Homo sapiens (human): 5350 Help Entry 5350              CDS       T01001                                  Symbol PLN, CMD1P, CMH18, PLB Name (RefSeq) phospholamban   KO K05852   phospholamban Organism hsa  Homo sapiens (human) Pathway hsa04020   Calcium signaling pathway hsa04022   cGMP-PKG signaling pathway hsa04024   cAMP signaling pathway hsa04261   Adrenergic signaling in cardiomyocytes hsa04919   Thyroid hormone signaling pathway hsa05414   Dilated cardiomyopathy hsa05415   Diabetic cardiomyopathy Network nt06234  cAMP signaling (cancer) nt06528  Calcium signaling   Element N01345   EP/NE-ADRB-cAMP signaling pathway N01646   Regulation of SERCA Disease H00292   Hypertrophic cardiomyopathy H00294   Dilated cardiomyopathy Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     5350 (PLN)    04024 cAMP signaling pathway     5350 (PLN)    04022 cGMP-PKG signaling pathway     5350 (PLN)  09150 Organismal Systems   09152 Endocrine system    04919 Thyroid hormone signaling pathway     5350 (PLN)   09153 Circulatory system    04261 Adrenergic signaling in cardiomyocytes     5350 (PLN)  09160 Human Diseases   09166 Cardiovascular disease    05414 Dilated cardiomyopathy     5350 (PLN)    05415 Diabetic cardiomyopathy     5350 (PLN)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     5350 (PLN) Transporters [BR:hsa02000]  Other transporters   Pores ion channels [TC:1]    5350 (PLN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Phospholamban Sarcolipin Motif Other DBs NCBI-GeneID:  5350 NCBI-ProteinID:  NP_002658 OMIM:  172405 HGNC:  9080 Ensembl:  ENSG00000198523 UniProt:  P26678 Q5R352 Structure PDBPDBj LinkDB All DBs Position 6:118548296..118561716 Genome browser AA seq 52 aa AA seqDB search MEKVQYLTRSAIRRASTIEMPQQARQKLQNLFINFCLILICLLLICIIVMLL NT seq 159 nt NT seq  +upstreamnt  +downstreamnt atggagaaagtccaatacctcactcgctcagctataagaagagcctcaaccattgaaatg cctcaacaagcacgtcaaaagctacagaatctatttatcaatttctgtctcatcttaata tgtctcttgctgatctgtatcatcgtgatgcttctctga

Homo sapiens (human): 6588 Help Entry 6588              CDS       T01001                                  Symbol SLN Name (RefSeq) sarcolipin   KO K22642   sarcolipin Organism hsa  Homo sapiens (human) Pathway hsa04020   Calcium signaling pathway Network nt06528  Calcium signaling   Element N01646   Regulation of SERCA Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     6588 (SLN)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     6588 (SLN) Transporters [BR:hsa02000]  Other transporters   Pores ion channels [TC:1]    6588 (SLN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Sarcolipin Phospholamban Motif Other DBs NCBI-GeneID:  6588 NCBI-ProteinID:  NP_003054 OMIM:  602203 HGNC:  11089 Ensembl:  ENSG00000170290 UniProt:  O00631 A0A158RFT9 Structure PDBPDBj LinkDB All DBs Position 11:complement(107707378..107712056) Genome browser AA seq 31 aa AA seqDB search MGINTRELFLNFTIVLITVILMWLLVRSYQY NT seq 96 nt NT seq  +upstreamnt  +downstreamnt atggggataaacacccgggagctgtttctcaacttcactattgtcttgattacggttatt cttatgtggctccttgtgaggtcctatcagtactga

Homo sapiens (human): 4295 Help Entry 4295              CDS       T01001                                  Symbol MLN Name (RefSeq) motilin   KO K05265   motilin Organism hsa  Homo sapiens (human) Pathway hsa04080   Neuroactive ligand-receptor interaction hsa04081   Hormone signaling Network nt06528  Calcium signaling   Element N01646   Regulation of SERCA Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09133 Signaling molecules and interaction    04080 Neuroactive ligand-receptor interaction     4295 (MLN)    04081 Hormone signaling     4295 (MLN)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04052 Cytokines and neuropeptides [BR:hsa04052]     4295 (MLN) Cytokines and neuropeptides [BR:hsa04052]  Neuropeptides   GPCR binding    4295 (MLN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Motilin_ghrelin Motilin_assoc Motif Other DBs NCBI-GeneID:  4295 NCBI-ProteinID:  NP_002409 OMIM:  158270 HGNC:  7141 Ensembl:  ENSG00000096395 CPD:  C16047 UniProt:  P12872 Structure PDBPDBj LinkDB All DBs Position 6:complement(33794673..33804003) Genome browser AA seq 115 aa AA seqDB search MVSRKAVAALLVVHVAAMLASQTEAFVPIFTYGELQRMQEKERNKGQKKSLSVWQRSGEE GPVDPAEPIREEENEMIKLTAPLEIGMRMNSRQLEKYPATLEGLLSEMLPQHAAK NT seq 348 nt NT seq  +upstreamnt  +downstreamnt atggtatcccgtaaggctgtggctgctctgctggtggtgcatgtagctgccatgctggcc tcccagacggaagccttcgtccccatcttcacctatggcgaactccagaggatgcaggaa aaggaacggaataaagggcaaaagaaatccctgagtgtatggcagaggtctggggaggaa ggtcctgtagaccctgcggagcccatcagggaagaagaaaacgaaatgatcaagctgact gctcctctggaaattggaatgaggatgaactccagacagctggaaaagtacccggccacc ctggaagggctgctgagtgagatgcttccccagcatgcagccaagtga

