Gene

ndnl2

ID
ZDB-GENE-031107-3
Name
necdin-like 2
Symbol
ndnl2 Nomenclature History
Previous Names
  • mage (1)
  • zgc:101850
Type
protein_coding_gene
Location
Chr: 23 Mapping Details/Browsers
Description
Human ortholog(s) of this gene implicated in Bartter disease type 5; Prader-Willi syndrome; and Schaaf-Yang syndrome. Orthologous to several human genes including MAGEF1 (MAGE family member F1) and NSMCE3 (NSE3 homolog, SMC5-SMC6 complex component).
Genome Resources
Note
None
Expression
All Expression Data
2 figures from 2 publications
Cross-Species Comparison
High Throughput Data
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 ndnl2 Human Ortholog
No data available
Associated With ndnl2 Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR002190 MAGE homology domain
Family IPR037445 Melanoma-associated antigen
Homologous_superfamily IPR041898 MAGE homology domain, winged helix WH1 motif
Homologous_superfamily IPR041899 MAGE homology domain, winged helix WH2 motif
Domain Details Per Protein
Protein Length MAGE homology domain MAGE homology domain, winged helix WH1 motif MAGE homology domain, winged helix WH2 motif Melanoma-associated antigen
UniProtKB:Q5PR97 260
UniProtKB:E9QE92 220
UniProtKB:Q7T3S8 71
UniProtKB:Q7T0K5 260
UniProtKB:F1Q5I8 120
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Ensembl Gene Tree
Citations