Gene

med27

ID

ZDB-GENE-040426-1601

Name

mediator complex subunit 27

Symbol

med27 Nomenclature History

Previous Names

crsp34
crsp8
trap37 (1)
zgc:66302 (1)

Type

protein_coding_gene

Location

Chr: 8 Mapping Details/Browsers

Description

Involved in retinal cone cell development. Predicted to localize to mediator complex. Orthologous to human MED27 (mediator complex subunit 27).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

2 figures from 2 publications

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

Thisse Expression Data

MGC:66302 (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 med27 Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
		Neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia	619286

Associated With med27 Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Family	IPR021627	Mediator complex, subunit Med27

Domain Details Per Protein

Protein	Length	Mediator complex, subunit Med27
UniProtKB:Q6PFL0 InterPro	311
UniProtKB:A0A8M9QDN3 InterPro	253
UniProtKB:B2GNU2 InterPro	311

Transcripts

Genome Browsers

Type	Name	Annotation Method	Has Havana Data	Length (nt)	Analysis
mRNA	med27-201 (1) Ensembl	Ensembl		1,242 nt	Select Tool
ncRNA	med27-002 (1) Ensembl	Ensembl		429 nt	Select Tool

Interactions and Pathways

No data available

Antibodies

No data available

Plasmids

No data available

Constructs

Marker Relationships

Sequences

Orthology

Comparative Orthology: Alliance
Gene Tree: Ensembl

Citations