Ensembl ID ENSG00000136492 Gene ID 83990 Accession 20473
Gene Symbol BRIP1 Alias OF;BACH1;FANCJ Full Name BRCA1 interacting helicase 1
Position 17 : 61679139 - 61863559 Length 184421 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary The protein encoded by this gene is a member of the RecQ DEAH helicase family and interacts with the BRCT repeats of breast cancer, type 1 (BRCA1). The bound complex is important in the normal double-strand break repair function of breast cancer, type 1 (BRCA1). This gene may be a target of germline cancer-inducing mutations. [provided by RefSeq, Jul 2008]

ENSG00000136492 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000136492 BRIP1 1.79 1.88e-49 KIRC
ENSG00000136492 BRIP1 1.02 2.53e-14 HNSC
ENSG00000136492 BRIP1 1.99 4.89e-18 BLCA
ENSG00000136492 BRIP1 2.19 1.45e-86 BRCA
ENSG00000136492 BRIP1 1.12 1.18e-19 COAD
ENSG00000136492 BRIP1 3.39 1.85e-176 LUSC
ENSG00000136492 BRIP1 3.22 9.79e-14 GBM
ENSG00000136492 BRIP1 1.88 1.83e-16 KIRP
ENSG00000136492 BRIP1 1.40 2.37e-17 LIHC
ENSG00000136492 BRIP1 1.60 3.83e-24 STAD
ENSG00000136492 BRIP1 2.27 6.92e-42 UCEC
ENSG00000136492 BRIP1 5.23 5.83e-41 CESC
ENSG00000136492 BRIP1 2.67 6.97e-78 LUAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000136492 BRIP1 breast cancer 16430786
ENSG00000136492 BRIP1 ovarian cancer 16493006
ENSG00000136492 BRIP1 HNSCC 17409780
ENSG00000136492 BRIP1 breast cancer 17420451
ENSG00000136492 BRIP1 tumor 17581638
ENSG00000136492 BRIP1 hereditary breast cancer 17596542
ENSG00000136492 BRIP1 breast cancer 17664283
ENSG00000136492 BRIP1 breast cancer 17768402
ENSG00000136492 BRIP1 breast cancer 18258506
ENSG00000136492 BRIP1 breast cancer 18302019
ENSG00000136492 BRIP1 breast cancer 18345034
ENSG00000136492 BRIP1 breast cancer 18414782
ENSG00000136492 BRIP1 breast cancer 18628483
ENSG00000136492 BRIP1 breast cancer 19099189
ENSG00000136492 BRIP1 prostate cancer 19127258
ENSG00000136492 BRIP1 breast cancer 19150983
ENSG00000136492 BRIP1 breast cancer 19419957
ENSG00000136492 BRIP1 tumor 19484476
ENSG00000136492 BRIP1 breast cancer 19519404
ENSG00000136492 BRIP1 breast cancer 19737859
ENSG00000136492 BRIP1 cancer 19861535
ENSG00000136492 BRIP1 breast cancer 20122882
ENSG00000136492 BRIP1 cancer 20173781
ENSG00000136492 BRIP1 hereditary breast cancer 20658644
ENSG00000136492 BRIP1 colon cancer 20978114
ENSG00000136492 BRIP1 Hereditary breast cancer 21345144
ENSG00000136492 BRIP1 breast cancer 21557222
ENSG00000136492 BRIP1 familial breast cancer 21605288
ENSG00000136492 BRIP1 ovarian cancer 21799032
ENSG00000136492 BRIP1 ovarian cancer 21964575
ENSG00000136492 BRIP1 breast cancer 22032289
ENSG00000136492 BRIP1 breast cancer 22287629
ENSG00000136492 BRIP1 colorectal cancer 22526901
ENSG00000136492 BRIP1 breast cancer 22582397
ENSG00000136492 BRIP1 cancer 22628295
ENSG00000136492 BRIP1 breast cancer 22629260
ENSG00000136492 BRIP1 cancer 22829014
ENSG00000136492 BRIP1 gastric cancer 22968820
ENSG00000136492 BRIP1 susceptibility to breast cancer 23021409
ENSG00000136492 BRIP1 ovarian cancer 23157317
ENSG00000136492 BRIP1 breast cancer 23161009
ENSG00000136492 BRIP1 breast cancer 23276657
