Homo sapiens (human): 390792 Help Entry 390792            CDS       T01001                                  Symbol KRT39, CK-39, K39, KA35 Name (RefSeq) keratin 39   KO K07604   type I keratin, acidic Organism hsa  Homo sapiens (human) Pathway hsa04915   Estrogen signaling pathway hsa05150   Staphylococcus aureus infection Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09152 Endocrine system    04915 Estrogen signaling pathway     390792 (KRT39)  09160 Human Diseases   09171 Infectious disease: bacterial    05150 Staphylococcus aureus infection     390792 (KRT39)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     390792 (KRT39)    04147 Exosome [BR:hsa04147]     390792 (KRT39) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Intermediate filaments    Intermediate filaments     Types I and II: Acidic and basic keratins      390792 (KRT39) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of epithelial cells    390792 (KRT39)   Exosomal proteins of other body fluids (saliva and urine)    390792 (KRT39)   Exosomal proteins of colorectal cancer cells    390792 (KRT39)   Exosomal proteins of melanoma cells    390792 (KRT39) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Filament Sec16 Motif Other DBs NCBI-GeneID:  390792 NCBI-ProteinID:  NP_998821 OMIM:  616678 HGNC:  32971 Ensembl:  ENSG00000196859 UniProt:  Q6A163 LinkDB All DBs Position 17:complement(40958417..40966948) Genome browser AA seq 491 aa AA seqDB search MDTKGCTTTNSPSTPCQNCSRITNVSTISSNNGCHPGGLTVNNCQPAGHVLRIPWDQGCQ PTPRFCRKPIYLMNNFNARFSLDDCSWYGEGINSNEKETMQILNERLANYLQKVRMLERE NAELESKIQEESNKELPVLCPDYLSYYTTIEELQQKILCTKAENSRLVSQIDNTKLTADD LRAKYEAEVSLRQLVESDANGLKQILNVLTLGKADLEAQVQSLKEELLCLKNNHKEEINS LQCQLGERLDIEVTAAPSADLNQVLQEMRCQYEPIMETNRKDVEQWFNTQIEELNQQVVT SSQQQQCCQKEIIELRRSVNTLEVELQAQHRMRDSQECILTETEARYTALLTQIQSLIDN LEAQLAEIRCALERQNQEYEILLDVKSRLECEITTYRSLLESSDGKRPCYPRATKCEPSP WTSCKSGAIESTAPACTSSSPCSLKEHCSACGPLSRILVKICTITKEIKDGKVISSYEHV QPCFIIRPAKV NT seq 1476 nt NT seq  +upstreamnt  +downstreamnt atggacaccaagggctgtacaacaaccaattctccttcaaccccatgtcaaaactgctct aggattacaaatgttagtaccatctcttctaacaacggctgccatcctggtggccttaca gtcaacaactgtcaaccagctggccacgttctcagaattccctgggaccagggctgccaa cccactcctcgcttttgtcgcaagcccatctacctaatgaacaacttcaatgcccgtttt tctctggatgactgcagctggtatggtgaaggcatcaacagtaatgagaaggagaccatg caaatcttgaacgagcgccttgctaactacctgcaaaaggtgcgaatgctagaacgagag aatgctgaactggaatctaaaatccaggaagaaagtaacaaagagctccctgttctatgt cctgattacctgtcttactacactaccattgaggagctccagcagaagatcttgtgtacc aaggccgagaattccagactggtctcgcaaattgacaacaccaaactgactgcagatgac ttgagagccaaatacgaagctgaggtgtctctacgccagctggtagagtcagatgccaat ggcctcaagcagatcctgaatgtgctgaccctgggcaaggccgacctagaggcacaagtc cagtctctgaaagaggagctcctttgcctcaagaacaaccacaaagaggaaatcaattct ttacagtgtcagcttggggagagacttgacattgaagtgactgctgccccttctgctgac ctaaaccaggttctacaagaaatgagatgtcaatatgagcccatcatggagacaaaccgc aaagatgtggaacagtggttcaacacgcagatagaggagctgaatcaacaagtggtgacc agctctcaacagcagcaatgctgccaaaaggagatcatagaactgagacgcagtgtgaac actctggaggttgaactgcaggcccagcatcgaatgagagattcccaagagtgcatccta acggagacagaggctcgctacacggccttgctgacccagatccagagtctgattgataac ctggaagctcagctggcagagatccggtgtgccctggaaagacagaaccaagaatacgag atcctgctggacgtcaagtcccggctggaatgtgagattaccacataccgcagccttctg gagagctcggatggcaagcgtccctgttacccacgtgccaccaaatgtgagccttcccct tggacatcttgtaagtccggagccatagaaagcacggccccagcttgcacatcctcatcc ccctgcagcttaaaggagcactgcagtgcctgcggacccctgtcccggatactggttaaa atttgcaccatcaccaaggagattaaggatgggaaggtcatttcttcttacgagcatgtg cagccttgtttcatcatcagacctgccaaagtctaa

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