Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8633
Gene name Gene Name - the full gene name approved by the HGNC.
Unc-5 netrin receptor C
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UNC5C
Synonyms (NCBI Gene) Gene synonyms aliases
UNC5H3
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4q22.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene product belongs to the UNC-5 family of netrin receptors. Netrins are secreted proteins that direct axon extension and cell migration during neural development. They are bifunctional proteins that act as attractants for some cell types and as rep
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017932 hsa-miR-335-5p Microarray 18185580
MIRT495575 hsa-miR-936 PAR-CLIP 22291592
MIRT495574 hsa-miR-199a-3p PAR-CLIP 22291592
MIRT495573 hsa-miR-199b-3p PAR-CLIP 22291592
MIRT495572 hsa-miR-3129-5p PAR-CLIP 22291592
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005042 Function Netrin receptor activity IBA
GO:0005042 Function Netrin receptor activity IEA
GO:0005042 Function Netrin receptor activity TAS 9782087
GO:0005043 Function Netrin receptor activity involved in chemorepulsion IEA
GO:0005043 Function Netrin receptor activity involved in chemorepulsion ISS
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603610 12569 ENSG00000182168
Protein
UniProt ID O95185
Protein name Netrin receptor UNC5C (Protein unc-5 homolog 3) (Protein unc-5 homolog C)
Protein function Receptor for netrin required for axon guidance (By similarity). Mediates axon repulsion of neuronal growth cones in the developing nervous system upon ligand binding (By similarity). NTN1/Netrin-1 binding might cause dissociation of UNC5C from p
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07679 I-set 167 257 Immunoglobulin I-set domain Domain
PF00090 TSP_1 264 313 Thrombospondin type 1 domain Domain
PF00090 TSP_1 317 367 Thrombospondin type 1 domain Domain
PF00791 ZU5 531 628 ZU5 domain Family
PF17217 UPA 678 817 UPA domain Domain
PF00531 Death 849 928 Death domain Domain
Tissue specificity TISSUE SPECIFICITY: Mainly expressed in brain (PubMed:9782087). Expressed in temporal lobe cortical neurons and in neurons of the hippocampal pyramidal layer (PubMed:25419706). Also expressed in kidney (PubMed:9782087). Not expressed in developing or adul
Sequence
MRKGLRATAARCGLGLGYLLQMLVLPALALLSASGTGSAAQDDDFFHELPETFPSDPPEP
LPHFLIEPEEAYIVKNKPVNLYCKASPATQIYFKCNSEWVHQKDHIVDERVDETSGLIVR
EVSIEISRQQVEELFGPEDYWCQCVAWSSAGTTKSRKAYVRIAYLRKTFEQEPLGKEVSL
EQEVLLQCRPPEGIPVAEVEWLKNEDIIDPVEDRNFYITIDHNLIIKQARLSDTANYTCV
AKNIVAKRKSTTATVIV
YVNGGWSTWTEWSVCNSRCGRGYQKRTRTCTNPAPLNGGAFCE
GQSVQKIACTTLC
PVDGRWTPWSKWSTCGTECTHWRRRECTAPAPKNGGKDCDGLVLQSK
NCTDGLC
MQTAPDSDDVALYVGIVIAVIVCLAISVVVALFVYRKNHRDFESDIIDSSALN
GGFQPVNIKAARQDLLAVPPDLTSAAAMYRGPVYALHDVSDKIPMTNSPILDPLPNLKIK
VYNTSGAVTPQDDLSEFTSKLSPQMTQSLLENEALSLKNQSLARQTDPSCTAFGSFNSLG
GHLIVPNSGVSLLIPAGAIPQGRVYEMYVTVHRKETMRPPMDDSQTLLTPVVSCGPPGAL
LTRPVVLTMHHCADPNTEDWKILLKNQA
AQGQWEDVVVVGEENFTTPCYIQLDAEACHIL
TENLSTYALVGHSTTKAAAKRLKLAIFGPLCCSSLEYSIRVYCLDDTQDALKEILHLERQ
MGGQLLEEPKALHFKGSTHNLRLSIHDIAHSLWKSKLLAKYQEIPFYHVWSGSQRNLHCT
FTLERFSLNTVELVCKLCVRQVEGEGQIFQLNCTVSE
EPTGIDLPLLDPANTITTVTGPS
AFSIPLPIRQKLCSSLDAPQTRGHDWRMLAHKLNLDRYLNYFATKSSPTGVILDLWEAQN
FPDGNLSMLAAVLEEMGRHETVVSLAAE
GQY
Sequence length 931
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Axon guidance  
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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
Coronary artery disease Coronary artery disease N/A N/A GWAS
Coronary Heart Disease Coronary heart disease N/A N/A GWAS
Diabetes Type 2 diabetes, Type 2 diabetes mellitus or coronary artery disease (pleiotropy) N/A N/A GWAS
Hypertension Hypertension (confirmatory factor analysis Factor 12) N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenomatous Polyps Associate 18054557
Adenomatous Polyps Inhibit 28378635
Alzheimer Disease Associate 27036079, 33522999, 35001095
Arthritis Rheumatoid Stimulate 19822088
Atrophy Associate 30883345
Brain Diseases Associate 33522999
Carcinogenesis Associate 18054557, 20032384, 24376576
Cognition Disorders Associate 30883345
Colonic Neoplasms Associate 19331160, 20032384
Colorectal Neoplasms Inhibit 18054557, 21893118, 33706130