Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
137970
Gene name Gene Name - the full gene name approved by the HGNC.
Unc-5 netrin receptor D
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
UNC5D
Synonyms (NCBI Gene) Gene synonyms aliases
PRO34692, Unc5h4
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8p12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT022228 hsa-miR-124-3p Microarray 18668037
MIRT651857 hsa-miR-129-5p HITS-CLIP 23824327
MIRT651856 hsa-miR-4328 HITS-CLIP 23824327
MIRT651855 hsa-miR-145-5p HITS-CLIP 23824327
MIRT651854 hsa-miR-5195-3p HITS-CLIP 23824327
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 21873635
GO:0005886 Component Plasma membrane IEA
GO:0006915 Process Apoptotic process IEA
GO:0007411 Process Axon guidance IBA 21873635
GO:0016021 Component Integral component of membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
616466 18634 ENSG00000156687
Protein
UniProt ID Q6UXZ4
Protein name Netrin receptor UNC5D (Protein unc-5 homolog 4) (Protein unc-5 homolog D)
Protein function Receptor for the netrin NTN4 that promotes neuronal cell survival (By similarity). Plays a role in cell-cell adhesion and cell guidance. Receptor for netrin involved in cell migration. Plays a role in axon guidance by mediating axon repulsion of
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07679 I-set 159 249 Immunoglobulin I-set domain Domain
PF00090 TSP_1 256 306 Thrombospondin type 1 domain Domain
PF00090 TSP_1 312 359 Thrombospondin type 1 domain Domain
PF00791 ZU5 543 639 ZU5 domain Family
PF17217 UPA 687 826 UPA domain Domain
PF00531 Death 858 936 Death domain Domain
Sequence
MGRAAATAGGGGGARRWLPWLGLCFWAAGTAAARGTDNGEALPESIPSAPGTLPHFIEEP
DDAYIIKSNPIALRCKARPAMQIFFKCNGEWVHQNEHVSEETLDESSGLKVREVFINVTR
QQVEDFHGPEDYWCQCVAWSHLGTSKSRKASVRIAYLRKNFEQDPQGREVPIEGMIVLHC
RPPEGVPAAEVEWLKNEEPIDSEQDENIDTRADHNLIIRQARLSDSGNYTCMAANIVAKR
RSLSATVVV
YVNGGWSSWTEWSACNVRCGRGWQKRSRTCTNPAPLNGGAFCEGMSVQKIT
CTSLCP
VDGSWEVWSEWSVCSPECEHLRIRECTAPPPRNGGKFCEGLSQESENCTDGLCI
LDKKPLHEIKPQSIENASDIALYSGLGAAVVAVAVLVIGVTLYRRSQSDYGVDVIDSSAL
TGGFQTFNFKTVRQGNSLLLNSAMQPDLTVSRTYSGPICLQDPLDKELMTESSLFNPLSD
IKVKVQSSFMVSLGVSERAEYHGKNHSRTFPHGNNHSFSTMHPRNKMPYIQNLSSLPTRT
ELRTTGVFGHLGGRLVMPNTGVSLLIPHGAIPEENSWEIYMSINQGEPSLQSDGSEVLLS
PEVTCGPPDMIVTTPFALTIPHCADVSSEHWNIHLKKRT
QQGKWEEVMSVEDESTSCYCL
LDPFACHVLLDSFGTYALTGEPITDCAVKQLKVAVFGCMSCNSLDYNLRVYCVDNTPCAF
QEVVSDERHQGGQLLEEPKLLHFKGNTFSLQISVLDIPPFLWRIKPFTACQEVPFSRVWC
SNRQPLHCAFSLERYTPTTTQLSCKICIRQLKGHEQILQVQTSILE
SERETITFFAQEDS
TFPAQTGPKAFKIPYSIRQRICATFDTPNAKGKDWQMLAQKNSINRNLSYFATQSSPSAV
ILNLWEARHQHDGDLDSLACALEEIGRTHTKLSNIS
ESQLDEADFNYSRQNGL
Sequence length 953
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Axon guidance  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Diabetes mellitus Diabetes Mellitus, Insulin-Dependent, Diabetes Mellitus, Non-Insulin-Dependent rs587776515, rs61730328, rs606231121, rs606231122, rs79020217, rs77625743, rs78378398, rs606231123, rs1362648752, rs104893649, rs80356624, rs80356616, rs80356625, rs80356611, rs104894237
View all (293 more)
28672053
Narcolepsy Narcolepsy rs104894574, rs387906655 19629137
Neuropathy Neuropathy, NEUROPATHY, CONGENITAL HYPOMYELINATING, 2, NEUROPATHY, CONGENITAL HYPOMYELINATING, 3 rs121913593, rs121913595, rs751050956, rs878853221, rs768554986, rs1553259568, rs1567973091, rs1560046845, rs1567969825, rs1567973088, rs756896276 28672053
Unknown
Disease term Disease name Evidence References Source
Neuroticism Neuroticism GWAS
Insomnia Insomnia GWAS
Psoriasis Psoriasis GWAS
Dyslexia Dyslexia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 38235871
Alzheimer Disease Associate 29282330
Anisometropia Associate 28614238
Carcinogenesis Associate 24519068
Cardiomyopathy Dilated Associate 19332114
Colonic Neoplasms Associate 38235871
Colorectal Neoplasms Associate 33078631, 38235871, 39186800
Leukoencephalopathies Associate 29282330
Neoplasms Inhibit 24519068, 38235871
Neoplasms Associate 33078631