ND5 (-)

Gene

• Entrez ID: 6775066
• Gene name: -
• Gene symbol: ND5
• Synonyms (NCBI Gene): -
• Chromosome: MT
• Chromosome location: -

Other IDs

• MIM: N/A
• HGNC: N/A
• e!Ensembl: N/A

Interactions View interactions

Associated diseases

Evidence Score:

• ★☆☆☆☆  Gene-disease association found in Text Mining only
• ★★☆☆☆  Found in Text Mining and Unknown/Other Associations
• ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources
• ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
• ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)

Unknown / Other Associations
Phenotype Name	Clinical Significance	Source	Evidence Score
CARCINOMA, HEPATOCELLULAR	—	CTD	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CEREBELLAR ATAXIA	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CLEFT PALATE AND BILATERAL CLEFT LIP	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CONGENITAL CARDIOMYOPATHY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DEVELOPMENTAL DELAY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
HEARING IMPAIRMENT	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
LEBER OPTIC ATROPHY AND DYSTONIA	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
LEIGH DISEASE	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MELAS SYNDROME	—	CTD, Disgenet CTD, Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MERRF SYNDROME	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MITOCHONDRIAL COMPLEX V DEFICIENCY, MITOCHONDRIAL TYPE 1	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MITOCHONDRIAL COMPLEX V DEFICIENCY, NUCLEAR TYPE 5	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MITOCHONDRIAL DISEASES	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
NEUROPATHY, ATAXIA, AND RETINITIS PIGMENTOSA	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OPTIC ATROPHY, HEREDITARY, LEBER	—	CTD, Disgenet CTD, Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PARKINSON DISEASE 6, AUTOSOMAL RECESSIVE EARLY-ONSET	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
ROD-CONE DYSTROPHY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
ULNAR POLYDACTYLY OF FINGERS	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining
Disease Name	Relationship Type	References	Evidence Score
Acidosis	Associate	21518340	★☆☆☆☆ Found in Text Mining only
Alzheimer Disease	Associate	36127429, 37905609	★☆☆☆☆ Found in Text Mining only
Atherosclerosis	Associate	22997526	★☆☆☆☆ Found in Text Mining only
Breast Diseases	Associate	20552226	★☆☆☆☆ Found in Text Mining only
Breast Neoplasms	Associate	20552226, 25925750	★☆☆☆☆ Found in Text Mining only
Carcinoma Ovarian Epithelial	Associate	26162681	★☆☆☆☆ Found in Text Mining only
Cardiomyopathies	Associate	30587702	★☆☆☆☆ Found in Text Mining only
Cholangiocarcinoma	Associate	40489465	★☆☆☆☆ Found in Text Mining only
Coronary Artery Disease	Associate	35328073	★☆☆☆☆ Found in Text Mining only
COVID 19	Associate	35421970, 39549291	★☆☆☆☆ Found in Text Mining only
Creutzfeldt Jakob Disease Sporadic	Associate	24667788	★☆☆☆☆ Found in Text Mining only
Cytochrome c Oxidase Deficiency	Associate	39549291	★☆☆☆☆ Found in Text Mining only
Deafness	Associate	32221064	★☆☆☆☆ Found in Text Mining only
Developmental Disabilities	Associate	26014388	★☆☆☆☆ Found in Text Mining only
Diabetes Mellitus	Associate	22780954, 30595373	★☆☆☆☆ Found in Text Mining only
Diabetes Mellitus Type 2	Inhibit	28730835	★☆☆☆☆ Found in Text Mining only
Drug Related Side Effects and Adverse Reactions	Associate	26014388	★☆☆☆☆ Found in Text Mining only
Endometriosis	Associate	22815783	★☆☆☆☆ Found in Text Mining only
Glaucoma Open Angle	Associate	23940637	★☆☆☆☆ Found in Text Mining only
Glucose Intolerance	Associate	30587702	★☆☆☆☆ Found in Text Mining only
HAIR AN syndrome	Associate	32601317	★☆☆☆☆ Found in Text Mining only
Hearing Loss	Associate	32221064	★☆☆☆☆ Found in Text Mining only
Huntington Disease	Associate	38447791	★☆☆☆☆ Found in Text Mining only
Hypertension Pulmonary	Associate	30587702	★☆☆☆☆ Found in Text Mining only
Hypertrophy	Associate	30587702	★☆☆☆☆ Found in Text Mining only
Lactation Disorders	Associate	40429710	★☆☆☆☆ Found in Text Mining only
Leigh Disease	Associate	12624137, 23847141, 23918514, 27345786, 29506874, 34928236, 36675121, 40429710	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Liver Neoplasms	Associate	37507754	★☆☆☆☆ Found in Text Mining only
MELAS Syndrome	Associate	12624137, 17940288, 21518340, 31996177, 9299505	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial complex I deficiency	Associate	12624137, 15250827, 16738010	★☆☆☆☆ Found in Text Mining only
Mitochondrial Diseases	Inhibit	16738010	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial Diseases	Associate	16738010, 16816025, 17898419, 23847141, 26014388, 26206091, 27110715, 30587702, 30622675, 34928236, 39549291, 40429710, 40489465	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial Encephalomyopathies	Associate	17940288, 40429710	★☆☆☆☆ Found in Text Mining only
Mitochondrial Myopathies	Associate	30587702	★☆☆☆☆ Found in Text Mining only
Mouth Neoplasms	Associate	27055661	★☆☆☆☆ Found in Text Mining only
Multiple Sclerosis	Associate	34002094	★☆☆☆☆ Found in Text Mining only
Muscle Hypotonia	Associate	21518340	★☆☆☆☆ Found in Text Mining only
Muscular Diseases	Associate	16738010, 16816025, 26501342	★☆☆☆☆ Found in Text Mining only
Myelodysplastic Syndromes	Associate	36899395	★☆☆☆☆ Found in Text Mining only
Myopathy with Lactic Acidosis Hereditary	Associate	26014388	★☆☆☆☆ Found in Text Mining only
Neoplasms	Associate	2173714	★☆☆☆☆ Found in Text Mining only
Neurologic Manifestations	Associate	29506874	★☆☆☆☆ Found in Text Mining only
Noninsulin dependent diabetes mellitus with deafness	Associate	22780954	★☆☆☆☆ Found in Text Mining only
Nonsyndromic sensorineural hearing loss	Associate	32221064	★☆☆☆☆ Found in Text Mining only
Obesity	Inhibit	28730835	★☆☆☆☆ Found in Text Mining only
Optic Atrophy Hereditary Leber	Associate	12624137, 16738010, 16816025, 1732158, 40429710	★☆☆☆☆ Found in Text Mining only
Parkinson Disease	Associate	28842646	★☆☆☆☆ Found in Text Mining only
Pathological Conditions Anatomical	Associate	23940637	★☆☆☆☆ Found in Text Mining only
Polycystic Ovary Syndrome	Associate	37674615	★☆☆☆☆ Found in Text Mining only
Pulmonary edema of mountaineers	Associate	31358833	★☆☆☆☆ Found in Text Mining only
Schizophrenia	Associate	17898419	★☆☆☆☆ Found in Text Mining only
Stroke	Associate	40429710	★☆☆☆☆ Found in Text Mining only
VLCAD deficiency	Associate	29736106	★☆☆☆☆ Found in Text Mining only
Walker Warburg Syndrome	Associate	35328073	★☆☆☆☆ Found in Text Mining only