ZMP
LOC100005951
Ensembl ID:
Human Orthologue:
IGSF10
Human Description:
immunoglobulin superfamily, member 10 [Source:HGNC Symbol;Acc:26384]
Mouse Orthologue:
Igsf10
Mouse Description:
immunoglobulin superfamily, member 10 Gene [Source:MGI Symbol;Acc:MGI:1923481]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22567 | Nonsense | Available for shipment | Available now |
sa35779 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22568 | Nonsense | Available for shipment | Available now |
sa35780 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10949 | Nonsense | Available for shipment | Available now |
sa16954 | Nonsense | Available for shipment | Available now |
sa42465 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22569 | Nonsense | Available for shipment | Available now |
sa24972 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18534 | Nonsense | Available for shipment | Available now |
sa9744 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22567
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 552 | 2497 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1092451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1135085 |
GRCz11 | 15 | 1095888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGGAATTCTTTCTGTAAAATCAGCTGAAATCTCAGACACGGGTGTCTA[T/A]CATTGCATTGCGACCAGCTATCTGGATGCAGATGTTCTTGCCTTTAGGGT
Long Flanking Sequence:
GATTTCCCAATGATCCTTGAGCGAGAATTAGCAATTTCTTTACAATCAGACGCAGTCTACACATATAAGCAGGCAGTGTCCACTGCAGAGGATGTTTTCACAGAAATCGAAGCAAAAATCAAAGCCATTCCTGAATGGTTAATGCAAGGTAGGGTTATGCTACAACTGGATCGTGCAACAACAGCATTCCCAACACTTACCATCAAGTATTTATCGACCATTCAAATAGATGTTGGGGGCAGCAAGAATAATAGAGATGAGTATAGTTGGACTATGATTAGAAGGGACAACCAGACCAGGACTGAGCACTTACTCCTTGTTGGTGGCATGACTGAATTAAATTGCCAGACTTTCGGGAATCCCAAACCCATAATTGAATGGATTCTACCAGATGGAAGTAAGATACGTGCACCATATAACAGCGAGGACCAAAGGATTGTAATAACTCATGAAGGAATTCTTTCTGTAAAATCAGCTGAAATCTCAGACACGGGTGTCTA[T/A]CATTGCATTGCGACCAGCTATCTGGATGCAGATGTTCTTGCCTTTAGGGTCACTGTGATGCCTCTGGATATTGAGGAGGAAGAGATTAACGGAATCAGAGTCTCACATCACCTTGGTCAGAACCTACGTCTTGATTGTACATCACTTAGCAGTCCACAGGCGTCCATCCAGTGGATACTTCCCGACCACACAGTTTTAGACAAATCTTATGGCAAAAGAACTCTCCATAGAAATGGCACTTTGGTCATACATGGATTGACTTACAGGGACATAGGGTTTTACAGATGCTTAGCTGGAAATTTTCTGGGAGCGGACTTGCTTGCTTCTCAAGTAACCATCTATGATGATTGGGTAAATAGCACAATGCCAACTCATGTAAAGGAATCTAACCATCGTGTTGTACAAATTATAGACAATAGTCAGACACTTGGAAGTAGGTATCTCTCTCAAAGGACAAGTGAGGAGTCAAGGAGTATTACCTCAGACAGGCCTTACACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35779
