| Type | Description |
|---|---|
| Definition | nuclear factor I X |
| Date | Results | Publications |
|---|---|---|
| 2020-08-12 13:02:00 | Malan syndrome due to shared NFIX variants was diagnosed in the brothers using exome sequencing. | 31369202 |
| 2020-05-16 12:29:00 | Knockdown of circNFIX inhibits progression of glioma in vitro and in vivo by increasing miR-378e and decreasing RPN2, providing a novel mechanism for understanding the pathogenesis of glioma. | 31888753 |
| 2020-03-28 10:50:00 | Secretory carcinoma of the skin associated with the presence of novel NFIX-PKN1 translocation. | 31045890 |
| 2019-10-26 10:04:00 | Data show that miR-744-5p expression directly downregulated mRNA and protein expression of nuclear factor I X (NFIX) and heterogeneous nuclear ribonucleoprotein C (HNRNPC). | 29899543 |
| 2019-08-10 10:46:00 | NFIX downregulation might independently predict poor prognosis in LUAD. DNA hypermethylation might be an important cause of the downregulation | 30418046 |
| Type | IDs |
|---|---|
| Synonymous | CTF, MRSHSS, NF-I/X, NF1-X, NF1A, SOTOS2 |
| Gene |
UniProtKB-ID:
NFIX_HUMAN,
B4DHW2_HUMAN
UniprotKB:
Q14938,
B4DHW2
UniParc:
UPI00017A70DE,
UPI000012FFCC,
UPI000003B460,
UPI000002AF1C,
UPI000002AF1F,
UPI000002AF1E,
UPI000002AF1D
EMBL:
CH471106,
U07811,
BT019732,
L31881,
AK295290,
KF456509,
AC004660,
AC007787,
BC117115,
AC022152,
BC117113,
U18759,
AC138474,
U18761,
AK297261
Ensembl:
ENSG00000008441
KO:
hsa:4784
|
| Nucleutide sequences |
EMBL-CDS:
AAB52371.1,
AAD38241.1,
AAD38240.1,
AAA53422.1,
AAB52369.1,
AAV38537.1,
AAC15752.1,
BAG59737.1,
EAW84340.1,
AAI17114.1,
AAI17116.1,
AAA93126.1,
BAG58274.1
Ensembl_TRS:
ENST00000587760,
ENST00000587260,
ENST00000585575,
ENST00000592199,
ENST00000397661,
ENST00000676441
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000467785,
ENSP00000467512,
ENSP00000380781,
ENSP00000466389,
ENSP00000468794,
ENSP00000502554
RefSeq:
NP_002492.2,
NP_001257972.1,
XP_005259974.1,
NP_001365334.1,
NP_001352912.1,
NP_001352911.1,
NP_001365333.1,
NP_001352913.1,
NP_001257973.1,
NP_001352914.1,
NP_001352831.1,
XP_006722823.1
|
| Others |
UniRef100:
UniRef100_Q14938,
UniRef100_B4DHW2
UniRef90:
UniRef90_F7DCY8,
UniRef90_Q14938
UniRef50:
UniRef50_Q14938,
UniRef50_F7DCY8
UniGene:
Hs.257970
CCDS:
CCDS45996.1,
CCDS59359.1
|
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|---|---|---|---|---|---|---|---|---|
| Refseq |
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