leukemia

Precursor T-Lymphoblastic Lymphoma/Leukemia

T Acute Lymphoblastic Leukemia

T-Cell Acute Lymphocytic Leukaemia

T-Cell Lymphoblastic Leukemia/Lymphoma

Leukemia T-Cell

Leukemia, T-Cell

Leukemia, Acute, Lymphoblastic, T-Cell

Leukemia, T-Cell Acute Lymphoblastic

Leukemia, Acute T-Cell

Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

Precursor T-Cell Lymphoblastic Lymphoma

Precursor T Cell Lymphoblastic Leukemia/Lymphoblastic Lymphoma

Ectodermal Dysplasia

Congenital Ectodermal Defect

Congenital Ectodermal Dysplasia

Ectodermal Dysplasia Syndrome

Dysplasia, Ectodermal

Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus MAP3K14 RGD RGD:1310487
Bos taurus MAP3K14 VGNC VGNC:31192
Felis catus MAP3K14 VGNC VGNC:99219
Mus musculus MAP3K14 MGD MGI:1858204
Macaca mulatta MAP3K14 VGNC VGNC:81459
Canis familiaris MAP3K14 VGNC VGNC:42970