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MDS1 myelodysplasia syndrome 1 [ Homo sapiens (human) ]

Gene ID: 4197, discontinued on 10-Aug-2009

Summary

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Official Symbol
MDS1provided by HGNC
Official Full Name
myelodysplasia syndrome 1provided by HGNC
Primary source
HGNC:HGNC:6979
See related
MIM:600049
Gene type
protein coding
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
PRDM3; MDS1-EVI1
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Genomic context

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See MDS1 in Genome Data Viewer
Location:
3q26

Bibliography

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GeneRIFs: Gene References Into Functions

General gene information

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Markers

General protein information

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Preferred Names
myelodysplasia syndrome 1
Names
myelodysplasia syndrome-associated protein 1
Nucleotide Protein
Heading Accession and Version
Protein Accession Links
GenPept Link UniProtKB Link
Q13465.1 GenPept UniProtKB/Swiss-Prot:Q13465

Gene LinkOut

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