Homo sapiens (human): 6406 Help Entry 6406              CDS       T01001                                  Symbol SEMG1, CT103, SEMG, SGI, dJ172H20.2 Name (RefSeq) semenogelin 1   KO K25736   semenogelin Organism hsa  Homo sapiens (human) Brite KEGG Orthology (KO) [BR:hsa00001]  09190 Not Included in Pathway or Brite   09193 Unclassified: signaling and cellular processes    99995 Signaling proteins     6406 (SEMG1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Semenogelin Motif Other DBs NCBI-GeneID:  6406 NCBI-ProteinID:  NP_002998 OMIM:  182140 HGNC:  10742 Ensembl:  ENSG00000124233 UniProt:  P04279 Structure PDBPDBj LinkDB All DBs Position 20:45207033..45209768 Genome browser AA seq 462 aa AA seqDB search MKPNIIFVLSLLLILEKQAAVMGQKGGSKGRLPSEFSQFPHGQKGQHYSGQKGKQQTESK GSFSIQYTYHVDANDHDQSRKSQQYDLNALHKTTKSQRHLGGSQQLLHNKQEGRDHDKSK GHFHRVVIHHKGGKAHRGTQNPSQDQGNSPSGKGISSQYSNTEERLWVHGLSKEQTSVSG AQKGRKQGGSQSSYVLQTEELVANKQQRETKNSHQNKGHYQNVVEVREEHSSKVQTSLCP AHQDKLQHGSKDIFSTQDELLVYNKNQHQTKNLNQDQQHGRKANKISYQSSSTEERRLHY GENGVQKDVSQSSIYSQTEEKAQGKSQKQITIPSQEQEHSQKANKISYQSSSTEERRLHY GENGVQKDVSQRSIYSQTEKLVAGKSQIQAPNPKQEPWHGENAKGESGQSTNREQDLLSH EQKGRHQHGSHGGLDIVIIEQEDDSDRHLAQHLNNDRNPLFT NT seq 1389 nt NT seq  +upstreamnt  +downstreamnt atgaagcccaacatcatctttgtactttccctgctcctcatcttggagaagcaagcagct gtgatgggacaaaaaggtggatcaaaaggccgattaccaagtgaattttcccaatttcca cacggacaaaagggccagcactattctggacaaaaaggcaagcaacaaactgaatccaaa ggcagtttttctattcaatacacatatcatgtagatgccaatgatcatgaccagtcccga aaaagtcagcaatatgatttgaatgccctacataagacgacaaaatcacaacgacatcta ggtggaagtcaacaactgctccataataaacaagaaggcagagaccatgataaatcaaaa ggtcattttcacagggtagttatacaccataaaggaggcaaagctcatcgtgggacacaa aatccttctcaagatcaggggaatagcccatctggaaagggaatatccagtcaatattca aacacagaagaaaggctgtgggttcatggactaagtaaagaacaaacttccgtctctggt gcacaaaaaggtagaaaacaaggcggatcccaaagcagttatgttctccaaactgaagag ctagtagctaacaaacaacaacgtgagactaaaaattctcatcaaaataaagggcattac caaaatgtggttgaagtgagagaggaacattcaagtaaagtacaaacctcactctgtcct gcgcaccaagacaaactccaacatggatccaaagacattttttctacccaagatgagctc ctagtatataacaagaatcaacaccagacaaaaaatctcaatcaagatcaacagcatggc cgaaaggcaaataaaatatcataccaatcttcaagtacagaagaaagacgactccactat ggagaaaatggtgtgcagaaagatgtatcccaaagcagtatttatagccaaactgaagag aaagcacagggcaagtctcaaaaacagataacaattcccagtcaagagcaagagcatagc caaaaggcaaataaaatatcataccaatcttcaagtacggaagaaagacgactccactat ggagaaaatggtgtgcagaaagatgtatcccaacgcagtatttatagccaaactgaaaag ctagtagcaggcaagtctcaaatccaggcaccaaatcctaagcaagagccatggcatggt gaaaatgcaaaaggagagtctggccaatctacaaatagagaacaagacctactcagtcat gaacaaaaaggcagacaccaacatggatctcatgggggattggatattgtaattatagag caggaagatgacagtgatcgtcatttggcacaacatcttaacaacgaccgaaacccatta tttacataa

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