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

Gene
Gene Gene ontology Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
100033413
Gene name Gene Name - the full gene name approved by the HGNC.
Small nucleolar RNA, C/D box 116-1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SNORD116-1
Synonyms (NCBI Gene) Gene synonyms aliases
HBII-85-1, PWCR1
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q11.2
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
Gene Gene ontology Other IDs Associated diseases
Show/Hide all(2)
GO ID Ontology Definition Evidence Reference
GO:0005730 Component Nucleolus IEA
GO:0006396 Process RNA processing IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Gene ontology Other IDs Associated diseases
MIM HGNC e!Ensembl
605436 33067 ENSG00000207063
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene Gene ontology Other IDs Associated diseases
Show/Hide Causal Diseases (9)
Causal
Disease term Disease name dbSNP ID References
Acromicric dysplasia Acromicric Dysplasia rs387906622, rs387906623, rs387906624, rs1131692052, rs387906626, rs587776863, rs1064797059, rs363806, rs1060501041, rs1555400049
Attention deficit hyperactivity disorder Attention deficit hyperactivity disorder rs786205019
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Developmental delay Global developmental delay rs28941770, rs199469464, rs281865469, rs143747297, rs398123009, rs587777428, rs786205133, rs606231459, rs797044854, rs797045027, rs864309504, rs878853160, rs886039902, rs886042046, rs886041291
View all (32 more)
Show/Hide Unknown Diseases (2)
Unknown
Disease term Disease name Evidence References Source
Prader-willi syndrome Prader-Willi Syndrome ClinVar
Specific learning disorder Specific learning disability ClinVar