ZMP
si:ch211-149m3.3
Ensembl ID:
ZFIN IDs:
Human Orthologue:
GRB10
Human Description:
growth factor receptor-bound protein 10 [Source:HGNC Symbol;Acc:4564]
Mouse Orthologue:
Grb10
Mouse Description:
growth factor receptor bound protein 10 Gene [Source:MGI Symbol;Acc:MGI:103232]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19132 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22755 | Nonsense | Available for shipment | Available now |
sa18384 | Nonsense | Available for shipment | Available now |
sa42661 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22754 | Nonsense | Available for shipment | Available now |
sa36043 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17433 | Nonsense | Available for shipment | Available now |
sa42660 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19132
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 9 | 594 | 1 | 16 |
ENSDART00000137365 | None | None | 578 | None | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9780100)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8566039 |
GRCz11 | 16 | 8479768 |
KASP Assay ID:
2260-9220.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGACACTAACAGAACGTGTATCATGGCTGTGGCCGGATGTCCGGATTA[T/A]TTTCTACACCATCCAAATTACAAGGTAGAAATTATTTTAATTTTTATTAA
Long Flanking Sequence:
TAATCTTACCCTCTGAAAATAAGGTACCATTATACGAGTGAAAATATATAATTTTGGTCTCGGTGGAAATGTTCACTATTTGGAGCTCCGTATGATTTGTTTGTTTAACATGTTCCTACTCTCCTCATATTGCAAGTGGAGCTGCTTTCCCAGTGTCTTGGGTTTTAAAAGCACAATCTAGAGATGGTTTCATATATTTTAACTGTGTGGCTGTCGGTCAGCTTTGGATTCAGTATTTTCCTGTTCGTATTCTTATGTTGTTTACTGACCCTGTGGAACTATTTGGGTTAAGATGTGCTCTGTGCTATATTGGTAGTAGCCACTTAGACTCAACTAATAAAGAGATTGCGTTTTTTTTTTTACCTTGAAAAACATTTGATGTAACATTTTTGTTTTGGTTTAATTTCAGACGCTTTTCCTCATCTATCTGAGGTGGATGTGATATCCGAGAGAGACACTAACAGAACGTGTATCATGGCTGTGGCCGGATGTCCGGATTA[T/A]TTTCTACACCATCCAAATTACAAGGTAGAAATTATTTTAATTTTTATTAATACGTTATTTACTCAGCCTTTATATTATCATTGTCACTTCACTTATTTTTGTGTCTGTATTATGTGAACTAGAGTTATTTCATAAACTGCTACAGTCAACCCTGTATAACCTTAAAGCGTAATGATGAAGGAACAATTATTATTTACTAAATCAGTGCATTGTCAAGAAATATTTGAATATGTTTTGAATATATGATTGTTTTTTTTTATCATATTTCCTTTCTTTTTCTGAATAGTTTTAATAATTAAAAAGTGTTTTTAATATTGTTATATTTGCAACCATATGAATGTAAAGTTTAAGGGAGCACACTTGTCAATATGAAGATCGCTGAAACTGAACTGTAAAAATATTTGAAAGCAAAGTACACTTTAAAGAGATGACTTTCATGTTTTATTTTTTGCTTTTAAAATCATTCTGAGTTTAAATGTTAGAATGTTCTAAACGAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22755
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 191 | 594 | 5 | 16 |
ENSDART00000137365 | Nonsense | 176 | 578 | 4 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9694813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8480752 |
GRCz11 | 16 | 8394481 |
