ZMP
LOC556807
Ensembl ID:
Human Orthologue:
FAT4
Human Description:
FAT tumor suppressor homolog 4 (Drosophila) [Source:HGNC Symbol;Acc:23109]
Mouse Orthologue:
Fat4
Mouse Description:
FAT tumor suppressor homolog 4 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:3045256]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15748 | Nonsense | Available for shipment | Available now |
sa40994 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40993 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34166 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40992 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34165 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15416 | Nonsense | Available for shipment | Available now |
sa40991 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21053 | Nonsense | Available for shipment | Available now |
sa27032 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27030 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45294 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15748
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 95 | 2532 | 2 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49150793)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47418412 |
GRCz11 | 7 | 47691491 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAAACGGRCACGTGCGGACRACAGGCCTCCCCCTTCAGAGAGACAGA[G/T]AGTATCTYCTAACAGTARTGGCTGCAGACCGGCAGGGCAGCCGCAGWCCT
Long Flanking Sequence:
GTGGAAACATTACTATTTTAGGTTTTGTAAGTTTAGTGGCTAATTCGTATGATTTCATAAGAGTTCATTACATTATAAGTTGTACAAATGAGATCATATAAATTCATACAAATACTAAATCAAAAAAAGTTACCAATTCACATTGAGTTAGTGCTGGATATATGCACGCTCTCAGCCTGATTAAGCCAATGGTTCTCACCTCTTGTCCTCAGTACCCAGTGCTCTGCACACTTTGTATGTCTTCATTATTTAACAGCTGATTCAGATCATCGGCTCGTCAGCAGAGAGCTCCATGAACTGTGTGTCAGATAAGAGAGGCATACTAAATGTGCCGTGATGGGTCCCCGGGACTGCAGTATAAAACTGCTGCACCAAGTCATCATTAAGCCTCTGAGCTGAATCTTTTTTTTTGTCATACAACAGGCGGTGATGGAAGATTTGAAGTGGACAGGAAAAACGGACACGTGCGGACAACAGGCCTCCCCCTTCAGAGAGACAGA[G/T]AGTATCTTCTAACAGTAGTGGCTGCAGACCGGCAGGGCAGCCGCAGTCCTCCTGCTGTACTCTCCATCATCGCAGGCCCGAGAGCTCCTCAGTTCACCAACGTGTCTTACACCATTCCCATACCAGAAAACACGCCAGAAGGACAGCCGTGAGTACAGCCATAGGGCGCACACAGCCAATCTCGTAAATGCAGCAAATCTTATTTCCATAGTGTAATTCTAGCGCACCCTAAATGCATCTCCCACGCTGCGAGAATGCTGCTTATCCATCAGGCTAACAAATAGAAACAGGATCATGCTGCACTTACAGCCATCTACGCGCCCTCTGCTTCTGCTGTGAGTCATCGTCTACTATACAATGCAAAATTCATGAAATAATGATCTTTGACTATGTCAGGCTACTGTGATATGCATTAAAGATGCATGAACATCAGATCTTTGGTCTGCAGTATAGACAGCCCTCAGTGGCTAACCATGCATTACAACAGGTAATATATACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40994
