Ensembl ID ENSG00000029363 Gene ID 9774 Accession 16863
Gene Symbol BCLAF1 Alias BTF;bK211L9.1 Full Name BCL2 associated transcription factor 1
Position 6 : 136256627 - 136289851 Length 33225 bases Strand Minus strand
Status Confidence Main interacting RNAsmRNARBP type Canonical_RBPs
Summary This gene encodes a transcriptional repressor that interacts with several members of the BCL2 family of proteins. Overexpression of this protein induces apoptosis, which can be suppressed by co-expression of BCL2 proteins. The protein localizes to dot-like structures throughout the nucleus, and redistributes to a zone near the nuclear envelope in cells undergoing apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

ENSG00000029363 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000029363 BCLAF1 -0.3 3.69e-14 KIRC
ENSG00000029363 BCLAF1 -0.3 4.32e-11 HNSC
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000029363 BCLAF1 tumor 10330179
ENSG00000029363 BCLAF1 bladder tumor 10999749
ENSG00000029363 BCLAF1 Bladder tumor 12964816
ENSG00000029363 BCLAF1 bladder cancer 15708039
ENSG00000029363 BCLAF1 tumor 17938203
ENSG00000029363 BCLAF1 tumour 18053169
ENSG00000029363 BCLAF1 tumour 18410436
ENSG00000029363 BCLAF1 oral cancer 18543609
ENSG00000029363 BCLAF1 tumor 21479368
ENSG00000029363 BCLAF1 cancers 22833098
ENSG00000029363 BCLAF1 bladder tumor 23735602
ENSG00000029363 BCLAF1 tumors 24402574
ENSG00000029363 BCLAF1 breast cancer 24746700
ENSG00000029363 BCLAF1 colon cancer 25091051
ENSG00000029363 BCLAF1 cancer 25182846
ENSG00000029363 BCLAF1 rectal cancer 26183150
ENSG00000029363 BCLAF1 bladder cancer 26676636
ENSG00000029363 BCLAF1 cancer 26794446
ENSG00000029363 BCLAF1 cancer 27125219
ENSG00000029363 BCLAF1 colon cancer 27928057
ENSG00000029363 BCLAF1 cancer 28078319
ENSG00000029363 BCLAF1 AMLs 28216661
ENSG00000029363 BCLAF1 tumors 29112714
ENSG00000029363 BCLAF1 tumor 29434030
ENSG00000029363 BCLAF1 tumor 29777453
ENSG00000029363 BCLAF1 tumor 30367150
ENSG00000029363 BCLAF1 breast cancer 30678233
ENSG00000029363 BCLAF1 tumor 31237058
ENSG00000029363 BCLAF1 tumor 31870774
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000029363 BCLAF1 clear cell renal carcinoma sequence_alteration 0.6977% (9/1290) 1 entry
ENSG00000029363 BCLAF1 head and neck squamous cell carcinoma missense_variant 0.639% (4/626) 2 entries
ENSG00000029363 BCLAF1 head and neck squamous cell carcinoma sequence_alteration 0.639% (4/626) 2 entries
ENSG00000029363 BCLAF1 esophageal squamous cell carcinoma sequence_alteration 1.333% (9/675) 3 entries
ENSG00000029363 BCLAF1 melanoma missense_variant 10.89% (11/101) 2 entries
ENSG00000029363 BCLAF1 clear cell renal carcinoma missense_variant 0.6977% (9/1290) 1 entry
ENSG00000029363 BCLAF1 prostate adenocarcinoma sequence_alteration 2.132% (31/1454) 1 entry
ENSG00000029363 BCLAF1 rectal adenocarcinoma missense_variant 2.715% (6/221) 1 entry
ENSG00000029363 BCLAF1 bladder transitional cell carcinoma sequence_alteration 1.46% (2/137) 2 entries
ENSG00000029363 BCLAF1 colorectal adenocarcinoma frameshift_variant 2.109% (24/1138) 2 entries
ENSG00000029363 BCLAF1 non-small cell lung carcinoma missense_variant 3.774% (2/53) 1 entry
ENSG00000029363 BCLAF1 small cell lung carcinoma missense_variant 2.201% (7/318) 2 entries
ENSG00000029363 BCLAF1 ovarian serous adenocarcinoma sequence_alteration 1.04% (7/673) 2 entries
ENSG00000029363 BCLAF1 lung adenocarcinoma sequence_alteration 4.815% (56/1163) 3 entries
ENSG00000029363 BCLAF1 hepatocellular carcinoma sequence_alteration 0.8889% (8/900) 1 entry
ENSG00000029363 BCLAF1 cecum adenocarcinoma sequence_alteration 5.6% (7/125) 1 entry
ENSG00000029363 BCLAF1 lung adenocarcinoma stop_gained 4.815% (56/1163) 2 entries
