| Type | Description |
|---|---|
| Definition | coiled-coil domain containing 136 |
| Date | Results | Publications |
|---|---|---|
| 2017-12-09 12:12:00 | Missense variant in CCDC136 gene is associated with reading disability. | 28866788 |
| 2015-05-23 10:41:00 | CCDC136 locus showed association with a comparable reading/language measure. | 25065397 |
| 2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
| 2010-01-21 00:00:00 | Data suggest that NAG6 may represent a candidate tumor suppressor gene at 7q31-32 loci associated with gastric carcinoma. | 15112360 |
| Type | IDs |
|---|---|
| Synonymous | NAG6 |
| Gene |
UniProtKB-ID:
CC136_HUMAN,
A0A024R758_HUMAN
UniprotKB:
Q96JN2,
A0A024R758
UniParc:
UPI00001AE462,
UPI0000E445DE,
UPI00001C09D9,
UPI0001AE70E5,
UPI0000EE405B
EMBL:
BC150331,
AF156971,
AL133027,
CH236950,
CH471070,
AK023500,
AB058696,
BC152408,
AC024952,
AK124447,
AC025594
Ensembl:
ENSG00000128596
KO:
hsa:64753
|
| Nucleutide sequences |
EMBL-CDS:
AAI52409.1,
EAW83684.1,
BAB47422.1,
BAB14590.1,
BAC85854.1,
CAB61359.1,
AAI50332.1,
EAL24111.1,
EAW83682.1,
EAW83685.1,
EAW83686.1
Gene_ORFName:
NAG6,
hCG_41665
Ensembl_TRS:
ENST00000297788,
ENST00000378685
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000367956,
ENSP00000297788
RefSeq:
XP_024302642.1,
NP_001188301.1,
XP_011514791.1,
XP_011514790.1,
XP_024302640.1,
NP_001354691.1,
NP_001354690.1,
NP_001354694.1,
XP_016868021.1,
NP_001354692.1,
NP_001350353.1,
XP_011514786.1,
NP_001354695.1,
XP_011514788.1,
XP_016868022.1,
NP_001350352.1,
XP_011514789.1,
XP_011514792.1,
XP_024302643.1,
XP_024302641.1,
XP_011514787.1,
NP_073579.5,
XP_011514785.1,
NP_001354693.1
|
| Others |
UniRef100:
UniRef100_A0A024R758,
UniRef100_Q96JN2
UniRef90:
UniRef90_Q96JN2
UniRef50:
UniRef50_Q96JN2
UniGene:
Hs.521178
CCDS:
CCDS56510.1,
CCDS47704.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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