Homo sapiens (human): 118788 Help Entry 118788            CDS       T01001                                  Symbol PIK3AP1, BCAP Name (RefSeq) phosphoinositide-3-kinase adaptor protein 1   KO K12230   phosphoinositide 3-kinase adapter protein 1 Organism hsa  Homo sapiens (human) Pathway hsa04151   PI3K-Akt signaling pathway hsa04662   B cell receptor signaling pathway Network nt06537  TCR/BCR signaling   Element N01695   BCR-BCAP/CD19-PI3K signaling pathway Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04151 PI3K-Akt signaling pathway     118788 (PIK3AP1)  09150 Organismal Systems   09151 Immune system    04662 B cell receptor signaling pathway     118788 (PIK3AP1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  DBB TIR_3 Motif Other DBs NCBI-GeneID:  118788 NCBI-ProteinID:  NP_689522 OMIM:  607942 HGNC:  30034 Ensembl:  ENSG00000155629 UniProt:  Q6ZUJ8 Q86YV3 Structure PDBPDBj LinkDB All DBs Position 10:complement(96593315..96720514) Genome browser AA seq 805 aa AA seqDB search MAASGVPRGCDILIVYSPDAEEWCQYLQTLFLSSRQVRSQKILTHRLGPEASFSAEDLSL FLSTRCVVVLLSAELVQHFHKPALLPLLQRAFHPPHRVVRLLCGVRDSEEFLDFFPDWAH WQELTCDDEPETYVAAVKKAISEDSGCDSVTDTEPEDEKVVSYSKQQNLPTVTSPGNLMV VQPDRIRCGAETTVYVIVRCKLDDRVATEAEFSPEDSPSVRMEAKVENEYTISVKAPNLS SGNVSLKIYSGDLVVCETVISYYTDMEEIGNLLSNAANPVEFMCQAFKIVPYNTETLDKL LTESLKNNIPASGLHLFGINQLEEEDMMTNQRDEELPTLLHFAAKYGLKNLTALLLTCPG ALQAYSVANKHGHYPNTIAEKHGFRDLRQFIDEYVETVDMLKSHIKEELMHGEEADAVYE SMAHLSTDLLMKCSLNPGCDEDLYESMAAFVPAATEDLYVEMLQASTSNPIPGDGFSRAT KDSMIRKFLEGNSMGMTNLERDQCHLGQEEDVYHTVDDDEAFSVDLASRPPVPVPRPETT APGAHQLPDNEPYIFKVFAEKSQERPGNFYVSSESIRKGPPVRPWRDRPQSSIYDPFAGM KTPGQRQLITLQEQVKLGIVNVDEAVLHFKEWQLNQKKRSESFRFQQENLKRLRDSITRR QREKQKSGKQTDLEITVPIRHSQHLPAKVEFGVYESGPRKSVIPPRTELRRGDWKTDSTS STASSTSNRSSTRSLLSVSSGMEGDNEDNEVPEVTRSRSPGPPQVDGTPTMSLERPPRVP PRAASQRPPTRETFHPPPPVPPRGR NT seq 2418 nt NT seq  +upstreamnt  +downstreamnt atggcagcctcaggggtgcccagaggatgcgacatcctcatcgtctacagcccggatgcc gaggaatggtgccagtacctgcagaccctgttcctgtccagtcggcaggtccgcagccag aagatactgactcacaggctgggccccgaggcctccttctcggcagaggacctaagcctt ttcctcagcacccgctgtgtcgtggtgctgctgtccgcggagctggtgcagcacttccac aagcccgccttgctgcccctgctgcagagagctttccatcctccgcaccgcgtggtcagg ctgctctgcggcgtgcgggacagcgaggagttcctagacttctttccagattgggcccat tggcaggagctcacctgtgacgatgagccagagacctacgtggcagctgtgaaaaaagcc atttccgaagattctggctgtgactcagtcactgacactgagcctgaggacgagaaggtt gtttcctactcgaagcagcagaacctgccgacggtgacttcacctgggaacctgatggtg gtgcagccggaccgcattcgctgtggggcagaaaccactgtctatgttattgtgagatgt aagctggatgacagggtggcgacagaagcagagttttctcctgaggattctccctctgta aggatggaagccaaggtggagaatgagtacaccatttcagtgaaggctcccaacctttca tctgggaacgtttctctgaagatatattctggagacttagtggtgtgtgaaaccgttatc agctattatactgacatggaagaaattgggaatttattgtccaatgccgcgaatcctgtg gaattcatgtgtcaggcctttaaaattgtgccctacaacacagagacccttgataaactg ctaaccgaatccctgaagaacaatatccctgcaagcggactgcacctctttggaatcaac cagctggaagaagaagatatgatgacaaatcagagggatgaagagctgcccaccctgttg cattttgctgcgaagtatggactgaagaacctcactgccttgttgctcacctgcccagga gccctgcaggcgtacagcgtggccaacaagcatggccactaccccaacaccatcgctgag aaacacggcttcagggacctgcggcagttcatcgacgagtatgtggaaacggtggacatg ctcaagagtcacattaaagaggaactgatgcacggggaggaggctgatgctgtgtacgag tccatggcccacctttccacagacctgcttatgaaatgctcgctcaaccccggctgtgac gaggatctctatgagtccatggctgcctttgtcccagctgccactgaagacctctatgtt gaaatgcttcaggccagtacatctaacccaatccctggagatggtttctctcgggccact aaggactctatgatccgcaagtttttagaaggcaacagcatgggaatgaccaatctggag agagatcagtgccatcttggtcaggaagaagatgtttatcacacggtggatgacgatgag gccttttctgtggacctggccagcaggccccctgtcccagtgcccagaccagagaccact gctcctggtgctcaccagctgcctgacaacgaaccatacatttttaaagtttttgcagaa aaaagtcaagagcggcctgggaatttctacgtttcctcagagagcatcaggaaagggccg cccgtcagaccatggagggacaggccccagtcgagtatatatgacccttttgcgggaatg aaaacgccaggccagcggcagcttatcaccctccaggagcaggtgaagctgggcattgtc aacgtggatgaggctgtgctccacttcaaagagtggcagctcaaccagaagaaacgatcg gagtcctttcgtttccagcaggaaaatcttaaacggctaagagacagcatcacccgaaga cagagagagaagcaaaaatcaggaaagcagacagacttggagatcacggtcccaattcgg cactcacagcacctgcctgcaaaagtggagtttggagtctatgagagtggccccaggaaa agtgtcattccccctaggacggagctgagacgaggagactggaaaacagacagcacctcc agcacagcaagtagcacaagtaaccgctccagcacccggagcctcctcagtgtgagcagc gggatggaaggggacaacgaggataatgaagtccctgaggttaccagaagtcgcagtcca ggccccccacaagtggatgggacacccaccatgtccctcgagagaccccccagggtgcct ccgagagctgcctcacagaggcctccgaccagggagaccttccatcctcctccacctgtt ccacccagaggacgctga

Homo sapiens (human): 930 Help Entry 930               CDS       T01001                                  Symbol CD19, B4, CVID3 Name (RefSeq) CD19 molecule   KO K06465   B-lymphocyte antigen CD19 Organism hsa  Homo sapiens (human) Pathway hsa04151   PI3K-Akt signaling pathway hsa04640   Hematopoietic cell lineage hsa04662   B cell receptor signaling pathway hsa05169   Epstein-Barr virus infection hsa05340   Primary immunodeficiency Network nt06537  TCR/BCR signaling   Element N01695   BCR-BCAP/CD19-PI3K signaling pathway Disease H00088   Common variable immunodeficiency Drug target Axicabtagene ciloleucel:  D11144<US> Blinatumomab:  D09325<JP/US> Brexucabtagene autoleucel:  D11880<US> Denintuzumab:  D11231 Denintuzumab mafodotin:  D11232 Duvortuxizumab:  D11372 Inebilizumab:  D11757<JP/US> Lisocabtagene maraleucel:  D11990<US> Loncastuximab:  D11333 Loncastuximab tesirine:  D11338<US> Obecabtagene autoleucel:  D13022<US> Obexelimab:  D11496 Tafasitamab:  D11601<JP/US> Tisagenlecleucel:  