ZMP
Q5RHN9_DANRE
Ensembl ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5RHN9]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32289 | Nonsense | Available for shipment | Available now |
sa37022 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23697 | Nonsense | Available for shipment | Available now |
sa11480 | Nonsense | Available for shipment | Available now |
sa11771 | Nonsense | Available for shipment | Available now |
sa29357 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43435 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11048 | Nonsense | Available for shipment | Available now |
sa32290 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32289
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 59 | 1995 | 3 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23931471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24050272 |
GRCz11 | 20 | 23949372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTTAACACTATCCTTTCTCCACGGACCATGGAATCTATGGATATATA[T/A]GAGGAAATTATCAGAGAAGAACAAGAAGAAAAGGAAGCAACTTACAATGA
Long Flanking Sequence:
AAAATTAAATAAATATATGATAATTACATTTAGCCATTCACCCGGGTTTGCTTTTTAATAGCTTTTATTTGTTTTTGCATATGAAAAGTACTTTATCCACATTAAAAAAAATCCTGATTCCATCCTGATTTTCTTATTTGTACAGGTTAGGTGTCCTAGCTATGTCAAAACCGAATATAAAAATGCATTAACATATTTGTGGGGCTTCTTTTTAATAATATGACTGTATCCGTGTTTTTTTTTGATGCAGGTACTCCTCTCCATCACAGTGAGGACTCTGTGGACATTTACTCTGGCCTGGAGAATAGCCCTAAGTGTGATGGGCACAGAGGTGGCTTTTATTAATGAATATGTTGTAATTAAAATAAAATTGTTGATGCGTGAATATCAGTGATATGTAGATGAAAACTTTCAGATTGTAATTCTTACCTTGTTGGTTTTTAATTGGTTACAGTTAACACTATCCTTTCTCCACGGACCATGGAATCTATGGATATATA[T/A]GAGGAAATTATCAGAGAAGAACAAGAAGAAAAGGAAGCAACTTACAATGAGGTTTGTTCAAAAAACAAGTTTTGCTCATGATATTGATTTGGTTATTCTTGAAAGTAAAGAAATGGACTTCATTTTGTCTTTAAATTCGACAATTTGTCTTTTATTACAGTTGAAGCAAAAATTTGATGGCGCACAAAAGCAAGTTAATGAACTCCTGTCAAAGTTACAGCTACTGCAGACAAAGGTGTGTTTGTTTTCATGGTTTCTGATAAATATCCTCATAACTTGTTTCAAAATAAAACTGAAAATGTATACTAAAAATGAAATGTTTTTTTTTTTATATATATCTAAAGAATTCAAGTTTAAGCTCTGAAAACATTCTTCTGAAGAAGAACATTTGCTCTCTCATCAAGACTGCTAGAATGGAAATTGTGCGTAAGGATGAGGAGATTAGCCGACTCAGCAATAGGTAAGAACTCAGGAGCTAATACTAAAATCAGCAAACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37022
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 204 | 1995 | 6 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23932240)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24051041 |
