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KCNV2

  • KCNV2
  • Protein-coding gene in the species Homo sapiens

    in humans is encoded by the KCNV2 gene. The protein encoded by this gene is a voltage-gated potassium channel subunit. KCNV2 retinopathy, historically referred

    KCNV2

    KCNV2

    KCNV2

  • Retinal cone dystrophy 3B
  • Medical condition

    This disorder is associated with autosomal recessive mutations in the KCNV2 and PDE6H genes. People with the disorder often start showing symptoms when

    Retinal cone dystrophy 3B

    Retinal cone dystrophy 3B

    Retinal_cone_dystrophy_3B

  • Voltage-gated potassium channel
  • Class of transport proteins

    Kv6.2 (KCNG2), Kv6.3 (KCNG3), Kv6.4 (KCNG4) Kvα8.x: Kv8.1 (KCNV1), Kv8.2 (KCNV2) Kvα9.x: Kv9.1 (KCNS1), Kv9.2 (KCNS2), Kv9.3 (KCNS3) Beta subunits are auxiliary

    Voltage-gated potassium channel

    Voltage-gated potassium channel

    Voltage-gated_potassium_channel

  • Cation channel superfamily
  • Family of ion channel proteins

    Kv6.2 (KCNG2), Kv6.3 (KCNG3), Kv6.4 (KCNG4) Kvα8.x: Kv8.1 (KCNV1), Kv8.2 (KCNV2) Kvα9.x: Kv9.1 (KCNS1), Kv9.2 (KCNS2), Kv9.3 (KCNS3) KCa1.1 (BK, Slo1, Maxi-K

    Cation channel superfamily

    Cation channel superfamily

    Cation_channel_superfamily

  • Potassium channel tetramerisation domain
  • Protein domain

    KCND3; KCNF1; KCNG1; KCNG2; KCNG3; KCNG4; KCNRG; KCNS1; KCNS2; KCNS3; KCNV1; KCNV2; KCTD1; KCTD10; KCTD11; KCTD12; KCTD13; KCTD14; KCTD15; KCTD16; KCTD17;

    Potassium channel tetramerisation domain

    Potassium channel tetramerisation domain

    Potassium_channel_tetramerisation_domain

  • List of human protein-coding genes 4
  • Q6UVM3 8060 KCNU1 HGNC:18867; A8MYU2 8061 KCNV1 HGNC:18861; Q6PIU1 8062 KCNV2 HGNC:19698; Q8TDN2 8063 KCP HGNC:17585; Q6ZWJ8 8064 KCTD1 HGNC:18249; Q719H9

    List of human protein-coding genes 4

    List_of_human_protein-coding_genes_4

  • Index of biophysics articles
  • Index of articles on biophysics

    KCNMB4 KCNN1 KCNN2 KCNN4 KCNQ4 KCNQ5 KCNS1 KCNS2 KCNS3 KCNT1 KCNT2 KCNV1 KCNV2 Kenneth Stewart Cole Kim Sung-Hou Kir2.1 Kir2.6 Kir6.2 Kv1.1 KvLQT1 KvLQT2

    Index of biophysics articles

    Index_of_biophysics_articles

  • List of OMIM disorder codes
  • Retinal cone dystrophy 3; 610024; PDE6H Retinal cone dystrophy 3B; 610356; KCNV2 Retinal cone dystrophy 4; 610478; CACNA2D4 Retinal degeneration, late-onset

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

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Online names & meanings

  • FLAVIU
  • Male

    Romanian

    FLAVIU

    Romanian form of Roman Latin Flavius, FLAVIU means "yellow hair."

  • BENETT
  • Male

    English

    BENETT

    Variant spelling of English Bennett, BENETT means "blessed."

  • Jayalakshmii
  • Girl/Female

    Indian, Kannada, Kashmiri

    Jayalakshmii

    Goddess Lakshmi Representing Victory

  • Hughes
  • Boy/Male

    Irish

    Hughes

    Surname.

  • Gulabi
  • Girl/Female

    Hindu, Indian, Parsi, Telugu

    Gulabi

    Colour Name; Rose-coloured

  • Jineen
  • Girl/Female

    French

    Jineen

    or Jeanne.

  • Chinthanaichelvan | சிஂதநைசேலவாந
  • Boy/Male

    Tamil

    Chinthanaichelvan | சிஂதநைசேலவாந

    Intelligent, Thoughtful

  • Shishidhar
  • Boy/Male

    Hindu

    Shishidhar

    Lord Shiva

  • Safi
  • Boy/Male

    Indian

    Safi

    Pure, Clear, Crystal

  • Abhipsita
  • Girl/Female

    Indian

    Abhipsita

    Desired

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