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84623 KIRREL3

84623

KIRREL3

kirre like nephrin family adhesion molecule 3

protein-coding

Homo sapiens

基因描述

Type Description
Definition kirre like nephrin family adhesion molecule 3

研究结论

Date Results Publications
2016-04-16 11:47:00 KIRREL3 interacting proteins MAP1B and MYO16 are potential candidates for intellectual disability and autism spectrum disorder. 25902260
2015-10-17 10:25:00 Results presented demonstrate for the first time that there are at least 3 splice variants of Kirrel3 expressed in adult human skeletal muscle, two of which have never previously been identified in human muscle. 25488023
2010-06-30 22:05:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614
2010-04-07 21:40:00 Observational study of gene-disease association. (HuGE Navigator) 20237496
2010-01-21 00:00:00 Alterations in KIRREL3 in patients with mild to severe intellectual disability are reported. 19012874

名称对应

Type IDs
Synonymous KIRRE, MRD4, NEPH2, PRO4502
Gene
UniProtKB-ID: KIRR3_HUMAN, E9PRX9_HUMAN
UniprotKB: Q8IZU9, E9PRX9
UniParc: UPI000058F1AA, UPI00000740A0, UPI0000048F5C
EMBL: AP001783, KF455565, AP000806, AP000741, AF480410, AY358743, AY358760, BC101801, AB058770, AP002832, KC877493, BC101775, KC877498
Ensembl: ENSG00000149571
KO: hsa:84623
Nucleutide sequences
EMBL-CDS: BAB47496.1, AAN73042.1, AAI01802.1, AAQ89120.1, AAI01776.1, AAQ89103.1
Gene_ORFName: UNQ5923/PRO4502/PRO19814
Ensembl_TRS: ENST00000525704, ENST00000525144, ENST00000529097
Protein sequencees
Ensembl_PRO: ENSP00000435466, ENSP00000435094, ENSP00000434081
RefSeq: XP_011541334.1, XP_011541329.1, XP_016873909.1, XP_016873908.1, NP_001155179.1, NP_001288026.1, NP_115920.1, XP_011541332.1, XP_011541333.1, XP_011541335.1, XP_011541330.1, XP_011541328.1
Others
UniRef100: UniRef100_Q8IZU9, UniRef100_E9PRX9
UniRef90: UniRef90_Q8BR86, UniRef90_E9PTD7
UniRef50: UniRef50_Q8BR86, UniRef50_E9PTD7
UniGene: Hs.376015
CCDS: CCDS53723.1, CCDS55796.1

全选

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