ZMP
EPHA2 (1 of 2)
Ensembl ID:
Description:
EPH receptor A2 [Source:HGNC Symbol;Acc:3386]
Human Orthologue:
EPHA2
Human Description:
EPH receptor A2 [Source:HGNC Symbol;Acc:3386]
Mouse Orthologue:
Epha2
Mouse Description:
Eph receptor A2 Gene [Source:MGI Symbol;Acc:MGI:95278]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24328 | Nonsense | Available for shipment | Available now |
sa6734 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12623 | Nonsense | Available for shipment | Available now |
sa12632 | Nonsense | Available for shipment | Available now |
sa16254 | Nonsense | Available for shipment | Available now |
sa13554 | Nonsense | Available for shipment | Available now |
sa11198 | Nonsense | Available for shipment | Available now |
sa10796 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24328
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 36 | 979 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24681333)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24467453 |
GRCz11 | 23 | 24393994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAAATTTTGCGTTATTGTCACAGAGGTGTTATTGGATATGGTGGCAT[C/A]GGGAGCTGAGTTGGGTTGGTTGACATCGCCTGTTAAGGATGGGGTGAGTT
Long Flanking Sequence:
GTGAGTACAAATGTTAAGTGTTTTAAATGTTAACGAGTTTGAACGTAGTCTAACCGGTGCGATTAATTGGGGATTTTAATTTGTACCAGCCTACTTTTTATAAATGTTGAAATTGTCAAAAATGTTTACTAAACACATTATACAAATTAAAATTGGCTAAATTCTCTCAATTAATTAAAACAAGACCTTTAGAATTTAAATCAAGTAAAAAAGCTAATTTCTAGTAAGCGAAGTGCGCAATTTCCCTAGCTACTACAAATAATTAACCTGGCGACTTTGCAACACGGGACGTTTGCTTTTTTATTATGACTGACGGAATGTTTTATTATCAGTAGTAACATAGCTTACATTTACTAATTTATTGTTTTGTATGAACCATGTGTATTTTGTGTGTAATCTAGTTAATATAGCTTTATAAATTGCTCTCTATTTTTAAGAAACATGTCATAAATGCAAATTTTGCGTTATTGTCACAGAGGTGTTATTGGATATGGTGGCAT[C/A]GGGAGCTGAGTTGGGTTGGTTGACATCGCCTGTTAAGGATGGGGTGAGTTCACTTCTTATGTACGAGTACTGTTGCATGCATTTCTTTTCGATTGTTTCACTTCATTTGCAAATGAAAAGACTTTTAGCTCTTGTATTTGACTCAAAACATTCCTGGGGACGATTAAAGGATTGCTGGTAGTTTCTTGACTGCTGAACACTTGTAGTCTCGTGCGAATTTAAAGCCCTGTTTTAGTGTCTGTAAAACTGAGGGTGTAATTAACTTTTAAAGTTTGGCGCATATGGTGCTTTGTGTGACGTGAGTTGAAGCTATAATGTTAACTAGAATTTAGAAAAGTAATGGGTTTTGAAATCAAAAGGATTTGCTTTAGTAGAACATAGCTGGTTTAGGTTATAGCTGGTCCTAGTTTAAATTAAATTTGTATTGCATATACCATTTTAGGATAGTCTGGGTTTTGAAACTGATATCTGGTTGACAAACCTAAATTAACTAGTGTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6734
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 42 | 979 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24681314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24467434 |
GRCz11 | 23 | 24393975 |
KASP Assay ID:
554-4960.1 (used for ordering genotyping assays)
KASP Sequence:
GTCACAGAGGTGTTATTGGATATGGTGGCATCGGGAGCTGAGTTGGGTTG[G/A]TTGACATCGCCTGTTAAGGATGGGGTGAGTTCACTTCTTATGTACGAGTA
Long Flanking Sequence:
GTTTTAAATGTTAACGAGTTTGAACGTAGTCTAACCGGTGCGATTAATTGGGGATTTTAATTTGTACCAGCCTACTTTTTATAAATGTTGAAATTGTCAAAAATGTTTACTAAACACATTATACAAATTAAAATTGGCTAAATTCTCTCAATTAATTAAAACAAGACCTTTAGAATTTAAATCAAGTAAAAAAGCTAATTTCTAGTAAGCGAAGTGCGCAATTTCCCTAGCTACTACAAATAATTAACCTGGCGACTTTGCAACACGGGACGTTTGCTTTTTTATTATGACTGACGGAATGTTTTATTATCAGTAGTAACATAGCTTACATTTACTAATTTATTGTTTTGTATGAACCATGTGTATTTTGTGTGTAATCTAGTTAATATAGCTTTATAAATTGCTCTCTATTTTTAAGAAACATGTCATAAATGCAAATTTTGCGTTATTGTCACAGAGGTGTTATTGGATATGGTGGCATCGGGAGCTGAGTTGGGTTG[G/A]TTGACATCGCCTGTTAAGGATGGGGTGAGTTCACTTCTTATGTACGAGTACTGTTGCATGCATTTCTTTTCGATTGTTTCACTTCATTTGCAAATGAAAAGACTTTTAGCTCTTGTATTTGACTCAAAACATTCCTGGGGACGATTAAAGGATTGCTGGTAGTTTCTTGACTGCTGAACACTTGTAGTCTCGTGCGAATTTAAAGCCCTGTTTTAGTGTCTGTAAAACTGAGGGTGTAATTAACTTTTAAAGTTTGGCGCATATGGTGCTTTGTGTGACGTGAGTTGAAGCTATAATGTTAACTAGAATTTAGAAAAGTAATGGGTTTTGAAATCAAAAGGATTTGCTTTAGTAGAACATAGCTGGTTTAGGTTATAGCTGGTCCTAGTTTAAATTAAATTTGTATTGCATATACCATTTTAGGATAGTCTGGGTTTTGAAACTGATATCTGGTTGACAAACCTAAATTAACTAGTGTATTTCAAAACGCTGTTCTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37702
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044918 | Essential Splice Site | 50 | 979 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24681288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24467408 |
GRCz11 | 23 | 24393949 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATCGGGAGCTGAGTTGGGTTGGTTGACATCGCCTGTTAAGGATGGGG[T/C]GAGTTCACTTCTTATGTACGAGTACTGTTGCATGCATTTCTTTTCGATTG
Long Flanking Sequence:
TAGTCTAACCGGTGCGATTAATTGGGGATTTTAATTTGTACCAGCCTACTTTTTATAAATGTTGAAATTGTCAAAAATGTTTACTAAACACATTATACAAATTAAAATTGGCTAAATTCTCTCAATTAATTAAAACAAGACCTTTAGAATTTAAATCAAGTAAAAAAGCTAATTTCTAGTAAGCGAAGTGCGCAATTTCCCTAGCTACTACAAATAATTAACCTGGCGACTTTGCAACACGGGACGTTTGCTTTTTTATTATGACTGACGGAATGTTTTATTATCAGTAGTAACATAGCTTACATTTACTAATTTATTGTTTTGTATGAACCATGTGTATTTTGTGTGTAATCTAGTTAATATAGCTTTATAAATTGCTCTCTATTTTTAAGAAACATGTCATAAATGCAAATTTTGCGTTATTGTCACAGAGGTGTTATTGGATATGGTGGCATCGGGAGCTGAGTTGGGTTGGTTGACATCGCCTGTTAAGGATGGGG[T/C]GAGTTCACTTCTTATGTACGAGTACTGTTGCATGCATTTCTTTTCGATTGTTTCACTTCATTTGCAAATGAAAAGACTTTTAGCTCTTGTATTTGACTCAAAACATTCCTGGGGACGATTAAAGGATTGCTGGTAGTTTCTTGACTGCTGAACACTTGTAGTCTCGTGCGAATTTAAAGCCCTGTTTTAGTGTCTGTAAAACTGAGGGTGTAATTAACTTTTAAAGTTTGGCGCATATGGTGCTTTGTGTGACGTGAGTTGAAGCTATAATGTTAACTAGAATTTAGAAAAGTAATGGGTTTTGAAATCAAAAGGATTTGCTTTAGTAGAACATAGCTGGTTTAGGTTATAGCTGGTCCTAGTTTAAATTAAATTTGTATTGCATATACCATTTTAGGATAGTCTGGGTTTTGAAACTGATATCTGGTTGACAAACCTAAATTAACTAGTGTATTTCAAAACGCTGTTCTAAAAGTGTTACTGGAATGATCTGAGATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12623
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 66 | 979 | 3 | 17 |
ENSDART00000044918 | Nonsense | 66 | 979 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24680111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24466231 |
