ZMP
ahnak
Ensembl ID:
ZFIN IDs:
Description:
Ahnak protein [Source:UniProtKB/TrEMBL;Acc:Q08BG5]
Human Orthologue:
AHNAK
Human Description:
AHNAK nucleoprotein [Source:HGNC Symbol;Acc:347]
Mouse Orthologue:
Ahnak
Mouse Description:
AHNAK nucleoprotein (desmoyokin) Gene [Source:MGI Symbol;Acc:MGI:1316648]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42400 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22488 | Nonsense | Available for shipment | Available now |
sa35698 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22489 | Nonsense | Available for shipment | Available now |
sa28316 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42401 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42402 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13008 | Essential Splice Site | Available for shipment | Available now |
sa17896 | Nonsense | Available for shipment | Available now |
sa6345 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22490 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42400
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 |
---|---|---|---|---|---|
ENSDART00000088484 | Nonsense | 211 | 848 | 5 | 5 |
ENSDART00000125289 | Nonsense | 211 | 5689 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27785826)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26478623 |
GRCz11 | 14 | 26776728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTCAAAATTCAGCTCTTGCAGCATGAGCAGGAAGGGGGTGATTCTTCA[C/T]AAATAGGATTACCACACAGCAGCCTTGTTAGCAGTGAACACGGGGGTAAA
Long Flanking Sequence:
GATTTTATTCTAGCCAAAATAAAACAAATAAGCCTTTCTCCAGAAGAAAAAATATTAGAGGAAATGCTGTTAAAATTCCATGCTCTGTTAAACATAATTTGGGAAATATTTATAAAAAAAAAACGCTATTAATTTTGACTTCAACTTATAGTCGTTTTGAATAATCGTGATTATGATTTTTCCCAAAATCGAGCAGCCCTATCTTATGTAATAATGTCCTTTTTTTCTTGTAGAGTGGGGATGATGAAGACTACAAGAGAATCTATAGCAAGAAGATTAAACCTAGACTGAAGTCTGAGGACCTTGCTGAGGGTGTTGATGTGCGCACAGAACGCCACAGCAGCACAAGCAGTGATGGTTGCACCATCACTACAATCACTCGACGAATAACTACCTACACAGTTGATATGCCTGGGGGCACTAGTCAGCAGATTGATCCCTCAAGTCCTGAGTTCAAAATTCAGCTCTTGCAGCATGAGCAGGAAGGGGGTGATTCTTCA[C/T]AAATAGGATTACCACACAGCAGCCTTGTTAGCAGTGAACACGGGGGTAAAAATTTAGGGGACATATCTTTTGGTGGGCCCCATGTCACTGGCTCGTCTGTGAAGCACTGTAGCACAGGATCTATCAGAGCAACAAGTGAATTAGATGGCAGTGGGAGAGAGATTACAATTAATGTGTCAGACACTGGACTTTCAGGGGGAAGAGGACAAAGATTTACAGAACATTTTGTAGGGACTGAAACTTCTCTAGAAGGTAATTTCTCTGGTAGAGTAACCACAGGGTTAGAAAAACAAGTGGGAAATATTTCTTCACCAGTAGAAGCTAGTTTTAAAGCTTTAAGTACGAAAGGAGGAACAGTAAAGGGCTCTGTTCTGGAAACGCATGGTTCAGGCTTTTCCATAATTGGAGGATCTAAGGGCAGTATTGGCAGAGAATCTTCTTCTGAAGTACTTAAGGATGGATCTGATGATCTAACCAAGCTGTCCAAGTTTAGCATAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22488