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 554 | 2497 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1092457)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1135091 |
GRCz11 | 15 | 1095894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCTTTCTGTAAAATCAGCTGAAATCTCAGACACGGGTGTCTATCATTG[C/A]ATTGCGACCAGCTATCTGGATGCAGATGTTCTTGCCTTTAGGGTCACTGT
Long Flanking Sequence:
CCAATGATCCTTGAGCGAGAATTAGCAATTTCTTTACAATCAGACGCAGTCTACACATATAAGCAGGCAGTGTCCACTGCAGAGGATGTTTTCACAGAAATCGAAGCAAAAATCAAAGCCATTCCTGAATGGTTAATGCAAGGTAGGGTTATGCTACAACTGGATCGTGCAACAACAGCATTCCCAACACTTACCATCAAGTATTTATCGACCATTCAAATAGATGTTGGGGGCAGCAAGAATAATAGAGATGAGTATAGTTGGACTATGATTAGAAGGGACAACCAGACCAGGACTGAGCACTTACTCCTTGTTGGTGGCATGACTGAATTAAATTGCCAGACTTTCGGGAATCCCAAACCCATAATTGAATGGATTCTACCAGATGGAAGTAAGATACGTGCACCATATAACAGCGAGGACCAAAGGATTGTAATAACTCATGAAGGAATTCTTTCTGTAAAATCAGCTGAAATCTCAGACACGGGTGTCTATCATTG[C/A]ATTGCGACCAGCTATCTGGATGCAGATGTTCTTGCCTTTAGGGTCACTGTGATGCCTCTGGATATTGAGGAGGAAGAGATTAACGGAATCAGAGTCTCACATCACCTTGGTCAGAACCTACGTCTTGATTGTACATCACTTAGCAGTCCACAGGCGTCCATCCAGTGGATACTTCCCGACCACACAGTTTTAGACAAATCTTATGGCAAAAGAACTCTCCATAGAAATGGCACTTTGGTCATACATGGATTGACTTACAGGGACATAGGGTTTTACAGATGCTTAGCTGGAAATTTTCTGGGAGCGGACTTGCTTGCTTCTCAAGTAACCATCTATGATGATTGGGTAAATAGCACAATGCCAACTCATGTAAAGGAATCTAACCATCGTGTTGTACAAATTATAGACAATAGTCAGACACTTGGAAGTAGGTATCTCTCTCAAAGGACAAGTGAGGAGTCAAGGAGTATTACCTCAGACAGGCCTTACACTTGGCTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22568
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 687 | 2497 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1092854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1135488 |
GRCz11 | 15 | 1096291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATAGCACAATGCCAACTCATGTAAAGGAATCTAACCATCGTGTTGTA[C/T]AAATTATAGACAATAGTCAGACACTTGGAAGTAGGTATCTCTCTCAAAGG
Long Flanking Sequence:
TACGTGCACCATATAACAGCGAGGACCAAAGGATTGTAATAACTCATGAAGGAATTCTTTCTGTAAAATCAGCTGAAATCTCAGACACGGGTGTCTATCATTGCATTGCGACCAGCTATCTGGATGCAGATGTTCTTGCCTTTAGGGTCACTGTGATGCCTCTGGATATTGAGGAGGAAGAGATTAACGGAATCAGAGTCTCACATCACCTTGGTCAGAACCTACGTCTTGATTGTACATCACTTAGCAGTCCACAGGCGTCCATCCAGTGGATACTTCCCGACCACACAGTTTTAGACAAATCTTATGGCAAAAGAACTCTCCATAGAAATGGCACTTTGGTCATACATGGATTGACTTACAGGGACATAGGGTTTTACAGATGCTTAGCTGGAAATTTTCTGGGAGCGGACTTGCTTGCTTCTCAAGTAACCATCTATGATGATTGGGTAAATAGCACAATGCCAACTCATGTAAAGGAATCTAACCATCGTGTTGTA[C/T]AAATTATAGACAATAGTCAGACACTTGGAAGTAGGTATCTCTCTCAAAGGACAAGTGAGGAGTCAAGGAGTATTACCTCAGACAGGCCTTACACTTGGCTACAGTCCCGATTTCATAAAGTTCCCATCGGTAGAAGAGGGAATGGAAGGAACTCTAGAAGAGTCTTTAATAAAAGGTTTCAGAAAGAGGGGAAAACGTTGATCAACAAGCCTCAAATCAAAGAAATAAATAAAGAGGCAGTAAACTTGTCTAAAACTCTCTTTAAAGAACAATCTGATGACAATAACGCAGCCTCGGGGGATGGTATAAATGAAGATGAATTTATTGTAATTTCAACAACTAAAACACTTGAGAAAAAACAAGTTAGCTCCATCAACACTGAAATCCCAAGGACTTACAAAACAGTTAACAGTGCTTTCATTCAAGTAACATCTGATGACACTAGTCATGTCTTAAGAACAAAGAAAAAAAGTAATTTGGTTACAGGAATAACAGACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35780
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 877 | 2497 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1093424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1136058 |
GRCz11 | 15 | 1096861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTCCAAGCTACACTTTAAGTAACTATGGAACACAAAGAAATTACAAA[A/T]AACAAAGTAAGACCAAGTCAGATTATAAATTAAATCAAACTGATGGAGAA
Long Flanking Sequence:
GTATTACCTCAGACAGGCCTTACACTTGGCTACAGTCCCGATTTCATAAAGTTCCCATCGGTAGAAGAGGGAATGGAAGGAACTCTAGAAGAGTCTTTAATAAAAGGTTTCAGAAAGAGGGGAAAACGTTGATCAACAAGCCTCAAATCAAAGAAATAAATAAAGAGGCAGTAAACTTGTCTAAAACTCTCTTTAAAGAACAATCTGATGACAATAACGCAGCCTCGGGGGATGGTATAAATGAAGATGAATTTATTGTAATTTCAACAACTAAAACACTTGAGAAAAAACAAGTTAGCTCCATCAACACTGAAATCCCAAGGACTTACAAAACAGTTAACAGTGCTTTCATTCAAGTAACATCTGATGACACTAGTCATGTCTTAAGAACAAAGAAAAAAAGTAATTTGGTTACAGGAATAACAGACTCTCAGACTCCTACCTCTCCAATAACTCCAAGCTACACTTTAAGTAACTATGGAACACAAAGAAATTACAAA[A/T]AACAAAGTAAGACCAAGTCAGATTATAAATTAAATCAAACTGATGGAGAAACCTCTTTATATGATACCGCAACAAGTAGACCCTCGGAGACACTTGTGACTCACAAACCTTCTCTGATCGAAGTTACAGAGCTTACGTTCTCTGGGGATTCAGAAGATGTTACCTCTGGGACAACACAGTATAACTTCCAAGGCCCAAATGTCACCAATGTGGAGCCTAAGAGTCAGACGATATTCACAGCAGTCACCACAACCGAAGATCAAGAGAAGATCACATTTCAGACAACTCAAAGGATCAAGTCAGAGCTCCTTCCTGGGTCTACCATCATCTCTAAACACCAGATCCAAATCGTTCCTTCCAGAAAAATGCAACCAGGAAAGAAGCGCAAGTTTAACGGCAGGCGTAGGATCATTCGTCCCAGCAAAATTTCAGACATACAGTCAATACTTGATAAATTTAAACTTCATTCTACAAACAAGGAAGACAACCTCCCAATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10949
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 1990 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1098400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1141034 |
GRCz11 | 15 | 1101837 |
KASP Assay ID:
2260-8026.1 (used for ordering genotyping assays)
KASP Sequence:
AATGGAACGCTGTACCTGAAYACAGTGGGTACYGACGAGGAAGGGGACTA[T/A]ACCTGTTATGCTGAWAACAAATTGGGTAAAGACAAGAWGCATGTTCACAW
Long Flanking Sequence:
TTATTTTTTCAAATCAACTGTTAACAGAATTCATTGTGTAAATGTGTTTTAAAATGTGTTTTAAAAACTGTGTTTTTATTATTTATTAAAACATCACATTCTCCTTTCAGAATGGGCAGTCGCATCAAAGTCCTGGAAAATGGTACCCTAATCATTGAATCACTCAATGAGAAAGATAGTGGGGACTTCCTCTGTGTTGCACGCAACAAAGTTGGAGATGACACACAGCTAATGAAGGTATCAGTATCTATGAAGCCAGCTCGAATTGAACCAAGTGTTTTCAGCAGGAAGCAAGTGCCTTATGGCAATGACCTAAAAGTGGACTGTGTGGCTGCTGGGGTGCCTATGCCAGAGATATCATGGGGACTCCCTGATGGTACGCTGCTCAATAGTGCCCTGCAGGCAGATGAAACGGAGGGGGACCAGTTGAAACGATACATCTTATTTAATAATGGAACGCTGTACCTGAATACAGTGGGTACTGACGAGGAAGGGGACTA[T/A]ACCTGTTATGCTGAAAACAAATTGGGTAAAGACAAGATGCATGTTCACATAAGTGTGCTAACAGCGGCGCCTTACATTCAGCACCCAAAGCTTTCTAATGCCAGAGTTAATCCAGGTGGAAATGTCCGCTTCGATTGTAAGGTTATCGGTGAGCCCAAGCCAAAGGTCTTTTGGATGCTGCCATCCAAAGACATAATCGCTGCCTCTAATGAGCGTTACTTTGTGCACGCTAATGGGTCTCTTGATATACGAAATGTTAAATTATCTGATGCTGGGGAGTATGTCTGCATGGCTCGTAATGCAGCAGGTGAGGAGAATAAAGTTTATAAACTGGACATCGATGGAAACCCACCCATAATCAATGGCTTCAAGCAAAACAGAACGGTGCTAAAAGATACAGCAATCAAATACACAAGAAAGCTAATAGACTGCAATGCTGAAGGGGATCCAGTGCCAAAGATCACGTGGATCATGCCTGACAATATATTTCTCACAGCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16954
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2074 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1098650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1141284 |
GRCz11 | 15 | 1102087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCTCTAATGAGCRTTACTTTGTGCACGCTAATGGGTCTCTKGWTATA[C/T]GAAATGTTAAATTATCTGATGCTGGGGAGTATGTCTGCATGGCTCGTAAT
Long Flanking Sequence:
TGAAGCCAGCTCGAATTGAACCAAGTGTTTTCAGCAGGAAGCAAGTGCCTTATGGCAATGACCTAAAAGTGGACTGTGTGGCTGCTGGGGTGCCTATGCCAGAGATATCATGGGGACTCCCTGATGGTACGCTGCTCAATAGTGCCCTGCAGGCAGATGAAACGGAGGGGGACCAGTTGAAACGATACATCTTATTTAATAATGGAACGCTGTACCTGAATACAGTGGGTACTGACGAGGAAGGGGACTATACCTGTTATGCTGAAAACAAATTGGGTAAAGACAAGATGCATGTTCACATAAGTGTGCTAACAGCGGCGCCTTACATTCAGCACCCAAAGCTTTCTAATGCCAGAGTTAATCCAGGTGGAAATGTCCGCTTCGATTGTAAGGTTATCGGTGAGCCCAAGCCAAAGGTCTTTTGGATGCTGCCATCCAAAGACATAATCGCTGCCTCTAATGAGCGTTACTTTGTGCACGCTAATGGGTCTCTTGATATA[C/T]GAAATGTTAAATTATCTGATGCTGGGGAGTATGTCTGCATGGCTCGTAATGCAGCAGGTGAGGAGAATAAAGTTTATAAACTGGACATCGATGGAAACCCACCCATAATCAATGGCTTCAAGCAAAACAGAACGGTGCTAAAAGATACAGCAATCAAATACACAAGAAAGCTAATAGACTGCAATGCTGAAGGGGATCCAGTGCCAAAGATCACGTGGATCATGCCTGACAATATATTTCTCACAGCTCCTTATTATGGGAGCAGGATCAATGTGCATGTCAATGGTACGCTAGAGATCCGTAATGTCCGGCCATCGGATACAGCAGAGTTTATTTGTATTGCTCAGAACGATGGAGGCGAGGCGGTCATGTTAGTTCAACTGGAAGTGACCGACAAGCTCATGAGACCCATTTTTAAGAACCCCTTTAATGAGAGAGTAGTGACTCGGGTTGGGAGAACTGCAGTGCTAAACTGTTCTGCTGATGGACAACCCACACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42465
