ZMP
ENSDARG00000016527
Ensembl ID:
Human Orthologue:
RP4-697K14.7
Human Description:
Peroxisomal proliferator-activated receptor A-interacting complex 285 kDa protein [Source:UniProtKB/
Mouse Orthologue:
BC006779
Mouse Description:
cDNA sequence BC006779 Gene [Source:MGI Symbol;Acc:MGI:2385169]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8413 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8867 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18418 | Nonsense | Available for shipment | Available now |
sa15330 | Nonsense | Available for shipment | Available now |
sa20836 | Nonsense | Available for shipment | Available now |
sa40812 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8462 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa7054 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20837 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa8413
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 1308 | 2507 | 9 | 21 |
ENSDART00000018498 | Nonsense | 1308 | 2507 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58497490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58600618 |
GRCz11 | 6 | 58594849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATCTCATTGATTATAGAAGTGGATGCRCAGACTAATCGCATAAAGAGA[A/T]GATTTWTCTGCAAGTCTGTGATTCACTCYAACAGGAAATTTTCCTAYGAT
Long Flanking Sequence:
GAAACGTTTTCAGATATCCTTTGGGGATTGTCGTAGGTGTGCTTCCTAAAATAGCAACTTTAGATGATGGATTGCATGTACTCAGCATTGAGTACCAGTTGAGAAGGACACTTTCCTCATCTCTGAGAAAGCAGATGCAATACTTACAACGTCTTGATATTTTCGAAAAAGGACGAAGAGATTTTCGCATGCTCCCAACCTTCACAGTTGATCCCGCACATTCGCAAGATCTCGATGATGCAATAAGTTTGCAGGATTTTGGTGAGTACCTTGAAATAGGAGTTCACATTTCTGATGTTGCAAGCTTTGTGGCTAAAGATAGCGAACTGGACAAATTTGCCAGACAGCTGTGTACTACATTCTACCCTCGTGAGAAGGAGCCAATATACATGTTTCCCAAAGAACTGAGCACCAATTTGTTAAGTTTAATCCCTAACCAGGACAGACGAGCAATCTCATTGATTATAGAAGTGGATGCACAGACTAATCGCATAAAGAGA[A/T]GATTTATCTGCAAGTCTGTGATTCACTCCAACAGGAAATTTTCCTACGATGAAGTTGAGGACATTCTTGAAAATGGTGAGCCGCTTTCCGACCTGCTTGAAATCTGTCTTGTAAAAGTGTCGAACTTTGCTGAGGTTCACCGAAGATACAGAAAGCAGGATGACTGGTGCTACAAGATGCCAGATGAGGATGTGACCCTTGGAAGAAGGAGATCTCACCAAATGGTGGAAGAGCTGATGGTCATGTTTAACCACATGGTTGCCGAACGTCTTTTATCTGATGGTGCAACAAGAAGCAAAACTCCATTGAGATGCCAGGACAGGCCTCAAACAGACAAACTCATTGAGATTTTTGACAAAAACGCAGCCTTGATTCCGCTGTCTGTTCACTTCTCAAGTCAAGCTCATGAACTGAATAAGCAAGGTTTGATCCAGCACAACCCTCAGACTGACTCAGACACGTTCCCTGTGTTAAAATCAATCCTCAGATGCCTGAAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8867
