Homo sapiens (human): 285489 Help Entry 285489            CDS       T01001                                  Symbol DOK7, C4orf25, CMS10, CMS1B, FADS3 Name (RefSeq) docking protein 7   KO K24038   docking protein 7 Organism hsa  Homo sapiens (human) Disease H00770   Congenital myasthenic syndrome H00987   Fetal akinesia deformation sequence Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04990 Domain-containing proteins not elsewhere classified [BR:hsa04990]     285489 (DOK7) Domain-containing proteins not elsewhere classified [BR:hsa04990]  Phosphotyrosine binding (PTB) domain-containing proteins   IRS related family proteins    285489 (DOK7) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  IRS PH Motif Other DBs NCBI-GeneID:  285489 NCBI-ProteinID:  NP_775931 OMIM:  610285 HGNC:  26594 Ensembl:  ENSG00000175920 UniProt:  Q18PE1 LinkDB All DBs Position 4:3463306..3501482 Genome browser AA seq 504 aa AA seqDB search MTEAALVEGQVKLRDGKKWKSRWLVLRKPSPVADCLLMLVYKDKSERIKGLRERSSLTLE DICGLEPGLPYEGLVHTLAIVCLSQAIMLGFDSHEAMCAWDARIRYALGEVHRFHVTVAP GTKLESGPATLHLCNDVLVLARDIPPAVTGQWKLSDLRRYGAVPSGFIFEGGTRCGYWAG VFFLSSAEGEQISFLFDCIVRGISPTKGPFGLRPVLPDPSPPGPSTVEERVAQEALETLQ LEKRLSLLSHAGRPGSGGDDRSLSSSSSEASHLDVSASSRLTAWPEQSSSSASTSQEGPR PAAAQAAGEAMVGASRPPPKPLRPRQLQEVGRQSSSDSGIATGSHSSYSSSLSSYAGSSL DVWRATDELGSLLSLPAAGAPEPSLCTCLPGTVEYQVPTSLRAHYDTPRSLCLAPRDHSP PSQGSPGNSAARDSGGQTSAGCPSGWLGTRRRGLVMEAPQGSEATLPGPAPGEPWEAGGP HAGPPPAFFSACPVCGGLKVNPPP NT seq 1515 nt NT seq  +upstreamnt  +downstreamnt atgaccgaggcggcgctggtggagggccaggtcaagctgcgggacggcaagaagtggaag agtaggtggctggtgctgcggaagccgtcgcccgtggcagactgcctgctgatgctggtc tacaaggacaagtcggagcgtatcaagggcctgcgggagcgcagcagcctgacgctagag gacatctgcgggctggagcccggcctgccctacgagggcctggtccacacgctggccatt gtctgcctgtcccaggccatcatgctgggctttgacagccacgaggccatgtgtgcgtgg gatgcccggatccgctatgcgctcggcgaggtgcataggttccatgtgacagtggctcca ggcaccaagttggagagcggcccggctaccctgcacctctgcaatgatgtcctcgtcttg gccagggacatccccccggctgtcacggggcagtggaagctgtctgacctccggcgctac ggggccgtgccaagcggattcatctttgaaggcgggaccaggtgtgggtactgggctggc gtcttcttcctgtcctcggccgagggggagcagatcagcttcctgttcgactgcatcgtc cgaggcatctcccccaccaagggcccctttgggctgcggccggttctaccagacccaagt cccccgggaccctcgactgtggaggagcgtgtggcccaggaagccctggaaaccctacag ctggagaagcggctgagcctcctctcacatgcgggcaggccgggcagtggaggggatgac cgcagcctgtccagctcatcctcagaggccagtcacttggacgtcagcgccagcagccgg ctcaccgcatggccagagcaatcctcgtcgtcagccagcacgtcacaggaggggcctaga ccagcagctgcccaggccgccggggaagccatggtgggtgcctcaaggccaccccccaag ccgctgcgtccgcggcagctgcaggaggttggccgccagagctcctcggacagcggcatc gccactggcagccactcctcttactccagcagcctctcgtcctacgcgggcagcagcctg gacgtgtggcgggccacagatgaactgggctcactgctcagcctgccagcagcgggggcc cccgagcccagcctgtgcacctgcctgcccgggacagtcgagtaccaggtgcccacctcc ctgcgggcccactatgacacaccacgcagcctttgcctggctcctagagaccacagcccc ccctcacagggcagccccggcaacagtgcggccagggactcaggcggccagacgtccgcc gggtgtccctctggctggctgggcacgagacggcggggcctggtgatggaggccccccag ggcagcgaggccacactgcctggccctgcccctggcgagccctgggaagcaggcggcccc cacgcggggccacccccggctttcttttcggcatgtccagtctgtggaggactcaaggta aacccccctccttga

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