ZMP
A5WUZ9_DANRE
Ensembl ID:
Description:
Novel protein similar to vertebrate ADAM metallopeptidase with thrombospondin type 1 motif, 7 (ADAMT
Human Orthologue:
ADAMTS12
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 12 [Source:HGNC Symbol;Acc:14605]
Mouse Orthologue:
Adamts12
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 12 Gene
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31415 | Essential Splice Site | Available for shipment | Available now |
| sa15083 | Essential Splice Site | Available for shipment | Available now |
| sa25290 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10586 | Essential Splice Site | Available for shipment | Available now |
| sa1731 | Nonsense | Available for shipment | Available now |
| sa40362 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33532 | Nonsense | Available for shipment | Available now |
| sa20346 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31415
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097221 | Essential Splice Site | 43 | 1499 | 2 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9303942)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8405830 |
| GRCz11 | 5 | 8910468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACGTCAAGAGCTCTGAACCGGACTACCTCTTTCCAGACACAGAGCAAG[G/A]TTTGTATCTTCATGCAAAACTATCATACAGCATGTGTTTAGGCTGTTTTT
Long Flanking Sequence:
TACCCACTGATAATATTACGCGTCTCAAGTTCTGAGTTTCACCGACATTTTCGAAATGATATGCACATTTTACTGTTTGATTTTCAAGAGGAAGTAAAGTACATTTAAGCGTGTAGTAATACCTCCCTTCAGCTCGTTGTTTTTGGGCTGTGAGGATTTCTCTCCTCCCGCGCCTGGAAACAGCAGGACAGTCAGTCAGTCAGTCAGCCACAGCAATCTCTCCTCCCACTCCACATCATATTCCCCTCATTCTCCCTTCACTTTCTTTCTCCGTTTCTCTGACCCCAGATGTCTCCAGCTTTCACCAGAAACTCCCCTCAGGACTGACTTTAACCAGTTCTCCGGCGTCGGAGCGTTACTTGCTCTTCTCATTTCGCGTTGTAGAAACATGCCAAGTCGGGTCAGCGTTGCGATTTTGCGGTTCAATTGTGTTTTGTTTCTGGCTGCGAGCCACGTCAAGAGCTCTGAACCGGACTACCTCTTTCCAGACACAGAGCAAG[G/A]TTTGTATCTTCATGCAAAACTATCATACAGCATGTGTTTAGGCTGTTTTTAATCCTAATATGCCGCCAAGTGTTGCACTGCTGAGGCGAGCGGTCAGTTGCTGCAAAAGTCCAGGTTTCTGTTCTGCAGTCCTGAACTTGCACAATCTCGTTTTGTAAAATTACTTTTAACCCTTTAATGCAAGTATGAATATTGATCAATTACAAAATGCATGATTAAAATGTTTCTCGTTTGACTCAGTGTAACCATGTTAAGTCTCTGTTGAACTACAGGAATCTTTGTGCATCAACATCAGTCACTTTGAGTGTTTTATGTATGACATGAAAGAGGACAGTGATGTATAATTATGTGCAAGGATCAAAGGTGGTGGCTTGGAGCTAAAGTTAGTCTCTTAATTGTTAAAACAGCTTGAGTGGTGATAAATCTTGTGAATGAATGGATGAATTATATTTCATTCTGTCTTAGGAAAAGTACTGAAAGTATATAAAATATAATGACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15083
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097221 | Essential Splice Site | 543 | 1499 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9268115)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8370003 |
