ZMP
cntnap5
Ensembl ID:
Human Orthologue:
CNTNAP5
Human Description:
contactin associated protein-like 5 [Source:HGNC Symbol;Acc:18748]
Mouse Orthologues:
Cntnap5a, Cntnap5b, Cntnap5c
Mouse Descriptions:
contactin associated protein-like 5A Gene [Source:MGI Symbol;Acc:MGI:3643623]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
contactin associated protein-like 5B Gene [Source:MGI Symbol;Acc:MGI:3664583]
contactin associated protein-like 5C Gene [Source:MGI Symbol;Acc:MGI:3646013]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13748 | Nonsense | Available for shipment | Available now |
sa21940 | Essential Splice Site | Available for shipment | Available now |
sa45432 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21941 | Essential Splice Site | Available for shipment | Available now |
sa13789 | Essential Splice Site | Available for shipment | Available now |
sa14172 | Essential Splice Site | Available for shipment | Available now |
sa9104 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13748
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Nonsense | 80 | 1310 | 3 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34313838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33214775 |
GRCz11 | 11 | 33477577 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGAGGTGGGGGGTGGTCTCCRAGCGGAGAAGACCAGCAMCCTTGGCTT[C/T]AGCTGGACCTACGGGAYAGGTTGAAGGTCACATCCATTGCCACCCAGGGT
Long Flanking Sequence:
GTCTGTGTGGGTGGACAAATATTTCCAAGAATTCTGTGAAGTTGTTGTGCGTGTGAGTCCTGCTTTTATTTTTACTCAATTCTGAACAAGAGCTGCAGGAATCCATGCAACTAGAAAATATAGTAAGACACACAAGTGTAGAACTGTGCCGCGTAATTTCCAAATTGCCTTTTTTATGTTATACTGCTTTGAGGCCTGTTTGCTGTCCCCTAGAGACAGATTGGTGATTTCTATCTCAAAAAAGAGTGACTGTGCCACAAAACTGCTAGAACAAATTTAATTCTTTTTTTTTTTTTACTCCTCTCTCTGACCGCTAAGCTTCAGTCCTGTCAGCATGATGAACAGGAGTATGAAATCTTAGCGAGTGCCTGAATTGTGAAGAGAATTACCCCCTGAATTCTGTTTCATTCCTCTGCAGTTTTTAAAGCACTGCCTCTTAATCTGTCCCCCTAGGAGGTGGGGGGTGGTCTCCGAGCGGAGAAGACCAGCAACCTTGGCTT[C/T]AGCTGGACCTACGGGATAGGTTGAAGGTCACATCCATTGCCACCCAGGGTCGCTGGGGCAGCTCTGACTGGGTGGCTCGGTACCAGCTACACTACAGTGACTCTGGACGAACCTGGAGACCGTATAGACAAGAGGACGTGATATGGGTGAGTCTTGTGAATCTGGCTGGAATATATCCATCTTGAGAGACTGCCTAGAAGTTTTTAGCCACAGTTTGAATAATGGCACACAAACGGTAAGAAGCATAGCACAAGTGGGAAATGAAAACCATAGCAACAACATCTAAATGGAAGAGACTTACAGATAAATCGTTTGAATTATACTGTAAATGCTGTTGTAACAGGCTAATTGGCACTACAGAGAATGCTATGAAATCTGTATATCAGATTTAGGACATTAGAATCAACTTTAAGGGCATCTTCAAGGGTTCTTCCTTTAATTATTCAAGTAAAGATTTTTACTGAGTCTTTACAGTATATTGGATATATTTACAGGAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21940
