ZMP
C0H5V7_DANRE
Ensembl ID:
Description:
Collagen type XXVIII alpha 1 b [Source:UniProtKB/TrEMBL;Acc:C0H5V7]
Alleles
There are 11 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10206 | Essential Splice Site | Available for shipment | Available now |
| sa9159 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40622 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40623 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14346 | Essential Splice Site | Available for shipment | Available now |
| sa40624 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1042 | Nonsense | F2 line generated | Not yet available |
| sa11556 | Nonsense | Available for shipment | Available now |
| sa16583 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10206
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | None | None | 806 | None | 24 |
| ENSDART00000113637 | Essential Splice Site | 35 | 491 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3446367)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3477591 |
| GRCz11 | 6 | 3638411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACGTAAAAGTAAACCAATCACCTCAAATGTGATCCCCAAAAACAAAGG[T/G]AAATATCACATGCTCTTCAGCACAAATGCTWTTTAAAACMCTCATTTTCA
Long Flanking Sequence:
CTCACAGCAAGAAGGTCGCTGGTTTGAGTCCCAACTGTGTGGACTTTGCATGTACTCCCTTTGTTGGTGTGGGTTTCCTCCAGGTGCTCTGGTTTTCCCCTCAGTCCAAGGGACTAAGTCGAAGGAAAATGAATGAATTGCATGCAACTTATACAACTTATATCCCTAACTTGCATTATAACCCTAAAATATGTACATGTAATCAATTAGTTAGTAAGTTTATGAATACACACAAGGACACCTTAAAATAAAGTTTGACCAAACAAAAGTGTAGCCATGCCTAATATTGAATATGCATCTGTTTGTCACTTTCCTGCTGTAGTGATGCTGCGGCTGTGTGTGCGTTGGCTGGTTTTGCTGTCGGCAGCGCAGCTTGTTTTGGCTCAGCTGAAGGATTTTGATGATGAAGATGAAGATCCTGAAGATTTTGTAGAAGACAATAGGAATGGAAGACGTAAAAGTAAACCAATCACCTCAAATGTGATCCCCAAAAACAAAGG[T/G]AAATATCACATGCTCTTCAGCACAAATGCTTTTTAAAACCCTCATTTTCAAAACACATTCATTTTATTTTAAAAACTCTAGTCATGTTTTATCTAAGCGGGTGGTGTGAGATAATCAGATTTCATTCTTGTATCTGTTTTTTTGGTTTCCAACAAATGAAACTGATTGAAATACTTCTCAAGAGCTAGAAGAAAAGTTCCTGCATGCAGTCTGCTGTGCTCTCCAGGGCTCCTGAGTTTGATCTAAACCCTGCTTGCTGTCCTGGGGCAAATTTCCTCTTTGACATGTTTCTTCTTTTTCTTCATAAATGTGATTTACTGTAGACCGGGGCCGTTTCAGCTGGTTCACATTTATCTTTAACATTACGTTTGGTTTTGACAGCCACTTTGAGGTATTTGCCTTGATTTTATTTGTATAAATAATCAAACAGTTGTCAAATTATTCATGGCAAATAAAAATCAGTGGCTGACCTTTTTTAATGAAAAAAAAAAAACAGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9159
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | None | None | 806 | None | 24 |
