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HYMAI hydatidiform mole associated and imprinted (non-protein coding) [ Homo sapiens (human) ]

Gene ID: 57061, updated on 9-Nov-2014
Official Symbol
HYMAIprovided by HGNC
Official Full Name
hydatidiform mole associated and imprinted (non-protein coding)provided by HGNC
Primary source
HGNC:HGNC:5326
See related
MIM:606546
Gene type
ncRNA
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NCRNA00020
Summary
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 transient neonatal diabetes mellitus (TNDM), which is a rare disease characterized by intrauterine growth retardation, dehydration, and failure to thrive due to a lack of normal insulin secretion. [provided by RefSeq, Oct 2010]
See HYMAI in Epigenomics, MapViewer
Location:
6q24.2
Exon count:
2
Annotation release Status Assembly Chr Location
106 current GRCh38 (GCF_000001405.26) 6 NC_000006.12 (144002886..144008730, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (144324023..144329867, complement)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene LTV1 ribosome biogenesis factor Neighboring gene zinc finger, C2HC-type containing 1B Neighboring gene pleiomorphic adenoma gene-like 1 Neighboring gene FK506 binding protein 7 pseudogene Neighboring gene splicing factor 3b, subunit 5, 10kDa

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Copy number response

Description
Copy number response
Haploinsufficency

No evidence available (Last evaluated (2012-09-06)

ClinGen Genome Curation Page
Triplosensitivity

No evidence available (Last evaluated (2012-09-06)

ClinGen Genome Curation Page

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_016174.1 

    Range
    5001..10845
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_002768.1 RNA Sequence

    Status: REVIEWED

    Source sequence(s)
    AF241534

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 106

The following sections contain reference sequences that belong to a specific genome build. Explain

Alternate HuRef

Genomic

  1. AC_000138.1 

    Range
    141887703..141893547
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38 Primary Assembly

Genomic

  1. NC_000006.12 

    Range
    144002886..144008730
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate CHM1_1.1

Genomic

  1. NC_018917.2 

    Range
    144586912..144592755
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)