TOP2B (DNA topoisomerase II beta)
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Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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7155 |
Gene nameGene Name - the full gene name approved by the HGNC.
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DNA topoisomerase II beta |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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TOP2B |
SynonymsGene synonyms aliases
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BILU, TOPIIB, top2beta |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3p24.2 |
SummarySummary of gene provided in NCBI Entrez Gene.
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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 |
SNPsSNP information provided by dbSNP.
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SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs886039770 |
G>A |
Likely-pathogenic |
Missense variant, non coding transcript variant, coding sequence variant |
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miRNAmiRNA information provided by mirtarbase database.
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Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
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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
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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 |
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Sequence |
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Sequence length |
1626 |
Interactions |
View interactions |
PathwaysPathway information has different metabolic/signaling pathways associated with genes. Each record is hyperlinked to a complete information page which also includes links to the KEGG/Reactome pathway database.
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Associated diseases
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Causal |
Disease name |
Disease term |
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, rs1452048149, rs370498156, rs756691187, rs1557863430, rs1557863440, rs1557863546, rs769581210, rs202098093, rs1276388879, rs778792467, rs760059077, rs373783340, rs1557867853, rs772572695, rs753214391, rs749270162, rs548226228, rs1557870645, rs1557874046, rs749548928, rs754532606, rs1557901347, rs1557902023, rs1557909572, rs574335012, rs1557909821, rs1372713010, rs561369202, rs1476293577, rs1557910728, rs1557911386, rs375045125, rs998675361, rs1557916296, rs1557935477, rs866632178, rs1561824498, rs1396313317, rs1564801388, rs1564801473, rs1564950387, rs1565527302, rs1569513495, rs1569305431, rs143944436, rs1563183492, rs1561846159, rs1565819425, rs1562957809, rs1585645641, rs1585016242, rs1595127294, rs1585667374, rs1585653028, rs1585653240, rs1592919048, rs1585645384, rs1789927813 |
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Chronic obstructive pulmonary disease |
Chronic Obstructive Airway Disease |
rs2227956, rs1008438, rs1043618, rs562047, rs1061581, rs2763979, rs6457452, rs13147758, rs1828591, rs13118928 |
30804561 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome |
B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome |
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Monocytic leukemia |
Leukemia, Monocytic, Chronic |
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16932348 |
Myeloid leukemia |
Myeloid Leukemia |
|
16932348 |
Prostatic neoplasms |
Prostatic Intraepithelial Neoplasias |
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20601956 |
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