| ENSDART00000113637 | Nonsense | 53 | 491 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3448391)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3479615 |
| GRCz11 | 6 | 3640435 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAACTGTAATTTGGAACTGGCRTTTTTGGTGGACAGCTCTGAAAGTGCC[A/T]AAGACAACCATGGCCAGGAGAAGAGCTTCGTTACTGATCTTGTCAACCRT
Long Flanking Sequence:
TAGATGGATTGATTGCTAGATAGATATATGGATATACAGTATGGATGGATTACTAGATAAATGGATGGACAGATGGATGGATGGATGGATTGATTACTAGATAGCTGATGGATGGATGGATGGATGGATTGATGGGTGGATGGTTTGATGGATGTATGATAGATGGGTCAGTAGAATAGATGGACGGATAGATGGATTACTAGATAGATGGATGGGTGGATGGACTACAAGATGGATAAATGGATTACTAGATAAATAGATGGACATATAGATGGATGGGTTACTGGAATAATGGATGGATGGATGGATGAATGGACTATTAGATAGATTACTGTTAGTAAATACATTATTCAACATCATCCTTATTTTAATGTATCACCAAACCTCTTTGACATAAAAATGTTTTAAATAAAGATGTTAATTATTTTTTTTCCCCCTTGTGTTCAGACGAGAACTGTAATTTGGAACTGGCGTTTTTGGTGGACAGCTCTGAAAGTGCC[A/T]AAGACAACCATGGCCAGGAGAAGAGCTTCGTTACTGATCTTGTCAACCGTATCCCGAACATCCGTCTCCAAACAGGCCAGGGCTTGAACTTCAGATCAGCTCTCCTTCAATACAGCAGTCATGTGATCACAGAGCAGTCCTTTAAAGACTGGAGGGGTGTGCCCAGCTTCCAGAGCCGCGTCGCCTCTATCCCGTTCATCGGGCATGGAACCTATACCACCTACGCCATCACCAACCTCACCCGCATCTACCTGGAGGAGTCCGGCCCAGGCACGGTCAAGGTGGCTATTCTGATGTACGGCGGCGCCTCGCATCCCAAGAATCCTGATATTTTCTCTGCTCTTGCTGATGCGAAGAACCAAGGGATTAAATTCTTCATAGTCGGTTTAACATCCGCAGCCAACATGGAGAAGCTGCAGCTTCTGGCCAGTGCTCCAGCCAGCCGATACGTGCACAATATACAGGACAAGGGCGTCGTGGACAAGATCATCAGAGAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40622
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | None | None | 806 | None | 24 |
| ENSDART00000113637 | Essential Splice Site | 219 | 491 | 2 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3448893)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3480117 |
| GRCz11 | 6 | 3640937 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCACAATATACAGGACAAGGGCGTCGTGGACAAGATCATCAGAGAGATTG[T/C]GAGTAATGTTTAAGGAGAATAAATGGAGGTGGAGTTTGACAGTTTTACAG
Long Flanking Sequence:
AGACAACCATGGCCAGGAGAAGAGCTTCGTTACTGATCTTGTCAACCGTATCCCGAACATCCGTCTCCAAACAGGCCAGGGCTTGAACTTCAGATCAGCTCTCCTTCAATACAGCAGTCATGTGATCACAGAGCAGTCCTTTAAAGACTGGAGGGGTGTGCCCAGCTTCCAGAGCCGCGTCGCCTCTATCCCGTTCATCGGGCATGGAACCTATACCACCTACGCCATCACCAACCTCACCCGCATCTACCTGGAGGAGTCCGGCCCAGGCACGGTCAAGGTGGCTATTCTGATGTACGGCGGCGCCTCGCATCCCAAGAATCCTGATATTTTCTCTGCTCTTGCTGATGCGAAGAACCAAGGGATTAAATTCTTCATAGTCGGTTTAACATCCGCAGCCAACATGGAGAAGCTGCAGCTTCTGGCCAGTGCTCCAGCCAGCCGATACGTGCACAATATACAGGACAAGGGCGTCGTGGACAAGATCATCAGAGAGATTG[T/C]GAGTAATGTTTAAGGAGAATAAATGGAGGTGGAGTTTGACAGTTTTACAGTGGCTTTTGGTGCATTTCTCACAACACTATTTTCATTTTCACAAGAGTTAATGCATTTCTCATAAAAGTTAGTCATTTGTGCACATCATAGTATCAGTTTCTCATTCCTTCCAGCAAACTGCAAATGCTTTTTTAACCTTTATAAGGTTATCATTTGCTTATGTCACGCCAGTCAAAAGTACAGTTTTTCTTGTTTGCTTTGACCTGGTTAAAGAAACTAGGAATAGGATGCTCTCTATTTTCCTCATCACTAACCCAGCAGAGCAGAAGACCTGTCTTGCAAATGTGTAAACCCTTTCTCATTGGATTGACACATTTTCCCGAACATTTTTCAAAACAGTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTTTGTTTAGGGGGGAGTGTCGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40623
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079675 | None | None | 806 | None | 24 |
| ENSDART00000113637 | Essential Splice Site | 264 | 491 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3464234)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3491921 |
| GRCz11 | 6 | 3652741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGGTCGTCCTGGAGATGACGGAAGTCCAGGCCCTAAAGGTCAAAAG[G/T]TCAGAGTTTTCTAAAACAACCATAAATAATTCAGAAATAATGTGTCCCCA
Long Flanking Sequence:
TTCTGTCTTCCAGTCATTTTGATCAAAGAGACAAAACACCCATCAAACGGTAACTGTAATTTGCTGGACATATTAGAATTTTTGCGTTTTATTAAAAATGTCAAAAAAATTATTTGCTCAGCCAACATTTTTTGCACGTATTTTTCTTTTTTGTCACACAGCTGTTGATCATACAGCTCCAATAAGGAACATTAAAGAGAAAAAACAAGCCTGTGATATAGACTTTTACACTATACAATAAATGTAAATATGGACAAAAAAACTGTAGTCGCACTAAATATATAATTCAGATACTGATAACATTTAAAAACAAAATTAAATTCTAGCATACATTAATTTTAATAGGTCTAAAAAGGAACATATAAACACTATTTCTATATGTTATCAGAATTAAATGCCAGTTTGAATCATTATTATTGTTAATGCTCTTCCGCTGAGAACTGCAGGGTAAAAAGGGTCGTCCTGGAGATGACGGAAGTCCAGGCCCTAAAGGTCAAAAG[G/T]TCAGAGTTTTCTAAAACAACCATAAATAATTCAGAAATAATGTGTCCCCATCTAAAACGAGCCGTTTGTCCTGCAGGGAGAGGGCGGTTCGAGCGGTGCTCCTGGACGAGATGGGACAGAGGTGAAGCTGACCAGAAAGAGGCCTCAATTCACAAATGTTTGACATTGTATGATTGCTCTTTTTCAGCATGTGTGTGTTTTTTTGTAGGGGAAAACTGGATACAAAGGAGAAAAGGTAAAATTATACCATAAACTGAGAGATTTATAATTGGAAAACAAGTCAAACATGATTCTAGCATGAGGCTGAATTGCCAAATAATGTATGAAACTTTGAAATGTATGAAAAAATTATTATAAAATTGTCTACAAAATGCACAAGGGTCAAAGACTTGACTAAATTTAGAAATGTAATGAAATTATAAGTGATTTTTTACAGAGCAAGCACAGTATGTGCAAATACATTGTCTACTTTAAGCTTTAATGTATAAAATATTGGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14346
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079675 | None | None | 806 | None | 24 |
| ENSDART00000113637 | Essential Splice Site | 264 | 491 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3464235)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3491922 |
| GRCz11 | 6 | 3652742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGGGTCGTCCTGGAGATGACGGAAGTCCAGGCCCTAAAGGTCAAAAGG[T/C]CAGAGTTTWCTAAAACAACCATAAATAATTCAGAAATAATGTGTCMMCAT
