QuickView for MYL3;jsessionid=A8BE1F5ED01BC44C7CC9201436BA3063 (gene)

Gene Symbol:

MYL3 Homo sapiens

Full name:

myosin light chain 3

Synonyms:

CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl, myosin light chain 3, CMLC1, cardiac myosin light chain 1, myosin light chain 1, slow-twitch muscle B/ventricular isoform, myosin, light chain 3, alkali; ventricular, skeletal, slow, myosin, light polypeptide 3, alkali; ventricular, skeletal, slow, ventricular myosin alkali light chain, ventricular myosin light chain 1, ventricular/slow twitch myosin alkali light chain

Genomic Location:

Chr 3: 46874361-46879977

Description:

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.

MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Danio rerio ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

TGGAAA_NFAT_Q4_01 ,  STAT4_01 ,  GNCF_01 ,  AREB6_02 ,  RSRFC4_01 ,  TGANNYRGCA_TCF11MAFG_01 ,  SYATTGTG_UNKNOWN ,  YTATTTTNR_MEF2_02 ,  CATTGTYY_SOX9_B1 ,  RSRFC4_Q2 ,  CTTTGA_LEF1_Q2 ,  IRF1_Q6 ,  NKX22_01 ,  TGACCTY_ERR1_Q2 ,  TAAWWATAG_RSRFC4_Q2 ,  TCF4_Q5 ,  GGGAGGRR_MAZ_Q6 ,  RP58_01 ,  RREB1_01 ,  P53_02 ,  CAGGTG_E12_Q6 ,  TGCCAAR_NF1_Q6 ,  SOX5_01 ,  RORA1_01 ,  CEBP_Q3 ,  GRE_C ,  CAGCTG_AP4_Q5 ,  PAX4_03 ,  ERR1_Q2 ,  COREBINDINGFACTOR_Q6 ,  TGACCTTG_SF1_Q6 ,  GGGTGGRR_PAX4_03

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Cytogenetic Map:

3p21.31

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