ZMP
epha6
Ensembl ID:
ZFIN ID:
Description:
Ephrin receptor [Source:UniProtKB/TrEMBL;Acc:B8A674]
Human Orthologue:
EPHA6
Human Description:
EPH receptor A6 [Source:HGNC Symbol;Acc:19296]
Mouse Orthologue:
Epha6
Mouse Description:
Eph receptor A6 Gene [Source:MGI Symbol;Acc:MGI:108034]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39638 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13485 | Nonsense | Available for shipment | Available now |
| sa38274 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39639 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39638
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042984 | Nonsense | 285 | 996 | 4 | 18 |
| ENSDART00000146042 | None | None | 213 | None | 6 |
| ENSDART00000146530 | Nonsense | 285 | 985 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 33767357)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33402108 |
| GRCz11 | 1 | 34134676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCCTGCAGACCTGGGTTCTACAAAGCCTTTGCAGGAAACATTAAATG[T/A]TCAAAGTGTCCCCCGCACAGCTCCAGCCACGCCGAGGGTTCAGCACAGTG
Long Flanking Sequence:
CTACCATTGAGCCCATTACAGTGAAAAAAAAAATTCCTATACTTACCTGATCTAAAATTGAATGCTTAGTCAAGTTAAAAAATGTGTTAATTCAAAATTCATCGTGTGCCTCACCCCCAAGTGAGTGGTGTCAAGTTTATATATATGTTATAATTTTAACCATGACAAGTCAACTATTGTTGCAAAGGTCTGATAGTCACGCTTTCTTATTTGGTATATGTTTTGAGATAGAAGTGATAACGTGAGAGAATTTGATGGTTTTGTTACATAAATACATAAAAAACATAAAAAAAACTACATTAAAGTGGTTCATAATTGACACACAATGTAATTCAGTTTAAAGGTACTATTTTTTTTTTTTTTAGAAATTTTGCTAATTAAAATAGGTCTGTTTATCCTACCTCTAAAACCTAGAACACACTGACTTTAATTTTCTCTTTGGTTTTGTCCACAGCCTGCAGACCTGGGTTCTACAAAGCCTTTGCAGGAAACATTAAATG[T/A]TCAAAGTGTCCCCCGCACAGCTCCAGCCACGCCGAGGGTTCAGCACAGTGTCACTGCGAGAAGAACTACTACAGAGCCAGCAAAGACCCTCCAACCATGGCCTGCACACGTTAGTCTGCCTACTGCTCTACTTTCATTTTAGTATTCTTTTAAAATGTAACAACAAAAACTGAACATTTCTAATTATACATTTTAATAGAAACAAATGTAAGCAATTTGCATGCTAGAATTTCAGCAGTATAAATATACAACTTACTCTTACAGTATAACCTTACCCAGTGAGTGTTACTTGTGTGTCACACGAGCTTCATGTTAAAGTCACATGTTAAACACTAATGAAATGTGTAGTTTTAAAACATTTCACAGACCAGACTTAAGACTTGTCCTGGACTAAGGGGGCAAATATTCTAAAACTGTAAACCTTGTCTGCATTTTACCTGTTCCTTTACTTCACATTAAAACAAAAAGCTTATACTTACATCTTACACACAGAAAATTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13485
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042984 | Nonsense | 443 | 996 | 6 | 18 |
| ENSDART00000146042 | None | None | 213 | None | 6 |
| ENSDART00000146530 | Nonsense | 443 | 985 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 33809159)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33443910 |
| GRCz11 | 1 | 34176478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACTAATTGTTTTTGTCYTTTAGGTCCGTCTCTGGTAGGTGTGGTGAGA[A/T]AAGACTGGGCATCTCAAACTAGTGTYGCCCTCTCATGGCAGGAAACTGAA
Long Flanking Sequence:
CCATAAGTGTTAACTATTGTCAGTTGTGTGCACCACTTGAGTCTCACAGAGGAGCTTTGAAAACTCGGGAAGAGACAGCAGTGAAAGATCAGAGAGGACCAGACCTAGAGCTTATGTTTGTTTTGCTTTCAGTTTGATGGTAGTTGTCATAAGGGACTCTTGCCGCCCATTTGTTTTGTGTTTATTTATTTATCAAAGTATTTTTAAGTTTGTTGGATCTCCGCCTTTTTCTTCCTGTCGGCCAGGGACTGATCAATCATTACAGTGGTGTCCAAAATGCAGGAGAAGGGTGGACATGTGGTCCAAATCCCCTCAAGGAGAGCAAGTGCTTGGGACTTAACCTAAGTGGGGAAGAAGCCTGTTGGTCTGCCACATGTTGTTGAACTGAGAATTAAACATGGTTTTACCCTGACCTGGGTCTATTCTTTTAATAAAACATAGTTTTATTACTAACTAATTGTTTTTGTCTTTTAGGTCCGTCTCTGGTAGGTGTGGTGAGA[A/T]AAGACTGGGCATCTCAAACTAGTGTCGCCCTCTCATGGCAGGAAACTGAACAGCCACATGCTGCCATCTTGGACTATGAGATTAAGTATTATGAAAAGGTAATTAAACTACTTGATTCTCTAATACTGTAATAATGAACTGTAGGTTAAATCGTTTCCTTTTTCACTTGTTTAGGAACAGGAACAGTTAAGTTATTCATCTACACGTACAAAATCTCCAAGCGTGATAGTGACAGGACTGAAGCCCTCCACAGTTTATGCGTTTCATGTGCGCGCTCGAACCCTCGCTGGCTACAGCAGTTACAGCCCCAAGTTTGAGTTCGCCACAGGAGATGAAGGTAAGCATTTCTCTAAAATGCTTCATTTCAATACCTGTTAGCCTAAAACGCTGTAGTTATGTCCAATTTTCTGAAATTGTGGTCATACCATGTCAGCTGCGTGAATAGAGTTTTAAACAAATGTTTGAAGAGAACGTTTTCTGTTTACTGTGAATGCCCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38274
