SNORD116-1 (small nucleolar RNA, C/D box 116-1)

2014-11-01  

Identity

HGNC
SNORD116-1
LOCATION
15q11.2
LOCUSID
100033413
ALIAS
HBII-85-1,PWCR1

Other Information

Locus ID:

NCBI: 100033413
MIM: 605436
HGNC: 33067
Ensembl: ENSG00000207063

Variants:

dbSNP: 100033413
ClinVar: 100033413
TCGA: ENSG00000207063
COSMIC: SNORD116-1

RNA/Proteins

Expression (GTEx)

0
1
Adipose - Subcutaneous
Adipose - Visceral
Adrenal Gland
Artery - Aorta
Artery - Tibial
Bladder
Brain - Amygdala
Brain - Anterior cingulate cortex
Brain - Caudate
Brain - Cerebellar Hemisphere
Brain - Cerebellum
Brain - Cortex
Brain - Frontal Cortex
Brain - Hippocampus
Brain - Hypothalamus
Brain - Nucleus accumbens
Brain - Putamen
Brain - Spinal cord
Brain - Substantia nigra
Breast - Mammary Tissue
Cells - Cultured fibroblasts
Cells - EBV - transformed lymphocytes
Cervix - Ectocervix
Cervix - Endocervix
Colon - Sigmoid
Colon - Transverse
Esophagus - Gastroesophageal Junction
Esophagus - Mucosa
Esophagus - Muscularis
Fallopian Tube
Heart - Atrial Appendage
Heart - Left Ventricle
Kidney - Cortex
Kidney - Medulla
Liver
Lung
Minor Salivary Gland
Muscle - Skeletal
Nerve - Tibial
Ovary
Pancreas
Pituitary
Prostate
Skin - Not Sun Exposed
Skin - Sun Exposed
Small Intestine - Terminal Ileum
Spleen
Stomach
Testis
Thyroid
Uterus
Vagina
Whole Blood

References

Pubmed IDYearTitleCitations
330825082021What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?14
340401952021SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.8
330825082021What can we learn from PWS and SNORD116 genes about the pathophysiology of addictive disorders?14
340401952021SNORD116 and growth hormone therapy impact IGFBP7 in Prader-Willi syndrome.8
324268212020Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndrome.7
324268212020Loss of Snord116 alters cortical neuronal activity in mice: a preclinical investigation of Prader-Willi syndrome.7
282660142017SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly.16
282660142017SNORD116 deletions cause Prader-Willi syndrome with a mild phenotype and macrocephaly.16
264461162016Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.30
276597132016Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.16
264461162016Deletion of the Snord116/SNORD116 Alters Sleep in Mice and Patients with Prader-Willi Syndrome.30
276597132016Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.16

Citation

Dessen P

SNORD116-1 (small nucleolar RNA, C/D box 116-1)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/73863