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 154 | 2532 | 3 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49145037)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47412656 |
GRCz11 | 7 | 47685735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTCTTTCTTTTCTCACCCAGCTTTCTTGTCACTCCTGCGGTGTCCTTC[C/T]AAAAGCAGCCAGTGACGTACAGCCTGCTCATCAATCCCAGCAGTCTTTTC
Long Flanking Sequence:
TAGACTGAAAAAATCCTTTTCTTATATTTTAGTTTAAAATAAGTACATTAATAGCGCACTTGAATATACTAATTCGTAAGTGAGCTCAAGTGTCCTTGGTGCACTAATAACTTTATTTTATTTATTTATTTAATTATTATTTTTTTTTTTCAAATTTGGCGTGAACTGATGCTGACTTTAATATAGTGACATATTTCCAGTTGAATTATTGAAAAGAAGATAATGGTCGAAAAGAACTGATTAGTCATATTCTTCCCAATCTGTCAAACAAAGAATTCATGTCATTTTAGACGATTTTCAGATATCCAAAATCCTTTTTTTCTAGATTAACTTAACCTCAAGATTAGCAGTGTTTGCTAACACACAAATAAATAGTATACATTTTGATTCCGTGAGGGCATTATTGTTTGCTTGCTTGTGTAACACCATTTTCAAAATAATAGTCACACTGACTCTTTCTTTTCTCACCCAGCTTTCTTGTCACTCCTGCGGTGTCCTTC[C/T]AAAAGCAGCCAGTGACGTACAGCCTGCTCATCAATCCCAGCAGTCTTTTCAGCATCCAGCCTGAGACGGGGGAGATCAGTCTGACCCGCTCTATAGACTATGAGAGTGATCAGCACCGCTACCTGCTGCTGGTGAGGGCCAGTGAGAACCAGGACAGTCTGAGTAGTGCTGCCGAGGTGAGTGTCAGCGCTGCAGGTGAATACAAAAACGTGAACATGCACTAGATTTATAGATTTCATGAATTGGGAAATCAGATATTTTGATCTTTTGAGTAACAAATAACTTTATTAAAAAATGAGTGGTGATCATGGTGATGTACACTGTTAGGGGAAACCTCAACATTCAAAGAGGTAGTGATGAAGAGGTTGTTTCTTCATGCAAAATAGATTTAAGCTAGCATATAGCTAATGTACTTTAAATTTTGAATGAAGGCCTAAAGGGCCTTAGGTGTATTTTAGACCTAAAGGGCGAATGGTGTATTTAGATTTATAAAACAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40993
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 187 | 2532 | 3 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49144936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47412555 |
GRCz11 | 7 | 47685634 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATCCAGCCTGAGACGGGGGAGATCAGTCTGACCCGCTCTATAGACTA[T/A]GAGAGTGATCAGCACCGCTACCTGCTGCTGGTGAGGGCCAGTGAGAACCA
Long Flanking Sequence:
CACTAATAACTTTATTTTATTTATTTATTTAATTATTATTTTTTTTTTTCAAATTTGGCGTGAACTGATGCTGACTTTAATATAGTGACATATTTCCAGTTGAATTATTGAAAAGAAGATAATGGTCGAAAAGAACTGATTAGTCATATTCTTCCCAATCTGTCAAACAAAGAATTCATGTCATTTTAGACGATTTTCAGATATCCAAAATCCTTTTTTTCTAGATTAACTTAACCTCAAGATTAGCAGTGTTTGCTAACACACAAATAAATAGTATACATTTTGATTCCGTGAGGGCATTATTGTTTGCTTGCTTGTGTAACACCATTTTCAAAATAATAGTCACACTGACTCTTTCTTTTCTCACCCAGCTTTCTTGTCACTCCTGCGGTGTCCTTCCAAAAGCAGCCAGTGACGTACAGCCTGCTCATCAATCCCAGCAGTCTTTTCAGCATCCAGCCTGAGACGGGGGAGATCAGTCTGACCCGCTCTATAGACTA[T/A]GAGAGTGATCAGCACCGCTACCTGCTGCTGGTGAGGGCCAGTGAGAACCAGGACAGTCTGAGTAGTGCTGCCGAGGTGAGTGTCAGCGCTGCAGGTGAATACAAAAACGTGAACATGCACTAGATTTATAGATTTCATGAATTGGGAAATCAGATATTTTGATCTTTTGAGTAACAAATAACTTTATTAAAAAATGAGTGGTGATCATGGTGATGTACACTGTTAGGGGAAACCTCAACATTCAAAGAGGTAGTGATGAAGAGGTTGTTTCTTCATGCAAAATAGATTTAAGCTAGCATATAGCTAATGTACTTTAAATTTTGAATGAAGGCCTAAAGGGCCTTAGGTGTATTTTAGACCTAAAGGGCGAATGGTGTATTTAGATTTATAAAACAACAGGAGATTTAAACATCCTTTAACTGCAACATTTCTTGTCAGTGTTAATTATTTAAAAAAAATATATATATATATTTTATTTTATTTTATTTTATTTTATGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34166
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 442 | 2532 | 9 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49076645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47344264 |
GRCz11 | 7 | 47617343 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTGTTCTTTGTTTTTGTCCCCTCCTCAATCCCTTAGTGTGCCGAGTA[T/A]AAGGAGAAGGCCTCAGTTCTGGAAAATAAGCCTGCAGGATCATTTGTGCT
Long Flanking Sequence:
TAAATAATTCATTCATTCATTCATTCATTCACTCTTGCATCCCTTTGTTACTTTGTTTGTTTATTCATTCATTCGTTAATCAAATCATTCATTCATTCATTCATTCATTCATTCATTCATTTGATTTAAAGCTGATAATACATCTCAAAACATCACATTTGTGTTTATATTAATATGCACATGCATTTCAGGCTGTATTGTTTTATTATTATTATCATAATTGTTGTTTACATTTTATTTTCTTTTTTTTGCTTCACAAACACTCAATCTAATAGCATCACCCAGAGATCTGTCTTTTAATAAATCCTATTGTGTTTTGACTGGAGATGTAGTTTCAAACAGCCTGTTTTCACCAAATGTAAGCAATGATGTATCTTCTGCCGAGAGAAATCCTAATACAAGTTTAATCCGCCTTTTGATTGTTTTACTGTACAGTACTGTACATCTCTCATTGTGTTCTTTGTTTTTGTCCCCTCCTCAATCCCTTAGTGTGCCGAGTA[T/A]AAGGAGAAGGCCTCAGTTCTGGAAAATAAGCCTGCAGGATCATTTGTGCTCCAGGTCCATGCTGATGATGCTGATGAAGGAGCCAATGGGAAAGTAACTTACGGTTTCATGCATAAAGACAGCACTGTTCCTGCCTTCAGCATTGACCCAGAAACAGGTAACGTTTCAAGCACACTTAAACATTCAATGAGCTCATTCATCATTAAATGTAAACCCATTTACTGCACCGAGGGCATAGATGAACTTCATTGTCATTCCTTTAAAAATAATCAGATGTCATTTAAGATAATGATCAGAGGACTTGAAATAGAACTTTTTAGGGCAAACGGTTAACTTTATATATATATATATATATATATATATATATATAATGTCTTATTTAGCACTCATTAGAAATATTGTCATCATCATCCCCTCTCTCTCTCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCAAATTTAAATTCAAATTCAAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40992
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109511 | Essential Splice Site | 791 | 2532 | 14 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49050056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47317675 |
