Homo sapiens (human): 101929726 Help Entry 101929726         CDS       T01001                                  Symbol MYMX, CFZS2, MINION, hMINION Name (RefSeq) myomixer, myoblast fusion factor   KO K24578   protein myomixer Organism hsa  Homo sapiens (human) Disease H01908   Carey-Fineman-Ziter syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99995 Signaling proteins     101929726 (MYMX) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  MINION Utp12 Motif Other DBs NCBI-GeneID:  101929726 NCBI-ProteinID:  NP_001302423 OMIM:  619912 HGNC:  52391 Ensembl:  ENSG00000262179 UniProt:  A0A1B0GTQ4 LinkDB All DBs Position 6:44192721..44218234 Genome browser AA seq 84 aa AA seqDB search MPTPLLPLLLRLLLSCLLLPAARLARQYLLPLLRRLARRLGSQDMREALLGCLLFILSQR HSPDAGEASRVDRLERRERLGPQK NT seq 255 nt NT seq  +upstreamnt  +downstreamnt atgcccacgccactgctcccgctgctgcttcgattgctgctgtcctgcctgctgctgcct gctgcccgcctggcccgccaatacctcctgcccctgctgcgccgattggcccgccgcctg ggctcccaggacatgcgagaggctttgctgggctgtctgctgttcattctcagccagcga cactcgccagacgctggggaggcctcaagagtggaccgcctggagaggagggagaggtta ggcccccaaaagtga

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