Detailed description page of humcfs

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ALPL details
Primary information
gene_nameALPL
Humcfs IdHumcfs_243
chromosome_numberchromosome1
nameFRA1A
chrlocation1-28000000
cytoband1p36
typeAphidicolin
frequencyCommon
gene_ensembl_idENSG00000162551
havana_transcript_idOTTHUMT00000008203
gene_location21551279-21578012
gene_orientation+
exon_idENSE00001464776, ENSE00001464850, ENSE00003585785, ENSE00003574693, ENSE00003569303, ENSE00001066206, ENSE00001066201, ENSE00001066195, ENSE00001066199, ENSE00003613168, ENSE00003735967, ENSE000014647
exon_number12
gene_descriptionalkaline phosphatase, liver/bone/kidney
disease_descriptionSeizures,Ankylosing spondylitis,Vitamin B 6 Deficiency,Adult hypophosphatasia (disorder),Meningioma,Infantile hypophosphatasia,Periodontal Diseases,Hyperostosis,Liver diseases,Osteoporosis, Postmenopausal,Alveolar Bone Loss,Disorder of skeletal system,Calcinosis,Osteochondrodysplasias,Uremia,Hyperparathyroidism, Secondary,Arthropathy,Metabolic Bone Disorder,Precursor Cell Lymphoblastic Leukemia Lymphoma,Osteosclerosis,Chromosome 1, monosomy 1p,Prostatic Neoplasms,Metabolic Diseases,Kidney Diseases,Alzheimer's Disease,Pathological fracture,ODONTOHYPOPHOSPHATASIA (disorder),Hypophosphatasia,Bone Diseases,Deformity of bone,Inborn Errors of Metabolism,Obesity,Osteoporosis, Age-Related,Hypertensive disease,Hypercholesterolemia,Epilepsy,HYPERPIGMENTATION, FAMILIAL PROGRESSIVE,Tobacco Use Disorder,Childhood hypophosphatasia (disorder),Osteoporosis,Inflammation
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueKaryotyping
PMID1322577
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