1581
|
|
|
SLC9A3 3' UTR overlapping transcript 1 |
PP7080 |
Curated: N/A
Unreviewed: N/A
|
1582
|
|
|
Solute carrier family 9 member 3 pseudogene 1 |
NHE3P, SLC9A3P, SLC9A3P4 |
Curated: N/A
Unreviewed: N/A
|
1583
|
|
|
Solute carrier family 9 member 3 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1584
|
|
|
Solute carrier family 9 member 3 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
|
1585
|
|
|
SLC9A3R1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1586
|
|
|
Solute carrier family 9 member A4 |
NHE4 |
Curated: Ankylosing spondylitis, Imperforate anus, Asthma, Eczema, Atypical femoral fracture, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Common variable immunodeficiency, Crohn disease, Aortic dissection, Inflammatory bowel disease, Juvenile idiopathic arthritis, Nasal polyp, Psoriasis, Respiratory system disease, Skin disease, Systemic lupus erythematosus, Diabetes mellitus type 1, Ulcerative colitis
Unreviewed: Diabetes mellitus, type 2, Graft-versus-host disease, Obesity, Obstructive azoospermia, Thrombosis
|
1587
|
|
|
Solute carrier family 9 member A5 |
NHE5 |
Curated: Kidney failure
Unreviewed: Congenital secretory diarrhea, Episodic Kinesigenic Dyskinesia, Glioma, Huntington Disease, Kidney Disease, Kidney Failure, Neoplasms, Neurodegenerative Disorders, Obstructive azoospermia, Thrombosis
|
1588
|
|
|
Solute carrier family 9 member A6 |
MRSA, MRXSCH, NDPACX, NHE6 |
Curated: Amblyopia, Astigmatism, Christianson syndrome, Global developmental delay, Hyperopia, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Leukodystrophy, Neurodegenerative disorder, x-linked, female-restricted, with parkinsonism and cognitive impairment, Neurodevelopmental disorder, Scoliosis, Strabismus
Unreviewed: N/A
|
1589
|
|
|
Solute carrier family 9 member A7 |
MRX108, NHE-7, NHE7, SLC9A6 |
Curated: Alzheimer disease, Intellectual developmental disorder, x-linked, X-linked intellectual disability
Unreviewed: Acne, Adenocarcinoma Of Colon, AL-Raqad Syndrome, Angelman Syndrome, Arthrogryposis multiplex congenita, Ataxia, Atrophy, Attention Deficit Hyperactivity Disorder, Autism, Baraitser-Winter Syndrome, Bowel incontinence, Brain disease, Breast Cancer, Breast Carcinoma, Camptodactyly of fingers, Cataract, Cerebellar atrophy, Cerebral cortical atrophy, Cerebral Infarction, Christianson Syndrome, Congenital Anomaly Of Nose, Congenital Pectus Excavatum, Congestive Heart Failure, Cystic Fibrosis, Cystinuria, Developmental Delay, Developmental disability, Developmental regression, Down Syndrome, Dysphagia, Dyssomnia, Endocarditis, Enteritis, Epilepsy, Epileptic encephalopathy, Esotropia, Exocrine pancreatic insufficiency, Facial paralysis, Gastroesophageal Reflux Disease, Head and neck neoplasm, Hyperkinesia, Hypoproteinemia, Intellectual developmental disorder, Kidney Disease, Kidney Failure, Language development disorders, Macrocephaly, Macrotia, Major depressive disorder, Malignant Neoplasm, Malocclusion, Meckel Diverticulum, Mental Depression, Mental retardation, Mental Retardation, X-Linked, Microcephaly, Movement disorder, Neoplasms, Nervous system disease, Nervous System Disorder, Neuroblastoma, Neuropathy, Neurosensory Hearing impairment, Non-Syndromic Intellectual Disability, X-Linked, Nystagmus, Obesity, Obstructive azoospermia, Osteomyelitis, Otitis Externa, Pharyngitis, Photosensitive tonic-clonic seizures, Pyruvate Dehydrogenase Complex Deficiency Disease, Retinitis, Scoliosis, Seizure, Seizures, Septicemia, Sinusitis, Skin Lesion, Sleep Disorders, Status Epilepticus, Stereotyped Behavior, Strabismus, Syndactyly Of The Toes, Thrombosis, Toxic Shock Syndrome, Trichohepatoenteric Syndrome
|
1590
|
|
|
Solute carrier family 9 member 7 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|