| GRCz11 | 5 | 8874641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTAAACKAGACTCACCGATYGACGGAACCAGGTGTGGACCTGAAAAG[G/A]TAGGAGAGATACACAATYARAAAGAAGCACATAGTATTTGTTCTGTTMTT
Long Flanking Sequence:
ATACAGCACCTTTAAACAGTGCAGTTGCCAACATTGTATAAAATACTTTTGTGTTCTTCAAAACAAAAAAAATATATTGAAAAAAGTGAGTAAATGACAGAATTTTTCATTTTTAGGTAAACCCTGCTTTTACATTTGACATTTTTAGGGATAATTTGGTAGTTTGGTACATTTCCAAAAATTCAATTTTAAGAAAACGCAAACAAAGTGTTAATTTCATGTGGACTTTTTTTTCTATTTGCCTGTGATCTGAAAATATTTCATGCTTTAGTAGAGAAATGTTCTGTTAGAGTTCAACTCATATTCATTCAGGAAGATTGCTTTGATTTGTATCTAAAGTATAACATATTTTCTTGTCTGGATTAACAAAAGGAGATCTTTATTAATTCAGCCTCTGCTGTTTGCAGAATGTGTGTCAGATTCTGTGGTGCTCAGTAAATGGATCGTGCCGCTCTAAACTAGACTCACCGATCGACGGAACCAGGTGTGGACCTGAAAAG[G/A]TAGGAGAGATACACAATTAGAAAGAAGCACATAGTATTTGTTCTGTTCTTATATCTTTAAAGGGTTACTTCACCCTAAAACGAATATTCTGTAACTAAATAGATGACCTTGTGGTATTTAGTCCTAGTACTGCTGGACTTCAGCAGAGTTTAAATATGTACACATATCATACGCTGATCCTTCATTCATTCATTTTCTTTTCGACTTAGTTCCTTTATTAATCTGGGGTTGCCACAGTGGAATGAACCGCCAACCTATCCAGCATATGTTTTACGCTGCTGATGCTCTTCCATCTGCGACCCATCACTGGGAAACATCCATGCACACTCATTCACACACATACACTACGGACAATTTAGCTTACCCAATTCACCTATAGCGCATGTCTTCGGACTTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACTCAGGCTGGGAGCGAACCAGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25290
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097221 | Essential Splice Site | 543 | 1499 | 11 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9268114)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8370002 |
| GRCz11 | 5 | 8874640 |
KASP Assay ID:
554-7440.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAAACTAGACTCACCGATCGACGGAACCAGGTGTGGACCTGAAAAGG[T/A]AGGAGAGATACACAATTAGAAAGAAGCACATAGTATTTGTTCTGTTCTTA
Long Flanking Sequence:
TACAGCACCTTTAAACAGTGCAGTTGCCAACATTGTATAAAATACTTTTGTGTTCTTCAAAACAAAAAAAATATATTGAAAAAAGTGAGTAAATGACAGAATTTTTCATTTTTAGGTAAACCCTGCTTTTACATTTGACATTTTTAGGGATAATTTGGTAGTTTGGTACATTTCCAAAAATTCAATTTTAAGAAAACGCAAACAAAGTGTTAATTTCATGTGGACTTTTTTTTCTATTTGCCTGTGATCTGAAAATATTTCATGCTTTAGTAGAGAAATGTTCTGTTAGAGTTCAACTCATATTCATTCAGGAAGATTGCTTTGATTTGTATCTAAAGTATAACATATTTTCTTGTCTGGATTAACAAAAGGAGATCTTTATTAATTCAGCCTCTGCTGTTTGCAGAATGTGTGTCAGATTCTGTGGTGCTCAGTAAATGGATCGTGCCGCTCTAAACTAGACTCACCGATCGACGGAACCAGGTGTGGACCTGAAAAGG[T/A]AGGAGAGATACACAATTAGAAAGAAGCACATAGTATTTGTTCTGTTCTTATATCTTTAAAGGGTTACTTCACCCTAAAACGAATATTCTGTAACTAAATAGATGACCTTGTGGTATTTAGTCCTAGTACTGCTGGACTTCAGCAGAGTTTAAATATGTACACATATCATACGCTGATCCTTCATTCATTCATTTTCTTTTCGACTTAGTTCCTTTATTAATCTGGGGTTGCCACAGTGGAATGAACCGCCAACCTATCCAGCATATGTTTTACGCTGCTGATGCTCTTCCATCTGCGACCCATCACTGGGAAACATCCATGCACACTCATTCACACACATACACTACGGACAATTTAGCTTACCCAATTCACCTATAGCGCATGTCTTCGGACTTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACTCAGGCTGGGAGCGAACCAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10586
