ZMP
prp
Ensembl ID:
ZFIN ID:
Human Orthologue:
COL22A1
Human Description:
collagen, type XXII, alpha 1 [Source:HGNC Symbol;Acc:22989]
Mouse Orthologue:
Col22a1
Mouse Description:
collagen, type XXII, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:1916950]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30459 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30458 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa19381 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30457 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38193 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45027 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24791 | Nonsense | Available for shipment | Available now |
| sa44408 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30459
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Nonsense | 497 | 1634 | 9 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 94368)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 94368 |
| GRCz11 | KN150214.1 | 94368 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCCTACAGGGTGATACAGGTCTACCGGGTGCCCCGGGGCCCAAGGGT[G/T]AAAAGGTCAATTAGCATTTTACAATCACAACATCCTCAATATGCATCTTC
Long Flanking Sequence:
TTTGACATGAGATTTTGAATAATTGCAATTATTGGATGTTATTATGTTAATGTTATATTATAGTTTTAGTTTGTGATATATTTAAATAATTTTAAAATAATAATAATAATAATTAACTAAATAATAAAAAAACAGTAGTACATAAATTATATCTATAACCTGTACAAAGTATTTGCCTAAGCATTTATTAAATATGAATTAAATAAGCATGTCATAGATATTCAAAATATAGCTTGACATTATTTGTTATTGTACAACAGCTTGACAATGTTTGACAGAAATTAATTGTATTCAACATGTAAAATTCAGTGCAGCATATAAGGCTAGATATCAATTTTTTTATGCTGAATTCATTTGTAATGCATTCACTTGCTTTTGTAATGCATTCGTTCTTTACGCTCTCGTTTTTCTTTCAAAATCTCTGTCATTTGCTATCTCTCTCAATCTTTTTCATCCTACAGGGTGATACAGGTCTACCGGGTGCCCCGGGGCCCAAGGGT[G/T]AAAAGGTCAATTAGCATTTTACAATCACAACATCCTCAATATGCATCTTCATATCTCCGGATTGTGTTTCTGATTTGTTTCCTCACCGGGTTACTGCATAAACTGTACATCTGCAGGGGGATCCTGGTCTTAAAGGGGCAGAAGGACCACCAGGACTCAAAGGGCTGAAAGGAGAACGTGTATGCCACCAATATTATTACTTAAAACAGTTTCTTGACTGTTTAAATGAACCTAAAACAGCATGGATATTTATTAGAATAATCAGCTGTTTCTACAGTATTGTGGATAGATTGTTAACAGTAAACCGATTTATTTTCATATGCTCTCGATTTTCATCTTCTGTTTCTTCCTCTATGGGCCTGGAGAATAATTGATCGGTGTTGATTGATTATTTGCAGGGTCAGGCTGTCTCTATCAAAGGTGATAGAGGAGAGAAGGTAAGGTCATGAGTTTAACAGTCAAACTCCTCCAGATGCAAAACAAAAACAGCGAATGTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30458
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Essential Splice Site | 586 | 1634 | 14 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 82139)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 82139 |
