Gene Gene information from NCBI Gene database.
Entrez ID 158586
Gene name Zinc finger X-linked duplicated B
Gene symbol ZXDB
Synonyms (NCBI Gene)
ZNF905dJ83L6.1
Chromosome X
Chromosome location Xp11.21
Summary The ZXDB gene is one of a pair of duplicated zinc finger genes on chromosome Xp11.21 (Greig et al., 1993 [PubMed 8268913]); see also ZXDA (MIM 300235).[supplied by OMIM, Jul 2010]
miRNA miRNA information provided by mirtarbase database.
298
miRTarBase ID miRNA Experiments Reference
MIRT327634 hsa-miR-24-3p PAR-CLIP 20371350
MIRT462882 hsa-miR-124-3p PAR-CLIP 20371350
MIRT462881 hsa-miR-506-3p PAR-CLIP 20371350
MIRT462880 hsa-miR-5692a PAR-CLIP 20371350
MIRT327636 hsa-miR-651-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
10
GO ID Ontology Definition Evidence Reference
GO:0003712 Function Transcription coregulator activity IBA
GO:0003713 Function Transcription coactivator activity IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300236 13199 ENSG00000198455
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P98169
Protein name Zinc finger X-linked protein ZXDB
Protein function Cooperates with CIITA to promote transcription of MHC class I and MHC class II genes.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 271 295 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 304 328 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 334 358 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 364 386 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 484 508 Zinc finger, C2H2 type Domain
Tissue specificity TISSUE SPECIFICITY: May be expressed in brain, heart, kidney, liver, lung, muscle and placenta. {ECO:0000269|PubMed:8268913}.
Sequence
MEIPKLLPARGTLQGGGGGGIPAGGGRVHRGPDSPAGQVPTRRLLLLRGPQDGGPGRRRE
EASTASRGPGPSLLAPRTDQPSGGGGGGGDDFFLVLLDPVGGDVETAGSGQAAGPVLREE
AEEGPGLQGGESGANPAGPTALGPRCLSAVPTPAPISAPGPAAAFAGTVTIHNQDLLLRF
ENGVLTLATPPPHAWEPGAAPAQQPGCLIAPQAGFPHAAHPGDCPELPPDLLLAEPAEPA
PAPAPEEEAEGPAAALGPRGPLGSGPGVVLYLCPEAQCGQTFAKKHQLKVHLLTHSSSQG
QRPFKCPLGGCGWTFTTSYKLKRHLQSHDKLRPFGCPAEGCGKSFTTVYNLKAHMKGHEQ
ENSFKCEVCEESFPTQAKLSAHQRSHFEPERPYQCAFSGCKKTFITVSALFSHNRAHFRE
QELFSCSFPGCSKQYDKACRLKIHLRSHTGERPFLCDFDGCGWNFTSMSKLLRHKRKHDD
DRRFMCPVEGCGKSFTRAEHLKGHSITHLGTKPFVCPVAGCCARFSARSSLYIHSKKHLQ
DVDTWKSRCPISSCNKLFTSKHSMKTHMVKRHKVGQDLLAQLEAANSLTPSSELTSQRQN
DLSDAEIVSLFSDVPDSTSAALLDTALVNSGILTIDVASVSSTLAGHLPANNNNSVGQAV
DPPSLMATSDPPQSLDTSLFFGTAATGFQQSSLNMDEVSSVSVGPLGSLDSLAMKNSSPE
PQALTPSSKLTVDTDALTPSSTLCENSVSELLTPTKAEWNVHPDSDFFGQEGETQFGFPN
AAGNHGSQKETDLITVTGSSFLV
Sequence length 803
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations