ZMP
si:ch211-141h12.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MXRA5
Human Description:
matrix-remodelling associated 5 [Source:HGNC Symbol;Acc:7539]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41561 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9164 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1691 | Nonsense | Available for shipment | Available now |
sa9588 | Nonsense | Available for shipment | Available now |
sa27514 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41562 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21620 | Nonsense | Available for shipment | Available now |
sa34797 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31754 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41561
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 77 | 2520 | 2 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | Nonsense | 68 | 652 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57757482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56189025 |
GRCz11 | 9 | 55539566 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATTTAACACCATCAGTCAGATCACAGACGCCTCTTTCAGTGGCCTT[C/T]GAAAGCTGGAGCTGCTGATGATGCACGGGAACAACGTGCAGAAGATACCA
Long Flanking Sequence:
ACTTGTTCTAGATCTGAGTTTTTTAAACTTTAAAAAACAAACACAAGATGAGCATTTTAAACTTTAACAAGTTTCTTTCTTATATTAAAAACAAAAGAAGATATATATTTTTAAAGTAAGCCATGAGGTAATTAATTTTAATGTGAACTATCCCTTTAAATCAGGGGTTCTCAATTCCGGTCTCAAATCCCCCCACCCCCCACTCCGCCCTGCACATTTTGTATGTCTTCCTTACTTAAAACCCCTGATTCAGATCATCAGCTCCTTATAAGAGAGAGATCAATGAACTGATCCTTGTAGGTCAGATAAGAGAGGGTGCCTGAGTACCAGAATTGAGTACCACTGCTTTAAATGTACACATTCATTGAAAGTATTGTTGTTGATCATGTGTTTGTATTGTACATGTTGATCATGTAAAAGTATTGTTGGTGATCATGTGTTTGTTCATGAACAGATTTAACACCATCAGTCAGATCACAGACGCCTCTTTCAGTGGCCTT[C/T]GAAAGCTGGAGCTGCTGATGATGCACGGGAACAACGTGCAGAAGATACCAGACGGTGCTTTTCAGGATCTGGTTTCATTACAGGTAAAATCACCTGCTGATGCTCACAAGTGCTAGTTTACTGTGAGTCCTCAACAAGAGTGTAAAGGTGACATTTAAAGGGTTGGTTCACTCAAAAATGAAAAATTACTTAAATTTACTCACTCTTAAAGGAGACCTATTATGCAGGAATCACATTTATGGGGGGTTTAACCCCAGTTGTGAGGCAGCAGTGTGTGAATATCTCCACACTCTGATGGTAAACATGAATAAATTGTATTTGTTCTAATCAGACTTGATATAAAGAGTCTGCAGAAACACTGTGATTGACATTCTCCCTTTGTACGTGTCACCAGAGGGGGAAAGCCCCGCCCACTAGTGCCCATCTCTTCCTCATTAGCATAAACAGCAGCCCTGAGTGAGAAGCAGCCGTCTGTCCATTAGCCATTAGAGTGTTTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9164