GRCz11 | 20 | 23950141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTAAATCAGCAAACGGACAGGATCACTTCAACATCAATTTCAGCATCA[C/T]AGCCATTTGAGGTGCTCCAGAGATGTCCAAGAACTGAAAGTGAAAATCCT
Long Flanking Sequence:
CTCATAACTTGTTTCAAAATAAAACTGAAAATGTATACTAAAAATGAAATGTTTTTTTTTTTATATATATCTAAAGAATTCAAGTTTAAGCTCTGAAAACATTCTTCTGAAGAAGAACATTTGCTCTCTCATCAAGACTGCTAGAATGGAAATTGTGCGTAAGGATGAGGAGATTAGCCGACTCAGCAATAGGTAAGAACTCAGGAGCTAATACTAAAATCAGCAAACAAATAATGAACTCTGGTTTGTTTGGTATTGGATGCCGTTCATGTTAAACTCATTTTGTTATGTTTCTGTGTTTCCTTTACAGGTCTGGTCGTGGAAGTTATGGTCACAGTTTCTATCAATCTCAAATGGGAAGTGCCTCTGCAAACACAAGACACACTTTAAACAATTCTACAGGTTCTGTTTTAGAGTCACGAGGTGCTAGACAAGAAAAAGTTATGGATGAAGTAAATCAGCAAACGGACAGGATCACTTCAACATCAATTTCAGCATCA[C/T]AGCCATTTGAGGTGCTCCAGAGATGTCCAAGAACTGAAAGTGAAAATCCTCTGCAAAGTCAGAATAAATCTGCTGCTAAAACTGATCGTGAGATCCTCAGTATTCAACCACAGCAAGAGTACCGACCAGTCCCTCCTTGCAGAACTTCCGAGAGTATAACAAATCCCACCACATTGCCCGATATCTTGAATACTTCCAAAACAAAAAACTATAAAAAGAGAGTTCCAGATGAAACTACTGATTGTCAATTAAGTAACTTGAAGGACAATAAGAATTGTCCCTCAAATCAGGATGACAAGCTAGAAAAGCCACAAAAATGCACAAGTAAGGATCAAATGTGTAACTCCAAAAATAAGGATGTGTCACCACAGAGTAAAGCAGACTTGAGCAAGCCAGTAAGAATGGAAAAAGAGCTGACAAAGGATAATTCTGTGTCTAGTGAAAACAGGAGTCAGCAGCTTGAGGTTCCAGTTGTTCTTAAAAGTTCAGAGCAATTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23697
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 408 | 1995 | 6 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 23932852)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24051653 |
GRCz11 | 20 | 23950753 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGAAAGCAGCAGACACGGAGGTGCAGAGTCAAGGGCACATGCATAAA[C/T]AAAACGCAGAAAGAACAAGCAGAGAAACGAGACAATCTGGATTGAGCAGT
Long Flanking Sequence:
AGCAAGAGTACCGACCAGTCCCTCCTTGCAGAACTTCCGAGAGTATAACAAATCCCACCACATTGCCCGATATCTTGAATACTTCCAAAACAAAAAACTATAAAAAGAGAGTTCCAGATGAAACTACTGATTGTCAATTAAGTAACTTGAAGGACAATAAGAATTGTCCCTCAAATCAGGATGACAAGCTAGAAAAGCCACAAAAATGCACAAGTAAGGATCAAATGTGTAACTCCAAAAATAAGGATGTGTCACCACAGAGTAAAGCAGACTTGAGCAAGCCAGTAAGAATGGAAAAAGAGCTGACAAAGGATAATTCTGTGTCTAGTGAAAACAGGAGTCAGCAGCTTGAGGTTCCAGTTGTTCTTAAAAGTTCAGAGCAATTGAAAAGTCATTCTTCCCAGTCACACAAATCCTTTTCATCTGCTTCGTCTCACTCCAGAACCTTAATTAAGAAAGCAGCAGACACGGAGGTGCAGAGTCAAGGGCACATGCATAAA[C/T]AAAACGCAGAAAGAACAAGCAGAGAAACGAGACAATCTGGATTGAGCAGTACAGAATGCACTGTGGTCAGTGAAGAAAACCATTCTCAAAGCCACAAAGGGAAGAAAAGAGATGCAAGTGGTTCTGAAAGAAAAGAGGAGAAACGTTCTAGTACAGAGAGGAGGAGCAGCAAAACTGAAAGAAGCCGAGACCATGAGCAAAAGAGGCCAAAGGAGAGTAACCGGAGCAAAAGAGATGAGGGTAACAGCTGCAGCAGCAGAGAAAGAAGAAGCAACAGGTCAGAGAGTAGCAGAGACCATGAGCGGAGAAGTACAAAGGGGAAGGATAATAAAGACCAAGATAAAAGATCTACAAAACAAGTGGATGGCTCAGATAGTAGGCGAGCTGTTTCTTCTCCCAAACATGATTCTCAACGGAAGGATGTTAATAAGGAGAAATCTTCAAGCAGACTTGATGAGGTTCCATCAAAAAGTAAGAGCTCTCATAGACATGACAAATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11480
