ZMP
h2afy
Ensembl ID:
ZFIN IDs:
Description:
H2A histone family, member Y [Source:RefSeq peptide;Acc:NP_001035451]
Human Orthologue:
H2AFY
Human Description:
H2A histone family, member Y [Source:HGNC Symbol;Acc:4740]
Mouse Orthologue:
H2afy
Mouse Description:
H2A histone family, member Y Gene [Source:MGI Symbol;Acc:MGI:1349392]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43732 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14475 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43732
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088826 | Essential Splice Site | 94 | 357 | 4 | 9 |
ENSDART00000124761 | Essential Splice Site | 94 | 357 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 44402269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45546171 |
GRCz11 | 21 | 45761513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATTCTTACTGAGGTTTTCCTCTTCAGATGTCTGTGTTTGTGTGTGCA[G/A]TTGCTGCGGGGCGTCACCATCTCCGCTGGGGGGGTTCTACCCAACATCCA
Long Flanking Sequence:
AAAGAGCATGCTATATCACTGCATTATGATGTCACTGTCCTCACTAAATATATGATATATATATATATATATTTTTTTTTTGCCCTTTTTTTTTTGCCCTTTTTTGTTTTCAAAATGTCCAATATAAGATAAACAAGCCTGCACTGATAACTAGAAGAATTAAAGGAAGTAAATATATATTGGGTGGGCTAATATGATTTGCCAGAGTGCATGTGTGATGCAATAACAGATCTAAGCGTACAGCCTTAACTATCTAATGATTAATTTGCTTAGTTCTATCATTTATAATTTGAATAAGAAAACAACACCAAGAAACTTAAGGTAATCAAAGAATGGTTTTATTAGCTACATCATAGATCAGACTTGATTATTTTTCTTTTCTGGAAGTGGCAGCCTAGAATAAAACGCCACACAGTAGCGACCAAAAATGGAAAATATCCAAAGTTTGATCTTATTCTTACTGAGGTTTTCCTCTTCAGATGTCTGTGTTTGTGTGTGCA[G/A]TTGCTGCGGGGCGTCACCATCTCCGCTGGGGGGGTTCTACCCAACATCCACCCAGAGCTGCTGGCCAAGAAGAGGGAGAGCCGAGGGAAGCTGGAGGCCGCCGTCACTGCTCCACCATCCAGGAAAACTAGCAAAACAGCCGCTGTCAGGAAACTGCACAGCCAGAAGCCCTCTACAGGAAAGGTGCCCACTGAACCACTGCTACTGACTAGTGCTAACCCGTCACCAGGAAACCCAAATCAGATGTGGGGAGGGGAGTAGGTTGTTAGGGGTGAGGTGTTTGAATAACACTGGGTTAGTAACTGTACTGTGGTGTTAGTAAGCTAAGTGTACTATGGACTGGGTTTCGGGTGGCCGCTGCGATCGGATGCTATACCAAAGTTGGCGACCTCTGCCTGATGGGGACAGTACTGTATGATGCTGATATATCTGCTGTGTTTCTGACAGAGGCAGTCTGCTAAAGCGTCCGGTGGACAGAGCGCTTCTGCCGGAGGATTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14475
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088826 | Splice Site, Nonsense | 94 | 357 | 4 | 9 |
ENSDART00000124761 | Splice Site, Nonsense | 94 | 357 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 44402271)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 45546169 |
GRCz11 | 21 | 45761515 |
KASP Assay ID:
2261-6140.1 (used for ordering genotyping assays)
KASP Sequence:
TATTCTTACTGAGRTYTTCCTCTTCAGAWGTCTGTGTTTGTGTGTGCAGT[T/A]GCTGCGGGGCGTCACCATCTCCGCTGGGGGGGTTCTACCCAAYATCCACC
Long Flanking Sequence:
AGAGCATGCTATATCACTGCATTATGATGTCACTGTCCTCACTAAATATATGATATATATATATATATATTTTTTTTTTGCCCTTTTTTTTTTGCCCTTTTTTGTTTTCAAAATGTCCAATATAAGATAAACAAGCCTGCACTGATAACTAGAAGAATTAAAGGAAGTAAATATATATTGGGTGGGCTAATATGATTTGCCAGAGTGCATGTGTGATGCAATAACAGATCTAAGCGTACAGCCTTAACTATCTAATGATTAATTTGCTTAGTTCTATCATTTATAATTTGAATAAGAAAACAACACCAAGAAACTTAAGGTAATCAAAGAATGGTTTTATTAGCTACATCATAGATCAGACTTGATTATTTTTCTTTTCTGGAAGTGGCAGCCTAGAATAAAACGCCACACAGTAGCGACCAAAAATGGAAAATATCCAAAGTTTGATCTTATTCTTACTGAGGTTTTCCTCTTCAGATGTCTGTGTTTGTGTGTGCAGT[T/A]GCTGCGGGGCGTCACCATCTCCGCTGGGGGGGTTCTACCCAACATCCACCCAGAGCTGCTGGCCAAGAAGAGGGAGAGCCGAGGGAAGCTGGAGGCCGCCGTCACTGCTCCACCATCCAGGAAAACTAGCAAAACAGCCGCTGTCAGGAAACTGCACAGCCAGAAGCCCTCTACAGGAAAGGTGCCCACTGAACCACTGCTACTGACTAGTGCTAACCCGTCACCAGGAAACCCAAATCAGATGTGGGGAGGGGAGTAGGTTGTTAGGGGTGAGGTGTTTGAATAACACTGGGTTAGTAACTGTACTGTGGTGTTAGTAAGCTAAGTGTACTATGGACTGGGTTTCGGGTGGCCGCTGCGATCGGATGCTATACCAAAGTTGGCGACCTCTGCCTGATGGGGACAGTACTGTATGATGCTGATATATCTGCTGTGTTTCTGACAGAGGCAGTCTGCTAAAGCGTCCGGTGGACAGAGCGCTTCTGCCGGAGGATTCACCG
Associated Phenotype:
Not determined