OMIA 002237-8090 : Coat colour, few melanophore in Oryzias latipes

Mendelian trait/disorder: yes

Mode of inheritance: Autosomal Recessive

Considered a defect: no

Key variant known: yes

Year key variant first reported: 2020

Associated gene:

Symbol Description Species Chr Location OMIA gene details page Other Links
kitlga Oryzias latipes - no genomic information (-..-) kitlga Ensembl

Variants

By default, variants are sorted chronologically by year of publication, to provide a historical perspective. Readers can re-sort on any column by clicking on the column header. Click it again to sort in a descending order. To create a multiple-field sort, hold down Shift while clicking on the second, third etc relevant column headers.

WARNING! Inclusion of a variant in this table does not automatically mean that it should be used for DNA testing. Anyone contemplating the use of any of these variants for DNA testing should examine critically the relevant evidence (especially in breeds other than the breed in which the variant was first described). If it is decided to proceed, the location and orientation of the variant sequence should be checked very carefully.

Breed(s) Variant Phenotype Gene Allele Type of Variant Reference Sequence Chr. g. or m. c. or n. p. Verbal Description EVA ID Year Published PubMed ID(s) Acknowledgements
Few melanophore kitlga indel, gross (>20) Otsuki et al. (2020): "the phenotype of fm medaka is attributable to insertion of a Tcb1-like transposon at the kitlga locus" 2019 31757930

Reference


2019 Otsuki, Y., Okuda, Y., Naruse, K., Saya, H. :
Identification of <i>kit-ligand a</i> as the Gene Responsible for the Medaka Pigment Cell Mutant <i>few melanophore</i>. G3 (Bethesda) :, 2019. Pubmed reference: 31757930. DOI: 10.1534/g3.119.400561.

Edit History


  • Created by Frank Nicholas on 30 Jan 2020
  • Changed by Frank Nicholas on 30 Jan 2020