Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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90381 |
Gene nameGene Name - the full gene name approved by the HGNC.
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TOPBP1 interacting checkpoint and replication regulator |
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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TICRR |
SynonymsGene synonyms aliases
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C15orf42, SLD3, Treslin |
ChromosomeChromosome number
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15 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q26.1 |
SummarySummary of gene provided in NCBI Entrez Gene.
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Treslin is involved in the initiation of DNA replication (Kumagai et al., 2010 [PubMed 20116089]).[supplied by OMIM, Apr 2010] |
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
|
UniProt ID |
Q7Z2Z1 |
Protein name |
Treslin (TopBP1-interacting checkpoint and replication regulator) (TopBP1-interacting, replication-stimulating protein) |
Protein function |
Regulator of DNA replication and S/M and G2/M checkpoints. Regulates the triggering of DNA replication initiation via its interaction with TOPBP1 by participating in CDK2-mediated loading of CDC45L onto replication origins. Required for the tran |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF15292 |
Treslin_N |
208 → 1004 |
Treslin N-terminus |
Family |
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Sequence |
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Sequence length |
1910 |
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 |
Acrocallosal syndrome |
Acrocallosal Syndrome |
rs752248403, rs387907044, rs387907045, rs797044463, rs797044464, rs794727316, rs797045093, rs778139192, rs202229910, rs886041531, rs1555425036, rs774403667, rs1555424505, rs1555424684, rs1555423165, rs569323391, rs781752990, rs1567057019, rs1235928535 |
26092869, 19666503, 26648833, 21633164, 21552264 |
Agenesis of corpus callosum |
Agenesis of corpus callosum |
rs754914260, rs1057519053, rs1057519056, rs1057519054, rs1057519055, rs1057519057, rs1384496494, rs1599017933 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Arachnoid cyst |
Arachnoid Cysts |
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Colpocephaly |
Colpocephaly |
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Congenital malrotation of intestine |
Congenital malrotation of intestine |
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Hypoplasia of the optic nerve |
Hypoplasia of the optic nerve |
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Liver carcinoma |
Liver carcinoma |
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28284560 |
Polycystic ovary syndrome |
Polycystic Ovary Syndrome |
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Syndactyly of the toes |
Syndactyly of the toes |
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Uterine anomalies |
Uterine Anomalies |
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