ENSG00000136492 BRIP1 breast cancer 23435420
ENSG00000136492 BRIP1 breast cancer 23530059
ENSG00000136492 BRIP1 breast cancer 23935105
ENSG00000136492 BRIP1 ovarian cancer 24086532
ENSG00000136492 BRIP1 breast cancer 24137204
ENSG00000136492 BRIP1 tumor 24301948
ENSG00000136492 BRIP1 skin cancer 24351291
ENSG00000136492 BRIP1 ovarian cancer 24573678
ENSG00000136492 BRIP1 cancer 25193968
ENSG00000136492 BRIP1 cancer 25374583
ENSG00000136492 BRIP1 ovarian cancer 26254775
ENSG00000136492 BRIP1 cancer 26336824
ENSG00000136492 BRIP1 Breast Cancer 26490168
ENSG00000136492 BRIP1 breast cancer 27107905
ENSG00000136492 BRIP1 cancer 27376332
ENSG00000136492 BRIP1 ovarian cancer 27399284
ENSG00000136492 BRIP1 breast cancer 27729585
ENSG00000136492 BRIP1 colon cancer 28007957
ENSG00000136492 BRIP1 tumor 28911102
ENSG00000136492 BRIP1 ovarian cancers 29186203
ENSG00000136492 BRIP1 breast cancer 29669169
ENSG00000136492 BRIP1 ovarian cancer 29788478
ENSG00000136492 BRIP1 tumors 30107528
ENSG00000136492 BRIP1 hereditary breast and ovarian cancer 30232006
ENSG00000136492 BRIP1 Breast cancer 30800220
ENSG00000136492 BRIP1 cancer 30813363
ENSG00000136492 BRIP1 AML 30998136
ENSG00000136492 BRIP1 breast cancers 31064327
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000136492 BRIP1 Ovarian Endometrioid Adenocarcinoma missense_variant 37.5% (6/16) 1 entry
ENSG00000136492 BRIP1 breast ductal adenocarcinoma sequence_alteration 6.448% (102/1582) 3 entries
ENSG00000136492 BRIP1 pancreatic ductal adenocarcinoma missense_variant 3.983% (67/1682) 2 entries
ENSG00000136492 BRIP1 breast ductal adenocarcinoma stop_gained 6.448% (102/1582) 1 entry
ENSG00000136492 BRIP1 esophageal adenocarcinoma missense_variant 6.055% (33/545) 1 entry
ENSG00000136492 BRIP1 breast ductal adenocarcinoma missense_variant 6.448% (102/1582) 1 entry
ENSG00000136492 BRIP1 Ovarian Endometrioid Adenocarcinoma sequence_alteration 37.5% (6/16) 1 entry
ENSG00000136492 BRIP1 lung adenocarcinoma missense_variant 2.017% (52/2578) 5 entries
ENSG00000136492 BRIP1 Endometrial Endometrioid Adenocarcinoma missense_variant 3.87% (25/646) 1 entry
ENSG00000136492 BRIP1 colorectal adenocarcinoma stop_gained 2.556% (31/1213) 2 entries
ENSG00000136492 BRIP1 colon adenocarcinoma frameshift_variant 2.401% (31/1291) 2 entries
ENSG00000136492 BRIP1 small cell lung carcinoma missense_variant 1.121% (5/446) 1 entry
ENSG00000136492 BRIP1 squamous cell lung carcinoma missense_variant 1.005% (10/995) 2 entries
ENSG00000136492 BRIP1 skin melanoma missense_variant 3.02% (35/1159) 5 entries
ENSG00000136492 BRIP1 Uterine Carcinosarcoma missense_variant 8.108% (12/148) 1 entry
ENSG00000136492 BRIP1 urothelial carcinoma missense_variant 2.326% (2/86) 1 entry
ENSG00000136492 BRIP1 lung adenocarcinoma frameshift_variant 2.017% (52/2578) 2 entries
ENSG00000136492 BRIP1 central nervous system primitive neuroectodermal neoplasm sequence_alteration 1.786% (8/448) 1 entry
ENSG00000136492 BRIP1 colorectal adenocarcinoma frameshift_variant 2.556% (31/1213) 2 entries
ENSG00000136492 BRIP1 esophageal squamous cell carcinoma missense_variant 1.308% (9/688) 5 entries