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042984 | Nonsense | 480 | 996 | 7 | 18 |
| ENSDART00000146042 | None | None | 213 | None | 6 |
| ENSDART00000146530 | Nonsense | 480 | 985 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 33809347)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33444098 |
| GRCz11 | 1 | 34176666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTAGGTTAAATCGTTTCCTTTTTCACTTGTTTAGGAACAGGAACAGT[T/A]AAGTTATTCATCTACACGTACAAAATCTCCAAGCGTGATAGTGACAGGAC
Long Flanking Sequence:
TTTATCAAAGTATTTTTAAGTTTGTTGGATCTCCGCCTTTTTCTTCCTGTCGGCCAGGGACTGATCAATCATTACAGTGGTGTCCAAAATGCAGGAGAAGGGTGGACATGTGGTCCAAATCCCCTCAAGGAGAGCAAGTGCTTGGGACTTAACCTAAGTGGGGAAGAAGCCTGTTGGTCTGCCACATGTTGTTGAACTGAGAATTAAACATGGTTTTACCCTGACCTGGGTCTATTCTTTTAATAAAACATAGTTTTATTACTAACTAATTGTTTTTGTCTTTTAGGTCCGTCTCTGGTAGGTGTGGTGAGAAAAGACTGGGCATCTCAAACTAGTGTCGCCCTCTCATGGCAGGAAACTGAACAGCCACATGCTGCCATCTTGGACTATGAGATTAAGTATTATGAAAAGGTAATTAAACTACTTGATTCTCTAATACTGTAATAATGAACTGTAGGTTAAATCGTTTCCTTTTTCACTTGTTTAGGAACAGGAACAGT[T/A]AAGTTATTCATCTACACGTACAAAATCTCCAAGCGTGATAGTGACAGGACTGAAGCCCTCCACAGTTTATGCGTTTCATGTGCGCGCTCGAACCCTCGCTGGCTACAGCAGTTACAGCCCCAAGTTTGAGTTCGCCACAGGAGATGAAGGTAAGCATTTCTCTAAAATGCTTCATTTCAATACCTGTTAGCCTAAAACGCTGTAGTTATGTCCAATTTTCTGAAATTGTGGTCATACCATGTCAGCTGCGTGAATAGAGTTTTAAACAAATGTTTGAAGAGAACGTTTTCTGTTTACTGTGAATGCCCTGTGATTTCAGTACTTCAGTATTGCTGTTGGGCTTATCTTAGCGCACAGTATGTAAATACCACAGACCTGTCAGCTGGCATTTAGCCGTTTCGGAGTCTTAATAAAATGAGCTTGCAAATGCATAAACACATGTCACTCACCTATCACAAACATGAACCTTATTGAAAAAAAGACTTTATTGTTTTTGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39639
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000042984 | Essential Splice Site | 784 | 996 | 13 | 18 |
| ENSDART00000146042 | Essential Splice Site | 159 | 213 | 4 | 6 |
| ENSDART00000146530 | Essential Splice Site | 784 | 985 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 1 (position 33821758)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 33456509 |
| GRCz11 | 1 | 34189077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTCCAGGGTGCTGGAGGACGACCCGGAGGCAGCTTACACCACCACAG[T/A]AAGCCACACATGCACCCTCTTCATTTACATTCAGGCCTGTTCACAGTTAA
Long Flanking Sequence:
TGAAAATATACTATAAATTTGCATGACATCACAGTTTTTACAATTTTTCATATTTATACTGTAGTTTACTCAAAGACAGACAGTAGGTTTTTCATACCATTGCACATTTTCATACCATTTTTCAGGGCAAACTTCAATGACAATAAGTGATTGGATGAATGAATTACATCCACAGCACTCTTAACATTATAGTCTCTTATTATTTCAAATAAATGTGAATATTTGCATCGTTCATTATGATACAATGCACACTCCTCTCATTTCCCTTTCTTTGGCTCTTCTTCTGTAGAAGCATGACGGGCACTTCACTGTGATCCAGCTGGTTGGTATGCTGCGTGGCATTGCCTCTGGTATGATGTACCTGTCCGACATCGGCTATGTCCACCGAGACCTGGCAGCCCGAAATATTCTAGTGGATGACAACCTGGTATGTAAGGTGTCGGACTTCGGTCTGTCCAGGGTGCTGGAGGACGACCCGGAGGCAGCTTACACCACCACAG[T/A]AAGCCACACATGCACCCTCTTCATTTACATTCAGGCCTGTTCACAGTTAATAACAATCCAGAGAGCCCAAGCTGATTCTCAATCTCTGGAGCTTAGCAGCAATCTGCTTGTTGTGTGTTACGGAATTGGATTGAGTTTATCTAAGCAGTATAACATGAGATTAAGGGCTTACTCTGAATACTGATTGAGTAATTAGTGTCATAATAAGATGCTAAGTGGGTCTGAATGCATCTGAACTTTTTAATACAGGGTTTTAGGGTGGCACAAACTATTGCATTTCAAGAAAACTATCTAACATTATGCAAAAAGCAATCAGAATTAATTTTAATTGGCTAGAAAAGCACAAAGTGATTGGTTGCTGGCAGTGTTGGGGGTATTGAATTGCAAGTAATGTGAGTTATGTAATCTGATTACATTTTTTTCTTATATATACTAGTAAAGTAGTTTTCTAGAAACATTTTTTTTACTAATTAGGAAATTATCTGAGGTATTTATTTTTT
Associated Phenotype:
Not determined