GRCz11 | 23 | 24392772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTA[T/A]TATGTATGTAACGTGGAKAAAGGAGAACAAGACAACTGGCTCCGTACTAC
Long Flanking Sequence:
TTATAGAAAGTTAATTGCACTCTTAATGAGCTGCTGTTTATTTAAAGAGTTCAACATCTTTCGAATGTATGAAATGCTTTAAACCACAAAGTTCCTTTTATATGGAAGCATTCATTTTACTGCCATGCCACACAATATGAAAACAATGCACCTCTCCTGTAATTAATATCACAGTGGCACATGAAATCAGAGCTAAAACACACATGCACACTGCATGTGAACAGATATGTTACAGCATATTACATCAGTCATGGTGTAGAAAGACTGCTGTATTGTTTCTTGCCAGAAGTTGGTGGGTAATTGACCAGCATCCTCACTACTACTTAAAATTCCACGGTCAGGACATTTTCGTCCTCAGCATTCGTTGGCATCTTTTCTTTGATTTCTTTTTTTTTTCCACAATCTTGGTTTTGACTTTATTGCTAACATCCATTTTTTTATTTCACATTGCAGTGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTA[T/A]TATGTATGTAACGTGGAGAAAGGAGAACAAGACAACTGGCTCCGTACTACATTTATCCAGCGCAACCCTGCTGCATCTCGGGTCTTTGTGGAGCTGCAATTCAATGTCCGCGACTGCAACACTTTCGAAGCAGTCCCGCTTAACTGCAAGGAGACCTTTAACTTGTACACCTCCGAGGCTGATGCGGACATTGGCACTGCTTTCCGCAAAGGCCTGTTCCGAAAGGTGGCCACCATTGCTCCAGATGAAATATCCGACCGTGGAAAGATGAAGATGAACACTGAGACTAAAGTGGTGGATAATCTTTCACGTAAGGGCTTCTACCTGGGCTTCCAGGACATTGGAGCCTGCGTAGCCATCTACTCTGTCAGGGTTTACTATAAAACATGTCCTGCAACAGTGCAGAGCTTGGCAGCATTCCCTGAGACAGTGGCAGGGGGCGAGAATCAAGCATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12632
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 66 | 979 | 3 | 17 |
ENSDART00000044918 | Nonsense | 66 | 979 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24680111)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24466231 |
GRCz11 | 23 | 24392772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTA[T/A]TATGTATGTAACGTGGAKAAAGGAGAACAAGACAACTGGCTCCGTACTAC
Long Flanking Sequence:
TTATAGAAAGTTAATTGCACTCTTAATGAGCTGCTGTTTATTTAAAGAGTTCAACATCTTTCGAATGTATGAAATGCTTTAAACCACAAAGTTCCTTTTATATGGAAGCATTCATTTTACTGCCATGCCACACAATATGAAAACAATGCACCTCTCCTGTAATTAATATCACAGTGGCACATGAAATCAGAGCTAAAACACACATGCACACTGCATGTGAACAGATATGTTACAGCATATTACATCAGTCATGGTGTAGAAAGACTGCTGTATTGTTTCTTGCCAGAAGTTGGTGGGTAATTGACCAGCATCCTCACTACTACTTAAAATTCCACGGTCAGGACATTTTCGTCCTCAGCATTCGTTGGCATCTTTTCTTTGATTTCTTTTTTTTTTCCACAATCTTGGTTTTGACTTTATTGCTAACATCCATTTTTTTATTTCACATTGCAGTGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTA[T/A]TATGTATGTAACGTGGAGAAAGGAGAACAAGACAACTGGCTCCGTACTACATTTATCCAGCGCAACCCTGCTGCATCTCGGGTCTTTGTGGAGCTGCAATTCAATGTCCGCGACTGCAACACTTTCGAAGCAGTCCCGCTTAACTGCAAGGAGACCTTTAACTTGTACACCTCCGAGGCTGATGCGGACATTGGCACTGCTTTCCGCAAAGGCCTGTTCCGAAAGGTGGCCACCATTGCTCCAGATGAAATATCCGACCGTGGAAAGATGAAGATGAACACTGAGACTAAAGTGGTGGATAATCTTTCACGTAAGGGCTTCTACCTGGGCTTCCAGGACATTGGAGCCTGCGTAGCCATCTACTCTGTCAGGGTTTACTATAAAACATGTCCTGCAACAGTGCAGAGCTTGGCAGCATTCCCTGAGACAGTGGCAGGGGGCGAGAATCAAGCATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16254
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 67 | 979 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24680108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24466228 |
