ZMP
adam10a
Ensembl ID:
ZFIN ID:
Description:
disintegrin and metalloproteinase domain-containing protein 10 [Source:RefSeq peptide;Acc:NP_001152
Human Orthologue:
ADAM10
Human Description:
ADAM metallopeptidase domain 10 [Source:HGNC Symbol;Acc:188]
Mouse Orthologue:
Adam10
Mouse Description:
a disintegrin and metallopeptidase domain 10 Gene [Source:MGI Symbol;Acc:MGI:109548]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12400 | Nonsense | Available for shipment | Available now |
sa18489 | Nonsense | Available for shipment | Available now |
sa18021 | Essential Splice Site | Available for shipment | Available now |
sa45281 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17467 | Nonsense | Available for shipment | Available now |
sa1909 | Nonsense | Available for shipment | Available now |
sa40917 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7067 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12400
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 29 | 690 | 1 | 14 |
ENSDART00000122259 | Nonsense | 101 | 763 | 3 | 16 |
ENSDART00000128654 | Nonsense | 95 | 751 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31778731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30171073 |
GRCz11 | 7 | 30442223 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTCACTCATAATCTGAAGGTGGAAGTTTCAGGTGTAGAGGTCCCCTA[T/A]GACACCTCTCACATTTACACTGGAGAAATATACGGTAGGCTTGGGACATT
Long Flanking Sequence:
TGTCAGTGTGTCAGTTTTTATTAGTGTGTCAAGCTTATAATGTAAAATGAATCATCCTGAACCAGTCATTCACCAGCACCTGGTATTTTCTGGAGAATCCTAATGACCTTACAGGCTGTTTGGAAATATAATAATCTGAAGGGAAGATTTAATTTGATAATAAATGCCAGAAAATAAGGGAAAAAATCTTTTTGGCAGTGAGAAATGCTGGTTGGCAGATTTCCATTATTTGCTCCCTTATCTCATAGTTCCAGTAATGCTCTGCATCATAACTCTTGGCTTAGACTATTAGTATTTTGGTGTGTTGCACAGCATCTTAAATATTGTGTCTTGTGTTTACCTCTGCTGGGACACATTGCATACATTCACAGGCAACTTCACAGTCCATTAATCTTGTTTTCTTTCTCTTCCATCAGGCATTTTAACCTTCGGATGAAGCGGGACACCTCTCTGTTCACTCATAATCTGAAGGTGGAAGTTTCAGGTGTAGAGGTCCCCTA[T/A]GACACCTCTCACATTTACACTGGAGAAATATACGGTAGGCTTGGGACATTTGCAGCACACACACACACACACACACACACACACACACTTTTGTATTTGTACACTGTTATAAATGAGATAAAGGGAATTTTTCATGTGTGGAAGAGGGCAATTAAGAAATGGCAGATATACAGTAGTGAGGTAGTCTTTTAAAAACAATGCCTTTTTAATGGGTTTATGATACAATCATATGATCCAGAGAAATTCTTCAAATGTATTCAGAAAAATAGCCATATAAATTATTCTCTGTGTTTATTGGGGACATCTGATACTGTTTTGTCGTGGCTAATGCAGTAACACAGGTGCCTCTGTAGTGTATTAGAAATATTTTGCTGTCATAAAGTAACAAAACAGTTTTATGTTGTTTAAAACAGAAAATCTATTATGATTTCTGACATTGAATTTTTGAGATCGCTACAAATGCTTGAGTTTTGGAGAAAAAATTATTTTGGGATATCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18489
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 185 | 690 | 5 | 14 |
ENSDART00000122259 | Nonsense | 258 | 763 | 7 | 16 |
ENSDART00000128654 | Nonsense | 252 | 751 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31761854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30154196 |