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 884 | 1995 | 6 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23934282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24053083 |
GRCz11 | 20 | 23952183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGAAGATGCAATTTCAGATAATGTTCCTCAGTCAATAGTTGATGGTTG[T/A]CTGCAACCARATCTTTTTGCCACCGTGTCTAAAGAGACTTCTCAGAAGGA
Long Flanking Sequence:
CATAACAGCAGATGTTCAGATTCCGGGGAGGAATTCTTTGTCATAGATGAATTAAAGAACAGCCAGAACAGTGTTGAGGAAATGGATGAGATCCCTGAGCTTACAAATGCAGAAGACCTTACCTGTTCTTTCAAACAGTCTGAAAATGCTTTGGATATGATGACAGCTGTAACCTCTGAGAAGCTCTCAACAGAAAAAATAGAAATAGCAATACAAAATAAGAATGTCACCGAAAATCAAGAGACTGTGGACGAAGTGGCAGCCATTGTTAACCCCTCAGAAGAGAAAAAAGACACATCTTTAGAATCCAAAATATTAGACACTGATTCAATTTCAGTAATAACTCTTACAAAAGAATCTCCCGATTTTGCAAGTCAGAGCCATGCGGAAGATTCTCCAGGAACTATAGATAATGCTGTTGCTGTTTTTAACACTTCACCTGCTAAACCATCAGAAGATGCAATTTCAGATAATGTTCCTCAGTCAATAGTTGATGGTTG[T/A]CTGCAACCAGATCTTTTTGCCACCGTGTCTAAAGAGACTTCTCAGAAGGAGTTTCAAGGAAACACCCTGCCAATGTCTAAAGATGTTCTACTAGAATCAAATGAGATTTGTCAGGGTGCTGTGTCATCCTCTGACAAGGAGCACAATAGTGCTACGATTAATTCCTCTGGGAATTCTGACAGTTCTGTCAGTATGGAAGTTTCGTCTAGCACAATTTGTGCAGATCTTAATGGCCCAAGCAAAGTAATTTGTGATTTTGAACAAGTTGATTCTGCAGAAGACGATAGAGAAAGGGAAATATTTGAAAATATAAAAATGATGGAAACACAGCAGACATCTGAAAATCTAAAAATATCTGAAACATCCCTTCAAAGTCCATTACGGAGTGAGAACACTAAGGCTCCAAATGATGGCACCAGTGTTGAAAAGGAGACCATATCATTCTCCCAGTCTAGTTTCTTAGAGCCAGATTCCACAGAGAAAGAGGAACAAATACCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11771
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 917 | 1995 | 6 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23934380)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24053181 |
GRCz11 | 20 | 23952281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGARTTTCAAGGAAACACCCTGCCAATGTCTAAAGATGTTCTACTAGAAT[C/A]AAATGAGATTTGTCAGGGTGCTGTGTCATCCTCTGACAAGGAGCACAATA
Long Flanking Sequence:
GCTTACAAATGCAGAAGACCTTACCTGTTCTTTCAAACAGTCTGAAAATGCTTTGGATATGATGACAGCTGTAACCTCTGAGAAGCTCTCAACAGAAAAAATAGAAATAGCAATACAAAATAAGAATGTCACCGAAAATCAAGAGACTGTGGACGAAGTGGCAGCCATTGTTAACCCCTCAGAAGAGAAAAAAGACACATCTTTAGAATCCAAAATATTAGACACTGATTCAATTTCAGTAATAACTCTTACAAAAGAATCTCCCGATTTTGCAAGTCAGAGCCATGCGGAAGATTCTCCAGGAACTATAGATAATGCTGTTGCTGTTTTTAACACTTCACCTGCTAAACCATCAGAAGATGCAATTTCAGATAATGTTCCTCAGTCAATAGTTGATGGTTGTCTGCAACCAGATCTTTTTGCCACCGTGTCTAAAGAGACTTCTCAGAAGGAGTTTCAAGGAAACACCCTGCCAATGTCTAAAGATGTTCTACTAGAAT[C/A]AAATGAGATTTGTCAGGGTGCTGTGTCATCCTCTGACAAGGAGCACAATAGTGCTACGATTAATTCCTCTGGGAATTCTGACAGTTCTGTCAGTATGGAAGTTTCGTCTAGCACAATTTGTGCAGATCTTAATGGCCCAAGCAAAGTAATTTGTGATTTTGAACAAGTTGATTCTGCAGAAGACGATAGAGAAAGGGAAATATTTGAAAATATAAAAATGATGGAAACACAGCAGACATCTGAAAATCTAAAAATATCTGAAACATCCCTTCAAAGTCCATTACGGAGTGAGAACACTAAGGCTCCAAATGATGGCACCAGTGTTGAAAAGGAGACCATATCATTCTCCCAGTCTAGTTTCTTAGAGCCAGATTCCACAGAGAAAGAGGAACAAATACCAAAGTCATCTAACTCTGTTCTGTTTTGCCATGATGAAGACTCTATGATGCTTACACTTAGAAACATCAGAGTTATTCCAGAGCCCATCAGCCCTCTCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29357
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 972 | 1995 | 6 | 9 |
ENSDART00000144195 | None | None | 937 | None | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23934544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24053345 |
GRCz11 | 20 | 23952445 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATTTGTGCAGATCTTAATGGCCCAAGCAAAGTAATTTGTGATTTTGAA[C/T]AAGTTGATTCTGCAGAAGACGATAGAGAAAGGGAAATATTTGAAAATATA
Long Flanking Sequence:
CCATTGTTAACCCCTCAGAAGAGAAAAAAGACACATCTTTAGAATCCAAAATATTAGACACTGATTCAATTTCAGTAATAACTCTTACAAAAGAATCTCCCGATTTTGCAAGTCAGAGCCATGCGGAAGATTCTCCAGGAACTATAGATAATGCTGTTGCTGTTTTTAACACTTCACCTGCTAAACCATCAGAAGATGCAATTTCAGATAATGTTCCTCAGTCAATAGTTGATGGTTGTCTGCAACCAGATCTTTTTGCCACCGTGTCTAAAGAGACTTCTCAGAAGGAGTTTCAAGGAAACACCCTGCCAATGTCTAAAGATGTTCTACTAGAATCAAATGAGATTTGTCAGGGTGCTGTGTCATCCTCTGACAAGGAGCACAATAGTGCTACGATTAATTCCTCTGGGAATTCTGACAGTTCTGTCAGTATGGAAGTTTCGTCTAGCACAATTTGTGCAGATCTTAATGGCCCAAGCAAAGTAATTTGTGATTTTGAA[C/T]AAGTTGATTCTGCAGAAGACGATAGAGAAAGGGAAATATTTGAAAATATAAAAATGATGGAAACACAGCAGACATCTGAAAATCTAAAAATATCTGAAACATCCCTTCAAAGTCCATTACGGAGTGAGAACACTAAGGCTCCAAATGATGGCACCAGTGTTGAAAAGGAGACCATATCATTCTCCCAGTCTAGTTTCTTAGAGCCAGATTCCACAGAGAAAGAGGAACAAATACCAAAGTCATCTAACTCTGTTCTGTTTTGCCATGATGAAGACTCTATGATGCTTACACTTAGAAACATCAGAGTTATTCCAGAGCCCATCAGCCCTCTCACAAGCCCAGTTCGTCAGGTTAAGAAAGTACAACCTCCACTTGCTGAGAAACAACCACATGTCAAAAGTCTTAGCAAAGGTGGGTGTGAGTTTTTCGTTGTCATGTTTTTTTTCTTTATAATTATCAGAATGGCACTAGTTTGACTGAAATGTATGCTCGTATAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43435
