Gene Gene information from NCBI Gene database.
Entrez ID 374946
Gene name Dorsal inhibitory axon guidance protein
Gene symbol DRAXIN
Synonyms (NCBI Gene)
AGPA3119C1orf187UNQ3119neucrin
Chromosome 1
Chromosome location 1p36.22
miRNA miRNA information provided by mirtarbase database.
175
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
27
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
612682 25054 ENSG00000162490
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Likely benign rs202026446 RCV005932840
Familial cancer of breast Likely benign rs202026446 RCV005932839
Malignant tumor of esophagus Likely benign rs112841098 RCV005932843
Malignant tumor of urinary bladder Likely benign rs202026446 RCV005932841
Associations from Text MiningDisease 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