ENSG00000136492 BRIP1 pancreatic neuroendocrine tumor missense_variant 5.085% (12/236) 1 entry
ENSG00000136492 BRIP1 bile duct adenocarcinoma frameshift_variant 0.5195% (2/385) 2 entries
ENSG00000136492 BRIP1 anaplastic oligodendroglioma missense_variant 2.353% (2/85) 1 entry
ENSG00000136492 BRIP1 hepatocellular carcinoma missense_variant 1.32% (13/985) 1 entry
ENSG00000136492 BRIP1 breast carcinoma sequence_alteration 1.085% (16/1474) 1 entry
ENSG00000136492 BRIP1 gastric adenocarcinoma missense_variant 0.8345% (6/719) 1 entry
ENSG00000136492 BRIP1 bladder transitional cell carcinoma missense_variant 1.794% (8/446) 2 entries
ENSG00000136492 BRIP1 Breast Carcinoma by Gene Expression Profile missense_variant 12.24% (6/49) 2 entries
ENSG00000136492 BRIP1 renal carcinoma missense_variant 10.0% (2/20) 2 entries
ENSG00000136492 BRIP1 melanoma missense_variant 3.448% (5/145) 3 entries
ENSG00000136492 BRIP1 colorectal adenocarcinoma sequence_alteration 2.556% (31/1213) 1 entry
ENSG00000136492 BRIP1 ovarian serous adenocarcinoma stop_gained 2.162% (19/879) 1 entry
ENSG00000136492 BRIP1 prostate adenocarcinoma sequence_alteration 2.932% (63/2149) 1 entry
ENSG00000136492 BRIP1 cecum adenocarcinoma frameshift_variant 3.717% (10/269) 1 entry
ENSG00000136492 BRIP1 brain glioblastoma missense_variant 0.495% (6/1212) 2 entries
ENSG00000136492 BRIP1 skin melanoma sequence_alteration 3.02% (35/1159) 1 entry
ENSG00000136492 BRIP1 Breast Carcinoma by Gene Expression Profile sequence_alteration 12.24% (6/49) 1 entry
ENSG00000136492 BRIP1 head and neck squamous cell carcinoma missense_variant 0.8011% (6/749) 1 entry
ENSG00000136492 BRIP1 pancreatic ductal adenocarcinoma frameshift_variant 3.983% (67/1682) 1 entry
ENSG00000136492 BRIP1 colon adenocarcinoma missense_variant 2.401% (31/1291) 8 entries
ENSG00000136492 BRIP1 bladder carcinoma missense_variant 3.02% (17/563) 1 entry
ENSG00000136492 BRIP1 basal cell carcinoma missense_variant 4.412% (3/68) 1 entry
ENSG00000136492 BRIP1 head and neck squamous cell carcinoma sequence_alteration 0.8011% (6/749) 1 entry
ENSG00000136492 BRIP1 prostate adenocarcinoma missense_variant 2.932% (63/2149) 2 entries
ENSG00000136492 BRIP1 melanoma frameshift_variant 3.448% (5/145) 1 entry
ENSG00000136492 BRIP1 skin melanoma stop_gained 3.02% (35/1159) 1 entry
ENSG00000136492 BRIP1 small cell lung carcinoma sequence_alteration 1.121% (5/446) 2 entries
ENSG00000136492 BRIP1 prostate carcinoma sequence_alteration 1.86% (9/484) 2 entries
ENSG00000136492 BRIP1 ovarian serous adenocarcinoma sequence_alteration 2.162% (19/879) 2 entries
ENSG00000136492 BRIP1 breast ductal adenocarcinoma frameshift_variant 6.448% (102/1582) 1 entry
ENSG00000136492 BRIP1 lung adenocarcinoma stop_gained 2.017% (52/2578) 3 entries
ENSG00000136492 BRIP1 cecum adenocarcinoma missense_variant 3.717% (10/269) 3 entries
ENSG00000136492 BRIP1 breast carcinoma missense_variant 1.085% (16/1474) 1 entry
ENSG00000136492 BRIP1 colon adenocarcinoma sequence_alteration 2.401% (31/1291) 2 entries
ENSG00000136492 BRIP1 rectal adenocarcinoma missense_variant 0.7326% (4/546) 1 entry