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 233 | 2520 | 3 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | Nonsense | 223 | 652 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57761618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56193161 |
GRCz11 | 9 | 55543702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCCWGGAGCTGTGACTGCCGCATGCGCTGGCTGCAGGACTGGAGCGCT[C/T]GACATCCAGGTCAGACATGATCATATTGTAATGGCGATCTWYTTCTTYAA
Long Flanking Sequence:
AAGACTCTAAATCAGCCCAGAATGGATAAAAATAACCCAATAGCACACAAGGGTTAACAACAACCTTATTGTAAAGTCTGACCATAATGACTCTTGTTTTCTCCTGTTTCTTTCTGCAGGTTTTAAAAATGAGCTACAATAAGCTGACAGTCATCACCGATCGCACCTTCTCTGGTCTGACGGGCATTATCAGACTCCATCTGGACCACAACCACATCTCCTCCATCCACCCGCAGGCATTCCTGGGCCTGACGTCTCTGCGTCTGCTGCACCTTGAGGCCAATCGTCTCCAGCAGCTTCATCCGCACACCTTCAGCACGTTCTCAGTGCTGCGGCGGTTCCCCGTGTCCACACTGAAGCACCTGCACATCTCTGATAACCTGCTGCAGACGCTGTCCCGGAGCGTGCTGGAGAACACACCTCAGCTGGAGACCCTACTGCTGACGGGGAACCCCTGGAGCTGTGACTGCCGCATGCGCTGGCTGCAGGACTGGAGCGCT[C/T]GACATCCAGGTCAGACATGATCATATTGTAATGGCGATCTACTTCTTCAAGTTCTTCACCGTTTCCATAGGGACTCGGCACAAAGGATTTGACGCGCAAAACCACAAACTTGCAATGCAACAGTTTACTTTTCGTTTGTCGAGAACAACAATAATCCAAATACAAACAAAAGAACTATGTACACTTTACCAAGCTTCCACATAAATATGGTTTTAGAACGGTCAAAAGACTGTCTACGATCAAGCCCCTTCCTCCTTTCTAATCCTTTTTTCCTGTTGCTTACGCATACATATGACGTATAACATTACTGAACACATAAAACATCATGCACATAATATAATATCACTAAATAAACATATTAAATACTGTATCAAATAGCAATAACTTTGTATCTTAATACAAATAATATAATATTATAGAAAAATATTACAAAAATTAAAAAGACAAATCTCTTAGTGCTCTTTATGGCTCTAACACGTATGCTGTCATGAGATTGCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1691
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 716 | 2520 | 4 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57763866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56195409 |
GRCz11 | 9 | 55545950 |
KASP Assay ID:
554-1637.1 (used for ordering genotyping assays)
KASP Sequence:
TAACACCGACTCGAAGAAGGCGTCCAAATRCACGTAGGTTTGGGAACATT[C/T]GACATAGACGGCCCTTTAGGAACAGAGCTGGTTTACCAAACCAAAGACCA
Long Flanking Sequence:
TTCTGCCTTTTCGTTTATCAGTAATCGAGTCTTCAAATCCTCTTCCCAATCAAGAAGTTGGGAATTCTTTAAGCAGATTTATCGGTCAGTCTGCGTTTTTGACTTGTCTTACTAAGGCATCACCAGATGCTGAAATAAATTGGGTGCTCCCTGATGGAAATGTGCTGAACGCAAAAGCAAACACATCCAGAGCTTTGCTCTTCCCCAATGGGACTTTATACATTCCTGTTTGCCAGCTTAATGATAATGGATATTATAAGTGTGTGGCGATGAATAACCACGGTGTGGATGTGTTTTCCACCAAACTAACAGTCATAAGGCGGAAGTTAATCCAGCCGCTGAGACAGTATCCCATCATCAGGCCACAGTCGGCCGCAGGAGTCTCCACTAAAGTAAAAGCATTTCTGGAGGACATGGAAGAAGCTTCTGGAGATATTTCTGAAACTCGATTAACACCGACTCGAAGAAGGCGTCCAAATGCACGTAGGTTTGGGAACATT[C/T