Ensembl ID ENSG00000100105 Gene ID 23598 Accession 13071
Gene Symbol PATZ1 Alias ZSG;MAZR;PATZ;RIAZ;ZBTB19;ZNF278;dJ400N23 Full Name POZ/BTB and AT hook containing zinc finger 1
Position 22 : 31325804 - 31346346 Length 20543 bases Strand Minus strand
Status Confidence Main interacting RNAsN.A.RBP type Canonical_RBPs
Summary The protein encoded by this gene contains an A-T hook DNA binding motif which usually binds to other DNA binding structures to play an important role in chromatin modeling and transcription regulation. Its Poz domain is thought to function as a site for protein-protein interaction and is required for transcriptional repression, and the zinc-fingers comprise the DNA binding domain. Since the encoded protein has typical features of a transcription factor, it is postulated to be a repressor of gene expression. In small round cell sarcoma, this gene is fused to EWS by a small inversion of 22q, then the hybrid is thought to be translocated (t(1;22)(p36.1;q12). The rearrangement of chromosome 22 involves intron 8 of EWS and exon 1 of this gene creating a chimeric sequence containing the transactivation domain of EWS fused to zinc finger domain of this protein. This is a distinct example of an intra-chromosomal rearrangement of chromosome 22. Four alternatively spliced transcript variants are described for this gene. [provided by RefSeq, Jul 2008]

ENSG00000100105 Expression In 33 Tumors

Ensembl ID Gene symbol Log2 Foldchange Pvaue Cancer
ENSG00000100105 -0.4 4.46e-16 KIRC
ENSG00000100105 0.58 1.02e-21 BRCA
ENSG00000100105 0.73 1.42e-16 COAD
Ensembl ID Gene symbol Cancer types Pubmed ID
ENSG00000100105 tumor 10949935
ENSG00000100105 tumours 18241078
ENSG00000100105 colorectal cancer 18401526
ENSG00000100105 cancer 20026299
ENSG00000100105 germ cell tumours 21381029
ENSG00000100105 cancer 22493480
ENSG00000100105 cancer 22886576
ENSG00000100105 tumour 24336083
ENSG00000100105 tumor 25515777
ENSG00000100105 thyroid cancer 25595894
ENSG00000100105 HNSCC 26840086
ENSG00000100105 thyroid cancer 27125250
ENSG00000100105 lung cancer 27391343
ENSG00000100105 tumor 27494852
ENSG00000100105 cancer 28607444
ENSG00000100105 tumor 28938636
ENSG00000100105 colorectal cancer 29039562
ENSG00000100105 thyroid cancer 29137300
ENSG00000100105 cancer 29186807
ENSG00000100105 tumour 29431183
ENSG00000100105 tumor 29584698
ENSG00000100105 tumor 29679497
ENSG00000100105 neuroepithelial tumor 29872694
ENSG00000100105 Ovarian Cancer 29926841
ENSG00000100105 tumor 30379650
ENSG00000100105 tumor 30744101
ENSG00000100105 cancer 31060775
ENSG00000100105 tumor 31099194
ENSG00000100105 tumor 31232935
ENSG00000100105 Glial Tumors 31614588
ENSG00000100105 thyroid cancer 31614935
ENSG00000100105 lung cancer 31620250
Ensembl ID Gene symbol Disease/phenotype Mutation type Mutated / Total samples Literature
ENSG00000100105 colorectal adenocarcinoma sequence_alteration 2.463% (28/1137) 2 entries
ENSG00000100105 colorectal adenocarcinoma frameshift_variant 2.463% (28/1137) 1 entry
ENSG00000100105 colorectal adenocarcinoma missense_variant 2.463% (28/1137) 3 entries
ENSG00000100105 lung adenocarcinoma sequence_alteration 0.9016% (11/1220) 2 entries
ENSG00000100105 bladder transitional cell carcinoma sequence_alteration 1.46% (2/137) 2 entries
ENSG00000100105 colon adenocarcinoma missense_variant 1.543% (11/713) 2 entries
ENSG00000100105 colon adenocarcinoma sequence_alteration 1.543% (11/713) 3 entries
ENSG00000100105 pancreatic ductal adenocarcinoma sequence_alteration 0.7149% (9/1259) 1 entry
ENSG00000100105 pancreatic ductal adenocarcinoma missense_variant 0.7149% (9/1259) 1 entry
ENSG00000100105 head and neck squamous cell carcinoma missense_variant 1.118% (7/626) 1 entry
ENSG00000100105 oral squamous cell carcinoma sequence_alteration 1.932% (4/207) 1 entry
ENSG00000100105 bladder transitional cell carcinoma missense_variant 1.46% (2/137) 2 entries
ENSG00000100105 skin melanoma missense_variant 0.9307% (9/967) 2 entries
