| Type | Description |
|---|---|
| Definition | DCC netrin 1 receptor |
| Date | Results | Publications |
|---|---|---|
| 2021-01-02 12:49:00 | A novel heterozygous loss-of-function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature. | 31697046 |
| 2020-12-26 13:13:00 | Association Between DCC Polymorphisms and Susceptibility to Autism Spectrum Disorder. | 32144606 |
| 2020-10-31 13:15:00 | Callosal agenesis and congenital mirror movements: outcomes associated with DCC mutations. | 32060908 |
| 2020-08-22 15:28:00 | Netrin-1 and Its Receptor DCC Are Causally Implicated in Melanoma Progression. | 31806640 |
| 2020-04-25 10:17:00 | Study provides evidence that a functional SNP rs12607853 in a putative miRNA binding site in the DCC 3 '-UTR may act by affecting the binding of hsa-miR-422a. This SNP-modified posttranscriptional gene regulation represents a potential pathogenic mechanism of opioid addiction. | 32092754 |
| Type | IDs |
|---|---|
| Synonymous | CRC18, CRCR1, HGPPS2, IGDCC1, MRMV1, NTN1R1 |
| Gene |
UniProtKB-ID:
DCC_HUMAN,
Q49AK4_HUMAN
UniprotKB:
P43146,
Q49AK4
UniParc:
UPI00001AEDC6,
UPI000056F172
EMBL:
AC078999,
M63696,
AC011155,
M32286,
AC110591,
M32292,
AC100777,
AC116002,
M32290,
AC016383,
BC036524,
M63718,
X76132,
M32288,
AC019239,
M63702,
AC021486,
AC027248,
M63700,
AC103949,
AC090660,
M63698
Ensembl:
ENSG00000187323
KO:
hsa:1630
|
| Nucleutide sequences |
EMBL-CDS:
AAA52181.1,
AAA52180.1,
CAA53735.1,
AAA52175.1,
AAA52174.1,
AAA52178.1,
AAA52176.1,
AAA52179.1,
AAA35751.1,
AAA52177.1,
AAH36524.1
Ensembl_TRS:
ENST00000442544
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000389140
RefSeq:
XP_016881058.1,
XP_011524146.1,
NP_005206.2,
XP_016881057.1,
XP_016881059.1,
XP_011524145.1
|
| Others |
UniRef100:
UniRef100_P43146,
UniRef100_Q49AK4
UniRef90:
UniRef90_H0Y2Q5,
UniRef90_P43146
UniRef50:
UniRef50_P43146,
UniRef50_H0Y2Q5
UniGene:
Hs.162025
CCDS:
CCDS11952.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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