ENSG00000136492 BRIP1 ovarian serous adenocarcinoma missense_variant 2.162% (19/879) 2 entries
ENSG00000136492 BRIP1 papillary thyroid carcinoma missense_variant 0.409% (2/489) 1 entry
ENSG00000136492 BRIP1 cecum adenocarcinoma stop_gained 3.717% (10/269) 1 entry
ENSG00000136492 BRIP1 clear cell renal carcinoma missense_variant 0.379% (6/1583) 2 entries
ENSG00000136492 BRIP1 colorectal adenocarcinoma missense_variant 2.556% (31/1213) 2 entries
ENSG00000136492 BRIP1 bladder transitional cell carcinoma stop_gained 1.794% (8/446) 1 entry
ENSG00000136492 BRIP1 glioma missense_variant 0.1669% (1/599) 1 entry
ENSG00000136492 BRIP1 adenosquamous lung carcinoma missense_variant 4.545% (1/22) 1 entry
ENSG00000136492 BRIP1 primary peritoneal carcinoma (disease) missense_variant 100.0% (1/1) 1 entry
ENSG00000136492 BRIP1 gastric intestinal type adenocarcinoma missense_variant 2.353% (2/85) 1 entry
ENSG00000136492 BRIP1 diffuse large B-cell lymphoma conservative_inframe_deletion 0.5405% (2/370) 1 entry
ENSG00000136492 BRIP1 gastric adenocarcinoma stop_gained 0.8345% (6/719) 1 entry
ENSG00000136492 BRIP1 small intestinal adenocarcinoma missense_variant 4.762% (1/21) 1 entry
ENSG00000136492 BRIP1 brain glioblastoma sequence_alteration 0.495% (6/1212) 1 entry
ENSG00000136492 BRIP1 colorectal adenocarcinoma conservative_inframe_deletion 2.556% (31/1213) 1 entry
ENSG00000136492 BRIP1 bronchoalveolar adenocarcinoma stop_gained 9.091% (2/22) 1 entry
ENSG00000136492 BRIP1 laryngeal squamous cell carcinoma missense_variant 4.878% (2/41) 1 entry
ENSG00000136492 BRIP1 colon adenocarcinoma stop_gained 2.401% (31/1291) 1 entry
ENSG00000136492 BRIP1 angiosarcoma sequence_alteration 2.128% (1/47) 1 entry
ENSG00000136492 BRIP1 gastric intestinal type adenocarcinoma frameshift_variant 2.353% (2/85) 1 entry
ENSG00000136492 BRIP1 prostate carcinoma missense_variant 1.86% (9/484) 1 entry
ENSG00000136492 BRIP1 adrenocortical adenoma missense_variant 2.439% (1/41) 1 entry
ENSG00000136492 BRIP1 Anal Squamous Cell Carcinoma missense_variant 1.22% (1/82) 1 entry
ENSG00000136492 BRIP1 large cell lung carcinoma missense_variant 5.263% (1/19) 1 entry
ENSG00000136492 BRIP1 neoplasm missense_variant 3.571% (1/28) 1 entry
ENSG00000136492 BRIP1 Endometrial Endometrioid Adenocarcinoma frameshift_variant 3.87% (25/646) 1 entry
ENSG00000136492 BRIP1 nasopharyngeal squamous cell carcinoma missense_variant 0.5556% (1/180) 1 entry
ENSG00000136492 BRIP1 small cell lung carcinoma stop_gained 1.121% (5/446) 1 entry
ENSG00000136492 BRIP1 basal cell carcinoma sequence_alteration 4.412% (3/68) 1 entry
ENSG00000136492 BRIP1 Thyroid Gland Undifferentiated (Anaplastic) Carcinoma stop_gained 0.3788% (1/264) 1 entry
ENSG00000136492 BRIP1 Gallbladder Adenocarcinoma sequence_alteration 1.227% (2/163) 1 entry
ENSG00000136492 BRIP1 Gallbladder Adenocarcinoma missense_variant 1.227% (2/163) 1 entry
ENSG00000136492 BRIP1 Adrenal Gland Neuroblastoma missense_variant 1.667% (1/60) 1 entry
ENSG00000136492 BRIP1 non-small cell lung carcinoma missense_variant 0.9524% (1/105) 1 entry
ENSG00000136492 BRIP1 bronchoalveolar adenocarcinoma missense_variant 9.091% (2/22) 1 entry
