Type | Description |
---|---|
Definition | CD99 molecule like 2 |
Date | Results | Publications |
---|---|---|
2016-03-05 10:31:00 | This study identified predicted pathogenic, hemizygous variants on chromosome X in disease genes CD99L2. | 25666757 |
Type | IDs |
---|---|
Synonymous | CD99B, MIC2L1 |
Gene |
UniProtKB-ID:
C99L2_HUMAN,
A0A024RC16_HUMAN
UniprotKB:
Q8TCZ2,
A0A024RC16
UniParc:
UPI0000034CC0,
UPI000006E348,
UPI000006D2CB,
UPI0001AE7005,
UPI0002065B16,
UPI000007145B
EMBL:
AL136580,
BC025729,
CH471169,
AY078166,
AK291375,
AY358837,
AK125020,
AY078167,
BC030536,
KU178797,
AF274573,
AF002223,
AK290200,
AK293244,
AY078165
Ensembl:
ENSG00000102181
KO:
hsa:83692
|
Nucleutide sequences |
EMBL-CDS:
BAG54124.1,
EAW99392.1,
AAL86617.1,
EAW99395.1,
EAW99393.1,
AAL86618.1,
BAG56778.1,
EAW99391.1,
AAQ89196.1,
BAF82889.1,
CAB66515.1,
BAF84064.1,
AAH25729.1,
AAH30536.1,
AAL86619.1,
EAW99394.1,
ALQ34255.1
Gene_ORFName:
UNQ1964/PRO4486,
hCG_39239
Ensembl_TRS:
ENST00000355149,
ENST00000613030,
ENST00000437787,
ENST00000346693,
ENST00000466436,
ENST00000370377
|
Protein sequencees |
Ensembl_PRO:
ENSP00000359403,
ENSP00000417697,
ENSP00000480322,
ENSP00000489222,
ENSP00000394858,
ENSP00000347275
RefSeq:
NP_604394.1,
XP_016885379.1,
NP_604395.1,
XP_016885380.1,
NP_001229543.1,
NP_001171737.1,
XP_011529504.1,
NP_113650.2
|
Others |
UniRef100:
UniRef100_Q8TCZ2
UniRef90:
UniRef90_Q8TCZ2
UniRef50:
UniRef50_Q8TCZ2
UniGene:
Hs.522805
CCDS:
CCDS14697.1,
CCDS55527.1,
CCDS76044.1,
CCDS35427.1,
CCDS14698.1
|
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