| GRCz11 | KN150214.1 | 82139 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAGGAGTTGCTGGTGAAGCTGGGCTGCCTGGACCACTCGGACCAAAG[G/A]TTAGACATTAACACTTACAGACAGAGTTACAGTGTTTCTTGATGAGCCCA
Long Flanking Sequence:
TTGCATTACACCCCTAGTATTTATGACCACATGTACCCTGAAAAAATTATTAATTGGATTTACTAATTTCTTTTAAGGTAAGTGGTTGCAAACGATTTATATAGGCTGAATTAAAGCAGACAAATTCAATTTAGTAATGTTCAACTTGTTTGTTTAAATTCAGATATAAATTGTTTGCAACCACTTACCTTCAAAGAAATGAGTAAATCCAATATTTTTTGCGTGTGTGTTGGCATCCATGATGAGCAGAAGATCAAATTTAACAAAAAGAAATGTTACTATCAGTGATATTAATATGTGTTTATATTTGGATATTTTTAGGGATCAGATGGTTTACCAGGTCTGGCTGGGAAAAAAGGCGATAAGGGTGAAAGAGTGAGTAACAGCTCATGTTGATGGTGTTTTTGGATCGATACTGTCTGTTAATTTAGCATGTTGATACACAGGGTGATCAAGGAGTTGCTGGTGAAGCTGGGCTGCCTGGACCACTCGGACCAAAG[G/A]TTAGACATTAACACTTACAGACAGAGTTACAGTGTTTCTTGATGAGCCCAGGGTCAGAAATTAACCACAAGAGTACATATTTATGCTTACTGCTTATAATGTAATCATTAGAGCTGTCAACATACTCATCGCATCCAAAATAAAAGCTTGTATTTACATAATTTACATACTGTCAAAAGTTTCAGGCCAACATTAAATCTGTTGATTTACTGATGGATATACAGTACAGTATGTGATCCTTTACCACAAAACAAATTATAAGTCAAAATTTTCTTGTCATTTTTAATTTAATTGAGATGTATATAAGGTGAATAAATGAAGGGTAGGAATTTTTTAGGTTTAATTGTTTAAGATAATGTATGAGGGAGGCTGGTTGTCCTGGGGTCCGTTCTTCGTACGTGGATTACTCGGTTAGCTGGATTTGGATATTGACGATTTGACACGATCCAGGATCGTTTCGTTCTTCAAAGCTGATCCGAGAGTTGTTGTCATAGCAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19381
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Essential Splice Site | 641 | 1634 | 17 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 76978)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 76978 |
| GRCz11 | KN150214.1 | 76978 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGAGGGCTGATTGGTGCTCCTGGTCCAAATGGAGTAAAAGGAGAAAAG[G/T]TAGAGTTGTGCAATTTATTATCTAATTTTATTATTTTATTTCATATTTTC
Long Flanking Sequence:
TACAAAAGTTGTCTATTTGAATATATTTAAAATTGCAGTTCATGTGATTTCAAAGCTGAATTTAAGTAATCATTCTAATATTGCTGCTAAAGAAACCTTTTTTATTTATAAAGTGCTGATAACAGTATTTTTATAGGAAACTTTATTTTCATGATTATACATTTCAAAAAGACAGCATTTGTGCAAAGTATATCTCTTGTGTAACATCGAGCATGTCTTTATTCTCACTCTCTGATGTTATTTAGGGTGAGCGGGGTGCAGATGGGTTTCCAGGGAAACCAGGTCTTCCAGGAAAAGAAGTAAGTGTTCTGATAGTTCTGAAATGTATATAATTTGTCATGTACCATTTTCCTCAGCATGCAGTTGCACTGGGGGGGCAGAAGATTTTATTGTGAGCTGATTTCAGGTATTGCTAAGTGACTCTTTTTTTTTTTTTGTAAAATCAGGGGGTTAGAGGGCTGATTGGTGCTCCTGGTCCAAATGGAGTAAAAGGAGAAAAG[G/T]TAGAGTTGTGCAATTTATTATCTAATTTTATTATTTTATTTCATATTTTCTTTTCTTTTATTTTTTGTTTCATTATTTTTATTTTGTTTTATCTTTTATTCTATTTTAATACATTTATTTGATTTATATATTTTTTTTTTGTTTTATTGTTTGTGTTTTATATTTTTTCTTTTATCTTATTTAGTTTTATTTTATTGCATTTTGTTTTGCTATTTTTTATTTTATTGTCAAATAACATGCAAATGGTCAATACAGGCAGGCAGCAGACAACGTAAACAAACTAACAAGGCTAGGGTAAAAACCAAGGCAGGACAAGGCAAGAAAAAGCATCATAATGTTAACTTGACAGATTAACAAGTCTTTGATAACTCTCCGGCTGTGTGTATGCAATCAGTCAGGATCAGGAACCGGTGTGAGTGTGTGTGGTGCATGACTGGACCTTGTAGTCCATCAGCGATCTGCAACCACTAAAACGCTGATCATCATAACAATTTTATATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30457