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 2806 | 5689 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27793611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26486408 |
GRCz11 | 14 | 26784513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACATTAAGGCACCTGATTTGGACATTAAATCTCCAGAGATTGACATT[G/T]AGGGACCTGAGGGAAAAGTAAAGGGGTCCAAGTTCAAAATACCTTTCTCT
Long Flanking Sequence:
GTGGTTTGAAAATGCCAACGATCAAAATGCCAAAATTCGGATTCAAGGGTCCAAAAGTTGAAGGACCAGGCATGGATGTGAAAAGCCCCAAGACTGACATTGATATTAAAGGACCTGATGTGGACATTAAGGCTCCAGAGCTTGACATTGAGGCACCTAAGGGAAACATCAAGGACCCCAAGCTGAAAATGCCTTCATTGTCCAGGCCAACAATTTCTATGCCAGATGTTGACTTTAACCTCAAAGGTCCGAAACTGAAAGGTGATGTTGATGTTTCTGTTCCAAAAGTGCAAGGAGATATTAAAGCACCAAAAGTCGAACTTGAAGGATCAGACATTGCGGGTCCTGAGGGTGGCTTTAAGATGCCAAAAATAAAAATGCCACAGATCGGATTCAAGGGTCCAAAAGTGGAAGGTCCAGATGTCGATGTAAAAATTCCCAAAACGGATATTGACATTAAGGCACCTGATTTGGACATTAAATCTCCAGAGATTGACATT[G/T]AGGGACCTGAGGGAAAAGTAAAGGGGTCCAAGTTCAAAATACCTTTCTCTGGGCCAAAAATTTCTATGCCTGATGTTGATTTCAACCTGAAAGGTCCGAAACTGAAAGGTGATGTTGATGTTTCTGTTCCTAAAGTGGAAGGAGATATTACAGCACCAAAAGTCCAACTTGAAGGCCCAGAAATTGAGGGTCCTGAGGGTGGTTTTAAAATGCCAACGATCAAAATGCCCAAATTCGGATTCAAGGGTCCAAAAGTTGAAGGACCAGGCATAGATGTAAAAAGCCCCAAGACTGACATTGATATTAAAGGATGTGATGTGGACATTAAGGCTCCAGAGCTTGACATTGAGGCACCTGAGGGAAACATCAAGGACCCCAAACTGAAAATGCCTTCATTGACCAGGCCAACAATTTCTATGCCAGATGTTGATTTTAACCTGAAAGGTCCAAAACTGAAAGGTGATGTTAATGTTTCTGTTCCAAAAGTGGAAGGAGATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35698
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 3269 | 5689 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27795000)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26487797 |
GRCz11 | 14 | 26785902 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAGGTGATGTTTCTGTTCCAAAAGTGGAAGGAGATATTAAAGCACCA[A/T]AAGTCGAACTTGAAGGCCCAGAAATTGAGGGTCCAGAAGGTGGCTTTAAG
Long Flanking Sequence:
TTGAGGGACCTGAAGGAAAACCTAAGGGCTCTAAATTCAGTATCCCATCAATATCTGGCCCAAATATTTCCATGCCAGATGCTGATTTTAGCCTCAAAGGTCCGAAACTGAAAGGTGATGTTGATGTTTCAGTTCCAAAAGTAGAAGGGGATATCAAAGCTCCAAACGTTGAAATTGAAGGCCCAGATATTAAAGGACCTGAGGGTGGTTTTAAGATGCCAAAGATCAAAATGCCAAGATTTGGGTTCAAAGGTCCAAAAGTGGAAGGTCCAGATGTCGAAGTCCCCAAAACTGATATTGACATCAAAGCACCTGATGTGGACATTAAATCTCCTGAGCTTGACTTTGAGGGACCTGAAGGCAAGGTCAAGGGCTCCAAGTTTAAAATGCCTTTCTCTGGGCCAACGATTTCTATGCCTGATGTTGATTTTAACCTGAAAAGTCCAAAACTGAAAGGTGATGTTTCTGTTCCAAAAGTGGAAGGAGATATTAAAGCACCA[A/T]AAGTCGAACTTGAAGGCCCAGAAATTGAGGGTCCAGAAGGTGGCTTTAAGATGCCAAATATCAAAATGCCAAAATTCGGATTCAAGGGTCCAAAAGTTGAAGGTCCAGATGTCGATATAAAAATTCCCAAAACTGATATCGACATTAAGGCACCTGATGTGGACATCAAAGGTCCAGAGATTGACATTGAGGGACCGGAGGGAAAAGTTAAGGGCTCCAAGTTCAAAATACCTTTCTCTGGGCCAACAATTTCTATGCCGGATGTTGATTTTAACCTGAAAGGTCCGAAACTGAAAGGTGATGTTGATGTTTCAGTTCCAAAAGTGAAAGGAGAGATTAAAGCACCTGACGTGGTTGTTAAAACCCCAAAAGTTGACATTGAGGGACCTGAAGGAAAACTTAAGGGCCCTAAATTTAACATTCCATCAATTTCTGGGCCAAATATTTCTATGCCTGATGTTGACTTTAACCTGAAAGGTCCAAAACTGAAAGGTGATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22489
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 4172 | 5689 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27799806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26492603 |
GRCz11 | 14 | 26790708 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATGCCAAAGATTTCTATGCCAGAAGTTGATTTCAATCTGAAAGGACCA[A/T]AACTGAAAGGTGATGTTGATTTTTCCGTTCCAAAAGTCGAAGGAGACGTA
Long Flanking Sequence:
TTGACATTGAGGGACCTGACGGAAAAGTCAAGGGCCCCACATTGAAAATGCCTTCTTTGTCCGGGCCAAAAATTTCTATGCCAGATGTTGATTTTAATCTGAAAGGTCCGAAAGTAAAAGGCGATGTTGATGTTTCTGTTCCAAAAGTGGAAGGAGATATAAAAGTCCCTGGTTTGGACATTAAAGCTCCAAAAGTTGACATTGAGGGACCAGAGGGAAAACTTAAGGGCCCTAAAATTAATATTCCTTCAATATCTGGCCCAAATATTTCCTTGCCAACTGTTGACTTTAACCTCAAAGGTCCAAAACTGAGAGGTGATGTTGATGTTTCTGTTCCCAAAGTGAAAGGAGATGTTAAAGCACCCGATCTGGATATTAAAACTCCTGAAATTGACATTGAGGGAGCTGAGGGAAAAATTAAGGGCCCTAAATTTAGGATACCATCTGTCTCCATGCCAAAGATTTCTATGCCAGAAGTTGATTTCAATCTGAAAGGACCA[A/T]AACTGAAAGGTGATGTTGATTTTTCCGTTCCAAAAGTCGAAGGAGACGTAAAGGCACCTGATGTTCATATCAAGGGTCCAGAGGTTGACGTAGAGACACCTGAAGGAAAAATCACAGGCTCCAAATTCAAGGGGCCATCATTTTCAGGTCCAAATATTTCTCTCCCAGATGTTGACTTCAACTTGAAAGGACCTAAACTAAAGGGTGGTGTTGATGTGTCCGTTCCAAAAGTTCAAGGGGATATTAAAGCCACAGATTTTAACATTAATCTGCCGAATATTGATGGTGATATACCTGAAGGAAAAGTAAAGGGCCCAAAACTTAAGATGCCATCTTTATCCGGCCCTGAAGGCTCCATTGAGGTTAATTTACCAGAAACAAATGTGAAAAAGCCAAAGTTTAAAATGCCAAAGTTTAAATTTCCGTCATTTGGGCACAAAGGTCCAAAAGTGGAAGGCCCTGATGTTGATGTAAAAATTCCTAAGGCTGATATCAAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28316
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 4600 | 5689 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27801090)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26493887 |
GRCz11 | 14 | 26791992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATATAAAGGTCCCTGGTATGGACATTAAAGGTCCACAAGTTGACATT[G/T]AGGGACCTGAGGGGAAAATCAAGGGCTCTAAATTCAGTATGCCTTCAATA
Long Flanking Sequence:
