ZMP
ENSDARG00000056781
Ensembl ID:
Mouse Orthologue:
Zan
Mouse Description:
zonadhesin Gene [Source:MGI Symbol;Acc:MGI:106656]
Alleles
There are 15 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1342 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa34069 | Essential Splice Site | Available for shipment | Available now |
sa25362 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30631 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa783 | Nonsense | Available for shipment | Available now |
sa11398 | Essential Splice Site | Available for shipment | Available now |
sa8476 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44661 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34070 | Nonsense | Available for shipment | Available now |
sa20943 | Essential Splice Site | Available for shipment | Available now |
sa40893 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1342
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 15 | 2214 | 1 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27452419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26055358 |
GRCz11 | 7 | 26326551 |
KASP Assay ID:
554-1256.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCCTCCTGCGACTTCAACGATAATGACGACCCTTTCTGCAACTTTCAA[C/T]AAGACACAGCAGATAATGGTGACTGGACACGACATTATGGACCAACTCCA
Long Flanking Sequence:
CCTCATAGCATAAATGTCATTGGTTCAAATTCTTACTCGACCATTAGATGTTTTTGTGTGGAGTTTACATGTTCTCCCTGTGCCCATGTGGGTTTCCCCCGGGTTCTCCGGTTTCCTCCTACAATCCAAAAACATGCGTAATAGATAAACTGACCAAACCAAATTGGCACCGTTTATGAGCTCTTAATCAGCAATTCCTAATTGCCATTAGCCATAAAATAAGCTCAAACTCCCCTTTTGCCTTACAAACGAGAGTGAGACCCAGGCTCAAGGATCTTATGAGCTCAGGGCTCTCTAGGAACAGTATGCCAAACATGGTATATAATCAATCATTATAGCGAATCGTGAACTCTTGAAATAAGTAATCTAAAATCAGAATTCTTAGTATAATCAATTCTAGGCAACGAAAAACATAAATGTCTCATGAAATATCTGTCTTTCAAACAGTGCTGGCCTCCTGCGACTTCAACGATAATGACGACCCTTTCTGCAACTTTCAA[C/T]AAGACACAGCAGATAATGGTGACTGGACACGACATTATGGACCAACTCCAAGCCAAGGCACTGGACCTGATGGAGACTATCCAGATGGAAGTGAGTATAAGTGCCAAATAACAAATCACAGTCAAAATGTACATTCACTGTCCAAAGACATGCAGCATAACGTGTTTCAGGTAACCTATGTGAACACTTTTTGCTAATTTCCATTCTCTCATTGATTGTAAACCAAACAATTCTCTGCCATAGATGGGTATTACATATACCATGAGGCTGACAACAATATAAATGGACAGAAAGTACGCCTTCTCAGCCCAACCATAACAAATGGACCTGCAGAGATCTGTGTACAGTTTGTTTACTTCATGTATGGTGTTGATCATACTAACACTTTGACTGTGCTGGCCAAACGACCTGGCTCTGAGGAACAACTGTGGCAAAAAATTGGCATACAGAGCCGGTCATGGCTTAGAGCTTCCATCACAGTGCCCATACCAGCCGGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34069