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111540 | Essential Splice Site | 682 | 1634 | 21 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 72887)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 72887 |
| GRCz11 | KN150214.1 | 72887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTGTTTTTAATCAGCCTATTGTTGATGCTGTTTTTTTTTTCTTCCAC[A/T]GGGTCCTCCTGGACCTCCAGGTTTGCCTGGTGAGACGGGTGACACTGGAC
Long Flanking Sequence:
ACCTGAGGTTAAATAAACTGTCATATTTAATAGACATGGCAGGGGGAAATGGAATTTAATGCAGTGCTTCTTGTCTGATCTGAGACCTACTTCATATTGTATATTTAACAGGCAGTGAAGATCACTCATTTTTTAAGATTTCAGATCTTAAACGTGACAGTTTTGTAATGAAAAGACAGTTCACCGGAAGCCCTTGGGTTGCCTGGCTGAAAATTAAAAGTCTGTGTGCATGTAGCCCATTGGCTAAATACATATAGATCCTGAAATATAGGATTTATCCTGATTTAATGCTGTTTAAATGTAGTGTTTTAAAATTAATAAGTTCTGAGAAGTATTTTAAAATAATTACATTTAATTCAATGGCAATCATACTTTAAAAATGGAGCTCAAATATATACTTGAATCACAATGCTCATCATGTTATGTTCCTGTCTTCCATTGTTGTTCACTTCATTGTTTTTAATCAGCCTATTGTTGATGCTGTTTTTTTTTTCTTCCAC[A/T]GGGTCCTCCTGGACCTCCAGGTTTGCCTGGTGAGACGGGTGACACTGGACCAAGGGTAAGACATTTGTAATTTTTATTATTGTTGTAACAATCCAGCTCGGCTGATTTTAATAGCTATGTAAGATGCTCTATAACCTGCTCTGTGGTCACTATAGAGACTGTGAGGATCTCAGTGCGGTTTGGTTCGTGTGTCTGGTGTTTCTGAGCTCAGATTAAAGCAAGGAGCCCATTAAGAAAAGAGATAGGAGATGTTCAGACGCCCTCAGACTGATAAAACCGCAACATCATTAAAATGCTCATTCTCCGACTTCTTGGAAAACACTGTTTCTTCCCAGAAATAATAGTGCTTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAACATAGGAAAGATAAAACAAGTAGGAGAAGGTTTGTGTGTATCGAGATAAATTTGGCCGACAGCTAGCTCTCTGAAACTCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38193
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111540 | Essential Splice Site | 887 | 1634 | 33 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 52505)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 52505 |
| GRCz11 | KN150214.1 | 52505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTAACTGTTAACATTAATATAATAATATCACAATATCTTTGATATTTCC[A/T]GGGTCAAAGAGGACTACCTGGAGAGCAAGGTTTCAGAGGACAACCAGGAC
Long Flanking Sequence:
TATTATATTATATTATATTATATTATTTTATATTATATTATATTATACACATTAAAAAAAAGTTAGATTTATGTAGCTGAATGCATTATTCTATTTTATTTCTAAGGCTGAATTCAAGAGTCTCTAATAAAATAGTCCAGCCACCATGCGATGCATCATTTACACAAGCACAGACAAGCTTGTTACAATGATGTATCTACTCTCACCTGAATTTATTAGTGTGAAATGAGAAATCTCATGTTGAACTACTGCATTTCTCACTAGTTCAGCCAAACGCAATCATTCCTGTCAGAGAAACTGCTTGACTTCATATTCAAAGAGAGCCAAGTTTCAGATTTCTGGAGTAAACTTTGAGAAAGGAAATTACAAAGTCAACACGACAGTAAAGTATACTAGAACAGAACAAAAATATCACACACTGTACACTTTATAGACATGAGTTCTGACTTTAGTAACTGTTAACATTAATATAATAATATCACAATATCTTTGATATTTCC[A/T]GGGTCAAAGAGGACTACCTGGAGAGCAAGGTTTCAGAGGACAACCAGGACCTGTGGTAAACCACAAACACGCTTTTAAAGAGACCCTATTTTGTTTTCATGCAATAGATTTGCATAAGGTTATATAAGCAATATCACATGAGTAGCAGTGCATTGTATGTATTGTTAAGAATTGTATTGTGTAATGTATTGTGATTTATGTTAGCTATGTATGCTATGCTATCTCAAACAGCACTCTTGTTCAGTAGCCAGTGCACTGATCAGGTGGTTAGCCATTTTAAATCTTGTCTCGAGCTCAAAAATACAGTGCACTGAAATGTTTGCAATGAATCGTGAAAATCAGGGCGTATTGATAAGTGTTATGCGGTTAAACATATACGCATTAAAGGTCAGCTGTGTTAGTGTTGCAGTTTCAGTTCATGTCCTCATCCTTTAAAAATGCATACAAAGTGAATTTGAAATAGAATTTGAGTATACAATCTTTGATCATTCACACAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45027
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Nonsense | 1374 | 1634 | 61 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 34096)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 34096 |
| GRCz11 | KN150214.1 | 34096 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAGCAGGGAGCCCAGGATTACCAGGCTTCCCAGGTCCAAAAGGGCCAT[C/A]GGTGAGTTGAGACGTTGGATCGGTTCTGATAGATTTTTTTTTTTGTTCTT
Long Flanking Sequence:
GGTCAACCTGGGAAAGACGTGAGTGAAGCTTCTGTCCATCTCTGTATGCAGATGTTACTAAATAGATAAAATGCTGTTGGTTTTAATTGGTGTGCTTGTGTTGTTCAGGGGAACTCCGGACCACCAGGGCCAGAGGGCATGAGAGGACCCCGAGGAGAATCTGTGAGGAAGCATTTCATCTTTTCAATCGCTAAATAAAACACCACCGGTTATTATACTGTTTGGGTCACTTTTTGTGTGTTTTAGGGCCAGCCAGGAGAACAAGGACCAACAGGCAAGCCTGGGTCTCAGGGAAATCCTGTGAGTTTTATTTCATCACGTGAAAACGGGTGGCCATATTGTAAATCGAGTTGAAATCATTCACAAAAATCGTCTTTCGCGTCATATAATTCATTAGTGGAAATGACCATGCTGCTTTACTATGTTTTAGGGTCAACCAGGACACAAAGGGGAAGCAGGGAGCCCAGGATTACCAGGCTTCCCAGGTCCAAAAGGGCCAT[C/A]GGTGAGTTGAGACGTTGGATCGGTTCTGATAGATTTTTTTTTTTGTTCTTGTATATCAGTATCATTAGCAAATTGCATAGCTGTAAAAACAAGTAATTCTGTAGAAGCTAACAGCAGTCTCTAGTAGGTGAAAATGAAGTGTTTTCACTGTCTGCCTGCCTAAGCATGAGCACTGTAAATATATTTAGACTATGTGTCTTTCTTCTAGGGTCCGCCTGGACCAATTGGCCCTGAGGGAAAACAAGTAAGGGATGGTTCTTTTTAAATTAATATTTTAGTACCACTTTTTATATTATTTGAACTAAACTTGTGTTTATCACAGGGCATGTTAGGAAAAGCTGGAGACCGAGGACAGAAGGGAGAAAAGGTTTGCATGCATAGGTCCACCTAATCATCTATCAGTCCATAATTTAACCATTCATACCCCCACCCACTAATACATCCATCCCTCCATCAGTCCTTCAACCCACCCAAGAATCCATTCATCCATCCAGTTGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24791
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Nonsense | 1393 | 1634 | 63 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 33755)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 33755 |
| GRCz11 | KN150214.1 | 33755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTATTTGAACTAAACTTGTGTTTATCACAGGGCATGTTAGGAAAAGCT[G/T]GAGACCGAGGACAGAAGGGAGAAAAGGTTTGCATGCATAGGTCCACCTAA
Long Flanking Sequence:
TAAATCGAGTTGAAATCATTCACAAAAATCGTCTTTCGCGTCATATAATTCATTAGTGGAAATGACCATGCTGCTTTACTATGTTTTAGGGTCAACCAGGACACAAAGGGGAAGCAGGGAGCCCAGGATTACCAGGCTTCCCAGGTCCAAAAGGGCCATCGGTGAGTTGAGACGTTGGATCGGTTCTGATAGATTTTTTTTTTTGTTCTTGTATATCAGTATCATTAGCAAATTGCATAGCTGTAAAAACAAGTAATTCTGTAGAAGCTAACAGCAGTCTCTAGTAGGTGAAAATGAAGTGTTTTCACTGTCTGCCTGCCTAAGCATGAGCACTGTAAATATATTTAGACTATGTGTCTTTCTTCTAGGGTCCGCCTGGACCAATTGGCCCTGAGGGAAAACAAGTAAGGGATGGTTCTTTTTAAATTAATATTTTAGTACCACTTTTTATATTATTTGAACTAAACTTGTGTTTATCACAGGGCATGTTAGGAAAAGCT[G/T]GAGACCGAGGACAGAAGGGAGAAAAGGTTTGCATGCATAGGTCCACCTAATCATCTATCAGTCCATAATTTAACCATTCATACCCCCACCCACTAATACATCCATCCCTCCATCAGTCCTTCAACCCACCCAAGAATCCATTCATCCATCCAGTTGTCCATCCATTTGCACATTCACCCACAGATTTATCTATCTAATCAGCCTTCCATATATCAACTCAGATCATTCACTTACAAGTTCATCCATCTGTTAGTCTATCCGTCCATCCATCCACAGACTCAAAAATTAATTCATCAGCATGTCTAGATCTGAGCAGTTGGTTGGTTGATTAGTTGGTTGGTTGTCGTACGAACAAATGAACAAACAAACCAAATTTCAACACTGTTTGGTAGCAGCTTCAGGACATGAAGCACCACATTTATCAAGTGTTGTCAATTAAATGCTAACATATCATCCCAAGCCTCCATTGCTAATACCTAAATGCCATTTTTGAGGTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44408
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 |
|---|---|---|---|---|---|
| ENSDART00000111540 | Essential Splice Site | 1401 | 1634 | 63 | 68 |
Genomic Location (Zv9):
Chromosome Zv9_NA466 (position 33728)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN150214.1 | 33728 |
| GRCz11 | KN150214.1 | 33728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACAGGGCATGTTAGGAAAAGCTGGAGACCGAGGACAGAAGGGAGAAAAG[G/A]TTTGCATGCATAGGTCCACCTAATCATCTATCAGTCCATAATTTAACCAT
Long Flanking Sequence:
ATCGTCTTTCGCGTCATATAATTCATTAGTGGAAATGACCATGCTGCTTTACTATGTTTTAGGGTCAACCAGGACACAAAGGGGAAGCAGGGAGCCCAGGATTACCAGGCTTCCCAGGTCCAAAAGGGCCATCGGTGAGTTGAGACGTTGGATCGGTTCTGATAGATTTTTTTTTTTGTTCTTGTATATCAGTATCATTAGCAAATTGCATAGCTGTAAAAACAAGTAATTCTGTAGAAGCTAACAGCAGTCTCTAGTAGGTGAAAATGAAGTGTTTTCACTGTCTGCCTGCCTAAGCATGAGCACTGTAAATATATTTAGACTATGTGTCTTTCTTCTAGGGTCCGCCTGGACCAATTGGCCCTGAGGGAAAACAAGTAAGGGATGGTTCTTTTTAAATTAATATTTTAGTACCACTTTTTATATTATTTGAACTAAACTTGTGTTTATCACAGGGCATGTTAGGAAAAGCTGGAGACCGAGGACAGAAGGGAGAAAAG[G/A]TTTGCATGCATAGGTCCACCTAATCATCTATCAGTCCATAATTTAACCATTCATACCCCCACCCACTAATACATCCATCCCTCCATCAGTCCTTCAACCCACCCAAGAATCCATTCATCCATCCAGTTGTCCATCCATTTGCACATTCACCCACAGATTTATCTATCTAATCAGCCTTCCATATATCAACTCAGATCATTCACTTACAAGTTCATCCATCTGTTAGTCTATCCGTCCATCCATCCACAGACTCAAAAATTAATTCATCAGCATGTCTAGATCTGAGCAGTTGGTTGGTTGATTAGTTGGTTGGTTGTCGTACGAACAAATGAACAAACAAACCAAATTTCAACACTGTTTGGTAGCAGCTTCAGGACATGAAGCACCACATTTATCAAGTGTTGTCAATTAAATGCTAACATATCATCCCAAGCCTCCATTGCTAATACCTAAATGCCATTTTTGAGGTAATAGCAGAGATTTGAGCCATTGGTTGGTTG
Associated Phenotype:
Not determined