TACTGTCAGGGCCAAATATTTCTATGCCACACGTTGACTTCAACCTCAAAGGTCCAAAATTGAAAAGTGATGTTGATGTTTCTGTCCTGAAAGTGGAAGGAGATATTAAAACACCAAAGATTGAACATGAAGGACCAGACATTGAGGGTCCTGAGGGTGGCTTTAAGATGCCAAAGCTCAAAATTCCACAGTTTGGATTCAAGGGCCCAAAAGTGGAAGGTCCAGACATGGATGTTAAAATCCCCAAAACCGATATTGACATTAATGCACCTGATGTCGACATTAAAGCTCCAGAGCTTGACATCGATGGACCTGAGGGAAAAATCAAGGGCCCTAAATTGACAAAGCCTTCTTTATCTGGGCCAACAATTTCTATGCCAGATGTTGATTTTAACCTAAAAGGTCGGAAAATGAAAGGTGATGTCGATGTGTCTGTTCCAAAATTGCAAGGAGATATAAAGGTCCCTGGTATGGACATTAAAGGTCCACAAGTTGACATT[G/T]AGGGACCTGAGGGGAAAATCAAGGGCTCTAAATTCAGTATGCCTTCAATATCTGGCCCAAAAATTTCCATGCCTAATGTTGACTTTAACCTCAAAGGGCCAAAACTAAAAGGTGATGTTGATGTTACAGTTCCAAAAGTAGAAGGAGACATGAAGGCACCAAAAGTTGAACTTGAAGGCCCAGACATTGAGGGTCCTGAGGGTGGTTTTAAGATGCCAAAGGTCAAAATGCCAAAAATTGGATTCAAGGGTCCAAAAGTTGAAGGTCCAGATGTTAATGTACAAATCCCTAAAACTGATATTGACATTAATGCACCCGATGTGGACATTAAATCTCCAGAGCTAGAAATTGAGGGACCTGAGGGTAAAGTCAAGGGCCACAAATTAAAAATGCCTTTCTCCGGCCCAACAATTTCTATGCCAGATGTTGATTTTAATCTAAAAGGTCTAAAACTGAAAGGTGATGTTGATGCATCTGCTCCGAAAGTGAAAGGAGATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42401
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 4663 | 5689 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27801279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26494076 |
GRCz11 | 14 | 26792181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGAAGGAGACATGAAGGCACCAAAAGTTGAACTTGAAGGCCCAGACATT[G/T]AGGGTCCTGAGGGTGGTTTTAAGATGCCAAAGGTCAAAATGCCAAAAATT
Long Flanking Sequence:
AGTTTGGATTCAAGGGCCCAAAAGTGGAAGGTCCAGACATGGATGTTAAAATCCCCAAAACCGATATTGACATTAATGCACCTGATGTCGACATTAAAGCTCCAGAGCTTGACATCGATGGACCTGAGGGAAAAATCAAGGGCCCTAAATTGACAAAGCCTTCTTTATCTGGGCCAACAATTTCTATGCCAGATGTTGATTTTAACCTAAAAGGTCGGAAAATGAAAGGTGATGTCGATGTGTCTGTTCCAAAATTGCAAGGAGATATAAAGGTCCCTGGTATGGACATTAAAGGTCCACAAGTTGACATTGAGGGACCTGAGGGGAAAATCAAGGGCTCTAAATTCAGTATGCCTTCAATATCTGGCCCAAAAATTTCCATGCCTAATGTTGACTTTAACCTCAAAGGGCCAAAACTAAAAGGTGATGTTGATGTTACAGTTCCAAAAGTAGAAGGAGACATGAAGGCACCAAAAGTTGAACTTGAAGGCCCAGACATT[G/T]AGGGTCCTGAGGGTGGTTTTAAGATGCCAAAGGTCAAAATGCCAAAAATTGGATTCAAGGGTCCAAAAGTTGAAGGTCCAGATGTTAATGTACAAATCCCTAAAACTGATATTGACATTAATGCACCCGATGTGGACATTAAATCTCCAGAGCTAGAAATTGAGGGACCTGAGGGTAAAGTCAAGGGCCACAAATTAAAAATGCCTTTCTCCGGCCCAACAATTTCTATGCCAGATGTTGATTTTAATCTAAAAGGTCTAAAACTGAAAGGTGATGTTGATGCATCTGCTCCGAAAGTGAAAGGAGATATTAAAATACCCAATGTGGATATTAAAGGTCCTGAAGTTGACATTGAGGGACCTGGGAGAAAATTTAAGGGCCCTAAATTTCAGATGCCATCAGTTTCTGGGCCAAATATTTCCATGCCTGATGTTGACTTTACGATGCCAGATGTTGATGTAAACCTGAAAGGCCCAAAACTGAAAGGTGATGTCGATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42402
