| Type | Description |
|---|---|
| Definition | lebercilin LCA5 like |
| Date | Results | Publications |
|---|---|---|
| 2016-05-09 12:09:00 | RNA-seq evidence of biallelic expression of LCA5L and 10 neighboring genes in at least one primary human tissue tested indicates that the expression of LCA5L is uncoupled from the control of the maternally inherited 5mCpG imprints at the WRB differentially methylated region (DMR) in disomic controls or trisomy (Down syndrome) individuals. | 27100087 |
| Type | IDs |
|---|---|
| Synonymous | C21orf13 |
| Gene |
UniProtKB-ID:
LCA5L_HUMAN
UniprotKB:
O95447
UniParc:
UPI00000015EE
EMBL:
CH471079,
AL163279,
AF121781,
BC043006,
BC031059
Ensembl:
ENSG00000157578
KO:
hsa:150082
|
| Nucleutide sequences |
EMBL-CDS:
AAH43006.1,
EAX09642.1,
AAH31059.1,
CAB90455.1,
EAX09644.1,
AAD12066.1,
EAX09641.1
Ensembl_TRS:
ENST00000288350,
ENST00000358268,
ENST00000380671
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000288350,
ENSP00000351008,
ENSP00000370046
RefSeq:
XP_011527767.1,
XP_011527773.1,
NP_001371224.1,
NP_001371227.1,
XP_011527761.1,
NP_001371222.1,
NP_001371240.1,
NP_001371238.1,
NP_001371216.1,
NP_001371223.1,
NP_001371220.1,
NP_001371235.1,
NP_001371226.1,
NP_001371218.1,
NP_001371221.1,
XP_011527763.1,
NP_001371214.1,
XP_011527760.1,
XP_011527771.1,
NP_001371215.1,
XP_011527770.1,
NP_001371229.1,
XP_011527765.1,
XP_011527762.1,
XP_011527772.1,
NP_001371217.1,
NP_001371233.1,
XP_011527766.1,
XP_011527769.1,
XP_016883766.1,
NP_001371236.1,
NP_001371232.1,
NP_001371237.1,
NP_001371242.1,
XP_016883763.1,
XP_011527764.1,
NP_001371241.1,
NP_001371231.1,
NP_001371234.1,
NP_001371225.1,
NP_001371228.1,
NP_001371230.1,
XP_016883765.1,
NP_689718.1,
NP_001371239.1,
XP_011527768.1
|
| Others |
UniRef100:
UniRef100_O95447
UniRef90:
UniRef90_O95447
UniRef50:
UniRef50_O95447
UniGene:
Hs.517284
CCDS:
CCDS13665.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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