GRCz11 | 23 | 24392769 |
KASP Assay ID:
2261-7738.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTAWTA[T/A]GTATGTAACGTGGAKAAAGGAGAACAAGACAACTGGCTCCGTACTACATT
Long Flanking Sequence:
TAGAAAGTTAATTGCACTCTTAATGAGCTGCTGTTTATTTAAAGAGTTCAACATCTTTCGAATGTATGAAATGCTTTAAACCACAAAGTTCCTTTTATATGGAAGCATTCATTTTACTGCCATGCCACACAATATGAAAACAATGCACCTCTCCTGTAATTAATATCACAGTGGCACATGAAATCAGAGCTAAAACACACATGCACACTGCATGTGAACAGATATGTTACAGCATATTACATCAGTCATGGTGTAGAAAGACTGCTGTATTGTTTCTTGCCAGAAGTTGGTGGGTAATTGACCAGCATCCTCACTACTACTTAAAATTCCACGGTCAGGACATTTTCGTCCTCAGCATTCGTTGGCATCTTTTCTTTGATTTCTTTTTTTTTTCCACAATCTTGGTTTTGACTTTATTGCTAACATCCATTTTTTTATTTCACATTGCAGTGGGAGATAGGCCAGCAGGCTGTGAATGGCTCTCTGTTGTATAACTATTA[T/A]GTATGTAACGTGGAGAAAGGAGAACAAGACAACTGGCTCCGTACTACATTTATCCAGCGCAACCCTGCTGCATCTCGGGTCTTTGTGGAGCTGCAATTCAATGTCCGCGACTGCAACACTTTCGAAGCAGTCCCGCTTAACTGCAAGGAGACCTTTAACTTGTACACCTCCGAGGCTGATGCGGACATTGGCACTGCTTTCCGCAAAGGCCTGTTCCGAAAGGTGGCCACCATTGCTCCAGATGAAATATCCGACCGTGGAAAGATGAAGATGAACACTGAGACTAAAGTGGTGGATAATCTTTCACGTAAGGGCTTCTACCTGGGCTTCCAGGACATTGGAGCCTGCGTAGCCATCTACTCTGTCAGGGTTTACTATAAAACATGTCCTGCAACAGTGCAGAGCTTGGCAGCATTCCCTGAGACAGTGGCAGGGGGCGAGAATCAAGCATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13554
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 234 | 979 | 3 | 17 |
ENSDART00000044918 | Nonsense | 234 | 979 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24679609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24465729 |
GRCz11 | 23 | 24392270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGRC[C/T]AACCTCGCATTYATTGCACCACGGATGGGGAATGGGTCGTACCTATGAGC
Long Flanking Sequence:
ATGTATGTAACGTGGAGAAAGGAGAACAAGACAACTGGCTCCGTACTACATTTATCCAGCGCAACCCTGCTGCATCTCGGGTCTTTGTGGAGCTGCAATTCAATGTCCGCGACTGCAACACTTTCGAAGCAGTCCCGCTTAACTGCAAGGAGACCTTTAACTTGTACACCTCCGAGGCTGATGCGGACATTGGCACTGCTTTCCGCAAAGGCCTGTTCCGAAAGGTGGCCACCATTGCTCCAGATGAAATATCCGACCGTGGAAAGATGAAGATGAACACTGAGACTAAAGTGGTGGATAATCTTTCACGTAAGGGCTTCTACCTGGGCTTCCAGGACATTGGAGCCTGCGTAGCCATCTACTCTGTCAGGGTTTACTATAAAACATGTCCTGCAACAGTGCAGAGCTTGGCAGCATTCCCTGAGACAGTGGCAGGGGGCGAGAATCAAGCATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGGC[C/T]AACCTCGCATTTATTGCACCACGGATGGGGAATGGGTCGTACCTATGAGCCAATGCCAGTGCGAATCCGGGTTCGAAGCCCTTGAAGATACTTGCCAAGGTGAGACATACATTTCTTTGTTTGCTTTTCACAGATCAAGGCCAGCAACAGCTGTTGTCACTTAAGATTTCGGGTCTGGGTCAGGAGTATTGACTAGAATTTCACATGGATTGTGATTAGCATTTCGAATTATATAATTAGGTGAATTTTTCTATTATGTTACAGAAATGATTTATACTATTGTGGATTTTATCTATCTTTACCATGCATGCTTGTGATTTGTTTTCTGTCTATAAAAGAAATGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATCTCCCCATTGTTGTTTTTATTCACTGTAATTATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11198
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 234 | 979 | 3 | 17 |
