Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
284346
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 575
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF575
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2160311 hsa-miR-140-3p CLIP-seq
MIRT2160312 hsa-miR-297 CLIP-seq
MIRT2160313 hsa-miR-3672 CLIP-seq
MIRT2160314 hsa-miR-3924 CLIP-seq
MIRT2160315 hsa-miR-567 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q86XF7
Protein name Zinc finger protein 575
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 63 85 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 91 113 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 119 141 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 147 170 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 177 199 Zinc finger, C2H2 type Domain
Sequence
MLERGAESAAGATDPSPTGKEPVTKEAPHQGPPQKPSQSAPGPTASAGSPPRPRRRPPPQ
RPHRCPDCDKAFSYPSKLATHRLAHGGARPHPCPDCPKAFSYPSKLAAHRLTHSGARPHP
CPHCPKSFGHRSKLAAHLWTH
APTRPYPCPDCPKSFCYPSKLAAHRHTHHATDARPYPCP
HCPKAFSFPSKLAAHRLCH
DPPTAPGSQATAWHRCSSCGQAFGQRRLLLLHQRSHHQVEH
KGERD
Sequence length 245
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Ethylmalonic encephalopathy Ethylmalonic encephalopathy rs28940289, rs119103249, rs387906987, rs267605525, rs863223954, rs745656120, rs863223955, rs935855792, rs756235299, rs1555762722, rs763799125, rs769259233, rs1284200516, rs1555765701, rs1555765689
View all (10 more)
14732903, 26917598, 19136963, 29526615, 18593870, 16183799
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Non Small Cell Lung Associate 24175795