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53870 Cntn6

53870

Cntn6

contactin 6

protein-coding

Mus musculus

基因描述

Type Description
Definition contactin 6

研究结论

Date Results Publications
2020-10-31 13:18:00 Time origin and structural analysis of the induced CRISPR/cas9 megabase-sized deletions and duplications involving the Cntn6 gene in mice. 31578377
2020-04-11 12:03:00 NB-3 deficiency promoted synapse reformation between sRST regenerative axons and motor neurons and enhanced the potential for electrical activity of muscle contraction and motor coordination. 30156464
2019-12-21 12:20:00 decrease of vermian SYP1 and CNTN6 in reln(+/-) mice displayed patterns compatible with the structural modifications of the autistic cerebellum. 31098770
2019-03-09 12:02:00 Cntn6 is expressed during postnatal hippocampal development. The absence of Cntn6 affects hippocampal Spatial Learning and memory, and affects allocentric navigation of the animals. 30106251
2018-02-10 11:15:00 The common phenotypic features of 40 patients with microdeletions and microduplications of CNTN6 appeared to be the autism spectrum disorders, developmental delay, intellectual disability, seizures, cognitive impairment, cardiological defects, and behavioral problems. 29369566

名称对应

Type IDs
Synonymous NB-3
Gene
UniProtKB-ID: CNTN6_MOUSE
UniprotKB: Q9JMB8
UniParc: UPI00000E9AAE, UPI00004650A7
EMBL: AK052972, AB032602, BC076594
Ensembl: ENSMUSG00000030092
KO: mmu:53870
Nucleutide sequences
EMBL-CDS: BAA92367.1, BAC35227.1, AAH76594.1
Ensembl_TRS: ENSMUST00000089215, ENSMUST00000162872
Protein sequencees
Ensembl_PRO: ENSMUSP00000124025, ENSMUSP00000086623
RefSeq: XP_036022181.1, XP_036022178.1, XP_017177167.1, XP_036022177.1, XP_036022179.1, XP_006506446.1, XP_006506447.1, XP_036022184.1, XP_006506445.1, NP_059079.2, XP_036022183.1, XP_036022185.1, XP_036022180.1, XP_036022182.1, XP_011239711.1, XP_006506444.1, XP_017177168.1
Others
UniRef100: UniRef100_Q9JMB8
UniRef90: UniRef90_Q9JMB8
UniRef50: UniRef50_Q9JMB8
UniGene: Mm.321671
CCDS: CCDS20394.1

全选

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