Genes?

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?All genes including those with curated and unreviewed disease associations.
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Chromosome:
Gene type:
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
190241 to 190250 of 193650 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

190241
-
-

Curated: N/A

Unreviewed: N/A

190242
-
-

Curated: N/A

Unreviewed: N/A

190243
-
-

Curated: N/A

Unreviewed: N/A

190244
TRNA selenocysteine 1 associated protein 1
PRO1902, SECP43, TRSPAP1

Curated: N/A

Unreviewed: N/A

190245
-
-

Curated: N/A

Unreviewed: N/A

190246
-
-

Curated: N/A

Unreviewed: N/A

190247
Mitochondrially encoded tRNA cysteine
MTTC

Curated: N/A

Unreviewed: Central Visual Impairment, Congestive Heart Failure, Dementia, Diabetes Mellitus, Epileptic encephalopathy, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Left Ventricular Hypertrophy, MELAS Syndrome, Migraine, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Seizure, Sensorineural hearing loss, Wolff-Parkinson-White Syndrome

190248
-
-

Curated: N/A

Unreviewed: Central Visual Impairment, Congestive Heart Failure, Dementia, Diabetes Mellitus, Epileptic encephalopathy, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Left Ventricular Hypertrophy, MELAS Syndrome, Migraine, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Seizure, Sensorineural hearing loss, Wolff-Parkinson-White Syndrome

190249
-
-

Curated: N/A

Unreviewed: Central Visual Impairment, Congestive Heart Failure, Dementia, Diabetes Mellitus, Epileptic encephalopathy, Hemianopsia, Hereditary Leber Optic Atrophy, Hypertension, Hypertrophic cardiomyopathy, Left Ventricular Hypertrophy, MELAS Syndrome, Migraine, Mitochondrial myopathy, Myoclonic epilepsy with ragged red fibers, Myopathy, Seizure, Sensorineural hearing loss, Wolff-Parkinson-White Syndrome

190250
-
-

Curated: N/A

Unreviewed: N/A