D11386<US> Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04151 PI3K-Akt signaling pathway     930 (CD19)  09150 Organismal Systems   09151 Immune system    04640 Hematopoietic cell lineage     930 (CD19)    04662 B cell receptor signaling pathway     930 (CD19)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     930 (CD19)   09163 Immune disease    05340 Primary immunodeficiency     930 (CD19)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04090 CD molecules [BR:hsa04090]     930 (CD19) CD molecules [BR:hsa04090]  Proteins   930 (CD19) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Ig_3 V-set Ig_2 Motif Other DBs NCBI-GeneID:  930 NCBI-ProteinID:  NP_001761 OMIM:  107265 HGNC:  1633 Ensembl:  ENSG00000177455 UniProt:  P15391 Structure PDBPDBj LinkDB All DBs Position 16:28931971..28939342 Genome browser AA seq 556 aa AA seqDB search MPPPRLLFFLLFLTPMEVRPEEPLVVKVEEGDNAVLQCLKGTSDGPTQQLTWSRESPLKP FLKLSLGLPGLGIHMRPLAIWLFIFNVSQQMGGFYLCQPGPPSEKAWQPGWTVNVEGSGE LFRWNVSDLGGLGCGLKNRSSEGPSSPSGKLMSPKLYVWAKDRPEIWEGEPPCLPPRDSL NQSLSQDLTMAPGSTLWLSCGVPPDSVSRGPLSWTHVHPKGPKSLLSLELKDDRPARDMW VMETGLLLPRATAQDAGKYYCHRGNLTMSFHLEITARPVLWHWLLRTGGWKVSAVTLAYL IFCLCSLVGILHLQRALVLRRKRKRMTDPTRRFFKVTPPPGSGPQNQYGNVLSLPTPTSG LGRAQRWAAGLGGTAPSYGNPSSDVQADGALGSRSPPGVGPEEEEGEGYEEPDSEEDSEF YENDSNLGQDQLSQDGSGYENPEDEPLGPEDEDSFSNAESYENEDEELTQPVARTMDFLS PHGSAWDPSREATSLGSQSYEDMRGILYAAPQLRSIRGQPGPNHEEDADSYENMDNPDGP DPAWGGGGRMGTWSTR NT seq 1671 nt NT seq  +upstreamnt  +downstreamnt atgccacctcctcgcctcctcttcttcctcctcttcctcacccccatggaagtcaggccc gaggaacctctagtggtgaaggtggaagagggagataacgctgtgctgcagtgcctcaag gggacctcagatggccccactcagcagctgacctggtctcgggagtccccgcttaaaccc ttcttaaaactcagcctggggctgccaggcctgggaatccacatgaggcccctggccatc tggcttttcatcttcaacgtctctcaacagatggggggcttctacctgtgccagccgggg cccccctctgagaaggcctggcagcctggctggacagtcaatgtggagggcagcggggag ctgttccggtggaatgtttcggacctaggtggcctgggctgtggcctgaagaacaggtcc tcagagggccccagctccccttccgggaagctcatgagccccaagctgtatgtgtgggcc aaagaccgccctgagatctgggagggagagcctccgtgtctcccaccgagggacagcctg aaccagagcctcagccaggacctcaccatggcccctggctccacactctggctgtcctgt ggggtaccccctgactctgtgtccaggggccccctctcctggacccatgtgcaccccaag gggcctaagtcattgctgagcctagagctgaaggacgatcgcccggccagagatatgtgg gtaatggagacgggtctgttgttgccccgggccacagctcaagacgctggaaagtattat tgtcaccgtggcaacctgaccatgtcattccacctggagatcactgctcggccagtacta tggcactggctgctgaggactggtggctggaaggtctcagctgtgactttggcttatctg atcttctgcctgtgttcccttgtgggcattcttcatcttcaaagagccctggtcctgagg aggaaaagaaagcgaatgactgaccccaccaggagattcttcaaagtgacgcctccccca ggaagcgggccccagaaccagtacgggaacgtgctgtctctccccacacccacctcaggc ctcggacgcgcccagcgttgggccgcaggcctggggggcactgccccgtcttatggaaac ccgagcagcgacgtccaggcggatggagccttggggtcccggagcccgccgggagtgggc