ZMP
epha3l
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate EPH receptor A3 (EPHA3) [Source:UniProtKB/TrEMBL;Acc:Q1L8W1]
Human Orthologue:
EPHA3
Human Description:
EPH receptor A3 [Source:HGNC Symbol;Acc:3387]
Mouse Orthologue:
Epha3
Mouse Description:
Eph receptor A3 Gene [Source:MGI Symbol;Acc:MGI:99612]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10403 | Essential Splice Site | Available for shipment | Available now |
| sa18943 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa25420 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11139 | Nonsense | Available for shipment | Available now |
| sa16865 | Nonsense | Available for shipment | Available now |
| sa38730 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41384 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10403
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006787 | Essential Splice Site | 52 | 712 | 1 | 14 |
| ENSDART00000006787 | Essential Splice Site | 52 | 712 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16828387)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16528322 |
| GRCz11 | 9 | 16536034 |
KASP Assay ID:
2260-1652.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAAAYTACTTTCGAGCAGACGAGGACCCTGCCTCCATGGCCTGCTCTC[G/A]TACGTGCTCTTATCTTACATACCCACATGTTTGTTTTGYTTAAACTTTAC
Long Flanking Sequence:
ATTTTGTAAGATGTTAAGATGTTTTCTAAAACTTTCACAGACACATATTACTGAGAACCAGTGTCGGGAAATATTAATTCACTTTTATGAGGTCATTAACATTCCCTTACATGTACATGTGGCCCACTGTACACACATCTTAGCACTGTTGGTACTGTTATTAGTTTGTTTAAGTCTGTGCAGATGATTAAATATCTTTCCATTGTGTCCGCCAATGCATATGCTCATGTGAAATGATTCGCTTCATTAAAAGTGGCAGTATTGTAATAGGGTAACGAATGGCCCTGTTTGCCATAGTCTCCCAGCACCCTAATTTGTCTTCCCTTCTGTTGTTGCACCCACAGCCTGCCGGCCCGGTTTCTATAAGGCTTCATCTGGGAACGTCAAGTGCTCCAAGTGTCCTCCACACAGCTACACACACCAGGAGGGATCTGTACACTGCGGCTGTGAGAAAAATTACTTTCGAGCAGACGAGGACCCTGCCTCCATGGCCTGCTCTC[G/A]TACGTGCTCTTATCTTACATACCCACATGTTTGTTTTGTTTAAACTTTACCTAAATTCATTGCAAAATCATGATGATTTACAGCATCATGTTGGTCTAAACCTGTATAAAAAATTTTATCTGTGGCTCTCAACCTAAATTTCGAGGAATTTTTGAAAAATTGTTGGTTTTCTTGGACAATAAATTAATGACCAAGTGAATAAATGTTTTTTAGAATAGATAACTTTAAACAATATGTTCAAGATAAGAGTCAATAGGTTGGAAAACACTTCAAAATCTCTTGTTCTGGAAAAAAATCAAAAATAACAAGTATAAAACAAATATAAAAAATCATATTTTAAAGAATGTTTATAGCCTAAGCTTCTCTTTTTTTTATCTATACAATAACTGCTTTCACGAAAGAACTTTTACATACATCCTGGAACTATTGGCCAGCTGTCTATGTACCCAGCTGTCTTCTCACTACACTGTAGTAAAATATCTGTAAATTGACAGTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18943
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 |
|---|---|---|---|---|---|
| ENSDART00000006787 | Essential Splice Site | 52 | 712 | 1 | 14 |
| ENSDART00000006787 | Essential Splice Site | 52 | 712 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16828387)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16528322 |
| GRCz11 | 9 | 16536034 |
KASP Assay ID:
2260-1652.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAATTACTTTCGAGCAGACGAGGACCCTGCCTCCATGGCCTGCTCTC[G/A]TACGTGCTCTTATCTTACATACCCACATGTTTGTTTTGTTTAAACTTTAC
Long Flanking Sequence:
ATTTTGTAAGATGTTAAGATGTTTTCTAAAACTTTCACAGACACATATTACTGAGAACCAGTGTCGGGAAATATTAATTCACTTTTATGAGGTCATTAACATTCCCTTACATGTACATGTGGCCCACTGTACACACATCTTAGCACTGTTGGTACTGTTATTAGTTTGTTTAAGTCTGTGCAGATGATTAAATATCTTTCCATTGTGTCCGCCAATGCATATGCTCATGTGAAATGATTCGCTTCATTAAAAGTGGCAGTATTGTAATAGGGTAACGAATGGCCCTGTTTGCCATAGTCTCCCAGCACCCTAATTTGTCTTCCCTTCTGTTGTTGCACCCACAGCCTGCCGGCCCGGTTTCTATAAGGCTTCATCTGGGAACGTCAAGTGCTCCAAGTGTCCTCCACACAGCTACACACACCAGGAGGGATCTGTACACTGCGGCTGTGAGAAAAATTACTTTCGAGCAGACGAGGACCCTGCCTCCATGGCCTGCTCTC[G/A]TACGTGCTCTTATCTTACATACCCACATGTTTGTTTTGTTTAAACTTTACCTAAATTCATTGCAAAATCATGATGATTTACAGCATCATGTTGGTCTAAACCTGTATAAAAAATTTTATCTGTGGCTCTCAACCTAAATTTCGAGGAATTTTTGAAAAATTGTTGGTTTTCTTGGACAATAAATTAATGACCAAGTGAATAAATGTTTTTTAGAATAGATAACTTTAAACAATATGTTCAAGATAAGAGTCAATAGGTTGGAAAACACTTCAAAATCTCTTGTTCTGGAAAAAAATCAAAAATAACAAGTATAAAACAAATATAAAAAATCATATTTTAAAGAATGTTTATAGCCTAAGCTTCTCTTTTTTTTATCTATACAATAACTGCTTTCACGAAAGAACTTTTACATACATCCTGGAACTATTGGCCAGCTGTCTATGTACCCAGCTGTCTTCTCACTACACTGTAGTAAAATATCTGTAAATTGACAGTGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25420
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006787 | Nonsense | 239 | 712 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16867048)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16566983 |
| GRCz11 | 9 | 16574695 |
KASP Assay ID:
554-7721.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTACACTGAACGGACTGAAACCTGACACCACCTACCTGCTGCAGATC[A/T]GAGCTCGTACTGCTGCCGGTTACGGCAGCAGCAGCCGCAAGTTTGAGTTC
Long Flanking Sequence:
GTCCAAAGACTTGCCTAATTAACTGAACTTGTATAGTTACGTTAAATTAACCTATGCTTTTTAATCAAATATTATGACAGTATCTTGCAAAATAATGTAAATTATACAAAACTACCATCATGGCAATGACAAAAGAAATGTGTAATTACTAAAAAAGTGTTATGTTAAAAAATGTCTAACAAGTCACAGGAAGGCTAATACGTTTGCCTTTATCTTTATGATTATGATCCAAACAGGTTTTTTAAACATTTCCTTTTAATATTGACTAAAAATTTTATTAAATACAAATAAAAAAAATGCATTTGCAGTTAATCCAATTCATTAATATGCCATTTATATTGCAAGCAAAACATACTCAAACTAACACATTTCTCTTGTTTCTGTTCTTACTTTGTTTTCTAAAGCAGGAACAAGAGACGAGCTACACCATCCTGAGGTCGAAGGGTACAAATGTTACACTGAACGGACTGAAACCTGACACCACCTACCTGCTGCAGATC[A/T]GAGCTCGTACTGCTGCCGGTTACGGCAGCAGCAGCCGCAAGTTTGAGTTCGAGACCAGCCCAGACTGTAAGCATTTACATATTTACTGTCATACTGCTTCCTATTTACAGTCCCATTCACCAGTCCATTCCCAGCTGTGCAGAACAAAGAACAATACAGACAACGACTCATGATTCCCTTGGCTTCTCAGCCCATACACCATGTTGCAAGTCATTCACACAGTATAAACCACTTGGTAAAACGATACAAGCTGCAGCTTTTGTCCCGTGATGGCAGCTGTTGTCTGCAGCACTATTAAGCACTTAGACTGAACATTCTGTAAACGTTGTATTGTGGAGCAGCATTGCTGAAGGCCTTTTATCTAATGAAAACCTTTATTGGAAATCAATGCACACTCATGTAATGAAATGATACCATGAGTGGCTCTCCACAGATTTCTGAGCACAATCTGGAATCTATAGGCGCCTCAGCGCATATAGCTAGTGTGAAATGTCCACCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11139
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006787 | Nonsense | 496 | 712 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16885671)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16585606 |
