Protein Ncoa4

URN urn:agi-llid:8031
Total Entities 0
Connectivity 135
Name Ncoa4
Description nuclear receptor coactivator 4
Notes This gene encodes an androgen receptor coactivator. The encoded protein interacts with the androgen receptor in a ligand-dependent manner to enhance its transcriptional activity. Chromosomal translocations between this gene and the ret tyrosine kinase gene, also located on chromosome 10, have been associated with papillary thyroid carcinoma. Alternatively spliced transcript variants have been described. Pseudogenes are present on chromosomes 4, 5, 10, and 14. [provided by RefSeq, Feb 2009]

GO Molecular Function transcription coactivator activity
androgen receptor binding

GO Cellular Component mitochondrion
nucleus

GO Biological Process male gonad development
androgen receptor signaling pathway
response to hormone
positive regulation of transcription, DNA-templated
transcription, DNA-templated

Pathway Prostate Cancer Overview
Proteins Involved in Pathogenesis of Prostate Cancer
iron homeostasis pathway

Group male gonad development
androgen receptor signaling pathway
response to hormone
positive regulation of transcription, DNA-templated
transcription coactivator activity
transcription, DNA-templated
androgen receptor binding
mitochondrion
nucleus

LocusLink ID 8031
27057
619385

GO ID 0050681
0003713
0030521
0008584
0045893
0009725
0006351
0005634
0005739

Alias RFG
ELE1
PTC3
ARA70
RP11-481A12.4
nuclear receptor coactivator 4
NCoA-4
ret fused
70 kDa AR-activator
RET-activating gene ELE1
70 kDa androgen receptor coactivator
androgen receptor-associated protein of 70 kDa
ELE1alpha
nuclear receptor coactivator IV
OTTHUMP00000019601
OTTHUMP00000019602
OTTHUMP00000019603
RET-activating gene ELE I
RIKEN cDNA 1110034E15 gene
androgen receptor-associated protein 70
RFG/ELE1alpha/ARA70
RIKEN cDNA 4432406M01 gene
4432406M01Rik
NCOA4
4432406M01
4432406M01Rik(2)
AI227008
MGC72479
DKFZp762E1112
ELE I
GNB:557270
1110034E15
1110034E15Rik

Mouse chromosome position 14

OMIM ID 601984
188550

Rat chromosome position 16p16

Hugo ID 7671

Human chromosome position 10q11.2

Swiss-Prot Accession Q13772
Q96E88
B2R5V0
B4DZ85
B4DF87
Q5U4H9
B1H215
A8K8W5
B4E260
E9PAV7
J3KQN8
Q14239

PIR ID S61532

GenBank ID NC_000010
NM_001145260
NP_001138732
NM_001145261
NP_001138733
NM_001145263
NP_001138735
XM_005270177
XP_005270234
XM_005270179
XP_005270236
XM_005270178
XP_005270235
XM_005270180
XP_005270237
NM_005437
NP_005428
NM_001145262
NP_001138734
NW_003871068
XM_005277658
XP_005277715
XM_005277657
XP_005277714
XM_005277659
XP_005277716
XM_005277656
XP_005277713
NG_023372
NC_018921
AC_000142
ABBA01033538
ABBA01033539
AL450342
AMYH02023033
AMYH02023034
CH471260
EAW53686
EAW53687
EAW53688
EAW53689
AB064669
BAB93520
AK129911
AK130612
AK292480
BAF85169
AK293978
BAG57348
AK302794
BAG63997
AK304123
BAG65022
AK310849
AK312325
BAG35247
AL162047
CAB82390
AY425959
AAR07952
BC001562
AAH01562
BC012736
AAH12736
DA415606
DA860108
DB075100
L49399
AAC37591
X71413
CAA50536
X77548
CAA54673
Q13772
AM393327
CAL38205
DQ891598
ABM82524
DQ894792
ABM85718
GQ129251
ACT64385
GQ129252
ACT64386
NC_000080
NM_001033988
NP_001029160
NM_001284319
NP_001271248
XM_006519068
XP_006519131
NM_019744
NP_062718
XM_006519067
XP_006519130
AC_000036
AAHY01112648
AC154532
CH466573
EDL24830
AF159461
AAD43136
AK004086
AK014479
BAB29382
AK016355
BAB30203
AK032951
BAC28095
AK129020
AK132981
AK143965
AK145070
BAE26220
AK145945
BAE26774
AK145954
BAE26782
AK146384
BAE27129
AK146498
BAE27214
AK146598
BAE27292
AK146646
BAE27327
AK146649
BAE27329
AK147036
AK147125
BAE27696
AK156999
BB750616
BC031528
AAH31528
BC085086
AAH85086
CF161810
CJ088075
NC_005115
NM_001034008
NP_001029180
NM_001034007
NP_001029179
XM_006252660
XP_006252722
AC_000084
AABR06086409
AAHX01086419
AAHX01086420
CH474046
EDL88925
EDL88926
AI031008
AI112421
BC160817
AAI60817
CB758330
CB806310
CV119475
CV795771
FQ220276
FQ226067
FQ226225
FQ226899
FQ227413
FQ228117
FQ230448
FQ232075
FQ232507
FQ233142
FQ234345
FQ235179

Unigene ID Hs.643658
Hs.709644
Mm.371598
Mm.477186
Rn.165968
Rn.198999

KEGG ID hsa:8031
mmu:27057
rno:619385

Swiss-Prot ID NCOA4_HUMAN

Ensembl ID ENSG00000138293
ENSP00000395465
ENST00000452682
ENSP00000405146
ENST00000438493
ENSP00000390713
ENST00000443446
ENSP00000363200
ENST00000374087
ENSP00000344552
ENST00000344348
ENSMUSG00000056234
ENSMUSP00000126071
ENSMUST00000163336
ENSMUSP00000107625
ENSMUST00000111994
ENSRNOG00000019768
ENSRNOP00000026803
ENSRNOT00000026803
ENSRNOP00000061299
ENSRNOT00000066062

Homologene ID 38052

Organism Homo sapiens
Mus musculus
Rattus norvegicus

MGI ID 1350932

RGD ID 1563014

MedScan ID 8031