Homo sapiens (human): 4635 Help Entry 4635              CDS       T01001                                  Symbol MYL4, ALC1, AMLC, GT1, PRO1957 Name (RefSeq) myosin light chain 4   KO K12750   myosin light chain 4 Organism hsa  Homo sapiens (human) Pathway hsa04260   Cardiac muscle contraction hsa04261   Adrenergic signaling in cardiomyocytes hsa04371   Apelin signaling pathway hsa04814   Motor proteins hsa04820   Cytoskeleton in muscle cells Network nt06539  Cytoskeleton in muscle cells   Element N01817   Myosin thick filament Disease H00731   Atrial fibrillation Drug target Aficamten:  D12253 Delocamten:  D12949 Brite KEGG Orthology (KO) [BR:hsa00001]  09140 Cellular Processes   09142 Cell motility    04814 Motor proteins     4635 (MYL4)    04820 Cytoskeleton in muscle cells     4635 (MYL4)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    04812 Cytoskeleton proteins [BR:hsa04812]     4635 (MYL4) Cytoskeleton proteins [BR:hsa04812]  Eukaryotic cytoskeleton proteins   Actin filaments / Microfilaments    Actin-binding proteins     Myosins      4635 (MYL4) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  EF-hand_9 EF-hand_6 EF-hand_7 EF-hand_1 AIF-1 Motif Other DBs NCBI-GeneID:  4635 NCBI-ProteinID:  NP_001002841 OMIM:  160770 HGNC:  7585 Ensembl:  ENSG00000198336 UniProt:  P12829 LinkDB All DBs Position 17:47189433..47227650 Genome browser AA seq 197 aa AA seqDB search MAPKKPEPKKEAAKPAPAPAPAPAPAPAPAPEAPKEPAFDPKSVKIDFTADQIEEFKEAF SLFDRTPTGEMKITYGQCGDVLRALGQNPTNAEVLRVLGKPKPEEMNVKMLDFETFLPIL QHISRNKEQGTYEDFVEGLRVFDKESNGTVMGAELRHVLATLGEKMTEAEVEQLLAGQED ANGCINYEAFVKHIMSG NT seq 594 nt NT seq  +upstreamnt  +downstreamnt atggctcccaagaagcctgagcctaagaaggaggcagccaagccagctccagctccagct ccagcccctgcaccagcccctgccccagctcctgaggctcccaaggaacctgcctttgac cccaagagtgtaaagatagacttcactgccgaccagattgaagagttcaaagaggccttt tcattgtttgaccggaccccgactggagagatgaagatcacctacggccagtgcggggat gtactgcgggccctgggccagaaccctaccaatgccgaggtgctgcgtgtgctgggcaag cccaagcctgaagagatgaatgtcaagatgctggactttgagacgttcttgcccatcctg cagcacatttcccgcaacaaggagcagggcacctatgaggacttcgtggagggcctgcgt gtctttgacaaggagagcaatggcacggtcatgggtgctgagcttcggcacgtccttgcc accctgggagagaagatgactgaggctgaagtggagcagctgttagctgggcaagaggat gccaatggctgcatcaattatgaagcctttgtcaagcacatcatgtcagggtga

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