Long Flanking Sequence:
TCTGTCTTCCAGTCATTTTGATCAAAGAGACAAAACACCCATCAAACGGTAACTGTAATTTGCTGGACATATTAGAATTTTTGCGTTTTATTAAAAATGTCAAAAAAATTATTTGCTCAGCCAACATTTTTTGCACGTATTTTTCTTTTTTGTCACACAGCTGTTGATCATACAGCTCCAATAAGGAACATTAAAGAGAAAAAACAAGCCTGTGATATAGACTTTTACACTATACAATAAATGTAAATATGGACAAAAAAACTGTAGTCGCACTAAATATATAATTCAGATACTGATAACATTTAAAAACAAAATTAAATTCTAGCATACATTAATTTTAATAGGTCTAAAAAGGAACATATAAACACTATTTCTATATGTTATCAGAATTAAATGCCAGTTTGAATCATTATTATTGTTAATGCTCTTCCGCTGAGAACTGCAGGGTAAAAAGGGTCGTCCTGGAGATGACGGAAGTCCAGGCCCTAAAGGTCAAAAGG[T/C]CAGAGTTTTCTAAAACAACCATAAATAATTCAGAAATAATGTGTCCCCATCTAAAACGAGCCGTTTGTCCTGCAGGGAGAGGGCGGTTCGAGCGGTGCTCCTGGACGAGATGGGACAGAGGTGAAGCTGACCAGAAAGAGGCCTCAATTCACAAATGTTTGACATTGTATGATTGCTCTTTTTCAGCATGTGTGTGTTTTTTTGTAGGGGAAAACTGGATACAAAGGAGAAAAGGTAAAATTATACCATAAACTGAGAGATTTATAATTGGAAAACAAGTCAAACATGATTCTAGCATGAGGCTGAATTGCCAAATAATGTATGAAACTTTGAAATGTATGAAAAAATTATTATAAAATTGTCTACAAAATGCACAAGGGTCAAAGACTTGACTAAATTTAGAAATGTAATGAAATTATAAGTGATTTTTTACAGAGCAAGCACAGTATGTGCAAATACATTGTCTACTTTAAGCTTTAATGTATAAAATATTGGTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40624
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | Essential Splice Site | 9 | 806 | 1 | 24 |
| ENSDART00000113637 | Essential Splice Site | 359 | 491 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3466446)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3494133 |
| GRCz11 | 6 | 3654953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCCCAGGGATACAAGGAGAGACTGGCATTGGACTTCAAGGACCAAAG[G/A]TTGGCTTATATACTTAAAATCTTCTGGTATTATGAGCCTATTTGAGTAGT
Long Flanking Sequence:
ATCAGTGAATCATTCACTGGAGAGCCATTCTGAACAGACAGTTTGAATCAGTGAGTTGTTATCTGGAGACTCTGATCGGATCATTTTAATTAGTTGGGGTTTTTGGTTCAGTTTTTTTTTTTTTTTTAAGTCATTTATAGCTAGAAAAAGGTTTTGTGCTTAAGAAATATTTGCTTAGTTATTACCAAAGTTCTTTCTATTTTTTTTACCAGTTACCTTGTATATGTTGCATAATAGGGCAGCAATGCGAGTCATCAAGCTTTCAGCCAAAATAGCAGTTACTCTGATTTATTTTGTGATTGCACGAGGTTTGAGCTCATTTTGAAAACACAGCATGAGTATAAATGTATTGTTGTGGTTTGATTGGTGGTCTAATCTTGTGTTTACATTTCAACTGATTATCAATGTTTGACATATTTCTGCGTCTTCAGGGTGAGAGAGGATTTCCCGGACCCCCAGGGATACAAGGAGAGACTGGCATTGGACTTCAAGGACCAAAG[G/A]TTGGCTTATATACTTAAAATCTTCTGGTATTATGAGCCTATTTGAGTAGTGTTGGTGATCATAACACATGTGATTTTATTATTTACTTTTAGGGTGATGTGGGATTTCAGGGAAGAATGGGTCCTCCTGGGCTTCCTGGGCTTGGGGAGCCAGGTTTACCGGTGAACAGCAAATAAAATGAATCAACACAGGCTCATTAGAAATATGTGCTTCAGCCTATACTTTAGTGGAACTGCAAAAATGTACTTCAACATACATTTGACTGCAGTTTCTAGGTAAAATTAATCGTATGACACCATCAACTTTTGTTCCTTTTCACACTAATGATATTTACAGGCACATATTATCGATGAAAAAAGGATTATTTTCATGCAGTTCATTGCACAACACCAAATAAACACCACAAATCAACTTAACAGGGTTTGTGATTTGAATACGTTTACGTCACCTATCTATGGTGTGGTCAGTTTGATCGTAGCTCACTTTGTATGGGCTTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1042
