ZMP
plekha7b
Ensembl ID:
ZFIN ID:
Human Orthologue:
PLEKHA7
Human Description:
pleckstrin homology domain containing, family A member 7 [Source:HGNC Symbol;Acc:27049]
Mouse Orthologue:
Plekha7
Mouse Description:
pleckstrin homology domain containing, family A member 7 Gene [Source:MGI Symbol;Acc:MGI:2445094]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18677 | Nonsense | Available for shipment | Available now |
sa11681 | Nonsense | Available for shipment | Available now |
sa11132 | Nonsense | Available for shipment | Available now |
sa31573 | Nonsense | Available for shipment | Available now |
sa18155 | Nonsense | Available for shipment | Available now |
sa40897 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20950 | Nonsense | Available for shipment | Available now |
sa9044 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34078 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18677
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 188 | 1267 | 7 | 27 |
ENSDART00000110605 | Nonsense | 188 | 1267 | 7 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28282325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26885264 |
GRCz11 | 7 | 27156457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTTAGGACAGCTCAGGCATGAGACTGTGGAAGAGGAAATGGTTTGTGT[T/A]GTCTGATTACTGCTTGTTTTATTATAAAGGTGAGTTATTGGATTCTACTT
Long Flanking Sequence:
ATCAAAAGGAACCCCAATGTCCCGGTGGTGGTGAGAGGATGGCTCTACAAACAGGTGCGAGTCTCAAAAGTAGATTACAGAGTTTGATTTTGATCTAAACTAAATGGTGCTCAGATGTTAGATTACATCTTAAATACGGCAGGCCTTATGACAAACTAAGACCCACAGTCACAGTAAACTGATTGATAGTTTTATTTAACATATATTAAACACATATTCTGTATGAAGGAGGAATTCATTTAAATGCAGCATACTGTATATTGGTTTGTAATAACAGATAGTGCCCTGACTGTTTTTAAATAATTATGAATGGGTCATTTAAAGTTGATGATTAGCGTAACAAAACATTTGCTACTAAATGTACCTTGTTATCTTATAATGTAGTTTATTAGATTATGCATACAGTTGAAACTGATAAATACTGTGAATTGAAATGTTATACTTCATCCACCCTTAGGACAGCTCAGGCATGAGACTGTGGAAGAGGAAATGGTTTGTGT[T/A]GTCTGATTACTGCTTGTTTTATTATAAAGGTGAGTTATTGGATTCTACTTAAATTAGCTGTAATTATCTAAAACAGGTCTCTAATTTTATTGCCTCATAATCACTTTTTTCATAAGTAAATCACTCTGTTTATGTAACACATTATTATGAGTGCCTATAATAAATGTTAATAGCAGATTTATATACTAAATAGCATTAAACAGTTTTGTTTTTAACATTGTTTATGTTAAGTAATGCATTATTTTTTATATAATTTCATCAGAAAAATTGGAATATCACTTGCTTACTGCCATTTGTTTCTGTTTAAGAATGAATTAATTGCATCATTTTTCAGCTGTAACTAACCATTTTCAGGCTTTTTCTTATAACATCTGTCCTTTATTCACAGATAGTCGAGAGGAGACTGTTTTGGGCAGTATACCTCTGCCCAGCTATGTAATTTCTCCCGTGGGACCCGAGGATCACATCAGCCGCAAGTATGCCTTCAAGGTAAGAGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11681
