Type | Description |
---|---|
Definition | netrin G1 |
Date | Results | Publications |
---|---|---|
2020-06-27 11:56:00 | A 117-base pair SARS-CoV-2 orf1b sequence matched a sequence in the human genome with 94.6% identity. The sequence was in chromosome 1p within an intronic region of the netrin G1 (NTNG1) gene, implicated in schizophrenia. | 32503821 |
2019-08-31 12:11:00 | Significant genetic family-based associations were detected between NTNG1 polymorphisms and cocaine dependence. NTNG1 expression in BA10, BA46 and the cerebellum, however, were not significantly associated with any allele or haplotype of this gene. | 28074533 |
2015-06-27 11:00:00 | examined the hypothesis that NTNG1 allelic variation contributes to the risk for schizophrenia | 25325217 |
2014-06-07 10:18:00 | Interaction between the tripartite NGL-1, netrin-G1 and LAR adhesion complex promotes development of excitatory synapses. | 23986473 |
2014-03-08 12:07:00 | Our finding nominates the minor G allele of the NTNG1 rs628117 single nucleotide polymorphism as a risk factor for ischemic stroke at least in Armenian population. | 23769687 |
Type | IDs |
---|---|
Synonymous | Lmnt1 |
Gene |
UniProtKB-ID:
NTNG1_HUMAN,
Q5IEC3_HUMAN,
Q5IEC8_HUMAN,
X5DNW2_HUMAN,
B4DKF0_HUMAN
UniprotKB:
Q9Y2I2,
Q5IEC3,
Q5IEC8,
X5DNW2,
B4DKF0
UniParc:
UPI00004B59A5,
UPI000006D0A8,
UPI00004B59AA,
UPI0000458A3E,
UPI0000035068,
UPI000006E519,
UPI0000458A40,
UPI0000458A3F,
UPI00004DE5C5
EMBL:
AL590427,
AY764265,
AK296533,
AC114491,
AY764260,
AY358365,
BX538348,
AL513187,
AB023193,
KJ534901,
BC030220
Ensembl:
ENSG00000162631
KO:
hsa:22854
|
Nucleutide sequences |
EMBL-CDS:
AAH30220.1,
BAA76820.2,
AAQ88731.1,
CAD98143.1,
AAW47412.1,
AAW47407.1,
AHW56541.1,
BAG59162.1
Gene_ORFName:
UNQ571/PRO1133
Ensembl_TRS:
ENST00000370066,
ENST00000370071,
ENST00000370065,
ENST00000370074,
ENST00000370073,
ENST00000370067,
ENST00000370068
|
Protein sequencees |
Ensembl_PRO:
ENSP00000359083,
ENSP00000359090,
ENSP00000359082,
ENSP00000359091,
ENSP00000359085,
ENSP00000359088,
ENSP00000359084
RefSeq:
NP_001359099.1,
NP_001359098.1,
NP_001106699.1,
NP_001106697.1,
NP_001359096.1,
NP_001317594.1,
XP_011539327.1,
NP_001299617.1,
XP_016856175.1,
NP_001359095.1,
XP_016856172.1,
NP_055732.2,
NP_001359097.1,
NP_001359100.1
|
Others |
UniRef100:
UniRef100_A0A2J8M4G5,
UniRef100_I3M559,
UniRef100_Q9Y2I2,
UniRef100_A0A1D5QLF9,
UniRef100_A0A5F8A3Q2
UniRef90:
UniRef90_A0A2I3MS97,
UniRef90_Q9Y2I2,
UniRef90_Q8R4G0-10,
UniRef90_A0A5F4C2I6
UniRef50:
UniRef50_Q9Y2I2,
UniRef50_Q8R4G0-10,
UniRef50_Q8R4G0
UniGene:
Hs.732535
CCDS:
CCDS81354.1,
CCDS30785.1,
CCDS44180.1,
CCDS44179.1
|
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