Type | Description |
---|---|
Definition | actin binding LIM protein 1 |
Date | Results | Publications |
---|---|---|
2015-09-26 20:41:00 | Exon 11 inclusion isoform of ABLIM1 may have a muscle-specific function, and its abnormal splicing could be related to muscle symptoms of myotonic dystrophy type 1. | 25403273 |
2012-09-15 10:17:00 | SNP rs727532 in ABLIM1 (10q25) had significant association in the multivariate test & strong associations with novelty seeking, harm avoidance, reward dependence and alcohol dependence in the COGA sample. | 21547531 |
2010-12-05 22:08:00 | Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) | 20970119 |
2010-09-15 22:07:00 | Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) | 20549515 |
2009-12-02 21:41:00 | Observational study of gene-disease association. (HuGE Navigator) | 16385451 |
Type | IDs |
---|---|
Synonymous | ABLIM, LIMAB1, LIMATIN, abLIM-1 |
Gene |
UniProtKB-ID:
ABLM1_HUMAN,
B3KSG3_HUMAN,
B4DQA3_HUMAN
UniprotKB:
O14639,
B3KSG3,
B4DQA3
UniParc:
UPI0000418D06,
UPI0000373525,
UPI0000425C63,
UPI00003E29FA,
UPI00005A7ABC,
UPI0000072AEB,
UPI0000418D07,
UPI00017A79BB
EMBL:
AK298709,
AL590109,
BC002448,
AL354873,
AK093471,
AL133384,
CR749819,
AK122891,
AF005654,
D31883,
AK098277
Ensembl:
ENSG00000099204
KO:
hsa:3983
|
Nucleutide sequences |
EMBL-CDS:
AAC51676.1,
CAH18679.1,
BAA06681.2,
AAH02448.1,
BAG53784.1,
BAG53605.1,
BAG52725.1,
BAG60865.1
Ensembl_TRS:
ENST00000369256,
ENST00000392952,
ENST00000392955,
ENST00000277895,
ENST00000369253
|
Protein sequencees |
Ensembl_PRO:
ENSP00000358257,
ENSP00000376682,
ENSP00000376679,
ENSP00000358260,
ENSP00000277895
RefSeq:
NP_001309811.1,
NP_001309815.1,
XP_016871745.1,
XP_024303789.1,
NP_006711.3,
XP_024303779.1,
XP_016871739.1,
NP_001339370.1,
NP_001309817.1,
NP_001309826.1,
NP_001309812.1,
NP_002304.3,
NP_001309823.1,
NP_001309825.1,
XP_016871736.1,
XP_024303780.1,
XP_024303781.1,
XP_024303785.1,
XP_006717910.1,
XP_024303788.1,
XP_005269884.1,
NP_001309818.1,
XP_011538104.2,
NP_001339369.1,
NP_001309824.1,
XP_024303778.1,
XP_024303786.1,
NP_001309821.1,
NP_001309814.1,
NP_001309820.1,
NP_001003407.1,
NP_001309819.1,
XP_024303787.1,
XP_024303784.1,
XP_016871748.1,
NP_001309816.1,
XP_016871744.1,
XP_024303782.1,
NP_001309827.1,
XP_006717909.1,
XP_011538107.1,
NP_001339372.1,
XP_024303790.1,
XP_005269883.1,
NP_001309828.1,
NP_001309813.1,
XP_016871734.1,
XP_024303783.1,
XP_011538103.2,
XP_016871737.1,
NP_001309829.1,
NP_001309822.1,
XP_006717900.1,
NP_001339371.1
|
Others |
UniRef100:
UniRef100_B4DQA3,
UniRef100_B3KSG3,
UniRef100_O14639
UniRef90:
UniRef90_B3KSG3,
UniRef90_O14639,
UniRef90_B4DQA3
UniRef50:
UniRef50_B3KSG3,
UniRef50_O14639,
UniRef50_O14639-5
UniGene:
Hs.438236,
Hs.538331,
Hs.593868
CCDS:
CCDS31288.1,
CCDS31289.1,
CCDS81508.1,
CCDS81509.1,
CCDS7590.1
|
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Refseq |
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