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CACNB2

  • CACNB2
  • Protein-coding gene in humans

    subunit beta-2 is a protein that in humans is encoded by the CACNB2 gene. Mutation in the CACNB2 gene are associated with Brugada syndrome, autism, attention

    CACNB2

    CACNB2

    CACNB2

  • Southeastern gentoo penguin
  • Species of bird

    GRIN2A, MEF2C) as well as muscle structural adaptations (such as BMP4, CACNB2, PDEV4B) supporting efficient movement and foraging behaviour. Vocal learning:

    Southeastern gentoo penguin

    Southeastern gentoo penguin

    Southeastern_gentoo_penguin

  • Voltage-gated calcium channel
  • Group of voltage-gated ion channels permeable to Ca2+

    activity. There are four known genes for the β subunit: CACNB1 (CACNB1), CACNB2 (CACNB2), CACNB3 (CACNB3), CACNB4 (CACNB4). It is hypothesized that the cytosolic

    Voltage-gated calcium channel

    Voltage-gated_calcium_channel

  • Brugada syndrome
  • Heart conduction disease

    genes encode ion channels that carry calcium or potassium ions (CACNA1C, CACNB2, KCND3, KCNE3, KCNJ8, KCNT1), while others generate proteins that interact

    Brugada syndrome

    Brugada syndrome

    Brugada_syndrome

  • N-type calcium channel
  • Protein family

    genes CACNA2D1, CACNA2D2 β – encoded by either one of four genes CACNB1, CACNB2, CACNB3, CACNB4 N-type calcium channels are important in neurotransmitter

    N-type calcium channel

    N-type calcium channel

    N-type_calcium_channel

  • List of human protein-coding genes 1
  • Q8IZS8 2033 CACNA2D4 HGNC:20202; Q7Z3S7 2034 CACNB1 HGNC:1401; Q02641 2035 CACNB2 HGNC:1402; Q08289 2036 CACNB3 HGNC:1403; P54284 2037 CACNB4 HGNC:1404; O00305

    List of human protein-coding genes 1

    List_of_human_protein-coding_genes_1

  • Index of biophysics articles
  • Index of articles on biophysics

    Brush border Bulk movement CACNA1G CACNA1H CACNA1I CACNA2D1 CACNA2D2 CACNB1 CACNB2 CACNB3 CACNB4 CACNG1 CACNG2 CACNG3 CACNG4 CD22 CD33 CHRNA10 CHRNA2 CHRNA3

    Index of biophysics articles

    Index_of_biophysics_articles

  • PLEKHA7
  • Protein-coding gene in the species Homo sapiens

    Huang H, Wen J, Chen G (December 2011). "Genetic variations in CYP17A1, CACNB2 and PLEKHA7 are associated with blood pressure and/or hypertension in She

    PLEKHA7

    PLEKHA7

    PLEKHA7

  • List of OMIM disorder codes
  • 611777; GPD1L Brugada syndrome 3; 611875; CACNA1C Brugada syndrome 4; 611876; CACNB2 Brugada syndrome 5; 612838; SCN1B Brugada syndrome 6; 613119; KCNE3 Brugada

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

  • MiR-137
  • RNA family

    type, alpha 1C subunit), DPYD (Dihydropyrimidine dehydrogenase [NADP+]), CACNB2 (Voltage-dependent L-type calcium channel subunit beta-2), TSSK6 (Testis-Specific

    MiR-137

    MiR-137

    MiR-137

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