Ensembl ID ENSG00000196588 Gene ID 57591 Accession 14334
Gene Symbol MRTFA Alias Full Name
Position 22 : 40410281 - 40636719 Length 226439 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary

ENSG00000196588 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000196588 0.57 5.06e-22 KIRC
ENSG00000196588 0.49 8.04e-13 LIHC
ENSG00000196588 1.49 2.79e-14 CHOL
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000196588 astrocytic tumors 14712485
ENSG00000196588 cancer 19625774
ENSG00000196588 AML with recurrent genetic abnormalities 19860179
ENSG00000196588 prostate cancer 19963382
ENSG00000196588 cancer 20338973
ENSG00000196588 cancer 20816842
ENSG00000196588 tumor 21538823
ENSG00000196588 cancer 22139079
ENSG00000196588 prostate cancer 23707258
ENSG00000196588 cancer 23766813
ENSG00000196588 tumour 23853104
ENSG00000196588 breast cancer 24084383
ENSG00000196588 breast cancer 24096006
ENSG00000196588 breast cancer 24189459
ENSG00000196588 breast cancer 24325915
ENSG00000196588 breast cancer 24721635
ENSG00000196588 breast cancer 25038455
ENSG00000196588 tumor 25079789
ENSG00000196588 breast cancer 25342443
ENSG00000196588 cancer 25381249
ENSG00000196588 cancer 25733820
ENSG00000196588 lung cancer 25746000
ENSG00000196588 AML 25794001
ENSG00000196588 breast cancer 25854163
ENSG00000196588 anaplastic thyroid cancer 25955685
ENSG00000196588 cancer 26071033
ENSG00000196588 breast cancer 26476216
ENSG00000196588 pancreatic cancer 26498848
ENSG00000196588 cancer 26872785
ENSG00000196588 cancer 27177343
ENSG00000196588 breast cancer 27432265
ENSG00000196588 Breast Cancer 27435395
ENSG00000196588 tumor 27708220
ENSG00000196588 tumor 28035058
ENSG00000196588 breast cancer 28069441
ENSG00000196588 breast cancer 28117334
ENSG00000196588 ovarian cancer 28385531
ENSG00000196588 cancer 28474808
ENSG00000196588 lung cancer 28536630
ENSG00000196588 Breast cancer 28592291
ENSG00000196588 breast cancer 28671673
ENSG00000196588 breast cancer 28822708
ENSG00000196588 cancer 28912487
ENSG00000196588 AML with minimal differentiation 28977979
ENSG00000196588 cancer 29065889
ENSG00000196588 breast cancer 29077787
ENSG00000196588 Cancer 29371938
ENSG00000196588 Cervical cancer 29391067
ENSG00000196588 tumor 29400712
ENSG00000196588 cancer 29483957
ENSG00000196588 breast cancer 29632640
ENSG00000196588 breast cancer 29807221
ENSG00000196588 tumor 29887596
ENSG00000196588 tumours 30068568
ENSG00000196588 colon cancer 30078679
ENSG00000196588 tumor 30106093
ENSG00000196588 tumor 30384218
ENSG00000196588 gastric cancer 30426547
ENSG00000196588 breast cancer 30642840
ENSG00000196588 Non-small Cell Lung Cancer 30827324
ENSG00000196588 pediatric AML 31024852
ENSG00000196588 pancreatic cancer 31068602
ENSG00000196588 papillary thyroid cancer 31363007
ENSG00000196588 tumour 31409840
ENSG00000196588 tumour 31414556
ENSG00000196588 colorectal cancer 31579420
ENSG00000196588 tumor 31759986
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000196588 prostate adenocarcinoma sequence_alteration 5.708% (83/1454) 1 entry
ENSG00000196588 esophageal adenocarcinoma sequence_alteration 10.05% (44/438) 1 entry
ENSG00000196588 melanoma sequence_alteration 12.87% (13/101) 2 entries
ENSG00000196588 breast ductal adenocarcinoma sequence_alteration 13.18% (77/584) 1 entry
ENSG00000196588 melanoma conservative_inframe_deletion 12.87% (13/101) 1 entry
ENSG00000196588 pancreatic ductal adenocarcinoma sequence_alteration 5.56% (70/1259) 1 entry
ENSG00000196588 melanoma missense_variant 12.87% (13/101) 2 entries
ENSG00000196588 colon adenocarcinoma missense_variant 2.078% (15/722) 3 entries
ENSG00000196588 oral squamous cell carcinoma missense_variant 2.427% (5/206) 2 entries