ENSG00000029363 BCLAF1 rectal adenocarcinoma sequence_alteration 2.715% (6/221) 1 entry
ENSG00000029363 BCLAF1 basal cell carcinoma sequence_alteration 31.03% (18/58) 1 entry
ENSG00000029363 BCLAF1 colorectal adenocarcinoma missense_variant 2.109% (24/1138) 2 entries
ENSG00000029363 BCLAF1 brain glioblastoma sequence_alteration 0.9719% (9/926) 1 entry
ENSG00000029363 BCLAF1 skin melanoma sequence_alteration 7.032% (68/967) 3 entries
ENSG00000029363 BCLAF1 basal cell carcinoma missense_variant 31.03% (18/58) 1 entry
ENSG00000029363 BCLAF1 rectal adenocarcinoma stop_gained 2.715% (6/221) 1 entry
ENSG00000029363 BCLAF1 squamous cell lung carcinoma missense_variant 2.362% (18/762) 2 entries
ENSG00000029363 BCLAF1 colon adenocarcinoma missense_variant 3.74% (27/722) 5 entries
ENSG00000029363 BCLAF1 melanoma sequence_alteration 10.89% (11/101) 2 entries
ENSG00000029363 BCLAF1 esophageal adenocarcinoma missense_variant 2.278% (10/439) 1 entry
ENSG00000029363 BCLAF1 pancreatic ductal adenocarcinoma missense_variant 1.271% (16/1259) 1 entry
ENSG00000029363 BCLAF1 esophageal squamous cell carcinoma missense_variant 1.333% (9/675) 2 entries
ENSG00000029363 BCLAF1 esophageal adenocarcinoma sequence_alteration 2.278% (10/439) 1 entry
ENSG00000029363 BCLAF1 Merkel cell skin cancer sequence_alteration 6.667% (2/30) 2 entries
ENSG00000029363 BCLAF1 Central Nervous System Lymphoma missense_variant 22.22% (2/9) 1 entry
ENSG00000029363 BCLAF1 prostate carcinoma sequence_alteration 2.113% (9/426) 1 entry
ENSG00000029363 BCLAF1 skin melanoma missense_variant 7.032% (68/967) 5 entries
ENSG00000029363 BCLAF1 lung adenocarcinoma frameshift_variant 4.815% (56/1163) 1 entry
ENSG00000029363 BCLAF1 breast carcinoma missense_variant 0.4252% (6/1411) 1 entry
ENSG00000029363 BCLAF1 ovarian serous adenocarcinoma missense_variant 1.04% (7/673) 2 entries
ENSG00000029363 BCLAF1 squamous cell lung carcinoma sequence_alteration 2.362% (18/762) 1 entry
ENSG00000029363 BCLAF1 small cell lung carcinoma sequence_alteration 2.201% (7/318) 2 entries
ENSG00000029363 BCLAF1 adenosquamous lung carcinoma missense_variant 27.27% (3/11) 1 entry
ENSG00000029363 BCLAF1 lung adenocarcinoma missense_variant 4.815% (56/1163) 3 entries
ENSG00000029363 BCLAF1 colon adenocarcinoma sequence_alteration 3.74% (27/722) 4 entries
ENSG00000029363 BCLAF1 prostate adenocarcinoma missense_variant 2.132% (31/1454) 3 entries
ENSG00000029363 BCLAF1 cecum adenocarcinoma missense_variant 5.6% (7/125) 2 entries
ENSG00000029363 BCLAF1 prostate carcinoma missense_variant 2.113% (9/426) 2 entries
ENSG00000029363 BCLAF1 hepatocellular carcinoma missense_variant 0.8889% (8/900) 1 entry
ENSG00000029363 BCLAF1 esophageal squamous cell carcinoma frameshift_variant 1.333% (9/675) 2 entries
ENSG00000029363 BCLAF1 colorectal adenocarcinoma sequence_alteration 2.109% (24/1138) 2 entries
ENSG00000029363 BCLAF1 colon adenocarcinoma stop_gained 3.74% (27/722) 1 entry
ENSG00000029363 BCLAF1 metaplastic breast carcinoma missense_variant 3.922% (2/51) 1 entry
ENSG00000029363 BCLAF1 breast ductal adenocarcinoma missense_variant 3.596% (21/584) 1 entry
ENSG00000029363 BCLAF1 rectal adenocarcinoma frameshift_variant 2.715% (6/221) 1 entry
ENSG00000029363 BCLAF1 mucosal melanoma sequence_alteration 7.143% (1/14) 1 entry
ENSG00000029363 BCLAF1 colon adenocarcinoma conservative_inframe_deletion 3.74% (27/722) 1 entry
ENSG00000029363 BCLAF1 small cell lung carcinoma frameshift_variant 2.201% (7/318) 1 entry
ENSG00000029363 BCLAF1 Mantle cell lymphoma sequence_alteration 4.878% (2/41) 1 entry
ENSG00000029363 BCLAF1 Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor missense_variant 3.704% (1/27) 1 entry
ENSG00000029363 BCLAF1 prostate carcinoma stop_gained 2.113% (9/426) 1 entry
