Busch Lab

ZMP

epha7

Ensembl ID:
ENSDARG00000004635
ZFIN ID:
ZDB-GENE-030131-3745
Description:
ephrin type-A receptor 7 [Source:RefSeq peptide;Acc:NP_001038444]
Human Orthologue:
EPHA7
Human Description:
EPH receptor A7 [Source:HGNC Symbol;Acc:3390]
Mouse Orthologue:
Epha7
Mouse Description:
Eph receptor A7 Gene [Source:MGI Symbol;Acc:MGI:95276]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa23700 Essential Splice Site Available for shipment Available now
sa37024 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa43437 Nonsense Mutation detected in F1 DNA Not yet available
sa3066 Essential Splice Site F2 line generated Not yet available
sa12035 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa23700
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102788 Essential Splice Site 277 1016 3 18
Genomic Location (Zv9):
Chromosome 20 (position 24989216)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 25060519
GRCz11 20 24959609
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATGTATATGCAAAGCTGGATTTCACCAGAAGGGAGATGCATGTGAACG[T/C]GAGTACTTTATTTTCATTTGCACAAATCTGTTGGCATGTATTAGAACCCA
Long Flanking Sequence:
CTTCCAGGGGTGGTTGGCTCTTGCAAGGAGACGTTCAACTTGTACTACCAGGAAACCGATGTGGAGGTGGGCAGGAATATAAGGGAGAGTCAGTATGTGAAAATTGACACTATAGCCGCGGACGAGAGTTTCACTCAGGGTGACCTGGGGGAAAGAAAGATGAAGCTCAACACAGAGGTGCGTATAATCGGGCCCCTTTCTCGCCGAGGCTTCTACTTAGCCTTTCAGGATGTAGGCGCCTGCATTGCTTTGGTCTCCGTCAAAGTGTATTATAAGAAGTGTTGGTCGATTATTGAGAACCTGGCCACGTTCCCAGATACAGTGACAGGTTCGGAGTTTTCATCTCTGGTGGAAGTGGAGGGCACATGCGTCAACGATGCAGAGGAGGAGGCCGACAATTCTCCCAAAATGCACTGCAGCGCAGAAGGAGAATGGCTGGTGCCCATTGGGAAATGTATATGCAAAGCTGGATTTCACCAGAAGGGAGATGCATGTGAACG[T/C]GAGTACTTTATTTTCATTTGCACAAATCTGTTGGCATGTATTAGAACCCAGCTGATTAACCTTATGTACGACAGAAGATAGGACAATGGAGCAATTAATAAGATATTATTATGTGTAAGACTCGTTTATGTGTGCATTCACCAAGACAGTCCTTGTTCCAATTGCTTGACTGAGTGCCCAAGCATAGAATTATCCCAATTTGAGGTAATTCATCCGAATTATACCAAACCAATGCGAAAGCAAAAACAAACCATGCTGAAAAACATGAAGCAGCTGATGAACGATTAATAAAAGAAAAGCTGAATGAAAAATAACCAGCAACAAAAAACGCATGCTTACTGGGCGAAGATAATAATGATGGATTAAATGTGGGGGCAAAAATCCTTGGCACAGTAATTGAAATCCCTGTAAGTCGTTTGATTTGTGGGCTTTTAATTTATTGCCTTATGCACATTGGCACATATTAAATGATAACTAGCACTCCAGTCTAGCTCTCAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37024
Status:
Mutation detected in F1 DNA
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
ENSDART00000102788 Essential Splice Site 659 1016 11 18
Genomic Location (Zv9):
Chromosome 20 (position 24871149)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 24942452
GRCz11 20 24841542
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGAGCTGGACGCCTCCTGCATTAAGATTGAGAGGGTTATCGGCGCAG[G/A]TGAGCTCTTTTCTTGTCTTCTCCGCTGCCTCGCTTTAGTCGCACACCTCG
Long Flanking Sequence:
