ZMP
bat2
Ensembl ID:
ZFIN ID:
Human Orthologue:
BAT2
Human Description:
HLA-B associated transcript 2 [Source:HGNC Symbol;Acc:13918]
Mouse Orthologue:
Bat2
Mouse Description:
HLA-B associated transcript 2 Gene [Source:MGI Symbol;Acc:MGI:1915467]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43293 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23536 | Nonsense | Available for shipment | Available now |
sa43292 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15913 | Nonsense | Available for shipment | Available now |
sa43291 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23535 | Nonsense | Available for shipment | Available now |
sa36848 | Nonsense | Available for shipment | Available now |
sa23534 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43293
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 392 | 1892 | 9 | 15 |
ENSDART00000138675 | Nonsense | 390 | 1890 | 10 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27234362)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27164474 |
GRCz11 | 19 | 26748697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCGAAGTTGAAATTCAGTGACGATGAAGGAGAGGATGATGGGGAGGAG[G/T]AACGGGGTGAAAATAAAAATGGAACCCGGTAAACATTTCTAAAATTTTCT
Long Flanking Sequence:
GCTCCTAGGTGAGTTATACGTGCTTAATTAAGCAGAAATTCAGATACTAATATTCATGTTCACAGTCATTTTATTGCCTTTTCTAAGTCTGTTGTAACTGTTTTTGCCAGGTTTTCTCGGAACCAGGGTGGAATAGGGCCAGATGGGCGACCCCCTGGAGGCCCCCGGGGTGAAGTGGTAAAACGCCCATCCATCCTCAAACAGGATGACCTAAAAGAGCTGGATGAGCTGGACCATGATGGAGATGAGGGCTGGGCTGGTAAGAGAAAATCTTTCCATTTATATGCCACATTAGAGTGGAATAAACCGTAGTAGTTAACACTATAAAATTGAGGGAAATGTGTAAAAGTAACTCTTTTAATACTGACACAGAAGTTGTAACTACAGTATTTAGTCCTTTTTCTTGATGGTTTACTTTGTTCTCAGGAGCTCAAGAGGAAATTGACTACTCCGCGAAGTTGAAATTCAGTGACGATGAAGGAGAGGATGATGGGGAGGAG[G/T]AACGGGGTGAAAATAAAAATGGAACCCGGTAAACATTTCTAAAATTTTCTCCCATTAGTTGTTTTTAACTGTTTATGTTTGCTTACTGAAGTTCTGGTTTAACAGGGAGTCAAGGGAACAGCAGAGATCCCAAGATGGACCTGTACCTGTTTCACGTTCCAGGGCATCCGACAGTGGAGGGGATTCGCGACGCACCCCTCCTTCCAGTACTGAAGATGGCTCTGTGTCCCCCTCCAGCAAGCCAGGCTGGGCCGAGGAGGGAGGTAGCAGCTGGAACAGTCAAGCAAATGCCGGATCTTATCAGGTATAAAAATCATAACCCCATCAAAGTCCAAGCCCTCAGTGCAACAACTTGCCTTTGCCAAATACTGTACAGTCATTGTGAGGACAGGAACATGCTCACGGTGTGTCCTGGATGACTCGCTGATTGATACATGTACCCCTATGCAGGGGCCTAGGCCTGGATTAGGTGGCACTAGGGAGCAGCCCTCTCCCCCACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23536
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 429 | 1892 | 10 | 15 |
ENSDART00000138675 | Nonsense | 427 | 1890 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27234174)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27164286 |
