Gene Gene information from NCBI Gene database.
Entrez ID 389840
Gene name Mitogen-activated protein kinase kinase kinase 15
Gene symbol MAP3K15
Synonyms (NCBI Gene)
ASK3bA723P2.3
Chromosome X
Chromosome location Xp22.12
Summary The protein encoded by this gene is a member of the mitogen-activated protein kinase (MAPK) family. These family members function in a protein kinase signal transduction cascade, where an activated MAPK kinase kinase (MAP3K) phosphorylates and activates a
miRNA miRNA information provided by mirtarbase database.
202
miRTarBase ID miRNA Experiments Reference
MIRT1128587 hsa-miR-181a CLIP-seq
MIRT1128588 hsa-miR-181b CLIP-seq
MIRT1128589 hsa-miR-181c CLIP-seq
MIRT1128590 hsa-miR-181d CLIP-seq
MIRT1128591 hsa-miR-1827 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0000165 Process MAPK cascade IEA
GO:0000166 Function Nucleotide binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004674 Function Protein serine/threonine kinase activity IEA
GO:0004709 Function MAP kinase kinase kinase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300820 31689 ENSG00000180815
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZN16
Protein name Mitogen-activated protein kinase kinase kinase 15 (EC 2.7.11.25) (Apoptosis signal-regulating kinase 3) (MAPK/ERK kinase kinase 15) (MEK kinase 15) (MEKK 15)
Protein function Serine/threonine kinase which acts as a component of the MAP kinase signal transduction pathway (PubMed:20362554, PubMed:26732173). Once activated, acts as an upstream activator of the p38 MAPK signal transduction cascade through the phosphoryla
PDB 6V0M
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13281 DUF4071 136 515 Domain of unknown function (DUF4071) Family
PF19039 ASK_PH 525 624 ASK kinase PH domain Domain
PF00069 Pkinase 653 908 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 2 and isoform 3 are widely expressed. Isoform 2 highest levels are observed in fetal brain, and isoform 3 highest levels in pancreas, peripheral blood leukocytes, fetal brain and spleen. {ECO:0000269|PubMed:20362554}.
Sequence
MESGGGNAPAGALGAASESPQCPPPPGVEGAAGPAEPDGAAEGAAGGSGEGESGGGPRRA
LRAVYVRSESSQGGAAGGPEAGARQCLLRACEAEGAHLTSVPFGELDFGETAVLDAFYDA
DVAVVDMSDVSRQPSLFYHLGVRESFDMANNVILYHDTDADTALSLKDMVTQKNTASSGN
YYFIPYIVTPCADYFCCESDAQRRASEYMQPNWDNILGPLCMPLVDRFISLLKDIHVTSC
VYYKETLLNDIRKAREKYQGEELAKELARIKLRMDNTEVLTSDIIINLLLSYRDIQDYDA
MVKLVETLEMLPTCDLADQHNIKFHYAFALNRRNSTGDREKALQIMLQVLQSCDHPGPDM
FCLCGRIYKDIFLDSDCKDDTSRDSAIEWYRKGFELQSSLYSGINLAVLLIVAGQQFETS
LELRKIGVRLNSLLGRKGSLEKMNNYWDVGQFFSVSMLAHDVGKAVQAAERLFKLKPPVW
YLRSLVQNLLLIRRFKKTIIEHSPRQERLNFWLDI
IFEATNEVTNGLRFPVLVIEPTKVY
QPSYVSINNEAEERTVSLWHVSPTEMKQMHEWNFTASSIKGISLSKFDERCCFLYVHDNS
DDFQIYFSTEEQCSRFFSLVKEMI
TNTAGSTVELEGETDGDTLEYEYDHDANGERVVLGK
GTYGIVYAGRDLSNQVRIAIKEIPERDSRYSQPLHEEIALHKYLKHRNIVQYLGSVSENG
YIKIFMEQVPGGSLSALLRSKWGPMKEPTIKFYTKQILEGLKYLHENQIVHRDIKGDNVL
VNTYSGVVKISDFGTSKRLAGVNPCTETFTGTLQYMAPEIIDQGPRGYGAPADIWSLGCT
IIEMATSKPPFHELGEPQAAMFKVGMFKIHPEIPEALSAEARAFILSCFEPDPHKRATTA
ELLREGFL
RQVNKGKKNRIAFKPSEGPRGVVLALPTQGEPMATSSSEHGSVSPDSDAQPD
ALFERTRAPRHHLGHLLSVPDESSALEDRGLASSPEDRDQGLFLLRKDSERRAILYKILW
EEQNQVASNLQECVAQSSEELHLSVGHIKQIIGILRDFIRSPEHRVMATTISKLKVDLDF
DSSSISQIHLVLFGFQDAVNKILRNHLIRPHWMFAMDNIIRRAVQAAVTILIPELRAHFE
PTCETEGVDKDMDEAEEGYPPATGPGQEAQPHQQHLSLQLGELRQETNRLLEHLVEKERE
YQNLLRQTLEQKTQELYHLQLKLKSNCITENPAGPYGQRTDKELIDWLRLQGADAKTIEK
IVEEGYTLSDILNEITKEDLRYLRLRGGLLCRLWSAVSQYRRAQEASETKDKA
Sequence length 1313
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
42
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Likely benign rs61744617 RCV005938632
Colorectal cancer Likely benign rs61744617 RCV005938633
Gastric cancer Likely benign rs34487219 RCV005871385
MAP3K15-related disorder Uncertain significance; Benign; Likely benign rs373501081, rs145004525, rs759538376, rs1296783815, rs952918430, rs141688905, rs61744617, rs748480121, rs56177884, rs140553102, rs5955788, rs56233219, rs141525900, rs139556701, rs200041074
View all (19 more)
RCV003395640
RCV003946367
RCV003408636
RCV003393082
RCV003399615
RCV003909490
RCV003919688
RCV003919806
RCV003929647
RCV003903905
RCV003912297
RCV003916776
RCV003916934
RCV003911465
RCV003911716
RCV003909669
RCV003909799
RCV003933892
RCV003942000
RCV003952001
RCV003952029
RCV003964088
RCV003919455
RCV003931413
RCV003924402
RCV003947240
RCV003961936
RCV003922263
RCV003926907
RCV003949205
RCV003956702
RCV003982151
RCV003968925
RCV003969039
RCV003925921
RCV003918462
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Azoospermia Nonobstructive Associate 36017582
Carcinoma Hepatocellular Associate 35311629
Diabetes Mellitus Inhibit 34662886
Diabetes Mellitus Associate 36383675
Diabetes Mellitus Type 2 Associate 36383675
Hypertension Inhibit 34662886
Insulin Resistance Associate 36383675
Melanocytic nevus syndrome congenital Associate 36085074
Obesity Associate 36383675
Polycystic Ovary Syndrome Associate 31745224