ZMP
zgc:171671
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100002269 [Source:RefSeq peptide;Acc:NP_001098611]
Human Orthologue:
ZNF292
Human Description:
zinc finger protein 292 [Source:HGNC Symbol;Acc:18410]
Mouse Orthologue:
Zfp292
Mouse Description:
zinc finger protein 292 Gene [Source:MGI Symbol;Acc:MGI:1353423]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9571 | Nonsense | Available for shipment | Available now |
sa10055 | Nonsense | Available for shipment | Available now |
sa18214 | Nonsense | Available for shipment | Available now |
sa23187 | Nonsense | Available for shipment | Available now |
sa23186 | Nonsense | Available for shipment | Available now |
sa23185 | Nonsense | Available for shipment | Available now |
sa10631 | Nonsense | Available for shipment | Available now |
sa10167 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9571
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 424 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49577230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49338314 |
GRCz11 | 17 | 49421289 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCT[T/G]AAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAAYTCTAA
Long Flanking Sequence:
TTTTGGAGTAAGCTTCTAATAAGGCTGGAATCAAAACAGGCCTTTTTGGAGCAATGCAGACTGTTAGCACGCCTCTCTGAGAGCGTGTACCATATTCTGCTCCTCATCAAAGTCATCCAGGCTGAGGTTAGAAAACCTTTCTTTTTTTTTATGCCAGCATGTTATGGAATCCAAATCTTTGGCAATCTGATGACTGACATTTTTGTTTCCCTAGGTTGACACCGATGGGCTTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCT[T/G]AAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAACGAATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10055
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49577000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49338084 |
GRCz11 | 17 | 49421059 |
KASP Assay ID:
2261-1579.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTTACGAACTCTTTGAAGTTGGARCAGAAAGAAAGAAGAAGAAGAAY[G/T]AAWTTAAGAAGGTRAAGGAGAAGGGATTWGTTTCTGCTCGATTCCGCAAT
Long Flanking Sequence:
TTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAAC[G/T]AATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18214
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
ENSDART00000004424 | Nonsense | 501 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49577000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49338084 |
GRCz11 | 17 | 49421059 |
KASP Assay ID:
2261-1579.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCTTACGAACTCTTTGAAGTTGGARCAGAAAGAAAGAAGAAGAAGAAY[G/T]AAWTTAAGAAGGTRAAGGAGAAGGGATTWGTTTCTGCTCGATTCCGCAAT
Long Flanking Sequence:
TTTCAGTGTGCATCGAAATGTGCATTCAAGCGCTGAAAATGGGAGTTCATGACAACGAGGACTGCAATATCACTATTTGCAAAACAATATCTTGTTTGCTGCCTTTAGACTTGGAAGTAAAACAGGCTTGCCAACTTACGGAGTTCCTGATAAAGCCATCTTTGGAATCTTATTATGCTGTTGAGACTCTTTTTAATGAGCCTGACCAAAAGCTTGACCAGGAGGATCCACCAATTCTAAATTCACTACGCTGTGACTTGTTGCTGGCCTTAAAGATAAAGTGGCCTTTTGATCCGGAGTTTTGGGACTGGAAAACTCTAAAACGTCAATGCCTTGCTTTGATGGGTCAGGAGGCAACCGCTATATTGTCTTCTGACAAATTCACTGACAGTGATGACAATGAGTTCCATGACCTGGATGAGAAATATTTCCAGCATTTTACTGATAACCCTTCTTACGAACTCTTTGAAGTTGGAACAGAAAGAAAGAAGAAGAAGAAC[G/T]AATTTAAGAAGGTGAAGGAGAAGGGATTTGTTTCTGCTCGATTCCGCAATTGGCAGGCTTATATGCAGTATTGTGTTTTGTGTGATAAAGAGTTCCTTGGACACCGAATCGTCAAGCATGCATTGAAGCATGTGCAAGACGGGGTTTTCCGTTGCCCGATATGTGCTAAAACCTTCGACAGCAGGACAGTGCTGGAGCCCCATGTGGCTTCACATGTAAAGCAGTCATGCAGTGAGCGCCTTGCTGCAATGGGTGTAAGCAAGAAACGCACTGACCCAAAGTTGACACCAGCTAGCAGCACCTTGAAAAAGGAAGAGCACTACAGCGACACGGCTGCAAAAGTTAGCCAAGAAAATACTTGCAATAACAATTTATATACTTCAATTGGTAGTACCAGCACAGATGTGAAAAGCAAAACGAAATCCTCATCATCATCGACGTCATCATCATCATCACCAAAGCAGGGCAACCCTATCCGGGATGTTAACAACACTAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23187
