ZMP
si:dkey-21e7.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC563665 [Source:RefSeq peptide;Acc:NP_001093483]
Human Orthologue:
C3
Human Description:
complement component 3 [Source:HGNC Symbol;Acc:1318]
Mouse Orthologue:
C3
Mouse Description:
complement component 3 Gene [Source:MGI Symbol;Acc:MGI:88227]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30732 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31073 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43860 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24189 | Nonsense | Available for shipment | Available now |
sa45772 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37529 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37528 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32404 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30732
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 7 | 1680 | 1 | 42 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 26827416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26216272 |
GRCz11 | 22 | 26236169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATATTGAGTGGCGGTTACTTCAGCAGGACGATGCTTCTTCAGCTGCTGT[T/A]ATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAAC
Long Flanking Sequence:
CAAAATATTCTAATAAATAAAAAATAAATAAATAAAAACATTTTACATATTGTCCCTTTAACCTGCTCAGGACATAACTTTAAATAATGATCCTTTTAAGTAGTAGGCTGACAGGTTGAGTAAACACTGCAATACAAAGTGCTGCATAAACTTTAATGTACCAATGACAACAAATGGCAATGCAGAGAATGCAACGCACACAGTTAAAATGTCCAAATAATAAATAAAAATAGCTTTTTTATAGCCTACCATTTTGTTTACAACACCTTAAACGTTTCTAATGCTGGGGGTCTGTGTGTTGTCAAGACAACTGATTTTGCCCAGAAAACACTGCAAACATTGCACAATTGCTTTACAAAGTTTCGAGATTCACTAAGCTCCCAGTTTAGTGGGTGGAGGGATTTGGGGATATGTCGATATTTTAGCTGTTTGTTTTCTAGTTATTTCTGACATATTGAGTGGCGGTTACTTCAGCAGGACGATGCTTCTTCAGCTGCTGT[T/A]ATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAACGACAGTGCGTTTAACTCTGCATTATTAACTTTTAATGTGTAAAAATATATTCTTATCTTGTCGACGTTGATTTTTATAATGTGTTTATCTTGTCAAATGAGCAGCAAGAGGACGGTTTGGAGACATATGCGACAAATGTAAGTAGCCTACCCTGTTTCGTTTTGTGTCCCGAAAATGAACGATCATATTAAAACAATATTAACCACAAATTAAGCATCAATATGTTTAACAATGTTGTTTGTTGTAAAATGTGCTTAAACTAATAAAGTCATTTCGGACTGTTATTTCTTTAGTATTTATAAGAGAATTGTGTGGAAAAATATTTATATATAAGTTATATATATATACTGTTGAAGTTCGAATTATTAGCCCTCTGATTTTTTTTTCTTTTTTTAAAAATTTTTCCAAATTATGTTTAACAGGGCAAGGAAATGTTCACAGTATGTCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31073
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 |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 24 | 1680 | 1 | 42 |
ENSDART00000138595 | Nonsense | 24 | 1680 | 1 | 42 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 26827366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26216222 |
GRCz11 | 22 | 26236119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAA[C/T]GACAGTGCGTTTAACTCTGCATTATTAACTTTTAATGTGTAAAAATATAT
Long Flanking Sequence:
TGTCCCTTTAACCTGCTCAGGACATAACTTTAAATAATGATCCTTTTAAGTAGTAGGCTGACAGGTTGAGTAAACACTGCAATACAAAGTGCTGCATAAACTTTAATGTACCAATGACAACAAATGGCAATGCAGAGAATGCAACGCACACAGTTAAAATGTCCAAATAATAAATAAAAATAGCTTTTTTATAGCCTACCATTTTGTTTACAACACCTTAAACGTTTCTAATGCTGGGGGTCTGTGTGTTGTCAAGACAACTGATTTTGCCCAGAAAACACTGCAAACATTGCACAATTGCTTTACAAAGTTTCGAGATTCACTAAGCTCCCAGTTTAGTGGGTGGAGGGATTTGGGGATATGTCGATATTTTAGCTGTTTGTTTTCTAGTTATTTCTGACATATTGAGTGGCGGTTACTTCAGCAGGACGATGCTTCTTCAGCTGCTGTTATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAA[C/T]GACAGTGCGTTTAACTCTGCATTATTAACTTTTAATGTGTAAAAATATATTCTTATCTTGTCGACGTTGATTTTTATAATGTGTTTATCTTGTCAAATGAGCAGCAAGAGGACGGTTTGGAGACATATGCGACAAATGTAAGTAGCCTACCCTGTTTCGTTTTGTGTCCCGAAAATGAACGATCATATTAAAACAATATTAACCACAAATTAAGCATCAATATGTTTAACAATGTTGTTTGTTGTAAAATGTGCTTAAACTAATAAAGTCATTTCGGACTGTTATTTCTTTAGTATTTATAAGAGAATTGTGTGGAAAAATATTTATATATAAGTTATATATATATACTGTTGAAGTTCGAATTATTAGCCCTCTGATTTTTTTTTCTTTTTTTAAAAATTTTTCCAAATTATGTTTAACAGGGCAAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTATTTTATTTCAACTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43860
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 |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 24 | 1680 | 1 | 42 |
ENSDART00000138595 | Nonsense | 24 | 1680 | 1 | 42 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 26827366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26216222 |
GRCz11 | 22 | 26236119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAA[C/T]GACAGTGCGTTTAACTCTGCATTATTAACTTTTAATGTGTAAAAATATAT
Long Flanking Sequence:
TGTCCCTTTAACCTGCTCAGGACATAACTTTAAATAATGATCCTTTTAAGTAGTAGGCTGACAGGTTGAGTAAACACTGCAATACAAAGTGCTGCATAAACTTTAATGTACCAATGACAACAAATGGCAATGCAGAGAATGCAACGCACACAGTTAAAATGTCCAAATAATAAATAAAAATAGCTTTTTTATAGCCTACCATTTTGTTTACAACACCTTAAACGTTTCTAATGCTGGGGGTCTGTGTGTTGTCAAGACAACTGATTTTGCCCAGAAAACACTGCAAACATTGCACAATTGCTTTACAAAGTTTCGAGATTCACTAAGCTCCCAGTTTAGTGGGTGGAGGGATTTGGGGATATGTCGATATTTTAGCTGTTTGTTTTCTAGTTATTTCTGACATATTGAGTGGCGGTTACTTCAGCAGGACGATGCTTCTTCAGCTGCTGTTATGGGCGACCCTGCTCTGTCAAATCTGCGATGGAAAGGCCTTCCCTCAA[C/T]GACAGTGCGTTTAACTCTGCATTATTAACTTTTAATGTGTAAAAATATATTCTTATCTTGTCGACGTTGATTTTTATAATGTGTTTATCTTGTCAAATGAGCAGCAAGAGGACGGTTTGGAGACATATGCGACAAATGTAAGTAGCCTACCCTGTTTCGTTTTGTGTCCCGAAAATGAACGATCATATTAAAACAATATTAACCACAAATTAAGCATCAATATGTTTAACAATGTTGTTTGTTGTAAAATGTGCTTAAACTAATAAAGTCATTTCGGACTGTTATTTCTTTAGTATTTATAAGAGAATTGTGTGGAAAAATATTTATATATAAGTTATATATATATACTGTTGAAGTTCGAATTATTAGCCCTCTGATTTTTTTTTCTTTTTTTAAAAATTTTTCCAAATTATGTTTAACAGGGCAAGGAAATGTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTATTTATTTTATTTCAACTAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24189