KASP Assay ID:
2260-9219.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGAAAGGTGGTGGAGATCCCAGCCGACATGACGGCGCGAGACCTGTG[C/A]CAGTTTCTCGTCTATAAAAACCATTGTGTGGACGATAACAGTTGGGCGCT
Long Flanking Sequence:
AGAACGTATGAAAGGTCTCAGAATTTTCGAGAAGAGCTAGAATGTGTGTGAGGAAGGGGGCACAATGACACGGGACACATTTCAAACTGTTTCAAATGAAATGCTTCTCTTTAGCTTCTCCCTCACATCAGTGAGGATGTAGTCTAGACATGGAATTTGCATGATAAGACCTAGATTTGAGCATTAATGGATTTGCACTACGACCCAAAGCCTTAAAAGAGTTTCTTTTTGCTTAAAGGTACGGTATCGTAACATCACATAAAATACCGATTGATTCATTTTGGGGCTCTGAAGATAAAATTTGTCCTGTGACGCAGTACACTTTTCTCCTGTCTAAATGTGATTTTTTTTTTCCATACTAGGAATTTTAGCTGTTTAAAACGAACCTCGAAGACATCTAATTTTTGTTGTTTTCTGTTTCAGATTATAAAAATATTCAGCGAGGACGGGATGGGAAAGGTGGTGGAGATCCCAGCCGACATGACGGCGCGAGACCTGTG[C/A]CAGTTTCTCGTCTATAAAAACCATTGTGTGGACGATAACAGTTGGGCGCTTGTGGAGCATCATCCAGCCCTGGGACTCGGTAACTAGCTTGCTCCTTTTCCAAGCTTGAGTGTAGCGAGTAAATTTATAGAGCTGTTTGAAAGTGTCTGTGTGTGTGCGTCAACCACTTTAGATGCACTAATTACAGGGTCTTTTGTGCTGGAGTTGAAATCAATGATGACCATGTAAGAGAAGAAGACAGACTTCCTTGATTCATGCTTTTATGTCTTCGGGCTGGGAGTAATTGATTACCAGTCGCCGGGGGGAAATCCCATATAATGAAGAGGCATAACAGGAAGTTAGGTTCCCTAAGAGTTGAAGTGCTTCCTTAAAGTTGAGCATTGTCATCATTTGTTACGTGCTATTGAGAGCGGTTTTCAGTGCGACTCATCTCTGCATCAAACCTGTTAAACTCGTTAATCCTAAACTATTGGATTTCAATTGCGTGCTTGGTTGATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18384
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 192 | 594 | 5 | 16 |
ENSDART00000137365 | Nonsense | 177 | 578 | 4 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9694812)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8480751 |
GRCz11 | 16 | 8394480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGAAAGGTGGTGGAGATCCCAGCCGACATGACGGCGCGAGACCTGTGC[C/T]AGTTTCTCGTCTATAAAAACCATTGTGTGGACGAYAACAGYTGGGCGCTT
Long Flanking Sequence:
GAACGTATGAAAGGTCTCAGAATTTTCGAGAAGAGCTAGAATGTGTGTGAGGAAGGGGGCACAATGACACGGGACACATTTCAAACTGTTTCAAATGAAATGCTTCTCTTTAGCTTCTCCCTCACATCAGTGAGGATGTAGTCTAGACATGGAATTTGCATGATAAGACCTAGATTTGAGCATTAATGGATTTGCACTACGACCCAAAGCCTTAAAAGAGTTTCTTTTTGCTTAAAGGTACGGTATCGTAACATCACATAAAATACCGATTGATTCATTTTGGGGCTCTGAAGATAAAATTTGTCCTGTGACGCAGTACACTTTTCTCCTGTCTAAATGTGATTTTTTTTTTCCATACTAGGAATTTTAGCTGTTTAAAACGAACCTCGAAGACATCTAATTTTTGTTGTTTTCTGTTTCAGATTATAAAAATATTCAGCGAGGACGGGATGGGAAAGGTGGTGGAGATCCCAGCCGACATGACGGCGCGAGACCTGTGC[C/T]AGTTTCTCGTCTATAAAAACCATTGTGTGGACGATAACAGTTGGGCGCTTGTGGAGCATCATCCAGCCCTGGGACTCGGTAACTAGCTTGCTCCTTTTCCAAGCTTGAGTGTAGCGAGTAAATTTATAGAGCTGTTTGAAAGTGTCTGTGTGTGTGCGTCAACCACTTTAGATGCACTAATTACAGGGTCTTTTGTGCTGGAGTTGAAATCAATGATGACCATGTAAGAGAAGAAGACAGACTTCCTTGATTCATGCTTTTATGTCTTCGGGCTGGGAGTAATTGATTACCAGTCGCCGGGGGGAAATCCCATATAATGAAGAGGCATAACAGGAAGTTAGGTTCCCTAAGAGTTGAAGTGCTTCCTTAAAGTTGAGCATTGTCATCATTTGTTACGTGCTATTGAGAGCGGTTTTCAGTGCGACTCATCTCTGCATCAAACCTGTTAAACTCGTTAATCCTAAACTATTGGATTTCAATTGCGTGCTTGGTTGATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42661