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097221 | Essential Splice Site | 649 | 1499 | 13 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9264315)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8366203 |
| GRCz11 | 5 | 8870841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCCGTATCACAATGAACTCTACCAGTGGATTCCTGTTTCAAGCCCTTG[T/A]AAGATCWCTTTGCATCAATATTCATTCATTCATTNNNNNNNNNNNNNNNNCATYNNNNTTATTTCGGGTT
Long Flanking Sequence:
GATCCAAAGCAGCTTTAAAGAGGTGAGAAAAGAAAATATATGCATGCTGCATTAAAACGAATATGCTAATATTCAACTATTATTCCTATATATCAGCCCATTTTCTGCACTACCAGTATAATGCACTAGAGGGCTCTCTTGTAGCTTTAACTAAACATTTCCTGTTTGGTCTGCAGTTACCAGTGCTGTCATATTTGACCAAATTTGTAAATATCACACTATTTCTTAAGTCTTAAATATCCATTTTACGTCTTTTTCTACTTTTTTGATACGTTGTTTTGCTGAACAGATGATCTAAAGCATGTTTTCTGTTTCTCCTGTTCACACAGGCCTGAGTTTGGTGGGAAGTATTGCACAGGAGAGCGGAAGCGCTACCGTGTTTGCAACACAAAGCTGTGTGTCAGAAAACATCCCAGCTTTAGAGAGATGCAGTGCAGTGAATTCAACACCGTGCCGTATCACAATGAACTCTACCAGTGGATTCCTGTTTCAAGCCCTTG[T/A]AAGATCTCTTTGCATCAATATTCATTCATTCATTCATTTTATTTCGGGTTAGTCGCTTATTTATCAGGGGTCGCCACAACGGAATGAACCGCCAACTATTCCGGCATATGTTTTACATAGCAGATGCCCTTCCAGCTGCAACCCAGTACTGGGAAATACTCATACACTCTCACATTCCAGGCTTGTAGGCAGCCTAGGGAAGGGTTGGGGGGGGGGGTCTTTTTTTCTTAAAGGGGACTTTTTTTGCATTTCCCCCCTCATTTTGTATTTGATTAGCTTGTCTTCTGGTATCATGTGTGAGCTTTTTCATACAAGTTCACAAAATTAAGTAATGACTTAATATGTACTTTAAAGTTCAAACAGGCTGCAAAAATCAACAAAACAAAAAAACATTTGCAATACTTCCTAAACAAGTGCTTTAGAATAAATGCATTGAATTGGGGTTTACCTTTAAAATTTTTTTTTGAGTTTTAGCTGATCCTAAATCCCCAATGATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1731
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 |
|---|---|---|---|---|---|
| ENSDART00000097221 | Nonsense | 797 | 1499 | 16 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9254807)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8356695 |
| GRCz11 | 5 | 8861333 |
KASP Assay ID:
554-1676.1 (used for ordering genotyping assays)
KASP Sequence:
GGAATGGAGAGTAYGAGGCTGGTGGCACAAAGTTTAACTACGAGCGCAGC[G/T]GAAATATAGAGAATCTCACCTCAGCGGGACCAACAACTGAACYTGTCATG
Long Flanking Sequence:
GTTGGGTTTGTCTCTGCAAGAACAACTGGCTGGATGTACATTATCCCTTATTTATTTTATAGAATACCTTTTATTTAAGGGGGCCTATTATGACCTTTTTATGACCTTCGAGTTCCCTACAGTGTAGTGTATATGTGAAGTTTCATCTCAAAATACCCCACAAATACTTTTTAAAACTCTTTGAAACTGCTCTTTTTAGGCAAAAAATGTTTTGGAGACTGTGTTTATAAAGTGTAAATTAAAAAAAAATATAATTCATTAATTTTTATCATTAGAGGCTGGTTAAATTTTTGTTAAACCCCTGTGATTTAGGGTACATGGACCTGGTTTTGATCCCGGCGGGAGCTCGGGATATCTACATTCAGGAAGTGGAAGAAGCTGGGAATTTCCTTGCGATGCGAGCGTCTGATTCAGATGAATATTACCTCAATGGGAATTACATCATTCAGTGGAATGGAGAGTACGAGGCTGGTGGCACAAAGTTTAACTACGAGCGCAGC[G/T]GAAATATAGAGAATCTCACCTCAGCGGGACCAACAACTGAACCTGTCATGATCCAGGTACCGACCATCATACACTTAAAGGAACACACCACTTATTTTGGAAATAGTCTCATTTTACAGCTCCCCTAGAGTTAAACAGTTACCATTTTTTAATCCATTAAGTCGATTTCCAGGTTTGGCGGAAGAACTTTTAGCTTAGCTTTGCATAAGTCATTGAATCAGATTAGACCATTAGCATTAAATGGGAACTTAAAAATGACAAAACAGAACAACACGAGAACTATTCTCTCATTCTGGCAATCTAGCTGGAGAATGGAGCTGTTGTCAGGTGCTGCGTAATAGCATTGCACAAAAAATGGGGTTAGCAAAATAATCTTGAATTGGATTTGAAATAAAATCATTTTGCTTACCTTTTAGACAGATTATTTTGCTTGTTTTAAGGACAAAATTTTTCTGAAAACAATGCTAAATGTTTTACTTGTCTAGAAAATACTTGTCTAA
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:
sa40362
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097221 | Nonsense | 911 | 1499 | 19 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9248205)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8350093 |
| GRCz11 | 5 | 8854731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGATCTGTATGAACTCTGTACTGACCTCAGGTGGTGGGTTGGAGGATG[G/A]CAGACGTGCTCGTCCACATGCGGTTCAACCGGAGTGAAAAAGCGCACCAT
Long Flanking Sequence:
AAAATGGCGACGATTAGCCACGCCTACTTGTTGCTTCATTTGCGCTCTTCAGAAACCTATGAGTGATGTCGCGGATACTATGTCTAATATCTTTTACAGTCAATGGTTAGCACATGGCCACTCATCTAGTTACCTGTTCATCATGTTAATTTGCCTCACCTGTCCTCCTCGTTTTAGTCTTCGTCTGCTCCTCTATTTATTCTCCCAGTGTGCTTTTGTCTCTTGTTGATTTATTTCTCATGTTATGTGATGTTTGATGTCTGTTTTTCTGCCCGGTTTGATTTTATTTTTGATTTAAAATGATGATTACTATCATGTTTTTTTTTTTGTTTTGTTTATTCCAGCCATATAAGCTGTTATCTGGGCTCTGTGTCCAGTTTTTTGTTGAGCGTATTTTTATTGCTGATCTGTGTCTGGGTTCTGTCCTCACACTTGACACCGTTGTATTAAAATGATCTGTATGAACTCTGTACTGACCTCAGGTGGTGGGTTGGAGGATG[G/A]CAGACGTGCTCGTCCACATGCGGTTCAACCGGAGTGAAAAAGCGCACCATTCTGTGTGTCCGTACGGTGGCTGGAGAAGAGCGAGTTCTGCACCCTGGTGACTGTAAGCAGCTGCTCAAACCCAAACCTGCAGTTCCTTGTAACCGAGACGTACCGTGTGGCTCAGAATGGACTGTGGGGAACTGGAGTGAGGTAGGCTGCTATATTACAAATGAACATGGATAATGTTCCTAAAGTACACATGAAACATGACTACAAACTTGGCCTAGCAACACATACATGGTGAACGCACAAAAGATGGCAAATGTTTTGTGTCTAAACCTAAAGTGATGTTCCTTTTTAAATGTGTGGCGTCTTGCAGTGCTCCCAGTCTTGTGATGGAGGAATAAAGTCGCGAATGGTCAAGTGTGTGGCAAAACAACCCAGCCGGTGCAACCCTGCCACTCGACCCCGCTCCACAATCCTCTGTAACCTCCAGAGCTGCTCATCCACTAACCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33532
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 |
|---|---|---|---|---|---|
| ENSDART00000097221 | Nonsense | 946 | 1499 | 19 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9248100)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8349988 |
| GRCz11 | 5 | 8854626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTCCGTACGGTGGCTGGAGAAGAGCGAGTTCTGCACCCTGGTGACTG[T/A]AAGCAGCTGCTCAAACCCAAACCTGCAGTTCCTTGTAACCGAGACGTACC
