Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10107
Gene name Gene Name - the full gene name approved by the HGNC.
Tripartite motif containing 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TRIM10
Synonyms (NCBI Gene) Gene synonyms aliases
HERF1, RFB30, RNF9
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.1
Summary Summary of gene provided in NCBI Entrez Gene.
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. This protein localizes to cytoplasmic bodies. Stud
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT643366 hsa-miR-4426 HITS-CLIP 23824327
MIRT643365 hsa-miR-4647 HITS-CLIP 23824327
MIRT643364 hsa-miR-4662b HITS-CLIP 23824327
MIRT643363 hsa-miR-454-5p HITS-CLIP 23824327
MIRT643362 hsa-miR-4778-3p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 25416956, 31515488
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005737 Component Cytoplasm ISS
GO:0008150 Process Biological_process ND
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605701 10072 ENSG00000204613
Protein
UniProt ID Q9UDY6
Protein name Tripartite motif-containing protein 10 (B30-RING finger protein) (RING finger protein 9)
Protein function E3 ligase that plays an essential role in the differentiation and survival of terminal erythroid cells. May directly bind to PTEN and promote its ubiquitination, resulting in its proteasomal degradation and activation of hypertrophic signaling (
PDB 7QS0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15227 zf-C3HC4_4 16 60 Domain
PF00643 zf-B_box 94 135 B-box zinc finger Domain
PF13765 PRY 312 360 SPRY-associated domain Family
PF00622 SPRY 364 481 SPRY domain Family
Sequence
MASAASVTSLADEVNCPICQGTLREPVTIDCGHNFCRACLTRYCEIPGPDLEESPTCPLC
KEPFRPGSFRPNWQLANVVENIERLQLVSTLGLGEEDVCQEHGEKIYFFCEDDEMQLCVV
CREAGEHATHTMRFL
EDAAAPYREQIHKCLKCLRKEREEIQEIQSRENKRMQVLLTQVST
KRQQVISEFAHLRKFLEEQQSILLAQLESQDGDILRQRDEFDLLVAGEICRFSALIEELE
EKNERPARELLTDIRSTLIRCETRKCRKPVAVSPELGQRIRDFPQQALPLQREMKMFLEK
LCFELDYEPAHISLDPQTSHPKLLLSEDHQRAQFSYKWQNSPDNPQRFDRATCVLAHTGI
TGGRHTWVVSIDLAHGGSCTVGVVSEDVQRKGELRLRPEEGVWAVRLAWGFVSALGSFPT
RLTLKEQPRQVRVSLDYEVGWVTFTNAVTREPIYTFTASFTRKVIPFFGLWGRGSSFSLS
S
Sequence length 481
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Interferon gamma signaling
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Dermatitis Dermatitis, Irritant rs61816761, rs150597413, rs138726443, rs201356558, rs149484917, rs372754256, rs747301529, rs567795279, rs745915174 27258892
Lung cancer Malignant neoplasm of lung rs121913530, rs121913529, rs878855122, rs1057519784, rs770315135 21725308
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 17804836, 19503088
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
28540026
Unknown
Disease term Disease name Evidence References Source
Psoriasis Psoriasis GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Diabetes Mellitus Type 1 Associate 19143812
Parkinson Disease Associate 28586827