Homo sapiens (human): 2162 Help Entry 2162              CDS       T01001                                  Symbol F13A1, F13A Name (RefSeq) coagulation factor XIII A chain   KO K03917   coagulation factor XIII A1 polypeptide [EC:2.3.2.13] Organism hsa  Homo sapiens (human) Pathway hsa04610   Complement and coagulation cascades hsa05171   Coronavirus disease - COVID-19 Network nt06514  Coagulation cascade   Element N01514   Common pathway of coagulation cascade, F13 activation Disease H00945   Factor XIII deficiency H01730   Myocardial infarction Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09151 Immune system    04610 Complement and coagulation cascades     2162 (F13A1)  09160 Human Diseases   09172 Infectious disease: viral    05171 Coronavirus disease - COVID-19     2162 (F13A1) Enzymes [BR:hsa01000]  2. Transferases   2.3  Acyltransferases    2.3.2  Aminoacyltransferases     2.3.2.13  protein-glutamine gamma-glutamyltransferase      2162 (F13A1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Transglut_C Transglut_N Transglut_core GtfA_EBD Motif Other DBs NCBI-GeneID:  2162 NCBI-ProteinID:  NP_000120 OMIM:  134570 HGNC:  3531 Ensembl:  ENSG00000124491 UniProt:  P00488 Structure PDB LinkDB All DBs Position 6:complement(6144084..6320662) Genome browser AA seq 732 aa AA seqDB search MSETSRTAFGGRRAVPPNNSNAAEDDLPTVELQGVVPRGVNLQEFLNVTSVHLFKERWDT NKVDHHTDKYENNKLIVRRGQSFYVQIDFSRPYDPRRDLFRVEYVIGRYPQENKGTYIPV PIVSELQSGKWGAKIVMREDRSVRLSIQSSPKCIVGKFRMYVAVWTPYGVLRTSRNPETD TYILFNPWCEDDAVYLDNEKEREEYVLNDIGVIFYGEVNDIKTRSWSYGQFEDGILDTCL YVMDRAQMDLSGRGNPIKVSRVGSAMVNAKDDEGVLVGSWDNIYAYGVPPSAWTGSVDIL LEYRSSENPVRYGQCWVFAGVFNTFLRCLGIPARIVTNYFSAHDNDANLQMDIFLEEDGN VNSKLTKDSVWNYHCWNEAWMTRPDLPVGFGGWQAVDSTPQENSDGMYRCGPASVQAIKH GHVCFQFDAPFVFAEVNSDLIYITAKKDGTHVVENVDATHIGKLIVTKQIGGDGMMDITD TYKFQEGQEEERLALETALMYGAKKPLNTEGVMKSRSNVDMDFEVENAVLGKDFKLSITF RNNSHNRYTITAYLSANITFYTGVPKAEFKKETFDVTLEPLSFKKEAVLIQAGEYMGQLL EQASLHFFVTARINETRDVLAKQKSTVLTIPEIIIKVRGTQVVGSDMTVTVEFTNPLKET LRNVWVHLDGPGVTRPMKKMFREIRPNSTVQWEEVCRPWVSGHRKLIASMSSDSLRHVYG ELDVQIQRRPSM NT seq 2199 nt NT seq  +upstreamnt  +downstreamnt atgtcagaaacttccaggaccgcctttggaggcagaagagcagttccacccaataactct aatgcagcggaagatgacctgcccacagtggagcttcagggcgtggtgccccggggcgtc aacctgcaagagtttcttaatgtcacgagcgttcacctgttcaaggagagatgggacact aacaaggtggaccaccacactgacaagtatgaaaacaacaagctgattgtccgcagaggg cagtctttctatgtgcagattgacttcagtcgtccatatgaccccagaagggatctcttc agggtggaatacgtcattggtcgctacccacaggagaacaagggaacctacatcccagtg cctatagtctcagagttacaaagtggaaagtggggggccaagattgtcatgagagaggac aggtctgtgcggctgtccatccagtcttcccccaaatgtattgtggggaaattccgcatg tatgttgctgtctggactccctatggcgtacttcgaaccagtcgaaacccagaaacagac acgtacattctcttcaatccttggtgtgaagatgatgctgtgtatctggacaatgagaaa