| Type | Description |
|---|---|
| Definition | trafficking protein particle complex 9 |
| Date | Results | Publications |
|---|---|---|
| 2020-11-21 13:13:00 | Trappc9 deficiency causes parent-of-origin dependent microcephaly and obesity. | 32877400 |
| 2020-07-25 10:40:00 | TRAPPC9 is associated with ADHD risk. | 32046534 |
| 2018-12-22 11:27:00 | CNVs significantly contribute to the mutational spectrum of TRAPPC9 gene associated with syndromic intellectual disability. | 29187737 |
| 2018-09-22 11:09:00 | Data show that NIBP expression level is high in gastric cancer (GC) patients and indicate that the NIBPregulated NFkappaB signaling pathway plays a pivotal role in the chemoresistance of GC cells by promoting EMT. | 29620292 |
| 2018-02-17 11:43:00 | Homozygous TRAPPC9 gene nonsense mutation in OXTR gene is associated with intellectual disability, speech disorder, and secondary microcephaly. | 29031008 |
| Type | IDs |
|---|---|
| Synonymous | IBP, IKBKBBP, MRT13, NIBP, T1, TRS120 |
| Gene |
UniProtKB-ID:
TPPC9_HUMAN
UniprotKB:
Q96Q05
UniParc:
UPI00001A46C7,
UPI0000E5AF77,
UPI0000DBEF2B
EMBL:
AY630619,
AK027689,
AL833973,
AK128755,
BC003650,
AB067469,
BC065288,
AY190606,
BC006206
Ensembl:
ENSG00000167632
KO:
hsa:83696
|
| Nucleutide sequences |
EMBL-CDS:
AAO38740.1,
AAH06206.3,
BAC87600.1,
CAH56384.1,
BAB55299.1,
AAV31908.1,
BAB67775.1,
AAH65288.1,
AAH03650.3
Gene_ORFName:
T1
Ensembl_TRS:
ENST00000648948,
ENST00000389328,
ENST00000438773
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000405060,
ENSP00000373979,
ENSP00000498020
RefSeq:
NP_001361611.1,
XP_011515632.1,
NP_113654.5,
XP_016869382.1,
XP_011515628.1,
XP_011515630.1,
NP_001361612.1,
XP_016869383.1,
NP_001361613.1,
NP_001308575.1,
NP_001153844.1
|
| Others |
UniRef100:
UniRef100_Q96Q05
UniRef90:
UniRef90_Q96Q05
UniRef50:
UniRef50_Q96Q05
UniGene:
Hs.654911,
Hs.733622
CCDS:
CCDS55278.1,
CCDS34946.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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