| GRCz11 | 9 | 16593318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAACATCCTGGTCAACAGCAATCTAKTGTGTAAAGTGTCAGACTTCGGCT[T/A]GTCCAGAGTGTTAGAGGATGACCCAGAAGCGGMCTACACAACAAGAGTAA
Long Flanking Sequence:
ACCAGTGTAAACACCGTGAGCCTGCCAGTGGGCTTCAGTTCAGATATGCAGTCGGCGATGGGTTCTTGTGTACATCCCATTTATATTCTTCAACAAGTTGCCACACACCAGAAAAACCAGAAAAGACAGTCAAACGTTCCTAAACATTCAAGGATCTGCTACTCTTAGCAAAATGATTCCATGAGTTGTGAGATGACTGGGAAATATTCAGGCAGTGTTTTGTAGATATGAGTCATCAAAAGTCCCTTTGTGTTTTGTAAAGCATAGCATGAATTATGTTTATACAGTAGACATTAAACACCTTATTTGACTTTTCCCTTCTTCCCATCTATGTCAGAAACACGACGCCCAGTTCACAGTGATTCAGCTGGTGGGCATGCTACGTGGCATTGCGTCTGGGATGAAGTATCTGTCGGATATGGGTTACGTGCACAGAGACCTAGCCGCTCGGAACATCCTGGTCAACAGCAATCTAGTGTGTAAAGTGTCAGACTTCGGCT[T/A]GTCCAGAGTGTTAGAGGATGACCCAGAAGCGGCCTACACAACAAGAGTAAGTTAACACCTGTAGGAACAAGGAGAGTTTTTTTTTTTTTTGTTTTGTTTTGTTTTTAAATAACAAGCCAATATTCTCTTTCAACATAAAGTTAAAGCTTATACCAGTAAAACTACTGGTATAATTTTTGATTTTTTTTTTATTAGTGCAATCAAATGATTTTCTGTCATAAATGTCCTTATACTGTGTATTTATAACTTACTTCACATACATACTGTACATAAAATACACAATATGTAAAAACAAAACTCACACATTTATACAGTATACACATTTTAAACATAGTTTTTTAAGAACTAATTTCTAAAAACTAATTTATTTTATCTGCAATAATCACAGTAAATATATTTATACTTATGTTACTTTGTAGATACTAATAGTCAGCCTAAAGTGCAATTTAAAGGCTTATTATGTTAACTAAAAAAAATAAAAACATATATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16865
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006787 | Nonsense | 508 | 712 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16885708)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16585643 |
| GRCz11 | 9 | 16593355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGACTTCGGCTWGTCCAGAGTGTTAGAGGATGACCCAGAAGCGGMCTA[C/A]ACAACAAGAGTAAGTTAACAYCTGTAGGAAMAAGGAGAGTTTTTTTTTTT
Long Flanking Sequence:
GTTCAGATATGCAGTCGGCGATGGGTTCTTGTGTACATCCCATTTATATTCTTCAACAAGTTGCCACACACCAGAAAAACCAGAAAAGACAGTCAAACGTTCCTAAACATTCAAGGATCTGCTACTCTTAGCAAAATGATTCCATGAGTTGTGAGATGACTGGGAAATATTCAGGCAGTGTTTTGTAGATATGAGTCATCAAAAGTCCCTTTGTGTTTTGTAAAGCATAGCATGAATTATGTTTATACAGTAGACATTAAACACCTTATTTGACTTTTCCCTTCTTCCCATCTATGTCAGAAACACGACGCCCAGTTCACAGTGATTCAGCTGGTGGGCATGCTACGTGGCATTGCGTCTGGGATGAAGTATCTGTCGGATATGGGTTACGTGCACAGAGACCTAGCCGCTCGGAACATCCTGGTCAACAGCAATCTAGTGTGTAAAGTGTCAGACTTCGGCTTGTCCAGAGTGTTAGAGGATGACCCAGAAGCGGCCTA[C/A]ACAACAAGAGTAAGTTAACACCTGTAGGAACAAGGAGAGTTTTTTTTTTTTTTGTTTTGTTTTGTTTTTAAATAACAAGCCAATATTCTCTTTCAACATAAAGTTAAAGCTTATACCAGTAAAACTACTGGTATAATTTTTGATTTTTTTTTTATTAGTGCAATCAAATGATTTTCTGTCATAAATGTCCTTATACTGTGTATTTATAACTTACTTCACATACATACTGTACATAAAATACACAATATGTAAAAACAAAACTCACACATTTATACAGTATACACATTTTAAACATAGTTTTTTAAGAACTAATTTCTAAAAACTAATTTATTTTATCTGCAATAATCACAGTAAATATATTTATACTTATGTTACTTTGTAGATACTAATAGTCAGCCTAAAGTGCAATTTAAAGGCTTATTATGTTAACTAAAAAAAATAAAAACATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38730
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 |
|---|---|---|---|---|---|
