Type | Description |
---|---|
Definition | kirre like nephrin family adhesion molecule 3 |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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