Homo sapiens (human): 8688 Help Entry 8688              CDS       T01001                                  Symbol KRT37, HA7, K37, KRTHA7 Name (RefSeq) keratin 37   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     8688 (KRT37)  09160 Human Diseases   09171 Infectious disease: bacterial    05150 Staphylococcus aureus infection     8688 (KRT37)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     8688 (KRT37)    04147 Exosome [BR:hsa04147]     8688 (KRT37) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Intermediate filaments    Intermediate filaments     Types I and II: Acidic and basic keratins      8688 (KRT37) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of epithelial cells    8688 (KRT37)   Exosomal proteins of other body fluids (saliva and urine)    8688 (KRT37)   Exosomal proteins of colorectal cancer cells    8688 (KRT37)   Exosomal proteins of melanoma cells    8688 (KRT37) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Filament KIF21A_2nd FANCL_d2 Motif Other DBs NCBI-GeneID:  8688 NCBI-ProteinID:  NP_003761 OMIM:  604541 HGNC:  6455 Ensembl:  ENSG00000108417 UniProt:  O76014 LinkDB All DBs Position 17:complement(41420547..41424585) Genome browser AA seq 449 aa AA seqDB search MTSFYSTSSCPLGCTMAPGARNVFVSPIDVGCQPVAEANAASMCLLANVAHANRVRVGST PLGRPSLCLPPTSHTACPLPGTCHIPGNIGICGAYGKNTLNGHEKETMKFLNDRLANYLE KVRQLEQENAELETTLLERSKCHESTVCPDYQSYFRTIEELQQKILCSKAENARLIVQID NAKLAADDFRIKLESERSLHQLVEADKCGTQKLLDDATLAKADLEAQQESLKEEQLSLKS NHEQEVKILRSQLGEKFRIELDIEPTIDLNRVLGEMRAQYEAMVETNHQDVEQWFQAQSE GISLQAMSCSEELQCCQSEILELRCTVNALEVERQAQHTLKDCLQNSLCEAEDRYGTELA QMQSLISNLEEQLSEIRADLERQNQEYQVLLDVKARLENEIATYRNLLESEDCKLPCNPC STPASCTSCPSCGPVTGGSPSGHGASMGR NT seq 1350 nt NT seq  +upstreamnt  +downstreamnt atgacctccttctacagcacctcctcatgccctctgggttgcaccatggctcctggagca agaaatgtctttgtctctcctatcgatgttgggtgccagcctgtggcagaggccaatgct gcctccatgtgcctcttggccaacgtggcacacgccaacagagtccgtgtggggtcgact cccctgggccgccccagcctctgtctgcccccaaccagtcacactgcttgtcccttgcca gggacctgtcacattcccggcaacatcggaatctgtggggcctacggcaaaaacaccctg aatggccatgagaaggagaccatgaagttcctgaatgaccgcctggccaactacctggag aaggtgcgccagctggagcaggagaatgcagagctggagaccacactcctcgagaggagc aagtgccacgagtccaccgtgtgccccgactaccagtcctacttccgtacaatcgaggag ctccagcagaagatcctgtgcagcaaggctgagaatgccaggctgattgtacaaattgac aacgcgaagctggctgctgatgactttaggatcaagctggagagtgagcgctcccttcac cagctggtggaggcggacaagtgcgggacgcagaagctcctggatgacgcgaccctggcc aaggccgacctggaggcccagcaggagtccctgaaggaggagcagctctccctcaagagc aaccacgagcaggaagtaaagattctgaggagtcagctgggggagaagttccggatcgag ctggacattgagcccaccattgacctgaacagggtgttgggggagatgcgggctcagtac gaggccatggtggagaccaaccaccaggatgtggaacagtggttccaagcccagtctgaa ggcatcagcctgcaggccatgtcctgctccgaggagctgcagtgctgccagtcggagatc ctggagctgagatgcacggtgaatgccctggaggtggagcgccaagcccagcacaccttg aaggactgtctgcagaactccctgtgtgaagcggaggaccgctacggcacagagctggcc cagatgcagagcctcattagcaacttggaagagcagttgtctgagatccgggccgacctg gagcggcagaaccaggagtaccaggtgctgctggacgtgaaggcccggttggagaacgag attgccacataccggaaccttctggagagcgaggactgcaaactcccctgcaatccctgt tccacgcctgcctcctgtacttcttgtccaagctgtggccctgtcaccggtgggtctccc tctggccatggagccagcatggggagatga

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