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 |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 158 | 1680 | 5 | 42 |
Genomic Location (Zv9):
Chromosome 22 (position 26821515)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26210371 |
GRCz11 | 22 | 26230268 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCGTTCCGCTCCGGACACATCTTCATTCAGACCGACAAACCTATTTA[C/A]AACCCTGGAGACAAAGGTCAGCTCTCACATGCTGCTATTGAGCTGTTTTC
Long Flanking Sequence:
TTTATATCATATGTCAATCCAGCGGTAACAATGGTTGATTTTTAGAGAAAACAGACCTTAAACGCGTCAATTTTTTTAACAGCATACAGTTCACTGGAAGCATTTGACCCAGGTTACTAAAGAATTAAAAGCCATTTTGCATACTTCTGCATATACCCTATAATTTATCGTATAAAATAAGCTACTTAATTGCTTATTCAATACAATTTTCCTACTTGGTGAGTTTCGTAACTACTGAAATTATTTTAGTGCTCATACTAGCCATTCGTAAATAAGGCCCTATGCTGAAGTTCTCTAATGTATGATCACGTCACTTGTTGCATGTAAATATAATCAATTACGTTCTTCTATCAGATCAACCCAAATTTGCTACTTCCAGATGGAAAAAAGAAGTATGTGAAGCTCGTTGCTCAGTTCAGCAACATCTATCGTGCAGAAAAAGTAATGGCGGTGTCGTTCCGCTCCGGACACATCTTCATTCAGACCGACAAACCTATTTA[C/A]AACCCTGGAGACAAAGGTCAGCTCTCACATGCTGCTATTGAGCTGTTTTCACAGTACTCATTTACATTTACAATTATTCCCCCTTTTCCCAGTACGTTTCAGGGCTTTTGTGTCTGATTTGGAATTTCGTTCTTCTGAGAGAACCATATCTCTGGAGATTCAGGTGATTTGTCACATTAACCTAACCTAATTTGTCACATTAACCTAAACATTACCATGTTTGCTAAACAATTGTTTGTTTGTTTGTTTTCTGGAATATTAATGCTTACAGCACAATTTGCTCGTGTTTCAGAATCCAGATGGAATTGCGGTGCATGGTATTGGGAGAGTTAAAGCAATCGATGGGGTCTTTTCTGACATTTTCTCACTGTCTACTGTAGTCAAGTATGCACTCAGAATAGTTCAGTTGTGTTGTGTAGAATATAAAACAGAGTATAATGCACCAAAAGATAAATAGAGTGTTGAGATTGTTTAAAGGATATTCAGATGTAGTTTAGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45772
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 1191 | 1680 | 29 | 42 |
Genomic Location (Zv9):
Chromosome 22 (position 26788626)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26177482 |
GRCz11 | 22 | 26197379 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTACTTGTATTTTTTTCTCCACAGGATAAGTCTAGACAGGCAGCAGGGTA[T/A]CTGACAGAGCATTTCTCCCGGCTGACCAGGCCATATACAGCAGCTATAGC
Long Flanking Sequence:
TGGAAGCTATATGAAATAATGATAACTGAATTAAATAATTAATATAATAGCTAAATTGAACGGTTTAAGAACAGAAGAACAGAAGCTAAATTAAATAGTTGTAGCTAAATTAAGTAGTAGTGATAGCTATTTGCAATAGTTAGAATAATTAGCACACTAGCTAAATTAAACAAGTAATATCTACATTAAATTGTTAAATGTTTCATTATATAATTTAGACATTATCTAAATACATAATTTGAATTATTGTTTATAAATAATTTGAACAATTCATTCTTTTCATCATCTCAAGGTCATGAAGTGTAAAAATATATATTATGTTAATAGGCTAAATTAGTAAACAAGTACAGCCCTGATCCATACTACCAGGCCTGTGAACTATGAATCTACAAGACCAAAACTATTTGTACTGGCTATAATAATGTACTTTTTTTTACATATTCAATGGTTTTACTTGTATTTTTTTCTCCACAGGATAAGTCTAGACAGGCAGCAGGGTA[T/A]CTGACAGAGCATTTCTCCCGGCTGACCAGGCCATATACAGCAGCTATAGCATGCTATGCGCTAGCCGTATCGAACAACGCCTGCGTGAAGAGCATGTTGCTCAAATTTGCCTCACCTGGTACTTACATTTTAAACGCACAAATATGAACACAATATGTCATCTTCTCTTTCTCATTATACTTTATTGTCTGTCCACAGATCATTCCCACTGGCCTGATTCAAACAATTATTTTTTCACACTGGAAGCTACAGGCTACGCACTGCTAGCGCTGATCAAAAGTGGCCACATGGAAGAGGCAGAAGCTCCATTTCGATGGTTGAATGAGCACCGTGGCATTGGTGGAGGATACGGCTCTACTCAGGTGAAGTAAACCTGTATGAATGATCTAAACTAACAGTCAAACGTTTGGGGTTTTAAAAGAAGCTTGTTCTGCTCGTTAAGGCTGCATTTATTTGACCAAATAATACAGTTAAAAATTGTATTTCTGTAATGTAATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37529
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 1224 | 1680 | 29 | 42 |
Genomic Location (Zv9):
Chromosome 22 (position 26788528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26177384 |
GRCz11 | 22 | 26197281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCATGCTATGCGCTAGCCGTATCGAACAACGCCTGCGTGAAGAGCATGT[T/A]GCTCAAATTTGCCTCACCTGGTACTTACATTTTAAACGCACAAATATGAA
Long Flanking Sequence:
TTGTAGCTAAATTAAGTAGTAGTGATAGCTATTTGCAATAGTTAGAATAATTAGCACACTAGCTAAATTAAACAAGTAATATCTACATTAAATTGTTAAATGTTTCATTATATAATTTAGACATTATCTAAATACATAATTTGAATTATTGTTTATAAATAATTTGAACAATTCATTCTTTTCATCATCTCAAGGTCATGAAGTGTAAAAATATATATTATGTTAATAGGCTAAATTAGTAAACAAGTACAGCCCTGATCCATACTACCAGGCCTGTGAACTATGAATCTACAAGACCAAAACTATTTGTACTGGCTATAATAATGTACTTTTTTTTACATATTCAATGGTTTTACTTGTATTTTTTTCTCCACAGGATAAGTCTAGACAGGCAGCAGGGTATCTGACAGAGCATTTCTCCCGGCTGACCAGGCCATATACAGCAGCTATAGCATGCTATGCGCTAGCCGTATCGAACAACGCCTGCGTGAAGAGCATGT[T/A]GCTCAAATTTGCCTCACCTGGTACTTACATTTTAAACGCACAAATATGAACACAATATGTCATCTTCTCTTTCTCATTATACTTTATTGTCTGTCCACAGATCATTCCCACTGGCCTGATTCAAACAATTATTTTTTCACACTGGAAGCTACAGGCTACGCACTGCTAGCGCTGATCAAAAGTGGCCACATGGAAGAGGCAGAAGCTCCATTTCGATGGTTGAATGAGCACCGTGGCATTGGTGGAGGATACGGCTCTACTCAGGTGAAGTAAACCTGTATGAATGATCTAAACTAACAGTCAAACGTTTGGGGTTTTAAAAGAAGCTTGTTCTGCTCGTTAAGGCTGCATTTATTTGACCAAATAATACAGTTAAAAATTGTATTTCTGTAATGTAATGTGTGTATTTATATAGCACATTTATTGTGTATGGCCATACACCCAAGGCACTTCACTATCACCACCACCAGTGTGCAGCATCCTCTTGGATGATGCAACGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37528
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 |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 1270 | 1680 | 30 | 42 |
Genomic Location (Zv9):
Chromosome 22 (position 26788309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26177165 |
GRCz11 | 22 | 26197062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCTGATCAAAAGTGGCCACATGGAAGAGGCAGAAGCTCCATTTCGATG[G/A]TTGAATGAGCACCGTGGCATTGGTGGAGGATACGGCTCTACTCAGGTGAA
Long Flanking Sequence:
ATGTTAATAGGCTAAATTAGTAAACAAGTACAGCCCTGATCCATACTACCAGGCCTGTGAACTATGAATCTACAAGACCAAAACTATTTGTACTGGCTATAATAATGTACTTTTTTTTACATATTCAATGGTTTTACTTGTATTTTTTTCTCCACAGGATAAGTCTAGACAGGCAGCAGGGTATCTGACAGAGCATTTCTCCCGGCTGACCAGGCCATATACAGCAGCTATAGCATGCTATGCGCTAGCCGTATCGAACAACGCCTGCGTGAAGAGCATGTTGCTCAAATTTGCCTCACCTGGTACTTACATTTTAAACGCACAAATATGAACACAATATGTCATCTTCTCTTTCTCATTATACTTTATTGTCTGTCCACAGATCATTCCCACTGGCCTGATTCAAACAATTATTTTTTCACACTGGAAGCTACAGGCTACGCACTGCTAGCGCTGATCAAAAGTGGCCACATGGAAGAGGCAGAAGCTCCATTTCGATG[G/A]TTGAATGAGCACCGTGGCATTGGTGGAGGATACGGCTCTACTCAGGTGAAGTAAACCTGTATGAATGATCTAAACTAACAGTCAAACGTTTGGGGTTTTAAAAGAAGCTTGTTCTGCTCGTTAAGGCTGCATTTATTTGACCAAATAATACAGTTAAAAATTGTATTTCTGTAATGTAATGTGTGTATTTATATAGCACATTTATTGTGTATGGCCATACACCCAAGGCACTTCACTATCACCACCACCAGTGTGCAGCATCCTCTTGGATGATGCAACGGCAGCCACAGGACAACAGTGCCAGTGCGTTCACCACACATCAGCTATAGGTGGAGTGGAGAGACAGTGATAGAGCCAATTCCGTGGATGGGGATGATTGGGAGGGCATGATGGTTAAGGGCCTATTGGGGCAATTTGGCCGGGACACCGAGGTTATACCCCTACTCTTTACAAGAAGTGGCATGGGATTTATTTATTTATGTTTAACTTTGTTTATTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32404
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 |
---|---|---|---|---|---|
ENSDART00000138595 | Nonsense | 1364 | 1680 | 33 | 42 |
Genomic Location (Zv9):
Chromosome 22 (position 26779319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26168175 |
GRCz11 | 22 | 26188072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGATGTAATTCATCGTTTATGTGTAATAGGTAGTGACGGTTTACCAT[C/T]AGCTTCCTGATGTGTATGAGAACAGCACATGCAACGGCTTTCAGCTGGAC
Long Flanking Sequence:
TTAAGCAACTTTTCTTTACTCATTCCAAACTTTTGACCAGTGGTGTAGTTGTGGTTCATTTGTTTTCATATAATGATCATATTCCTCCATCAGTCCACCATGGTGGTTCTTCAGGCCCTGTCTGAGTATCTAGTGAAGAGGCCTCCTCCGTCAGACCTCAATTTGTTGGTTCAGCTCAGCGTTCCTGGTCGGAGTGATGTTCGCTGGACCTTCAATCCCAACTTGGCTTATGTGGCCCGTTCTTCACGAGTGAGTTTATGGATGTTCCATCTTTTGAATTCCTTTTTGAAGACAAAGACAAGTTTGGTATGAAATATGACACACTTTTAATGTCTTCCAGGTCCCTCTTGATCAGGAATTCTCAGTGGCGGCTTCTGGGAACGGCAAGGGTGTTTTGGAGGTGCTAAATGTCAATGTTTACCAAGAATATCTTGAACTAGAATATAAAAATTTAGATGTAATTCATCGTTTATGTGTAATAGGTAGTGACGGTTTACCAT[C/T]AGCTTCCTGATGTGTATGAGAACAGCACATGCAACGGCTTTCAGCTGGACGTCTCTATCGCTGAGACTAATGGTGAGTTGACAAAAGTTTGCAGTGTTTTCCCCCATACCGAGATGTACAGTGCAGGATTTATGAACTGTTGATTCTTTCAGAAATAATGTAACTTTCACAGTATTTTTTATAAAGGGATTTCTCCCTCCTCTGACATCATGGGGTGAAAACTTCAGTTGTATAGGCCACACGATGACACTATACCCAGGGTTTCAGAAAATCTTTTTTTTTAGAAATGTTTTTTTTTTTTTTGTTAGAAATGTTTGGTTTTAGTCACCTGGGGCCTCATGTACGAAGACTTGCGTGGAAATCTTACTAAAACATTGCGTACGCACAAAGCTGTAAATGTGCGTACGCAGAAAAAATGTCAGATGTATGAAACACTGCGTACGCCGAATCCCACGCATATTCTTTTGTACCTCCGAATGAACGTGAAACTGAGCGCAACA
Associated Phenotype:
Not determined