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079322 | Essential Splice Site | 577 | 2214 | 10 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27467393)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26070332 |
GRCz11 | 7 | 26341525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTGAAAGAAAACACATGTGGTTGCACCTTTAATGATCATTATTATAAG[G/A]TAAACAAAACATGTGTTTTAATATCAAACAATGGTTTGTTTTAGTCTAAA
Long Flanking Sequence:
ATCTCATGTGTGTATAGGGTTACTTCCAAAACTGTCTGTTTGATGTGTGTGAGCTGGACGGAGCTCATTCAGCATTGTGTGAAGCAATAGAGTCGTACGTCAATGAATGTCAGGACCGTGGCGTCACAATTGGACCCTGGAGAAACAGCACCTTCTGTCGTAAGTCTAATAAATACATAGCAATTAAAACTCAATTAAAACCATTTAGAGGGATTGACTTTTCCACCATACTCTTACAAATTAACATTTTTAAGTAAAAATAAAAATTGTGATTACCACTTACACACACTCCTTTTTCTTCAGCTCTGAAATGCCCACCCAATAGTCACTATGATTCATGCGCACCGGTTTGCCAGCCGTCTTGTACACCAGTTCCACCAAGTCAGTGCACTGGACCTTGTTCTGAAGGATGTGTTTGTGACCCTGGATACATCCTCAGTGCTGGCCAGTGTGTGAAAGAAAACACATGTGGTTGCACCTTTAATGATCATTATTATAAG[G/A]TAAACAAAACATGTGTTTTAATATCAAACAATGGTTTGTTTTAGTCTAAAACTAATAATTTTCATCAGACTAACACTATGTTTCCTCTCTATGTGGATTTAGCCAGGTGAAGAGTTCTACACTAAAGACTGTGATCTGCTGTGTAAGTGTGATCCTCCATTTGTTACCTGTAATGCTGCTGACTGCCCACCAATGGAGCAATGTGGAGTTCAGGATGGAATAACTGGGTGTTACCCACAAGGTAAGAACCATATTTAGGCAAGTGAATAGCATGGTCATAGACTTCACATATTCTTCATCATTTAAAAACTCTTCTTTTTACAATCCCTCAGGATCTCAAGACTGTGTCGTCTCTGGTGATCCTCATTACAACACATTTGATGGCAAATTCTACAGCTACATGGGCACTTGCACATACACACTGGCTCGCACCTGCAAAAACAACACCGGTAAGAGATTGCCAAAGACAAGTTTTACTATTCTGCTGTGACATTAATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25362
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Essential Splice Site | 624 | 2214 | 11 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27467636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26070575 |
GRCz11 | 7 | 26341768 |
KASP Assay ID:
554-7552.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGCAATGTGGAGTTCAGGATGGAATAACTGGGTGTTACCCACAAGG[T/C]AAGAACCATATTTAGGCAAGTGAATAGCATGGTCATAGACTTCACATATT
Long Flanking Sequence:
ACATTTTTAAGTAAAAATAAAAATTGTGATTACCACTTACACACACTCCTTTTTCTTCAGCTCTGAAATGCCCACCCAATAGTCACTATGATTCATGCGCACCGGTTTGCCAGCCGTCTTGTACACCAGTTCCACCAAGTCAGTGCACTGGACCTTGTTCTGAAGGATGTGTTTGTGACCCTGGATACATCCTCAGTGCTGGCCAGTGTGTGAAAGAAAACACATGTGGTTGCACCTTTAATGATCATTATTATAAGGTAAACAAAACATGTGTTTTAATATCAAACAATGGTTTGTTTTAGTCTAAAACTAATAATTTTCATCAGACTAACACTATGTTTCCTCTCTATGTGGATTTAGCCAGGTGAAGAGTTCTACACTAAAGACTGTGATCTGCTGTGTAAGTGTGATCCTCCATTTGTTACCTGTAATGCTGCTGACTGCCCACCAATGGAGCAATGTGGAGTTCAGGATGGAATAACTGGGTGTTACCCACAAGG[T/C]AAGAACCATATTTAGGCAAGTGAATAGCATGGTCATAGACTTCACATATTCTTCATCATTTAAAAACTCTTCTTTTTACAATCCCTCAGGATCTCAAGACTGTGTCGTCTCTGGTGATCCTCATTACAACACATTTGATGGCAAATTCTACAGCTACATGGGCACTTGCACATACACACTGGCTCGCACCTGCAAAAACAACACCGGTAAGAGATTGCCAAAGACAAGTTTTACTATTCTGCTGTGACATTAATGCTTTCGTCATCAGTTGGTTTTATGGAGTCACCCAAAAAATTCTAGCATTCTTACAAATGATTCTCAAAGTACATTAAATGCCTCAAAAACATCCAAAAATATTGACATTAAATACGAATTTAAGTCCTGACAAAAGCCTGAGTCACTTCCCTCTCTGGTCCACAGGCCCCTGGTTCTCCATAGAGGGTAAAAATGAAGAGAGAGGAGCTTCTGGCGTTTCCTACCTGAGAAAACTGTACGTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30631
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 652 | 2214 | 12 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27467811)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26070750 |
GRCz11 | 7 | 26341943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAACACATTTGATGGCAAATTCTACAGCTACATGGGCACTTGCACATA[C/A]ACACTGGCTCGCACCTGCAAAAACAACACCGGTAAGAGATTGCCAAAGAC
Long Flanking Sequence:
TGACCCTGGATACATCCTCAGTGCTGGCCAGTGTGTGAAAGAAAACACATGTGGTTGCACCTTTAATGATCATTATTATAAGGTAAACAAAACATGTGTTTTAATATCAAACAATGGTTTGTTTTAGTCTAAAACTAATAATTTTCATCAGACTAACACTATGTTTCCTCTCTATGTGGATTTAGCCAGGTGAAGAGTTCTACACTAAAGACTGTGATCTGCTGTGTAAGTGTGATCCTCCATTTGTTACCTGTAATGCTGCTGACTGCCCACCAATGGAGCAATGTGGAGTTCAGGATGGAATAACTGGGTGTTACCCACAAGGTAAGAACCATATTTAGGCAAGTGAATAGCATGGTCATAGACTTCACATATTCTTCATCATTTAAAAACTCTTCTTTTTACAATCCCTCAGGATCTCAAGACTGTGTCGTCTCTGGTGATCCTCATTACAACACATTTGATGGCAAATTCTACAGCTACATGGGCACTTGCACATA[C/A]ACACTGGCTCGCACCTGCAAAAACAACACCGGTAAGAGATTGCCAAAGACAAGTTTTACTATTCTGCTGTGACATTAATGCTTTCGTCATCAGTTGGTTTTATGGAGTCACCCAAAAAATTCTAGCATTCTTACAAATGATTCTCAAAGTACATTAAATGCCTCAAAAACATCCAAAAATATTGACATTAAATACGAATTTAAGTCCTGACAAAAGCCTGAGTCACTTCCCTCTCTGGTCCACAGGCCCCTGGTTCTCCATAGAGGGTAAAAATGAAGAGAGAGGAGCTTCTGGCGTTTCCTACCTGAGAAAACTGTACGTGACTGTTGACGGTATCACTGTGACAATGATGAAAAACAAGAGAACTCTGGTCAGTATTCACAGCAGCAGTCATCATTACACCAAGTCATTCAATAATCTTGGATAGAGAACTGAGATTAAGTCAGCAGATAAAATATATTTTAGTCTTACATTATAATCTCTTAGATTATATAACAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa783
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 956 | 2214 | 18 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27470072)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26073011 |
GRCz11 | 7 | 26344204 |
KASP Assay ID:
554-0688.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTGACAACAAATGTGTCCCTGTTAAAGACTGTGGCTGTGTGGACTCTT[C/A]AGGCTCCTACCATCCAGTGAGTTTAACACYAGGGCTGACCCATTGGGCTC
Long Flanking Sequence:
GGCAACTTACAGCCATGCTAGAATAACATTTCAATTCCTAGTGACAAGCCTGCTTTTAGCGCTCTCTAATGCACTATATGAATTATTGAAATGAATAGAGTTCAAGAAGTTGGAATAGGAAATCCAGAGCTGAACACTTACCTTAACTTAGCTATATCGTTTAGATTATTTATGAGGCTTTTAGGAGCTGAAGACAGAAATGCTGTCATAGAGGGAGGGGGACAAGGAATTGGGAAACACTCTCTATAATGCATCCCTAATTTCATCTCAGTTCCACCGTCATTTAATGGCATTTCCTCTCATTTTTCCTTCAGCTCTGGTGTGTCCTCCAAACAGCCACTACTCCATATGTGTAAGCTCCTGCCCAGAGACCTGTCTGGGCATCAATGGACCACCGGGCTGCAGTGAAAAGTGTGTAGAGGGATGTGAATGTGACCCCGGCTTCATCCTCAGTGACAACAAATGTGTCCCTGTTAAAGACTGTGGCTGTGTGGACTCTT[C/A]AGGCTCCTACCATCCAGTGAGTTTAACACTAGGGCTGACCCATTGGGCTCTTGCACTGTAGAAGACATTTTTAAAGTGTAAAACTTCCATAAAATTACAGAACACAGCGTGATTAACAGTAGTTTGACAAATACATACAAATAAATGGATTTTAAAAAGCCACATATGCAGACCTCTTAAATACTAAAAACATTTTTTTACCTTACTTTTGAGAAAAAGTGTCAAACTAATTCATTCATTTATTTTCCTTTGGCTTAGTCTCTATTTCAGCCACCTATTCCAGCATGTTTTACGCAGCAGATACCAGGGATATAGGCATGGGCTGGTTTAAGTTTCTGCCGGTATGACAGCCTTGGATAAAAATTTCACGGTTTCACAGTATTGTGATTACTGCTGTAAAATACATTATTTTTAAATGGTTTAGTAAAAAAAAAAATAAATTAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATTTTTTT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa11398
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079322 | Essential Splice Site | 961 | 2214 | 18 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27470090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26073029 |
GRCz11 | 7 | 26344222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YCCWGTTAAAGACTGTGGCTGTGTGGACTCTTMAGGCTCCTACCATCCAG[T/C]GAGTTTAACACYAGGGCTGACCCATTGGGCTCTTGCACTGTRGAAGACAY
Long Flanking Sequence:
TAGAATAACATTTCAATTCCTAGTGACAAGCCTGCTTTTAGCGCTCTCTAATGCACTATATGAATTATTGAAATGAATAGAGTTCAAGAAGTTGGAATAGGAAATCCAGAGCTGAACACTTACCTTAACTTAGCTATATCGTTTAGATTATTTATGAGGCTTTTAGGAGCTGAAGACAGAAATGCTGTCATAGAGGGAGGGGGACAAGGAATTGGGAAACACTCTCTATAATGCATCCCTAATTTCATCTCAGTTCCACCGTCATTTAATGGCATTTCCTCTCATTTTTCCTTCAGCTCTGGTGTGTCCTCCAAACAGCCACTACTCCATATGTGTAAGCTCCTGCCCAGAGACCTGTCTGGGCATCAATGGACCACCGGGCTGCAGTGAAAAGTGTGTAGAGGGATGTGAATGTGACCCCGGCTTCATCCTCAGTGACAACAAATGTGTCCCTGTTAAAGACTGTGGCTGTGTGGACTCTTCAGGCTCCTACCATCCAG[T/C]GAGTTTAACACTAGGGCTGACCCATTGGGCTCTTGCACTGTAGAAGACATTTTTAAAGTGTAAAACTTCCATAAAATTACAGAACACAGCGTGATTAACAGTAGTTTGACAAATACATACAAATAAATGGATTTTAAAAAGCCACATATGCAGACCTCTTAAATACTAAAAACATTTTTTTACCTTACTTTTGAGAAAAAGTGTCAAACTAATTCATTCATTTATTTTCCTTTGGCTTAGTCTCTATTTCAGCCACCTATTCCAGCATGTTTTACGCAGCAGATACCAGGGATATAGGCATGGGCTGGTTTAAGTTTCTGCCGGTATGACAGCCTTGGATAAAAATTTCACGGTTTCACAGTATTGTGATTACTGCTGTAAAATACATTATTTTTAAATGGTTTAGTAAAAAAAAAAATAAATTAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTCCAATTGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8476
