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21
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|
|
X inactive specific transcript |
DXS1089, DXS399E, LINC00001, NCRNA00001, SXI1, swd66 |
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22
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|
X-linked Kx blood group antigen, Kell and VPS13A binding protein |
KX, NA, NAC, X1k, XKR1 |
Abetalipoproteinemia, Anxiety disorder, Atrial fibrillation, Behavior disorders, Benign fasciculation-cramp syndrome, Cardiomyopathy, Chorea, Dysarthria, Dyskinetic syndrome, Hematological disease, Mcleod neuroacanthocytosis syndrome, Mental disorders, Mental depression, Mental retardation, Movement disorders, Myopathy, Nervous system diseases, Neuromuscular diseases, Obsessive-compulsive disorder, Oppenheim`s disease, Personality disorders, Seizure, Status marmoratusView all (8 more) |
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23
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XPA, DNA damage recognition and repair factor |
XP1, XPAC |
Actinic keratosis, Alopecia, Apraxia, Brain atrophy, Carcinoma, Cataract, Cerebral cortical atrophy, Choreoathetosis, Congenital ankyloblepharon, Conjunctival telangiectasis, Conjunctivitis, Convergence insufficiency, Cryptorchidism, Developmental regression, Dwarfism, Dysarthria, Ectropion, Entropion, Exotropia, Eye neoplasms, Hearing loss, Hyperkeratosis, Hypogonadism, Impaired cognition, Intestinal neoplasms, Intestinal cancer, Keratitis, Liver neoplasms, Liver cancer, Melanocytic nevus, Melanoma, Mental retardation, Microcephaly, Nervous system diseases, Nystagmus, Optic atrophy, Papilloma, Poikiloderma, Pterygium, Seborrheic dermatitis, Sensorimotor neuropathy, Skin cancer, Skin neoplasms, Strabismus, Supranuclear gaze palsy, Xeroderma pigmentosumView all (31 more) |
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24
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XPC complex subunit, DNA damage recognition and repair factor |
RAD4, XP3, XPCC, p125 |
Alopecia, Autism, Carcinoma, Cataract, Cerebral cortical atrophy, Congenital ankyloblepharon, Conjunctival telangiectasis, Conjunctivitis, Cryptorchidism, Developmental regression, Disorder of amino acid metabolism, Dwarfism, Ectropion, Entropion, Eye neoplasms, Hearing loss, Hyperkeratosis, Hypogonadism, Hypopigmentation disorder, Impaired cognition, Inherited errors of amino acid metabolism, Keratitis, Liver neoplasms, Liver cancer, Lung carcinoma, Lung neoplasms, Lung adenocarcinoma, Lung cancer, Melanocytic nevus, Melanoma, Microcephaly, Nervous system diseases, Optic atrophy, Papilloma, Poikiloderma, Pterygium, Skin carcinoma, Strabismus, Xeroderma pigmentosumView all (24 more) |
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25
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|
|
X-prolyl aminopeptidase 2 |
AEACEI, APP2 |
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26
|
|
|
Exportin 1 |
CRM-1, CRM1, emb, exp1 |
Atrial fibrillation, B-cell lymphoma, Mammary neoplasms, Colorectal neoplasms, Lymphocytic leukemia, Malignant uterine corpus neoplasm, Paroxysmal atrial fibrillation, Mediastinal b-cell lymphoma, Prostate adenocarcinoma, Prostatic neoplasms, Prostate cancer |
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27
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|
|
X-ray repair cross complementing 1 |
RCC, SCAR26 |
Cerebellar atrophy, Colorectal cancer, Dysarthria, Dysphagia, Esophagus neoplasm, Gastric cancer, Glioma, Lymphoblastic leukemia, Mesothelioma, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral mucositis, Prostatic neoplasms, Prostate cancer, Schizophrenia, Sensorimotor neuropathy, Spinocerebellar ataxia, Stomach neoplasms, StomatitisView all (5 more) |
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28
|
|
|
X-ray repair cross complementing 2 |
FANCU, POF17, SPGF50 |
Astigmatism, Atrial septal defect, Azoospermia, Breast cancer, Mammary neoplasms, Breast carcinoma, Cafe-au-lait spot, Camptodactyly of fingers, Hereditary cancer syndrome, Cataract, Choanal atresia, Congenital arteriovenous malformation, Congenital epicanthus, Congenital exomphalos, Cranial nerve paralysis, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Fanconi anemia, Frontal bossing, Hereditary breast cancer, High palate, Hirschsprung disease, Hydrocephalus, Hypertrophic cardiomyopathy, Hypogonadism, Hypospadias, Imperforate anus, Leukemia, Leukopenia, Male infertility, Marfan syndrome, Meckel diverticulum, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Miller dieker syndrome, Monocytic leukemia, Myelodysplasia, Myelodysplastic syndrome, Non-obstructive azoospermia, Nystagmus, Obstructive azoospermia, Ovarian neoplasm, Patent ductus arteriosus, Proptosis, Ptosis, Renal insufficiency, Scoliosis, Spina bifida, Strabismus, Syndactyly of fingers, Syndactyly of the toes, Tetralogy of fallotView all (41 more) |
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29
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|
|
X-ray repair cross complementing 3 |
CMM6 |
Breast cancer, Mammary neoplasms, Breast carcinoma, Carcinoma, Esophagus neoplasm, Gastric cancer, Head and neck neoplasms, Head neoplasms, Neck cancer, Neoplasm of head, Head and neck cancer, Marfan syndrome, Melanoma, Mesothelioma, Neck neoplasms, Skin cancer, Skin neoplasms, Stomach neoplasms, Upper aerodigestive tract neoplasmsView all (4 more) |
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30
|
|
|
X-ray repair cross complementing 4 |
SSMED, hXRCC4 |
Acanthosis nigricans, Anemia, Apraxia, Brachycephaly, Camptodactyly of fingers, Colorectal neoplasms, Colorectal cancer, Congenital blindness, Congenital epicanthus, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Dysarthria, Ectopic kidney, Fanconi anemia, Fatty liver, Hereditary nonpolyposis colorectal cancer, Hypertension, Hypothyroidism, Immunologic deficiency syndromes, Impaired cognition, Insulin-resistant diabetes mellitus, Leukemia, Lig4 syndrome, Lymphoma, Lymphopenia, Malabsorption syndrome, Mental retardation, Microcephalic primordial dwarfism-insulin resistance syndrome, Microcephaly, Micrognathism, Myeloproliferative disorder, Nystagmus, Pancytopenia, Penis agenesis, Pituitary dwarfism, Renal aplasia, Renal hypoplasia, Retinal detachment, Schizophrenia, Seckel syndrome, Sensory neuropathy, Severe combined immunodeficiency disease, Short stature, microcephaly, and endocrine dysfunction, Short-limb dwarfism, Speech delayView all (33 more) |