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 1804 | 1995 | 7 | 9 |
ENSDART00000144195 | Nonsense | 746 | 937 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23937182)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24055983 |
GRCz11 | 20 | 23955083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGGTAAACAAGCCCTGTCACATTTCAGAAACGGTAGAATCTCAACCAT[C/A]AAGCCAAAAGTCTTCATCTGAAGGTGATAAAACATTCTGCAACAATGCCA
Long Flanking Sequence:
CCTTACCATTCCCTCACCACTGAAGTCAGATAGCCACTTGAGTTTCCTGCATCCTGGAACTGGACAGCCACTGTCTGCCCCAAACAGTGTCCTTAGTGCTCATTATAGTGAAGATGCTCTTCTTGATGGAGAAGATGCCACTGAGCAGGATATCCACCTTTCACTGGACACTGACAACTCTAGTTGTGGGTCGAGCCCCAGCAGGACTTGGGAGGGTTCTGATCAATTGGGTTTCCAGTTTCAGCCGAATTTGCCAATGCAGGCGGTGGTAATGGAGAGATCAAATGATCACTTCATTGTGCGGATAAGGCGGACATCCACTAGCCCAAGTGAAGGGAAAGCAGTACCAACATTAGCTAAATGTCCAGAGCCATCTCTTAAGCCTAATGTCAATCTGACCCATGAAGACTTGAGTTCTGCACCTGGAGAGATGTTGACCAAAAGTCCAACCAAGGTAAACAAGCCCTGTCACATTTCAGAAACGGTAGAATCTCAACCAT[C/A]AAGCCAAAAGTCTTCATCTGAAGGTGATAAAACATTCTGCAACAATGCCAAGCCTGTTTCCAAAGAAGTGTGTTTCCAAAGAAGCAGGGATATTGAGGAAAACAGTGCAACAGAGGTTAAAACATCAGAGAAGGTGTCAGAAAGTTTAAGCAACAACATTCAGAGCTTAAGTGCACCAGAAACGGAACCCGAGAGGGTGTCAAGGAAACGCAAGGACCGCCAATCGGAGTCAAAATCAAAGCGCTCAAAGGTAGAAAAATCTAAAGAAAAACATTCCAAGTCCAGACATAAGAAAAAGTCAAAACCCTCTAAAGAAAAAGTCTTAAAAACTGCAACACCCCCAGTGTCTCCTAGCAGCCTTTCTGCTAAGAATGTAATCCGAAAGAAAGGGGAAGTGGTGGTGTCATGGACCAGGTGAGTTTACTTCAATTCCAATGCAGTTATGGGTTGTTTTTTGTTTGTATGCAAATAAAATTGTTTAAGCATCCAGTTAAACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11048
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 1853 | 1995 | 7 | 9 |
ENSDART00000144195 | Nonsense | 795 | 937 | 2 | 4 |
ENSDART00000062686 | Nonsense | 1853 | 1995 | 7 | 9 |
ENSDART00000144195 | Nonsense | 795 | 937 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23937329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24056130 |
GRCz11 | 20 | 23955230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAACAGTGCAACAGARGTTAAAACATCAGAGAAGGYGTCAGAAAGTT[T/G]AAGCAASAACATTCAGAGCTTAAGTGCACCAGAAACGGAACCCRAGAGGG
Long Flanking Sequence:
