Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
28988
Gene name Gene Name - the full gene name approved by the HGNC.
Drebrin like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DBNL
Synonyms (NCBI Gene) Gene synonyms aliases
ABP1, HIP-55, HIP55, SH3P7
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7p13
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022629 hsa-miR-124-3p Microarray 18668037
MIRT025775 hsa-miR-7-5p Microarray 19073608
MIRT028810 hsa-miR-26b-5p Microarray 19088304
MIRT051893 hsa-let-7b-5p CLASH 23622248
MIRT046641 hsa-miR-222-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0001726 Component Ruffle ISS
GO:0002102 Component Podosome ISS
GO:0002250 Process Adaptive immune response IEA
GO:0003779 Function Actin binding ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
610106 2696 ENSG00000136279
Protein
UniProt ID Q9UJU6
Protein name Drebrin-like protein (Cervical SH3P7) (Cervical mucin-associated protein) (Drebrin-F) (HPK1-interacting protein of 55 kDa) (HIP-55) (SH3 domain-containing protein 7)
Protein function Adapter protein that binds F-actin and DNM1, and thereby plays a role in receptor-mediated endocytosis. Plays a role in the reorganization of the actin cytoskeleton, formation of cell projections, such as neurites, in neuron morphogenesis and sy
PDB 1X67
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00241 Cofilin_ADF 12 131 Cofilin/tropomyosin-type actin-binding protein Domain
PF14604 SH3_9 378 427 Variant SH3 domain Domain
Sequence
MAANLSRNGPALQEAYVRVVTEKSPTDWALFTYEGNSNDIRVAGTGEGGLEEMVEELNSG
KVMYAFCRVKDPNSGLPKFVLINWTGEGVNDVRKGACASHVSTMASFLKGAHVTINARAE
EDVEPECIMEK
VAKASGANYSFHKESGRFQDVGPQAPVGSVYQKTNAVSEIKRVGKDSFW
AKAEKEEENRRLEEKRRAEEAQRQLEQERRERELREAARREQRYQEQGGEASPQRTWEQQ
QEVVSRNRNEQESAVHPREIFKQKERAMSTTSISSPQPGKLRSPFLQKQLTQPETHFGRE
PAAAISRPRADLPAEEPAPSTPPCLVQAEEEAVYEEPPEQETFYEQPPLVQQQGAGSEHI
DHHIQGQGLSGQGLCARALYDYQAADDTEISFDPENLITGIEVIDEGWWRGYGPDGHFGM
FPANYVE
LIE
Sequence length 430
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Caspase-mediated cleavage of cytoskeletal proteins
Neurexins and neuroligins
Neutrophil degranulation
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Glycogen storage disease Glycogen storage disease type X rs10250779, rs387906244, rs113994126, rs113994129, rs113994134, rs369973784, rs199922945, rs118203964, rs113994132, rs387906246, rs113994128, rs267606639, rs267606640, rs755419857, rs895690691
View all (721 more)
27612597, 8447317
Associations from Text Mining
Disease Name Relationship Type References
Aortic Dissection Associate 39738466
Bipolar Disorder Associate 22760556, 35821008
Common Variable Immunodeficiency Associate 36220400
Leukemia Promyelocytic Acute Associate 15637062
Rosacea Associate 37437773