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 1066 | 2214 | 20 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27472437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26075376 |
GRCz11 | 7 | 26346569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCATACTTCTCTGTGGAGACACAAAACGAGCACAGAGACAATAATAAA[A/T]AAGTGTCRTATGTAAGATCTGTTATCGTCAAAGTTCACAACACAACAGTC
Long Flanking Sequence:
AAATACAACAAATGGGATGTCAATTTTTGACATTCATAAAATTGTGGTCATTTTTAGGTTGACGAGAGCTGGTATCTGGAGGGCTGTAAGCAGAAGTGCACTTGTGAGGGAGGAGGATCTATTAAGTGTTATGACACCAGCTGTCTTCCTACTGAGAGCTGCCAGCTTCAAGATGGAGACTACATCTGCAAACCACTTGGTAAAAACACTGTTTGACACAAACAGTTGGTTTAACATACACATTTTTTTTTTCACATACACCAATGCAGCTCTGCACAAACATGTCAAGACATCTTATTATCTCTCATTTTTAAACTCTTTCTGTTTTAGGTTCAGGCATTTGCTCGGTTTCTGGTGACCCTCATTATACCACCTTTGATGATAAAGTACATCACTTCATGGGTGCCTGCTCCTACACTCTCACCAAGCCCTGTAATGAGACCTCCGGCATGCCATACTTCTCTGTGGAGACACAAAACGAGCACAGAGACAATAATAAA[A/T]AAGTGTCGTATGTAAGATCTGTTATCGTCAAAGTTCACAACACAACAGTCATTTTGGGCAAGGGCCGCAAAATACAGGTGAGAGACATTTCCAGGGATTTGTGAAGCCTCATTAACAGATTAGAGGGGATTAAAAGAGCAGTGCATTCATTTGCTTACCTTCGTCCTGCAGGTGAATGGAGTTCAGGTCACTGCGCCTGTAACACTTTCTAATGGTATTAAGATCTTCATGAGTGGCAAATTTGTGGTGCTTGAGACCAACTTTGGACTGCGTGTCCGCTTTGATGGAAATCATCATGCAGATGTCACCCTGCCTTCCTCTTACAACGGACTGTTATGTGGACTTTGTGGTAAAGATAGCACACTAAATTATCATGTAGCAACTTAATCTTAATAGTTTGGTGTGTTAAATCCTACTTACTGTATTAAAGGAAACTTTAATGGTAATCCTAATGACGACAACATCAAGTTAGATGGGAAGCCCACAGACAGCACCAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44661
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 1076 | 2214 | 20 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27472467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26075406 |
GRCz11 | 7 | 26346599 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCACAGAGACAATAATAAAAAAGTGTCGTATGTAAGATCTGTTATCGTC[A/T]AAGTTCACAACACAACAGTCATTTTGGGCAAGGGCCGCAAAATACAGGTG
Long Flanking Sequence:
CATTCATAAAATTGTGGTCATTTTTAGGTTGACGAGAGCTGGTATCTGGAGGGCTGTAAGCAGAAGTGCACTTGTGAGGGAGGAGGATCTATTAAGTGTTATGACACCAGCTGTCTTCCTACTGAGAGCTGCCAGCTTCAAGATGGAGACTACATCTGCAAACCACTTGGTAAAAACACTGTTTGACACAAACAGTTGGTTTAACATACACATTTTTTTTTTCACATACACCAATGCAGCTCTGCACAAACATGTCAAGACATCTTATTATCTCTCATTTTTAAACTCTTTCTGTTTTAGGTTCAGGCATTTGCTCGGTTTCTGGTGACCCTCATTATACCACCTTTGATGATAAAGTACATCACTTCATGGGTGCCTGCTCCTACACTCTCACCAAGCCCTGTAATGAGACCTCCGGCATGCCATACTTCTCTGTGGAGACACAAAACGAGCACAGAGACAATAATAAAAAAGTGTCGTATGTAAGATCTGTTATCGTC[A/T]AAGTTCACAACACAACAGTCATTTTGGGCAAGGGCCGCAAAATACAGGTGAGAGACATTTCCAGGGATTTGTGAAGCCTCATTAACAGATTAGAGGGGATTAAAAGAGCAGTGCATTCATTTGCTTACCTTCGTCCTGCAGGTGAATGGAGTTCAGGTCACTGCGCCTGTAACACTTTCTAATGGTATTAAGATCTTCATGAGTGGCAAATTTGTGGTGCTTGAGACCAACTTTGGACTGCGTGTCCGCTTTGATGGAAATCATCATGCAGATGTCACCCTGCCTTCCTCTTACAACGGACTGTTATGTGGACTTTGTGGTAAAGATAGCACACTAAATTATCATGTAGCAACTTAATCTTAATAGTTTGGTGTGTTAAATCCTACTTACTGTATTAAAGGAAACTTTAATGGTAATCCTAATGACGACAACATCAAGTTAGATGGGAAGCCCACAGACAGCACCAATGAGCTTGGAGAGAGTTGGCAGGTGCCTGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34070
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 1416 | 2214 | 27 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27476286)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26079225 |
GRCz11 | 7 | 26350418 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGCTGGGGATCCTCACTATTACACCTTCGATGGCATCATGCACACCTA[C/A]ATGGGCACCTGTACTTACACACTGGTGGAAGTGTGCAACACCTCTATGGT
Long Flanking Sequence:
GACAGCACTACCCATTACGCCACTGTGCTGCCAAAACGCAAAACTTAACTGCAGAAAATTGTAAAGAAGCAGCAAGATCTTTTTTTTAAAGGAAAAACTTCCACAGTGCCAACTTCTAATTATCCTTCTAGCATAAGCTACTAAAATGTGCACCTGCTGCGTGCAACATGTCATGTCATGTCATAAAGGCACCACTCATGGCCAGCAGCACACATCTTAAGCAGATCATCCAGCAGAAATAATCCATAATTTATGACCCGATATTATTTTCTTAACAATAAAACTATGCATTAAACATAAAAAATAAACATTTATCAGCTGATATCGATATGGTGGCCATTTTGCATTACCAATATCTCATTATCTCTCTCTTTACACTGAATCTGTGTTCAAATATTTTTTATGCAATTATGCTAACTGATCTTCTTTGCAGGAGTGGGCATTTGCCACATCGCTGGGGATCCTCACTATTACACCTTCGATGGCATCATGCACACCTA[C/A]ATGGGCACCTGTACTTACACACTGGTGGAAGTGTGCAACACCTCTATGGTGACACCCTTCACCATTGTGGCCAAGAACGAAGAGCGCGGCCAACCAGAAGCTTCATATGTTCGCTCTGTGACCGTCTACCTGCCCACTGCCAACATCACCATCAGCAAGAGTGGACGAGTTCTGGTGAGTGGCAGAAAAAAGATGAAGAAATTATTGCATTTGTCTTCTTCTGATTAGACTTTGGGGTAAAACTTTACAATAAAAGTATTAACATGAACAGTTTAACACAGGAGTTCATGAGTAGTTAATGTGATATGCCCCTCCAAGTAAAGTCATGATATAATTATAGATTAACAGCTTATGAGATCTTGATGGTTACATTTAGCTTAAGCCTAAATGTTAATTAATACATTAACTAGCATGAACTAACAAGTAATTAAGGTAGCCATTATTTACACATTAAAGTCACGTGACTCATGTTGTAGTTAAAGTTAGTTCATGATTAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20943
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000079322 | Essential Splice Site | 1732 | 2214 | 31 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27480227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26083166 |
GRCz11 | 7 | 26354359 |
KASP Assay ID:
2259-8858.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCTCTCAAGCTGTGGATGCGTTGACAGCAATGGAGAGTATCACGAC[G/A]TGAGTACAATTTGCACCTAAGTACCAAGCAAAACTCAGCTTTTCTCAATT
Long Flanking Sequence:
