Detailed description page of humcfs

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INSL3 details
Primary information
gene_nameINSL3
Humcfs IdHumcfs_4720
chromosome_numberchromosome19
nameFRA19B
chrlocation1-20000000
cytoband19p13
typeFolic acid
frequencyRare
gene_ensembl_idENSG00000248099
havana_transcript_idOTTHUMT00000466837
gene_location17816513-17821505
gene_orientation-
exon_idENSE00002996093, ENSE00001320565
exon_number2
gene_descriptioninsulin-like 3 (Leydig cell)
disease_descriptionMalignant neoplasm of stomach,Congenital Abnormality,Prostatic Intraepithelial Neoplasias,Leydig cell hyperplasia,Thyroid carcinoma,Stomach Carcinoma,Congenital absence of germinal epithelium of testes,Prostate carcinoma,Pituitary Diseases,Cyst,Klinefelter Syndrome,Testicular dysgenesis syndrome,Oligospermia,Polycystic Ovary Syndrome,ovarian neoplasm,Bilateral Cryptorchidism,Hyperandrogenism,Adenoma,Small cell carcinoma of lung,Diabetes,Medullary carcinoma of thyroid,Hypogonadism,Hyperplasia,Carcinogenesis,Eclampsia,Breast Fibrocystic Disease,Secondary malignant neoplasm of lymph node,Cryptorchidism,Malignant neoplasm of testis,Thyroid Diseases,Diabetes Mellitus,Testicular malignant germ cell tumor,Unilateral Cryptorchidism,Adrenal Rest Tumor,Male infertility,Benign Prostatic Hyperplasia,Thyroid Neoplasm,Ductal Carcinoma,Klinefelter's syndrome - male with more than two X chromosomes,Leydig Cell Tumor,Leydig cell tumor, benign,Osteoporosis
miRNA_locationNA
miRNA_strandNA
miRNA_idNA
miRNA_nameNA
miRNA_derived NA
TechniqueFISH
PMID3568428
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