Gene

znf711

ID

ZDB-GENE-081107-49

Name

zinc finger protein 711

Symbol

znf711 Nomenclature History

Previous Names

sb:eu767
si:dkey-152p16.4
vitelline envelope protein
zvep (1)

Type

protein_coding_gene

Location

Chr: 14 Mapping Details/Browsers

Description

Predicted to have RNA polymerase II regulatory region sequence-specific DNA binding activity. Predicted to be involved in positive regulation of transcription, DNA-templated. Localizes to cytoplasm and vitelline envelope. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability. Is expressed in brain and ovary. Orthologous to human ZNF711 (zinc finger protein 711).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

5 figures from 2 publications

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Thisse Expression Data

eu767 (1 image)

Wild Type Expression Summary

Phenotype

All Phenotype Data: No data available
Cross-Species Comparison: Alliance

Phenotype Summary

Mutations

Mutants

Sequence Targeting Reagents

Human Disease

Associated With znf711 Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
non-syndromic X-linked intellectual disability 97	Alliance	Intellectual developmental disorder, X-linked 97	300803

Associated With znf711 Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Domain	IPR006794	Transcriptional activator, Zfx / Zfy domain
Domain	IPR013087	Zinc finger C2H2-type
Homologous_superfamily	IPR036236	Zinc finger C2H2 superfamily