Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
374946
Gene name Gene Name - the full gene name approved by the HGNC.
Dorsal inhibitory axon guidance protein
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
DRAXIN
Synonyms (NCBI Gene) Gene synonyms aliases
AGPA3119, C1orf187, UNQ3119, neucrin
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.22
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT051878 hsa-let-7b-5p CLASH 23622248
MIRT714655 hsa-miR-140-3p HITS-CLIP 19536157
MIRT714658 hsa-miR-28-3p HITS-CLIP 19536157
MIRT714657 hsa-miR-6502-3p HITS-CLIP 19536157
MIRT658894 hsa-miR-4714-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 26190107
GO:0005576 Component Extracellular region IBA
GO:0005576 Component Extracellular region IEA
GO:0005576 Component Extracellular region ISS
GO:0007411 Process Axon guidance IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612682 25054 ENSG00000162490
Protein
UniProt ID Q8NBI3
Protein name Draxin (Dorsal inhibitory axon guidance protein) (Dorsal repulsive axon guidance protein) (Neucrin)
Protein function Chemorepulsive axon guidance protein required for the development of spinal cord and forebrain commissures. Acts as a chemorepulsive guidance protein for commissural axons during development. Able to inhibit or repel neurite outgrowth from dorsa
PDB 6FKQ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15550 Draxin 37 349 Draxin Family
Sequence
Sequence length 349
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Glioma Associate 36040678
Neoplasms Associate 36040678
Precancerous Conditions Associate 36040678
Stress Disorders Post Traumatic Associate 36631443