ND4 (-)

Gene

• Entrez ID: 6775072
• Gene name: -
• Gene symbol: ND4
• 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
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
DEMENTIA	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DEVELOPMENTAL DELAY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
EPILEPSY	—	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
LEBER PLUS DISEASE	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MACULAR DEGENERATION	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MELAS SYNDROME	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MITOCHONDRIAL COMPLEX I DEFICIENCY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MITOCHONDRIAL COMPLEX V DEFICIENCY, MITOCHONDRIAL TYPE 1	—	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	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OPTIC ATROPHY, HEREDITARY, LEBER	—	CTD, Disgenet CTD, Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OPTIC NEURITIS	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
OPTIC NEUROPATHY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PARKINSON DISEASE	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
PERIPHERAL NEUROPATHY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
ROD-CONE DYSTROPHY	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SCHIZOPHRENIA	—	CTD, Disgenet CTD, Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
ULNAR POLYDACTYLY OF FINGERS	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
VENOUS THROMBOEMBOLISM	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining
Disease Name	Relationship Type	References	Evidence Score
Alzheimer Disease	Associate	30040709	★☆☆☆☆ Found in Text Mining only
Ataxia	Associate	31776719	★☆☆☆☆ Found in Text Mining only
Autistic Disorder	Associate	24002085, 33731054	★☆☆☆☆ Found in Text Mining only
Autoimmune Diseases	Associate	30949164	★☆☆☆☆ Found in Text Mining only
Blindness	Associate	26606867	★☆☆☆☆ Found in Text Mining only
Breast Neoplasms	Associate	35082309	★☆☆☆☆ Found in Text Mining only
Cardiomyopathy Dilated	Associate	33303703	★☆☆☆☆ Found in Text Mining only
Cholangiocarcinoma	Associate	40489465	★☆☆☆☆ Found in Text Mining only
Colitis Ulcerative	Associate	27716073	★☆☆☆☆ Found in Text Mining only
Coronary Artery Disease	Associate	35328073	★☆☆☆☆ Found in Text Mining only
Creutzfeldt Jakob Disease Sporadic	Associate	24667788	★☆☆☆☆ Found in Text Mining only
Deafness	Associate	17723226	★☆☆☆☆ Found in Text Mining only
Diabetes Mellitus Type 2	Associate	37371486	★☆☆☆☆ Found in Text Mining only
Dysarthria	Associate	31776719	★☆☆☆☆ Found in Text Mining only
Dystonia	Associate	31776719	★☆☆☆☆ Found in Text Mining only
Esophageal Neoplasms	Associate	16620376	★☆☆☆☆ Found in Text Mining only
Fatigue	Associate	30949164	★☆☆☆☆ Found in Text Mining only
Fatigue Syndrome Chronic	Inhibit	37569433	★☆☆☆☆ Found in Text Mining only
HAIR AN syndrome	Associate	32601317	★☆☆☆☆ Found in Text Mining only
Hearing Loss	Associate	17723226	★☆☆☆☆ Found in Text Mining only
Heart Diseases	Associate	30949164	★☆☆☆☆ Found in Text Mining only
Huntington Disease	Associate	38447791	★☆☆☆☆ Found in Text Mining only
Infertility Male	Associate	33895935	★☆☆☆☆ Found in Text Mining only
Inflammation	Associate	30730541	★☆☆☆☆ Found in Text Mining only
Macular Degeneration	Associate	25592585	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
MELAS Syndrome	Associate	30949164	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial complex I deficiency	Associate	33879611, 8644732, 9685604	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial Diseases	Associate	17518546, 29587845, 37371486	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Mitochondrial Myopathy with Diabetes	Associate	37371486	★☆☆☆☆ Found in Text Mining only
Mouth Neoplasms	Associate	27055661	★☆☆☆☆ Found in Text Mining only
Mucocutaneous Lymph Node Syndrome	Associate	35154107	★☆☆☆☆ Found in Text Mining only
Myelitis Transverse	Associate	31776719	★☆☆☆☆ Found in Text Mining only
Neoplasms	Associate	16620376	★☆☆☆☆ Found in Text Mining only
Neuroblastoma	Associate	35134187	★☆☆☆☆ Found in Text Mining only
Neurodegenerative Diseases	Associate	30040709	★☆☆☆☆ Found in Text Mining only
Nonsyndromic sensorineural hearing loss	Associate	23805034	★☆☆☆☆ Found in Text Mining only
Oligospermia	Associate	17069814	★☆☆☆☆ Found in Text Mining only
Optic Atrophy Hereditary Leber	Associate	10933019, 16137960, 17300996, 17320357, 17366829, 17518546, 18513491, 19167085, 1959619, 20454697, 20627642, 20837795, 22879922, 22893673, 23170061, 23805034, 26606867, 26892229, 27426279, 28392196, 30730541, 31234430, 31718067, 31776719, 31888524, 31939618, 32771908, 33451738, 33566264, 33720041, 33911213, 34310464, 34415265, 35035206, 35623556, 35820885, 36074687, 36350566, 36827238, 37071596, 7926004, 8344246, 8593537, 8644732, 9055542, 9685604	★☆☆☆☆ Found in Text Mining only
Optic Nerve Diseases	Associate	17366829, 20627642, 31776719, 35623556	★☆☆☆☆ Found in Text Mining only
Ovarian Neoplasms	Associate	24148579	★☆☆☆☆ Found in Text Mining only
Pemphigoid Bullous	Associate	31824475	★☆☆☆☆ Found in Text Mining only
Polyendocrinopathies Autoimmune	Associate	30949164	★☆☆☆☆ Found in Text Mining only
Ptosis Hereditary Congenital 2	Associate	31776719	★☆☆☆☆ Found in Text Mining only
Retinitis	Associate	24525545	★☆☆☆☆ Found in Text Mining only
Stomach Neoplasms	Associate	37482618	★☆☆☆☆ Found in Text Mining only
Syndrome	Associate	30949164	★☆☆☆☆ Found in Text Mining only
Thyroid Neoplasms	Associate	33035689, 35464760, 37047426	★☆☆☆☆ Found in Text Mining only
Toxoplasmosis	Associate	33731054	★☆☆☆☆ Found in Text Mining only
Vision Disorders	Associate	17300996, 17723226, 19167085, 20837795, 23805034, 33451738, 33911213, 35035206	★☆☆☆☆ Found in Text Mining only
Vision Disorders	Inhibit	33451738	★☆☆☆☆ Found in Text Mining only
VLCAD deficiency	Associate	29736106	★☆☆☆☆ Found in Text Mining only
Walker Warburg Syndrome	Associate	35328073	★☆☆☆☆ Found in Text Mining only