]GACATAGACGGCCCTTTAGGAACAGAGCTGGTTTACCAAACCAAAGACCAGTTAATACCAAAAATAAAATCGACCCTCAGAAATGGGCTGATCTTTTATCCAAAATCAGAGCGAAAACATCAGAAAGCAACAAAAGTCTACAGTCGGGATTAATCGACAACACTGAAAGCTCTTCAGGAGACTCTGGACCACAGGAGAAGACTTTCAACACGGATGTTTACCACACACCTCAAATTAAAGAACGTGATGATGATAACATTTACCGAACCACACCTTCACAATTACACACTACTAGATCAAACCAAGTGCTTTACATCTCACATCCCACATCTGCACCTCATTATGTTACGACACATGTACAAGACAGACACGCGAGCACTGTAAATGCTGAAAATAACCAAATATACTCCGAGTCTGTCATCAGTCCAGAGTTAGAGACAGAAAATGAGCTTAATTTGCCTGGCGTCAAGTCTCAGATCGGGGGTTTTGATTCTGGAGGG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa9588
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1006 | 2520 | 5 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57764803)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56196346 |
GRCz11 | 9 | 55546887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CMAAGTGAAGGAAAGTAACTTCCAACAAACTCAGCAAGTGATGCCAAACT[C/A]GAGGYTTCACCCCACAATAKCAACAAATGYATCTGCGGTTTTGAGGTTAG
Long Flanking Sequence:
GACAGAAAATGAGCTTAATTTGCCTGGCGTCAAGTCTCAGATCGGGGGTTTTGATTCTGGAGGGATCGACAGAAATGTGTTTGCAACAGCAAGCAGTGTTAGATTGAGTTCTGCACCAAATTCAACACAATCGAGAGGGAGGGATAGATGGAGATTTGGAGGTAGGCGACGGATAAAATTTCGAAGGCCAATCTCAAACCTTCCTACAAGCAGAGTATGGTCAACATCAACAACTGCAAGAGTAACTCTGAAAACAGATGACCAAGATGCATCAATCTATCCAACAACTCCATCCAAAGTTCCATCAGTCAGTCAGACTATTCCAGTTACATTGCATGTTTACTCTACTACCTTATCTAGAGGTATTCCAATCAATCCAACTCAATCGTCTCACATTTATCCTACAAAACACAACGAGTTAACAAATGAAGTTGAGGAGAATATTAATCACAAAGTGAAGGAAAGTAACTTCCAACAAACTCAGCAAGTGATGCCAAACT[C/A]GAGGTTTCACCCCACAATATCAACAAATGCATCTGCGGTTTTGAGGTTAGCAAATGAAGACTTTAATTCTTTAGAGAAAGAGGAGCAGGACGGTAGCTTTGCATCTGCAGAGGAGATGGATGAGTATATAGTTCCCACGAGAAAACATCCAACATCTCGACTTGGCGCTAAAACCGTCCCACTGACAACTCCTCGGCTGGAGTTCACAAGCAGGCTTTCTGCAGACATACCGAAGATGGATCCAACAGAGATCAGCGTTACTGTACACACAGACAGACTGGATGACTTCCACTTACCTGAATCACATTTTAGAGATGTTTTGAGAGAGAACAAATCTGTGGACTTTACTAGTGCAAGAGAGGGTGTTACTTCTACTGAAGAGTCTGTAGTCTCCTCCATACTACAATCTCAAACCTATCCTCTTTCAAACCCAAATCAAAGCTTCAAAGAGGAAGAATCCATACCTTTATTAACAACATCCACCCAAAAACAATCTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27514
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1141 | 2520 | 5 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57765207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56196750 |
GRCz11 | 9 | 55547291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGAGAGGGTGTTACTTCTACTGAAGAGTCTGTAGTCTCCTCCATACTA[C/T]AATCTCAAACCTATCCTCTTTCAAACCCAAATCAAAGCTTCAAAGAGGAA