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2274 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1099252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1141886 |
GRCz11 | 15 | 1102689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGAAGGCTCAAGATACCACCTAGGTAGGGATGGAACATTTGTGATTTA[T/G]AACTCCAGCATAGAAGACTCTGGTAAATACCGCTGCGCTGCCAAAAACAA
Long Flanking Sequence:
CCCATAATCAATGGCTTCAAGCAAAACAGAACGGTGCTAAAAGATACAGCAATCAAATACACAAGAAAGCTAATAGACTGCAATGCTGAAGGGGATCCAGTGCCAAAGATCACGTGGATCATGCCTGACAATATATTTCTCACAGCTCCTTATTATGGGAGCAGGATCAATGTGCATGTCAATGGTACGCTAGAGATCCGTAATGTCCGGCCATCGGATACAGCAGAGTTTATTTGTATTGCTCAGAACGATGGAGGCGAGGCGGTCATGTTAGTTCAACTGGAAGTGACCGACAAGCTCATGAGACCCATTTTTAAGAACCCCTTTAATGAGAGAGTAGTGACTCGGGTTGGGAGAACTGCAGTGCTAAACTGTTCTGCTGATGGACAACCCACACCCGACATCATATGGACACTACCCAACAAGACTCGATTCACTAGAGCGCAAGGGCTTGAAGGCTCAAGATACCACCTAGGTAGGGATGGAACATTTGTGATTTA[T/G]AACTCCAGCATAGAAGACTCTGGTAAATACCGCTGCGCTGCCAAAAACAAAGTGGGATATATTGAAAAGCTTGTCGTTCTTGAGGTGATTCAAAAGCCTTATATTCTAACACGGCCAAAGGGGATTATTCGGGGTATTTCTGGACAGTCTCTCTTCCTACATTGCCTGACAGATGAAATAAAGTCCACTATTTCTTGGACCATGCCAGGAGGTTTTGTTCTCGCAAGTCCACAGGTGAGTGGACGCTATCAGTTAATGGAAAATGGGACACTTGTTGTACATGAGACAACCATGCAAGATCGTGGGAATTATGTGTGCAAAGCAACAAACGACGCTGGTGAGGCTGTTCTCACTGTGTCCGTCATAATTCTTGCATATCCAGCTCGAATTACCAATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTGCAGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCTGATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22569
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2423 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1099697)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1142331 |
GRCz11 | 15 | 1103134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTG[C/T]AGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCT
Long Flanking Sequence:
AAGGGCTTGAAGGCTCAAGATACCACCTAGGTAGGGATGGAACATTTGTGATTTATAACTCCAGCATAGAAGACTCTGGTAAATACCGCTGCGCTGCCAAAAACAAAGTGGGATATATTGAAAAGCTTGTCGTTCTTGAGGTGATTCAAAAGCCTTATATTCTAACACGGCCAAAGGGGATTATTCGGGGTATTTCTGGACAGTCTCTCTTCCTACATTGCCTGACAGATGAAATAAAGTCCACTATTTCTTGGACCATGCCAGGAGGTTTTGTTCTCGCAAGTCCACAGGTGAGTGGACGCTATCAGTTAATGGAAAATGGGACACTTGTTGTACATGAGACAACCATGCAAGATCGTGGGAATTATGTGTGCAAAGCAACAAACGACGCTGGTGAGGCTGTTCTCACTGTGTCCGTCATAATTCTTGCATATCCAGCTCGAATTACCAATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTG[C/T]AGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCTGATCGCTCGATTCTTGCTACGAATGGAAAGGGACAACCTGTCGGCAGTGAGCTTCTCCAAGCACAAGGGACACTTATAATTCGAAATCCTACAAGAATGCATTCTGGGAATTACAAGTGTATCGCCTTTAATTACCTGGGCAGAGATACCAGAACAACATACATGACAATACTATAATTCACAACTTAATGACTTTACAGCGGTGACTATTCAAAAGAGATGTGTGCCAGGTAGTGTAAATATTTACCTAAAGTTAAATGGATTAAACATTGGTAGGTATGCTGCCTAAAAGAACACAAAGTGTGAGATATTCAGCCTTTGGGGGAAAAAAAAAACATCCATGTGAAGTTTTTTTATTAACTAATTTCGAGAGGATCACATGCTTATGATTGAACACAGCAGGTGATGCATTAGCCAATTTATGATTGAACAATCAGACGATTCCTAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24972
