Myo15a<sup>ci2</sup> (myosin XVA; ci2 mutant) - Rat Genome Database

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Gene: Myo15aci2 (myosin XVA; ci2 mutant) Rattus norvegicus
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Symbol: Myo15aci2
Name: myosin XVA; ci2 mutant
RGD ID: 150404269
Description: This allele is a spontaneous mutation of Myo15a containing a base substitution (T->C) in exon 56 of Myo15, leading to an amino acid exchange from leucine (Leu) to proline (Pro) within the carboxy-terminal MyTH4 domain in the proteins' tail region.
ASSOCIATED WITH abnormal a-wave implicit time; abnormal b-wave implicit time; abnormal vision; ASSOCIATED WITH blindness
Type: allele  of Myo15a  
Previously known as: Myo15a^[ci2]
Is Marker For: Strains:   LEW-Myo15aci2/Ztm  
Latest Assembly: mRatBN7.2 - mRatBN7.2 Assembly
Position: No map positions available.


Disease Annotations     Click to see Annotation Detail View
blindness  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
References

References - curated
# Reference Title Reference Citation
1. A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats. Held N, etal., PLoS One. 2011 Mar 29;6(3):e15669. doi: 10.1371/journal.pone.0015669.

Genomics


Related Rat Strains
The following Strains have been annotated to Myo15aci2
LEW-Myo15aci2/Ztm    


Expression

RNA-SEQ Expression


Sequence

Nucleotide Sequences


Additional Information