ENSG00000136492 BRIP1 head and neck squamous cell carcinoma frameshift_variant 0.8011% (6/749) 1 entry
ENSG00000136492 BRIP1 Merkel cell skin cancer missense_variant 1.075% (1/93) 1 entry
ENSG00000136492 BRIP1 Extraskeletal Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor conservative_inframe_deletion 3.03% (1/33) 1 entry
ENSG00000136492 BRIP1 bladder transitional cell carcinoma frameshift_variant 1.794% (8/446) 1 entry
ENSG00000136492 BRIP1 hemangioblastoma missense_variant 2.857% (1/35) 1 entry
ENSG00000136492 BRIP1 clear cell renal carcinoma sequence_alteration 0.379% (6/1583) 1 entry
ENSG00000136492 BRIP1 Malignant Urinary System Neoplasm missense_variant 100.0% (1/1) 1 entry
ENSG00000136492 BRIP1 metaplastic breast carcinoma missense_variant 3.333% (2/60) 1 entry
ENSG00000136492 BRIP1 endometrial carcinoma stop_gained 4.167% (1/24) 1 entry
ENSG00000136492 BRIP1 laryngeal squamous cell carcinoma sequence_alteration 4.878% (2/41) 1 entry
ENSG00000136492 BRIP1 squamous cell lung carcinoma stop_gained 1.005% (10/995) 1 entry
ENSG00000136492 BRIP1 esophageal squamous cell carcinoma sequence_alteration 1.308% (9/688) 1 entry
ENSG00000136492 BRIP1 oral squamous cell carcinoma missense_variant 0.3817% (1/262) 1 entry
ENSG00000136492 BRIP1 brain astrocytoma missense_variant 2.083% (1/48) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000136492 BRIP1 SARC 0.018 low
ENSG00000136492 BRIP1 STAD 0.0033 low
ENSG00000136492 BRIP1 CHOL 0.022 high
ENSG00000136492 BRIP1 UVM 0.044 high
ENSG00000136492 BRIP1 PAAD 0.0018 high
ENSG00000136492 BRIP1 UCEC 0.00068 low
ENSG00000136492 BRIP1 THCA 0.019 low
ENSG00000136492 BRIP1 LUSC 0.039 low
ENSG00000136492 BRIP1 HNSC 0.00014 low
ENSG00000136492 BRIP1 READ 0.0032 low
ENSG00000136492 BRIP1 LUAD 0.00072 high
ENSG00000136492 BRIP1 PCPG 0.0012 high
ENSG00000136492 BRIP1 COAD 0.00094 low
ENSG00000136492 BRIP1 UCS 0.019 low
ENSG00000136492 BRIP1 DLBC 0.049 low
ENSG00000136492 BRIP1 KIRC 0.0011 high
ENSG00000136492 BRIP1 PRAD 0.0048 low
ENSG00000136492 BRIP1 BLCA 0.019 low
ENSG00000136492 BRIP1 SKCM 0.0032 low
ENSG00000136492 BRIP1 LIHC 0.0038 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000136492 BRIP1 LUAD Amp 1.053615 0.126748 0.390472 0.478682
ENSG00000136492 BRIP1 LGG Amp 1.826458 0.060525 0.558766 0.070175
ENSG00000136492 BRIP1 CESC Amp 1.000276 0.140491 0.549310 0.237288
ENSG00000136492 BRIP1 KIRP Amp 0.829705 0.057342 0.720131 0.690972
ENSG00000136492 BRIP1 COAD Amp 0.754246 0.068373 0.511951 0.226164
ENSG00000136492 BRIP1 SARC Amp 1.111421 0.284037 0.622792 0.303502
ENSG00000136492 BRIP1 PAAD Amp 0.847891 0.086697 0.484522 0.141304
ENSG00000136492 BRIP1 PAAD Del 3.563306 0.095320 0.372496 0.211957
ENSG00000136492 BRIP1 SKCM Amp 5.058794 0.244168 0.563064 0.332425
ENSG00000136492 BRIP1 LIHC Amp 4.474974 0.197416 0.641795 0.351351
ENSG00000136492 BRIP1 BLCA Amp 3.526813 0.253866 0.514627 0.470588
ENSG00000136492 BRIP1 BRCA Amp 52.632482 0.564502 0.862655 0.387963
ENSG00000136492 BRIP1 STAD Amp 1.058496 0.142576 0.445592 0.224490
ENSG00000136492 BRIP1 PRAD Amp 2.400791 0.069160 0.625603 0.050813
ENSG00000136492 BRIP1 UVM Amp 0.721460 0.165534 0.811066 0.162500