GRCz11 | 7 | 47590754 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTCTCCAAGTGTCAGCCAATGATCTTGACCTGGGGCTGAATGGAAAG[G/A]TATGTAATTTTGAGTTGAATTAGCTATTCACTGAATCTGCCTCCGCATAA
Long Flanking Sequence:
GAGTTTTAATTTCCCTCAAGCTACCGAGAATATTTCTGCATATCTGCATATATACGAGGGCAAACTTTCGCATTAAGACTGTAAACAATGCACAAACATCGATTCAGGTGAATAATGTTTTGTTAAACGACATCTGTTCTGTGTAACAAAAGCCACATTATTCCGTTTCTTTGAATGGCAGAGAGTCTGCATTCATATCAGCGTGCAGCAGACTTGCAATATTCTTTCTTTATGTGACAGCCGAAGAAAAGCGATGGAAATATTATACCAGTTGTCTGTCGGGTTTTATAACTGATACCCCACAAGGGACCACAGAGATATGGCGCTGTTTTGGTTTGTTAAATTAACATTGCGACCGTCTGCTTTTGACAGATGTCAACGACAACGTTCCGTTCTTCACCTCCTCCATATACGAGGCATCTGTGACGGAAGGAGTGGAAATAGGGACTTTGGTTCTCCAAGTGTCAGCCAATGATCTTGACCTGGGGCTGAATGGAAAG[G/A]TATGTAATTTTGAGTTGAATTAGCTATTCACTGAATCTGCCTCCGCATAAACCTGTAAACACTGCACACATTACTACACTGACTATTGTGCTCACTGTGGAAAGATCTATACAATTCTGAGAACATTCGTGATATAACTCAGCATGAATAGCATGATATTCTGTGACCTCCAGAACTCACTTATTTATTCTGATAAACTGACTACCTTTTCTCAGCCTTGTTTTGGAAGGGCGAACGTGTCTGCAGTGCTTAGGTTTCATTATTGTGTACATAATAGCATTCTGTGCTGTACACATTCTGTTCAGATATTTCTTATAAAGGCTTTGAGAAAAAGGTATGTTTAATATATCAATTTGCAGAGTTTCTATCATTATGTATATCATTTATTCAACACTACTGTTCAAAAGATTGGGGTAGGAATTAAATTTTTCTTCTTTATTTATTCATTCGTTCATTTTCCTTCGGCTTAGTCTTCAGAATGAACTGCCAACTATTCCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34165
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 877 | 2532 | 16 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49034200)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47301819 |
GRCz11 | 7 | 47574898 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATCAGTGACGTGAACGATAACAAGCCGGTGTTTGCCCAGCCTGTATA[T/G]GAAGTGGACGTGGATGAGGATGCTGACGTGGGCTCCACCGTCCTCACAGT
Long Flanking Sequence:
CCCACCTGAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGGCCCAGTCTGGGACTCGAACCAGCGACCTTTTTGCTGTAAAAGTGCTAACCATTAATGTGGGGGAAGCATCACAAATTTTTACTTGCCTGCATGAGTAAACACAGAACCCCTAAGGTTTTTGACGGCACCTGATGCGTTAAGACCCAAAATAGAGTCACATGCGAGAAGTAGATAGAGAGATGAAGATAGGCAGAAAATAAATGAGACAAACAGAATTCTCATGAATTTGATGGAATTGGAAATGGCAGTTATTTACAAAGATGGGAGGAAAAGGCAAGAGGAAACGAGAGACAAGCACTTGAACGTAAGAAAGGAAAGAAAGGTAAAGGTAAGATAAGAGCGCACTGATTGCTAGTAATGTGTTTTTACTCTCCTCAGATACGGCATACGTGCGCATTTTCATCAGTGACGTGAACGATAACAAGCCGGTGTTTGCCCAGCCTGTATA[T/G]GAAGTGGACGTGGATGAGGATGCTGACGTGGGCTCCACCGTCCTCACAGTCAGCGCTAATGATGAAGATGAAGGTAGGTGAAGATCAAGAGCAGGATATTTTGGTGCGCAGATTAGAACAATATGCAGATTGCAGGAAACAGAGTGTTCATTTGGTGAAAATGAGGGTTTGTACATTTGACAACCTGACATCACAGCTCAGGTGTGATCATTTACACCTGGTGAATACATGTTCTGCCGAGTGTGAGGAAGACATGTTAATTAATATATTAACTAATTAGAGACACGGAATGTCATTTTTGCTGCCAGAAGGTACCTATTCACAAAAATCCAAATGCATAGATTGTTTTGTTGTGACATAGGGCTCATGGTCTAACAGGGTTGTGCTTATTCTCTTATTGAGTTATGGGTGTGTTTTGAGCATAGCGTGCATTAAACCAACCAGACTCTCATCCTCCATTCCCTTTAATAGTAAAGTGCGCCACACCATGGTGCATTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15416
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 939 | 2532 | 17 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49026457)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47294076 |
GRCz11 | 7 | 47567155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAGCCTGAGGTGGGGACCAYCTTCAWCGCCCAGCCATTGGATTATGAA[C/T]AAAACAAGCTCTACAAGTTGCACGTCTTGGCCTCGGATGGCAAGTGGGAG
Long Flanking Sequence:
TTTTTTTTAGACCATTGTTAAACATTCGGAAAAAAAGAAATAGAGAATTTTTAATTCTAGACATATCTTCACCTAATTTAAGGTTTATTGGTCTGTTTCCATGGTGGCGAGTGTCCAAGGCTGCTCTTAACAATAACCTCTAAAGGCCATCAAAGCAGTTTATTGTTCACCTGCAGCAAAAAGCTTGTTATCATGCTTTAAATATATATCGTTTTTCCTGCTAAGCATTTTTTGACACTTTAAGAAATGCCTGACTTTTAGCCTTTTGTCCAATAGCTTTTACATCCGCTTAAATGAAGATATTTCACTTCCTCGTTGTTCTTCTTGAGATTTTATTCAAGCCATAGCAAAAAGCATTCTCTCTGTTCAGTAACTGTTCTTATTCTTTAGGTGCTAATGCCAAGTTACGCTACCAGATTACCTCAGGAAATGTCGGAGGTGTTTTTGACATGGAGCCTGAGGTGGGGACCATCTTCATCGCCCAGCCATTGGATTATGAA[C/T]AAAACAAGCTCTACAAGTTGCACGTCTTGGCCTCGGATGGCAAGTGGGAGCATTATGCTACAGTGATAGTTACAATTGTGAATAAAAATGATGAGGCACCTGTTTTCTCTGTGAATGAGTACTACGGCAGTGTGACAGAGGAGCTGGATGGTTCTCCTGTCTTTGTGCTACAGGTACAGTTTCTAGTTTCTCTTCTTGGATTCCATCAGCTCTGTGTTATTTTTCAGCTCATATTTTTGTTATTTCAAAATGTCATTTGAGGCTTTTATTTCTTTTTGGGAAAAAAAGTGTGTTAGTAGTCTCTCTAAATGTAATAAAAAAAGGTCATTGATGTGTGAATTAACACATTCTTCTTTCATTATTACGCTTGTTACAAATTAATAATACAACATCATTGGAAATTGCCCAAGCACTCATTTGCATGTCCTTGTCAGGGTATTTTGTGTTTTGTTTTTTGTTGTTATTATTATTATTATTATGGTGAAAATTGGGATTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40991
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 1094 | 2532 | 18 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49023740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47291359 |
GRCz11 | 7 | 47564438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTCCTATTTTTGCGTGTGCTCCGGACAGTTGCCATGGAGATGTGGCT[G/T]AAAATTCTCCCCCTGGCACCTCTGTCATGGAGATGACGGCCACTGATCTG
Long Flanking Sequence:
AGATGTATGAACAGACAGTTGGAAAGATGCACAGAAGGTTGTGCAGATAAAATAGATGATAGATCAATACACATAGAGAAATATATGGATGACTAGAACATGTACAGATAAAATGAGTATATATGGATGGATGGTTGGAGGAATAGAGTGATTTTTGTTTTTGCTAAGTGTGCAGAATAATCTTCAATATATTCTCTTTGATGTTGCAGGTAACAGCTTCTGACCCAGATAAGGATGCTGACCAGGAGGCTTTGAGATATTCCCTTCATGGTCAAGGTGCTGAGAGCGAGTTCATCATTGACGAGGTGACTGGGAAGATTTATGCCCAGAGAACATTAGACCGCGAGGTCCGGGCAGTGTGGCGTTTTGTGGTCCTGGCTACAGATGAGGGTGGCGAGGGGCTGACAGGATTCACAGATGTCATCATCAACGTATGGGACATAAACGACAATGCTCCTATTTTTGCGTGTGCTCCGGACAGTTGCCATGGAGATGTGGCT[G/T]AAAATTCTCCCCCTGGCACCTCTGTCATGGAGATGACGGCCACTGATCTGGATGATGCAGCTGTCGGACAAAACGCAATGCTGGCCTATAGGATTGTAGGTAATGCTGCTCTTAATGGAGCTAACAATGGAGCAGATATGTTTAACATCAATCCGGCAACTGGGACTGTTTCTGTATCGATGTCTGGCCTGGACAGGGAACAGATTGACTCGTATGTATTGGTGGTGGAGGCACGGGATGGTGGAGGTATGATTGGATCAGCCACCGCCACTATCCACGTAACAGACGTTAATGACCACATACCTCGTTTCCTGGACCGCTCCTGCTTCGTGCGCATCCCTGAAAGCAGTGAGCCCAACACGGCCGTAATTGAGCTCGCCGCAGAGGATGCAGATGCTGGAGAAAATGGCCAGCTTACCTTCAGCGTAGTGGCTGGTGATCCCGAACAGAAGTTTTACATGGTAAGCCATCGACAGGAGCAGCGTGGGACTCTTCGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21053
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 1153 | 2532 | 18 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49023562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47291181 |
GRCz11 | 7 | 47564260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCAGATATGTTTAACATCAATCCGGCAACTGGGACTGTTTCTGTAT[C/A]GATGTCTGGCCTGGACAGGGAACAGATTGACTCGTATGTATTGGTGGTGG
Long Flanking Sequence:
AATCTTCAATATATTCTCTTTGATGTTGCAGGTAACAGCTTCTGACCCAGATAAGGATGCTGACCAGGAGGCTTTGAGATATTCCCTTCATGGTCAAGGTGCTGAGAGCGAGTTCATCATTGACGAGGTGACTGGGAAGATTTATGCCCAGAGAACATTAGACCGCGAGGTCCGGGCAGTGTGGCGTTTTGTGGTCCTGGCTACAGATGAGGGTGGCGAGGGGCTGACAGGATTCACAGATGTCATCATCAACGTATGGGACATAAACGACAATGCTCCTATTTTTGCGTGTGCTCCGGACAGTTGCCATGGAGATGTGGCTGAAAATTCTCCCCCTGGCACCTCTGTCATGGAGATGACGGCCACTGATCTGGATGATGCAGCTGTCGGACAAAACGCAATGCTGGCCTATAGGATTGTAGGTAATGCTGCTCTTAATGGAGCTAACAATGGAGCAGATATGTTTAACATCAATCCGGCAACTGGGACTGTTTCTGTAT[C/A]GATGTCTGGCCTGGACAGGGAACAGATTGACTCGTATGTATTGGTGGTGGAGGCACGGGATGGTGGAGGTATGATTGGATCAGCCACCGCCACTATCCACGTAACAGACGTTAATGACCACATACCTCGTTTCCTGGACCGCTCCTGCTTCGTGCGCATCCCTGAAAGCAGTGAGCCCAACACGGCCGTAATTGAGCTCGCCGCAGAGGATGCAGATGCTGGAGAAAATGGCCAGCTTACCTTCAGCGTAGTGGCTGGTGATCCCGAACAGAAGTTTTACATGGTAAGCCATCGACAGGAGCAGCGTGGGACTCTTCGTCTCAAAAAGCGACTGGATTACGAAAGACCAGGCGAGCAACGTTTCAACCTTACCATCAAAGTGGAGGATATGCAGTACTCCACTCTTCTACACTGCACACTCGAAATCGAGGACTGCAATGACCACGTGCCGGTCTTCATTCCTCACTTCCTCCAGCTTCCTGCCATACGAGAGGACGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27032