| ENSDART00000006787 | Nonsense | 527 | 712 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16891912)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16591847 |
| GRCz11 | 9 | 16599559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGTGGCAAGATTCCAATCCGATGGACTGCGCCAGAAGCCATCGCCTA[T/A]CGCAAGTTCACCTCAGCCAGTGACGTATGGAGCTATGGGATTGTGCTATG
Long Flanking Sequence:
AAACAACATTTGCACTGATACTTTCTTGAAAATAATTATTTTGTTATTGACTTAATTCCTTAAGAATTTATTTTTAAACATGTTGAACCCTTACATAACCCAAAAAGTATCCTTAAAGAAAAAGATTTGTTTTTTAATGTTTTTATATTTTAAATCATCTGAACATGTACGTTGTATGTGTACATTTTAATAAATTGTTTCACTTAAAACTCAAGTTCTAATGCTACCTTATTAGAGCTTGTTTGTTTAGAATTTCATTCATAAGATGCCACTGTCAGAAATTCGACACCATACATATGTCTTGATTTAAACTCCGCTGCACACAAATTACACTATCTGGCATCTGAAAGTTAGAGTATGTGCTTGTTATTCCACTAATTGTAAAAATATTTGTTTGAATATTGCCACAGATGGCAAAATTTTCCCTGACAGATGGTTTTTGTCTGTTTACAGGGTGGCAAGATTCCAATCCGATGGACTGCGCCAGAAGCCATCGCCTA[T/A]CGCAAGTTCACCTCAGCCAGTGACGTATGGAGCTATGGGATTGTGCTATGGGAGGTCATGTCTTACGGAGAAAGGCCTTATTGGGAGATGTCCAATCAGGACGTGAGTAAAACGACTGTCAGCAAAGAAATCCAACATCTTCCTTGCCAAAATATAGCAGTGTGGCATATGTTCAGAGGTCGATTTGATTTGAAAAGCTTTCAAAAATGCACATTTTATATTCCACAGAAAGAAAGAAAACGGCATGAAAATGAGCCCTTAAATAAACTTTTAAATAAGGGATATGTAATGTTAGTTAATGTATTTATTAACATGAGCAATGCTTGTACTGCATTTTCTCATTATAGTTTAACTTTTACTAATAAATTACCACCCCTGTGCTTAATAACATTAGTTAATGCACTGTGAGTTAACATGAAGAGTGAACAACTCATAGTTAATTACTTGTTCATGCTAGTAAATACATGAACGAATATTATCTACATGCCCCATGTTGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41384
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006787 | Nonsense | 658 | 712 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 9 (position 16904915)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 16604850 |
| GRCz11 | 9 | 16612562 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTCACACAATGGGAGATTGGCTGGAGAGTGCGAGGACGTTGCCCTGT[A/T]AAGATGCATTCAGCGGTGTTAGCTACAGCTCCTGTGATACACTGGCCAAA
Long Flanking Sequence:
AAGGTTGCTGGTTCGAGCCTTAGCTTGCATGTTCTCCCAGTGTTCGCTTGGGTTTCCTCTGGGTGCTCCAGTTTCTACCACAAGTCCAAAGACAGGTGAATTGAGTATAGGTGAATTGGGTAAGCTAAATTGTCTGTCTTGTATGTGAGTGTGTATGGATGTTTCCCAGTGATGGGTAACAGCTGTAAAGGCATACGCTGCATAAAACTGTATAAAATATACTGGATAGGTTGACAGTTTATTCAGCTGTGGTGACCCCAGATTAATAAAAGGACCAAGCCAAAAATGAATGAATACATTTTATTGAGACTACTGGTGCAGAAATGCTTATTTGCAGTTTTGATTTTTAATATGTATACTGTATAACTAACAGTACATCCTGCATGTGTTTTTAATCTGTTTCTAGACCGGTAAATTTACTTCTGGACAGGAACAGCACTGATATCACTTCTTTTCACACAATGGGAGATTGGCTGGAGAGTGCGAGGACGTTGCCCTGT[A/T]AAGATGCATTCAGCGGTGTTAGCTACAGCTCCTGTGATACACTGGCCAAAACCTCAGCAGAGTAAGAAACTTTCACAATACATGCTTTCAGGTTTTATATTATACTTGCAAAAATGATTGACATAATTAGGATGTCATTAAAAGAAGGTTCTTTTGATTGAAAGTAGTTATTTTAAAAAGTAAAACTGTTCAGATGTCTACAGTTTTCACTGTACATTGCATTAATTAAATGTGGCCTTGGTAGACAAAAGAGACTTCTTTTATAAACCTTTAAAAAATCTTAATTCTTCTTAATTGGAGATTGGTGTATATTCAAATACCATTGCTCAAAGGTTTTAGAAAAACATACATTTAATTAGTTTTTATTTATTTATTTTTTTTTTTAAGAAGTCCACCAAGCATGCATTTATTTCAGTCAAAGGTGGGGTTTTCTCCGAGTGCTCTGGTTTCCCCCACAGCTCAAAGACAGGCGGTATAAGTCAATTGGATTAACTAAATTG
Associated Phenotype:
Not determined