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 1308 | 2507 | 9 | 21 |
ENSDART00000018498 | Nonsense | 1308 | 2507 | 9 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58497490)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58600618 |
GRCz11 | 6 | 58594849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAATCTCATTGATTATAGAAGTGGATGCRCAGACTAATCGCATAAAGAGA[A/T]GATTTWTCTGCAAGTCTGTGATTCACTCYAACAGGAAATTTTCCTAYGAT
Long Flanking Sequence:
GAAACGTTTTCAGATATCCTTTGGGGATTGTCGTAGGTGTGCTTCCTAAAATAGCAACTTTAGATGATGGATTGCATGTACTCAGCATTGAGTACCAGTTGAGAAGGACACTTTCCTCATCTCTGAGAAAGCAGATGCAATACTTACAACGTCTTGATATTTTCGAAAAAGGACGAAGAGATTTTCGCATGCTCCCAACCTTCACAGTTGATCCCGCACATTCGCAAGATCTCGATGATGCAATAAGTTTGCAGGATTTTGGTGAGTACCTTGAAATAGGAGTTCACATTTCTGATGTTGCAAGCTTTGTGGCTAAAGATAGCGAACTGGACAAATTTGCCAGACAGCTGTGTACTACATTCTACCCTCGTGAGAAGGAGCCAATATACATGTTTCCCAAAGAACTGAGCACCAATTTGTTAAGTTTAATCCCTAACCAGGACAGACGAGCAATCTCATTGATTATAGAAGTGGATGCACAGACTAATCGCATAAAGAGA[A/T]GATTTATCTGCAAGTCTGTGATTCACTCCAACAGGAAATTTTCCTACGATGAAGTTGAGGACATTCTTGAAAATGGTGAGCCGCTTTCCGACCTGCTTGAAATCTGTCTTGTAAAAGTGTCGAACTTTGCTGAGGTTCACCGAAGATACAGAAAGCAGGATGACTGGTGCTACAAGATGCCAGATGAGGATGTGACCCTTGGAAGAAGGAGATCTCACCAAATGGTGGAAGAGCTGATGGTCATGTTTAACCACATGGTTGCCGAACGTCTTTTATCTGATGGTGCAACAAGAAGCAAAACTCCATTGAGATGCCAGGACAGGCCTCAAACAGACAAACTCATTGAGATTTTTGACAAAAACGCAGCCTTGATTCCGCTGTCTGTTCACTTCTCAAGTCAAGCTCATGAACTGAATAAGCAAGGTTTGATCCAGCACAACCCTCAGACTGACTCAGACACGTTCCCTGTGTTAAAATCAATCCTCAGATGCCTGAAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18418
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 1448 | 2507 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58497934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58601062 |
GRCz11 | 6 | 58595293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAGTCAAGCTYATGAACTGAATAAGCAAGGTTTGATCCAGCACAACCCT[C/T]AGACYGACTCAGACACGTTCCCWGTGTTAAAATCAAWCCTCAGATGCCTG
Long Flanking Sequence:
GACGAGCAATCTCATTGATTATAGAAGTGGATGCACAGACTAATCGCATAAAGAGAAGATTTATCTGCAAGTCTGTGATTCACTCCAACAGGAAATTTTCCTACGATGAAGTTGAGGACATTCTTGAAAATGGTGAGCCGCTTTCCGACCTGCTTGAAATCTGTCTTGTAAAAGTGTCGAACTTTGCTGAGGTTCACCGAAGATACAGAAAGCAGGATGACTGGTGCTACAAGATGCCAGATGAGGATGTGACCCTTGGAAGAAGGAGATCTCACCAAATGGTGGAAGAGCTGATGGTCATGTTTAACCACATGGTTGCCGAACGTCTTTTATCTGATGGTGCAACAAGAAGCAAAACTCCATTGAGATGCCAGGACAGGCCTCAAACAGACAAACTCATTGAGATTTTTGACAAAAACGCAGCCTTGATTCCGCTGTCTGTTCACTTCTCAAGTCAAGCTCATGAACTGAATAAGCAAGGTTTGATCCAGCACAACCCT[C/T]AGACTGACTCAGACACGTTCCCTGTGTTAAAATCAATCCTCAGATGCCTGAAGTCAGCAGCAGAGCAGGAAAACATCTACAAAATAATTGACTTTGTTGCAACTGATGACATTCATCCTCAGCTTCTGCCTTTTGCTGTTGCATTTAGGCGGTTGTTTCACAAGGCGTGCATTCAGCGCTCAAACTCAACGCATGTCTCAAGAATAGGGCACTATGATTTAGATCTTGACAGCTATACATGGGCCTCATCTCCAGTTCGCCGATACTTAGATGTAATTGTGCAGCGCCTTCTTCATTCTGTGATTGACAAGACAGATGTTAAGTACACAACTCTAGACATTAACCTGTCTTGTTTGGAATTCTCCAGGAAAAATGATCAACAGTCGGCCTATGAGAGGAAGGCAAATGCTCTGCATTTCGCATTAAAACTGTCAAGCCAAAGTGAAAGGAAGGTGGCTTATATTGTGGAGCTCAATCCATTAGGGACAAACTTCAAAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15330
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 1589 | 2507 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58498358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58601486 |
GRCz11 | 6 | 58595717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGATCAACARTCGGCCTATGAGAGGAAGGCAAATGCTCTGCATTTYGCAT[T/A]AAARCTKTCAAGCCAAAGTGAAAGGAAGGTGGCTTATATTGTGGAGCTCA
Long Flanking Sequence:
CTTGATTCCGCTGTCTGTTCACTTCTCAAGTCAAGCTCATGAACTGAATAAGCAAGGTTTGATCCAGCACAACCCTCAGACTGACTCAGACACGTTCCCTGTGTTAAAATCAATCCTCAGATGCCTGAAGTCAGCAGCAGAGCAGGAAAACATCTACAAAATAATTGACTTTGTTGCAACTGATGACATTCATCCTCAGCTTCTGCCTTTTGCTGTTGCATTTAGGCGGTTGTTTCACAAGGCGTGCATTCAGCGCTCAAACTCAACGCATGTCTCAAGAATAGGGCACTATGATTTAGATCTTGACAGCTATACATGGGCCTCATCTCCAGTTCGCCGATACTTAGATGTAATTGTGCAGCGCCTTCTTCATTCTGTGATTGACAAGACAGATGTTAAGTACACAACTCTAGACATTAACCTGTCTTGTTTGGAATTCTCCAGGAAAAATGATCAACAGTCGGCCTATGAGAGGAAGGCAAATGCTCTGCATTTCGCAT[T/A]AAAACTGTCAAGCCAAAGTGAAAGGAAGGTGGCTTATATTGTGGAGCTCAATCCATTAGGGACAAACTTCAAAGTGTCCTTTCCACTTAACAGATCCTCTATATCAGAAAACTTAGACATTATGAGCAGGGATCTTCTGCTGGCTGTTCAGCCAGAGTTTGATGTAACAAACAACAGCATGATCCTGAAATGGGAGCGAAGGATATATTCATTCTCCAATTCTCACATCCATGCTGAAGTGAAGCAACAAAACCCAAACTCAGTTATGGCCTATGTCCCTGCAAAGACCTGGAAATGCATTGCAGATGCTATCAGAGAACAAAACTGGAATGCCATTTTTCCTCTTATTGAGGAACTTCAACGCAACTCTGGCATCAATGCAAGACAATTTCACGAAACACTGAGTGCTTCAAAATGCACGAAAAATTATGACCCCTTGCATGCTGAGCATTATGCTGAACTGTATCTGAGAATTAAGCAAGGTGAGGCGGTCGAAGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20836
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 1948 | 2507 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58499434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58602562 |