GRCz11 | 7 | 30425346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTATGTTTATAGGGTTGTTTTTNGTGCTATCCAGATTTCCAGTCATGTG[A/T]AGGCGATTAACTCCATCTATCAAGGCACAGAKTTTCAGGGCATTMGGAAT
Long Flanking Sequence:
TGACCTCACCAACTAATGCCATCATTCTGATCTCACAATGCAAACACGGAAGTCTCACCACATGGCGAGATTTCTTATTTCTCTTTGTTCTGATGTTCAGAAATCAACTTGAAGCCTGAATACATCCATAATTCATTAGAGAGAAAAAAAAGTCATTTTGTCAGTGCGCCCAAACATAGCAAATGTCTTCTCAGCCTCCTCAGCTAAATTGTAATGCATCCTGCTATTTTGTGTTCAGCAGACGAACCACATCATTGATGAAGAGGTGGCTGATGGGCCAGTGATCCTGAGGACACGTCGTGCAGCACAGGCAGAGAAAAACACCTGTCAGCTCTTCATCCAGACAGATCACCTCTTCTTTAAATACTACGGCAGTAGGGAAGCTGTAATTGCTCAGGTACACAGAAATAGCAGGTGTAGTCATGGCATATTCTGTCTACTTTTTTATATCGTATGTTTATAGGGTTGTTTTTTGTGCTATCCAGATTTCCAGTCATGTG[A/T]AGGCGATTAACTCCATCTATCAAGGCACAGATTTTCAGGGCATTAGGAATATCAGCTTTATGGTGAAGAGAATCAAAGTAAGTGTGTTTTCGTGTTTTCTCTGTGTTCATGTAGGTTTCCTCTGGGTGCTCCGGTTTCCTAAACTCCAAAGACAAGCGCTATAGGTGAATTGAATAAGCTAAATTGTCTGTAGTGTATATGTGTGAATGAGTGTATATAAAGTTTTCCAGTACTGGCTAGCAGCTGGAAGGACATCCGCTGTGTAGAACATATGCTGGATAAGTTGGCAGTTCATTCCGCTGTGGCGACCCCTGATGGGGACTAAGCCCAAAGAAAATGAATTAATGTTGTAACATTATTCGTTATGCCTGTCTGTATGTGGTTTTGTCTTTCTGTCATGCCTGTCTATGTTGTTATGTCTGTCTGTCATCATGCTTTTCTTTTTGTTGTCATGTTTGTCAATATGTTTGTATGTTATGTGTGTCATTCCTTGTTGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18021
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099639 | Essential Splice Site | 326 | 690 | 7 | 14 |
ENSDART00000122259 | Essential Splice Site | 399 | 763 | 9 | 16 |
ENSDART00000128654 | Essential Splice Site | 393 | 751 | 12 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31754448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30146790 |
GRCz11 | 7 | 30417940 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTCACATCACCTTCGCTCATGAAGTCGGACATAACTTCGGCTCTCCGG[T/G]GAGTYCTTTTCACTATATGTGCTGCATCCTAGACACATTAGYCGTAAASA
Long Flanking Sequence:
AAAAAATAAATAAAAAATAGAGCTGTTTGACAGAGCTGCAGCATTAATAATTTTGATGAATTATAGCTGGCTCTGCACATTCAATTAGGATAGAAGTTTGGCTTTTAAGATTTGACACTTTAATTCGTTTGAATGTCTTAGCTTGGATGTTTGTATAAATGTTTCATTTTAGTTCACAAGTAGAGCAAAAGAGCGTATTTTGTGCATTGTTTTGTTTTAATGACTTTTAAATTTGTTTCTGAACTTTTTGTTTTGTCATTTTTTAGTTAATATAGTTAATGTTTTTAATTTTATATTTTGTATTTGATTAATGCCTTTCTATTGTGTCATTTCAGGCAGCTCCGGTGGAATCTGTGAGAAGAATAAACAGTACTCTGATGGGAAAAAGAAGTCTCTGAACACCGGCATCATCACAGTGCAAAACTATGCATCACACGTTCCTCCTAAAGTCTCTCACATCACCTTCGCTCATGAAGTCGGACATAACTTCGGCTCTCCGG[T/G]GAGTCCTTTTCACTATATGTGCTGCATCCTAGACACATTAGCCGTAAACAACACACCTTAGCTGAATCCTTTATGAACAAATCAATTTTACTCTTCGATGCTTCGCGAAATTAGAAATTGCACACTATTGCCTTTGAGACCTCAAATTGTCAGATTGATCTAGCCAAGCTTTTATAATAACCTGACTTGGTATTCACTCTATCCTCAGTTCAGTTTAAAAGCTAATGCCGAGAACTGGCCGATGGCCAACTAAAAACAGTGTTGGAATATTTTCAGGATGAATTATAGCAGCAGGCTAATTAAGATCTTGTTATATAATTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATTTATTGTGTGTGTGTCTGTGTGTGTCTGTGTGTGTCTGTGTGTGTGTGTGTCTGTGTGTGTGTCTGTGTGTGTGTGTGTGCACACAAGCAGTTTTTTTTAATCTTCCATTCAGGCCACACTAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45281
