Gene
zgc:101715
- ID
- ZDB-GENE-040912-59
- Name
- zgc:101715
- Symbol
- zgc:101715 Nomenclature History
- Previous Names
-
- c19orf12b2 (1)
- Type
- protein_coding_gene
- Location
- Chr: 7 Mapping Details/Browsers
- Description
- Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 43 and neurodegeneration with brain iron accumulation 4. Orthologous to human C19orf12 (chromosome 19 open reading frame 12).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 4 figures from 2 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:101715 (1 image)
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hereditary spastic paraplegia 43 | Alliance | ?Spastic paraplegia 43, autosomal recessive | 615043 |
| neurodegeneration with brain iron accumulation 4 | Alliance | Neurodegeneration with brain iron accumulation 4 | 614298 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR033369 | Protein C19orf12 |
Domain Details Per Protein
| Protein | Length | Protein C19orf12 |
|---|---|---|
|
UniProtKB:Q66ID9
|
141 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
zgc:101715-201
(1)
|
Ensembl | 942 nt | ||
| mRNA |
zgc:101715-202
(1)
|
Ensembl | 1,113 nt | ||
| ncRNA |
zgc:101715-002
(1)
|
Ensembl | 775 nt |
Interactions and Pathways
No data available
Plasmids
No data available
- Comparative Orthology
- Alliance