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MAGEL2 MAGE-like 2 [Homo sapiens (human)]


RefSeq Accession Definition Service Stock Status Price *Turnaround time Order
NM_019066 Homo sapiens MAGE-like 2 (MAGEL2), mRNA. GenEZ ORF Cloning On-demand TBD TBD

*Business Day

Related Services

Gene Symbol MAGEL2
Entrez Gene ID 54551
Full Name MAGE-like 2
Synonyms NDNL1, nM15
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

15

15q11-q12

Summary Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010].
Disorder

MIM: 605283

mRNA Protein Product Sequence Price Select
NM_019066, 257900507 NP_061939, 257900508 MAGE-like protein 2 ORF Sequence $1500.00
Homo sapiens (human)MAGEL2NP_061939.3
Macaca mulatta (Rhesus monkey)MAGEL2XP_001114423.2
Canis lupus familiaris (dog)LOC100684492XP_003434387.1
Bos taurus (cattle)MAGEL2XP_002696517.1
Mus musculus (house mouse)Magel2NP_038807.4
Rattus norvegicus (Norway rat)Magel2XP_001054803.1
GeneCards MAGEL2
MIM 605283
Ensembl ENSG00000254585
HGNC 6814
HPRD 12008

GeneRIFs: Gene References Into Functions What's a GeneRIF?

General protein information

Preferred Names
MAGE-like protein 2
Names
MAGE-like protein 2
protein nM15
necdin-like protein 1

Interactant



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