Type | Description |
---|---|
Definition | nucleolar protein 4 |
Date | Results | Publications |
---|---|---|
2018-09-22 10:04:00 | the cosegregation of an intronic rare variant in NOL4 in one family, and a haplotype consisting of three variants in the noncoding region of IRF6 (introns 1, 8 and 3'UTR) in the other family, are reported. | 29666346 |
2014-09-06 12:48:00 | NOL4 was identified as a highly specific promoter methylated gene associated with head and neck squamous cell carcinoma | 24337411 |
2010-06-30 22:06:00 | Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) | 20379614 |
Type | IDs |
---|---|
Synonymous | CT125, HRIHFB2255, NOLP |
Gene |
UniProtKB-ID:
NOL4_HUMAN,
B4DLW2_HUMAN,
B3KRF4_HUMAN
UniprotKB:
O94818,
B4DLW2,
B3KRF4
UniParc:
UPI0000E24CE6,
UPI00017A73E7,
UPI000059D504,
UPI0001880C22,
UPI0000E24CE5,
UPI00003E2890
EMBL:
AC104985,
AK091463,
AK297185,
BT006763,
AC018972,
AB017800,
AC087397,
AK296539,
CR456730,
BC000313,
AC010798,
CH471088,
AK299850,
AB015339
Ensembl:
ENSG00000101746
KO:
hsa:8715
|
Nucleutide sequences |
EMBL-CDS:
BAA34576.1,
CAG33011.1,
BAG61712.1,
AAP35409.1,
BAH12383.1,
BAA34797.1,
AAH00313.1,
BAG59674.1,
EAX01312.1,
BAG52366.1
Gene_ORFName:
HRIHFB2255,
hCG_2021864
Ensembl_TRS:
ENST00000538587,
ENST00000535384,
ENST00000589544,
ENST00000261592
|
Protein sequencees |
Ensembl_PRO:
ENSP00000445733,
ENSP00000465450,
ENSP00000443472,
ENSP00000261592
RefSeq:
XP_016881542.1,
NP_001185475.1,
XP_011524541.1,
NP_001371399.1,
NP_001185478.1,
XP_016881544.1,
NP_003778.2,
NP_001371397.1,
XP_006722626.1,
NP_001371398.1,
NP_001269456.1,
XP_016881547.1,
NP_001371402.1,
XP_016881543.1,
NP_001340162.1,
NP_001340161.1,
NP_001371401.1,
XP_011524540.1,
XP_016881541.1,
NP_001185477.1,
NP_001185476.1,
NP_001340163.1,
NP_001340166.1,
NP_001340164.1,
XP_011524539.1,
NP_001371400.1,
NP_001340165.1,
XP_016881548.1,
NP_001371396.1,
XP_024307047.1
|
Others |
UniRef100:
UniRef100_B4DLW2,
UniRef100_B3KRF4,
UniRef100_O94818
UniRef90:
UniRef90_A0A5G2RHK3,
UniRef90_O94818,
UniRef90_A0A383YW68
UniRef50:
UniRef50_P60954,
UniRef50_O94818,
UniRef50_A0A4W3JLD3
UniGene:
Hs.514795
CCDS:
CCDS59308.1,
CCDS11907.2,
CCDS56059.1,
CCDS56058.1
|
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Refseq |
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