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 188 | 1267 | 7 | 27 |
ENSDART00000110605 | Nonsense | 188 | 1267 | 7 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28282325)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26885264 |
GRCz11 | 7 | 27156457 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTTAGGACAGCTCAGGCATGAGACTGTGGAAGAGGAAATGGTTTGTGT[T/A]GTCTGATTACTGCTTGTTTTATTATAAAGGTGAGTTATTGGATTCTACTT
Long Flanking Sequence:
ATCAAAAGGAACCCCAATGTCCCGGTGGTGGTGAGAGGATGGCTCTACAAACAGGTGCGAGTCTCAAAAGTAGATTACAGAGTTTGATTTTGATCTAAACTAAATGGTGCTCAGATGTTAGATTACATCTTAAATACGGCAGGCCTTATGACAAACTAAGACCCACAGTCACAGTAAACTGATTGATAGTTTTATTTAACATATATTAAACACATATTCTGTATGAAGGAGGAATTCATTTAAATGCAGCATACTGTATATTGGTTTGTAATAACAGATAGTGCCCTGACTGTTTTTAAATAATTATGAATGGGTCATTTAAAGTTGATGATTAGCGTAACAAAACATTTGCTACTAAATGTACCTTGTTATCTTATAATGTAGTTTATTAGATTATGCATACAGTTGAAACTGATAAATACTGTGAATTGAAATGTTATACTTCATCCACCCTTAGGACAGCTCAGGCATGAGACTGTGGAAGAGGAAATGGTTTGTGT[T/A]GTCTGATTACTGCTTGTTTTATTATAAAGGTGAGTTATTGGATTCTACTTAAATTAGCTGTAATTATCTAAAACAGGTCTCTAATTTTATTGCCTCATAATCACTTTTTTCATAAGTAAATCACTCTGTTTATGTAACACATTATTATGAGTGCCTATAATAAATGTTAATAGCAGATTTATATACTAAATAGCATTAAACAGTTTTGTTTTTAACATTGTTTATGTTAAGTAATGCATTATTTTTTATATAATTTCATCAGAAAAATTGGAATATCACTTGCTTACTGCCATTTGTTTCTGTTTAAGAATGAATTAATTGCATCATTTTTCAGCTGTAACTAACCATTTTCAGGCTTTTTCTTATAACATCTGTCCTTTATTCACAGATAGTCGAGAGGAGACTGTTTTGGGCAGTATACCTCTGCCCAGCTATGTAATTTCTCCCGTGGGACCCGAGGATCACATCAGCCGCAAGTATGCCTTCAAGGTAAGAGCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11132
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 300 | 1267 | 10 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28305082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26908021 |
GRCz11 | 7 | 27179214 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAACTCWCTTTTWCTCCACAGAGAAGCTGAAAGAAGCTCCAAACCTGAG[C/T]AGCATGCCGTCCCACAGACCAACCATTTCAGCAGCAKCAAAGGCTCATCC
Long Flanking Sequence:
TAAGGTCTGATTTAATCAGAGTAAATTGTACTCTTTCATTATGTATGTATTGTGCTTTTTATGCAGAAAAAAGTCATTCAGGCTTTGTCTTGTTGCGTTTAGAATGGAAATAGCTTTCATGAGGTAGGCCATCAGCACAAGGTCAGATAATTGTACATTGGGACTGTAGACTCAAAATTAATGCAGTCTAAACTCATTTCTGTCGTGTTTTGCTTCTTTGTGCCGAAAGAAACACTTAAAAAATGCTTAATTGTCATTGATGTTTACATAAAGTCTTTTCATTGCCTATAAAAAATTTCTTTATAGTGGGTAAGGTTCTTCAGGTCATTGAAAATGCTTTTTATTCTAAGAAAAATGGTTCATTTAAGAACTGTTCGCTGAATGGTTTTTTAGAACGCTTGTTTTTTTTAAGAGTGAAGGTCAAATATATATTTGTGTTCTGACTTTTAAATAACTCTCTTTTTCTCCACAGAGAAGCTGAAAGAAGCTCCAAACCTGAG[C/T]AGCATGCCGTCCCACAGACCAACCATTTCAGCAGCATCAAAGGCTCATCCCAGGCAGAGAGCGCCCAGCAAACACATATAGAGGTGGCGGAGCTGAGACCGCAGCGAGATGGAGACGAGTGTTACGTTTACAGCAAGGATATAACCGAGGATCCTGTTAAACTCATGTCCCCTGGAGAAATGGAGATGGAGGCGCTTTCCCAATCAGGTGCTCATTCACGGCCTCCGTCCACGGTGCCCACTCAAAGGAACGGACTGCCCTCTTCAGGCATTCCTCCTGATCAGAACGGCAACGTAGTGTATAAGAGAGGTCTCGTCCCACGTACAGACACTGAGAAAAAGGTACAGAGAAAAACTGCGCTTGCTCAGGTCGAGCACTGGGTGAAAGTACAGAAAGGAGACCCCAAAAGGTCAGTTTTTTTTGGATAATGTAAACACCTTTAAATATGCTGCGGTTGAGTAAAAAATACTTGGAATACATAAAGGTATTTTTGTAATACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31573
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 802 | 1267 | 18 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28332022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26934961 |
GRCz11 | 7 | 27206154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAAACGTAAATCTGTGTTTGTGTGCAGCAGGAGAAATCTCAAATGAGG[A/T]AGGAACTGTGGCGGATCGAAGATGTGCTCGCAGGCCTGAGCTCAAGCAAA
Long Flanking Sequence:
CGAACCAATATCCAATCCAAGTACTGTGATCGGTGCATCCCTAATACACACACCGCTGTTTGACACTATTCTCTCCACCTATCGAGTCAATGAAGGACCAAAGATGCCTGCATTGTGAAAAGTGGAGGGTTTTTCCCATATGGCGTCCATTAAAACAACACTCTTCCAGCAGTTCATACTCGCATCCAATATCTTGTTTGTCACAGGGAGAATGCATTAAATGTTCCTGAATGAAAGTGTAAGTCTCAAACTGCTGTTAAAGTCAACAAATAAAAATGAAACACCCTAAATTATATGCTAAATGTGGATAGCATGGTGACACAATGATGTTAATTGAATTATGTGCTATTACATAAAAAATGGGATCATGAAAAGCAACTCATGTAAACACCTTAATCGTATTATTGTCCTTATTTAGATTAAGGCAAATAATTCAATCAATGATGTCCATGCAAACGTAAATCTGTGTTTGTGTGCAGCAGGAGAAATCTCAAATGAGG[A/T]AGGAACTGTGGCGGATCGAAGATGTGCTCGCAGGCCTGAGCTCAAGCAAAGCAAACTACAGAGTGATCATTGACTCAGTGCGTAATCCAGGTGAGAGCGGCCCCCTTCCTGCCATCACCCCCATGCACTGGAACACAGCCAGAGGTATTGAGGCCAAACGTCATCACATGCGACCCCACATACAGATCATACTGATAATAATACCTGTGTTTTTGTTTTTGTAAACATTTGGGATGTTTGTGTGACCCAGAGAGGAAACTCGTGCCTTCAGCGTCATTGTCCGCAGTGCCTTCGCTCTCCGACAGCCCGTCCATGGGGGAACTAAAAGCTGCTCAACCCAGCCCACATCTCAGCCCTGTGCAGCCATGTACCCAACAGCCTCTGCAACTCTCGCACACAGCCCTCAAGCCAAAATGGGTAAGTTATTGGGTGAAATTGAATAACCAGCAGTGATGCACTGATCTTGAATTTTACAGTGAAATTAACTAATTCTGATACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18155
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 821 | 1267 | 18 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28332081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26935020 |