ccagaagaagaggaaggggagggctatgaggaacctgacagtgaggaggactccgagttc tatgagaacgactccaaccttgggcaggaccagctctcccaggatggcagcggctacgag aaccctgaggatgagcccctgggtcctgaggatgaagactccttctccaacgctgagtct tatgagaacgaggatgaagagctgacccagccggtcgccaggacaatggacttcctgagc cctcatgggtcagcctgggaccccagccgggaagcaacctccctggggtcccagtcctat gaggatatgagaggaatcctgtatgcagccccccagctccgctccattcggggccagcct ggacccaatcatgaggaagatgcagactcttatgagaacatggataatcccgatgggcca gacccagcctggggaggagggggccgcatgggcacctggagcaccaggtga

Homo sapiens (human): 1380 Help Entry 1380              CDS       T01001                                  Symbol CR2, C3DR, CD21, CR, CVID7, SLEB9 Name (RefSeq) complement C3d receptor 2   KO K04012   complement receptor type 2 Organism hsa  Homo sapiens (human) Pathway hsa04610   Complement and coagulation cascades hsa04640   Hematopoietic cell lineage hsa04662   B cell receptor signaling pathway hsa05169   Epstein-Barr virus infection Network nt06165  Epstein-Barr virus (EBV) nt06537  TCR/BCR signaling   Element N00225   EBV EBNA2 to RBP-Jk-mediated transcription N01695   BCR-BCAP/CD19-PI3K signaling pathway Disease H00080   Systemic lupus erythematosus H00088   Common variable immunodeficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09151 Immune system    04640 Hematopoietic cell lineage     1380 (CR2)    04610 Complement and coagulation cascades     1380 (CR2)    04662 B cell receptor signaling pathway     1380 (CR2)  09160 Human Diseases   09172 Infectious disease: viral    05169 Epstein-Barr virus infection     1380 (CR2)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04090 CD molecules [BR:hsa04090]     1380 (CR2) CD molecules [BR:hsa04090]  Proteins   1380 (CR2) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Sushi F54D1_6_C Motif Other DBs NCBI-GeneID:  1380 NCBI-ProteinID:  NP_001868 OMIM:  120650 HGNC:  2336 Ensembl:  ENSG00000117322 UniProt:  P20023 Structure PDBPDBj LinkDB All DBs Position 1:207454328..207489892 Genome browser AA seq 1033 aa AA seqDB search MGAAGLLGVFLALVAPGVLGISCGSPPPILNGRISYYSTPIAVGTVIRYSCSGTFRLIGE KSLLCITKDKVDGTWDKPAPKCEYFNKYSSCPEPIVPGGYKIRGSTPYRHGDSVTFACKT NFSMNGNKSVWCQANNMWGPTRLPTCVSVFPLECPALPMIHNGHHTSENVGSIAPGLSVT YSCESGYLLVGEKIINCLSSGKWSAVPPTCEEARCKSLGRFPNGKVKEPPILRVGVTANF FCDEGYRLQGPPSSRCVIAGQGVAWTKMPVCEEIFCPSPPPILNGRHIGNSLANVSYGSI VTYTCDPDPEEGVNFILIGESTLRCTVDSQKTGTWSGPAPRCELSTSAVQCPHPQILRGR MVSGQKDRYTYNDTVIFACMFGFTLKGSKQIRCNAQGTWEPSAPVCEKECQAPPNILNGQ KEDRHMVRFDPGTSIKYSCNPGYVLVGEESIQCTSEGVWTPPVPQCKVAACEATGRQLLT KPQHQFVRPDVNSSCGEGYKLSGSVYQECQGTIPWFMEIRLCKEITCPPPPVIYNGAHTG SSLEDFPYGTTVTYTCNPGPERGVEFSLIGESTIRCTSNDQERGTWSGPAPLCKLSLLAV QCSHVHIANGYKISGKEAPYFYNDTVTFKCYSGFTLKGSSQIRCKADNTWDPEIPVCEKE TCQHVRQSLQELPAGSRVELVNTSCQDGYQLTGHAYQMCQDAENGIWFKKIPLCKVIHCH PPPVIVNGKHTGMMAENFLYGNEVSYECDQGFYLLGEKKLQCRSDSKGHGSWSGPSPQCL RSPPVTRCPNPEVKHGYKLNKTHSAYSHNDIVYVDCNPGFIMNGSRVIRCHTDNTWVPGV PTCIKKAFIGCPPPPKTPNGNHTGGNIARFSPGMSILYSCDQGYLLVGEALLLCTHEGTW SQPAPHCKEVNCSSPADMDGIQKGLEPRKMYQYGAVVTLECEDGYMLEGSPQSQCQSDHQ WNPPLAVCRSRSLAPVLCGIAAGLILLTFLIVITLYVISKHRARNYYTDTSQKEAFHLEA REVYSVDPYNPAS NT seq 3102 nt NT seq  +upstreamnt  +downstreamnt atgggcgccgcgggcctgctcggggttttcttggctctcgtcgcaccgggggtcctcggg atttcttgtggctctcctccgcctatcctaaatggccggattagttattattctaccccc attgctgttggtaccgtgataaggtacagttgttcaggtaccttccgcctcattggagaa aaaagtctattatgcataactaaagacaaagtggatggaacctgggataaacctgctcct aaatgtgaatatttcaataaatattcttcttgccctgagcccatagtaccaggaggatac aaaattagaggctctacaccctacagacatggtgattctgtgacatttgcctgtaaaacc aacttctccatgaacggaaacaagtctgtttggtgtcaagcaaataatatgtgggggccg acacgactaccaacctgtgtaagtgttttccctctcgagtgtccagcacttcctatgatc cacaatggacatcacacaagtgagaatgttggctccattgctccaggattgtctgtgact tacagctgtgaatctggttacttgcttgttggagaaaagatcattaactgtttgtcttcg ggaaaatggagtgctgtcccccccacatgtgaagaggcacgctgtaaatctctaggacga tttcccaatgggaaggtaaaggagcctccaattctccgggttggtgtaactgcaaacttt ttctgtgatgaagggtatcgactgcaaggcccaccttctagtcggtgtgtaattgctgga cagggagttgcttggaccaaaatgccagtatgtgaagaaattttttgcccatcacctccc cctattctcaatggaagacatataggcaactcactagcaaatgtctcatatggaagcata gtcacttacacttgtgacccggacccagaggaaggagtgaacttcatccttattggagag agcactctccgttgtacagttgatagtcagaagactgggacctggagtggccctgcccca cgctgtgaactttctacttctgcggttcagtgtccacatccccagatcctaagaggccga atggtatctgggcagaaagatcgatatacctataacgacactgtgatatttgcttgcatg tttggcttcaccttgaagggcagcaagcaaatccgatgcaatgcccaaggcacatgggag ccatctgcaccagtctgtgaaaaggaatgccaggcccctcctaacatcctcaatgggcaa aaggaagatagacacatggtccgctttgaccctggaacatctataaaatatagctgtaac cctggctatgtgctggtgggagaagaatccatacagtgtacctctgagggggtgtggaca ccccctgtaccccaatgcaaagtggcagcgtgtgaagctacaggaaggcaactcttgaca aaaccccagcaccaatttgttagaccagatgtcaactcttcttgtggtgaagggtacaag ttaagtgggagtgtttatcaggagtgtcaaggcacaattccttggtttatggagattcgt ctttgtaaagaaatcacctgcccaccaccccctgttatctacaatggggcacacaccggg agttccttagaagattttccatatggaaccacggtcacttacacatgtaaccctgggcca gaaagaggagtggaattcagcctcattggagagagcaccatccgttgtacaagcaatgat caagaaagaggcacctggagtggccctgctcccctgtgtaaactttccctccttgctgtc cagtgctcacatgtccatattgcaaatggatacaagatatctggcaaggaagccccatat ttctacaatgacactgtgacattcaagtgttatagtggatttactttgaagggcagtagt cagattcgttgcaaagctgataacacctgggatcctgaaataccagtttgtgaaaaagaa acatgccagcatgtgagacagagtcttcaagaacttccagctggttcacgtgtggagcta gttaatacgtcctgccaagatgggtaccagttgactggacatgcttatcagatgtgtcaa gatgctgaaaatggaatttggttcaaaaagattccactttgtaaagttattcactgtcac cctccaccagtgattgtcaatgggaagcacacaggcatgatggcagaaaactttctatat