ENSG00000029363 BCLAF1 Pleural Biphasic Mesothelioma missense_variant 3.333% (1/30) 1 entry
ENSG00000029363 BCLAF1 esophageal squamous cell carcinoma stop_gained 1.333% (9/675) 1 entry
ENSG00000029363 BCLAF1 female breast carcinoma missense_variant 0.3745% (1/267) 1 entry
ENSG00000029363 BCLAF1 osteosarcoma missense_variant 1.724% (2/116) 1 entry
ENSG00000029363 BCLAF1 clear cell renal carcinoma frameshift_variant 0.6977% (9/1290) 1 entry
ENSG00000029363 BCLAF1 melanoma frameshift_variant 10.89% (11/101) 1 entry
ENSG00000029363 BCLAF1 cecum adenocarcinoma frameshift_variant 5.6% (7/125) 1 entry
ENSG00000029363 BCLAF1 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000029363 BCLAF1 basal cell carcinoma stop_gained 31.03% (18/58) 1 entry
ENSG00000029363 BCLAF1 brain glioblastoma conservative_inframe_deletion 0.9719% (9/926) 1 entry
ENSG00000029363 BCLAF1 colorectal adenocarcinoma stop_gained 2.109% (24/1138) 1 entry
ENSG00000029363 BCLAF1 Pancreatic Acinar Cell Carcinoma sequence_alteration 5.0% (1/20) 1 entry
ENSG00000029363 BCLAF1 head and neck squamous cell carcinoma stop_gained 0.639% (4/626) 1 entry
ENSG00000029363 BCLAF1 cecum adenocarcinoma stop_gained 5.6% (7/125) 1 entry
ENSG00000029363 BCLAF1 non-small cell lung carcinoma sequence_alteration 3.774% (2/53) 1 entry
ENSG00000029363 BCLAF1 Pancreatic Acinar Cell Carcinoma stop_gained 5.0% (1/20) 1 entry
ENSG00000029363 BCLAF1 Mantle cell lymphoma missense_variant 4.878% (2/41) 1 entry
ENSG00000029363 BCLAF1 papillary renal cell carcinoma stop_gained 0.2985% (1/335) 1 entry
ENSG00000029363 BCLAF1 colon adenocarcinoma frameshift_variant 3.74% (27/722) 1 entry
ENSG00000029363 BCLAF1 head and neck squamous cell carcinoma frameshift_variant 0.639% (4/626) 1 entry
ENSG00000029363 BCLAF1 osteosarcoma sequence_alteration 1.724% (2/116) 1 entry
ENSG00000029363 BCLAF1 mucosal melanoma missense_variant 7.143% (1/14) 1 entry
ENSG00000029363 BCLAF1 Central Nervous System Lymphoma sequence_alteration 22.22% (2/9) 1 entry
ENSG00000029363 BCLAF1 Merkel cell skin cancer missense_variant 6.667% (2/30) 1 entry
ENSG00000029363 BCLAF1 central nervous system primitive neuroectodermal neoplasm missense_variant 0.2252% (1/444) 1 entry
ENSG00000029363 BCLAF1 oral squamous cell carcinoma missense_variant 0.4878% (1/205) 1 entry
ENSG00000029363 BCLAF1 large cell lung carcinoma missense_variant 5.556% (1/18) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000029363 BCLAF1 ACC 0.00051 high
ENSG00000029363 BCLAF1 LUSC 0.048 low
ENSG00000029363 BCLAF1 READ 0.0045 low
ENSG00000029363 BCLAF1 KIRP 0.038 high
ENSG00000029363 BCLAF1 KICH 0.015 high
ENSG00000029363 BCLAF1 PCPG 0.0033 high
ENSG00000029363 BCLAF1 THYM 0.027 low
ENSG00000029363 BCLAF1 BRCA 0.00057 high
ENSG00000029363 BCLAF1 COAD 0.0043 low
ENSG00000029363 BCLAF1 ESCA 0.0056 high
ENSG00000029363 BCLAF1 KIRC 0.0024 low
ENSG00000029363 BCLAF1 BLCA 0.011 low
ENSG00000029363 BCLAF1 LAML 0.034 low
ENSG00000029363 BCLAF1 GBM 0.0015 low
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000029363 BCLAF1 LGG Del 1.244694 0.044952 0.580083 0.155945
ENSG00000029363 BCLAF1 SARC Amp 2.624781 0.357442 0.957559 0.256809
ENSG00000029363 BCLAF1 GBM Del 7.441237 0.109391 0.560358 0.287695
ENSG00000029363 BCLAF1 SKCM Del 5.200298 0.124195 0.557350 0.596730
ENSG00000029363 BCLAF1 LIHC Del 1.658913 0.081052 0.590314 0.351351
ENSG00000029363 BCLAF1 DLBC Del 1.405491 0.164653 0.555628 0.312500
ENSG00000029363 BCLAF1 MESO Del 1.141442 0.143109 0.534029 0.459770
ENSG00000029363 BCLAF1 KIRC Del 5.842127 0.050237 0.457795 0.282197
ENSG00000029363 BCLAF1 UVM Del 0.890814 0.063606 0.842531 0.287500
ENSG00000029363 BCLAF1 OV Del 9.903896 0.298991 0.611925 0.590674