IPW (imprinted in Prader-Willi syndrome)

Gene
Gene Other IDs Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3653
Gene name Gene Name - the full gene name approved by the HGNC.
Imprinted in Prader-Willi syndrome
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IPW
Synonyms (NCBI Gene) Gene synonyms aliases
NCRNA00002
Chromosome Chromosome number
15
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
15q11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is non-protein coding, is expressed exclusively from the paternal allele, and may play a role in the imprinting process. Mutations in this gene are associated with Prader-Willi syndrome. [provided by RefSeq, May 2010]
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
Gene Other IDs Associated diseases
MIM HGNC e!Ensembl
601491 6109 HGNC
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Gene 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
Show/Hide Text Mining Associations (3)
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Intraductal Noninfiltrating Inhibit 35078502
Neoplasms Inhibit 35078502
Prader Willi Syndrome Associate 8542279