Type | Description |
---|---|
Definition | tectonic family member 2 |
Date | Results | Publications |
---|---|---|
2020-02-22 10:48:00 | Data suggest that TCTN2 enhances autophagy by targeting the miR-216b-Beclin-1 pathway, thereby ameliorating neuronal apoptosis and relieving spinal cord injury. | 31050183 |
2019-09-07 10:03:00 | TCTN2 Depletion-Induced IFT88 Lumen Leakage and Ciliary Weakening | 29866362 |
2011-09-24 11:31:00 | a truncating mutation in TCTN2 linked to Meckel Gruber syndrome was shown. | 21462283 |
2011-07-23 11:08:00 | Network building strategy led to the proposal of candidates for new ciliopathy disease genes, leading to the identification of the first human mutations in the Nephronophthisis gene Ataxin10 (ATXN10) and Joubert syndrome gene Tectonic2 (TCTN2). | 21565611 |
Type | IDs |
---|---|
Synonymous | C12orf38, JBTS24, MKS8, TECT2 |
Gene |
UniProtKB-ID:
TECT2_HUMAN
UniprotKB:
Q96GX1
UniParc:
UPI00015DAA21,
UPI0000038A56
EMBL:
CH471054,
AC117503,
BC009112,
AK023037,
AK292153,
AK056924,
DQ278870
Ensembl:
ENSG00000168778
KO:
hsa:79867
|
Nucleutide sequences |
EMBL-CDS:
BAB14370.1,
BAF84842.1,
AAH09112.1,
BAG51827.1,
ABB90562.1,
EAW98430.1
Ensembl_TRS:
ENST00000303372,
ENST00000426174
|
Protein sequencees |
Ensembl_PRO:
ENSP00000395171,
ENSP00000304941
RefSeq:
XP_016875463.1,
XP_016875464.1,
XP_006719668.1,
NP_079085.2,
NP_001137322.1,
XP_005253680.1
|
Others |
UniRef100:
UniRef100_Q96GX1
UniRef90:
UniRef90_Q96GX1
UniRef50:
UniRef50_Q2MV57
UniGene:
Hs.167165
CCDS:
CCDS9253.1,
CCDS45007.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
---|---|---|---|---|---|---|---|---|
Refseq |
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