ggaaatgaagtctcttatgaatgtgaccaaggattctatctcctgggagagaaaaaattg cagtgcagaagtgattctaaaggacatggatcttggagcgggccttccccacagtgctta cgatctcctcctgtgactcgctgccctaatccagaagtcaaacatgggtacaagctcaat aaaacacattctgcatattcccacaatgacatagtgtatgttgactgcaatcctggcttc atcatgaatggtagtcgcgtgattaggtgtcatactgataacacatgggtgccaggtgtg ccaacttgtatcaaaaaagccttcatagggtgtccacctccgcctaagacccctaacggg aaccatactggtggaaacatagctcgattttctcctggaatgtcaatcctgtacagctgt gaccaaggctacctgctggtgggagaggcactccttctttgcacacatgagggaacctgg agccaacctgcccctcattgtaaagaggtaaactgtagctcaccagcagatatggatgga atccagaaagggctggaaccaaggaaaatgtatcagtatggagctgttgtaactctggag tgtgaagatgggtatatgctggaaggcagtccccagagccagtgccaatcggatcaccaa tggaaccctcccctggcggtttgcagatcccgttcacttgctcctgtcctttgtggtatt gctgcaggtttgatacttcttaccttcttgattgtcattaccttatacgtgatatcaaaa cacagagcacgcaattattatacagatacaagccagaaagaagcttttcatttagaagca cgagaagtatattctgttgatccatacaacccagccagctga

Homo sapiens (human): 975 Help Entry 975               CDS       T01001                                  Symbol CD81, CVID6, S5.7, TAPA1, TSPAN28 Name (RefSeq) CD81 molecule   KO K06508   CD81 antigen Organism hsa  Homo sapiens (human) Pathway hsa03272   Virion - Hepatitis viruses hsa04662   B cell receptor signaling pathway hsa05144   Malaria hsa05160   Hepatitis C Network nt06537  TCR/BCR signaling   Element N01695   BCR-BCAP/CD19-PI3K signaling pathway Disease H00088   Common variable immunodeficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09120 Genetic Information Processing   09125 Information processing in viruses    03272 Virion - Hepatitis viruses     975 (CD81)  09150 Organismal Systems   09151 Immune system    04662 B cell receptor signaling pathway     975 (CD81)  09160 Human Diseases   09172 Infectious disease: viral    05160 Hepatitis C     975 (CD81)   09174 Infectious disease: parasitic    05144 Malaria     975 (CD81)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04147 Exosome [BR:hsa04147]     975 (CD81)    04090 CD molecules [BR:hsa04090]     975 (CD81) Exosome [BR:hsa04147]  Exosomal proteins   Proteins found in most exosomes    975 (CD81) CD molecules [BR:hsa04090]  Proteins   975 (CD81) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  Tetraspanin Motif Other DBs NCBI-GeneID:  975 NCBI-ProteinID:  NP_004347 OMIM:  186845 HGNC:  1701 Ensembl:  ENSG00000110651 UniProt:  P60033 Structure PDBPDBj LinkDB All DBs Position 11:2376180..2397397 Genome browser AA seq 236 aa AA seqDB search MGVEGCTKCIKYLLFVFNFVFWLAGGVILGVALWLRHDPQTTNLLYLELGDKPAPNTFYV GIYILIAVGAVMMFVGFLGCYGAIQESQCLLGTFFTCLVILFACEVAAGIWGFVNKDQIA KDVKQFYDQALQQAVVDDDANNAKAVVKTFHETLDCCGSSTLTALTTSVLKNNLCPSGSN IISNLFKEDCHQKIDDLFSGKLYLIGIAAIVVAVIMIFEMILSMVLCCGIRNSSVY NT seq 711 nt NT seq  +upstreamnt  +downstreamnt atgggagtggagggctgcaccaagtgcatcaagtacctgctcttcgtcttcaatttcgtc ttctggctggctggaggcgtgatcctgggtgtggccctgtggctccgccatgacccgcag accaccaacctcctgtatctggagctgggagacaagcccgcgcccaacaccttctatgta ggcatctacatcctcatcgctgtgggcgctgtcatgatgttcgttggcttcctgggctgc tacggggccatccaggaatcccagtgcctgctggggacgttcttcacctgcctggtcatc ctgtttgcctgtgaggtggccgccggcatctggggctttgtcaacaaggaccagatcgcc aaggatgtgaagcagttctatgaccaggccctacagcaggccgtggtggatgatgacgcc aacaacgccaaggctgtggtgaagaccttccacgagacgcttgactgctgtggctccagc acactgactgctttgaccacctcagtgctcaagaacaatttgtgtccctcgggcagcaac atcatcagcaacctcttcaaggaggactgccaccagaagatcgatgacctcttctccggg aagctgtacctcatcggcattgctgccatcgtggtcgctgtgatcatgatcttcgagatg atcctgagcatggtgctgtgctgtggcatccggaacagctccgtgtactga

Homo sapiens (human): 8519 Help Entry 8519              CDS       T01001                                  Symbol IFITM1, 9-27, CD225, DSPA2a, IFI17, LEU13 Name (RefSeq) interferon induced transmembrane protein 1   KO K19831   interferon induced transmembrane protein 1 Organism hsa  Homo sapiens (human) Pathway hsa04662   B cell receptor signaling pathway Network nt06537  TCR/BCR signaling   Element N01695   BCR-BCAP/CD19-PI3K signaling pathway Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09151 Immune system    04662 B cell receptor signaling pathway     8519 (IFITM1)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     8519 (IFITM1)    04147 Exosome [BR:hsa04147]     8519 (IFITM1)    04090 CD molecules [BR:hsa04090]     8519 (IFITM1) Transporters [BR:hsa02000]  Other transporters   Accessory factors involved in transport [TC:8]    8519 (IFITM1) Exosome [BR:hsa04147]  Exosomal proteins   Exosomal proteins of colorectal cancer cells    8519 (IFITM1) CD molecules [BR:hsa04090]  Proteins   8519 (IFITM1) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  CD225 MamF_MmsF Motif Other DBs NCBI-GeneID:  8519 NCBI-ProteinID:  NP_003632 OMIM:  604456 HGNC:  5412 Ensembl:  ENSG00000185885 UniProt:  P13164 LinkDB All DBs Position 11:314040..315272 Genome browser AA seq 125 aa AA seqDB search MHKEEHEVAVLGPPPSTILPRSTVINIHSETSVPDHVVWSLFNTLFLNWCCLGFIAFAYS VKSRDRKMVGDVTGAQAYASTAKCLNIWALILGILMTIGFILLLVFGSVTVYHIMLQIIQ EKRGY NT seq 378 nt NT seq  +upstreamnt  +downstreamnt atgcacaaggaggaacatgaggtggctgtgctggggccaccccccagcaccatccttcca aggtccaccgtgatcaacatccacagcgagacctccgtgcccgaccatgtcgtctggtcc ctgttcaacaccctcttcttgaactggtgctgtctgggcttcatagcattcgcctactcc gtgaagtctagggacaggaagatggttggcgacgtgaccggggcccaggcctatgcctcc accgccaagtgcctgaacatctgggccctgattctgggcatcctcatgaccattggattc atcctgttactggtattcggctctgtgacagtctaccatattatgttacagataatacag gaaaaacggggttactag

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