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2467 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1099829)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1142463 |
GRCz11 | 15 | 1103266 |
KASP Assay ID:
554-7574.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAACCTGTCGGCAGTGAGCTTCTCCAAGCACAAGGGACACTTATAATT[C/T]GAAATCCTACAAGAATGCATTCTGGGAATTACAAGTGTATCGCCTTTAAT
Long Flanking Sequence:
TTCTTGAGGTGATTCAAAAGCCTTATATTCTAACACGGCCAAAGGGGATTATTCGGGGTATTTCTGGACAGTCTCTCTTCCTACATTGCCTGACAGATGAAATAAAGTCCACTATTTCTTGGACCATGCCAGGAGGTTTTGTTCTCGCAAGTCCACAGGTGAGTGGACGCTATCAGTTAATGGAAAATGGGACACTTGTTGTACATGAGACAACCATGCAAGATCGTGGGAATTATGTGTGCAAAGCAACAAACGACGCTGGTGAGGCTGTTCTCACTGTGTCCGTCATAATTCTTGCATATCCAGCTCGAATTACCAATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTGCAGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCTGATCGCTCGATTCTTGCTACGAATGGAAAGGGACAACCTGTCGGCAGTGAGCTTCTCCAAGCACAAGGGACACTTATAATT[C/T]GAAATCCTACAAGAATGCATTCTGGGAATTACAAGTGTATCGCCTTTAATTACCTGGGCAGAGATACCAGAACAACATACATGACAATACTATAATTCACAACTTAATGACTTTACAGCGGTGACTATTCAAAAGAGATGTGTGCCAGGTAGTGTAAATATTTACCTAAAGTTAAATGGATTAAACATTGGTAGGTATGCTGCCTAAAAGAACACAAAGTGTGAGATATTCAGCCTTTGGGGGAAAAAAAAAACATCCATGTGAAGTTTTTTTATTAACTAATTTCGAGAGGATCACATGCTTATGATTGAACACAGCAGGTGATGCATTAGCCAATTTATGATTGAACAATCAGACGATTCCTAAGCCACTATATATACACCCTGAGTTCCATATCACAGCCATCTTTGTTTTGAAGAATCCCCCCTTCCTCCCCTCCTCCTCCTCCTTGTCTAGATGGGTGGCCCAGTGGTTAGCACTGTTGCTTCAAAGCAAGAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18534
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2479 | 2497 | 6 | 6 |
ENSDART00000113091 | Nonsense | 2479 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1099867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1142501 |
GRCz11 | 15 | 1103304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTTMTMATTCGAAATCCTWCAAGAATGCATTCTGGGAWTTACAAGTG[T/A]ATCGCCTTTAATTACCTGGRCAGAGATACCAGAACAACATACATGACAAT
Long Flanking Sequence:
CCAAAGGGGATTATTCGGGGTATTTCTGGACAGTCTCTCTTCCTACATTGCCTGACAGATGAAATAAAGTCCACTATTTCTTGGACCATGCCAGGAGGTTTTGTTCTCGCAAGTCCACAGGTGAGTGGACGCTATCAGTTAATGGAAAATGGGACACTTGTTGTACATGAGACAACCATGCAAGATCGTGGGAATTATGTGTGCAAAGCAACAAACGACGCTGGTGAGGCTGTTCTCACTGTGTCCGTCATAATTCTTGCATATCCAGCTCGAATTACCAATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTGCAGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCTGATCGCTCGATTCTTGCTACGAATGGAAAGGGACAACCTGTCGGCAGTGAGCTTCTCCAAGCACAAGGGACACTTATAATTCGAAATCCTACAAGAATGCATTCTGGGAATTACAAGTG[T/A]ATCGCCTTTAATTACCTGGGCAGAGATACCAGAACAACATACATGACAATACTATAATTCACAACTTAATGACTTTACAGCGGTGACTATTCAAAAGAGATGTGTGCCAGGTAGTGTAAATATTTACCTAAAGTTAAATGGATTAAACATTGGTAGGTATGCTGCCTAAAAGAACACAAAGTGTGAGATATTCAGCCTTTGGGGGAAAAAAAAAACATCCATGTGAAGTTTTTTTATTAACTAATTTCGAGAGGATCACATGCTTATGATTGAACACAGCAGGTGATGCATTAGCCAATTTATGATTGAACAATCAGACGATTCCTAAGCCACTATATATACACCCTGAGTTCCATATCACAGCCATCTTTGTTTTGAAGAATCCCCCCTTCCTCCCCTCCTCCTCCTCCTTGTCTAGATGGGTGGCCCAGTGGTTAGCACTGTTGCTTCAAAGCAAGAACGTCACTGGTTCTAGTCCTTACCAAGCCAGCCAACGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9744
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 |
---|---|---|---|---|---|
ENSDART00000113091 | Nonsense | 2479 | 2497 | 6 | 6 |
ENSDART00000113091 | Nonsense | 2479 | 2497 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 15 (position 1099867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 1142501 |
GRCz11 | 15 | 1103304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACACTTMTMATTCGAAATCCTACAAGAATGCATTCTGGGAWTTACAAGTG[T/A]ATCGCCTTTAATTACCTGGRCAGAGATACCAGAACAACATACATGACAAT
Long Flanking Sequence:
CCAAAGGGGATTATTCGGGGTATTTCTGGACAGTCTCTCTTCCTACATTGCCTGACAGATGAAATAAAGTCCACTATTTCTTGGACCATGCCAGGAGGTTTTGTTCTCGCAAGTCCACAGGTGAGTGGACGCTATCAGTTAATGGAAAATGGGACACTTGTTGTACATGAGACAACCATGCAAGATCGTGGGAATTATGTGTGCAAAGCAACAAACGACGCTGGTGAGGCTGTTCTCACTGTGTCCGTCATAATTCTTGCATATCCAGCTCGAATTACCAATGGGCCACCTCCGGCTTTGAAAGGAGTGACGGGAGTTCCTGTTCATCTGCAGTGTGTTGCTAATGGTATACCTACACCAGATATAGTCTGGGAGCTGCCTGATCGCTCGATTCTTGCTACGAATGGAAAGGGACAACCTGTCGGCAGTGAGCTTCTCCAAGCACAAGGGACACTTATAATTCGAAATCCTACAAGAATGCATTCTGGGAATTACAAGTG[T/A]ATCGCCTTTAATTACCTGGGCAGAGATACCAGAACAACATACATGACAATACTATAATTCACAACTTAATGACTTTACAGCGGTGACTATTCAAAAGAGATGTGTGCCAGGTAGTGTAAATATTTACCTAAAGTTAAATGGATTAAACATTGGTAGGTATGCTGCCTAAAAGAACACAAAGTGTGAGATATTCAGCCTTTGGGGGAAAAAAAAAACATCCATGTGAAGTTTTTTTATTAACTAATTTCGAGAGGATCACATGCTTATGATTGAACACAGCAGGTGATGCATTAGCCAATTTATGATTGAACAATCAGACGATTCCTAAGCCACTATATATACACCCTGAGTTCCATATCACAGCCATCTTTGTTTTGAAGAATCCCCCCTTCCTCCCCTCCTCCTCCTCCTTGTCTAGATGGGTGGCCCAGTGGTTAGCACTGTTGCTTCAAAGCAAGAACGTCACTGGTTCTAGTCCTTACCAAGCCAGCCAACGTTTT
Associated Phenotype:
Not determined