Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
7155
|
Gene name
Gene Name - the full gene name approved by the HGNC.
|
DNA topoisomerase II beta |
Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
|
TOP2B |
Synonyms (NCBI Gene)
Gene synonyms aliases
|
BILU, TOPIIB, top2beta |
Disease Acronyms (UniProt)
Disease acronyms from UniProt database
|
BILU |
Chromosome
Chromosome number
|
3 |
Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
3p24.2 |
Summary
Summary of gene provided in NCBI Entrez Gene.
|
This gene encodes a DNA topoisomerase, an enzyme that controls and alters the topologic states of DNA during transcription. This nuclear enzyme is involved in processes such as chromosome condensation, chromatid separation, and the relief of torsional str |
UniProt ID |
Q02880
|
Protein name |
DNA topoisomerase 2-beta (EC 5.6.2.2) (DNA topoisomerase II, beta isozyme) |
Protein function |
Key decatenating enzyme that alters DNA topology by binding to two double-stranded DNA molecules, generating a double-stranded break in one of the strands, passing the intact strand through the broken strand, and religating the broken strand. Pl |
PDB |
3QX3
,
4G0U
,
4G0V
,
4G0W
,
4J3N
,
5GWI
,
5GWJ
,
5ZAD
,
5ZEN
,
5ZQF
,
5ZRF
,
7QFN
,
7QFO
,
7YQ8
,
7ZBG
,
8KE7
|
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF02518
|
HATPase_c |
97 → 246 |
Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase |
Domain |
PF00204
|
DNA_gyraseB |
287 → 451 |
DNA gyrase B |
Domain |
PF01751
|
Toprim |
477 → 592 |
Toprim domain |
Family |
PF16898
|
TOPRIM_C |
594 → 732 |
C-terminal associated domain of TOPRIM |
Family |
PF00521
|
DNA_topoisoIV |
734 → 1190 |
DNA gyrase/topoisomerase IV, subunit A |
Family |
PF08070
|
DTHCT |
1508 → 1610 |
DTHCT (NUC029) region |
Family |
|
Tissue specificity |
TISSUE SPECIFICITY: Expressed in the tonsil, spleen, lymph node, thymus, skin, pancreas, testis, colon, kidney, liver, brain and lung (PubMed:9155056). Also found in breast, colon and lung carcinomas, Hodgkin's disease, large-cell non-Hodgkin's lymphoma, |
Sequence |
|
Sequence length |
1626 |
Interactions |
View interactions
|
Causal |
Disease term |
Disease name |
dbSNP ID |
References |
Autism spectrum disorder |
Autism Spectrum Disorders |
rs724159978, rs75184679, rs119103221, rs9332964, rs121912562, rs1594344233, rs727504317, rs111033204, rs1801086, rs587784464, rs724159948, rs764659822, rs794727977, rs796052733, rs796052728, rs762292772, rs864321694, rs869312878, rs758432471, rs750896617, rs886039692, rs886039770, rs201037487, rs200483989, rs1057518198, rs1057517708, rs780267761, rs1555910143, rs1057519632, rs775225727, rs751037529, rs1064794848, rs1064795655, rs1131691548, rs1135401811, rs1553248081, rs1454466097, rs1554480537, rs1553578503, rs1553518509, rs774152851, rs1554481395, rs1554464807, rs1554401434, rs1561824498, rs1396313317, rs1564801388, rs1564801473, rs1564950387, rs1565527302, rs1569513495, rs1569305431, rs143944436, rs1563183492, rs1561846159, rs1565819425, rs1562957809, rs1585645641, rs1585016242, rs1595127294, rs1585667374, rs1585653028, rs1585653240, rs1592919048, rs1585645384, rs1789927813 View all (51 more) |
|
|
Unknown |
Disease term |
Disease name |
Evidence |
References |
Source |
Chronic obstructive pulmonary disease |
Chronic Obstructive Airway Disease |
|
30804561 |
ClinVar |
Neurodevelopmental Disorders |
neurodevelopmental disorder |
|
|
GenCC |
|
Associations from Text Mining |
Disease Name |
Relationship Type |
References |
Adenocarcinoma |
Stimulate
|
28355294 |
Adenomatous Polyposis Coli |
Associate
|
31663907 |
Astrocytoma |
Associate
|
36503484 |
Autism Spectrum Disorder |
Associate
|
31953910, 36450898 |
Autistic Disorder |
Associate
|
26612825 |
Carcinoma Hepatocellular |
Associate
|
15526362 |
Carcinoma Non Small Cell Lung |
Associate
|
28355294, 9765623 |
Carcinoma Ovarian Epithelial |
Associate
|
25846551 |
Carcinoma Renal Cell |
Associate
|
34784933 |
Cardiotoxicity |
Associate
|
26237429, 27142468, 31399497 |
Cell Transformation Viral |
Associate
|
27974636 |
Chromosome Xp11.3 Deletion Syndrome |
Associate
|
34784933 |
Colorectal Neoplasms |
Associate
|
25009397, 37453058 |
Developmental Disabilities |
Associate
|
31953910 |
Drug Related Side Effects and Adverse Reactions |
Associate
|
12105221, 26237429, 34576262 |
Inflammation |
Associate
|
32218491 |
Leukemia |
Associate
|
22894901, 38508753 |
Leukemia Biphenotypic Acute |
Associate
|
22615413 |
Leukemia Myeloid Acute |
Associate
|
10233413, 23696245, 32218491, 7904487 |
Leukemia Promyelocytic Acute |
Associate
|
18212063 |
Lung Neoplasms |
Associate
|
10879730, 8398710 |
Multiple Myeloma |
Associate
|
33375771 |
Neoplasms |
Associate
|
10879730, 15526362, 16807458, 18596031, 37406101, 7797575, 8664122, 9155056 |
Neuroblastoma |
Associate
|
20886683, 35831557 |
Neurodegenerative Diseases |
Associate
|
29695291 |
Ovarian Neoplasms |
Associate
|
10070864, 21542140 |
Pathological Conditions Anatomical |
Associate
|
26612825 |
Precursor T Cell Lymphoblastic Leukemia Lymphoma |
Associate
|
22627319 |
Prostatic Intraepithelial Neoplasia |
Associate
|
20601956 |
Prostatic Neoplasms |
Associate
|
20601956, 28055971 |
Schizophrenia |
Associate
|
26612825 |
Small Cell Lung Carcinoma |
Associate
|
8980384 |
Translocation Genetic |
Associate
|
22894901 |
|