Long Flanking Sequence:
CAAAACACAACGAGTTAACAAATGAAGTTGAGGAGAATATTAATCACAAAGTGAAGGAAAGTAACTTCCAACAAACTCAGCAAGTGATGCCAAACTCGAGGTTTCACCCCACAATATCAACAAATGCATCTGCGGTTTTGAGGTTAGCAAATGAAGACTTTAATTCTTTAGAGAAAGAGGAGCAGGACGGTAGCTTTGCATCTGCAGAGGAGATGGATGAGTATATAGTTCCCACGAGAAAACATCCAACATCTCGACTTGGCGCTAAAACCGTCCCACTGACAACTCCTCGGCTGGAGTTCACAAGCAGGCTTTCTGCAGACATACCGAAGATGGATCCAACAGAGATCAGCGTTACTGTACACACAGACAGACTGGATGACTTCCACTTACCTGAATCACATTTTAGAGATGTTTTGAGAGAGAACAAATCTGTGGACTTTACTAGTGCAAGAGAGGGTGTTACTTCTACTGAAGAGTCTGTAGTCTCCTCCATACTA[C/T]AATCTCAAACCTATCCTCTTTCAAACCCAAATCAAAGCTTCAAAGAGGAAGAATCCATACCTTTATTAACAACATCCACCCAAAAACAATCTGTAGTATCTGTTGGAACTCAAATCAAGTCTTTAGATGCAAATTTGCCAAACGTCTTATATGAAAGTGTTACTTCTACAGAAGAATCTGTAGTCTCCTCCATACCACAAACTCAAAACTATCCTCTTGCAAAACAAAATCAAAGCTTTAAAGAATCAGTGCCTTCATTTACAACAACATCAACTCCAAAACAATCCAGAATATCTGTTGGAACTCAAATCAAGACTTTAGACAGAGATATACCAATGAAAGTGTTAAATAAAAGCATTACTTCCTCCATACTATCTCAAAACCCTCCTCTTTTAAAACCAAATCAAAGCTTCACAGAAGAAGAATCAATACCTTTATTATCATCAACTCCAAAACCATCTATAAAATCTGTTGGAACTCAAATCAAGACCTTAGACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41562
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1387 | 2520 | 6 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57765975)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56197518 |
GRCz11 | 9 | 55548059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAACCAGACTTGGATTCTAAGGTGGGCCAAAGGAACAGATTAATCCCC[G/T]AACTTGAACTTACAACATCAGTTAACACTCCACCTGCAACTACCAGCATG
Long Flanking Sequence:
CATCAACTCCAAAACAATCCAGAATATCTGTTGGAACTCAAATCAAGACTTTAGACAGAGATATACCAATGAAAGTGTTAAATAAAAGCATTACTTCCTCCATACTATCTCAAAACCCTCCTCTTTTAAAACCAAATCAAAGCTTCACAGAAGAAGAATCAATACCTTTATTATCATCAACTCCAAAACCATCTATAAAATCTGTTGGAACTCAAATCAAGACCTTAGACACAAGTTTACCAGTTAAAGTGTTGAATAAAAGTATTATTTTACAACAATCTCAAAACTATCTCCTTTCAACACCAAATCAAAGATTAGAAGAAGAATCAATATCTGTATTAACTTCAAATCAATCCATAATAGCTGTTGAAACTCAAACAGAGTCTTTACATGCAAGTTCTCCAATGCCCACGTTTACTACTCATAAAGAAACCAATGAGATTGCTTTCTTACAACCAGACTTGGATTCTAAGGTGGGCCAAAGGAACAGATTAATCCCC[G/T]AACTTGAACTTACAACATCAGTTAACACTCCACCTGCAACTACCAGCATGATTCCCAATACAACCGAATTCATGAGAACAACACCACCATTAACTACATCTACATTATACTCTACTACTACATCTACTACTACTCCTGTTGTAAAGTTAGCACCCAGGTATCCCTTACCGGACAACCGAATCCCAATTTACTCCAAAAATCCAGGAACAAACTACATAGGGGGAAGAATTCCTAGTACTAATCATAGGTATCCATACTATCACAGTAGAAATATTAAACCCAATATTGACAGAACGCCATCTCTGACCACTTCACCTGTGGATCTAAGCATCATCAGATCAACTATAACACCTAAAACACTTACTAGATTGAGGATTTCAAGTTTCACAACTGCAAGCACCACTCAACCAAACAACCAAATTCAGATCCAGGATTCAATGAACAGACAGTTGAATTTTCCAGTCCTGCAGATGAGAGCCAGGATTACAGATGATAAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21620
