KEGG   Homo sapiens (human): 101929726
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)
SSDB
Motif
Pfam: Utp12
Other DBs
NCBI-GeneID: 101929726
NCBI-ProteinID: NP_001302423
OMIM: 619912
HGNC: 52391
Ensembl: ENSG00000262179
UniProt: A0A1B0GTQ4
Position
6:44192721..44218234
AA seq 84 aa
MPTPLLPLLLRLLLSCLLLPAARLARQYLLPLLRRLARRLGSQDMREALLGCLLFILSQR
HSPDAGEASRVDRLERRERLGPQK
NT seq 255 nt   +upstreamnt  +downstreamnt
atgcccacgccactgctcccgctgctgcttcgattgctgctgtcctgcctgctgctgcct
gctgcccgcctggcccgccaatacctcctgcccctgctgcgccgattggcccgccgcctg
ggctcccaggacatgcgagaggctttgctgggctgtctgctgttcattctcagccagcga
cactcgccagacgctggggaggcctcaagagtggaccgcctggagaggagggagaggtta
ggcccccaaaagtga

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