Type | Description |
---|---|
Definition | cAMP regulated phosphoprotein 21 |
Date | Results | Publications |
---|---|---|
2020-09-12 16:04:00 | Mutation analysis of GLT8D1 and genes in amyotrophic lateral sclerosis patients from mainland China. | 31653410 |
2014-08-09 10:11:00 | Interstitial deletion of 3p22.3p22.2 encompassing and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability. | 24127197 |
2010-06-30 22:06:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
Type | IDs |
---|---|
Synonymous | ARPP-21, R3HDM3, RCS, TARPP |
Gene |
UniProtKB-ID:
ARP21_HUMAN,
A8K1F3_HUMAN,
A8K0T4_HUMAN
UniprotKB:
Q9UBL0,
A8K1F3,
A8K0T4
UniParc:
UPI0000209B3D,
UPI00015DA559,
UPI0000125BC2,
UPI000056F13E,
UPI0000253B24,
UPI0000192731,
UPI00004570DC
EMBL:
BC051828,
CH471055,
BC017805,
AL133109,
AK055064,
AK294484,
BC041385,
AF112220,
BC066651,
BC031106,
AK289868,
AK289649,
BC036399
Ensembl:
ENSG00000172995
KO:
hsa:10777
|
Nucleutide sequences |
EMBL-CDS:
EAW64471.1,
AAH51828.1,
AAF17207.1,
AAH66651.1,
AAH36399.1,
AAH31106.1,
BAG57707.1,
CAB61414.1,
AAH41385.1,
AAH17805.1,
BAF82557.1,
EAW64472.1,
EAW64470.1,
BAG51459.1,
BAF82338.1
Gene_ORFName:
hCG_1996238
Ensembl_TRS:
ENST00000438071,
ENST00000396482,
ENST00000427542,
ENST00000412048,
ENST00000428373,
ENST00000436702,
ENST00000441454,
ENST00000396481,
ENST00000417925,
ENST00000474696,
ENST00000444190,
ENST00000187397,
ENST00000432682
|
Protein sequencees |
Ensembl_PRO:
ENSP00000405276,
ENSP00000417838,
ENSP00000406964,
ENSP00000389754,
ENSP00000390151,
ENSP00000379741,
ENSP00000187397,
ENSP00000412411,
ENSP00000410171,
ENSP00000397720,
ENSP00000401602,
ENSP00000412326,
ENSP00000379742
RefSeq:
XP_011531605.1,
NP_001254546.1,
NP_001372424.1,
XP_016861064.1,
NP_001020240.1,
NP_001372514.1,
NP_001372524.1,
XP_011531601.1,
NP_001372413.1,
XP_011531602.1,
XP_024309088.1,
NP_001372523.1,
NP_001372494.1,
NP_001372420.1,
NP_001372485.1,
NP_057384.2,
NP_001254548.1,
NP_001254547.1,
NP_001372516.1,
NP_938409.1,
NP_001372503.1,
XP_024309092.1,
NP_001020239.1,
NP_001372491.1,
NP_001372506.1,
NP_001372421.1,
NP_001372495.1,
XP_016861080.1,
NP_001372487.1,
XP_016861087.1,
XP_016861096.1,
XP_024309090.1,
NP_001254545.1,
NP_001372419.1,
NP_001372496.1,
XP_016861079.1,
XP_011531604.1,
NP_001372511.1,
NP_001372519.1,
XP_016861069.1,
XP_016861101.1,
NP_001372502.1,
NP_001372517.1,
NP_001372425.1,
NP_001372465.1,
NP_001372521.1,
NP_001372513.1,
NP_001372416.1,
XP_016861077.1,
NP_001372507.1,
XP_016861063.1,
NP_001372415.1,
XP_011531603.1,
NP_001372522.1,
XP_016861068.1,
NP_001372520.1,
NP_001372418.1,
NP_001372414.1,
XP_016861085.1,
NP_001372426.1,
NP_001372510.1,
NP_001372493.1,
NP_001372518.1,
NP_001372446.1,
NP_001372492.1,
NP_001372417.1,
NP_001372509.1,
NP_001372505.1,
XP_024309091.1,
XP_016861073.1
|
Others |
UniRef100:
UniRef100_Q5R6X9,
UniRef100_A8K0T4,
UniRef100_Q9UBL0
UniRef90:
UniRef90_Q9UBL0-6,
UniRef90_Q9UBL0
UniRef50:
UniRef50_Q9UBL0-6,
UniRef50_Q9UBL0
UniGene:
Hs.475902
CCDS:
CCDS43063.1,
CCDS58824.1,
CCDS2661.1,
CCDS58823.1
|
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Refseq |
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