Type | Description |
---|---|
Definition | SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4 |
Date | Results | Publications |
---|---|---|
2021-04-17 13:18:00 | [Clinicopathological and molecular features of SMARCA4-deficient carcinoma of the intestinal tract]. | 33831999 |
2021-04-17 13:13:00 | Clinical impact of EZH2 and its antagonist SMARCA4 in ovarian cancer. | 33230143 |
2021-04-13 10:15:00 | Small Cell Carcinoma of the Ovary, Hypercalcemic Type (SCCOHT) beyond SMARCA4 Mutations: A Comprehensive Genomic Analysis. | 32575483 |
2021-04-13 10:13:00 | Acute BAF perturbation causes immediate changes in chromatin accessibility. | 33558760 |
2021-04-13 10:10:00 | Re-expression of SMARCA4/BRG1 in small cell carcinoma of ovary, hypercalcemic type (SCCOHT) promotes an epithelial-like gene signature through an AP-1-dependent mechanism. | 33355532 |
Type | IDs |
---|---|
Synonymous | BAF190, BAF190A, BRG1, CSS4, MRD16, RTPS2, SNF2, SNF2L4, SNF2LB, SWI2, hSNF2b |
Gene |
UniProtKB-ID:
SMCA4_HUMAN,
Q9HBD4_HUMAN,
A7E2E1_HUMAN,
B3KNW7_HUMAN
UniprotKB:
P51532,
Q9HBD4,
A7E2E1,
B3KNW7
UniParc:
UPI000165D5FA,
UPI000165D5FB,
UPI000006F973,
UPI000006FF7A,
UPI000165D5FC,
UPI0000EE5FF6,
UPI0000E042EF
EMBL:
CH471106,
AC011442,
AK290033,
EU430757,
AC006127,
BC150298,
KC877700,
U29175,
AF254822,
AC011485,
EU430756,
AK055168,
D26156,
EU430758,
EU430759
Ensembl:
ENSG00000127616
KO:
hsa:6597
|
Nucleutide sequences |
EMBL-CDS:
AAG24789.1,
AAB40977.1,
ACA09750.1,
ACA09752.1,
EAW84167.1,
ACA09751.1,
ACA09753.1,
AAC97986.1,
AAC97987.1,
BAA05143.1,
AAG24790.1,
EAW84164.1,
EAW84162.1,
BAF82722.1,
AAI50299.1,
BAG51479.1
Gene_ORFName:
hCG_29955,
hCG_29955
Ensembl_TRS:
ENST00000643296,
ENST00000344626,
ENST00000646484,
ENST00000647230,
ENST00000541122,
ENST00000589677,
ENST00000590574,
ENST00000644737,
ENST00000444061,
ENST00000645460,
ENST00000429416,
ENST00000646510,
ENST00000646693,
ENST00000450717
|
Protein sequencees |
Ensembl_PRO:
ENSP00000495548,
ENSP00000494772,
ENSP00000392837,
ENSP00000464778,
ENSP00000395654,
ENSP00000343896,
ENSP00000445036,
ENSP00000495536,
ENSP00000494463,
ENSP00000466963,
ENSP00000494676,
ENSP00000496635,
ENSP00000495368,
ENSP00000397783
RefSeq:
XP_024307435.1,
XP_024307429.1,
XP_024307432.1,
XP_006722909.1,
XP_024307427.1,
NP_001122319.1,
XP_024307430.1,
NP_001122317.1,
XP_024307431.1,
NP_003063.2,
XP_024307433.1,
NP_001374212.1,
NP_001122318.1,
NP_001122320.1,
XP_011526500.1,
NP_001122316.1,
NP_001122321.1,
NP_001361386.1,
XP_024307426.1,
XP_024307428.1
|
Others |
UniRef100:
UniRef100_P51532,
UniRef100_K7CA21,
UniRef100_Q9HBD4
UniRef90:
UniRef90_P51532,
UniRef90_K7CA21,
UniRef90_Q9HBD4
UniRef50:
UniRef50_Q3TKT4
UniGene:
Hs.327527
CCDS:
CCDS54217.1,
CCDS54218.1,
CCDS12253.1,
CCDS45972.1,
CCDS45973.1
|
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Refseq |
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