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111193 | Essential Splice Site | 246 | 1310 | 6 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34347148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33248085 |
GRCz11 | 11 | 33510887 |
KASP Assay ID:
2260-4486.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTTTGCTTATGTTGTCCAGTCTATGTTTCTAGTGTCTTTCTCTGTAC[A/T]GATGATGCCAAGCCCCAGTCTGGTGGTCGCTCATCATCTGTCATGTTAGG
Long Flanking Sequence:
GACGGACGGATGGACTGATAATAGATGGATGGATGGATGGATGGATGGACGGTCGGATGGATGGATGGATGGATGGATGGATGGATGGATAGATGGATGGATGGATGGATGGATGGATGGATGGATTGACGGACGGACGGACAGTCAGATAGATAGATGGATGGATGGATGGATGGATGGATGGATGGACAGATGAACAGACACAATGATGGACAGATATATGGATATTTCAATTGATAGATGGATGAATGGACAGATAGACAGATATGGACAATGGTGTAAATGAATGATGCACAGAGGAATGTATGGACTATTTAATGAGTGAATGTAGGTTTGCAATAATTAGATGGATTTGTGGATGGAAAGTTATTGTAGATGGACAGATTGAAGATTGGTGAAACAGTTTGCATAAATGATGCAAATGACTGCCTTTGCTAGACTGCTTGGCTAAATGTTTGCTTATGTTGTCCAGTCTATGTTTCTAGTGTCTTTCTCTGTAC[A/T]GATGATGCCAAGCCCCAGTCTGGTGGTCGCTCATCATCTGTCATGTTAGGAAGTCTGCTGGATGACCACCACTGGCATTCTGTTCAGATTGAGCGCTTTAACAAACACGTCAACTTTACCGTGGATGGACACACTCAACACTTCCGTAGTCTAGGACAAGAGGACACCCTGGAGATCGACTATGAGGTGAGATCTGAGTGTATATTTCCGTAAATCTGAATTTATAGTTAATTAGTTTCCATCCAGAGCTTGTTTATGTTATTGGTTTAGATAACGGAAAATATTACTACACAACGGACGCTTGAACAAAGAAATATTTAAAAAGTAATCCTTGTCAAAACAGCAAGAAGAAAAAAGAATAAGATCTATTACTGTGACATGCATAAATATATCCCACTCCCTTGTTATCTGAAACCAAGTTTCAAAACATTTTATTCAATCACTGTCACCGCAAACTTATGAAAGCCTGAAACAAAGTACCACAGAGAACAAAGTCAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45432
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Nonsense | 336 | 1310 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34350993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33251930 |
GRCz11 | 11 | 33514732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGACGTTTCTTCATGAAAATTTCCATGGCTGCATAGAGAACCTCAACTA[C/A]AACGGCGTCAATGTCATCGACATGGCAAAGAGACGAAAGCCACAGATTTA
Long Flanking Sequence:
TTTACCACTTCCTTTCCTTTTTCCTATCCCTTGTTTTTTTTTTTTTTTTTTCCAATCTTGACAAGAGCAGCAAAGTTTATAATTTTCTTATGGAGATTTTGAGTGCCTATTTGATACTTTGTACCATTACTGTCAGGGTGCAGCACTCAAAATAACTAGGGAATGTGCAGCAATGCTATTAAAATACAAAACTATTAAAACCGGATAGACAATTGTTTCAATTGGTCTCAGTTTTTACATAATAAATAGTTGTAATTCATGGATAAAAAAACAGGTTACAGGTTAAAGTAGTCTCTTGTCTGCTATACAAGCAGTATTGTTACTGATCTCTGGGATATGTGTTTGCTTTGTGTCTTTGTTTGCTTGTGTGTGTGTGTGTGTTTGTGTTTCTGTGTTTGCGTGGCCTTATTCAAGCTCAGTTTCGGGGGAATACCTTTGCCTGGCAAACCTGGGACGTTTCTTCATGAAAATTTCCATGGCTGCATAGAGAACCTCAACTA[C/A]AACGGCGTCAATGTCATCGACATGGCAAAGAGACGAAAGCCACAGATTTATACCGTGGTAAGTTTGAAGTTGAACAATCGCAATTACAAGTGAAACTGTAAATAACACTTTTCAACATGCCCGTCTATTGTAAGAATCAAACACCACCCTAGCTTGTTTGTTTGAAAATCATCAAATCCCACTCGCTGTCAAAGTTGAGATTCGAAATCTTGCTTTTCACAAGTCAATGTGAGACCACACTTTGTTGACGTTTTTGTTGCGTTGCCACTTAAACAACTTCATTCACACAACATGCATTTATATCCGGTGCAATTTACAACCATGTCACTTGGCAAATTACAGTAGCTCAGTGTGTATTGCAGTTGTGTGAAGTTGTGTGCATCGCACCATAAAAGAGCTCTCTTTCTCTAATTAACAGGCTGTGAAGTCTCTCGTCTTGTCCATTTCTCTCGCACGCTCTCCGGGTGGTTTAATACACTTATCACAGACAGGAAAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8838