GRCz11 | 6 | 58596793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGAATTGATTTTCTGATTAATCACATGCCCATGACAAACATTCCAGAA[C/T]AAATATTCCACGAGAGGACGAGATTTACGCTGGAGCTGATTCCAAAGCTT
Long Flanking Sequence:
TTTGCGTGGAGCATGTAAGAGATCCAGTCAAGTGTTTTTCTGAATACGCACTAAGCTCATCAAGGAGTTCATACAACTTGTACAAGGATTATCAGGCAATATGGAGACCTATGTGCGAGATGGAGTCAGCCTCCAGCGCTGTGGCTGAAAATGAGAGCATTCTTATTGTAGATGTGCCCTTGAAATGGGAAAACTCCAATCCGAAGAGGCTACAGGGGTTTTTTCTGCTCCCGCTTGACAAGAAATCTCAGTGGTCAATAGACTGTGATCTCAGAAACAGCTTCCTATGCATTCGAACGAGGATTCAGAAACAGAGTAGCCCATTTCTGGAGAGCGCTCAGAACACAGCGCTCATGGATATTCCTTCTTTCACTTGGGTAGTTCATGGTGTGATTACAGAAGCTGAAGAAACAGAGTCCAAAGAATCAACGAATCAAGAACCAAAGAGTTTGCGAATTGATTTTCTGATTAATCACATGCCCATGACAAACATTCCAGAA[C/T]AAATATTCCACGAGAGGACGAGATTTACGCTGGAGCTGATTCCAAAGCTTCTGCCAGACGTGTAAGTTTGCAAATAATATACCTTACAACTATAGTTTAAAATGCTAAATAATACAGAGTTAATCATTGCAAATTTATTTGTGAATACATTGTATAGTTTAATACGGTTGAAGATAGAAGTATTAGCCTTCCTTTGAAATTGTAATTCAGTAAGAAAAAATTGTGAAGTTTCAAGAGTTTACACTTAGCTCATGATTTATCACATAGCTTGTTTGGCGTGCTGTCCCGGGAGAGAGCCCTGAGCTCAAGGGATCCTTGGGCCCAGGGCTTCCCCCTTTTCAAGGGGCGAGGGGAAATTCCCCCGCTGCTAAGGCCAAGGTGAACTTCCTGAGAGTAAGACATTAGAAAAAAGATTTAGGCTTATTTTATCTATAGTATGGAGCATATATGGACAGTGGGAGGAAACCAGGGAACCCGGGGGAAACCCACGCGGACACGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40812
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 2066 | 2507 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58502183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58605311 |
GRCz11 | 6 | 58599542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTGTTGTTGGTGTCCATATTTTGTACTGGCTGCACAAGAATATCCAA[C/T]AGCTCCAAGCTTCTGGTTCAAAGAAGAGAGCTATTCTGTACTGTGGCCCG
Long Flanking Sequence:
CAGTCTAACCAAAGCCAACCAGCTTGTAAAAAACATTGCCATGGGCAGGAGAATCACTTCGGACAGAGGTACTACAGTTTCACATCCACTGTTAATTTGAATGCATTTAGCATTATACTCTAAATTAGTGTTTTACTAGTCATCTTCATCAAATATATCACTTCAGAAGTAGTTCAATTTTGTTTAAAAGTAAACTGTATCTCTCCAAAAGGATGTAAAATACCAAATCAGAATACAGGCAGGTTTGAGATCAACAGTTATCATCCTTCTGGGTTATCCCATCTAAACAACAGCCAAAGTAAAGCAATAAGAGAAGCACTGACTAACCCATTCACACTTATCCAAGGACCACCGGGTGAGCCTCTCTTTGTTTTCTCAAAGTTCATTGAAATTCTCAAAGTCCTTTTTTGATTACTTTATAATTTATCTTCATTTTCTCAGGGACTGGAAAAACTGTTGTTGGTGTCCATATTTTGTACTGGCTGCACAAGAATATCCAA[C/T]AGCTCCAAGCTTCTGGTTCAAAGAAGAGAGCTATTCTGTACTGTGGCCCGTCAAATAAATCTGTTGATGTTGTTGCAGGTAATGCAAAATTTTGTTTATAAAGCTTTTATATTATTTGTATTCATGCATTGTGTTGTGAAAGGGATGCTATGCAAACCGGGGTAGTTCCAAATGCAGCTTTATTAAAAGAATGGTCAATCAGGCAAGGGTCAAATACCAGTATAAACAGTGTAGTAGACAATCCAGAAGCAAATCCAATAAAACAGGCTAAAGGTTCGGGGCAGGCAGAAAAGGGTCAAAACACAATAATCAGTCCAAAAGTCAAAAACACAGGCAACAAGGAAAAATGCTTACGTAAGGACAGCAACAGCTTAACAATACTCAGCAACATGTGTGTGGAACAGAGGGGTTTAAATAGTCCAAATAATCATTGTGTGAGTGGCTTCAACTGTGAGAGTTTAATCAGTCTGGATCTTGAACCGGTTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8462
