Phenotype ontology term - FYPO:0007477 - abnormal epigenetic heterochromatin inheritance
Term summary
- ID
- FYPO:0007477
- Name
- abnormal epigenetic heterochromatin inheritance
- Ontology or CV name
- Phenotype
- Definition
- A phenotype in which the stable inheritance of heterochromatic structure is abnormal in regions of the genome where heterochromatin is normally maintained over successive generations.
Annotation
Multi-locus phenotype
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Single locus phenotype
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- clr3delta
- clr4-F449Y(aa)
- clr4-I418P(aa)
- clr4-W31G(aa)
- dpb3delta
- dpb4delta
- fft3delta
- hht1-K14R(K15R aa)
- hht3-K9R(K10R aa)
- mcm2-2a(Y80A,Y89A aa)
- mcm2-G221V(aa)
- mrc1-784-788A(R784A,K785A,R786A,R788A aa)
- mrc1-806-811A(R806A,R807A,K809A,K811A aa)
- mrc1-E712K(aa)
- mrc1-E763R,D767K(aa)
- mrc1-K769*(aa)[Overexpression]
- mrc1-K785E(aa)
- mrc1-L774P(aa)
- mrc1-M755A,F758A,L774A(aa)
- mrc1-V752*(aa)
- mrc1-W620*(aa)
- mrc1-delta(730-797)(aa)
- mrc1delta
- pds5delta
- pob3delta
- snf5-CDx2(Chromodomain fusion)
- swi1-delta832-894(aa)
- swi1delta
- swi3delta
- swi7-2A(F61A,D65A aa)
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