Type | Description |
---|---|
Definition | IQ motif containing E |
Date | Results | Publications |
---|---|---|
2017-12-16 10:02:00 | Frameshift and a premature stop codon 22 in IQCE completely co-segregated with post-axial polydactyly phenotype within the family. | 28488682 |
2010-12-05 22:08:00 | Observational study of gene-disease association. (HuGE Navigator) | 20877624 |
Type | IDs |
---|---|
Synonymous | 1700028P05Rik, PAPA7 |
Gene |
UniProtKB-ID:
IQCE_HUMAN,
A0A087WX19_HUMAN,
A0A087WX45_HUMAN,
A0A024R853_HUMAN,
B4DXN1_HUMAN,
B4DDX4_HUMAN,
B3KRY4_HUMAN
UniprotKB:
Q6IPM2,
A0A087WX19,
A0A087WX45,
A0A024R853,
B4DXN1,
B4DDX4,
B3KRY4
UniParc:
UPI000020E9F6,
UPI00017A81F6,
UPI00003E2945,
UPI0000EE76A1,
UPI000006F2AB,
UPI000387B0A2,
UPI000020E9EF,
UPI00017A6C00,
UPI000020E9F7
EMBL:
AK293372,
AC092488,
AL136792,
CH471144,
AB028946,
AK092404,
BC043150,
AC073462,
BC061518,
BC071858,
AK302053
Ensembl:
ENSG00000106012
KO:
hsa:23288
|
Nucleutide sequences |
EMBL-CDS:
BAA82975.2,
CAB66726.1,
AAH61518.1,
AAH43150.1,
AAH71858.1,
EAW87263.1,
EAW87262.1,
EAW87264.1,
BAG63443.1,
BAG56885.1,
BAG52546.1
Gene_ORFName:
hCG_1788871,
hCG_1788871
Ensembl_TRS:
ENST00000438376,
ENST00000404984,
ENST00000623361,
ENST00000402050,
ENST00000325979,
ENST00000611775,
ENST00000476665
|
Protein sequencees |
Ensembl_PRO:
ENSP00000313772,
ENSP00000385945,
ENSP00000485601,
ENSP00000396178,
ENSP00000385597,
ENSP00000480668,
ENSP00000480715
RefSeq:
NP_001274431.1,
NP_001274429.1,
XP_024302466.1,
XP_011513545.1,
XP_016867391.1,
NP_689771.3,
NP_001274430.1,
XP_024302468.1,
XP_006715739.1,
XP_011513544.1,
XP_024302467.1,
XP_011513546.1,
NP_001274428.1,
XP_016867392.1
|
Others |
UniRef100:
UniRef100_A0A087WX45,
UniRef100_A0A024R853,
UniRef100_B3KRY4,
UniRef100_Q6IPM2,
UniRef100_A0A087WX19,
UniRef100_B4DDX4
UniRef90:
UniRef90_Q6IPM2
UniRef50:
UniRef50_Q6IPM2
UniGene:
Hs.520627
CCDS:
CCDS75560.1,
CCDS43542.1
|
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