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Essential Splice Site | 2091 | 2507 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58502262)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58605390 |
GRCz11 | 6 | 58599621 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTATTCTGTACTGTGGCCCGTCAAATAAATCTGTTGATGTTGTTGCAG[G/A]YAATGCAAAATTTTGTTTATAAAGCTTTTNTATWATTTGTATWCATGCAT
Long Flanking Sequence:
TCACATCCACTGTTAATTTGAATGCATTTAGCATTATACTCTAAATTAGTGTTTTACTAGTCATCTTCATCAAATATATCACTTCAGAAGTAGTTCAATTTTGTTTAAAAGTAAACTGTATCTCTCCAAAAGGATGTAAAATACCAAATCAGAATACAGGCAGGTTTGAGATCAACAGTTATCATCCTTCTGGGTTATCCCATCTAAACAACAGCCAAAGTAAAGCAATAAGAGAAGCACTGACTAACCCATTCACACTTATCCAAGGACCACCGGGTGAGCCTCTCTTTGTTTTCTCAAAGTTCATTGAAATTCTCAAAGTCCTTTTTTGATTACTTTATAATTTATCTTCATTTTCTCAGGGACTGGAAAAACTGTTGTTGGTGTCCATATTTTGTACTGGCTGCACAAGAATATCCAACAGCTCCAAGCTTCTGGTTCAAAGAAGAGAGCTATTCTGTACTGTGGCCCGTCAAATAAATCTGTTGATGTTGTTGCAG[G/A]TAATGCAAAATTTTGTTTATAAAGCTTTTATATTATTTGTATTCATGCATTGTGTTGTGAAAGGGATGCTATGCAAACCGGGGTAGTTCCAAATGCAGCTTTATTAAAAGAATGGTCAATCAGGCAAGGGTCAAATACCAGTATAAACAGTGTAGTAGACAATCCAGAAGCAAATCCAATAAAACAGGCTAAAGGTTCGGGGCAGGCAGAAAAGGGTCAAAACACAATAATCAGTCCAAAAGTCAAAAACACAGGCAACAAGGAAAAATGCTTACGTAAGGACAGCAACAGCTTAACAATACTCAGCAACATGTGTGTGGAACAGAGGGGTTTAAATAGTCCAAATAATCATTGTGTGAGTGGCTTCAACTGTGAGAGTTTAATCAGTCTGGATCTTGAACCGGTTGTGTGTGTGTGTGTGGCCTGACTGGGTGTTGTAGTCCATAACATGGCAGATATGTAGTTCAAGGAGTGTGAATGTTTACCAGTGACCTCTGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7054
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018498 | Essential Splice Site | 2092 | 2507 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58502263)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58605391 |
GRCz11 | 6 | 58599622 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTATTCTGTACTGTGGCCCGTCAAATAAATCTGTTGATGTTGTTGCAGG[T/C]AATGCAAAATTTTGTTTATAAAGCTTTTNTATTATTTGTATWCATGCATT
Long Flanking Sequence:
CACATCCACTGTTAATTTGAATGCATTTAGCATTATACTCTAAATTAGTGTTTTACTAGTCATCTTCATCAAATATATCACTTCAGAAGTAGTTCAATTTTGTTTAAAAGTAAACTGTATCTCTCCAAAAGGATGTAAAATACCAAATCAGAATACAGGCAGGTTTGAGATCAACAGTTATCATCCTTCTGGGTTATCCCATCTAAACAACAGCCAAAGTAAAGCAATAAGAGAAGCACTGACTAACCCATTCACACTTATCCAAGGACCACCGGGTGAGCCTCTCTTTGTTTTCTCAAAGTTCATTGAAATTCTCAAAGTCCTTTTTTGATTACTTTATAATTTATCTTCATTTTCTCAGGGACTGGAAAAACTGTTGTTGGTGTCCATATTTTGTACTGGCTGCACAAGAATATCCAACAGCTCCAAGCTTCTGGTTCAAAGAAGAGAGCTATTCTGTACTGTGGCCCGTCAAATAAATCTGTTGATGTTGTTGCAGG[T/C]AATGCAAAATTTTGTTTATAAAGCTTTTATATTATTTGTATTCATGCATTGTGTTGTGAAAGGGATGCTATGCAAACCGGGGTAGTTCCAAATGCAGCTTTATTAAAAGAATGGTCAATCAGGCAAGGGTCAAATACCAGTATAAACAGTGTAGTAGACAATCCAGAAGCAAATCCAATAAAACAGGCTAAAGGTTCGGGGCAGGCAGAAAAGGGTCAAAACACAATAATCAGTCCAAAAGTCAAAAACACAGGCAACAAGGAAAAATGCTTACGTAAGGACAGCAACAGCTTAACAATACTCAGCAACATGTGTGTGGAACAGAGGGGTTTAAATAGTCCAAATAATCATTGTGTGAGTGGCTTCAACTGTGAGAGTTTAATCAGTCTGGATCTTGAACCGGTTGTGTGTGTGTGTGTGGCCTGACTGGGTGTTGTAGTCCATAACATGGCAGATATGTAGTTCAAGGAGTGTGAATGTTTACCAGTGACCTCTGGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20837
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 |
---|---|---|---|---|---|
ENSDART00000018498 | Nonsense | 2200 | 2507 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 58509742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 58612870 |
GRCz11 | 6 | 58607101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAAAAGGCTCGAAAGCATGAATTATTGCACCATGACGTAATCTTATG[C/A]ACGTGCACCGCAGCTTCACATCCAGCACTGGCGGAAACCCTTGACTTTAA
Long Flanking Sequence:
TAAATGCATCCAATATAAAAGTTTATATTTACATAATATATACAAGTGTACTGTGTTTATTTATGTGTATACTGTACGTATAAACACACAAACATACTGTACATAAAATACAAAATAAATTAATTTGAGTATATATTAATATAGAGTTTCTATTATATATAAATATTGTTTATATTTTTGTGTATAAATATACATGAATAACTATAATGTATAAAATATTAGTTTGTATATAAATATAACCATATATTTTATACAATATAGTCATGCATATATTTACACACAAAATATAGACAGTACGCACAAATATATTTTGTTTTGGATGTGATTAATCACAATTAGCACTACTTCAAATCTATTTTCTGTGCTGTGTTATTATTACTTCATTGTTGTAAATTTATGGACACATTTTAATTGATATGAAAACCTAATTTTTACAGCTTCAGAGAAATCCTCAAAAAGGCTCGAAAGCATGAATTATTGCACCATGACGTAATCTTATG[C/A]ACGTGCACCGCAGCTTCACATCCAGCACTGGCGGAAACCCTTGACTTTAAGCAGATCATCATTGATGAATGTGCCATGGCCACTGAACCTGAAGCCTTTATTCCTCTCGTGGCTCATAAACCTGAGCAGGTATGATTGCAAACCACTGTTGTATTTAGCCAAACTCTAAATACTGGATATTAGCAGCACATTAAAGGCTACTGGAGACTTTTTTGCAGTTTGCAATGAACAAAGAATGCATTTTTATGTTCTTATTAAACTAATTCATGTTTTAGATTGTCCTTCTTGGCGATCACAAACAGCTTCAACCAGTGGTCCACTGCGAGGTGGCGGAGCGATTAGGAATGAGCAGATCTCTTTTTGAACGTTACATGGAGAACGCACTCATGCTTGACACCCAGTACAGAATGGTAATATATTATTAGAACATATAGCTTCAATACTGTTTTTTATCTACACACATTTACTGTTCTTTGCTTTAGAAGTCTATATCAATTCAT
Associated Phenotype:
Not determined