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 |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 1342 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49574475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49335559 |
GRCz11 | 17 | 49418534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGAAAATAGGAAATGCAAAAAAATTAAATCATCAAAAAGAACCAAATG[G/A]CCTGCCATAATACAGGATGGGAAGGTCATTTGCTGCAGGTGCTACAGAGA
Long Flanking Sequence:
CCCTCAGGCGTGATGAATGAAGCCTCAAAATATGTCTCAAGCTCTCTTAGGGTGCTGCATGCTCTTAATGGCGATCAGACTTGTGACCTGTCACAGGTTGAGTCGAGCGTTAATCTCGAAGATATTTCCATCAGCAATGATTTGCATGCAGGAGCTCTGTCCGGACAGAACGTCAGCCTGTATTTTCCTTCAGAGGCAAGTTCTGTTTCAATGCAGTCAATGGAAAATTCGAACAAAGAAATGAGCTCGGAGTGTACCGATGCAGCGTTCGCATCAGAAATCAAATGCATGTCAGATATTTTAAACCCTAACTTTAAGGAATCATCAGAAGATTTCTTTGGTGCTACCCCTGTGAACGATGATAAAACTCCAGATGATTTTTGTAATCATGAAATGGCCCTGGAAGGACCGGAAGGAATCACTTCAGATGATCAGACTGTTTTAGATTCTGGTGAAAATAGGAAATGCAAAAAAATTAAATCATCAAAAAGAACCAAATG[G/A]CCTGCCATAATACAGGATGGGAAGGTCATTTGCTGCAGGTGCTACAGAGAGTTTTCAAGCACAAAGTCTCTAGGAGGTCATTTGTCAAAACGTTCCCAGTGCAAACCTGTAGACGAAATAGATCTTACTGCTGATTTACCAGTATCGTTTCTCGATTTTCTAAATGATCCTGACATTTCAACAGTACAAATGCCTCTACCAGCTAATGATATACTTGAGGACAATCACAAATCCTTCATCTATGCACCATCAGAATCAAGTACCTTTAACGATAACACCTTAACAAGTGTGCATGGCACAGAGAGCATCCCCAACATTAATGCTAATGAGCCCTCTCAAGACCACTCTGAGATAGCTACAAATCCCAATTTGTTTAATTCCCCTGTATCTAACACAGCCACAGAAATGATAGCTGATACTGAAATTATCCCTGAAAATGCTGGTGAGGATGGAATTATCTTAGAAATTGAAAGGGCATTACAACGCCTTGATTTAGTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23186
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 |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 1967 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49572601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49333685 |
GRCz11 | 17 | 49416660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGT[C/A]GAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCA
Long Flanking Sequence:
GATGGCAGTTGGTAACACTGATTGTGGTGATTCGGTTGATGTGTATCGGCCATATCGATGCATTCATGAGGGATGTGTGGCTGCCTTTTCAATCCAACAAAATCTCATCCTCCATTATAGGGCTATGCATCAGTCAGAATGTGATGAAAAGAACAGCGCTAAAGCTACCGATGGAGTGTTCCCGGTGCAGGAATACAGATGCCAAGTCAAACAATGCTCAAAAGTTGTGTCGAAAGTTACCAGCTTGCTGAAACACTATCTTTTGCTCCACAGATGCACATTGGAAAAGGCAAGTGCGTTGCTCTCTGGTGTTGAGGTAGGCACGTTTCAGTGTGACCAGTCCAAATGTTCTGCTCACTTCACGTGCCATTTGAAGTACATTGATCATATCAAAAACGATCACAAAGCAATAAAGGTTTCAGTCGATGGGGACTTTGAGAGCGTGAACCTCACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGT[C/A]GAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCATGAAAGCGAAACAAGAACATGTGGGGGACAGTGTTCAAACCAAGAAGTCAAGTGCAAATCCTAATTCCAACAATGGGAAGGAAAATATTGCGAAAGACAAAACTAAAACGAAGAAGAAAAGTTCCAAAAAGAAAGAGGACAAGGCTCAAAGCCAACGGGTAACCTTAGAGAAGCCTGCGCTTAAATCCAACGAGGAAGCATCTGCTTTGTGCACTCAAACATTTCCTCTACAGTACCCATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTACACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23185
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 |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 2083 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49572252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49333336 |
GRCz11 | 17 | 49416311 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTA[C/A]ACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTT
Long Flanking Sequence:
TCTGCTCACTTCACGTGCCATTTGAAGTACATTGATCATATCAAAAACGATCACAAAGCAATAAAGGTTTCAGTCGATGGGGACTTTGAGAGCGTGAACCTCACATTCGGATGTCAATTCAAAGGTTGCGACCGGGTATATACGACAAAGTCGAACCTTCTTCGACATCTCATGAAGAAGCATGATGCTACTTTCGAAACCATGAAAGCGAAACAAGAACATGTGGGGGACAGTGTTCAAACCAAGAAGTCAAGTGCAAATCCTAATTCCAACAATGGGAAGGAAAATATTGCGAAAGACAAAACTAAAACGAAGAAGAAAAGTTCCAAAAAGAAAGAGGACAAGGCTCAAAGCCAACGGGTAACCTTAGAGAAGCCTGCGCTTAAATCCAACGAGGAAGCATCTGCTTTGTGCACTCAAACATTTCCTCTACAGTACCCATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTA[C/A]ACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTTCAGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10631
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 |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 2230 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49571813)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49332897 |
GRCz11 | 17 | 49415872 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTT[C/T]AGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAA
Long Flanking Sequence:
CATGCATGATCAAGAACTGTGATTCAGTAATGAATGATGAACGGAATATATTGCATCATTACACCACTCATGGCCTCACGGAACAATACATTGAGGATCAGAGAAGCCAGTTCATATTTTGCATTAAAAGCAGTGAGATCCCCGCAGCAGATAGTACCTCACAAAATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTT[C/T]AGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAAACTCAAACCGATCATCCGAACGAAAGATCAAGTCAAGCGCGTCGTTAATTTCCGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTATAAAAACCAGTCCCCTGGTTCTAGACTTCTGCTGAAGCAACTTCAAGATATGCAGCCTAGGGTCATCCTGGAAAAGAGGCTGCACAGTTGATGGTTAGAGTAGAGACGTTAAAAACAAGGCCTTGCTCTCAGGACCACATACTGTGTCACATGCTGCTGACAGGTACATCCAGATACTCTCTTGCATTTATAGTAGTTCCAACACATTGTTAATGACTTTTAATTAGTAGAAGAGAAAGCAAAGTTTTGTACAATATTTAACGTTTTGATGTACTATTATGGTTGTGCTAAAAAAAAAACCTTTTGTATTTCTGAAATTCTCTGATGAAAATTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10167
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004424 | Nonsense | 2284 | 2313 | 8 | 8 |
ENSDART00000111678 | None | None | 200 | None | 9 |
Genomic Location (Zv9):
Chromosome 17 (position 49571649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 49332733 |
GRCz11 | 17 | 49415708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTA[T/G]AAAAACCAGTCCCCTGGTYCTAGACTTCTGCTGAAGCAACTTCAAGATAT
Long Flanking Sequence:
AATGTTGAGGTGAAGGAAGCTCAAATCTCTGAAGCTCAAAACCCGAATTCCGACGTCAGTTCTCAAGATGTAGGCCCAGAGCCTGCAAAAGAGGTTGAAGTCAATGAAGCTGTTACCGCAGTTCCACCAGTAGTCAAGAGGAAAAGGGGTCGTCCGCGCAAGTCAGATTGTAGAAACAAGGTTTCTGTAGAACGAAAACAAAGTCTTCGCAACTGCTCCGATGAGCACGTTAAGTGTATGCTGAAAGTCTCAGGATCCATATTGAGAGCATCCAACTCCCAAGGAAACCACAGAAAGAATAAAGTCGCACTAAAACTTTACAAGTCCTCGAAGTTTCAGACTACCGTCCTGAAGTTCAGCCAAAATCCTCTGTCCAATCCATCGAAACGACTGCGAAAACTCAAACCGATCATCCGAACGAAAGATCAAGTCAAGCGCGTCGTTAATTTCCGAAATCCTCTAAAGATCGAGAGAGTGAACAATGTTAAAATTGTCATGTA[T/G]AAAAACCAGTCCCCTGGTTCTAGACTTCTGCTGAAGCAACTTCAAGATATGCAGCCTAGGGTCATCCTGGAAAAGAGGCTGCACAGTTGATGGTTAGAGTAGAGACGTTAAAAACAAGGCCTTGCTCTCAGGACCACATACTGTGTCACATGCTGCTGACAGGTACATCCAGATACTCTCTTGCATTTATAGTAGTTCCAACACATTGTTAATGACTTTTAATTAGTAGAAGAGAAAGCAAAGTTTTGTACAATATTTAACGTTTTGATGTACTATTATGGTTGTGCTAAAAAAAAAACCTTTTGTATTTCTGAAATTCTCTGATGAAAATTAGATGAATTTTTTTTAAATGTACAGTTTTGTGTAGAATGAAAAAGTTATCATCTATCCCTGTGGGATTTTTTTTTCTTTATTTTTTTTCCTTTATTCGAAAGTATTTATTTTTAACTTAACAGTAGTGTTTCAACGTACTTGTCTTCCACCTAACATTCAATTTAAGT
Associated Phenotype:
Not determined