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79600 TCTN1

79600

TCTN1

tectonic family member 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition tectonic family member 1

研究结论

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

名称对应

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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