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1470 | 2520 | 6 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57766226)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56197769 |
GRCz11 | 9 | 55548310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGAACAAACTACATAGGGGGAAGAATTCCTAGTACTAATCATAGGTA[T/G]CCATACTATCACAGTAGAAATATTAAACCCAATATTGACAGAACGCCATC
Long Flanking Sequence:
TTGAATAAAAGTATTATTTTACAACAATCTCAAAACTATCTCCTTTCAACACCAAATCAAAGATTAGAAGAAGAATCAATATCTGTATTAACTTCAAATCAATCCATAATAGCTGTTGAAACTCAAACAGAGTCTTTACATGCAAGTTCTCCAATGCCCACGTTTACTACTCATAAAGAAACCAATGAGATTGCTTTCTTACAACCAGACTTGGATTCTAAGGTGGGCCAAAGGAACAGATTAATCCCCGAACTTGAACTTACAACATCAGTTAACACTCCACCTGCAACTACCAGCATGATTCCCAATACAACCGAATTCATGAGAACAACACCACCATTAACTACATCTACATTATACTCTACTACTACATCTACTACTACTCCTGTTGTAAAGTTAGCACCCAGGTATCCCTTACCGGACAACCGAATCCCAATTTACTCCAAAAATCCAGGAACAAACTACATAGGGGGAAGAATTCCTAGTACTAATCATAGGTA[T/G]CCATACTATCACAGTAGAAATATTAAACCCAATATTGACAGAACGCCATCTCTGACCACTTCACCTGTGGATCTAAGCATCATCAGATCAACTATAACACCTAAAACACTTACTAGATTGAGGATTTCAAGTTTCACAACTGCAAGCACCACTCAACCAAACAACCAAATTCAGATCCAGGATTCAATGAACAGACAGTTGAATTTTCCAGTCCTGCAGATGAGAGCCAGGATTACAGATGATAAACTTCACACAGTGTCTGTGAATGCTGGGACGGATGTGCAGTTACCGTGCAATTCTGTGGGGGAGCCGAGACCACTCTTAACTTGGACTAAAGTCTCAACAGGTAACTTTCTTACAGGACACATAAGACATTCATCTCATCACGTTAAAGTGGGTTCCATGTAGAAATGGCCGTATATGGCTATATATGCAAATGACATGAGACCCTGAACCACATAACCAATCAGAAGAATCAGTTTTCTGAAAAATCCTGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34797
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1473 | 2520 | 6 | 8 |
ENSDART00000144757 | None | None | 967 | None | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57766235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56197778 |
GRCz11 | 9 | 55548319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTACATAGGGGGAAGAATTCCTAGTACTAATCATAGGTATCCATACTA[T/G]CACAGTAGAAATATTAAACCCAATATTGACAGAACGCCATCTCTGACCAC
Long Flanking Sequence:
