Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57061
Gene name Gene Name - the full gene name approved by the HGNC.
Hydatidiform mole associated and imprinted
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HYMAI
Synonyms (NCBI Gene) Gene synonyms aliases
NCRNA00020
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q24.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene, which encodes a non-protein coding transcript, exhibits differential DNA methylation between the two parental alleles at an adjacent CpG island, and is expressed only from the paternal allele. It is believed to be one of the causative genes for
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
606546 5326 ENSG00000283122
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Apraxia Apraxias rs121908377, rs121908378, rs1135401820, rs1178491246, rs1584969672
Arthrogryposis multiplex congenita Arthrogryposis rs1586285494, rs80358233, rs137853305, rs1559154278, rs398124167, rs398124172, rs587780399, rs786204576, rs786204430, rs769345284, rs749355583, rs793888524, rs793888525, rs878854368, rs555445835
View all (138 more)
Congenital heart defects Congenital Heart Defects rs267607101, rs121434422, rs387906498, rs397509416, rs587777371, rs587777372, rs587777374, rs367537998, rs797044882, rs886041730, rs768027510, rs1064793873, rs1555447012, rs1554263268, rs1554263321
View all (13 more)
Cryptorchidism Cryptorchidism rs121912555, rs104894697, rs104894698, rs398122886
Associations from Text Mining
Disease Name Relationship Type References
Chromosome Aberrations Associate 16971482
Diabetes Mellitus Associate 24993786
Diabetes Mellitus Transient Neonatal 1 Stimulate 27075368
Fetal Growth Retardation Associate 24993786