| Type | Description |
|---|---|
| Definition | necdin, MAGE family member |
| Date | Results | Publications |
|---|---|---|
| 2020-10-31 13:17:00 | The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry. | 32529326 |
| 2019-05-18 11:50:00 | We focused on three important regulatory DNA elements which are all differentially methylated regions (DMRs), methylated on the maternal allele: the PWS imprinting center (PWS-IC), which is a germline DMR and the somatic NDN and MKRN3 DMRs, hierarchically controlled by PWS-IC. | 30102380 |
| 2018-12-22 10:28:00 | the single-nucleotide polymorphism rs850807, which is putatively functional and linked with MAGEL2 and NDN Genetic variation in rs850807 was strongly and exclusively associated with the ideas of reference subscale of the schizophrenia spectrum, which is best typified as paranoia | 29343559 |
| 2018-04-21 10:14:00 | this study shows that hypermethylation of NDN promotes cell proliferation by activating the Wnt signaling pathway in colorectal cancer | 28521288 |
| 2017-06-24 10:12:00 | One candidate variant was located in an alpha helix of Necdin (NDN), phased to the paternally inherited allele. NDN is maternally imprinted within the 15q11.2 Prader-Willi Syndrome (PWS) region | 28213671 |
| Type | IDs |
|---|---|
| Synonymous | HsT16328, PWCR |
| Gene |
UniProtKB-ID:
NECD_HUMAN,
X5D982_HUMAN
UniprotKB:
Q99608,
X5D982
UniParc:
UPI000012FEF1
EMBL:
U35139,
KU178221,
AB007828,
BC008750,
KJ534888,
AK312779
Ensembl:
ENSG00000182636
KO:
hsa:4692
|
| Nucleutide sequences |
EMBL-CDS:
BAA22660.1,
AAB39469.1,
BAG35642.1,
AAH08750.1,
ALQ33679.1,
AHW56528.1
Ensembl_TRS:
ENST00000649030
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000497916
RefSeq:
NP_002478.1
|
| Others |
UniRef100:
UniRef100_Q99608
UniRef90:
UniRef90_Q99608
UniRef50:
UniRef50_P25233
UniGene:
Hs.50130
CCDS:
CCDS10014.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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