Gene id |
51127 |
Gene Summary Protein Summary Gene ontology Diseases PubMed |
Gene Summary
|
Gene Symbol |
TRIM17 Gene UCSC Ensembl |
Aliases |
RBCC, RNF16, terf |
Gene name |
tripartite motif containing 17 |
Alternate names |
E3 ubiquitin-protein ligase TRIM17, RING finger protein terf, RING-type E3 ubiquitin transferase TRIM17, ring finger protein 16, testis RING finger protein, tripartite motif-containing protein 17, |
Gene location |
1q42.13 (228416881: 228406876) Exons: 7 NC_000001.11
|
Gene summary(Entrez) |
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. The protein localizes to cytoplasmic bodies. The p
|
OMIM |
606123 |
Protein Summary
|
Protein general information
| Q9Y577
Name: E3 ubiquitin protein ligase TRIM17 (EC 2.3.2.27) (RING finger protein 16) (RING type E3 ubiquitin transferase TRIM17) (Testis RING finger protein) (Tripartite motif containing protein 17)
Length: 477 Mass: 54418
Tissue specificity: Almost exclusively in the testis. {ECO
|
Sequence |
MEAVELARKLQEEATCSICLDYFTDPVMTTCGHNFCRACIQLSWEKARGKKGRRKRKGSFPCPECREMSPQRNLL PNRLLTKVAEMAQQHPGLQKQDLCQEHHEPLKLFCQKDQSPICVVCRESREHRLHRVLPAEEAVQGYKLKLEEDM EYLREQITRTGNLQAREEQSLAEWQGKVKERRERIVLEFEKMNLYLVEEEQRLLQALETEEEETASRLRESVACL DRQGHSLELLLLQLEERSTQGPLQMLQDMKEPLSRKNNVSVQCPEVAPPTRPRTVCRVPGQIEVLRGFLEDVVPD ATSAYPYLLLYESRQRRYLGSSPEGSGFCSKDRFVAYPCAVGQTAFSSGRHYWEVGMNITGDALWALGVCRDNVS RKDRVPKCPENGFWVVQLSKGTKYLSTFSALTPVMLMEPPSHMGIFLDFEAGEVSFYSVSDGSHLHTYSQATFPG PLQPFFCLGAPKSGQMVISTVTMWVKG
|
Structural information |
|
Other Databases |
GeneCards: TRIM17  Malacards: TRIM17 |
|
GO accession | Term name | Evidence code | Go category |
---|
GO:0061630 |
ubiquitin protein ligase activity
|
IBA |
molecular function |
GO:0045087 |
innate immune response
|
IBA |
biological process |
GO:0005829 |
cytosol
|
IBA |
cellular component |
GO:0005654 |
nucleoplasm
|
IBA |
cellular component |
GO:0016567 |
protein ubiquitination
|
IBA |
biological process |
GO:0010468 |
regulation of gene expres sion
|
IBA |
biological process |
GO:0005737 |
cytoplasm
|
IBA |
cellular component |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0004842 |
ubiquitin-protein transfe rase activity
|
IEA |
molecular function |
GO:0008270 |
zinc ion binding
|
IEA |
molecular function |
GO:0006914 |
autophagy
|
IEA |
biological process |
GO:0016567 |
protein ubiquitination
|
IEA |
biological process |
GO:0046872 |
metal ion binding
|
IEA |
molecular function |
GO:0016740 |
transferase activity
|
IEA |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0016567 |
protein ubiquitination
|
IEA |
biological process |
GO:0004842 |
ubiquitin-protein transfe rase activity
|
IDA |
molecular function |
GO:0051865 |
protein autoubiquitinatio n
|
IDA |
biological process |
GO:0006914 |
autophagy
|
IDA |
biological process |
GO:0005575 |
cellular_component
|
ND |
cellular component |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0032880 |
regulation of protein loc alization
|
IMP |
biological process |
GO:0005515 |
protein binding
|
IPI |
molecular function |
GO:0030674 |
protein-macromolecule ada ptor activity
|
IPI |
molecular function |
GO:0005515 |
protein binding
|
IPI |
molecular function |
|
|
Associated diseases |
References |
Aberrant CpGs in Low Motility Sperm | MIK: 21674046 |
Hypospadias | MIK: 31219235 |
Spermatogenic defects | MIK: 31037746 |
|
|
PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
31219235 |
Hypospadia s
|
c.C109T(p.R37X) |
Chinese
|
133 cases
|
Male infertility |
NGS
|
Show abstract |
21674046 |
Aberrant C pGs in Low Motility Sperm
|
|
|
18
|
Male infertility |
GSE26881
|
Show abstract |
31037746 |
Spermatoge nic defect s
|
|
|
16 (1 control, 15 cases)
|
Male infertility |
GSE6023 analyzed using GEO2R
|
Show abstract |
|