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Essential Splice Site | 5299 | 5689 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27803272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26496069 |
GRCz11 | 14 | 26794174 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGTTGATTTGCCATCGGCAAGCCTTAAAACTGACATTCAGACACCAG[A/G]TGCTAGTTTGGACAGTCCAGATTTGAAAACGAAAGGGGCAAAAGTAAAAA
Long Flanking Sequence:
TTCGGGTGGCAGTCTTTCAGTTCCTGAACAGGATGTTGAGGCAACCATAGATGCCAAAAGCCCTGATGTTACCCTCAGTGGACCAGATGCAAACATCAAAGTGCCAAAAACTAAGAAATCTAAATTTTCACTTGGAGTTAGGAGCCCAAAGTTAGATGCAGATATCCCTGATGCTGGTGGTAATTTTGAAGGACCTGACATGAATGTAGATGTCAAAGGAAAAAAGGGTAAATTCAAATTGCCAAAAGGGAAAGGGAAGTCTAAAACATTTGATGCTGATTTAAAGACGGAAATGGTCGAGTTGGAGACAAATGAACCTGAAATTCACATAAAGTCCACCAAAGTAAAGAAACCTTTTTTTGGAAGGTTACATTTTCCTGATGTGGAATTTGACATAAAATCTCCAAAAGTTAAAGCTAGTTCATCTGCATCTGGAACCATGAAATCATCAGATGTTGATTTGCCATCGGCAAGCCTTAAAACTGACATTCAGACACCAG[A/G]TGCTAGTTTGGACAGTCCAGATTTGAAAACGAAAGGGGCAAAAGTAAAAATGTCAAAATACAGCATGTCTAGCTCCAAACTAAAAACTTCAGACTTGGATGTTAGAGATGCAACATTGGAGATTCCAGAGAAGACCATGCATTCTCCAGATGTCAGTGTAGCAGGATCAGGGATTAATGGAAAACGCAGTGCTAAAATTGACATAGAAGGAAAAGTACAAAGTGTTGAGTCGGCAGTGCCATCTACAAATGTCAGCGGGGGGGTTATAGATGCTGATTTAGGTATCGCTGAACAGAAAGGAGTAAAAGGGAGCATTGGAATAGCTGGCTTTAATGTAGGAGGACAAAAGGAAGATACTGCAAGTGGGATAGGCTTGAAGTCAGATGCATCATTATCTGGTGGGATAGAGAATCAAGAAGGTAATTTAACATTTCCTAAAGTCAAAGTACCAAAGTTTGGTATTGCATTGCCTAGAGTAGAACCAAGAGAAATGCGAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13008
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Essential Splice Site | 5299 | 5689 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27803273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26496070 |
GRCz11 | 14 | 26794175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGTTGATTTGCCATCGGCAAGCCTTAAAACTGACATTCAGACACCAGA[T/G]GCTAGTTTGGACAGTCCAGATTTGAAAACGAAAGGGGCAAAAGTAAAAAT
Long Flanking Sequence:
TCGGGTGGCAGTCTTTCAGTTCCTGAACAGGATGTTGAGGCAACCATAGATGCCAAAAGCCCTGATGTTACCCTCAGTGGACCAGATGCAAACATCAAAGTGCCAAAAACTAAGAAATCTAAATTTTCACTTGGAGTTAGGAGCCCAAAGTTAGATGCAGATATCCCTGATGCTGGTGGTAATTTTGAAGGACCTGACATGAATGTAGATGTCAAAGGAAAAAAGGGTAAATTCAAATTGCCAAAAGGGAAAGGGAAGTCTAAAACATTTGATGCTGATTTAAAGACGGAAATGGTCGAGTTGGAGACAAATGAACCTGAAATTCACATAAAGTCCACCAAAGTAAAGAAACCTTTTTTTGGAAGGTTACATTTTCCTGATGTGGAATTTGACATAAAATCTCCAAAAGTTAAAGCTAGTTCATCTGCATCTGGAACCATGAAATCATCAGATGTTGATTTGCCATCGGCAAGCCTTAAAACTGACATTCAGACACCAGA[T/G]GCTAGTTTGGACAGTCCAGATTTGAAAACGAAAGGGGCAAAAGTAAAAATGTCAAAATACAGCATGTCTAGCTCCAAACTAAAAACTTCAGACTTGGATGTTAGAGATGCAACATTGGAGATTCCAGAGAAGACCATGCATTCTCCAGATGTCAGTGTAGCAGGATCAGGGATTAATGGAAAACGCAGTGCTAAAATTGACATAGAAGGAAAAGTACAAAGTGTTGAGTCGGCAGTGCCATCTACAAATGTCAGCGGGGGGGTTATAGATGCTGATTTAGGTATCGCTGAACAGAAAGGAGTAAAAGGGAGCATTGGAATAGCTGGCTTTAATGTAGGAGGACAAAAGGAAGATACTGCAAGTGGGATAGGCTTGAAGTCAGATGCATCATTATCTGGTGGGATAGAGAATCAAGAAGGTAATTTAACATTTCCTAAAGTCAAAGTACCAAAGTTTGGTATTGCATTGCCTAGAGTAGAACCAAGAGAAATGCGAGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17896