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 |
---|---|---|---|---|---|
ENSDART00000109511 | Nonsense | 1536 | 2532 | 20 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 49017373)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47284992 |
GRCz11 | 7 | 47558071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTACACCTGATGCGCAATCTATGTTTTGACACATGGTTTTTTTTTATAA[T/A]GACAGGGAGAATGCCAACCAATGTGCTGGGAAAGGTTTACTCTCCAGATC
Long Flanking Sequence:
TGTTTATTCTTAGTTCATGTAATTAAATGGATTAACTCAAATGAACTAGTTGAATGTTATTGTAAAGTGTGACCACTGATTCTCCTTAATAATTAACCCTTCCATGGGGCTATTTATCTTTTTATTAAATAACTACTATTTATTTCTAGATTATTTAAGGCTAAAATCATTTAATATAATTTGCTTTGTACATCTGACCTTTGACTTTTATTTATTTATATCATTTATAACTGATTTTGTCCCATTTAGGGTAAATCATTTTTGTAAACTTGTCTGAAACTGGCTATTGTGACACGACTATTTACATTTATACAGACTCCGCATATAGAGCACAGCATGTCTGTTTACAGTTGTCAGTTCACATAAGTCTATAGACAGTTCTGAATTCTTGCAGTGGCATACTGTAGTGTTTTTACAGACACAAACATGCATTTATATACTGTACTGTATCCTACACCTGATGCGCAATCTATGTTTTGACACATGGTTTTTTTTTATAA[T/A]GACAGGGAGAATGCCAACCAATGTGCTGGGAAAGGTTTACTCTCCAGATCCAGATGACTGGGATAACAAGACGTATGCCTTCGAGGGACATGTTCCTAAGTGAGACTTTTTCTTTTCTTCTCCACTCTATTTTCTAGCACCTTTTCCTTTCTGTCCACATCGTTGCATCATCCCCTCCACCTTGTTAACATGTTTATACACCTCTCACTGCACCCTTGCTCTCAAACATTTTTTTTTTCTGCACCTTTTGTGATGCTAAGGGGTCAGGGGGTCTCTAAAAAACAATGTCTAATCCATGGTTCTCACATCCAAGCATCATTCATCTTCACTTTTTCTTTTCTACTGATGTTGTACATTTTTCTTGAGAGGTGAATACAATGATTAGATATTCTTGACAGGACCAGTCTTGATGTTTTGAGCACACAGGCACCTGAGCTCTCGCTTTCTGAAAGAACTCAATATACACATCAAAAATTCGGATTATTCCATTAGGAAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27030
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109511 | Essential Splice Site | 2414 | 2532 | 35 | 35 |
ENSDART00000109511 | Essential Splice Site | 2414 | 2532 | 35 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 48879327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 47146946 |
GRCz11 | 7 | 47420025 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCCTCCCGAGCGGGAACAGCCACCACCACCACCTCCTCCATCTCCTC[A/G]GGATCTGCCACCATCCGCAGGGATGTCCCCCCCTGCCGCTCTCCGGCTCA
Long Flanking Sequence:
TCAGGATTCTTCCTCTCAGGTGCAGGAAGGCACACATAAAGGTGTTAATCATAACGCAGTGTTAGCAGCTTGAATCCGGATTAATGCCATTAACAGTTTAGGGGATAATAAATTACGTGATGAAGAAGTACAGACAAGCTGCTTATTTTGTCAGTGAGCTCAGACTTATTAGTCGTAGCAGTTTTTGTGACAGACGCTGTTGTTATTACACCAGTTCCTGAATGTAATGGCGGGTTATGTAAGGCTAATGATCTTGTTATTTGTCAGCGCTTTATGCATTTCATTTCCCCCTCTCTCTTTCTCGCCCTCCTTTAGAATGCCTATGACATGGCGGAGCTCCAGAAGTCCCTGCAGCCGAGTCCAGCACAGTCGGTGCAGTACAGCCGCTCGAGGGCCATCCACCACCACCCACCCTCCCAGCAGCAACAGCAACACTTTTGCCAGCCTGACCCTCCCTCCCGAGCGGGAACAGCCACCACCACCACCTCCTCCATCTCCTC[A/C]GGATCTGCCACCATCCGCAGGGATGTCCCCCCCTGCCGCTCTCCGGCTCAAGGCCAGACTGCAAATCCCAGTCGGGCGGCACAGCTGGCCCGCAAGAGCCTGTCATTCTCCAGCCAGGACCTGGCCCGCTACCTGTGTGAAATTATCCGTGATGCCGACCAGCACCCAGAGACGGCGCCCTTCGACTCCCTGCAGGTCTTCTCCACGGAGGGGGGCGGCTCGCTGGCTGGGTCACTGAGTTCCTTCAGCTCCGCTGGGCTGGAAGAAGGAATGGCAGCAGGGCATGAGTGTTTGAAAGAGTGGGGGCCTCGTTTTGAGAAGCTGAAAGCTCTCTATGAGCGGGCCGAGGGCAGCGACCTCTAAGGAACTGCCGGGAAGTGTTCTTGCAGCTCGAGGAGAGGAGGGAGACCACTAAAGACATGCCTAAAAACCAGAGAGCTTTTTCTTATGCTGAAAAGTCCTACGCTCCGACTTTCTCTGGATGTATTACTTCACACGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45294
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109511 | Essential Splice Site | 2414 | 2532 | 35 | 35 |
ENSDART00000109511 | Essential Splice Site | 2414 | 2532 | 35 | 35 |
Genomic Location (Zv9):
Chromosome 7 (position 48879327)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCCTCCCGAGCGGGAACAGCCACCACCACCACCTCCTCCATCTCCTC[A/G]GGATCTGCCACCATCCGCAGGGATGTCCCCCCCTGCCGCTCTCCGGCTCA
Long Flanking Sequence:
TCAGGATTCTTCCTCTCAGGTGCAGGAAGGCACACATAAAGGTGTTAATCATAACGCAGTGTTAGCAGCTTGAATCCGGATTAATGCCATTAACAGTTTAGGGGATAATAAATTACGTGATGAAGAAGTACAGACAAGCTGCTTATTTTGTCAGTGAGCTCAGACTTATTAGTCGTAGCAGTTTTTGTGACAGACGCTGTTGTTATTACACCAGTTCCTGAATGTAATGGCGGGTTATGTAAGGCTAATGATCTTGTTATTTGTCAGCGCTTTATGCATTTCATTTCCCCCTCTCTCTTTCTCGCCCTCCTTTAGAATGCCTATGACATGGCGGAGCTCCAGAAGTCCCTGCAGCCGAGTCCAGCACAGTCGGTGCAGTACAGCCGCTCGAGGGCCATCCACCACCACCCACCCTCCCAGCAGCAACAGCAACACTTTTGCCAGCCTGACCCTCCCTCCCGAGCGGGAACAGCCACCACCACCACCTCCTCCATCTCCTC[A/G]GGATCTGCCACCATCCGCAGGGATGTCCCCCCCTGCCGCTCTCCGGCTCAAGGCCAGACTGCAAATCCCAGTCGGGCGGCACAGCTGGCCCGCAAGAGCCTGTCATTCTCCAGCCAGGACCTGGCCCGCTACCTGTGTGAAATTATCCGTGATGCCGACCAGCACCCAGAGACGGCGCCCTTCGACTCCCTGCAGGTCTTCTCCACGGAGGGGGGCGGCTCGCTGGCTGGGTCACTGAGTTCCTTCAGCTCCGCTGGGCTGGAAGAAGGAATGGCAGCAGGGCATGAGTGTTTGAAAGAGTGGGGGCCTCGTTTTGAGAAGCTGAAAGCTCTCTATGAGCGGGCCGAGGGCAGCGACCTCTAAGGAACTGCCGGGAAGTGTTCTTGCAGCTCGAGGAGAGGAGGGAGACCACTAAAGACATGCCTAAAAACCAGAGAGCTTTTTCTTATGCTGAAAAGTCCTACGCTCCGACTTTCTCTGGATGTATTACTTCACACGAG
Associated Phenotype:
Not determined