Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
126208
Gene name Gene Name - the full gene name approved by the HGNC.
Zinc finger protein 787
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ZNF787
Synonyms (NCBI Gene) Gene synonyms aliases
TIP20
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.43
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1539911 hsa-miR-1181 CLIP-seq
MIRT1539912 hsa-miR-296-5p CLIP-seq
MIRT1539913 hsa-miR-3184 CLIP-seq
MIRT1539914 hsa-miR-431 CLIP-seq
MIRT1539915 hsa-miR-4749-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0005634 Component Nucleus IBA 21873635
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA 21873635
GO:0043565 Function Sequence-specific DNA binding IBA 21873635
GO:0046872 Function Metal ion binding IEA
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 Q6DD87
Protein name Zinc finger protein 787 (TTF-I-interacting peptide 20)
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00096 zf-C2H2 66 88 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 95 116 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 122 144 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 150 172 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 178 200 Zinc finger, C2H2 type Domain
PF13912 zf-C2H2_6 316 340 Domain
Sequence
MELREEAWSPGPLDSEDQQMASHENPVDILIMDDDDVPSWPPTKLSPPQSAPPAGPPPRP
RPPAPYICNECGKSFSHWSKLTRHQRTHTGERPNACADCGKTFSQSSHLVQHRRIHTGEK
PYACLECGKRFSWSSNLMQHQRIHTGEKPYTCPDCGRSFTQSKSLAKHRRSHSGLKPFVC
PRCGRGFSQPKSLARHLRLH
PELSGPGVAAKVLAASVRRAKGPEEAVAADGEIAIPVGDG
EGIIVVGAPGEGAAAAAAMAGAGAKAAGPRSRRAPAPKPYVCLECGKGFGHGAGLLAHQR
AQHGDGLGAAGGEEPAHICVECGEGFVQGAALRRHKKIHAVGAPSVCSSCGQSYYRAGGE
EEDDDDEAAGGRCPECRGGEGR
Sequence length 382
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Coronary artery disease Coronary artery disease GWAS