Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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55521 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Tripartite motif containing 36 |
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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TRIM36 |
SynonymsGene synonyms aliases
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ANPH, ANPH1, HAPRIN, RBCC728, RNF98 |
ChromosomeChromosome number
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5 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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5q22.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Multiple alternatively spliced transcript variants |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs773607884 |
G>T |
Pathogenic |
Coding sequence variant, non coding transcript variant, missense variant, genic downstream transcript 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 |
Q9NQ86 |
Protein name |
E3 ubiquitin-protein ligase TRIM36 (EC 2.3.2.27) (RING finger protein 98) (RING-type E3 ubiquitin transferase TRIM36) (Tripartite motif-containing protein 36) (Zinc-binding protein Rbcc728) |
Protein function |
E3 ubiquitin-protein ligase which mediates ubiquitination and subsequent proteasomal degradation of target proteins. Involved in chromosome segregation and cell cycle regulation (PubMed:28087737). May play a role in the acrosome reaction and fer |
PDB |
7QS4
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Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF13445 |
zf-RING_UBOX |
33 → 86 |
RING-type zinc-finger |
Domain |
PF00643 |
zf-B_box |
207 → 249 |
B-box zinc finger |
Domain |
PF18568 |
COS |
359 → 408 |
TRIM C-terminal subgroup One Signature domain |
Domain |
PF00041 |
fn3 |
426 → 500 |
Fibronectin type III domain |
Domain |
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Sequence |
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Sequence length |
728 |
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 |
Anencephaly |
Anencephaly |
rs773607884 |
28087737 |
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Aprosencephaly |
Aprosencephaly |
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Incomplete anencephaly, hemicrania |
incomplete anencephaly, hemicrania |
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Spina bifida |
Spina Bifida |
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