951
|
|
|
ALG10 alpha-1,2-glucosyltransferase B |
ALG10, KCR1 |
Curated: Atypical femoral fracture, Long qt syndrome, Diabetes mellitus type 2
Unreviewed: Colorectal neoplasm, Developmental and epileptic encephalopathy, Long QT Syndrome, Torsades de Pointes, Ventricular Fibrillation
|
952
|
|
|
ALG11 alpha-1,2-mannosyltransferase |
CDG1P, GT8 |
Curated: Congenital disorder of glycosylation, Crohn disease, Hepatolenticular degeneration, Inflammatory bowel disease, Ulcerative colitis, ALG11-congenital disorder of glycosylation
Unreviewed: Cerebral Atrophy, Chordoma, Congenital Microcephaly, Developmental Delay, Epilepsy, Glycogen storage disease, Hypotonia, Inborn Errors Of Metabolism, Mental retardation, Microcephaly, Neuronal Heterotopia, Psychiatric disorders, Scoliosis, Social Communication Disorder, Strabismus
|
953
|
|
|
ALG12 alpha-1,6-mannosyltransferase |
CDG1G, ECM39, PP14673, hALG12 |
Curated: Congenital disorder of glycosylation, Desbuquois syndrome, Osteoarthritis, Schizophrenia, ALG12-congenital disorder of glycosylation
Unreviewed: Cerebral palsy, Congenital Clubfoot, Congenital Hypoplasia Of Radius, Cryptorchidism, Developmental Delay, Glycogen storage disease, Hearing Loss, Hypospadias, Impaired Cognition, Patent ductus arteriosus, Patent foramen ovale, Penis Agenesis, Retinal Detachment, Retinitis Pigmentosa, Rhizomelia, Short femur
|
954
|
|
|
ALG13 UDP-N-acetylglucosaminyltransferase subunit |
CDG1S, CXorf45, DEE36, EIEE36, GLT28D1, MDS031, TDRD13, YGL047W |
Curated: Congenital disorder of glycosylation, Developmental and epileptic encephalopathy, Epilepsy, Focal glomerulosclerosis, Intellectual developmental disorder, Intellectual developmental disorder, x-linked, Neurodevelopmental disorder, X-linked intellectual disability, Scoliosis, genetic developmental and epileptic encephalopathy
Unreviewed: Attention Deficit Hyperactivity Disorder, Autism, Brachycephaly, Brain atrophy, Brain disease, Cataract-microcornea syndrome, Cerebral Atrophy, Cerebral cortical atrophy, Developmental Delay, Developmental disability, Endocrine system disease, Epileptic encephalopathy, Facial paralysis, Glomerulosclerosis, Glycogen storage disease, Horizontal nystagmus, Hypersensitivity, Impaired Cognition, Infantile Spasms, Leiomyoma, Lung carcinoma, Macrocephaly, Meckel Diverticulum, Mental retardation, Mental Retardation, X-Linked, Microcephaly, Micrognathism, Movement disorder, Neurodevelopmental Disorders, Neurosensory Hearing impairment, Non-Syndromic Intellectual Disability, X-Linked, Nonobstructive azoospermia, Nystagmus, Obesity, Optic Atrophy, Osteopenia, Osteoporosis, Seizure, Syndactyly Of The Toes, Visual disorder, West Syndrome
|
955
|
|
|
ALG13 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
956
|
|
|
ALG14 UDP-N-acetylglucosaminyltransferase subunit |
CMS15, IDDEBF, MEPCA |
Curated: Bipolar disorder, Congenital disorder of glycosylation, Congenital myasthenic syndrome, Congenital myopathy, Intellectual developmental disorder seizures behavioral, Myasthenic syndrome, Scoliosis, Tourette syndrome
Unreviewed: Congenital Myasthenic Syndromes With Glycosylation Defect, Epilepsy, Facial paralysis, High palate, Mental retardation, Motor delay, Multiple system atrophy, Myasthenia Gravis, Myasthenic Syndrome, Myopathy, Neurodegenerative disorder, Ptosis
|
957
|
|
|
ALG14 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Myasthenic Syndrome
|
958
|
|
|
ALG1 like 10, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|
959
|
|
|
ALG1 like 11, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|
960
|
|
|
ALG1 like 12, pseudogene |
- |
Curated: N/A
Unreviewed: N/A
|