MuScle-logoMuScle - Molecule ID B0611

geneAMMECR1
nameAMME syndrome candidate gene 1 protein
speciesHomo sapiens

Molecule reference

SwissProtUniProtEnsEMBLGeneIDUniGeneOMIM
AMMR1_HUMANQ9Y4X0ENSG000001019359949Hs.656243300194, 300195

Functions and classifications

UniProtAlport syndrome, Alternative splicing, Complete proteome, Deafness, Elliptocytosis, Hereditary hemolytic anemia, Mental retardation, Reference proteome
PADBDIS: disease

Studies, tissues and diseases

Study IDSpeciesNTissue / SourceCompartmentDiseaseFold change in diseaseP-valuePubMed/DOI
Exp17467740Homo sapiens10Blood RRMS_(IFN-Beta-1a_1_day_follow-up) (Multiple sclerosis)0.551.09E-0217467740
Exp20136355Homo sapiens50Blood RRMS_(rIFN-Beta-1b_1_month_follow-up) (Multiple sclerosis)1.262.48E-0320136355
Exp21886806Homo sapiens12Blood RRMS_(IFN-Beta-1a_24_month_follow-up) (Multiple sclerosis)0.680.048357721886806
Exp22021740Homo sapiens27Blood MS (Multiple sclerosis)1.234.19E-0222021740
Exp22021740Homo sapiens27Blood MS (Multiple sclerosis)1.741.60E-0422021740
Exp22252466AHomo sapiens16BloodCD34+/CD34- HPCRRMS_SPMS (Multiple sclerosis)1.209.09E-0322252466
Exp23895517AHomo sapiens19BloodT-cellsRRMS_(relapsing-remitting_MS) (Multiple sclerosis)0.796.81E-0323895517

Compile date 09-07-2016© MuScle project