AGTATTATTTTACAACAATCTCAAAACTATCTCCTTTCAACACCAAATCAAAGATTAGAAGAAGAATCAATATCTGTATTAACTTCAAATCAATCCATAATAGCTGTTGAAACTCAAACAGAGTCTTTACATGCAAGTTCTCCAATGCCCACGTTTACTACTCATAAAGAAACCAATGAGATTGCTTTCTTACAACCAGACTTGGATTCTAAGGTGGGCCAAAGGAACAGATTAATCCCCGAACTTGAACTTACAACATCAGTTAACACTCCACCTGCAACTACCAGCATGATTCCCAATACAACCGAATTCATGAGAACAACACCACCATTAACTACATCTACATTATACTCTACTACTACATCTACTACTACTCCTGTTGTAAAGTTAGCACCCAGGTATCCCTTACCGGACAACCGAATCCCAATTTACTCCAAAAATCCAGGAACAAACTACATAGGGGGAAGAATTCCTAGTACTAATCATAGGTATCCATACTA[T/G]CACAGTAGAAATATTAAACCCAATATTGACAGAACGCCATCTCTGACCACTTCACCTGTGGATCTAAGCATCATCAGATCAACTATAACACCTAAAACACTTACTAGATTGAGGATTTCAAGTTTCACAACTGCAAGCACCACTCAACCAAACAACCAAATTCAGATCCAGGATTCAATGAACAGACAGTTGAATTTTCCAGTCCTGCAGATGAGAGCCAGGATTACAGATGATAAACTTCACACAGTGTCTGTGAATGCTGGGACGGATGTGCAGTTACCGTGCAATTCTGTGGGGGAGCCGAGACCACTCTTAACTTGGACTAAAGTCTCAACAGGTAACTTTCTTACAGGACACATAAGACATTCATCTCATCACGTTAAAGTGGGTTCCATGTAGAAATGGCCGTATATGGCTATATATGCAAATGACATGAGACCCTGAACCACATAACCAATCAGAAGAATCAGTTTTCTGAAAAATCCTGCTTAAAGATGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31754
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 |
---|---|---|---|---|---|
ENSDART00000110561 | Nonsense | 1656 | 2520 | 7 | 8 |
ENSDART00000144757 | Nonsense | 103 | 967 | 2 | 3 |
ENSDART00000147209 | None | None | 652 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 57768591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 56200134 |
GRCz11 | 9 | 55550675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCACGTTCCCAGGATGACGAGTCCACGCCATCAAGACGTAACGGTGTA[T/A]ATAGGAAACACTGCACTCCTGCAATGCCAAGCACAAGGACTCCCAATCCC
Long Flanking Sequence:
ATTTTTTTTAGCCTAATGCACTACAAAAGATGCTTTTCTTACTTTTCCAAATATCTAAAAACTCCGAAATCAAGAAGCTTCTGCATTATAACCAATCAGTTTTATTAAACTGTTCAAGTCAAATAATCTGCCAAAGGGATAAGCAAAATAATTTAATGTCAAAAGGAAAAGCAAGATTATTTTTTTACCCCTTGGCAGATTATTTGGGAAACAATATACAGGAGGGGGTAAATAATTTGACTTCAACTCTATATTAATCATTTAATAGATATTTATACATTGTCCACAGGAGCCGTGATGTCAACCAACACCAAAGTCCAGCGGTTTGAGGTCCACCCCAATGGCACTTTTACCATCAGAAACGTCCATCTTCAGGACCGCGGTCAGTATCTCTGCAGCGCTAGCAATGCTCACGGCACAGATAAGATGATGGTGACGCTAGTGGTGTTGGCTCACGTTCCCAGGATGACGAGTCCACGCCATCAAGACGTAACGGTGTA[T/A]ATAGGAAACACTGCACTCCTGCAATGCCAAGCACAAGGACTCCCAATCCCCAACATCAGCTGGATGCTTCCGGACCGCTCAATGCTGCGAAGTGTTAGCAACACCCAACAGAAGATCATGCTATTGGCTAACGGCACGCTTCAAATCAAGCAGACTAATTATTTAGACACGGGTGTTTATAAATGCATAGCGAGCAACGCAGCTGGAGCCGACATGCTTTCTGTGAGGCTTCAGATTACAGCATTGGCTCCAGTTATTCAAGAGCAGCGCTGGGAAAACTATACGCTTTCTGATGGCCATGCTGCGCTAATTCATTGCACTGCTAACGGTGCACCAAATCCAACGGTCCGTTGGGTTACATCTTCAGGCATGCAGCTTCGGCCGTCTCAGTTTGTGAACAGCAACTTATTCGTGTTTCCCAATGGGACGCTGTTTATCCGTAACCCCACAGTGAAGGATTCTGGGATTTATGAGTGCGTGGCGGTCAGTTCAGTGGGCAT
Associated Phenotype:
Not determined