ZMP
eya1
Ensembl ID:
ZFIN ID:
Description:
eyes absent homolog 1 [Source:RefSeq peptide;Acc:NP_571268]
Human Orthologue:
EYA1
Human Description:
eyes absent homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:3519]
Mouse Orthologue:
Eya1
Mouse Description:
eyes absent 1 homolog (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:109344]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11723 | Nonsense | Available for shipment | Available now |
sa10957 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11723
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012253 | Nonsense | 344 | 587 | 10 | 17 |
ENSDART00000081595 | Nonsense | 366 | 609 | 11 | 19 |
ENSDART00000134221 | Nonsense | 349 | 592 | 10 | 17 |
ENSDART00000136443 | Nonsense | 366 | 609 | 11 | 18 |
ENSDART00000142058 | None | None | 86 | None | 4 |
The following transcripts of ENSDARG00000014259 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 13875949)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 13827397 |
GRCz11 | 24 | 13971816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATCATCGTTTTCCATTCCTTGCTCACAGGATCTTACGYCAACCGATTC[G/T]GAAGGGTAAGTCGTGTATTTTAAATGCAAACACAGGYAAATATTGCGGCA
Long Flanking Sequence:
TTTTTGTTGATTATTTTTATTGAAACTTATACAAGTGTTCACTTTTTATAGTGTACATTCTACACATAAATGTTTACAAGTGCTATATATATCTTGATCATGCAGTTCAGATTTAGAGTTGCGGTCATTTCATTAATGAAACCTAAATCTCAGCAAGGTTTCGGCCCCATTAGCGAGCTGACATCATAGCATGTTAACAAATCTAGTTAATTAGTTTGTTGGTATTGATTGTGTTAATGCATTGAGGGCAGGAGACGGATGGTCCGAAGGTGGTTGGTCTCGCAGTCGAGGGCTTCTGTGGTGACCATCAGTGCTGTGTATCTAGTGATCCCAGAGCGCATGAATCTGTGCACCCTTCATATTGACTATCAGATCGTCTTGCATGCTGAGTGAAGCATTGATTTTGCTCTTTCTTTTCTCAGCGCGTGTTCATTTGGGACTTGGATGAAACAATCATCGTTTTCCATTCCTTGCTCACAGGATCTTACGCCAACCGATTC[G/T]GAAGGGTAAGTCGTGTATTTTAAATGCAAACACAGGCAAATATTGCGGCAGAGTTTAGAAAAATACACAGAAAAGAGGGTCTGTTTGGGTACACGGTCCAGCTTCGAGGAACTTGGAGTTCAGTGTAATTGTTTCTTTTTTTAATAAGATTGTGGAGGCCTCGCAGGCATTCGGCTCGGCCTGCAGCTGTCTCAGTTATGTAGCTGCTACAGGCATGGATTACAAACCAGTTGCACAGAGAATGTCCATTGACACTTCCTAAGGGTTTTTTTTTTTTTTTTAGACCTTCAGAAACGTTTCATTGTTAAGTTTAATTAAGTGTTTGTCTTAACTGCACTTTAAGTCAGGGTTGTGTATTGTGGCATAATTAAAGAAAAAAGTTCACTTTAAATAAACAAAGTTGACTTTTGGTCTTCGGGCATTAAAATGACTAAACTTAATTCATTACAAAAATCAAATAATAAAGAAAAGGTACACTGTAAAAAAAAGTTGACTCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10957
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012253 | Nonsense | 420 | 587 | 13 | 17 |
ENSDART00000081595 | Nonsense | 442 | 609 | 14 | 19 |
ENSDART00000134221 | Nonsense | 425 | 592 | 13 | 17 |
ENSDART00000136443 | Nonsense | 442 | 609 | 14 | 18 |
ENSDART00000142058 | None | None | 86 | None | 4 |
The following transcripts of ENSDARG00000014259 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 13910278)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 13861726 |
GRCz11 | 24 | 14006145 |
KASP Assay ID:
2261-8534.1 (used for ordering genotyping assays)
KASP Sequence:
GATTCCACGCTGCTGCCACCAGTGCCAAYCTGTGTCTGGCCACCGGYGTA[C/T]GAGGAGGCGTGGACTGGATGAGAAAGCTCGCGTTCCGCTACAGACGAGTA
Long Flanking Sequence:
GAGAGATCCCCCTAGTGGTAGTGGCCAAATGGGTTGGACCCCGGTCCCCTGATGATGGTGTTTATTTTTATTAAGATTTAGCAGGTGGGGGGTTACAGGCTGGAAGTGGTTGAGGGTTGATTTGAGCTTAGCCTTCAGTTGGGAATTCCTCAGTTGTTGACATTATTCACTTCATGGATTCAAGCTGCCAAATCTCACAAAGTTCTGCACATGAACACCATTCACTAAATCACTATGTTTTAATAATCCAATCAGCTCATCGTGTTGTTTCTGCTTGTTTTCAGGAATGCGATCAAGTCCATATTGACGATGTGTCGTCGGATGACAATGGGCAGGATTTAAGGTACACTTAGCACAGTATTAGCCATTTCACAGTTCACTTTGACCGAAGTCAAACTCATTGTCTCTTTCTCTCCTCTCTGTTTAGCACATACAATTTTAGCACAGACGGATTCCACGCTGCTGCCACCAGTGCCAACCTGTGTCTGGCCACCGGCGTA[C/T]GAGGAGGCGTGGACTGGATGAGAAAGCTCGCGTTCCGCTACAGACGAGTAAAAGAAATTTACACCACCTATAAAAATAACGTCGGAGGTAATCCCCCAATAAACTGCTTTGCTAAAATTGCTAGGGAAGAGGGGTGGCGTGTCAACAAAAGCACTCATAGGTTTCTCAAATAATCCCTTATGTAGAAACCACTTGGTCTGAGTAAATTTCGAAATTTCTTAAAGTATTTGCGGGACGGTCCAACTCAAACAATGTTTCTGTTCATTTCAGGTCTGCTTGGCCCGGCCAAAAGGGAAGCCTGGTTGCAATTGCGAGCAGAAATTGAAGCCCTGACTGACTCCTGGTTAACACTGGCACTGAAAGCACTAACATTAATCCACTCAAGGTAGGCCTTAGCACAAGCAAATTATATAGAGCCCATCAGTGATACACATAAATCAGCGAGAGGCATGAATAATGGTGCGCTTCATACTCCAGTGCCCTTAAGGATGATTATTATT
Associated Phenotype:
Not determined