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Nonsense | 348 | 1310 | 7 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34351027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33251964 |
GRCz11 | 11 | 33514766 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAGAAYCTCAACTACAACGGCGTCAATGTCATCGACATGGCAAAGMGA[C/T]GAAAGCCACAGATTTATACCGTGGTAAGTTTGAANNNGAACAATCGCAWT
Long Flanking Sequence:
TTTTTTTTTTTTTTTTTCCAATCTTGACAAGAGCAGCAAAGTTTATAATTTTCTTATGGAGATTTTGAGTGCCTATTTGATACTTTGTACCATTACTGTCAGGGTGCAGCACTCAAAATAACTAGGGAATGTGCAGCAATGCTATTAAAATACAAAACTATTAAAACCGGATAGACAATTGTTTCAATTGGTCTCAGTTTTTACATAATAAATAGTTGTAATTCATGGATAAAAAAACAGGTTACAGGTTAAAGTAGTCTCTTGTCTGCTATACAAGCAGTATTGTTACTGATCTCTGGGATATGTGTTTGCTTTGTGTCTTTGTTTGCTTGTGTGTGTGTGTGTGTTTGTGTTTCTGTGTTTGCGTGGCCTTATTCAAGCTCAGTTTCGGGGGAATACCTTTGCCTGGCAAACCTGGGACGTTTCTTCATGAAAATTTCCATGGCTGCATAGAGAACCTCAACTACAACGGCGTCAATGTCATCGACATGGCAAAGAGA[C/T]GAAAGCCACAGATTTATACCGTGGTAAGTTTGAAGTTGAACAATCGCAATTACAAGTGAAACTGTAAATAACACTTTTCAACATGCCCGTCTATTGTAAGAATCAAACACCACCCTAGCTTGTTTGTTTGAAAATCATCAAATCCCACTCGCTGTCAAAGTTGAGATTCGAAATCTTGCTTTTCACAAGTCAATGTGAGACCACACTTTGTTGACGTTTTTGTTGCGTTGCCACTTAAACAACTTCATTCACACAACATGCATTTATATCCGGTGCAATTTACAACCATGTCACTTGGCAAATTACAGTAGCTCAGTGTGTATTGCAGTTGTGTGAAGTTGTGTGCATCGCACCATAAAAGAGCTCTCTTTCTCTAATTAACAGGCTGTGAAGTCTCTCGTCTTGTCCATTTCTCTCGCACGCTCTCCGGGTGGTTTAATACACTTATCACAGACAGGAAAATAAGGAAGAGCAATGTCACATAGTGATCTTCATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21941
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Essential Splice Site | 495 | 1310 | 9 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34357764)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33258701 |
GRCz11 | 11 | 33521503 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCACTGGACGTAGCCAAACCCCCCAGAGAACAACCATCTACATTGGAG[G/A]TACAGCATTAGAAATGCAAAAAGTCAGTTTATTCTTACTAGCTGTATTCA
Long Flanking Sequence:
ACCCCTTCACGTGAACGTGCAAAACGAGGGGTACGGCTACACTGCAAAGTAATCTTGTTTTTCCTTTTGACTCCTTTTGAATATTTTGCTTAACCCATTGGCAGATTATTTTGCTTGTTTTAAGGAAACACTCACTTAATTTTAGGCATATTTTTTCTATAACAATACAATATGTTTTTCTATAACAATACAATATGCATGATTTAAGAATTTTTAGATTTTTGGACAAGAAACAAGACAAAAAAGTAAGAAAAGCATTTTTTCCAGTGTAAGGGGTAGAATTGGGTTTGGGCCTAAATTATATATTCACTTTCATTCTACCTTATATACCCTGTCTCTTTGTGTTACAGGTCAGAATTTAAATGATGGACAGTGGCACTCCATATCCGTTGAGGTCAAAGGTGAGAAGGTGTCTTTAACAGTCAACAACCAAAAGCCTGCCACCATGGAAATCACTGGACGTAGCCAAACCCCCCAGAGAACAACCATCTACATTGGAG[G/A]TACAGCATTAGAAATGCAAAAAGTCAGTTTATTCTTACTAGCTGTATTCAAATTTAGAAATAGTAACTTATTTTGATCTATTATCTACAAAGCTCAGTTCTGAACTAGCCTAATAGCTGCGGGCAAAGAGCAGTTATTATCCGAAACATTTTCCTGAATGCAAGGGACAATTTTCTTCTACATTATTAACTCTAACCTCCATCAACCAAACGTTCCTCATATTCCTGAGTAAAATACAGGCTTGACAAGCTGAGAGCATTCTTAGAGTCTATTCATTTCACACGTACAGCTGTTATTCCCAAATGTCCTTCTTTTTTTTCTGCCTTTTTTAGTTCATTCTGGCAGCTTTAACCACATTCAATTACTGTAGAGGATAAACGCGTTTTCTTTAAAGCTGTTGCTGAAATCTCTGACTCAAAACTTCCAATGTCTTAACTAAGACCGCTAAATCTCTCATTTTGCTTGCTTCTGGGACAATGCTGAGTCCTGCTGAGATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13789
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Essential Splice Site | 553 | 1310 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34358554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33259491 |
GRCz11 | 11 | 33522293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGGCAACTTTAGCCAGATTAGCTTTGATGTTTGCAACATACAAGWTAG[G/A]TCTGTTTCMCTGTGTGTGCNNGTGTGTGTGTCTGTGTTTATGTGAATCAT
Long Flanking Sequence:
CTGTTATTCCCAAATGTCCTTCTTTTTTTTCTGCCTTTTTTAGTTCATTCTGGCAGCTTTAACCACATTCAATTACTGTAGAGGATAAACGCGTTTTCTTTAAAGCTGTTGCTGAAATCTCTGACTCAAAACTTCCAATGTCTTAACTAAGACCGCTAAATCTCTCATTTTGCTTGCTTCTGGGACAATGCTGAGTCCTGCTGAGATTTTATAAGCTGCTTTGCATGAATTCCTCAGAACAGAGATTTGTCTTTGTGCGACTTGGTATTAGTTGTGGATGTTGTTTTTGATTTAAAAGACAGTAAGTTGGAATTTTCCATTATTTTAGGCTGCCCTTTATTCCAGAGCAATTTCAACTGTGAGAACCCCGGCAGAGGATACCAGGGCTGCTTTCGTCTCCTTTTAATCAACAACCATCCGGTCAACTTCCTTCAGATCCAACAGGAAAACATGGGCAACTTTAGCCAGATTAGCTTTGATGTTTGCAACATACAAGATAG[G/A]TCTGTTTCACTGTGTGTGCGTGTGTGTGTGTCTGTGTTTATGTGAATCATCTGCATGAAATGTACAGATCTGTTTCATCTCTGTTAGAGGTCTGTGATATTGACAAAAACATACACTCACCGGTCACTTTATTAGGTACATCTGTCCAACTGCTCCAAATTCCTAATCAGCCAATCACATGGCAGCAGGTCAATGCATTTAGGCATGGTCAAGATGTTCTGCTGCCGATCAAACCGAGCATCAAAATAGGGAAGAAAGGTGATTCAAGTGACTTTGATCGTGGCATGGTTGTTGGTGCCAGATGGGCTGGTCTGAGTATTTCAGAAACTTCTGACCTACTGGGACTTTCACACACAACCATCTCAAAGGTTTACAGAGAATAGTGCAAAAAAGAGAAAATATCCAGTGAATGGCAGTTTTGTGGGCACAAATGCCTTGTTGATGCCAGAGGCTAGAGGAGAAAGGCCAGATTGGTTTGTGCCGATAGAAAGGCAACAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14172
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111193 | Essential Splice Site | 921 | 1310 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34373505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33274442 |
GRCz11 | 11 | 33537244 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGGCTTTGTAAATTGCCRAGACAAYTAATCATTGTAATCTCCCCATTA[G/T]GAGGAACGGCTTCAAGGCAGAGGGGCTTCGTGGGCTGCTTACGCGCKCTC