GRCz11 | 7 | 27206213 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGYGGATCGAAGATGTGCTCGCAGGCCTGAGCTCAAGCAAAGCAAACTA[C/A]AGAGTGAKCATTGACTCAGTGCGTAATCCAGGTGAGAGCGGCYCCCTTCC
Long Flanking Sequence:
TTGACACTATTCTCTCCACCTATCGAGTCAATGAAGGACCAAAGATGCCTGCATTGTGAAAAGTGGAGGGTTTTTCCCATATGGCGTCCATTAAAACAACACTCTTCCAGCAGTTCATACTCGCATCCAATATCTTGTTTGTCACAGGGAGAATGCATTAAATGTTCCTGAATGAAAGTGTAAGTCTCAAACTGCTGTTAAAGTCAACAAATAAAAATGAAACACCCTAAATTATATGCTAAATGTGGATAGCATGGTGACACAATGATGTTAATTGAATTATGTGCTATTACATAAAAAATGGGATCATGAAAAGCAACTCATGTAAACACCTTAATCGTATTATTGTCCTTATTTAGATTAAGGCAAATAATTCAATCAATGATGTCCATGCAAACGTAAATCTGTGTTTGTGTGCAGCAGGAGAAATCTCAAATGAGGAAGGAACTGTGGCGGATCGAAGATGTGCTCGCAGGCCTGAGCTCAAGCAAAGCAAACTA[C/A]AGAGTGATCATTGACTCAGTGCGTAATCCAGGTGAGAGCGGCCCCCTTCCTGCCATCACCCCCATGCACTGGAACACAGCCAGAGGTATTGAGGCCAAACGTCATCACATGCGACCCCACATACAGATCATACTGATAATAATACCTGTGTTTTTGTTTTTGTAAACATTTGGGATGTTTGTGTGACCCAGAGAGGAAACTCGTGCCTTCAGCGTCATTGTCCGCAGTGCCTTCGCTCTCCGACAGCCCGTCCATGGGGGAACTAAAAGCTGCTCAACCCAGCCCACATCTCAGCCCTGTGCAGCCATGTACCCAACAGCCTCTGCAACTCTCGCACACAGCCCTCAAGCCAAAATGGGTAAGTTATTGGGTGAAATTGAATAACCAGCAGTGATGCACTGATCTTGAATTTTACAGTGAAATTAACTAATTCTGATACTGATGAATGAAAAACTTTACATGAAAAATTTACTTAAAATAAAACTATTAACTCTCTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40897
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 892 | 1267 | 19 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28332398)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26935337 |
GRCz11 | 7 | 27206530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGCTCAACCCAGCCCACATCTCAGCCCTGTGCAGCCATGTACCCAA[C/T]AGCCTCTGCAACTCTCGCACACAGCCCTCAAGCCAAAATGGGTAAGTTAT
Long Flanking Sequence:
AACTCATGTAAACACCTTAATCGTATTATTGTCCTTATTTAGATTAAGGCAAATAATTCAATCAATGATGTCCATGCAAACGTAAATCTGTGTTTGTGTGCAGCAGGAGAAATCTCAAATGAGGAAGGAACTGTGGCGGATCGAAGATGTGCTCGCAGGCCTGAGCTCAAGCAAAGCAAACTACAGAGTGATCATTGACTCAGTGCGTAATCCAGGTGAGAGCGGCCCCCTTCCTGCCATCACCCCCATGCACTGGAACACAGCCAGAGGTATTGAGGCCAAACGTCATCACATGCGACCCCACATACAGATCATACTGATAATAATACCTGTGTTTTTGTTTTTGTAAACATTTGGGATGTTTGTGTGACCCAGAGAGGAAACTCGTGCCTTCAGCGTCATTGTCCGCAGTGCCTTCGCTCTCCGACAGCCCGTCCATGGGGGAACTAAAAGCTGCTCAACCCAGCCCACATCTCAGCCCTGTGCAGCCATGTACCCAA[C/T]AGCCTCTGCAACTCTCGCACACAGCCCTCAAGCCAAAATGGGTAAGTTATTGGGTGAAATTGAATAACCAGCAGTGATGCACTGATCTTGAATTTTACAGTGAAATTAACTAATTCTGATACTGATGAATGAAAAACTTTACATGAAAAATTTACTTAAAATAAAACTATTAACTCTCTTTCAGTAGGTGGCTGAATTCCTTGGTTAGTGCTGTAAACAAAAAAAGCTGTGCTGTTATTTTCAAATAAATATCAAAATAAGATATCATCTTAAATTTTCTGAAGACAGAGAATCTACCCTGTTGATACTTCAGTGTGTCTGCTGGCTTTTAAAAAGTCTTAAAATGTCTCAAATATCAAAATAAAAAATTTAGGCCTTAAAAGGCTTAAATTGACTGAAATATTGTGTTTTAGGTCTTAAGTCTTTTTAACACAGGCCTTCATTTAAGAAAAAAATATTTTTTTCACATTTTTCGAGTGCCTTGGACTGATTTTTGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20950
