Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
23500 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Dishevelled associated activator of morphogenesis 2 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
DAAM2 |
SynonymsGene synonyms aliases
|
NPHS24, dJ90A20A.1 |
ChromosomeChromosome number
|
6 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
6p21.2 |
miRNAmiRNA information provided by mirtarbase database.
|
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
GO ID |
Ontology |
Definition |
Evidence |
Reference |
GO:0003779 |
Function |
Actin binding |
IEA |
|
GO:0016055 |
Process |
Wnt signaling pathway |
IEA |
|
GO:0021516 |
Process |
Dorsal spinal cord development |
ISS |
|
GO:0030036 |
Process |
Actin cytoskeleton organization |
IEA |
|
GO:0048715 |
Process |
Negative regulation of oligodendrocyte differentiation |
IBA |
21873635 |
GO:0048715 |
Process |
Negative regulation of oligodendrocyte differentiation |
ISS |
|
GO:0060828 |
Process |
Regulation of canonical Wnt signaling pathway |
ISS |
|
GO:0070062 |
Component |
Extracellular exosome |
HDA |
18570454 |
GO:0090263 |
Process |
Positive regulation of canonical Wnt signaling pathway |
IBA |
21873635 |
GO:0090263 |
Process |
Positive regulation of canonical Wnt signaling pathway |
ISS |
|
GO:2000050 |
Process |
Regulation of non-canonical Wnt signaling pathway |
IBA |
21873635 |
GO:2000050 |
Process |
Regulation of non-canonical Wnt signaling pathway |
ISS |
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|
Protein
|
UniProt ID |
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 |
|
Sequence |
|
Sequence length |
1068 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
|
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Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Osteoporosis |
Osteoporosis, Age-Related, Osteoporosis, Osteoporosis, Senile, Post-Traumatic Osteoporosis |
rs72658152, rs72667023, rs587776916, rs72656370, rs768615287 |
30598549 |
Schizophrenia |
Schizophrenia |
rs74315508, rs74315509, rs13447324, rs1558507406, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346, rs863223347, rs863223351, rs863223352, rs61734270, rs797045205, rs869312829, rs869312830, rs770913157, rs869312832, rs869312831, rs781720548, rs1262969313 |
19358997 |
|