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 423 | 690 | 9 | 14 |
ENSDART00000122259 | Nonsense | 496 | 763 | 11 | 16 |
ENSDART00000128654 | Nonsense | 490 | 751 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31752716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30145058 |
GRCz11 | 7 | 30416208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGTGGCTATAACGATCAGTGCAAAGACCAATGCTGCTATAGTGCAGAT[G/T]AACCAGAGGGAAAGAAATGTAAATTGAAGCCAGAGACAGAGTCAAAGTCA
Long Flanking Sequence:
ACATCGTTTACAAATGCCCTAAAGTCATAATACACATTTGAATATTAAATACAGTTCTTTACAGTATCATACTGAAGCGTTTACAAAGAGTTCTGTTCACTAGATGAGAAGCTCTGCATGTTCTTTGTCCTAAAACCCAAACATTGAAATTTTGTAAAATAACAGCCATTGTTTTTTATTATTTTCCTGGTTTATATCTCCATAGTTTGGCGTTTCTCTGAACAATAAACATAGTTAAGAGATTATAGTTTTTTTTTTATTAATTGCTTATTTTATTTCTTTTTTGACAAAAAAACTTCACCTGTAAGACTTGTAGGAGTAATAAGGTAATGTAACTTTGTCCTCATTCTGTGTCCCTTTTGCTAACTTACATTTTTTACTCTCATTTGTATCCAGAATCTGGACAGCCCATCTGTGGTAATGGTTTGGTTGAGACTAATGAAGAGTGTGACTGTGGCTATAACGATCAGTGCAAAGACCAATGCTGCTATAGTGCAGAT[G/T]AACCAGAGGGAAAGAAATGTAAATTGAAGCCAGAGACAGAGTCAAAGTCAAAGGTTTTTTGCAGGTAAGAAAATCTTAACAGTCTGTTTTTGCTCATTGATGTAAATCTTAATTTAAATAAAATAAAATTAAATTAAATTAAATTAAATTTTAAATCTAAATTAGAATTGGCATTTGTTGAGGACCAAAACTGCTAAAATGGAAAGAAAATTAATAGGAGTAAACATTTTTAAAACCTATATTAATAATACTGTATTACTAAATAATTAAACCCCTGTTCTGTAGAATCTTATATCCTTGTGACAGTTTGCTTAACACTCATTTGTGACTGACAGACTCTGCAGTAATTTATTATTAAAGAGTTAGTTTGCCCCCAAGAAAAAATTTTATCGTTTACCTACCCTCATGTCATTTTAAACCCATAAGACATTTGTTCATCTTTAGAACACAGCTTAAGACATTTTAAATGAAATCCAAGAGATCAGAAACTAAATTATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17467
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 455 | 690 | 10 | 14 |
ENSDART00000122259 | Nonsense | 528 | 763 | 12 | 16 |
ENSDART00000128654 | Nonsense | 516 | 751 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31751956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30144298 |
GRCz11 | 7 | 30415448 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCTTTTCTTTTGCAGTCCCAGTCAGGGTCCATGCTGCACACCACAGTG[C/A]ACGTATAGGACCGGTAAKGAATGTAGGCCGGAATCAGACTGTGCATTTAA
Long Flanking Sequence:
TAAATAATTAAACCCCTGTTCTGTAGAATCTTATATCCTTGTGACAGTTTGCTTAACACTCATTTGTGACTGACAGACTCTGCAGTAATTTATTATTAAAGAGTTAGTTTGCCCCCAAGAAAAAATTTTATCGTTTACCTACCCTCATGTCATTTTAAACCCATAAGACATTTGTTCATCTTTAGAACACAGCTTAAGACATTTTAAATGAAATCCAAGAGATCAGAAACTAAATTATGAATTAAGCAGTTTATTTAAAGCTTTCTGAAGAGGCATAATTGCTTCACATGTTGAATGGATTTTAGGATTTATATCTTTCTAACTTTTTCTGTCCCGAGTAAATGATAGAATTCAGCGGATAAATGAAATGATCGTAATGTTTTAATGGGGTGAACTAACCCTTTGAGTGAACACATTTTTCATTGAGAGAAATAAAGTCTTCATTTTTTCAATCTTTTCTTTTGCAGTCCCAGTCAGGGTCCATGCTGCACACCACAGTG[C/A]ACGTATAGGACCGGTAATGAATGTAGGCCGGAATCAGACTGTGCATTTAAGGGCTTGTGCAATGGACTCTCTGCCCAATGCCCTGCCTCAACACCCAAAGAAAACTATACAGCCTGCCATGCAAATACACAAGTCTGCATTAATGGGGTAGGTGATGCATTATGGCCTGTGTCAGAAAATGTATCACATGGTCATAGTCCAGCAAGTCAATGGCAAGATTTATCAAGCTGAAACTGTGAAAGAAGGAGTAGACTATACACAGTGATTTGCCCCTCAGGCTTGAATAATAATCATTATTAGCTTTAATTATGATGTGTATTTTAAGGTTTCCTTTGGTGGTTTGGATTTTGAAAGATGTTATACATACATTGAAAGTGAAGGACTTTTATATATTATTTGTCTATTTCATGTTTATCATTAAATAATTTAACTTCTCATTTTTTAAAATCTTTTTTTATACCCTATTTTTAACACATTGTTTTTTGGCGATATTTGCAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1909
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 475 | 690 | 10 | 14 |
ENSDART00000122259 | Nonsense | 548 | 763 | 12 | 16 |
ENSDART00000128654 | Nonsense | 536 | 751 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31751896)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30144238 |
GRCz11 | 7 | 30415388 |
KASP Assay ID:
554-1899.1 (used for ordering genotyping assays)
KASP Sequence:
ACCGGTAATGAATGTAGGCCGGAATCAGACTGTGCATTTAAGGGCTTGTG[C/A]AATGGACTCTCTGCCCAATGCCCTGCCTCAACACCCAAAGAAAACTATAC
Long Flanking Sequence:
CATTTGTGACTGACAGACTCTGCAGTAATTTATTATTAAAGAGTTAGTTTGCCCCCAAGAAAAAATTTTATCGTTTACCTACCCTCATGTCATTTTAAACCCATAAGACATTTGTTCATCTTTAGAACACAGCTTAAGACATTTTAAATGAAATCCAAGAGATCAGAAACTAAATTATGAATTAAGCAGTTTATTTAAAGCTTTCTGAAGAGGCATAATTGCTTCACATGTTGAATGGATTTTAGGATTTATATCTTTCTAACTTTTTCTGTCCCGAGTAAATGATAGAATTCAGCGGATAAATGAAATGATCGTAATGTTTTAATGGGGTGAACTAACCCTTTGAGTGAACACATTTTTCATTGAGAGAAATAAAGTCTTCATTTTTTCAATCTTTTCTTTTGCAGTCCCAGTCAGGGTCCATGCTGCACACCACAGTGCACGTATAGGACCGGTAATGAATGTAGGCCGGAATCAGACTGTGCATTTAAGGGCTTGTG[C/A]AATGGACTCTCTGCCCAATGCCCTGCCTCAACACCCAAAGAAAACTATACAGCCTGCCATGCAAATACACAAGTCTGCATTAATGGGGTAGGTGATGCATTATGGCCTGTGTCAGAAAATGTATCACATGGTCATAGTCCAGCAAGTCAATGGCAAGATTTATCAAGCTGAAACTGTGAAAGAAGGAGTAGACTATACACAGTGATTTGCCCCTCAGGCTTGAATAATAATCATTATTAGCTTTAATTATGATGTGTATTTTAAGGTTTCCTTTGGTGGTTTGGATTTTGAAAGATGTTATACATACATTGAAAGTGAAGGACTTTTATATATTATTTGTCTATTTCATGTTTATCATTAAATAATTTAACTTCTCATTTTTTAAAATCTTTTTTTATACCCTATTTTTAACACATTGTTTTTTGGCGATATTTGCAGCAAGAACCTTAAGAGCCATTGCTCTCTGTAATTTGTAAAAAGGGGACTATGAGGGAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40917
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 680 | 690 | 14 | 14 |
ENSDART00000122259 | Nonsense | 753 | 763 | 16 | 16 |
ENSDART00000128654 | Nonsense | 741 | 751 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31747691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30140033 |
GRCz11 | 7 | 30411183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCCAGAATCCTTCTGCACAGACGCAACCACAGCGCCCGCGCCAACAG[A/T]GAGAGAACTATCAGATGGGACAAATGCGACGCTGAGGCAGCTTCCTCATT
