ZMP
epha8
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate Eph family of receptors [Source:UniProtKB/TrEMBL;Acc:Q5SPQ0]
Human Orthologue:
EPHA8
Human Description:
EPH receptor A8 [Source:HGNC Symbol;Acc:3391]
Mouse Orthologue:
Epha8
Mouse Description:
Eph receptor A8 Gene [Source:MGI Symbol;Acc:MGI:109378]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21965 | Nonsense | Available for shipment | Available now |
sa35149 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21965
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 |
---|---|---|---|---|---|
ENSDART00000041800 | Nonsense | 764 | 1027 | 13 | 17 |
ENSDART00000136107 | Nonsense | 466 | 729 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 40099557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 38600967 |
GRCz11 | 11 | 38867863 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTCTCTCCTCCTGCAAACAGAGACACGACGGTCAGTTCACCATTATT[C/T]AGCTGGTTGGGATTCTGCGTGGCATCGCGGCTGGCATGACTTACTTGGCT
Long Flanking Sequence:
AGTAAGTAGTCTTGTATTATATATATATATATATATATATATAATCTGCACTGTAAACCCTATTGTGTTGAAATATAAAACCCCTTCAGCTTCCTGATCACCCTGTCTAGGTTTATCTCTTAATAATGACCGGCTGAATGTACACTGGTCCTCAAGTAAATCAATAATTCACCCACAGCAGAGTAAAAAGTGAAGAAAACAAAAAAACTCCAATTTCTCTTGCATCATCTCTCCAATCTCCTGACATCTTCTTCTCCGTCTTTTTTTCTTCTCTGTGTTTTCTGCGTTCTCCACCAAGGCAAACCGGTAATGATCATCACAGAGTACATGGAGAACGGCTCCTTGGACTCTTTCTTGAGGGTCTGTAAACACGTTTCCGTTTGTTCTCTTATATCTCTGCAGTTCAGCTTCGCCTCAGCGAATCTCCCTGTGAAGCCCAGTTCAATCTTTTCTTTCTCTCCTCCTGCAAACAGAGACACGACGGTCAGTTCACCATTATT[C/T]AGCTGGTTGGGATTCTGCGTGGCATCGCGGCTGGCATGACTTACTTGGCTGATCTGGGTTACGTCCACCGGGATTTGGCCGCCAGAAACGTTCTGGTCAACAGTAATCTGGTGTGCAAGATCTCAGACTTCGGGCTTTCACGAGTGCTGGAGGACGATCCTGATGCAGCGTATACCACCAGCGTGAGTTTAACACACTGTTTACTGTTGTAAAGCATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGAGCCCTTATTAATAAAAAGATTAGGCCGAAAAGAAAATGAATGAATGAATGAATAAAATATAAAACTAAATTTAATGAATAAAATAAAATTAGATTAACACTGCACAACACGGGTAAGATGTCTGATACCGCTTTAATTATTATTGTGAAAAGGCTATATTTTATGTAAACACATGCGCTATTAGTAAATTGCATGTAGTGTATAAGTGCATGTGTAAATGGTGTATGTGTAACGGAGGCCAGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35149
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041800 | Essential Splice Site | 875 | 1027 | 15 | 17 |
ENSDART00000136107 | Essential Splice Site | 577 | 729 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 11 (position 40101993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 38603403 |
GRCz11 | 11 | 38870299 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCAATATCTCACATATAAATTCTTTCTTTTTTTTTTTTTTTTACCTC[A/G]GGTGATCAAGTCCGTAGAGGAGGGTTACCGTCTCCCAGCCCCCATGGGCT
Long Flanking Sequence:
GCCTTTAAACCAAAATAATTTTAAAACGTTTTATTAATAAAAGTATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAATGATATTGTTGTTGTTTTTTGTTGTTGTTATTGATAATAAGCCTTAAAACCAAAATAACATTACAAAACACAAGATAACTAACTATTATTATTATTATTATTATTATTATTATTATTATTATTCTAACAATATCAAGAAGAAGAATAATGACAAAAAAAAAGTAATTTTAACAATCATTTTAATTGTTTCCACAGCTATTAAGGTAGTATTTTTTTATTTTAATTAAAATGAATTATAATATTCTTAACACCTTTGGCTAAATTTATTTTGGCATTAAATTGCAGTAAACTAGAACAAAAATGAACCTGTCTTCATAGAAATGCTACTTTTTTGACAAACTGAAAAGTTAATGCAATATCTCACATATAAATTCTTTCTTTTTTTTTTTTTTTTACCTC[A/G]GGTGATCAAGTCCGTAGAGGAGGGTTACCGTCTCCCAGCCCCCATGGGCTGCCCCGGGGCCCTCCACACCCTCATGCTGGACTGCTGGCAGAAAGACCGCAACGAAAGACCCAAATTCTGCCAGATCGTCACAGTCCTGGACAAACTGATCCGCACTCCTGAAACACTCAAATCAGTGGAAACATTGTGCAGGTGAGCTCCTGTAATTAATACAATCCTAATGGATAATAAAAGCAATGTGTCATTCAATAAAATTATAAATAAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATTTATATATCACTTTAATAATGCACACATCTAACATTATAATGAAAAGCATTCGACTGCTTTCTTAACTTTTTATGCTCATTTAAGACAAAATTAGCTGTTTTGAAAAAAAAAACACCAAGATTGAGATATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAT
Associated Phenotype:
Not determined