Homo sapiens (human): 2006 Help Entry 2006              CDS       T01001                                  Symbol ELN, ADCL1, SVAS, WBS, WS Name (RefSeq) elastin   KO K14211   elastin Organism hsa  Homo sapiens (human) Pathway hsa04820   Cytoskeleton in muscle cells hsa04974   Protein digestion and absorption Network nt06528  Calcium signaling nt06539  Cytoskeleton in muscle cells   Element N01646   Regulation of SERCA N01814   Extracellular matrix - Basal lamina Disease H00553   Congenital supravalvular aortic stenosis H00557   Cutis laxa H01439   Williams-Beuren syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04820 Cytoskeleton in muscle cells     2006 (ELN)  09150 Organismal Systems   09154 Digestive system    04974 Protein digestion and absorption     2006 (ELN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Other DBs NCBI-GeneID:  2006 NCBI-ProteinID:  NP_001265868 OMIM:  130160 HGNC:  3327 Ensembl:  ENSG00000049540 UniProt:  P15502 LinkDB All DBs Position 7:74028173..74069907 Genome browser AA seq 786 aa AA seqDB search MAGLTAAAPRPGVLLLLLSILHPSRPGGVPGAIPGGVPGGVFYPGAGLGALGGGALGPGG KPLKPVPGGLAGAGLGAGLGAFPAVTFPGALVPGGVADAAAAYKAAKAGAGLGGVPGVGG LGVSAGAVVPQPGAGVKPGKVPGVGLPGVYPGGVLPGARFPGVGVLPGVPTGAGVKPKAP GVGGAFAGIPGVGPFGGPQPGVPLGYPIKAPKLPGGYGLPYTTGKLPYGYGPGGVAGAAG KAGYPTGTGVGPQAAAAAAAKAAAKFGAGAAGVLPGVGGAGVPGVPGAIPGIGGIAGVGT PAAAAAAAAAAKAAKYGAAAGLVPGGPGFGPGVVGVPGAGVPGVGVPGAGIPVVPGAGIP GAAVPGVVSPEAAAKAAAKAAKYGARPGVGVGGIPTYGVGAGGFPGFGVGVGGIPGVAGV PGVGGVPGVGGVPGVGISPEAQAAAAAKAAKYGAAGAGVLGGLVPGAPGAVPGVPGTGGV PGVGTPAAAAAKAAAKAAQFGLVPGVGVAPGVGVAPGVGVAPGVGLAPGVGVAPGVGVAP GVGVAPGIGPGGVAAAAKSAAKVAAKAQLRAAAGLGAGIPGLGVGVGVPGLGVGAGVPGL GVGAGVPGFGAGADEGVRRSLSPELREGDPSSSQHLPSTPSSPRVPGALAAAKAAKYGAA VPGVLGGLGALGGVGIPGGVVGAGPAAAAAAAKAAAKAAQFGLVGAAGLGGLGVGGLGVP GVGGLGGIPPAAAAKAAKYGAAGLGGVLGGAGQFPLGGVAARPGFGLSPIFPGGACLGKA CGRKRK NT seq 2361 nt NT seq  +upstreamnt  +downstreamnt atggcgggtctgacggcggcggccccgcggcccggagtcctcctgctcctgctgtccatc ctccacccctctcggcctggaggggtccctggggccattcctggtggagttcctggagga gtcttttatccaggggctggtctcggagcccttggaggaggagcgctggggcctggaggc aaacctcttaagccagttcccggagggcttgcgggtgctggccttggggcagggctcggc gccttccccgcagttacctttccgggggctctggtgcctggtggagtggctgacgctgct gcagcctataaagctgctaaggctggcgctgggcttggtggtgtcccaggagttggtggc ttaggagtgtctgcaggtgcggtggttcctcagcctggagccggagtgaagcctgggaaa gtgccgggtgtggggctgccaggtgtatacccaggtggcgtgctcccaggagctcggttc cccggtgtgggggtgctccctggagttcccactggagcaggagttaagcccaaggctcca ggtgtaggtggagcttttgctggaatcccaggagttggaccctttgggggaccgcaacct ggagtcccactggggtatcccatcaaggcccccaagctgcctggtggctatggactgccc tacaccacagggaaactgccctatggctatgggcccggaggagtggctggtgcagcgggc aaggctggttacccaacagggacaggggttggcccccaggcagcagcagcagcggcagct aaagcagcagcaaagttcggtgctggagcagccggagtcctccctggtgttggaggggct ggtgttcctggcgtgcctggggcaattcctggaattggaggcatcgcaggcgttgggact ccagctgcagctgcagctgcagcagcagccgctaaggcagccaagtatggagctgctgca ggcttagtgcctggtgggccaggctttggcccgggagtagttggtgtcccaggagctggc gttccaggtgttggtgtcccaggagctgggattccagttgtcccaggtgctgggatccca ggtgctgcggttccaggggttgtgtcaccagaagcagctgctaaggcagctgcaaaggca gccaaatacggggccaggcccggagtcggagttggaggcattcctacttacggggttgga gctgggggctttcccggctttggtgtcggagtcggaggtatccctggagtcgcaggtgtc cctggtgtcggaggtgttcccggagtcggaggtgtcccgggagttggcatttcccccgaa gctcaggcagcagctgccgccaaggctgccaagtacggtgctgcaggagcaggagtgctg ggtgggctagtgccaggtgccccaggcgcagtcccaggtgtgccgggcacgggaggagtg ccaggagtggggaccccagcagctgcagctgctaaagcagccgccaaagccgcccagttt gggttagttcctggtgtcggcgtggctcctggagttggcgtggctcctggtgtcggtgtg gctcctggagttggcttggctcctggagttggcgtggctcctggagttggtgtggctcct ggcgttggcgtggctcccggcattggccctggtggagttgcagctgcagcaaaatccgct gccaaggtggctgccaaagcccagctccgagctgcagctgggcttggtgctggcatccct ggacttggagttggtgtcggcgtccctggacttggagttggtgctggtgttcctggactt ggagttggtgctggtgttcctggcttcggggcaggtgcagatgagggagttaggcggagc ctgtcccctgagctcagggaaggagatccctcctcctctcagcacctccccagcaccccc tcatcacccagggtacctggagccctggctgccgctaaagcagccaaatatggagcagca gtgcctggggtccttggagggctcggggctctcggtggagtaggcatcccaggcggtgtg gtgggagccggacccgccgccgccgctgccgcagccaaagctgctgccaaagccgcccag tttggcctagtgggagccgctgggctcggaggactcggagtcggagggcttggagttcca ggtgttgggggccttggaggtatacctccagctgcagccgctaaagcagctaaatacggt gctgctggccttggaggtgtcctagggggtgccgggcagttcccacttggaggagtggca gcaagacctggcttcggattgtctcccattttcccaggtggggcctgcctggggaaagct tgtggccggaagagaaaatga

