Homo sapiens (human): 374393 Help Entry 374393            CDS       T01001                                  Symbol FAM111B, CANP, POIKTMP Name (RefSeq) FAM111 trypsin like peptidase B   KO K24275   protein FAM111B Organism hsa  Homo sapiens (human) Disease H01906   Poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99995 Signaling proteins     374393 (FAM111B) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Trypsin_2 Peptidase_S7 Trypsin Motif Other DBs NCBI-GeneID:  374393 NCBI-ProteinID:  NP_945185 OMIM:  615584 HGNC:  24200 Ensembl:  ENSG00000189057 UniProt:  Q6SJ93 LinkDB All DBs Position 11:59107237..59127412 Genome browser AA seq 734 aa AA seqDB search MNSMKTEENKSFSAMEDDQRTRPEVSKDTVMKQTHADTPVDHCLSGIRKCSSTFKLKSEV NKHETALEMQNPNLNNKECCFTFTLNGNSRKLDRSVFTAYGKPSESIYSALSANDYFSER IKNQFNKNIIVYEEKTIDGHINLGMPLKCLPSDSHFKITFGQRKSSKEDGHILRQCENPN MECILFHVVAIGRTRKKIVKINELHEKGSKLCIYALKGETIEGALCKDGRFRSDIGEFEW KLKEGHKKIYGKQSMVDEVSGKVLEMDISKKKALQQKDIHKKIKQNESATDEINHQSLIQ SKKKVHKPKKDGETKDVEHSREQILPPQDLSHYIKDKTRQTIPRIRNYYFCSLPRKYRQI NSQVRRRPHLGRRYAINLDVQKEAINLLKNYQTLNEAIMHQYPNFKEEAQWVRKYFREEQ KRMNLSPAKQFNIYKKDFGKMTANSVSVATCEQLTYYSKSVGFMQWDNNGNTGNATCFVF NGGYIFTCRHVVHLMVGKNTHPSLWPDIISKCAKVTFTYTEFCPTPDNWFSIEPWLKVSN ENLDYAILKLKENGNAFPPGLWRQISPQPSTGLIYLIGHPEGQIKKIDGCTVIPLNERLK KYPNDCQDGLVDLYDTTSNVYCMFTQRSFLSEVWNTHTLSYDTCFSDGSSGSPVFNASGK LVALHTFGLFYQRGFNVHALIEFGYSMDSILCDIKKTNESLYKSLNDEKLETYDEEKGKQ ESSLQDHQIEPMEC NT seq 2205 nt NT seq  +upstreamnt  +downstreamnt atgaattccatgaagactgaagaaaacaagtcatttagcgctatggaagatgaccagagg actagacctgaagtttcaaaggatactgtcatgaagcagacacatgctgacacacctgtt gatcattgtctatctggcataagaaagtgtagcagcacctttaagcttaaaagtgaagtc aacaagcatgaaacagcccttgaaatgcagaatccaaatttgaacaataaagaatgttgt ttcacctttacgttgaatggaaactccagaaaattagaccgtagtgtgtttacagcatat ggtaaacccagcgagagtatctactcagccctgagtgctaatgactatttcagtgaaagg ataaagaatcagtttaataagaacattattgtttatgaagaaaagacaatagatggacat ataaatttaggaatgcctctcaagtgcctgcctagtgattctcattttaaaattacattt ggtcaaagaaagagtagcaaagaagatggacacatattacgccaatgtgaaaatccaaac atggaatgcattctttttcatgttgttgctataggaaggacaagaaagaagattgttaag atcaacgaacttcatgaaaaaggaagtaaactttgtatttatgccttgaagggtgagact attgaaggagccttatgcaaggatggccgttttcggtctgacataggtgaatttgaatgg aaactaaaggaaggtcataagaaaatttatggaaaacagtccatggtggatgaagtatct ggaaaagtcttagaaatggacatttcaaaaaaaaaagcattacaacagaaagatatccat aaaaaaattaaacagaatgaaagtgccactgatgaaattaatcaccagagtctgatacag tctaagaaaaaagtccacaaaccaaagaaagatggagagaccaaagatgtagaacacagc agagagcaaattctcccacctcaggatctaagccattatattaaagataaaactcgccag acaattcccaggattagaaattattacttttgtagtttgccccgaaaatataggcaaata aactcacaagttagacggaggccgcatctgggtaggcggtatgctattaatctggatgtc caaaaggaggcaattaatctcttaaagaattatcaaacgttgaatgaagccataatgcat cagtatccgaattttaaagaggaggcacagtgggtaagaaaatattttcgggaagaacaa aagagaatgaatctttcaccagctaagcaattcaacatatataaaaaggacttcggaaaa atgactgcaaattctgtttcagttgcaacctgcgaacagcttacatattatagcaagtca gttgggttcatgcaatgggacaataatggaaacacaggtaatgctacttgctttgtcttc aatggtggttatattttcacctgtcgacatgttgtacatcttatggtgggtaaaaacaca catccaagtttgtggccagatataattagcaaatgtgcgaaggtaaccttcacttataca gagttctgccctactcctgacaattggttttccattgagccatggcttaaagtgtccaat gaaaatctagattatgccattttaaaactaaaagaaaatggaaatgcgtttcctccagga ctatggcgacagatttctcctcaaccatctactggtttgatttatttaattggtcatcct gaaggccagatcaagaaaatagatggttgtactgtgattcctctaaacgaacgattgaaa aaatatccaaacgattgtcaagatgggttggtagatctctatgataccaccagtaatgta tactgtatgtttacccaaagaagtttcctatcagaggtttggaacacacacacgcttagt tatgatacttgtttctctgatgggtcctcaggctccccagtgtttaatgcatctggcaaa ttggttgctttgcatacctttgggcttttttatcaacgaggatttaatgtgcatgccctt attgaatttggttattctatggattctattctttgtgatattaaaaagacaaatgagagc ttgtataaatcattaaatgatgagaaacttgagacctacgatgaagagaaaggtaaacaa gagtcatcacttcaagatcatcagattgaacccatggaatgttag

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