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 284 | 594 | 8 | 16 |
ENSDART00000137365 | Nonsense | 269 | 578 | 7 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9679544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8465483 |
GRCz11 | 16 | 8379212 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTATCTGTGTGTTTTATTGAATCCATCTTCTTTCATCACCAGAACTTCT[T/A]GAACTCCAGCAGTTGTCCTGAGATCCAGGGATATTTGTATGTGAAAGAGA
Long Flanking Sequence:
TGGTGGTTCATTTCACTGTGGTGACCTCTGAAATACAGACTAAAGGAAATGATTGAGTTACATTGAGCTAACAATGAACAGCTTTATTCTCATTAACTAATGTTAACAAACAGGAATAAATTCTGTAATAAATGTATTTTTCATTGTTTGATTGTGTTTAGCTAACATTATCTAATACAGCATTATTGTTAAGTGTTACCATTTTATTTACAATACATAATATTTGTGTTTAAAAAGAATTTACCTACATATTCATAAGATTGTCTTATTTAATCTTTTATTAATGGATGAACTGATGTTAGATCAAAATGTTGCTAAATTTGACATGCAGGTCAGTATTTTTTGGGAAAAAAAAAACTTTTAATCAGTGATTTGTTGCTCCATTCAGATTTCAAAAAACTTCAACTGGTGGTGAAGAGTTCACATTGAAACGAATCAATCCACTGCAATCTTATCTGTGTGTTTTATTGAATCCATCTTCTTTCATCACCAGAACTTCT[T/A]GAACTCCAGCAGTTGTCCTGAGATCCAGGGATATTTGTATGTGAAAGAGATGGGCAGGAAATCGTGGAAGAAACTGTATGTGTTTTTAAGACGGTCAGGGTTGTATTTTTCGACGAAAGGAACGTCAAAGGTAAGTTAACTTCTATAAAAGTTAGTAAAAAAAAAAACAATCTTTAACTGCCTGCTCTACCAAAAGGAGGACCATATTTTGACTGTTTTCAATAATGACTGTTAAATAATGGTTTACACACAGCATTGTTGGTTTACAAAAAAATAAATAAAATCTAACATAATCCTGTTGCACTTGTAACAGGGTTATATTGTATCTCTCCACTTGCAAACATTGAAATACTAATGGAAAGGAAGGGGTTAACATTTGTTTTATTGTTTTACATGTAGAGCGCCCCCTCTGTTACCTTAAAAAGAAAATTCATTGTAGTATATATAAGAGGAAGCCAGTGCATGAGGCTGGTTGAATAGATCTGCGCTCATTTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22754
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 310 | 594 | 8 | 16 |
ENSDART00000137365 | Nonsense | 295 | 578 | 7 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9679465)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8465404 |
GRCz11 | 16 | 8379133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATATTTGTATGTGAAAGAGATGGGCAGGAAATCGTGGAAGAAACTGTA[T/A]GTGTTTTTAAGACGGTCAGGGTTGTATTTTTCGACGAAAGGAACGTCAAA
Long Flanking Sequence:
AGCTTTATTCTCATTAACTAATGTTAACAAACAGGAATAAATTCTGTAATAAATGTATTTTTCATTGTTTGATTGTGTTTAGCTAACATTATCTAATACAGCATTATTGTTAAGTGTTACCATTTTATTTACAATACATAATATTTGTGTTTAAAAAGAATTTACCTACATATTCATAAGATTGTCTTATTTAATCTTTTATTAATGGATGAACTGATGTTAGATCAAAATGTTGCTAAATTTGACATGCAGGTCAGTATTTTTTGGGAAAAAAAAAACTTTTAATCAGTGATTTGTTGCTCCATTCAGATTTCAAAAAACTTCAACTGGTGGTGAAGAGTTCACATTGAAACGAATCAATCCACTGCAATCTTATCTGTGTGTTTTATTGAATCCATCTTCTTTCATCACCAGAACTTCTTGAACTCCAGCAGTTGTCCTGAGATCCAGGGATATTTGTATGTGAAAGAGATGGGCAGGAAATCGTGGAAGAAACTGTA[T/A]GTGTTTTTAAGACGGTCAGGGTTGTATTTTTCGACGAAAGGAACGTCAAAGGTAAGTTAACTTCTATAAAAGTTAGTAAAAAAAAAAACAATCTTTAACTGCCTGCTCTACCAAAAGGAGGACCATATTTTGACTGTTTTCAATAATGACTGTTAAATAATGGTTTACACACAGCATTGTTGGTTTACAAAAAAATAAATAAAATCTAACATAATCCTGTTGCACTTGTAACAGGGTTATATTGTATCTCTCCACTTGCAAACATTGAAATACTAATGGAAAGGAAGGGGTTAACATTTGTTTTATTGTTTTACATGTAGAGCGCCCCCTCTGTTACCTTAAAAAGAAAATTCATTGTAGTATATATAAGAGGAAGCCAGTGCATGAGGCTGGTTGAATAGATCTGCGCTCATTTTTGTGTTCTGACTGTTTTCACAACAATAAATCGATTAAAGACATATTAAAGTGAATATTTATTTATACAACGCAGAAGAGATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36043
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 319 | 594 | 8 | 16 |
ENSDART00000137365 | Nonsense | 304 | 578 | 7 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9679438)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8465377 |
GRCz11 | 16 | 8379106 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAATCGTGGAAGAAACTGTATGTGTTTTTAAGACGGTCAGGGTTGTA[T/A]TTTTCGACGAAAGGAACGTCAAAGGTAAGTTAACTTCTATAAAAGTTAGT
Long Flanking Sequence:
CAAACAGGAATAAATTCTGTAATAAATGTATTTTTCATTGTTTGATTGTGTTTAGCTAACATTATCTAATACAGCATTATTGTTAAGTGTTACCATTTTATTTACAATACATAATATTTGTGTTTAAAAAGAATTTACCTACATATTCATAAGATTGTCTTATTTAATCTTTTATTAATGGATGAACTGATGTTAGATCAAAATGTTGCTAAATTTGACATGCAGGTCAGTATTTTTTGGGAAAAAAAAAACTTTTAATCAGTGATTTGTTGCTCCATTCAGATTTCAAAAAACTTCAACTGGTGGTGAAGAGTTCACATTGAAACGAATCAATCCACTGCAATCTTATCTGTGTGTTTTATTGAATCCATCTTCTTTCATCACCAGAACTTCTTGAACTCCAGCAGTTGTCCTGAGATCCAGGGATATTTGTATGTGAAAGAGATGGGCAGGAAATCGTGGAAGAAACTGTATGTGTTTTTAAGACGGTCAGGGTTGTA[T/A]TTTTCGACGAAAGGAACGTCAAAGGTAAGTTAACTTCTATAAAAGTTAGTAAAAAAAAAAACAATCTTTAACTGCCTGCTCTACCAAAAGGAGGACCATATTTTGACTGTTTTCAATAATGACTGTTAAATAATGGTTTACACACAGCATTGTTGGTTTACAAAAAAATAAATAAAATCTAACATAATCCTGTTGCACTTGTAACAGGGTTATATTGTATCTCTCCACTTGCAAACATTGAAATACTAATGGAAAGGAAGGGGTTAACATTTGTTTTATTGTTTTACATGTAGAGCGCCCCCTCTGTTACCTTAAAAAGAAAATTCATTGTAGTATATATAAGAGGAAGCCAGTGCATGAGGCTGGTTGAATAGATCTGCGCTCATTTTTGTGTTCTGACTGTTTTCACAACAATAAATCGATTAAAGACATATTAAAGTGAATATTTATTTATACAACGCAGAAGAGATGCAAAAGACTAGTTACATTGGTGCCGTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17433
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 461 | 594 | 12 | 16 |
ENSDART00000137365 | Nonsense | 446 | 578 | 11 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9672764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8458703 |
GRCz11 | 16 | 8372432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGACAATCCTKTGGAGGCACAGAGTGCTGCCATGGAGGAGGGACATGCCT[G/A]GAGAGTGAGTTACAATAATATTTTTTGGTCATTTAARTTACATGTTARAA
Long Flanking Sequence:
TCCTGCATTCAGTTTCTGTACCTCACAGATGGAGCATTAATCACACGTGTCAGTATGTGGGCCATGATGTCACATTATGGAATGATTGTTCGAGTGTTGGCAGTAAAGTTATTATTACAGCTTGTTCTATGGATATTATGCAGCGATTCTATAATAAATGAGCACAGAGATGCAAAATATGTCTGCATTTAGCATGCATGTTTTGATATGTGTAAATGTTTTTAGTATTGCACGACTCTTTATATTCTATATTTAATCTACTGCCATATGATCGAATGTACTGTAAATGGAAGAGTAGAAGACATAAGAGACTAGATCATTGTCATAAGACAACACACCTGCAACAAAGCAAACAAAGTCATTGTCACTGTGTGATCTTATTTTCCAGAGGAGTGTTTCAGAGAGCTCTCTGGTTGCCATGGATTTCTCAGGGAGGATAGGCAGAGTGATCGACAATCCTGTGGAGGCACAGAGTGCTGCCATGGAGGAGGGACATGCCT[G/A]GAGAGTGAGTTACAATAATATTTTTTGGTCATTTAAGTTACATGTTAAAAAAACACTCCACTTTTTTTGGAAATAAGCTCATTTTTTTCAACTACCCTAGAGTATAACAGTATAAAAGGACATTTGCCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGTTTTTTTGCTGGTCAACCAGGCTGGTTTTAGAGGGGTTTTGGCCATATTCAGGCTGCTTTCCAGTCATTTCCAGCCTGGTCTTAGCTGGTCAGACTAGAAAATGACCTGCTAAATCCAGCTAAAACCAGCTTGACCAGCCTGGTTTAAGCTGGAAATAGCTGGTTTTGACTGGACTCCCAGCCTGGCTAGGCTAGTCAAGTTGGTTTTAGCTGGTCATTTCCCAGCCTGACCAGCTAACACCAGGCTGGAGATGACTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGGCTGGTCGACAAGCTAATACCGGTCAACCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42660
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 |
---|---|---|---|---|---|
ENSDART00000051166 | Nonsense | 462 | 594 | 12 | 16 |
ENSDART00000137365 | Nonsense | 447 | 578 | 11 | 15 |
The following transcripts of ENSDARG00000035308 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 16 (position 9672762)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 8458701 |
GRCz11 | 16 | 8372430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATCCTGTGGAGGCACAGAGTGCTGCCATGGAGGAGGGACATGCCTGG[A/T]GAGTGAGTTACAATAATATTTTTTGGTCATTTAAGTTACATGTTAAAAAA
Long Flanking Sequence:
CTGCATTCAGTTTCTGTACCTCACAGATGGAGCATTAATCACACGTGTCAGTATGTGGGCCATGATGTCACATTATGGAATGATTGTTCGAGTGTTGGCAGTAAAGTTATTATTACAGCTTGTTCTATGGATATTATGCAGCGATTCTATAATAAATGAGCACAGAGATGCAAAATATGTCTGCATTTAGCATGCATGTTTTGATATGTGTAAATGTTTTTAGTATTGCACGACTCTTTATATTCTATATTTAATCTACTGCCATATGATCGAATGTACTGTAAATGGAAGAGTAGAAGACATAAGAGACTAGATCATTGTCATAAGACAACACACCTGCAACAAAGCAAACAAAGTCATTGTCACTGTGTGATCTTATTTTCCAGAGGAGTGTTTCAGAGAGCTCTCTGGTTGCCATGGATTTCTCAGGGAGGATAGGCAGAGTGATCGACAATCCTGTGGAGGCACAGAGTGCTGCCATGGAGGAGGGACATGCCTGG[A/T]GAGTGAGTTACAATAATATTTTTTGGTCATTTAAGTTACATGTTAAAAAAACACTCCACTTTTTTTGGAAATAAGCTCATTTTTTTCAACTACCCTAGAGTATAACAGTATAAAAGGACATTTGCCCTGCTGAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGTTTTTTTGCTGGTCAACCAGGCTGGTTTTAGAGGGGTTTTGGCCATATTCAGGCTGCTTTCCAGTCATTTCCAGCCTGGTCTTAGCTGGTCAGACTAGAAAATGACCTGCTAAATCCAGCTAAAACCAGCTTGACCAGCCTGGTTTAAGCTGGAAATAGCTGGTTTTGACTGGACTCCCAGCCTGGCTAGGCTAGTCAAGTTGGTTTTAGCTGGTCATTTCCCAGCCTGACCAGCTAACACCAGGCTGGAGATGACTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGGCTGGTCGACAAGCTAATACCGGTCAACCAGCC
Associated Phenotype:
Not determined