GRCz11 | 19 | 26748509 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCTGTACCTGTTTCACGTTCCAGGGCATCCGACAGTGGAGGGGATTCG[C/T]GACGCACCCCTCCTTCCAGTACTGAAGATGGCTCTGTGTCCCCCTCCAGC
Long Flanking Sequence:
ATCCATCCTCAAACAGGATGACCTAAAAGAGCTGGATGAGCTGGACCATGATGGAGATGAGGGCTGGGCTGGTAAGAGAAAATCTTTCCATTTATATGCCACATTAGAGTGGAATAAACCGTAGTAGTTAACACTATAAAATTGAGGGAAATGTGTAAAAGTAACTCTTTTAATACTGACACAGAAGTTGTAACTACAGTATTTAGTCCTTTTTCTTGATGGTTTACTTTGTTCTCAGGAGCTCAAGAGGAAATTGACTACTCCGCGAAGTTGAAATTCAGTGACGATGAAGGAGAGGATGATGGGGAGGAGGAACGGGGTGAAAATAAAAATGGAACCCGGTAAACATTTCTAAAATTTTCTCCCATTAGTTGTTTTTAACTGTTTATGTTTGCTTACTGAAGTTCTGGTTTAACAGGGAGTCAAGGGAACAGCAGAGATCCCAAGATGGACCTGTACCTGTTTCACGTTCCAGGGCATCCGACAGTGGAGGGGATTCG[C/T]GACGCACCCCTCCTTCCAGTACTGAAGATGGCTCTGTGTCCCCCTCCAGCAAGCCAGGCTGGGCCGAGGAGGGAGGTAGCAGCTGGAACAGTCAAGCAAATGCCGGATCTTATCAGGTATAAAAATCATAACCCCATCAAAGTCCAAGCCCTCAGTGCAACAACTTGCCTTTGCCAAATACTGTACAGTCATTGTGAGGACAGGAACATGCTCACGGTGTGTCCTGGATGACTCGCTGATTGATACATGTACCCCTATGCAGGGGCCTAGGCCTGGATTAGGTGGCACTAGGGAGCAGCCCTCTCCCCCACCAGGTCCACTTCTTGGACAAGGGCCCCACTCCTACTACCGCCAGGTACATGGGGAAAGAGTCCGAGAAATAGGGCAGAAGTGACATCAAGCACTAACATAAGCATGTTGGGTGTAATGGAGGTAATGTTTGTATTTGTGAACTTGACTAACCCACCTTATGTCAACAGGACCGGCCTTCAAACCAGTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43292
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 718 | 1892 | 12 | 15 |
ENSDART00000138675 | Nonsense | 716 | 1890 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27232784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27162896 |
GRCz11 | 19 | 26747119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACAGGACGGCAGGGAAGTGGTCCTTCTGGGCAAGGCTTTTCCAAGTAT[C/T]AAAAATCGCTTCCTCCTCGCTTTCAGAGGCAACAACAGGTTGGTTTTTAT
Long Flanking Sequence:
GCCATCATCACCCTGCGTGGACACTGAAGAACCACCTCTGTTATCCGCTCAAGGAAGTGGTGCAACTCTAGGGCTTACTAATAATAACAGACAGAGAGCTGGTAGCAACAGCAGCCACGACTCCAACAATGGTTAGTTTTTTATTTTATTTAAATTATTACATAAAAGTATGTTTGGCACTTTTGTTAAAATGTTTCCTAACTTTTCTGAAATGTCAATTTTGTTCAAGATCAGCAAACAGCTTGAGTATGATTATTTTTAAGGTAATTGCATGATTTCCTTTCTATTCAGAGTCCCAGCAGGTTCTGCAACCTCAAGCCACCCAGCATCCACAATCCCAGGATGTCCCAGGGCCTGGAGATATCAAGGAGGAGCATGTGGTGGGCGGTCCACACATCCGCAGTACTAGAGTTGGAGATGATTCAGTGAAGGTGGTTGAATGTGTTGGTGTAACAGGACGGCAGGGAAGTGGTCCTTCTGGGCAAGGCTTTTCCAAGTAT[C/T]AAAAATCGCTTCCTCCTCGCTTTCAGAGGCAACAACAGGTTGGTTTTTATTTTTTCAAATCTGTAAGAAAAGCTCATTAAATTCAATGAGTTGTTTTAGTTTGTGTTGTTAAAATTTGCTAGAAACATCTTGACCTGTTTTAACGTTCCCACTAGGACTGTAGAATTATGATGCAGAGTGACAAGAATATTTTTATAGATTGTGTAGATGTAAATATTCATCACCAGAGCTGAAACATTAGAAACCTTGAATGCTTTAAAGTACTAAATGGTTCACATGGTGTACTATAATGATAAATGCATAGTTCTAAATATTTTTCTACTTAGAAAATGTCACACAACAGCTATAAAGGTAACAGCAGAGCGGAACAATTAGCAGAATCATTTTTTCAACCAGAATCTTTTCTGTGTAAGCTTGAGCATTTAAAGTGGCAGATGAACTTTTAAAAATGTTCTATATAAAATCTGCCTTGTATCATTTATCAACAGGAGCAACTTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15913