Long Flanking Sequence:
GTTAGCACATGGCCACTCATCTAGTTACCTGTTCATCATGTTAATTTGCCTCACCTGTCCTCCTCGTTTTAGTCTTCGTCTGCTCCTCTATTTATTCTCCCAGTGTGCTTTTGTCTCTTGTTGATTTATTTCTCATGTTATGTGATGTTTGATGTCTGTTTTTCTGCCCGGTTTGATTTTATTTTTGATTTAAAATGATGATTACTATCATGTTTTTTTTTTTGTTTTGTTTATTCCAGCCATATAAGCTGTTATCTGGGCTCTGTGTCCAGTTTTTTGTTGAGCGTATTTTTATTGCTGATCTGTGTCTGGGTTCTGTCCTCACACTTGACACCGTTGTATTAAAATGATCTGTATGAACTCTGTACTGACCTCAGGTGGTGGGTTGGAGGATGGCAGACGTGCTCGTCCACATGCGGTTCAACCGGAGTGAAAAAGCGCACCATTCTGTGTGTCCGTACGGTGGCTGGAGAAGAGCGAGTTCTGCACCCTGGTGACTG[T/A]AAGCAGCTGCTCAAACCCAAACCTGCAGTTCCTTGTAACCGAGACGTACCGTGTGGCTCAGAATGGACTGTGGGGAACTGGAGTGAGGTAGGCTGCTATATTACAAATGAACATGGATAATGTTCCTAAAGTACACATGAAACATGACTACAAACTTGGCCTAGCAACACATACATGGTGAACGCACAAAAGATGGCAAATGTTTTGTGTCTAAACCTAAAGTGATGTTCCTTTTTAAATGTGTGGCGTCTTGCAGTGCTCCCAGTCTTGTGATGGAGGAATAAAGTCGCGAATGGTCAAGTGTGTGGCAAAACAACCCAGCCGGTGCAACCCTGCCACTCGACCCCGCTCCACAATCCTCTGTAACCTCCAGAGCTGCTCATCCACTAACCGATGGACAGGACCACGATTCAGACCACGCAAAATCCCAACCCAGCCCCCCGGGACCCAAACAACACAATACAGCCCTACTATCACACCTCCAAACACCTCTACACCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20346
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 |
|---|---|---|---|---|---|
| ENSDART00000097221 | Nonsense | 995 | 1499 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 5 (position 9247786)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 8349674 |
| GRCz11 | 5 | 8854312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTTGTGATGGAGGAATAAAGTCGCGAATGGTCAAGTGTGTGGCAAAA[C/T]AACCCAGCCGGTGCAACCCTGCCACTCGACCCCGCTCCACAATCCTCTGT
Long Flanking Sequence:
TCTGTCCTCACACTTGACACCGTTGTATTAAAATGATCTGTATGAACTCTGTACTGACCTCAGGTGGTGGGTTGGAGGATGGCAGACGTGCTCGTCCACATGCGGTTCAACCGGAGTGAAAAAGCGCACCATTCTGTGTGTCCGTACGGTGGCTGGAGAAGAGCGAGTTCTGCACCCTGGTGACTGTAAGCAGCTGCTCAAACCCAAACCTGCAGTTCCTTGTAACCGAGACGTACCGTGTGGCTCAGAATGGACTGTGGGGAACTGGAGTGAGGTAGGCTGCTATATTACAAATGAACATGGATAATGTTCCTAAAGTACACATGAAACATGACTACAAACTTGGCCTAGCAACACATACATGGTGAACGCACAAAAGATGGCAAATGTTTTGTGTCTAAACCTAAAGTGATGTTCCTTTTTAAATGTGTGGCGTCTTGCAGTGCTCCCAGTCTTGTGATGGAGGAATAAAGTCGCGAATGGTCAAGTGTGTGGCAAAA[C/T]AACCCAGCCGGTGCAACCCTGCCACTCGACCCCGCTCCACAATCCTCTGTAACCTCCAGAGCTGCTCATCCACTAACCGATGGACAGGACCACGATTCAGACCACGCAAAATCCCAACCCAGCCCCCCGGGACCCAAACAACACAATACAGCCCTACTATCACACCTCCAAACACCTCTACACCCATTACCACACAATCCAACACTTCCCCAACATCGGATATCATCCACGAAGACGACAAAGACTTTATACTAGTAAAAAAAAACAATGTAGCAGTTCCCACAATTACTGAAGACGAGGAGGGAAGCACAGACCTGCAGCCTCCTGATAAAAGCTATACACCAGGTTATGATTACATAGAAGATCCAGAACGGATACGTGAGGATGATTTGTTCACCAGCAAACCTGAAGAAGTGCTCATATCCAGTGTGCAACCAATAACAATGAGTGCACCAGTTAGCACAACAAAACCAGCCATTACTACTACCATTCGGACGCAA
Associated Phenotype:
Not determined