ENSG00000196588 ovarian serous adenocarcinoma sequence_alteration 0.8915% (6/673) 1 entry
ENSG00000196588 bladder carcinoma missense_variant 1.622% (9/555) 1 entry
ENSG00000196588 lung adenocarcinoma missense_variant 1.148% (14/1220) 4 entries
ENSG00000196588 colorectal adenocarcinoma frameshift_variant 4.394% (50/1138) 1 entry
ENSG00000196588 acute myeloid leukemia sequence_alteration 1.544% (14/907) 1 entry
ENSG00000196588 chronic lymphocytic leukemia missense_variant 1.802% (16/888) 1 entry
ENSG00000196588 lung adenocarcinoma sequence_alteration 1.148% (14/1220) 6 entries
ENSG00000196588 prostate carcinoma sequence_alteration 2.686% (13/484) 3 entries
ENSG00000196588 colon adenocarcinoma frameshift_variant 2.078% (15/722) 2 entries
ENSG00000196588 embryonal rhabdomyosarcoma sequence_alteration 2.632% (2/76) 1 entry
ENSG00000196588 gastric adenocarcinoma sequence_alteration 2.509% (14/558) 1 entry
ENSG00000196588 chronic lymphocytic leukemia sequence_alteration 1.802% (16/888) 2 entries
ENSG00000196588 skin melanoma sequence_alteration 2.068% (20/967) 3 entries
ENSG00000196588 colon adenocarcinoma sequence_alteration 2.078% (15/722) 5 entries
ENSG00000196588 melanoma frameshift_variant 12.87% (13/101) 1 entry
ENSG00000196588 hepatocellular carcinoma sequence_alteration 1.667% (15/900) 1 entry
ENSG00000196588 esophageal squamous cell carcinoma missense_variant 0.8889% (6/675) 3 entries
ENSG00000196588 head and neck squamous cell carcinoma sequence_alteration 0.6369% (4/628) 2 entries
ENSG00000196588 skin melanoma missense_variant 2.068% (20/967) 3 entries
ENSG00000196588 female breast carcinoma sequence_alteration 1.79% (7/391) 2 entries
ENSG00000196588 squamous cell lung carcinoma sequence_alteration 1.212% (10/825) 1 entry
ENSG00000196588 colorectal adenocarcinoma missense_variant 4.394% (50/1138) 4 entries
ENSG00000196588 gastric intestinal type adenocarcinoma sequence_alteration 2.353% (2/85) 1 entry
ENSG00000196588 embryonal rhabdomyosarcoma missense_variant 2.632% (2/76) 1 entry
ENSG00000196588 gastric adenocarcinoma missense_variant 2.509% (14/558) 1 entry
ENSG00000196588 bladder carcinoma sequence_alteration 1.622% (9/555) 1 entry
ENSG00000196588 head and neck squamous cell carcinoma missense_variant 0.6369% (4/628) 1 entry
ENSG00000196588 clear cell renal carcinoma missense_variant 0.6074% (8/1317) 1 entry
ENSG00000196588 brain glioblastoma missense_variant 0.324% (3/926) 1 entry
ENSG00000196588 gastric intestinal type adenocarcinoma missense_variant 2.353% (2/85) 1 entry
ENSG00000196588 hepatocellular carcinoma missense_variant 1.667% (15/900) 1 entry
ENSG00000196588 pancreatic ductal adenocarcinoma frameshift_variant 5.56% (70/1259) 1 entry
ENSG00000196588 clear cell renal carcinoma sequence_alteration 0.6074% (8/1317) 2 entries
ENSG00000196588 anaplastic astrocytoma sequence_alteration 4.545% (2/44) 1 entry
ENSG00000196588 colorectal adenocarcinoma sequence_alteration 4.394% (50/1138) 4 entries
ENSG00000196588 esophageal squamous cell carcinoma sequence_alteration 0.8889% (6/675) 4 entries
ENSG00000196588 ovarian serous adenocarcinoma missense_variant 0.8915% (6/673) 1 entry
ENSG00000196588 papillary renal cell carcinoma sequence_alteration 1.201% (4/333) 1 entry
ENSG00000196588 oral squamous cell carcinoma sequence_alteration 2.427% (5/206) 3 entries
ENSG00000196588 brain glioblastoma sequence_alteration 0.324% (3/926) 2 entries
ENSG00000196588 nasopharyngeal squamous cell carcinoma sequence_alteration 1.198% (2/167) 1 entry
ENSG00000196588 ganglioneuroblastoma sequence_alteration 100.0% (1/1) 1 entry