TTGTTATTATTATTATTCTGTTGGCCACTTGCCTAGAAACAACACAGTCTTGTGAAACCCATTATCCAATTGAGTGACAGCTATGAACACCACTGCCATGCTGTACTGCTAATACCCTTCCGGCTCCATTGTAAGAAGGTTAACAAGAAAATGTAATAGCGCTTCCAACGGAATATGCAAGGAAAAATAAGAGCATAGGTTTTGTTATTTGATGAAAGAGACCTTTTTGACACTCTATCTCCCTGTTTAGCCCACCGCCCGGCATTTCTACCCTCCAGTAATCGCATCCGTCCATCAAGTAAAACTCTCTGTGTGTATGTGTGTTTGCGGTCTGCATATTTAATCGTAACAGTAATCCTCTTACCCTTCTACAGTCAAATTTCCAGGCACCAAAACCTACATTGACCCTGAAACCTACGAGGACCCGAACAGGGCCGTCCATCAGTTCGCCAAAGAGCTGGACGCCTCCTGCATTAAGATTGAGAGGGTTATCGGCGCAG[G/A]TGAGCTCTTTTCTTGTCTTCTCCGCTGCCTCGCTTTAGTCGCACACCTCGCTCATTTATCACAATGACAACCAAATATTTACACTCTCAATAGCGGCCGGAGCATCTCTCTGGCCTCTTGTTATTGATAGCGCCGCTGTAAGATTGCTTTATAATTAATATGTCTTCTCTTAAGGCCAGGATGCACATAAATGCATCGCCATTGATGAATTGCTGCCGCATCCCTTTTAGTTATAAAGCGTATAACTGTGTTAGCGCGTCCTCTATGTAGCATATCCAATTATCTGAGGTCTCTAGTGTACTGACGCATAGCATGAATGCTGCTGCTAGCGTGACGGATGTGAATGAAGCAGCACAGGTACAGGTGACGTGTTTAACTTGGCCCGGATCACTTTAAACTCAGCTTGCGGGTGGTTTTGTGCTTCACAGGAGAGTTTGGAGAGGTGTGCAGTGGACGACTCAAGCTGCCGGGGAAGAGGGACGTGTCGGTGGCCATTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43437
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102788 Nonsense 949 1016 17 18
Genomic Location (Zv9):
Chromosome 20 (position 24851148)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 24922451
GRCz11 20 24821541
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGACCAGAACACTCCAGATTTCACCTCTTTCCGATTGGTCAGCGAGTG[G/A]TTGGAAGCCATCAAGATGGAGAGATACATGGACAACTTCACAGCCGCCGG
Long Flanking Sequence:
CCTGATAAATAAAGGACTAAGCCGAAGTAAAATCAATGAAGCTGCTTCTAGCCATGATATTTTCAAACCTAAATGGTTATAAGAGACGTATTTAACGTATTATATGCAGCATCTTCTATCAAGGTTCATACTTGGAGGAAAAATGTGCTTAATGCCTTATAAAGCTTGAAGCATTAGACTCGGTACACGATATTTTCCGATCACCATGACACAGAATAGGTACTTGATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTTTATGTTAACTGAGTACAGTACTATATACCATTAGTAATGATACTGCACCTTCTATAGCTCTTATTTTTCTCTTTTTATAACATTTTGTTTATCTTCTTCTTCCTCAGACCCATAAGTCCACTACTTGACCAGAACACTCCAGATTTCACCTCTTTCCGATTGGTCAGCGAGTG[G/A]TTGGAAGCCATCAAGATGGAGAGATACATGGACAACTTCACAGCCGCCGGCTACAGCTCGCTTGAATCTGTGGCTCGAATGACTATCGAGTAAGAGCTCTGATCCCTCGCTCACACTGTCACGCTCCACAGAAATGCATGATCTTTCTAGGAGTCATTTCAGCCCTCAGCTCTCATTCACAATACCATCCTGACATTGCGCTGAATTTTAATCAGATCTCTTTGATTCATCGTGTTGTAGTTAATATGGCTTTTTCTCAGTTTCCTTTTTTGCTTTGCTAATGAAATAGCTCTCGGGCGCTTCATGCTCCATTGCTGTGATTTATGAACGTTGTGTTTCTGCTTTAGGGACGTAATGAGTTTGGGAATCTCCTTGGTGGGCCATCAGAAGAAGATCATGAGCAGTATACAGACTATGAGAGCGCAGATGTTGCATCTTCACGGGACGGGCGTTCAAGTGTGATGGGCATCCACAGCCCCTTCCCAGTTGGATGAAGCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa3066
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102788 Essential Splice Site 979 1016 17 18
Genomic Location (Zv9):
Chromosome 20 (position 24851057)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 24922360
GRCz11 20 24821450
