Log In|Sign Up
ENMitochondrial Complex I Deficiency, Nuclear Type 21 (MC1DN21)
Alias:
Mc1dn21
Mitochondrial Complex 1 Deficiency, Nuclear Type 21
Nuclear Type Mitochondrial Complex I Deficiency 21
Favorite
Mitochondrial Complex I Deficiency, Nuclear Type 21, is also known as mc1dn21. An important gene associated with Mitochondrial Complex I Deficiency, Nuclear Type 21 is NUBPL (NUBP Iron-Sulfur Cluster Assembly Factor, Mitochondrial). Affiliated tissues include liver and cerebellum, and related phenotypes are spasticity and nystagmus
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