gaaagagaagagtatgtcctgaatgacatcggggtaattttttatggagaggtcaatgac atcaagaccagaagctggagctatggtcagtttgaagatggcatcctggacacttgcctg tatgtgatggacagagcacaaatggacctctctggaagagggaatcccatcaaagtcagc cgtgtggggtctgcaatggtgaatgccaaagatgacgaaggtgtcctcgttggatcctgg gacaatatctatgcctatggcgtccccccatcggcctggactggaagcgttgacattcta ttggaataccggagctctgagaatccagtccggtatggccaatgctgggtttttgctggt gtctttaacacatttttacgatgccttggaataccagcaagaattgttaccaattatttc tctgcccatgataatgatgccaatttgcaaatggacatcttcctggaagaagatgggaac gtgaattccaaactcaccaaggattcagtgtggaactaccactgctggaatgaagcatgg atgacaaggcctgaccttcctgttggatttggaggctggcaagctgtggacagcaccccc caggaaaatagcgatggcatgtatcggtgtggccccgcctcggttcaagccatcaagcac ggccatgtctgcttccaatttgatgcaccttttgtttttgcagaggtcaacagcgacctc atttacattacagctaagaaagatggcactcatgtggtggaaaatgtggatgccacccac attgggaaattaattgtgaccaaacaaattggaggagatggcatgatggatattactgat acttacaaattccaagaaggtcaagaagaagagagattggccctagaaactgccctgatg tacggagctaaaaagcccctcaacacagaaggtgtcatgaaatcaaggtccaacgttgac atggactttgaagtggaaaatgctgtgctgggaaaagacttcaagctctccatcaccttc cggaacaacagccacaaccgttacaccatcacagcttatctctcagccaacatcaccttc tacaccggggtcccgaaggcagaattcaagaaggagacgttcgacgtgacgctggagccc ttgtccttcaagaaagaggcggtgctgatccaagccggcgagtacatgggtcagctgctg gaacaagcgtccctgcacttctttgtcacagctcgcatcaatgagaccagggatgttctg gccaagcaaaagtccaccgtgctaaccatccctgagatcatcatcaaggtccgtggcact caggtagttggttctgacatgactgtgacagttgagtttaccaatcctttaaaagaaacc ctgcgaaatgtctgggtacacctggatggtcctggagtaacaagaccaatgaagaagatg ttccgtgaaatccggcccaactccaccgtgcagtgggaagaagtgtgccggccctgggtc tctgggcatcggaagctgatagccagcatgagcagtgactccctgagacatgtgtatggc gagctggacgtgcagattcaaagacgaccttccatgtga

Homo sapiens (human): 2165 Help Entry 2165              CDS       T01001                                  Symbol F13B, FXIIIB Name (RefSeq) coagulation factor XIII B chain   KO K03906   coagulation factor XIII B polypeptide Organism hsa  Homo sapiens (human) Pathway hsa04610   Complement and coagulation cascades hsa05171   Coronavirus disease - COVID-19 Network nt06514  Coagulation cascade   Element N01514   Common pathway of coagulation cascade, F13 activation Disease H00945   Factor XIII deficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09151 Immune system    04610 Complement and coagulation cascades     2165 (F13B)  09160 Human Diseases   09172 Infectious disease: viral    05171 Coronavirus disease - COVID-19     2165 (F13B) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Sushi Sushi_2 Motif Other DBs NCBI-GeneID:  2165 NCBI-ProteinID:  NP_001985 OMIM:  134580 HGNC:  3534 Ensembl:  ENSG00000143278 UniProt:  P05160 LinkDB All DBs Position 1:complement(197038741..197067260) Genome browser AA seq 661 aa AA seqDB search MRLKNLTFIIILIISGELYAEEKPCGFPHVENGRIAQYYYTFKSFYFPMSIDKKLSFFCL