ENSG00000196588 prostate carcinoma missense_variant 2.686% (13/484) 1 entry
ENSG00000196588 head and neck squamous cell carcinoma frameshift_variant 0.6369% (4/628) 1 entry
ENSG00000196588 osteosarcoma sequence_alteration 0.8621% (1/116) 1 entry
ENSG00000196588 lung adenocarcinoma frameshift_variant 1.148% (14/1220) 1 entry
ENSG00000196588 lung adenocarcinoma stop_gained 1.148% (14/1220) 1 entry
ENSG00000196588 Mantle cell lymphoma missense_variant 2.439% (1/41) 1 entry
ENSG00000196588 bile duct adenocarcinoma missense_variant 0.5291% (1/189) 1 entry
ENSG00000196588 large cell lung carcinoma missense_variant 5.556% (1/18) 1 entry
ENSG00000196588 Mantle cell lymphoma sequence_alteration 2.439% (1/41) 1 entry
ENSG00000196588 ovarian serous adenocarcinoma frameshift_variant 0.8915% (6/673) 1 entry
ENSG00000196588 small cell lung carcinoma missense_variant 0.3106% (1/322) 1 entry
ENSG00000196588 renal cell carcinoma sequence_alteration 9.091% (1/11) 1 entry
ENSG00000196588 acute lymphoblastic leukemia missense_variant 0.3115% (1/321) 1 entry
ENSG00000196588 large cell lung carcinoma sequence_alteration 5.556% (1/18) 1 entry
ENSG00000196588 non-small cell lung carcinoma sequence_alteration 1.613% (1/62) 1 entry
ENSG00000196588 female breast carcinoma missense_variant 1.79% (7/391) 1 entry
ENSG00000196588 renal cell carcinoma missense_variant 9.091% (1/11) 1 entry
ENSG00000196588 alveolar rhabdomyosarcoma missense_variant 1.695% (1/59) 1 entry
ENSG00000196588 adrenocortical adenoma sequence_alteration 2.5% (1/40) 1 entry
ENSG00000196588 bile duct adenocarcinoma sequence_alteration 0.5291% (1/189) 1 entry
ENSG00000196588 basal cell carcinoma missense_variant 1.724% (1/58) 1 entry
ENSG00000196588 acute lymphoblastic leukemia sequence_alteration 0.3115% (1/321) 1 entry
ENSG00000196588 adrenocortical adenoma missense_variant 2.5% (1/40) 1 entry
ENSG00000196588 nasopharyngeal squamous cell carcinoma missense_variant 1.198% (2/167) 1 entry
ENSG00000196588 alveolar rhabdomyosarcoma sequence_alteration 1.695% (1/59) 1 entry
ENSG00000196588 papillary renal cell carcinoma frameshift_variant 1.201% (4/333) 1 entry
ENSG00000196588 ependymoma sequence_alteration 2.174% (1/46) 1 entry
ENSG00000196588 acute myeloid leukemia frameshift_variant 1.544% (14/907) 1 entry
ENSG00000196588 small cell lung carcinoma sequence_alteration 0.3106% (1/322) 1 entry
ENSG00000196588 ganglioneuroblastoma missense_variant 100.0% (1/1) 1 entry
ENSG00000196588 non-small cell lung carcinoma missense_variant 1.613% (1/62) 1 entry
ENSG00000196588 oral squamous cell carcinoma conservative_inframe_deletion 2.427% (5/206) 1 entry
ENSG00000196588 basal cell carcinoma sequence_alteration 1.724% (1/58) 1 entry
ENSG00000196588 acute myeloid leukemia missense_variant 1.544% (14/907) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000196588 SARC 0.0011 low
ENSG00000196588 UVM 0.042 high
ENSG00000196588 UCEC 0.0032 low
ENSG00000196588 THCA 0.0017 high
ENSG00000196588 LGG 0.00021 low
ENSG00000196588 LUSC 0.048 high
ENSG00000196588 READ 0.0094 low
ENSG00000196588 KIRP 0.011 high
ENSG00000196588 LUAD 0.0019 high
ENSG00000196588 THYM 0.00048 low
ENSG00000196588 BRCA 0.0054 low
ENSG00000196588 ESCA 0.0011 low
ENSG00000196588 PRAD 0.0019 low
ENSG00000196588 LAML 0.0066 high
ENSG00000196588 GBM 0.032 low
ENSG00000196588 SKCM 0.006 high
ENSG00000196588 CESC 0.046 low
ENSG00000196588 LIHC 0.006 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000196588 SKCM Amp 5.079943 0.244675 0.671167 0.389646
ENSG00000196588 PCPG Del 0.648111 0.056806 0.618450 0.395062
ENSG00000196588 BLCA Del 1.597275 0.092344 0.367135 0.455882
ENSG00000196588 OV Del 0.848851 0.178011 0.648849 0.803109