ENSG00000100105 cecum adenocarcinoma missense_variant 4.0% (5/125) 2 entries
ENSG00000100105 melanoma missense_variant 4.95% (5/101) 2 entries
ENSG00000100105 skin melanoma sequence_alteration 0.9307% (9/967) 2 entries
ENSG00000100105 oral squamous cell carcinoma missense_variant 1.932% (4/207) 3 entries
ENSG00000100105 lung adenocarcinoma missense_variant 0.9016% (11/1220) 5 entries
ENSG00000100105 HER2 Positive Breast Carcinoma sequence_alteration 1.899% (3/158) 1 entry
ENSG00000100105 cecum adenocarcinoma sequence_alteration 4.0% (5/125) 2 entries
ENSG00000100105 colon adenocarcinoma frameshift_variant 1.543% (11/713) 1 entry
ENSG00000100105 esophageal adenocarcinoma sequence_alteration 1.37% (6/438) 1 entry
ENSG00000100105 esophageal squamous cell carcinoma missense_variant 0.2963% (2/675) 1 entry
ENSG00000100105 rectal adenocarcinoma sequence_alteration 0.9091% (2/220) 1 entry
ENSG00000100105 parathyroid adenoma sequence_alteration 6.25% (1/16) 1 entry
ENSG00000100105 rectal adenocarcinoma missense_variant 0.9091% (2/220) 1 entry
ENSG00000100105 Ampulla of Vater Carcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000100105 breast ductal adenocarcinoma missense_variant 1.396% (8/573) 1 entry
ENSG00000100105 Brain Stem Glioblastoma sequence_alteration 1.786% (1/56) 1 entry
ENSG00000100105 brain glioblastoma missense_variant 0.108% (1/926) 1 entry
ENSG00000100105 malignant soft tissue neoplasm gene_fusion 100.0% (1/1) 1 entry
ENSG00000100105 T-cell acute lymphoblastic leukemia missense_variant 0.2632% (1/380) 1 entry
ENSG00000100105 rectal adenocarcinoma frameshift_variant 0.9091% (2/220) 1 entry
ENSG00000100105 acute lymphoblastic leukemia sequence_alteration 0.3115% (1/321) 1 entry
ENSG00000100105 small cell lung carcinoma sequence_alteration 0.3096% (1/323) 1 entry
ENSG00000100105 Sarcomatoid Mesothelioma missense_variant 100.0% (1/1) 1 entry
ENSG00000100105 cecum adenocarcinoma frameshift_variant 4.0% (5/125) 1 entry
ENSG00000100105 nasopharyngeal squamous cell carcinoma missense_variant 0.5988% (1/167) 1 entry
ENSG00000100105 multiple myeloma missense_variant 2.273% (1/44) 1 entry
ENSG00000100105 prostate carcinoma sequence_alteration 0.2066% (1/484) 1 entry
ENSG00000100105 Breast Carcinoma by Gene Expression Profile missense_variant 5.263% (1/19) 1 entry
ENSG00000100105 clear cell renal carcinoma sequence_alteration 0.2177% (3/1378) 1 entry
ENSG00000100105 chronic lymphocytic leukemia sequence_alteration 0.1126% (1/888) 1 entry
ENSG00000100105 non-small cell lung carcinoma missense_variant 1.613% (1/62) 1 entry
ENSG00000100105 Endometrial Clear Cell Adenocarcinoma sequence_alteration 8.333% (1/12) 1 entry
ENSG00000100105 gastric intestinal type adenocarcinoma missense_variant 1.176% (1/85) 1 entry
ENSG00000100105 acute lymphoblastic leukemia missense_variant 0.3115% (1/321) 1 entry
ENSG00000100105 female breast carcinoma missense_variant 0.2558% (1/391) 1 entry
ENSG00000100105 ovarian serous adenocarcinoma missense_variant 0.1486% (1/673) 1 entry
ENSG00000100105 melanoma sequence_alteration 4.95% (5/101) 1 entry
ENSG00000100105 small cell lung carcinoma missense_variant 0.3096% (1/323) 1 entry
ENSG00000100105 Ampulla of Vater Carcinoma sequence_alteration 1.176% (1/85) 1 entry
Ensembl ID Gene symbol Cancer P-value Which worse show
ENSG00000100105 MESO 0.035 low
ENSG00000100105 UVM 0.0027 low
ENSG00000100105 PAAD 0.0053 low
ENSG00000100105 UCEC 0.00058 low
ENSG00000100105 THCA 0.042 high
ENSG00000100105 LUSC 0.00059 low
ENSG00000100105 READ 0.023 low
ENSG00000100105 KIRP 0.00087 low
ENSG00000100105 KICH 8e-04 low
ENSG00000100105 THYM 0.021 low
ENSG00000100105 BRCA 0.0027 low
ENSG00000100105 ESCA 0.025 low
ENSG00000100105 KIRC 0.00054 low
ENSG00000100105 LIHC 0.026 high
Ensembl ID Gene symbol Cancer CNV type -log10(q-value) G-score average amplitude frequency
ENSG00000100105 BLCA Amp 1.786699 0.202972 0.593655 0.203431
ENSG00000100105 UCEC Amp 0.908641 0.108308 0.561604 0.107607