AGYTTESGRQEEQTTCTTEGWSPEPRCFKKCTKPDLSNGYISDVKLLYKIQENMRYGCAS GYKTTGGKDEEVVQCLSDGWSSQPTCRKEHETCLAPELYNGNYSTTQKTFKVKDKVQYEC ATGYYTAGGKKTEEVECLTYGWSLTPKCTKLKCSSLRLIENGYFHPVKQTYEEGDVVQFF CHENYYLSGSDLIQCYNFGWYPESPVCEGRRNRCPPPPLPINSKIQTHSTTYRHGEIVHI ECELNFEIHGSAEIRCEDGKWTEPPKCIEGQEKVACEEPPFIENGAANLHSKIYYNGDKV TYACKSGYLLHGSNEITCNRGKWTLPPECVENNENCKHPPVVMNGAVADGILASYATGSS VEYRCNEYYLLRGSKISRCEQGKWSSPPVCLEPCTVNVDYMNRNNIEMKWKYEGKVLHGD LIDFVCKQGYDLSPLTPLSELSVQCNRGEVKYPLCTRKESKGMCTSPPLIKHGVIISSTV DTYENGSSVEYRCFDHHFLEGSREAYCLDGMWTTPPLCLEPCTLSFTEMEKNNLLLKWDF DNRPHILHGEYIEFICRGDTYPAELYITGSILRMQCDRGQLKYPRCIPRQSTLSYQEPLR T NT seq 1986 nt NT seq  +upstreamnt  +downstreamnt atgaggttgaaaaacctgacttttatcatcatattgataatctcaggagaactctatgca gaagagaaaccctgtggttttcctcatgtggaaaatggaagaattgcccaatattactat acttttaaaagcttttactttccaatgagcatagacaaaaaattgtcatttttctgcttg gctggttataccactgaaagtggaagacaagaagagcaaaccacgtgtacaacagaaggc tggtctccagagccaaggtgcttcaaaaaatgcactaagcctgacctgagtaatggttac atctctgatgtaaagttattgtataaaattcaagagaacatgcgttatggttgcgcttca gggtacaaaaccactggagggaaggatgaagaagtggttcaatgtctctctgatggatgg tcttctcaaccaacctgtaggaaagaacatgaaacatgtttggctcctgaattatataat ggaaattattccacaacacagaaaacattcaaagtgaaggacaaagtacaatacgaatgt gctactggctactacacagctggaggaaagaagacagaggaggtagaatgtctcacatac ggatggtctctcacaccaaaatgtaccaaattaaagtgctcttctttaagattaattgaa aatggttattttcatcctgtaaagcaaacctatgaagaaggagatgtcgttcagtttttc tgtcatgaaaattattatctaagtggatctgatttaattcaatgctataactttggttgg tacccagaatctcctgtatgcgaaggaagaagaaacagatgtcctcctccacctctgccc ataaactccaaaattcaaacacattcaacaacttatcgtcatggagaaatagttcatata gaatgtgaacttaattttgagatccatgggtcagcagaaatacgttgtgaagatggaaaa tggacagaacctccaaaatgcattgaaggacaggagaaggtagcctgtgaggaaccaccc ttcattgaaaatggtgcagcaaatttacactctaagatttattacaatggggataaagtg acatatgcatgtaaaagcggctaccttctccatggatcgaatgagataacttgtaatcgt ggaaaatggacacttcctcctgagtgtgttgaaaataatgagaattgtaagcatcctcct gttgtaatgaatggggctgttgcagacgggatattggcaagctatgcaacaggatcctca gtggaatatagatgcaatgaatattacttactgaggggatcaaaaatatctcgttgcgaa caaggaaaatggtcatccccacctgtttgcttggaaccatgtactgttaatgtggattac atgaacagaaataacatagaaatgaagtggaaatatgaagggaaagtcttacatggagat ttaatagattttgtatgtaaacagggatatgacttatctccattaaccccattgtctgaa ttatctgtgcagtgcaacagaggagaagtgaaatatcctttatgtactagaaaagaatct aaaggaatgtgcacatctcctcctcttattaaacatggagtcattattagttcaacagta gacacctatgaaaatggctcttcagtagaatacagatgttttgatcaccatttcctagaa ggatctagggaggcctattgtttagatggaatgtggactacaccaccattgtgtttagag ccatgcacattatcttttactgaaatggaaaagaataatttacttctgaaatgggatttt gacaatagaccacacattttgcatggtgaatatattgagtttatttgtagaggagatact tatccagctgaattatatattactggatctatacttagaatgcaatgtgacagagggcag ttaaaatatccaagatgtattccaagacaaagcactctgtcttatcaagaacccttaaga acatag

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