| Type | Description |
|---|---|
| Definition | MN1 proto-oncogene, transcriptional regulator |
| Date | Results | Publications |
|---|---|---|
| 2021-02-06 13:52:00 | MN1 Linked to Syndrome Characterized by Craniofacial Abnormalities and Severe Developmental Delay. | 32153127 |
| 2021-02-06 13:49:00 | Spinal cord astroblastoma with an EWSR1-BEND2 fusion classified as a high-grade neuroepithelial tumour with MN1 alteration. | 31863478 |
| 2020-11-21 13:29:00 | Frequent MN1 Gene Mutations in Malignant Peripheral Nerve Sheath Tumor. | 33109559 |
| 2020-10-03 12:59:00 | Allogeneic stem cell transplantation mitigates the adverse prognostic impact of high diagnostic BAALC and MN1 expression in AML. | 32862286 |
| 2020-08-22 15:29:00 | MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. | 31834374 |
| Type | IDs |
|---|---|
| Synonymous | MGCR, MGCR1, MGCR1-PEN, dJ353E16.2 |
| Gene |
UniProtKB-ID:
MN1_HUMAN,
A0A024R1C3_HUMAN
UniprotKB:
Q10571,
A0A024R1C3
UniParc:
UPI0000207445
EMBL:
AL031591,
Z70218,
FO393416,
X82209,
CH471095
Ensembl:
ENSG00000169184
KO:
hsa:4330
|
| Nucleutide sequences |
EMBL-CDS:
EAW59741.1,
CAA57693.2,
CAA94179.1,
EAW59742.1
Gene_ORFName:
hCG_40087
Ensembl_TRS:
ENST00000302326
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000304956
RefSeq:
NP_002421.3
|
| Others |
UniRef100:
UniRef100_Q10571
UniRef90:
UniRef90_Q10571
UniRef50:
UniRef50_Q10571
UniGene:
Hs.268515
CCDS:
CCDS42998.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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