Gene Gene information from NCBI Gene database.
Entrez ID 441234
Gene name Zinc finger protein 716
Gene symbol ZNF716
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7p11.2
miRNA miRNA information provided by mirtarbase database.
603
miRTarBase ID miRNA Experiments Reference
MIRT706184 hsa-miR-1910-3p HITS-CLIP 22927820
MIRT706183 hsa-miR-6511a-5p HITS-CLIP 22927820
MIRT706182 hsa-miR-4257 HITS-CLIP 22927820
MIRT706181 hsa-miR-6840-3p HITS-CLIP 22927820
MIRT706180 hsa-miR-6719-3p HITS-CLIP 22927820
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:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0003677 Function DNA binding IEA
GO:0005634 Component Nucleus IEA
GO:0006355 Process Regulation of DNA-templated transcription 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.
A6NP11
Protein name Zinc finger protein 716
Protein function May be involved in transcriptional regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01352 KRAB 15 56 KRAB box Family
PF00096 zf-C2H2 213 235 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 241 263 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 296 318 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 324 346 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 352 374 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 380 402 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 408 430 Zinc finger, C2H2 type Domain
PF00096 zf-C2H2 436 458 Zinc finger, C2H2 type Domain
Sequence
MAKRPGPPGSREMGLLTFRDIAIEFSLAEWQCLDHAQQNLYRDVMLENYRNLVSLGIAVS
KPDLITCLEQNKEPQNIKRNEMVAKHPVTCSHFTQDLQSEQGIKDSLQKVILRRYGKCGQ
EDLQVKKCCKSVGECEVHKGGYNYVNQCLSATQNKTFQTHKCVKVFGKFSNSNRHKTRHT
GKKHFKCKNDGKSFCMLSRLNQHQIIHTREKSYKCEECGKSFNCSSTLTRHKRIHTGEKP
YRCEECGKAFSWSASLTKHKRIHTGEKPYTCEERGKVFSRSTLTNYKRIHTGEKPYTCEE
CGKAFSRSSTLTNHKRIH
TGERPYKCEECGKAFSLSSTLKKHKIVHTGEKLYTCEECGKA
FTFSSTLNTHKRIH
TGEKPYTCEECGKAFSLPSTFTYHKRTHTGEKPYKCEECGKAFNCS
STLKKHKIIH
TGEKLYKCKECGKAFTFSSTLNTHKRIHTGEKPYKCEECDQTFKWHSSLA
NHKNMHTGEKPYKYE
Sequence length 495
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Generic Transcription Pathway
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
AUTISM SPECTRUM DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations