{"results":[{"entryType":"UniProtKB reviewed (Swiss-Prot)","primaryAccession":"O43318","secondaryAccessions":["B2RE27","E1P523","O43317","O43319","Q5TDN2","Q5TDN3","Q5TDT7","Q9NTR3","Q9NZ70"],"uniProtkbId":"M3K7_HUMAN","entryAudit":{"firstPublicDate":"2000-12-01","lastAnnotationUpdateDate":"2026-11-04","lastSequenceUpdateDate":"1998-06-01","entryVersion":250,"sequenceVersion":1},"annotationScore":5.0,"organism":{"scientificName":"Homo sapiens","commonName":"Human","taxonId":9606,"lineage":["Eukaryota","Metazoa","Chordata","Craniata","Vertebrata","Euteleostomi","Mammalia","Eutheria","Euarchontoglires","Primates","Haplorrhini","Catarrhini","Hominidae","Homo"]},"proteinExistence":"1: Evidence at protein level","proteinDescription":{"recommendedName":{"fullName":{"value":"Mitogen-activated protein kinase kinase kinase 7"},"ecNumbers":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10094049"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10838074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12589052"}],"value":"2.7.11.25"}]},"alternativeNames":[{"fullName":{"value":"Transforming growth factor-beta-activated kinase 1"},"shortNames":[{"value":"TGF-beta-activated kinase 1"}]}]},"genes":[{"geneName":{"evidences":[{"evidenceCode":"ECO:0000303","source":"PubMed","id":"28397838"},{"evidenceCode":"ECO:0000312","source":"HGNC","id":"HGNC:6859"}],"value":"MAP3K7"},"synonyms":[{"value":"TAK1"}]}],"comments":[{"texts":[{"evidences":[{"evidenceCode":"ECO:0000250","source":"UniProtKB","id":"Q62073"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10094049"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11460167"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12589052"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16845370"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16893890"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"21512573"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"37832545"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"8663074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"9079627"}],"value":"Serine/threonine kinase which acts as an essential component of the MAP kinase signal transduction pathway (PubMed:10094049, PubMed:11460167, PubMed:12589052, PubMed:16845370, PubMed:16893890, PubMed:21512573, PubMed:8663074, PubMed:9079627). Plays an important role in the cascades of cellular responses evoked by changes in the environment (PubMed:10094049, PubMed:11460167, PubMed:12589052, PubMed:16845370, PubMed:16893890, PubMed:21512573, PubMed:8663074, PubMed:9079627). Mediates signal transduction of TRAF6, various cytokines including interleukin-1 (IL-1), transforming growth factor-beta (TGFB), TGFB-related factors like BMP2 and BMP4, toll-like receptors (TLR), tumor necrosis factor receptor CD40 and B-cell receptor (BCR) (PubMed:16893890, PubMed:9079627). Once activated, acts as an upstream activator of the MKK/JNK signal transduction cascade and the p38 MAPK signal transduction cascade through the phosphorylation and activation of several MAP kinase kinases like MAP2K1/MEK1, MAP2K3/MKK3, MAP2K6/MKK6 and MAP2K7/MKK7 (PubMed:11460167, PubMed:8663074). These MAP2Ks in turn activate p38 MAPKs and c-jun N-terminal kinases (JNKs); both p38 MAPK and JNK pathways control the transcription factors activator protein-1 (AP-1) (PubMed:11460167, PubMed:12589052, PubMed:8663074). Independently of MAP2Ks and p38 MAPKs, acts as a key activator of NF-kappa-B by promoting activation of the I-kappa-B-kinase (IKK) core complex (PubMed:12589052, PubMed:8663074). Mechanistically, recruited to polyubiquitin chains of RIPK2 and IKBKG/NEMO via TAB2/MAP3K7IP2 and TAB3/MAP3K7IP3, and catalyzes phosphorylation and activation of IKBKB/IKKB component of the IKK complex, leading to NF-kappa-B activation (PubMed:10094049, PubMed:11460167). In osmotic stress signaling, plays a major role in the activation of MAPK8/JNK1, but not that of NF-kappa-B (PubMed:16893890). Promotes TRIM5 capsid-specific restriction activity (PubMed:21512573). Phosphorylates RIPK1 at 'Ser-321' which positively regulates RIPK1 interaction with RIPK3 to promote necroptosis but negatively regulates RIPK1 kinase activity and its interaction with FADD to mediate apoptosis (By similarity). Phosphorylates STING1 in response to cGAMP-activation, promoting association between STEEP1 and STING1 and STING1 translocation to COPII vesicles (PubMed:37832545)"}],"commentType":"FUNCTION"},{"commentType":"CATALYTIC ACTIVITY","reaction":{"name":"L-seryl-[protein] + ATP = O-phospho-L-seryl-[protein] + ADP + H(+)","reactionCrossReferences":[{"database":"Rhea","id":"RHEA:17989"},{"database":"Rhea","id":"RHEA-COMP:9863"},{"database":"Rhea","id":"RHEA-COMP:11604"},{"database":"ChEBI","id":"CHEBI:15378"},{"database":"ChEBI","id":"CHEBI:29999"},{"database":"ChEBI","id":"CHEBI:30616"},{"database":"ChEBI","id":"CHEBI:83421"},{"database":"ChEBI","id":"CHEBI:456216"}],"ecNumber":"2.7.11.25","evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10094049"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10838074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12589052"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"37832545"}]}},{"commentType":"CATALYTIC ACTIVITY","reaction":{"name":"L-threonyl-[protein] + ATP = O-phospho-L-threonyl-[protein] + ADP + H(+)","reactionCrossReferences":[{"database":"Rhea","id":"RHEA:46608"},{"database":"Rhea","id":"RHEA-COMP:11060"},{"database":"Rhea","id":"RHEA-COMP:11605"},{"database":"ChEBI","id":"CHEBI:15378"},{"database":"ChEBI","id":"CHEBI:30013"},{"database":"ChEBI","id":"CHEBI:30616"},{"database":"ChEBI","id":"CHEBI:61977"},{"database":"ChEBI","id":"CHEBI:456216"}],"ecNumber":"2.7.11.25","evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10094049"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10838074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12589052"}]}},{"commentType":"COFACTOR","cofactors":[{"name":"Mg(2+)","evidences":[{"evidenceCode":"ECO:0000305","source":"PubMed","id":"16289117"}],"cofactorCrossReference":{"database":"ChEBI","id":"CHEBI:18420"}}]},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10702308"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11104763"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11460167"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16893890"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17079228"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"29291351"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"37832545"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"9079627"}],"value":"Activated by pro-inflammatory cytokines and in response to physical and chemical stresses, including osmotic stress, oxidative stress, arsenic and ultraviolet light irradiation (PubMed:16893890). Activated by 'Lys-63'-linked polyubiquitination and by autophosphorylation (PubMed:10702308, PubMed:11460167, PubMed:12242293, PubMed:29291351). Association with TAB1/MAP3K7IP1 and TAB2/MAP3K7IP2 promotes activation through autophosphorylation, whereas PPM1B/PP2CB, PP2A and PPP6C dephosphorylation leads to inactivation (PubMed:11104763, PubMed:17079228, PubMed:37832545). Ceramides are also able to activate MAP3K7/TAK1 (PubMed:9079627)"}],"commentType":"ACTIVITY REGULATION"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000250","source":"UniProtKB","id":"Q62073"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10094049"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10838074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11104763"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11460167"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12589052"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12804775"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12874243"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"14670075"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"15894542"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16289117"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16845370"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16893890"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17079228"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17449468"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17548520"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"18286207"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"18758450"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"19521662"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"19675569"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"21512573"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"22084099"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"23776175"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"26334375"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"27426733"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"8638164"}],"value":"Can form homodimer (PubMed:27426733). Binds both upstream activators and downstream substrates in multimolecular complexes. Interacts with TAB1/MAP3K7IP1, TAB2/MAP3K7IP2 and TAB3/MAP3K7IP3 (PubMed:10838074, PubMed:11460167, PubMed:12242293, PubMed:14670075, PubMed:16289117, PubMed:19675569, PubMed:8638164). Identified in the TRIKA2 complex composed of MAP3K7/TAK1, TAB1/MAP3K7IP1 and TAB2/MAP3K7IP2 (PubMed:11460167). Interacts with PPM1L and PPM1B/PP2CB (PubMed:11104763). Interaction with PP2A and PPP6C leads to its repressed activity (PubMed:17079228). Interacts with TRAF6 and TAB1/MAP3K7IP1; during IL-1 signaling (PubMed:10094049, PubMed:12242293). Interacts with TAOK1 and TAOK2; interaction with TAOK2 interferes with MAP3K7 interaction with IKKA, thus preventing NF-kappa-B activation (PubMed:16893890). Interacts with DYNC2I2 (via WD domains) (PubMed:19521662). Interacts with CYLD and RBCK1 (PubMed:17449468, PubMed:17548520). Interacts with TGFBR1; induces MAP3K7/TAK1 activation by TRAF6 (PubMed:18758450). Interacts with MAPK8IP1 and SMAD6 (By similarity). Interacts with isoform 1 of VRK2 (PubMed:18286207). Interacts with DAB2; the interaction is induced by TGF-beta stimulation and may mediate TGF-beta stimulated JNK activation (PubMed:15894542). Interacts with TRIM5 (PubMed:21512573). Part of a complex containing ITCH, NDFIP1 and MAP3K7 (By similarity). Interacts with IFIT5; the interaction synergizes the recruitment of IKK to MAP3K7 and enhances IKK phosphorylation (PubMed:26334375). Interacts with PLEKHM1 (via N- and C-terminus) (By similarity). Interacts with TRIM8 (PubMed:22084099). Found in a complex with SH3RF1, RAC2, MAP2K7/MKK7, MAPK8IP1/JIP1, MAPK8/JNK1 and MAPK9/JNK2 (By similarity). Interacts with SASH1 (PubMed:23776175). Interacts with RIPK1 (By similarity)"}],"commentType":"SUBUNIT"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"28827540"}],"value":"(Microbial infection) Interacts with herpes simplex virus 2 protein US2; this interaction induces MAP3K7 phosphorylation and subsequent activation"}],"commentType":"SUBUNIT"},{"commentType":"INTERACTION","interactions":[{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q16543","geneName":"CDC37","intActId":"EBI-295634"},"numberOfExperiments":4,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"O14920","geneName":"IKBKB","intActId":"EBI-81266"},"numberOfExperiments":6,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"O14733","geneName":"MAP2K7","intActId":"EBI-492605"},"numberOfExperiments":3,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q9UQF2","geneName":"MAPK8IP1","intActId":"EBI-78404"},"numberOfExperiments":11,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"O00743","geneName":"PPP6C","intActId":"EBI-359751"},"numberOfExperiments":4,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"P40763","geneName":"STAT3","intActId":"EBI-518675"},"numberOfExperiments":4,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q15750","geneName":"TAB1","intActId":"EBI-358643"},"numberOfExperiments":10,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q9NYJ8","geneName":"TAB2","intActId":"EBI-358708"},"numberOfExperiments":9,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q8N5C8","geneName":"TAB3","intActId":"EBI-359964"},"numberOfExperiments":6,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q9UKE5","geneName":"TNIK","intActId":"EBI-1051794"},"numberOfExperiments":3,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"Q9Y4K3","geneName":"TRAF6","intActId":"EBI-359276"},"numberOfExperiments":2,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"P0CG48","geneName":"UBC","intActId":"EBI-3390054"},"numberOfExperiments":5,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"B5Z6S0","geneName":"cagA","intActId":"EBI-7287204"},"numberOfExperiments":4,"organismDiffer":true},{"interactantOne":{"uniProtKBAccession":"O43318","intActId":"EBI-358684"},"interactantTwo":{"uniProtKBAccession":"P0DTC9","geneName":"N","intActId":"EBI-25475856"},"numberOfExperiments":4,"organismDiffer":true},{"interactantOne":{"uniProtKBAccession":"O43318-2","intActId":"EBI-358700"},"interactantTwo":{"uniProtKBAccession":"Q16543","geneName":"CDC37","intActId":"EBI-295634"},"numberOfExperiments":5,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318-2","intActId":"EBI-358700"},"interactantTwo":{"uniProtKBAccession":"P07900","geneName":"HSP90AA1","intActId":"EBI-296047"},"numberOfExperiments":5,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318-2","intActId":"EBI-358700"},"interactantTwo":{"uniProtKBAccession":"Q15750","geneName":"TAB1","intActId":"EBI-358643"},"numberOfExperiments":3,"organismDiffer":false},{"interactantOne":{"uniProtKBAccession":"O43318-2","intActId":"EBI-358700"},"interactantTwo":{"uniProtKBAccession":"Q9NYJ8","geneName":"TAB2","intActId":"EBI-358708"},"numberOfExperiments":2,"organismDiffer":false}]},{"commentType":"SUBCELLULAR LOCATION","note":{"texts":[{"value":"Although the majority of MAP3K7/TAK1 is found in the cytosol, when complexed with TAB1/MAP3K7IP1 and TAB2/MAP3K7IP2, it is also localized at the cell membrane"}]},"subcellularLocations":[{"location":{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"}],"value":"Cytoplasm","id":"SL-0086"}},{"location":{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"}],"value":"Cell membrane","id":"SL-0039"},"topology":{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"}],"value":"Peripheral