Gene Gene information from NCBI Gene database.
Entrez ID 8633
Gene name Unc-5 netrin receptor C
Gene symbol UNC5C
Synonyms (NCBI Gene)
UNC5H3
Chromosome 4
Chromosome location 4q22.3
Summary 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.
192
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
45
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
603610 12569 ENSG00000182168
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
24
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Colon adenocarcinoma Uncertain significance rs139372477 RCV005930709
UNC5C-related disorder Benign; Uncertain significance; Likely benign rs61741188, rs929930790, rs34585936, rs146932015, rs147827953, rs773385589, rs201589427, rs187902349, rs146123204, rs4699423, rs2276322, rs1339815696, rs141315686, rs3733212, rs145013421
View all (8 more)
RCV003975856
RCV003402449
RCV003980923
RCV003938999
RCV003966407
RCV003919192
RCV003907101
RCV003923939
RCV003917311
RCV003974326
RCV003974548
RCV003974185
RCV003974272
RCV003984687
RCV003916845
RCV003964414
RCV003973856
RCV003909374
RCV003927364
RCV003939597
RCV003932325
RCV003956682
RCV003982213
Associations from Text MiningDisease 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