Gene Gene information from NCBI Gene database.
Entrez ID 23500
Gene name Dishevelled associated activator of morphogenesis 2
Gene symbol DAAM2
Synonyms (NCBI Gene)
NPHS24dJ90A20A.1
Chromosome 6
Chromosome location 6p21.2
miRNA miRNA information provided by mirtarbase database.
258
miRTarBase ID miRNA Experiments Reference
MIRT031230 hsa-miR-19b-3p Sequencing 20371350
MIRT031355 hsa-miR-18a-5p Sequencing 20371350
MIRT609347 hsa-miR-8485 HITS-CLIP 23824327
MIRT609346 hsa-miR-329-3p HITS-CLIP 23824327
MIRT609345 hsa-miR-362-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
25
GO ID Ontology Definition Evidence Reference
GO:0003779 Function Actin binding IEA
GO:0005515 Function Protein binding IPI 33232676
GO:0007368 Process Determination of left/right symmetry IEA
GO:0016055 Process Wnt signaling pathway IEA
GO:0021516 Process Dorsal spinal cord development IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
606627 18143 ENSG00000146122
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86T65
Protein name Disheveled-associated activator of morphogenesis 2
Protein function Key regulator of the Wnt signaling pathway, which is required for various processes during development, such as dorsal patterning, determination of left/right symmetry or myelination in the central nervous system. Acts downstream of Wnt ligands
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06371 Drf_GBD 40 228 Diaphanous GTPase-binding Domain Family
PF06367 Drf_FH3 231 435 Diaphanous FH3 Domain Family
PF02181 FH2 595 969 Formin Homology 2 Domain Family
Tissue specificity TISSUE SPECIFICITY: Expressed in most tissues examined. Expressed in kidney glomeruli (PubMed:33232676). {ECO:0000269|PubMed:33232676, ECO:0000269|PubMed:9205841}.
Sequence
MAPRKRSHHGLGFLCCFGGSDIPEINLRDNHPLQFMEFSSPIPNAEELNIRFAELVDELD
LTDKNREAMFALPPEKKWQIYCSKKKEQEDPNKLATSWPDYYIDRINSMAAMQSLYAFDE
EETEMRNQVVEDLKTALRTQPMRFVTRFIELEGLTCLLNFLRSMDHATCESRIHTSLIGC
IKALMNNSQGRAHVLAQPEAISTIAQSLRTENSKTKVAVLEILGAVCL
VPGGHKKVLQAM
LHYQVYAAERTRFQTLLNELDRSLGRYRDEVNLKTAIMSFINAVLNAGAGEDNLEFRLHL
RYEFLMLGIQPVIDKLRQHENAILDKHLDFFEMVRNEDDLELARRFDMVHIDTKSASQMF
ELIHKKLKYTEAYPCLLSVLHHCLQMPYKRNGGYFQQWQLLDRILQQIVLQDERGVDPDL
APLENFNVKNIVNML
INENEVKQWRDQAEKFRKEHMELVSRLERKERECETKTLEKEEMM
RTLNKMKDKLARESQELRQARGQVAELVAQLSELSTGPVSSPPPPGGPLTLSSSMTTNDL
PPPPPPLPFACCPPPPPPPLPPGGPPTPPGAPPCLGMGLPLPQDPYPSSDVPLRKKRVPQ
PSHPLKSFNWVKLNEERVPGTVWNEIDDMQVFRILDLEDFEKMFSAYQRHQKELGSTEDI
YLASRKVKELSVIDGRRAQNCIILLSKLKLSNEEIRQAILKMDEQEDLAKDMLEQLLKFI
PEKSDIDLLEEHKHEIERMARADRFLYEMSRIDHYQQRLQALFFKKKFQERLAEAKPKVE
AILLASRELVRSKRLRQMLEVILAIGNFMNKGQRGGAYGFRVASLNKIADTKSSIDRNIS
LLHYLIMILEKHFPDILNMPSELQHLPEAAKVNLAELEKEVGNLRRGLRAVEVELEYQRR
QVREPSDKFVPVMSDFITVSSFSFSELEDQLNEARDKFAKALMHFGEHDSKMQPDEFFGI
FDTFLQAFS
EARQDLEAMRRRKEEEERRARMEAMLKEQRERERWQRQRKVLAAGSSLEEG
GEFDDLVSALRSGEVFDKDLCKLKRSRKRSGSQALEVTRERAINRLNY
Sequence length 1068
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Wnt signaling pathway
Cytoskeleton in muscle cells
 
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
71
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Nephrotic syndrome, type 24 Pathogenic rs1391253919, rs200668867, rs1764951663 RCV001363214
RCV001363217
RCV001363218
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Cervical cancer Benign rs199767843 RCV005906506
Cholangiocarcinoma Benign rs199767843 RCV005906508
Clear cell carcinoma of kidney Benign rs201309255 RCV005933207
DAAM2-related disorder Uncertain significance; Conflicting classifications of pathogenicity; Likely benign; Benign rs150676991, rs111950018, rs370518716, rs181701991, rs370112679, rs148294935, rs780925746, rs138611904, rs1035310700, rs775379327, rs114233535, rs61748650, rs3003929, rs2481858103, rs531101009
View all (33 more)
RCV003918890
RCV004756222
RCV003420427
RCV003954036
RCV003946495
RCV003896753
RCV003897111
RCV003894677
RCV003894691
RCV003907188
RCV003921698
RCV003919658
RCV003919752
RCV003974739
RCV003964512
RCV003902067
RCV003902103
RCV003916942
RCV003907265
RCV003977277
RCV003984494
RCV003911560
RCV003909711
RCV003909773
RCV003914087
RCV003939852
RCV003941899
RCV003934546
RCV003931488
RCV003927037
RCV003941402
RCV003941563
RCV003941692
RCV003927251
RCV003939751
RCV003927305
RCV003951685
RCV003914401
RCV003914571
RCV003956708
RCV003954334
RCV003954400
RCV003944644
RCV003981938
RCV003981997
RCV003971735
RCV003969410
RCV003972315
RCV003925935
RCV003922923
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 40179422
Adenoma Associate 27245242
Ataxia Telangiectasia Stimulate 32772041
Bone Diseases Associate 36720443
Carcinogenesis Associate 29053101
Carcinoma Hepatocellular Associate 32772041
Carcinoma Squamous Cell Associate 40179422
Colonic Neoplasms Associate 27245242
Demyelinating Diseases Associate 26293489
Femoral Fractures Associate 35052486