GGAGTCACTATCAGCTGGAGGAACAGCACCTTCTGCCGTAAGTGGAAGAGAAACAGAGAAGTAAAGTAATGCTGAGCTGGCTGACAGGAGGAAGAATCATTTGTGAAAATGAAACAGAGCCCAAGTTTTATGCAGATGAAATTAAGCATTTATGAGATTCTCAGTTGATAACCTCCAGGCATCATATAAATATTAATGGATTTTTCTGCACATTTTAAATGTGTCTGAATATGTCAGAAAATCATTTCTATTCGGATTCAGTGTTTTAAATGTCTTTCGTTTTTTTTCCAGCTCTCCCGTGCCCACCCAACAGTCACTACTCTGAGTGCACACCTCCATGTCCTCCTACTTGTGCTGACCTCTTCCCCATTTTCTGCCCATTACCACCCAATAGCTGTGTTGAAGGCTGTCAGTGTAATGCAGGTTTTGTGCTAAGTGATGGCAAGTGCGTTCCTCTCTCAAGCTGTGGATGCGTTGACAGCAATGGAGAGTATCACGAC[G/A]TGAGTACAATTTGCACCTAAGTACCAAGCAAAACTCAGCTTTTCTCAATTTTAGCTGAACAATGATCACTTTTAATGTTTTATAAGCAGCAAATCATCATATTAGAATTCAAATTAGAAAAACAAAAGGATCTCCTAAGCCTATATATACAGATATGTATACAGTGCTTATAAAAAATCATCATACCTTACTACTCAGATTACACCCTGCTTTCAGAAGAACTTCAGGATAAAGTTTTAAAGAGGCAGAGGTTAGGAGAAAATTACTAAAACATTTCAAAGGTTGGAATGTAATTTAATTTCAGGCTGTATAACAAAGTAATTATTTCAAAGAGGTGTGATGATTTTTAATAGGCACTATACATATATATGAGCAATATCACACTAGTAGCAGTGCGTGCGATGGCCTGTGGCTGCAGGCTTAGTGCCTTAGTGCCCCCCACCAGTGTCGATATACAGTCATATCGCACTGCTACGAGTGTGATATTGAGTTTATACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40893
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 |
---|---|---|---|---|---|
ENSDART00000079322 | Nonsense | 2158 | 2214 | 41 | 42 |
Genomic Location (Zv9):
Chromosome 7 (position 27488340)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26091279 |
GRCz11 | 7 | 26362472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGCGCACAGAGTTGCGAATGTACAAAGACTGGCGCTGTGTGCCAAGTC[A/T]AGGGCTGCCAGGAGAACGAGATCTGCACTGTGTTCGAAACCAAACTGGAC
Long Flanking Sequence:
AATAGAGGCTCGGACATTCTATATGTACATAACAAGTGAATAATTGACATTTACATCATTTACAAGCACAAACTTATCAACTCAATCACCTGTACTGTCCTGATTGCATGTGTGTTTGTGATCACCTGTAGGTCTGCAGTGTGGAGCCAACAGCACCTACTTCGCCAGTATGACTCCCTGCCCGGCGTCCTGCGGAGATCTGGCAGCTCCATCCGAATGCGAGCAAACGCAGTTGGTGGAGGGATGTCAGTGTAACGCCGGCTTCGTCCTGAGCGACCAGGACTGTGTGCCTTACAGCCAGTGTGGATGCACTTATCTCAATCGCTACCATGTGGTGAGTCTATTGACGCATGTACAAGACTGCAGGCGGTGATGTGAAATGAATTGCAAAGAAAGCTAAAACAAGACTTTGTTACTCTACACAGCTCGGGGAGATGTTTGTGACTGAAGATTGCGCACAGAGTTGCGAATGTACAAAGACTGGCGCTGTGTGCCAAGTC[A/T]AGGGCTGCCAGGAGAACGAGATCTGCACTGTGTTCGAAACCAAACTGGACTGTTATAGAGGTGAGCTTATTGAGACTAACATTCTTCAATTCAATTAAATTTACTTTATTTCTAAAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGATTAACATAGAAGTTCAAGTAAATGAAAACTTTGTCAGTTCAGTTTTTAGAGTTGAAGTTTAGTTTAGTTTAGTTCAGTTCGGTGGTTTCATTTTTACTGCTAAAAGTCCAAACACTGAAGAGCAAATCCATCAATGCACAGCTCCACAAGTCCAAAACCAAGCAAGCCAGTGGTGAGGAACAAACTTCACCAATTGACCAAAGTGAAGGAACAAACTTTGAAAGAAACCAGGCTCAGTTGGTTGTACTTTTAGGGGGCACATTTCAAAGTCATTTCAGTCTTTTTTTTTCATGCATCACTCTGCGGTCTTCACAAACAAGCTAATTAAATAACTTAAACTCAAAATAATCT
Associated Phenotype:
Not determined