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 1130 | 1892 | 15 | 15 |
ENSDART00000138675 | Nonsense | 1128 | 1890 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27230858)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27160970 |
GRCz11 | 19 | 26745193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGGASAAGACAGGAAATGCGCATAATCAGCCCCCACAAMATTCTGGG[C/T]AGCAGCACCACCCTAGAGCCAACCCTCGCAAYCGGGAACACAAAACTGAG
Long Flanking Sequence:
GTTACAGCAGCTACCCTGACAATGGATCAAGAATGGGCTCCCACCTGCAGCAAAGGGCTAACAGTGGAGGGACACTGCATGGTTTTGGCCATCAGGAAGGTAGTCAGCCGAACCAAATCTGGGGGACTCCTCATCCTCATTATGACCGTTCTGATCACTCAGCCTTGGAGAGCAACTCTCATCACCAACATCATGGTCCTCCCTCTCACGCCCCTCATTTTTCTCTTCATCCTCATAAGCAAGAGAATGGCAGGGAGCGAGAAAAAATGGTGGAGCCAAAGAAGAATGACCCTTCACCTCCACTCCATCAGCCGTCCCTCTCCTCTTCCTGTTCATCATCATCCTCGTCTTCCTCTGCCAGAGAAGATGGCAGTGGAAAACAGTCTTTACATAATCAAGTTCCACCACTGCATGAGCATGATACTGGATCCACTCATGCTTCAGGAAGGAAGCAGGACAAGACAGGAAATGCGCATAATCAGCCCCCACAACATTCTGGG[C/T]AGCAGCACCACCCTAGAGCCAACCCTCGCAATCGGGAACACAAAACTGAGACGCACTGGGGCCCGAGGCCTGGTAGCAGTAGTGTGAGTGGAAGCTCTACTCACAACAGAAAGACAGGCTCTGGAATTATTGCAATTACAGAACCATCTGGAAACCAGGGTGCTGAGAACAAGTCCTTTAACCAATCAGATGGCATCACAGTCAAGCGGGCAGGTCCTATTAAGAGACCAGTTCTTAAAGAGATTAAAAGGGAGGGTGGTGAAGGAGGAGGAGAAAAGACTACTGGAGGCTCTGGTAAAGATAAAGAACAAGATGCAAGTCAAACCACAACCAAACAAGAACCTGCCACTGGGAATCAAGTCATATTAGCACCCAGTGGAAAAGATGATGCCGTCTCATCAAATAAACCCAGAACTGGTGGAAAGGAGCGAGGTAACACTGGGGGTTCAGGCAAAGGATCCAAAAATGGGGAAAGCTCCATGCAGAATTCTGGTTATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43291
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 1233 | 1892 | 15 | 15 |
ENSDART00000138675 | Nonsense | 1231 | 1890 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27230549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27160661 |
GRCz11 | 19 | 26744884 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAAGGAGGAGGAGAAAAGACTACTGGAGGCTCTGGTAAAGATAAAGAA[C/T]AAGATGCAAGTCAAACCACAACCAAACAAGAACCTGCCACTGGGAATCAA
Long Flanking Sequence:
AGCCGTCCCTCTCCTCTTCCTGTTCATCATCATCCTCGTCTTCCTCTGCCAGAGAAGATGGCAGTGGAAAACAGTCTTTACATAATCAAGTTCCACCACTGCATGAGCATGATACTGGATCCACTCATGCTTCAGGAAGGAAGCAGGACAAGACAGGAAATGCGCATAATCAGCCCCCACAACATTCTGGGCAGCAGCACCACCCTAGAGCCAACCCTCGCAATCGGGAACACAAAACTGAGACGCACTGGGGCCCGAGGCCTGGTAGCAGTAGTGTGAGTGGAAGCTCTACTCACAACAGAAAGACAGGCTCTGGAATTATTGCAATTACAGAACCATCTGGAAACCAGGGTGCTGAGAACAAGTCCTTTAACCAATCAGATGGCATCACAGTCAAGCGGGCAGGTCCTATTAAGAGACCAGTTCTTAAAGAGATTAAAAGGGAGGGTGGTGAAGGAGGAGGAGAAAAGACTACTGGAGGCTCTGGTAAAGATAAAGAA[C/T]AAGATGCAAGTCAAACCACAACCAAACAAGAACCTGCCACTGGGAATCAAGTCATATTAGCACCCAGTGGAAAAGATGATGCCGTCTCATCAAATAAACCCAGAACTGGTGGAAAGGAGCGAGGTAACACTGGGGGTTCAGGCAAAGGATCCAAAAATGGGGAAAGCTCCATGCAGAATTCTGGTTATTCAGCCTCTCAGTCCAGGAGGGAAAGAGAACATTCACCTGAAAGAGGGAGCACAACCTACCATTCGTCCTCATCCAGAGGTAGCCGATCCAATCGTGGCAGAGGAGAGTTCTATGGTCGAGGCAGAGGCTATAGGGGCACTTACGTGGGTAGTGCAGGTGGTGGCAACCGTGGAAAGGCTGGTGGCAGGAACAGCAGGGATTATAGGCCAGCTGCCAATAGTGGTTACCACCATCCATCTTCTAATCAAGATTACAAAAGAGAGGCATCATCTGGGAGTGGCAGACATGGCACATCTCAACCCAATCCTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23535
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 1353 | 1892 | 15 | 15 |
ENSDART00000138675 | Nonsense | 1351 | 1890 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27230189)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27160301 |
GRCz11 | 19 | 26744524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGGCTATAGGGGCACTTACGTGGGTAGTGCAGGTGGTGGCAACCGT[G/T]GAAAGGCTGGTGGCAGGAACAGCAGGGATTATAGGCCAGCTGCCAATAGT
Long Flanking Sequence:
ACAAGTCCTTTAACCAATCAGATGGCATCACAGTCAAGCGGGCAGGTCCTATTAAGAGACCAGTTCTTAAAGAGATTAAAAGGGAGGGTGGTGAAGGAGGAGGAGAAAAGACTACTGGAGGCTCTGGTAAAGATAAAGAACAAGATGCAAGTCAAACCACAACCAAACAAGAACCTGCCACTGGGAATCAAGTCATATTAGCACCCAGTGGAAAAGATGATGCCGTCTCATCAAATAAACCCAGAACTGGTGGAAAGGAGCGAGGTAACACTGGGGGTTCAGGCAAAGGATCCAAAAATGGGGAAAGCTCCATGCAGAATTCTGGTTATTCAGCCTCTCAGTCCAGGAGGGAAAGAGAACATTCACCTGAAAGAGGGAGCACAACCTACCATTCGTCCTCATCCAGAGGTAGCCGATCCAATCGTGGCAGAGGAGAGTTCTATGGTCGAGGCAGAGGCTATAGGGGCACTTACGTGGGTAGTGCAGGTGGTGGCAACCGT[G/T]GAAAGGCTGGTGGCAGGAACAGCAGGGATTATAGGCCAGCTGCCAATAGTGGTTACCACCATCCATCTTCTAATCAAGATTACAAAAGAGAGGCATCATCTGGGAGTGGCAGACATGGCACATCTCAACCCAATCCTGGACGTGCTAGGAACCGTAGTGAGACTCGAAGCGAAGGCTCTGAATATGAAGAGGTGCCAAAGAGAAGGAGACAACGAGGATCTGAAACAGGCAGTGAGAGTGCTGGAAGTGACCTTGCTCACTCTGACAAGGAAGATCGCAAGCTCAACACCAAGGCTGGAACAGTAGGAGAGAACCCTACAACTGGCCCTTCATCTTCTGCTTCAGTCAGAAACACTCAGACTAGAGTATTCACACCAAGGGGAGTACCATCAAGACGTGGTAGAGGTGGAGGTGGTGCTGGAGGGGGTCTCCATAGAAGCGGAGGTGGTGCTGGAGTGTCTGGTGGACAAAGACCTGGACCTGGCTCTTCTTCCCATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36848
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 1531 | 1892 | 15 | 15 |
ENSDART00000138675 | Nonsense | 1529 | 1890 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27229655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27159767 |
GRCz11 | 19 | 26743990 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTTCTTCCCATGGCTGGTCGGCAAAGTCTGCAAATGTGCGAAAGCCA[C/T]AGACATCCTCACAGCCACCCCCTGCTAAAGATTTAAGCCGTGGAGTGAAT
Long Flanking Sequence:
GGCCAGCTGCCAATAGTGGTTACCACCATCCATCTTCTAATCAAGATTACAAAAGAGAGGCATCATCTGGGAGTGGCAGACATGGCACATCTCAACCCAATCCTGGACGTGCTAGGAACCGTAGTGAGACTCGAAGCGAAGGCTCTGAATATGAAGAGGTGCCAAAGAGAAGGAGACAACGAGGATCTGAAACAGGCAGTGAGAGTGCTGGAAGTGACCTTGCTCACTCTGACAAGGAAGATCGCAAGCTCAACACCAAGGCTGGAACAGTAGGAGAGAACCCTACAACTGGCCCTTCATCTTCTGCTTCAGTCAGAAACACTCAGACTAGAGTATTCACACCAAGGGGAGTACCATCAAGACGTGGTAGAGGTGGAGGTGGTGCTGGAGGGGGTCTCCATAGAAGCGGAGGTGGTGCTGGAGTGTCTGGTGGACAAAGACCTGGACCTGGCTCTTCTTCCCATGGCTGGTCGGCAAAGTCTGCAAATGTGCGAAAGCCA[C/T]AGACATCCTCACAGCCACCCCCTGCTAAAGATTTAAGCCGTGGAGTGAATGTTGACAAGAAGAAACCTGCAGAACAGAATCAGCCTCAAAGTCAAAGTGCAAATCCCACCACAACTGTTGCCTCTGTGCCTACAACTATCCAACAGGGGTCCACTGAGAATGGAAATGTTGGAGCACCAATGTCTTCAACTAATGCTCCATCAAATCCCGCTGGTGCACCTACACAGTCTCTTCCTCTGCCTGCCCCAGATGGGCGGAACTTCCCTAACAGGGGATTTGAGCGCCCTCCTCGTCGTAGGCGCCATGGCCGATCCCAGCATCAGCAGGACAAGCCTCCAAGATTCCGCAGACTTAAACAAGAGCGAGAGAATGCAGCCCGTATAAATGGAAGCAGTGGATTAATTGAAGTCATAGCTGCACAACAGCAACGCACTGCTCCACTGTTGCAAAATTCCCTGCAACAAGCCAACAGCACTCCCAATGTACCCGATGCAGTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23534
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 |
---|---|---|---|---|---|
ENSDART00000043776 | Nonsense | 1558 | 1892 | 15 | 15 |
ENSDART00000138675 | Nonsense | 1556 | 1890 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 19 (position 27229574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 27159686 |
GRCz11 | 19 | 26743909 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAAGCCGTGGAGTGAATGTTGACAAGAAGAAACCTGCAGAACAGAAT[C/T]AGCCTCAAAGTCAAAGTGCAAATCCCACCACAACTGTTGCCTCTGTGCCT
Long Flanking Sequence:
ATGGCACATCTCAACCCAATCCTGGACGTGCTAGGAACCGTAGTGAGACTCGAAGCGAAGGCTCTGAATATGAAGAGGTGCCAAAGAGAAGGAGACAACGAGGATCTGAAACAGGCAGTGAGAGTGCTGGAAGTGACCTTGCTCACTCTGACAAGGAAGATCGCAAGCTCAACACCAAGGCTGGAACAGTAGGAGAGAACCCTACAACTGGCCCTTCATCTTCTGCTTCAGTCAGAAACACTCAGACTAGAGTATTCACACCAAGGGGAGTACCATCAAGACGTGGTAGAGGTGGAGGTGGTGCTGGAGGGGGTCTCCATAGAAGCGGAGGTGGTGCTGGAGTGTCTGGTGGACAAAGACCTGGACCTGGCTCTTCTTCCCATGGCTGGTCGGCAAAGTCTGCAAATGTGCGAAAGCCACAGACATCCTCACAGCCACCCCCTGCTAAAGATTTAAGCCGTGGAGTGAATGTTGACAAGAAGAAACCTGCAGAACAGAAT[C/T]AGCCTCAAAGTCAAAGTGCAAATCCCACCACAACTGTTGCCTCTGTGCCTACAACTATCCAACAGGGGTCCACTGAGAATGGAAATGTTGGAGCACCAATGTCTTCAACTAATGCTCCATCAAATCCCGCTGGTGCACCTACACAGTCTCTTCCTCTGCCTGCCCCAGATGGGCGGAACTTCCCTAACAGGGGATTTGAGCGCCCTCCTCGTCGTAGGCGCCATGGCCGATCCCAGCATCAGCAGGACAAGCCTCCAAGATTCCGCAGACTTAAACAAGAGCGAGAGAATGCAGCCCGTATAAATGGAAGCAGTGGATTAATTGAAGTCATAGCTGCACAACAGCAACGCACTGCTCCACTGTTGCAAAATTCCCTGCAACAAGCCAACAGCACTCCCAATGTACCCGATGCAGTAGTTGCAAATGCAAATCACAGTGTGTCCACAACTCCTAACAGTAATAATAATAGCAGCAACCTTGCAGGTGGAAACCAAAATTTC
Associated Phenotype:
Not determined