Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
56980
Gene name Gene Name - the full gene name approved by the HGNC.
PR/SET domain 10
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PRDM10
Synonyms (NCBI Gene) Gene synonyms aliases
BHD2, PFM7, TRIS
Disease Acronyms (UniProt) Disease acronyms from UniProt database
BHD2
Chromosome Chromosome number
11
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q24.3
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a transcription factor that contains C2H2-type zinc-fingers. It also contains a positive regulatory domain, which has been found in several other zinc-finger transcription factors including those involved in B cell diff
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT619472 hsa-miR-6826-5p HITS-CLIP 19536157
MIRT619471 hsa-miR-7110-3p HITS-CLIP 19536157
MIRT619470 hsa-miR-6817-3p HITS-CLIP 19536157
MIRT619469 hsa-miR-6873-3p HITS-CLIP 19536157
MIRT713839 hsa-miR-4768-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IDA 31143550
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 25416956
GO:0005634 Component Nucleus IBA 21873635
GO:0008168 Function Methyltransferase activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
618319 13995 ENSG00000170325
Protein
UniProt ID Q9NQV6
Protein name PR domain zinc finger protein 10 (PR domain-containing protein 10) (Tristanin)
Protein function Transcriptional activator, essential for early embryonic development and survival of embryonic stem cells (ESCs) (By similarity). Supports cell growth and survival during early development by transcriptionally activating the expression of the tr
PDB 3IHX
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12171 zf-C2H2_jaz 354 378 Zinc-finger double-stranded RNA-binding Family
PF16638 Tristanin_u2 380 510 Disordered
PF12874 zf-met 560 580 Domain
PF00096 zf-C2H2 644 666 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 672 695 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 772 795 Zinc finger, C2H2 type Domain
Sequence
MDSKDESSHVWPTSAEHEQNAAQVHFVPDTGTVAQIVYTDDQVRPPQQVVYTADGASYTS
VDGPEHTLVYIHPVEAAQTLFTDPGQVAYVQQDATAQQASLPVHNQVLPSIESVDGSDPL
ATLQTPLGRLEAKEEEDEDEDEDTEEDEEEDGEDTDLDDWEPDPPRPFDPHDLWCEECNN
AHASVCPKHGPLHPIPNRPVLTRARASLPLVLYIDRFLGGVFSKRRIPKRTQFGPVEGPL
VRGSELKDCYIHLKVSLDKGDRKERDLHEDLWFELSDETLCNWMMFVRPAQNHLEQNLVA
YQYGHHVYYTTIKNVEPKQELKVWYAASYAEFVNQKIHDISEEERKVLREQEKNWPCYEC
NRRFISSEQLQQHLNSHD
EKLDVFSRTRGRGRGRGKRRFGPGRRPGRPPKFIRLEITSEN
GEKSDDGTQDLLHFPTKEQFDEAEPATLNGLDQPEQTTIPIPQLPQETQSSLEHEPETHT
LHLQPQHEESVVPTQSTLTADDMRRAKRIR
LELQNAALQHLFIRKSFRPFKCLQCGKAFR
EKDKLDQHLRFHGREGNCPLTCDLCNKGFISSTSLESHMKLHSDQKTYSCIFCPESFDRL
DLLKDHVAIHINDGYFTCPTCKKRFPDFIQVKKHVRSFHSEKIYQCTECDKAFCRPDKLR
LHMLRH
SDRKDFLCSTCGKQFKRKDKLREHMQRMHNPEREAKKADRISRSKTFKPRITST
DYDSFTFKCRLCMMGFRRRGMLVNHLSKRHPDMKIEEVPELTLPIIKPNRDYFCQYCDKV
YKSASKRKAHILKNH
PGAELPPSIRKLRPAGPGEPDPMLSTHTQLTGTIATPPVCCPHCS
KQYSSKTKMVQHIRKKHPEFAQLSNTIHTPLTTAVISATPAVLTTDSATGETVVTTDLLT
QAMTELSQTLTTDYRTPQGDYQRIQYIPVSQSASGLQQPQHIQLQVVQVASATSPHQSQQ
STVDVGQLHDPQPYPQHAIQVQHIQVSGQPLSPSAQQAQQGLSPSHIQGSSSTQGQALQQ
QQQQQQNSSVQHTYLPSAWNSFRGYSSEIQMMTLPPGQFVITDSGVATPVTTGQVKAVTS
GHYVLSESQSELEEKQTSALSGGVQVEPPAHSDSLDPQTNSQQQTTQYIITTTTNGNGSS
EVHITKP
Sequence length 1147
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 30251476
Unknown
Disease term Disease name Evidence References Source
Birt-Hogg-Dube Syndrome Birt-Hogg-Dube syndrome 2 GenCC
Dementia Dementia GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Birt Hogg Dube Syndrome Associate 36440963, 37331486, 40028672
Carcinoma Associate 36734437
Carcinoma Hepatocellular Associate 29843214
Carcinoma Renal Cell Associate 36440963, 37331486
Coronary Artery Disease Associate 22951892
Craniocerebral Trauma Associate 34969957
Diabetes Mellitus Type 1 Associate 22951892
Dyslexia Associate 36514817
Esophageal Squamous Cell Carcinoma Associate 32662828
Extranodal Extension Associate 36440963