Homo sapiens (human): 401152 Help Entry 401152            CDS       T01001                                  Symbol ARLN, ALN, C4orf3, HCVFTP1 Name (RefSeq) allregulin   KO K26467   another-regulin Organism hsa  Homo sapiens (human) Pathway hsa04020   Calcium signaling pathway Network nt06528  Calcium signaling   Element N01646   Regulation of SERCA Brite KEGG Orthology (KO) [BR:hsa00001]  09130 Environmental Information Processing   09132 Signal transduction    04020 Calcium signaling pathway     401152 (ARLN)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     401152 (ARLN) Transporters [BR:hsa02000]  Other transporters   Pores ion channels [TC:1]    401152 (ARLN) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  ALN Motif Other DBs NCBI-GeneID:  401152 NCBI-ProteinID:  NP_001001701 OMIM:  620530 HGNC:  19225 Ensembl:  ENSG00000164096 UniProt:  Q8WVX3 LinkDB All DBs Position 4:complement(119296419..119304445) Genome browser AA seq 66 aa AA seqDB search MEVDAPGVDGRDGLRERRGFSEGGRQNFDVRPQSGANGLPKHSYWLDLWLFILFDVVVFL FVYFLP NT seq 201 nt NT seq  +upstreamnt  +downstreamnt atggaggtggacgcaccgggtgttgatggtcgagatggtctccgggagcggcgaggcttt agcgagggagggaggcagaacttcgatgtgaggcctcagtctggggcaaatgggcttccc aaacactcctactggttggacctctggcttttcatccttttcgatgtggtggtgtttctc tttgtgtattttttgccatga

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