ENSDART00000044918 | Nonsense | 234 | 979 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24679609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24465729 |
GRCz11 | 23 | 24392270 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGRC[C/T]AACCTCGCATTYATTGCACCACGGATGGGGAATGGGTCGTACCTATGAGC
Long Flanking Sequence:
ATGTATGTAACGTGGAGAAAGGAGAACAAGACAACTGGCTCCGTACTACATTTATCCAGCGCAACCCTGCTGCATCTCGGGTCTTTGTGGAGCTGCAATTCAATGTCCGCGACTGCAACACTTTCGAAGCAGTCCCGCTTAACTGCAAGGAGACCTTTAACTTGTACACCTCCGAGGCTGATGCGGACATTGGCACTGCTTTCCGCAAAGGCCTGTTCCGAAAGGTGGCCACCATTGCTCCAGATGAAATATCCGACCGTGGAAAGATGAAGATGAACACTGAGACTAAAGTGGTGGATAATCTTTCACGTAAGGGCTTCTACCTGGGCTTCCAGGACATTGGAGCCTGCGTAGCCATCTACTCTGTCAGGGTTTACTATAAAACATGTCCTGCAACAGTGCAGAGCTTGGCAGCATTCCCTGAGACAGTGGCAGGGGGCGAGAATCAAGCATTGCGGGAGGTGGCTGGAAGTTGTGTCAAAAATGCTATCAGTGAGGGC[C/T]AACCTCGCATTTATTGCACCACGGATGGGGAATGGGTCGTACCTATGAGCCAATGCCAGTGCGAATCCGGGTTCGAAGCCCTTGAAGATACTTGCCAAGGTGAGACATACATTTCTTTGTTTGCTTTTCACAGATCAAGGCCAGCAACAGCTGTTGTCACTTAAGATTTCGGGTCTGGGTCAGGAGTATTGACTAGAATTTCACATGGATTGTGATTAGCATTTCGAATTATATAATTAGGTGAATTTTTCTATTATGTTACAGAAATGATTTATACTATTGTGGATTTTATCTATCTTTACCATGCATGCTTGTGATTTGTTTTCTGTCTATAAAAGAAATGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATATCTCCCCATTGTTGTTTTTATTCACTGTAATTATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10796
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 |
---|---|---|---|---|---|
ENSDART00000044918 | Nonsense | 671 | 979 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 23 (position 24650380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 24436690 |
GRCz11 | 23 | 24363231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACAGAGAAACAGAGGCAAGACTTCCTGAGTGAGGCCAGTATCATGGGA[C/T]AGTTCTCACACCAGAACATCATCCGGCTGGAAGGGGTTGTCACTAAATGT
Long Flanking Sequence:
ACTTACAAATAAAACAAACAAACACTAAATTAGCCCTAAATCATTTAAAATTTTTTATAGTATACATCTCAAGCATCAGCATTAAATGAGAAGATCTGTGTGTTGTGGTCAGGTTTTCACTCTTATTATCCCTCAGCAACTCTCCTCTAGTTTCTGTTCGCTTGTTATACACAGATTCTCATGGCCTTTCTGACCTCCCGTCCCATGAATCCACTCGCTAACTGTGCATGCTGGTTATAATTTCAAAGGATCTCCTGCATGTTGTTAAATAACCCCTATTTGTCAGGGGACGTGTTTGAGGAGTTTCCGTGTGGAATGTGTTTTATCTGATGGCGTTTGGTGGTGTGTGTTTTTATGCTGTAGGTGAGTTTGGAGAGGTGTATCGAGGAATCCTCAAAGCTCCCAGCCGGAAAGAAGTGGCTGTAGCTATTAAAACGCTAAAGCCGGGATACACAGAGAAACAGAGGCAAGACTTCCTGAGTGAGGCCAGTATCATGGGA[C/T]AGTTCTCACACCAGAACATCATCCGGCTGGAAGGGGTTGTCACTAAATGTAAGTGCAGTCGACTGCTAATTGTTAAAATAGTAATAATAATAATCATTATCATCATCATATTTAACAACATAATAATAATACTATTTATTAACATTACAAATAATAAAATAATATAGTAATACTTTAAAATAGTTATGTAACAGATTGACATTAATAAAATAAACAATAAAAAGAGGTAATAATGGTCAAATTATGTTAATTGAATAATGGTCCTAATGATGCATTTTATGTAATTTTATGTAATTCAAATGAACACGTAACTATATTATACTAAAATAAATATGACCAAAAAATGAATTAATTTGTATTAAGTCGTCGGGGTGACAACAGAGGTGATGGTCCAAGCACAGTTTTTACAGCTTAATCAGACAGGCAATGGTCACACAGGAGCAAACAGTATCATGAGGGTAATCCAAAGAGTAGTCGTGGTCACAGGCAAAGAGATTAAT
Associated Phenotype:
Not determined