GGATATCCACCTTTCACTGGACACTGACAACTCTAGTTGTGGGTCGAGCCCCAGCAGGACTTGGGAGGGTTCTGATCAATTGGGTTTCCAGTTTCAGCCGAATTTGCCAATGCAGGCGGTGGTAATGGAGAGATCAAATGATCACTTCATTGTGCGGATAAGGCGGACATCCACTAGCCCAAGTGAAGGGAAAGCAGTACCAACATTAGCTAAATGTCCAGAGCCATCTCTTAAGCCTAATGTCAATCTGACCCATGAAGACTTGAGTTCTGCACCTGGAGAGATGTTGACCAAAAGTCCAACCAAGGTAAACAAGCCCTGTCACATTTCAGAAACGGTAGAATCTCAACCATCAAGCCAAAAGTCTTCATCTGAAGGTGATAAAACATTCTGCAACAATGCCAAGCCTGTTTCCAAAGAAGTGTGTTTCCAAAGAAGCAGGGATATTGAGGAAAACAGTGCAACAGAGGTTAAAACATCAGAGAAGGTGTCAGAAAGTT[T/G]AAGCAACAACATTCAGAGCTTAAGTGCACCAGAAACGGAACCCGAGAGGGTGTCAAGGAAACGCAAGGACCGCCAATCGGAGTCAAAATCAAAGCGCTCAAAGGTAGAAAAATCTAAAGAAAAACATTCCAAGTCCAGACATAAGAAAAAGTCAAAACCCTCTAAAGAAAAAGTCTTAAAAACTGCAACACCCCCAGTGTCTCCTAGCAGCCTTTCTGCTAAGAATGTAATCCGAAAGAAAGGGGAAGTGGTGGTGTCATGGACCAGGTGAGTTTACTTCAATTCCAATGCAGTTATGGGTTGTTTTTTGTTTGTATGCAAATAAAATTGTTTAAGCATCCAGTTAAACAGTTGGTGTCTTTTGTAGGGATGAAGATCGGGATATCCTTGTCGAGCTTAAAATGAAGGGAACTTCACCCAAGACATTTGCTGCTCTGTCGAAAAAGTTGAAGAAATCAACAGAGCAGGTATGCTCCCTAATTATTTTTTGATTGACATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32290
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 |
---|---|---|---|---|---|
ENSDART00000062686 | Nonsense | 1853 | 1995 | 7 | 9 |
ENSDART00000144195 | Nonsense | 795 | 937 | 2 | 4 |
ENSDART00000062686 | Nonsense | 1853 | 1995 | 7 | 9 |
ENSDART00000144195 | Nonsense | 795 | 937 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 23937329)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 24056130 |
GRCz11 | 20 | 23955230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACAGTGCAACAGAGGTTAAAACATCAGAGAAGGTGTCAGAAAGTT[T/A]AAGCAACAACATTCAGAGCTTAAGTGCACCAGAAACGGAACCCGAGAGGG
Long Flanking Sequence:
GGATATCCACCTTTCACTGGACACTGACAACTCTAGTTGTGGGTCGAGCCCCAGCAGGACTTGGGAGGGTTCTGATCAATTGGGTTTCCAGTTTCAGCCGAATTTGCCAATGCAGGCGGTGGTAATGGAGAGATCAAATGATCACTTCATTGTGCGGATAAGGCGGACATCCACTAGCCCAAGTGAAGGGAAAGCAGTACCAACATTAGCTAAATGTCCAGAGCCATCTCTTAAGCCTAATGTCAATCTGACCCATGAAGACTTGAGTTCTGCACCTGGAGAGATGTTGACCAAAAGTCCAACCAAGGTAAACAAGCCCTGTCACATTTCAGAAACGGTAGAATCTCAACCATCAAGCCAAAAGTCTTCATCTGAAGGTGATAAAACATTCTGCAACAATGCCAAGCCTGTTTCCAAAGAAGTGTGTTTCCAAAGAAGCAGGGATATTGAGGAAAACAGTGCAACAGAGGTTAAAACATCAGAGAAGGTGTCAGAAAGTT[T/A]AAGCAACAACATTCAGAGCTTAAGTGCACCAGAAACGGAACCCGAGAGGGTGTCAAGGAAACGCAAGGACCGCCAATCGGAGTCAAAATCAAAGCGCTCAAAGGTAGAAAAATCTAAAGAAAAACATTCCAAGTCCAGACATAAGAAAAAGTCAAAACCCTCTAAAGAAAAAGTCTTAAAAACTGCAACACCCCCAGTGTCTCCTAGCAGCCTTTCTGCTAAGAATGTAATCCGAAAGAAAGGGGAAGTGGTGGTGTCATGGACCAGGTGAGTTTACTTCAATTCCAATGCAGTTATGGGTTGTTTTTTGTTTGTATGCAAATAAAATTGTTTAAGCATCCAGTTAAACAGTTGGTGTCTTTTGTAGGGATGAAGATCGGGATATCCTTGTCGAGCTTAAAATGAAGGGAACTTCACCCAAGACATTTGCTGCTCTGTCGAAAAAGTTGAAGAAATCAACAGAGCAGGTATGCTCCCTAATTATTTTTTGATTGACATAT
Associated Phenotype:
Not determined