Type | Description |
---|---|
Definition | tectonic family member 1 |
Date | Results | Publications |
---|---|---|
2019-09-14 10:48:00 | Two novel TCTN1 mutations were identified in a family with Joubert syndrome | 31302911 |
2017-12-02 12:26:00 | we describe the phenotype of a patient with Varadi syndrome who is homozygous for a previously reported mutation in TCTN1 (NM_001082538.2:c.342-2A>G, p.Gly115Lysfs*8) and suggest that allelic disorders linked to TCTN1 include Varadi syndrome, in addition to Joubert syndrome and Meckel-Gruber syndrome. | 28631893 |
2017-06-10 11:15:00 | Flow cytometry analysis showed that depletion of TCTN1 could cause cell cycle arrest at the G2/M phase. This indicates that TCTN1 may be crucial for CRC cell growth. | 28123172 |
2016-10-29 10:47:00 | High TCTN1 expression is associated with Pancreatic Cancer. | 26844847 |
2016-06-28 12:00:00 | These findings confirmed the direct association between the TCTN1 gene and prostate cancer growth in vitro. | 26310786 |
Type | IDs |
---|---|
Synonymous | JBTS13, TECT1 |
Gene |
UniProtKB-ID:
TECT1_HUMAN,
A8MW34_HUMAN,
B4DIB9_HUMAN,
Q05BR9_HUMAN
UniprotKB:
Q2MV58,
A8MW34,
B4DIB9,
Q05BR9
UniParc:
UPI0000072EAD,
UPI0000039EA9,
UPI0000073CA1,
UPI00006E2260,
UPI0000E5745D,
UPI0001639260,
UPI000056F1DD,
UPI00017A72A9,
UPI00006E225F
EMBL:
AK092775,
BC040113,
AK301732,
DQ278868,
AK055891,
AK295514,
AY358184,
BC044885,
BC062611,
BC033811,
AC144522,
AC002350,
AK024780
Ensembl:
ENSG00000204852
KO:
hsa:79600
|
Nucleutide sequences |
EMBL-CDS:
ABB90560.1,
BAB71036.1,
BAB15000.1,
BAC03973.1,
AAH62611.1,
AAH40113.1,
AAQ88551.1,
BAH13543.1,
BAG58431.1,
AAH33811.1
Gene_ORFName:
UNQ9369/PRO34160
Ensembl_TRS:
ENST00000397655,
ENST00000551590,
ENST00000397659,
ENST00000550703
|
Protein sequencees |
Ensembl_PRO:
ENSP00000448735,
ENSP00000380775,
ENSP00000380779,
ENSP00000473789
RefSeq:
NP_001076006.1,
XP_006719657.1,
NP_001306610.1,
XP_006719661.1,
XP_011537039.1,
XP_006719659.1,
NP_001167447.1,
XP_006719658.1,
XP_016875458.1,
XP_011537035.1,
XP_011537040.1,
XP_016875453.1,
NP_001306609.1,
XP_006719663.1,
NP_078825.2,
NP_001306611.1,
XP_016875455.1,
XP_011537036.1,
XP_006719660.1,
XP_011537037.1,
XP_005253991.1,
NP_001076007.1,
XP_006719662.1,
XP_005253992.1,
XP_016875457.1,
NP_001167446.1
|
Others |
UniRef100:
UniRef100_Q05BR9,
UniRef100_Q2MV58,
UniRef100_B4DIB9
UniRef90:
UniRef90_Q2MV58,
UniRef90_Q05BR9,
UniRef90_A0A2K6M102
UniRef50:
UniRef50_Q05BR9,
UniRef50_A0A1D5Q1F3,
UniRef50_Q2MV58
UniGene:
Hs.211511
CCDS:
CCDS41835.1,
CCDS41834.1,
CCDS41833.1
|
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Refseq |
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