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 987 | 1267 | 21 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28334731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26937670 |
GRCz11 | 7 | 27208863 |
KASP Assay ID:
2259-8883.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAGATACGGGCATTCCTCAGCGAGCCTGAACTGCTGGTGGTCGGTGGA[C/T]AGATTGGGAGCTTGAGCCGTGATAGTGGCTACCAAACTCTACCAAACAGA
Long Flanking Sequence:
CAAACATGTCCTCTCTCCATATTTTCTCAACTTTCAGCATCCCTCTGTTACTCCAGCCCCACACCTTTAAACATGATTCCTACTTAAATCGGAGCAAGGGAAGCATTATGTAACCAAATGCCACTTCAGTCCATTTATCTAAACTTATAGATGTTTTATCTGTATGTATTCAGCCTGAAGAAGATGCTCCTCCCAGACCGCCTCTCCCTCACCTCTACAGCCCAGACGAACACCCTCCAGCTGTGCCCCCTCTGCCCAAAGAGACCTCTGTCATCCGACACACTTCAGTTCGGGGTCTGAAACGGCAGTCTGATGAGCGCAAGCGCGATCGTGAAATCGGACAGTTCTCTAACGGAGATCACAAGGTTTGTGCCAAGCTGAACAGTACCAAGATAAAGCCACATTTCAATGTTAATTGAGTCCTGAGATCTTTTTTCCTGGAAATCTAGGTTGAGATACGGGCATTCCTCAGCGAGCCTGAACTGCTGGTGGTCGGTGGA[C/T]AGATTGGGAGCTTGAGCCGTGATAGTGGCTACCAAACTCTACCAAACAGAGGTACACACATGATAGAATATATATATGTACACTAATTGGAGCTTGGTTAATGCAAACCACTGCCTGATTCAATGGTAATGTGAAAACATGCAAGTAAATAGTTGATTATTATGTGTACTTAATTATTGTATTCCTAAATGAAGCAGAAATTTTGACTAATTTTTCAAGTTTGAAAGTTGTTGTTAAATGTGTGTAGCTTAGACCAGGGGTTTCCCAAACTTTTCAGCCTGCAACCCTTTAAAAAATAATGCCAGTGACTTGTGAACCCCAACATTCTGGTGGTGGTTATAAATATACAATCCTTACAAATAAAGGTGCACAAACACCAATTCTATTCTTGGTGTAATTTTGGCGACCGCCACTCGGAGACCATCCTTCATGTTCAGTAGTGGCCTGTATTTATTTTTAATGTACGTGATTCAATTCAATTCAATTCAATTAATCTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9044
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:
C > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 1015 | 1267 | 22 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28336119)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26939058 |
GRCz11 | 7 | 27210251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTCCAATTCTGCTAGGTTTGACAAGCTCCTCTTCAAGACTGAACCAGT[C/G]ATCAAACATTTCATCATTTGTCACCCTCAGAAGAGGACTCACCACCACAA
Long Flanking Sequence:
AATGGCAGAATGCTGTTAAACACATTTTGTCATTTGAGACTTATGGAAATGTAATGAATGTTTTCATGATTTTTTTTTTTAGAAAAATTATAATTTTGTGCATTATCACATTCTACAACAGTTTCAGACAGGTTGAATTTTTGTCAAGATATTGGTACTTTCATTTTGTACTGATGCATTAAATTGATTAAAAATAACAGTAAAGGCATTCAATGACACAAGCACAACTTACCAGTTTAAATAATGACTGCCAAAAACGGACTTGCCTTCAAAAAGATAAATAAATGAATAAAAAAAGTTGAAGTAGTTATTTAAATAAATACTATTATTTAATTCAAAAATCTTTGTGATAAAACAGTGCAGTCTTGTCATACATTTCTGACTCAGTGAGCACAATAAAGATGGACAATTATAGAAGTATTTTAGCAGGTCTGAAACATTTGCCTAATCCAGTCCAATTCTGCTAGGTTTGACAAGCTCCTCTTCAAGACTGAACCAGT[C/G]ATCAAACATTTCATCATTTGTCACCCTCAGAAGAGGACTCACCACCACAAGCTTGAAGGTAGGACGTCAAACAAGTCCCAGAGATGTCTATTGGGAGGCAGAGGGACATAAAGAGTCTGTCATGGTTTGCTTTGGCGGAGTCGATGAGATACAGCAGCAGTGCAAACCGCTGAGCGCATGAAATAAAAGCAGCCAGTGTGGGTTTGAGCACGACTGTACTTTTTGCGAATAAATTACTGTGGTAGTGTTGCCATGCAGAGTGAACACAGTGTGTGTCTCCCACCCTGATGGATTCATGTAGAAATTGTTAACACAAATAAGCATAGCGGCTTCAAAATGCACTCCTGAAACTTTCCTCTCTTCCCTGTCTCTTGCCAACTGACAATTTTACATGCATTTAAAACAGCACACTTTAATAAAAATGTATATGCAGACAGATACGGAAAAATTTGCGACCATTTGATTCTAATGTTACAATCTTTGTATTTACAATCTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34078
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 |
---|---|---|---|---|---|
ENSDART00000110605 | Nonsense | 1077 | 1267 | 23 | 27 |
Genomic Location (Zv9):
Chromosome 7 (position 28338599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26941538 |
GRCz11 | 7 | 27212731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCTGGAGAGGATGAAGCGCCACCAAAAGGCTCTGGTACGAGAGCGC[A/T]AGAGAACCCTCAGCCAGGGCGAGCGGCAGGCCTCCACGTCTCGCGCTTCT
Long Flanking Sequence:
GCATGCCAAACAAGCTTTATAGTTAATCATCAGCTAAGTGTGAACTCTTAAAGTGCCCTTGATAGAGTGCACAGTTTAATTAATGCAGAAAGGTACCTTAGTGCTGGTCCATGTAGGGATTTAAAAAGTAAAACTAAAATCTTAAAACGTACTCTAAAAATGAACAGGAAGCCAGTAAAGAGAAACACACAAAAAAAGGTAAAAAACAAATTTTAGCACAACATGAAATTAATAAAAAAATGACTCTACATTCTTCTCCACATCTTCAATTTGGCATACAATATTGCTCCCGTTTCAGCACATTCTCTCTATCCGTGCTGTTCTTTAGCGCAGTTCATTCTGGCAATATTAACTCATCCTTCGATGTCTCCTAGGAGAGACCAAAGAGTGCCTTGGAGCGTCTTTACTCCGGAGAGCCTGTGCAGCAGCGCGGACGCATGAGCGCAGAAGAGCAGCTGGAGAGGATGAAGCGCCACCAAAAGGCTCTGGTACGAGAGCGC[A/T]AGAGAACCCTCAGCCAGGGCGAGCGGCAGGCCTCCACGTCTCGCGCTTCTTCCTCCTCCACCTCCAGACCCGTCTCTGCAGACCTGGGATCAGTACGTTAAGAGCACAATGACACATTTGATCCTCCAGAGAGGACCGTCACCCTGACGTTAATGCACGTTCAGCTATTTACACTGTTTTGATGGAGAACTGTAAGATTTGGTGTTAAAGCGATCAGCGTTTTTAATGAGGTAGCGTTTGCCGCAGGTAAGTGTGTTTGCGGGAGGTGTTGCAGAAGGAGATGGGAGAGATTTTTTTATCATATGTTGTTGAGCCACATGGATAGGCTTTGGGATAAGAACAGACAGAATGCTATTTGCCAATGAAAGACTTATTATTATGTGTTTAGAGGAGTATTAATGAAAGTTGATGTGCTGTTCATTCTTATTACACTCTGAGGATGGTTCAAAATGTTCAAATGACATGTAGGAGTGTTTAATTTTAACCATCTCTTCTGGTAT
Associated Phenotype:
Not determined