Gene Gene information from NCBI Gene database.
Entrez ID 126208
Gene name Zinc finger protein 787
Gene symbol ZNF787
Synonyms (NCBI Gene)
TIP20
Chromosome 19
Chromosome location 19q13.43
miRNA miRNA information provided by mirtarbase database.
25
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
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 identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Oromandibular-limb hypogenesis spectrum Uncertain significance rs202243737 RCV000240210