Long Flanking Sequence:
TAAAGTTCATCTTAATTTTCTTGTTTAAATTCACCCCATATAAATTGTTTGCAACCACTTACCATTTTTTTTTTTTTTAGCGCATGTTAATGTAAATAAAAGCAATATAGCAAAGACCTATATAACATTTTTAAGTATAACAGTGACAAATAGGAACATGTAAATCATTTAACGTTAGCCAGGATTTTAGGCAAGGCAAGGCAAGTTTATTTATATAGCACATTTCATACACAGTGGCAAATCAAAGTGCTTTACATAGACAAGAATAAGAGAAACAAGTTTTCAATAAACAAATTTTAATAAAACCTTTCCCACTAATTTATCTTTTACAGTTTACACTAAACTCTCAAATTATGTCAAAATGTGGTTAATTATGTCAGTAGATTGGGCACACATAGCACACAAATGGCATCGTTTCCTGAGAATGACACTATTATCGACTTCTAAGGGCTTGGCTTTGTAAATTGCCAAGACAATTAATCATTGTAATCTCCCCATTA[G/T]GAGGAACGGCTTCAAGGCAGAGGGGCTTCGTGGGCTGCTTACGCGCTCTCACCATTAATGGGGTTACCCTTGACCTTTTCGAACGTGCAAAGACCACCCCGGGGGTGAATTCAGGCTGCCCGGGTCACTGCACCAGTGACAGCGTCTGCCATAATGGAGGACGATGTGTTGAAGAGCGCAGCAGTTACGCCTGTGACTGCACACAAACAGCCTTCGATGGGCCACACTGCAGAAAAGGTGAGGTTACAATGGCTTCTGGGCAAATTCATAGGCTTTCATAGGCCTTAATGCACCAATCAAAATAAGCTGAATGAGAAGGGCACAATGGATTAAAGCATGACTGTTTCTCAATTCCAAGAATGCAGATAATGGACGTCCTTGCAATCTTGCTAATTTACCACAGAAGAACAAACTCGAGGGCTAATGTTTTTGACTTTAACTGTATATATACAGTAACATGCACAAAAGCTTTACAAATATACTTCGCACAATACAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9104
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 |
---|---|---|---|---|---|
ENSDART00000111193 | Nonsense | 1025 | 1310 | 19 | 24 |
Genomic Location (Zv9):
Chromosome 11 (position 34375845)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 33276782 |
GRCz11 | 11 | 33539584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCTTCAGTCCTGTATACTCTCCAKGAGCCATTTTCTGGGATACTAAAC[G/T]AGGAAGCCAGAAGWWCGCCGGCTGGTTTCCATGATGCAGAAGTTGCCAAG
Long Flanking Sequence:
GAATTCATTGAGGCTGGGCTGACAGGCTTTGGCAGAAAAGCTTTAACTGACAAATGGAATTTAATTACAGCGTCCATCCCTCTGCCTCAAACCCATCCAGGAGCCTGTCAGTCAGATTACCAATGTAATGGCTTTGTTTCTTTACAATGTGATGTCACAACGGGTCTGCTCCAGCCACGGGTGTTTACTGCTAACTAGAATAGATGACCAGAAAATGAGAAGAGACAGAGAAAATCAGGAGGACAGCGGTCTCAGCTGTGGCTGGGGAGGAAGCAATGCTAATGTTGTTGTTTTTTATAGCTCTAATAATGAAAAATAAGATGTTAGAGTTCATTGGTACGCTAAATTTGCATAGAGATGATGATGATGATGATGATTGCAGTGGAGTTACACGGAGATTGCTTTGTCTCTCCATGTCCATCACAGCTCTTGCAGCTTCTTTTGAAAGTGGGTCTTCAGTCCTGTATACTCTCCAGGAGCCATTTTCTGGGATACTAAAC[G/T]AGGAAGCCAGAAGATCGCCGGCTGGTTTCCATGATGCAGAAGTTGCCAAGTCTCAAGAGAAAGTGTCATTTGGGTTCTTGACGCGTCACGTGCCAGCCTTGATCCTGATGGCTCACACTCTGGACCAGAACTACATGGCTGTTATGCTCACATCAAACGGTACTAAATCAAACATTACTGAAGAACTTGCAAAATAATAGAGCTGTCACAATAGAGATTTTTCATTATATGATTATATGGCTAGAAGAATTCACGGTAACAACCAGTGTTGTCTAAGTTACTTAAAGTAATTGATTACAAGTTACTGATTACTACCCTGTTCCCAATTTGGTTGCGCAAGCCGCACACCTCCATTGGAAATAATAAACTTGTATGTGCAAAAGACGTGATATTTGAACGGCCCATAAGCTCCTATGCTTCTTTTTACACTTTTAGATGTTACCTTACCTTACCAATCCTGCACAAAAAAAAAAAATATATATATATATATATATATATAT
Associated Phenotype:
Not determined