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
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA
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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Coronary artery disease Coronary artery disease N/A N/A GWAS