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 5538 | 5689 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27803992)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26496789 |
GRCz11 | 14 | 26794894 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGATGCTGATGCTACTAGTAAAGGTGCTGCTAAAGTGTCTAAGGAGT[T/A]GAGTCTTAGTTCTGGGGAACTGACAAGTGGCAAGTTAACAGTAGAGGAAA
Long Flanking Sequence:
AAGTGTTGAGTCGGCAGTGCCATCTACAAATGTCAGCGGGGGGGTTATAGATGCTGATTTAGGTATCGCTGAACAGAAAGGAGTAAAAGGGAGCATTGGAATAGCTGGCTTTAATGTAGGAGGACAAAAGGAAGATACTGCAAGTGGGATAGGCTTGAAGTCAGATGCATCATTATCTGGTGGGATAGAGAATCAAGAAGGTAATTTAACATTTCCTAAAGTCAAAGTACCAAAGTTTGGTATTGCATTGCCTAGAGTAGAACCAAGAGAAATGCGAGAAGATATAGGTTCGGGTGAATTGGCTGGTGGAGCTAAAGTTAGTTCTCAAGGTTTAGAAATGCAGAAAACTGATGTCAAAAGCAGTGGTGGCAAAGTGAAAGTAAAAATGCCGAAGCTGTTTGTCAAATCTAAATCTAAAGGTGGCAGTGCAGCTGATCTAACTGTTGAGGGAGAAGATGCTGATGCTACTAGTAAAGGTGCTGCTAAAGTGTCTAAGGAGT[T/A]GAGTCTTAGTTCTGGGGAACTGACAAGTGGCAAGTTAACAGTAGAGGAAAGCTCTGGATTTAAAGTTTCTCCAAAGAGTAAATCTGCCTCTCTTGACTTCTTTAAAAAGTCACGACATCACTCATCCTCTGTCAGTGAAGAGGGAGCCTTAGCTTCACCTGTTTCTACTGAAGGGCACTTACAAGCAGAAGCTGGCAATGTTTCTCTAGATGTTGGAGACACTAAGGTTAAAGGCAAAAAAGGAAAGTTGAAGTTCTCTACAATTGGAGGTTTTAGTTCAAAAAGTAAAGGTTCATATGAAGTGACTGATGAGAGTGAGGCTATGACTGAGAGTGCTAGTGGGGTTGCTCAGCCTTCAAAGAAGTCCAGAATGTCATCGTCATCTAGCAGTGATAGTGGTACAAAAGGTAGTATTCGGTTACCACAACTCGAGATATCAGTTTCACCAAAAAAATAAGTTTTTACGTTGATATCTAGGCACAGTTCAAATACATTTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6345
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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 5598 | 5689 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27804172)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26496969 |
GRCz11 | 14 | 26795074 |
KASP Assay ID:
554-4773.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCAGTGAAGAGGGAGCCTTAGCTTCACCTGTTTCTACTGAAGGGCAMT[T/G]ACAAGCAGAAGCTGGCAATGTTTCTCTAGATGTTGGAGACACTAAGGTTA
Long Flanking Sequence:
TGGGATAGAGAATCAAGAAGGTAATTTAACATTTCCTAAAGTCAAAGTACCAAAGTTTGGTATTGCATTGCCTAGAGTAGAACCAAGAGAAATGCGAGAAGATATAGGTTCGGGTGAATTGGCTGGTGGAGCTAAAGTTAGTTCTCAAGGTTTAGAAATGCAGAAAACTGATGTCAAAAGCAGTGGTGGCAAAGTGAAAGTAAAAATGCCGAAGCTGTTTGTCAAATCTAAATCTAAAGGTGGCAGTGCAGCTGATCTAACTGTTGAGGGAGAAGATGCTGATGCTACTAGTAAAGGTGCTGCTAAAGTGTCTAAGGAGTTGAGTCTTAGTTCTGGGGAACTGACAAGTGGCAAGTTAACAGTAGAGGAAAGCTCTGGATTTAAAGTTTCTCCAAAGAGTAAATCTGCCTCTCTTGACTTCTTTAAAAAGTCACGACATCACTCATCCTCTGTCAGTGAAGAGGGAGCCTTAGCTTCACCTGTTTCTACTGAAGGGCACT[T/G]ACAAGCAGAAGCTGGCAATGTTTCTCTAGATGTTGGAGACACTAAGGTTAAAGGCAAAAAAGGAAAGTTGAAGTTCTCTACAATTGGAGGTTTTAGTTCAAAAAGTAAAGGTTCATATGAAGTGACTGATGAGAGTGAGGCTATGACTGAGAGTGCTAGTGGGGTTGCTCAGCCTTCAAAGAAGTCCAGAATGTCATCGTCATCTAGCAGTGATAGTGGTACAAAAGGTAGTATTCGGTTACCACAACTCGAGATATCAGTTTCACCAAAAAAATAAGTTTTTACGTTGATATCTAGGCACAGTTCAAATACATTTATTTTATTATGTCAGTCTAGATGATTATCGTAAATCTGGCTTTCATTGTAATTATAATGCACTGCCTTATAAACTGTTTCTTCAGTTTCCAAAAATGCTCTTTACAGGCATTGATATTATTTGAATCACAATTTAACTGTAAATAAGAGAAAACTGTAGGTAATTTTAAATTTTTTTTGTAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22490
Status:
Available for shipment
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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 |
---|---|---|---|---|---|
ENSDART00000088484 | None | None | 848 | None | 5 |
ENSDART00000125289 | Nonsense | 5615 | 5689 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 14 (position 27804222)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 26497019 |
GRCz11 | 14 | 26795124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAAGCAGAAGCTGGCAATGTTTCTCTAGATGTTGGAGACACTAAGGTT[A/T]AAGGCAAAAAAGGAAAGTTGAAGTTCTCTACAATTGGAGGTTTTAGTTCA
Long Flanking Sequence:
CAAAGTTTGGTATTGCATTGCCTAGAGTAGAACCAAGAGAAATGCGAGAAGATATAGGTTCGGGTGAATTGGCTGGTGGAGCTAAAGTTAGTTCTCAAGGTTTAGAAATGCAGAAAACTGATGTCAAAAGCAGTGGTGGCAAAGTGAAAGTAAAAATGCCGAAGCTGTTTGTCAAATCTAAATCTAAAGGTGGCAGTGCAGCTGATCTAACTGTTGAGGGAGAAGATGCTGATGCTACTAGTAAAGGTGCTGCTAAAGTGTCTAAGGAGTTGAGTCTTAGTTCTGGGGAACTGACAAGTGGCAAGTTAACAGTAGAGGAAAGCTCTGGATTTAAAGTTTCTCCAAAGAGTAAATCTGCCTCTCTTGACTTCTTTAAAAAGTCACGACATCACTCATCCTCTGTCAGTGAAGAGGGAGCCTTAGCTTCACCTGTTTCTACTGAAGGGCACTTACAAGCAGAAGCTGGCAATGTTTCTCTAGATGTTGGAGACACTAAGGTT[A/T]AAGGCAAAAAAGGAAAGTTGAAGTTCTCTACAATTGGAGGTTTTAGTTCAAAAAGTAAAGGTTCATATGAAGTGACTGATGAGAGTGAGGCTATGACTGAGAGTGCTAGTGGGGTTGCTCAGCCTTCAAAGAAGTCCAGAATGTCATCGTCATCTAGCAGTGATAGTGGTACAAAAGGTAGTATTCGGTTACCACAACTCGAGATATCAGTTTCACCAAAAAAATAAGTTTTTACGTTGATATCTAGGCACAGTTCAAATACATTTATTTTATTATGTCAGTCTAGATGATTATCGTAAATCTGGCTTTCATTGTAATTATAATGCACTGCCTTATAAACTGTTTCTTCAGTTTCCAAAAATGCTCTTTACAGGCATTGATATTATTTGAATCACAATTTAACTGTAAATAAGAGAAAACTGTAGGTAATTTTAAATTTTTTTTGTAGATAGGAAATTCAGATTCAATCCAAAAATGTGTGTACTTAATATAAAAAAGAA
Associated Phenotype:
Not determined