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | Nonsense | 670 | 806 | 22 | 24 |
| ENSDART00000113637 | None | None | 491 | None | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3482299)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3509982 |
| GRCz11 | 6 | 3670802 |
KASP Assay ID:
554-0945.1 (used for ordering genotyping assays)
KASP Sequence:
TCAATGGTAACGGCGGGCATAATTTCGACACCAGCACATATAAAGGCAGC[A/T]GAGAAAACACAGGAACACCGTCTGCCACCAACACYGTGATCACTGAGAGA
Long Flanking Sequence:
ACTACGGCCAGTTTATCCAATTCCCCTATAGCGCATGTGTTTGGACTGTGGGGGACACTGGAGCACCCAAAGGAAACCCAGGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATACTAACTGATCCAATAGGGACTCGAACCAGCAACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTAAACCATCGCGCCCATTATTATGTTTAAAAATGTTTTAAAATCTTTCTATCAAACAGCTCTTTGGAGATATTAATAAAATAATAATTAAAATTAATATAAATTTTGCCTTCAACTGTATTTCTCTAATAAATATCCTTCCTCTATTTTTAATCTCAGCTCTGGAGTCCAAACTAGTCAATCAGCTCTGCGAAGATGAAAGTAGAGCGCTTATCTTCAACCGCATTAATGATTTTGAAAACGGATATGGTCTGAACGGAAACCGCATCAATGGTAACGGCGGGCATAATTTCGACACCAGCACATATAAAGGCAGC[A/T]GAGAAAACACAGGAACACCGTCTGCCACCAACACCGTGATCACTGAGAGAGGCAGAGGAGGCACGTTTGCTTCAACAGCTGGTCCAGACATTAAACAGGTTAGTGCAGACATGATTATGAAATGAGCCTTTGGTTTGTGTATTGATTATGGTTTGTTTCATTAACATTTTGTCAGGAGGTTGAGCGTGTACCTAAAACACCAGACATAAGAGGAGCTCCTGCAGTCACTGGGACATCCACACCTAGCAAACCTTCATCAGGGACAACAACATCATCATCATCTGTGAACACATATTCAACTTCAATGCAGTTTATAGCAGCACCACGACCACCTTTACCTAAAGGTACAAACGAAACACACTCGCTAACTTACCGCAAAACATATTTTGAGTCTAGGATTTATTTTGTTGAAAGAAATTCATACTTTTATTTGACAGGGATCCATTAATTCAATCTAAAGTGACGGTAAAGAAAGGTATTGGGCCCTATCATACACCCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11556
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 |
|---|---|---|---|---|---|
| ENSDART00000079675 | Nonsense | 701 | 806 | 22 | 24 |
| ENSDART00000113637 | None | None | 491 | None | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3482392)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3510075 |
| GRCz11 | 6 | 3670895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGAGAGGCAGAGGAGGCACGTTTGCTTCAACAGCTGGTCCAGACATT[A/T]AACAGGTTAGTGCAGACATGATTATGAAATGAGCYTTTGGTTTGTGTATT
Long Flanking Sequence:
AGAACATGCAAACTCCACACAGAAATACTAACTGATCCAATAGGGACTCGAACCAGCAACCTTCTTGCTGTGAGGCAACAGTGCTAACCACTAAACCATCGCGCCCATTATTATGTTTAAAAATGTTTTAAAATCTTTCTATCAAACAGCTCTTTGGAGATATTAATAAAATAATAATTAAAATTAATATAAATTTTGCCTTCAACTGTATTTCTCTAATAAATATCCTTCCTCTATTTTTAATCTCAGCTCTGGAGTCCAAACTAGTCAATCAGCTCTGCGAAGATGAAAGTAGAGCGCTTATCTTCAACCGCATTAATGATTTTGAAAACGGATATGGTCTGAACGGAAACCGCATCAATGGTAACGGCGGGCATAATTTCGACACCAGCACATATAAAGGCAGCAGAGAAAACACAGGAACACCGTCTGCCACCAACACCGTGATCACTGAGAGAGGCAGAGGAGGCACGTTTGCTTCAACAGCTGGTCCAGACATT[A/T]AACAGGTTAGTGCAGACATGATTATGAAATGAGCCTTTGGTTTGTGTATTGATTATGGTTTGTTTCATTAACATTTTGTCAGGAGGTTGAGCGTGTACCTAAAACACCAGACATAAGAGGAGCTCCTGCAGTCACTGGGACATCCACACCTAGCAAACCTTCATCAGGGACAACAACATCATCATCATCTGTGAACACATATTCAACTTCAATGCAGTTTATAGCAGCACCACGACCACCTTTACCTAAAGGTACAAACGAAACACACTCGCTAACTTACCGCAAAACATATTTTGAGTCTAGGATTTATTTTGTTGAAAGAAATTCATACTTTTATTTGACAGGGATCCATTAATTCAATCTAAAGTGACGGTAAAGAAAGGTATTGGGCCCTATCATACACCCGGCGCAATGTGGCGCAAGGCGCGGCGCAATACTCTTTTGCTACTTTTAGCTCGGCGCAAGGGTCATTTTGAGGTGTTGCGCCACGCTGTTTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16583
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079675 | Nonsense | 783 | 806 | 24 | 24 |
| ENSDART00000113637 | None | None | 491 | None | 17 |
Genomic Location (Zv9):
Chromosome 6 (position 3485204)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 3512886 |
| GRCz11 | 6 | 3673706 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTAAGCTGCTCCTGGATCAGGGWCCTTGTCGAGAATATAACATYCGATG[G/A]TACTAYGTACCACAAGCCAACGCCTGTGCACAGTTCTGGTACGGTGGCTG
Long Flanking Sequence:
AACGTGGTAAAAATCAGGCAAGGGCCTTTTCTTTTCTTTTTTGGATTGCTTTTTTACAATTGTTGGTTGGGTTTAGCAAAGTGGCTGGGCGGGTCAATCCGTGCTTTTTAAAACACTATTGGTTGGGTTTAGGGAAGGAGGAGGGTGGATCAGTCGTCGCTCAGTCAGTCAACAGTGACCTCTGGTGGATTCACGAAAACAAAAACTGCAATAAAAAAAACAAACAAAAAAAAAAACGTACCTCCTGGGATGTATTTGGGGCTCTCCAGAAATGTATATAGGGGTGCATTTTCAGAATGAGCCTGCGTTGGACTGAAACTAATATCTTAAATTTCTTATTTGAATTTCACTGGACCTTCTAATAATTACATTAATAACATTTTAGTTGACTCTTGCTTAATATTTTATATTTTTTATCTGTGTTCAGAGGTTGTGCTTTTGGACCCCCTTTGTAAGCTGCTCCTGGATCAGGGTCCTTGTCGAGAATATAACATCCGATG[G/A]TACTATGTACCACAAGCCAACGCCTGTGCACAGTTCTGGTACGGTGGCTGTGAAGGAAACCGTAATCGCTTTGACACAGAAGAAGAGTGCAAGAAGACGTGTGTGGTCGTGTGAGCAGGTAAAACACACACCTGAAAACCTTTCGCTGGTAAATATTACTGCAAATGAAAAGGGACAGTAGTTTTTTCCTTTTGGTCACGGTTGTTTCTTTGCATCCAGGGGGCTGACATCCATTATGGACAAATTTACCTTTGTCTGTAATTCCTCATTCTCAACTTCAATGGACCTGCACTGAAATAAACAGATGTTAAATAAATTGACGTCTGCAAGAAACTAGTGGTCCTGCTTTATATTAAGTGGCCTTAACTACTATGTACTTATATGTAAATTAATCATGTAGTACAATACTTATTTGTAATAATATTAGTAAAATAAGAATATTAGTACAATACTTTTGTGTAATAACAATTGTGTAAAAACACTTTATTTAAAAGGCTTTT
Associated Phenotype:
Not determined