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
- Comparative Information
-
- All Expression Data
- 2 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:101850 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
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:Q7T0K5
|
260 |
Interactions and Pathways
No data available
Plasmids
No data available