KASP Assay ID:
554-2847.1 (used for ordering genotyping assays)
KASP Sequence:
CMGCCGCCGGCTACAGCTCGCTTGAATCTGTGGCTCGAATGACTATCGAG[T/C]AAGAGCTCTGATMCCTCGCTCACACTGTCACGCTCCACAGAAATGCATGA
Long Flanking Sequence:
TTAACGTATTATATGCAGCATCTTCTATCAAGGTTCATACTTGGAGGAAAAATGTGCTTAATGCCTTATAAAGCTTGAAGCATTAGACTCGGTACACGATATTTTCCGATCACCATGACACAGAATAGGTACTTGATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTTTATGTTAACTGAGTACAGTACTATATACCATTAGTAATGATACTGCACCTTCTATAGCTCTTATTTTTCTCTTTTTATAACATTTTGTTTATCTTCTTCTTCCTCAGACCCATAAGTCCACTACTTGACCAGAACACTCCAGATTTCACCTCTTTCCGATTGGTCAGCGAGTGGTTGGAAGCCATCAAGATGGAGAGATACATGGACAACTTCACAGCCGCCGGCTACAGCTCGCTTGAATCTGTGGCTCGAATGACTATCGAG[T/C]AAGAGCTCTGATCCCTCGCTCACACTGTCACGCTCCACAGAAATGCATGATCTTTCTAGGAGTCATTTCAGCCCTCAGCTCTCATTCACAATACCATCCTGACATTGCGCTGAATTTTAATCAGATCTCTTTGATTCATCGTGTTGTAGTTAATATGGCTTTTTCTCAGTTTCCTTTTTTGCTTTGCTAATGAAATAGCTCTCGGGCGCTTCATGCTCCATTGCTGTGATTTATGAACGTTGTGTTTCTGCTTTAGGGACGTAATGAGTTTGGGAATCTCCTTGGTGGGCCATCAGAAGAAGATCATGAGCAGTATACAGACTATGAGAGCGCAGATGTTGCATCTTCACGGGACGGGCGTTCAAGTGTGATGGGCATCCACAGCCCCTTCCCAGTTGGATGAAGCAGAAGTCTCCAGGACAGCACAGCAAAGTGTGTGACACAGCAAACAAAAATCGGAAAAACTAAACATTTCTCAAAAAAAAAAAAAAAAAATGTTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12035
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000102788 Nonsense 1007 1016 18 18
Genomic Location (Zv9):
Chromosome 20 (position 24850717)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 24922020
GRCz11 20 24821110
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATCAGAAGAAGATCATGAGCAGTATACAGACTATGAGAGCGCAGATGT[T/A]GCATCTTCACGGGACRGGCGTTCAAGTGTGATGGGCAYCCACARCCCCTT
Long Flanking Sequence:
CAGACCCATAAGTCCACTACTTGACCAGAACACTCCAGATTTCACCTCTTTCCGATTGGTCAGCGAGTGGTTGGAAGCCATCAAGATGGAGAGATACATGGACAACTTCACAGCCGCCGGCTACAGCTCGCTTGAATCTGTGGCTCGAATGACTATCGAGTAAGAGCTCTGATCCCTCGCTCACACTGTCACGCTCCACAGAAATGCATGATCTTTCTAGGAGTCATTTCAGCCCTCAGCTCTCATTCACAATACCATCCTGACATTGCGCTGAATTTTAATCAGATCTCTTTGATTCATCGTGTTGTAGTTAATATGGCTTTTTCTCAGTTTCCTTTTTTGCTTTGCTAATGAAATAGCTCTCGGGCGCTTCATGCTCCATTGCTGTGATTTATGAACGTTGTGTTTCTGCTTTAGGGACGTAATGAGTTTGGGAATCTCCTTGGTGGGCCATCAGAAGAAGATCATGAGCAGTATACAGACTATGAGAGCGCAGATGT[T/A]GCATCTTCACGGGACGGGCGTTCAAGTGTGATGGGCATCCACAGCCCCTTCCCAGTTGGATGAAGCAGAAGTCTCCAGGACAGCACAGCAAAGTGTGTGACACAGCAAACAAAAATCGGAAAAACTAAACATTTCTCAAAAAAAAAAAAAAAAAATGTTCCACACCCTTCCGGTGAGATTAACCTTCCAGAACTGGCTGAACAGAATCATTCCTTTGTTTTGGCGAAGGATTTGGGTGAAGGTGCTGAAAACCAAGAGACGAGGACACAGATGAGGACAAAGAACACAGGCGGACAGACCTCCGGATGCTCTCAAGAACTCTTCACGTCACTGAGACGGAGCATTCCAGAGGATTTTTATGCTTTGTACGAACTGTCTTTATCGTCAAAAAAGATTGATTTGCTCATAGTTGCTATAGATTTCATTGATTTTGTTTTTTTTTTTTTTTAATATAAAATAAGCAAATCCGGTTCATAAGGAGTGAATTTGGAGATTTCGTT
Associated Phenotype:
Not determined