membrane protein","id":"SL-9903"},"orientation":{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"12242293"}],"value":"Cytoplasmic side","id":"SL-9910"}}]},{"commentType":"ALTERNATIVE PRODUCTS","events":["Alternative splicing"],"isoforms":[{"name":{"value":"1B"},"isoformIds":["O43318-1"],"isoformSequenceStatus":"Displayed"},{"name":{"value":"1A"},"isoformIds":["O43318-2"],"sequenceIds":["VSP_004886"],"isoformSequenceStatus":"Described"},{"name":{"value":"1C"},"isoformIds":["O43318-3"],"sequenceIds":["VSP_004887","VSP_004888"],"isoformSequenceStatus":"Described"},{"name":{"value":"1D"},"isoformIds":["O43318-4"],"sequenceIds":["VSP_004886","VSP_004887","VSP_004888"],"isoformSequenceStatus":"Described"}]},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"11118615"}],"value":"Isoform 1A is the most abundant in ovary, skeletal muscle, spleen and blood mononuclear cells. Isoform 1B is highly expressed in brain, kidney and small intestine. Isoform 1C is the major form in prostate. Isoform 1D is the less abundant form"}],"commentType":"TISSUE SPECIFICITY"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10702308"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"10838074"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"16845370"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17548520"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"19675569"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"21512573"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"37832545"}],"value":"Association with TAB1/MAP3K7IP1 promotes autophosphorylation at Ser-192 and subsequent activation. Association with TAB2/MAP3K7IP2, itself associated with free unanchored Lys-63 polyubiquitin chain, promotes autophosphorylation and subsequent activation of MAP3K7. Dephosphorylation at Ser-192 by PPM1B/PP2CB and at Thr-187 by PP2A and PPP6C leads to inactivation"}],"commentType":"PTM"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000250","source":"UniProtKB","id":"Q62073"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"17548520"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"22406003"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"24356957"}],"value":"'Lys-48'-linked polyubiquitination at Lys-72 is induced by TNFalpha, and leads to proteasomal degradation. Undergoes 'Lys-48'-linked polyubiquitination catalyzed by ITCH (By similarity). Requires 'Lys-63'-linked polyubiquitination for autophosphorylation and subsequent activation. 'Lys-63'-linked ubiquitination does not lead to proteasomal degradation. Deubiquitinated by CYLD, a protease that selectively cleaves 'Lys-63'-linked ubiquitin chains. Deubiquitinated by Y.enterocolitica YopP. Deubiquitinated by USP19; leading to negative regulation of TNF- and IL-1beta-triggered NF-kappa-B activation (PubMed:24356957)"}],"commentType":"PTM"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"28424289"}],"value":"(Microbial infection) Cleaved and inactivated by the proteases 3C of coxsackievirus A16 and human enterovirus D68, allowing the virus to disrupt TRAF6-triggered NF-kappa-B induction"}],"commentType":"PTM"},{"texts":[{"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"22520462"},{"evidenceCode":"ECO:0000269","source":"PubMed","id":"22802624"}],"value":"(Microbial infection) Acetylation of Thr-184 and Thr-187 by Yersinia YopJ prevents phosphorylation and activation, thus blocking the MAPK signaling pathway"}],"commentType":"PTM"},{"commentType":"DISEASE","disease":{"diseaseId":"Frontometaphyseal dysplasia 2","diseaseAccession":"DI-04852","acronym":"FMD2","description":"A form of frontometaphyseal dysplasia, a progressive sclerosing skeletal dysplasia affecting the long bones and skull. Characteristic features include supraorbital hyperostosis, cranial hyperostosis, undermodeling of the small bones, flared metaphyses, and digital anomalies. Extra-skeletal manifestations include hearing loss, cardiac malformations, and stenosis, particularly of the upper airway and urinary tract. FMD2 inheritance is autosomal dominant.","diseaseCrossReference":{"database":"MIM","id":"617137"},"evidences":[{"evidenceCode":"ECO:0000269","source":"PubMed","id":"27426733"}]},"note":{"texts":[{"value":"The disease is caused by variants affecting the gene represented in this entry"}]}},{"commentType":"DISEASE","disease":{"diseaseId":"Cardiospondylocarpofacial syndrome","diseaseAccession":"DI-04853","acronym":"CSCF","description":"A syndrome characterized by growth retardation, dysmorphic facial features, brachydactyly with carpal-tarsal fusion and extensive posterior cervical vertebral synostosis, cardiac septal defects with valve dysplasia, and deafness with inner ear malformations. 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