Long Flanking Sequence:
CATTGTTTTAACCCACTTTTCCAATTTCCATCTGGACAAAGATCTTGCTTAAAACAATGCATGTAGGGGTGCAAAGTTAAGGAATATGCCAAAGGAAAAAAACAAACCCAGCCCGAATACTTTTTTTTTTCCCCTTTAAAATAAAGCAATAGACCATTTTAATGTGGTAATGTCATTGGCCCATAAATATTTCCTATTGCCAAACTATTTCATAACTGTAAAAAATTTGTTTCTTTCCAATGACTTTCTTTCTAGAAGTTATGAACAACAACAACAAACTTTTTGTGCACTCCATCCCAGTCAGAAGTCATAGTTTAATATTTATTATAGTGGTGAACTCTGGTAGAGGTGACATTCAGCAGGGCTTCTTTCCCCCAATACCTCGGTTAACCCCTGCACAGAGAGTGATTAATCTTACCTGTTATTCTCCAGGCACGCTAAAGAGAAGAAGAGCCCAGAATCCTTCTGCACAGACGCAACCACAGCGCCCGCGCCAACAG[A/T]GAGAGAACTATCAGATGGGACAAATGCGACGCTGAGGCAGCTTCCTCATTGCCTTGGTTCTTCCTAGTGCCTACAGTGGGAAACACTTCACTCCAAAGAGTTACCTGAATCAGTCAACGAGTCCCATCTAGAAACTAAGAAACTGGCAAAATCAAATGGACTTCAGAAAAGCCTACACTTCAGAACACAACCGTTTTAAAGAGTAAGAAACCACTGCTCTGGGAGCCAGCAAAGCGTAGCTCAGAGAATAATACAGAAGCTAGATATGAGGAAGAGGATTTTCAGTCAATGATTTTTTTTTTTTTGTTCTATTTTCCCCTCCTGCTTTTCATTTTCTTTCTCAAGTGATTAAATCATTATTACTCTTCACTAAAGTTTTCCCCCTTTTATTTTGCTAGTTTTGTTTGTTTTTAAAACATTTTTAATGATTAGTATTTGGAATTACCACCCTCCTGTGGAGCTGAGCATGATGGGAAGTCAATAGTTTTTTCTGCCAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7067
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 |
---|---|---|---|---|---|
ENSDART00000099639 | Nonsense | 683 | 690 | 14 | 14 |
ENSDART00000122259 | Nonsense | 756 | 763 | 16 | 16 |
ENSDART00000128654 | Nonsense | 744 | 751 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 31747680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30140022 |
GRCz11 | 7 | 30411172 |
KASP Assay ID:
554-5268.1 (used for ordering genotyping assays)
KASP Sequence:
CCTTCTGCACAGACGCAACCACAGCGCCCGCGCCARCAGAGAGAGAACTA[T/A]CAGATGGGACAAATGCGACGCTGAGGCAGCTTCCTCATTGCCTTGGTTCT
Long Flanking Sequence:
CCCACTTTTCCAATTTCCATCTGGACAAAGATCTTGCTTAAAACAATGCATGTAGGGGTGCAAAGTTAAGGAATATGCCAAAGGAAAAAAACAAACCCAGCCCGAATACTTTTTTTTTTCCCCTTTAAAATAAAGCAATAGACCATTTTAATGTGGTAATGTCATTGGCCCATAAATATTTCCTATTGCCAAACTATTTCATAACTGTAAAAAATTTGTTTCTTTCCAATGACTTTCTTTCTAGAAGTTATGAACAACAACAACAAACTTTTTGTGCACTCCATCCCAGTCAGAAGTCATAGTTTAATATTTATTATAGTGGTGAACTCTGGTAGAGGTGACATTCAGCAGGGCTTCTTTCCCCCAATACCTCGGTTAACCCCTGCACAGAGAGTGATTAATCTTACCTGTTATTCTCCAGGCACGCTAAAGAGAAGAAGAGCCCAGAATCCTTCTGCACAGACGCAACCACAGCGCCCGCGCCAACAGAGAGAGAACTA[T/A]CAGATGGGACAAATGCGACGCTGAGGCAGCTTCCTCATTGCCTTGGTTCTTCCTAGTGCCTACAGTGGGAAACACTTCACTCCAAAGAGTTACCTGAATCAGTCAACGAGTCCCATCTAGAAACTAAGAAACTGGCAAAATCAAATGGACTTCAGAAAAGCCTACACTTCAGAACACAACCGTTTTAAAGAGTAAGAAACCACTGCTCTGGGAGCCAGCAAAGCGTAGCTCAGAGAATAATACAGAAGCTAGATATGAGGAAGAGGATTTTCAGTCAATGATTTTTTTTTTTTTGTTCTATTTTCCCCTCCTGCTTTTCATTTTCTTTCTCAAGTGATTAAATCATTATTACTCTTCACTAAAGTTTTCCCCCTTTTATTTTGCTAGTTTTGTTTGTTTTTAAAACATTTTTAATGATTAGTATTTGGAATTACCACCCTCCTGTGGAGCTGAGCATGATGGGAAGTCAATAGTTTTTTCTGCCAATCACTGGCGGCCGA
Associated Phenotype:
Not determined