ZMP
cntn2
Ensembl ID:
ZFIN IDs:
Description:
contactin-2 [Source:RefSeq peptide;Acc:NP_571521]
Human Orthologue:
CNTN2
Human Description:
contactin 2 (axonal) [Source:HGNC Symbol;Acc:2172]
Mouse Orthologue:
Cntn2
Mouse Description:
contactin 2 Gene [Source:MGI Symbol;Acc:MGI:104518]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41829 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19006 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9412 | Nonsense | Available for shipment | Available now |
sa41830 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35078 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41831 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21903 | Nonsense | Available for shipment | Available now |
sa12173 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41829
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 40 | 853 | 2 | 18 |
ENSDART00000103800 | Nonsense | 38 | 412 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24886566)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23725865 |
GRCz11 | 11 | 23963722 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGGGATGTGTGTGTGTCGGGTCATGACAGTGGGCCGGTGTTTGAAGAG[C/T]AGCCATCTAGTCTGATTTACCCAGAGGGGATGCCAGAAGGCAAGGTGACC
Long Flanking Sequence:
TAATACAAGGCTATATAAGCTTAAAAATAAGGGGAAATTATCATTGTTGTCATCTCAGATGGAAACATTGTAGCCAATCAAACGCTGCCTGGTAATTGTATTAATTGTATTAAATTGTATTTTTAATTTTTTTTTTTGTAAAAAGTCAGAGACTGTGTTTTGCTCGAATTGGCACGTGTTTCACTGGGCTTTTAAACTCAGGATTTAAATGAGAACAAGGGAACAATGGTATTTGAGGCTCACAGTTTGTCATTTCCATGTTCTGAACTCTTATTATTTAGCTATGCCTAGGCATATCCAGATTTTCATTCTATGGCTTTTTAACATTTAAAATTAGCTTTGGTGCACTGCATTAAACTGTGAATGCTTTGTGAAAGTGTACACCTCATTAGGTGTTTAACCTGTTTAGACTCTTTCTGAAAGACATTGTTTGTTACTTTTTTTTGGTAGGTGGGGATGTGTGTGTGTCGGGTCATGACAGTGGGCCGGTGTTTGAAGAG[C/T]AGCCATCTAGTCTGATTTACCCAGAGGGGATGCCAGAAGGCAAGGTGACCCTGAGCTGCCAGGCTCGCTCCAGCCCTGCTGCTGTTTACCGGTACTCACATCACATTTTTGTCATTTACACGTGAACGAACAAAACACGACCTTTACTTGCTTTGTATGACTCATAGTTAAACAAAAACCAACATATTTTACTAAATAGCATATTAAAATTAAATATTTTATGTGTTTGAAGTATCTGTTTAATAAAGCTGCTTTACAAAATTAGTAAAATATTCAAATATGTCAAATATTAATCCAATTTCAGTTAATTTCTGTTTTAATACATTTTTAAATAAAGTTTTGGTTTGTGATGGCTAAACTGAACTTTACAGTCTACATTGTGTCACATGATCCCTCAGAAAACTGGTTCTCAAATTTAAATAAATATATGGTTATTATTATTATTATTATTATTATTATTATTATTATTATTAGTGGTGTAACAGATAACAAATCTCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19006
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 109 | 853 | 3 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
ENSDART00000000486 | Nonsense | 109 | 853 | 3 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24888728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23728027 |
GRCz11 | 11 | 23965884 |
KASP Assay ID:
2260-4257.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTGATCAACAACCCTCAGAATGGGCGAGATGGCGGCTCGTACCAGTG[T/A]CTCGCAATCAACCGATGCGGCACCATTGTTAGCCGCGTCGCTAATCTCAA
Long Flanking Sequence:
GTTCCGATCTGTACGAATCACAGATCAACTGTGATCCATTAACACCCCTAATTATTATTAATGATTAAAAAAGCTGTGCTGCTTAATTTGTTTATGGAACATGGAATTTTTTTGCTATTTAGTACTTCTGATTTCCAAAGTGATTTCCAAAGTTTTTTATCATACTGTTTTTTTATATATATTATATAATTGAGATCCAGTTTTATATGTAATTTTGACAAAGAAAACTTGAAGATACAATGTATTTGATGAGAGCAGTTTTTAAGTAGATTATTGATATTTCAATAAAATCAATAAAAATATACTATATATATGGCAAATTGGTTATTGACTTTCCTTTACTCTGGTAATAAAGTCAGATCTTGTGTGTGATTTCCTCCCAGGTGGCGTGTGAATGGCACTGACATATCATTTGCTGAAGAGTCGCACTACACACAGGTTGCAGGAAACCTTGTGATCAACAACCCTCAGAATGGGCGAGATGGCGGCTCGTACCAGTG[T/A]CTCGCAATCAACCGATGCGGCACCATTGTTAGCCGCGTCGCTAATCTCAAGTTCGGCTGTGAGTAACCATTGTCCAAGTAGAAAACTGGGTCTTGTCTACTACTCGTGCTTGATTTATACTGTGCTTTCTTCCAGACCTGCATGATTTTCCCCCTGAGAGCAGAAGTCCTCAGACGGTCCATGAAGGAATGGGAACATTTCTTGCCTGCCAGCCACCAGCTCATTACCCAGGTAAACACACACACATATCAGTTAGCAAAACATTTCACTCTTTTTTTATTTCGTTAACTCTTGCATCCCTTCTGTTTGTTAGCTTTGTCCTACCGCTGGTTTATCAACGAGTTCCCTAACTTCATCCAGCCAGAAGCGGGCAGGTGGTTTGTTTCTCAGGTCACTGGTAACTTGTATCTTGCTAACGCGAGAGCCAATGACACGGGCAACTATTTCTGCTTCACCACCATCAACATGGATGTCAGCACCAAGAGCATCTTCAGCAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9412
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 109 | 853 | 3 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
ENSDART00000000486 | Nonsense | 109 | 853 | 3 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24888728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23728027 |
GRCz11 | 11 | 23965884 |
KASP Assay ID:
2260-4257.1 (used for ordering genotyping assays)
KASP Sequence:
CTTGTGATCAACAACCCTCAGAATGGGCGAGATGGCGGCTCGTACCAGTG[T/A]CTCGCAATCAACCGATGCRGCACCATTGTTAGCCGCGTCGCTAATCTCAA
Long Flanking Sequence:
GTTCCGATCTGTACGAATCACAGATCAACTGTGATCCATTAACACCCCTAATTATTATTAATGATTAAAAAAGCTGTGCTGCTTAATTTGTTTATGGAACATGGAATTTTTTTGCTATTTAGTACTTCTGATTTCCAAAGTGATTTCCAAAGTTTTTTATCATACTGTTTTTTTATATATATTATATAATTGAGATCCAGTTTTATATGTAATTTTGACAAAGAAAACTTGAAGATACAATGTATTTGATGAGAGCAGTTTTTAAGTAGATTATTGATATTTCAATAAAATCAATAAAAATATACTATATATATGGCAAATTGGTTATTGACTTTCCTTTACTCTGGTAATAAAGTCAGATCTTGTGTGTGATTTCCTCCCAGGTGGCGTGTGAATGGCACTGACATATCATTTGCTGAAGAGTCGCACTACACACAGGTTGCAGGAAACCTTGTGATCAACAACCCTCAGAATGGGCGAGATGGCGGCTCGTACCAGTG[T/A]CTCGCAATCAACCGATGCGGCACCATTGTTAGCCGCGTCGCTAATCTCAAGTTCGGCTGTGAGTAACCATTGTCCAAGTAGAAAACTGGGTCTTGTCTACTACTCGTGCTTGATTTATACTGTGCTTTCTTCCAGACCTGCATGATTTTCCCCCTGAGAGCAGAAGTCCTCAGACGGTCCATGAAGGAATGGGAACATTTCTTGCCTGCCAGCCACCAGCTCATTACCCAGGTAAACACACACACATATCAGTTAGCAAAACATTTCACTCTTTTTTTATTTCGTTAACTCTTGCATCCCTTCTGTTTGTTAGCTTTGTCCTACCGCTGGTTTATCAACGAGTTCCCTAACTTCATCCAGCCAGAAGCGGGCAGGTGGTTTGTTTCTCAGGTCACTGGTAACTTGTATCTTGCTAACGCGAGAGCCAATGACACGGGCAACTATTTCTGCTTCACCACCATCAACATGGATGTCAGCACCAAGAGCATCTTCAGCAAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41830
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 261 | 853 | 6 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24889426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23728725 |
GRCz11 | 11 | 23966582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCCCGCTGAGACATACGCTTTATCAGGGCAAACCGCACAGCTGGAATG[C/A]TTTGCCTATGGCAAGTAAGTCCCCCTTAACTCCTAGAGATCACTGCAGCA
Long Flanking Sequence:
TTTCTTGCCTGCCAGCCACCAGCTCATTACCCAGGTAAACACACACACATATCAGTTAGCAAAACATTTCACTCTTTTTTTATTTCGTTAACTCTTGCATCCCTTCTGTTTGTTAGCTTTGTCCTACCGCTGGTTTATCAACGAGTTCCCTAACTTCATCCAGCCAGAAGCGGGCAGGTGGTTTGTTTCTCAGGTCACTGGTAACTTGTATCTTGCTAACGCGAGAGCCAATGACACGGGCAACTATTTCTGCTTCACCACCATCAACATGGATGTCAGCACCAAGAGCATCTTCAGCAAAGCTGTCCAGCTCACAGTTCACCCTGATGGTTAGTTCAAAGCCTTATATTTCCTTCAGCAACAAGCTCAAAAACTGAATCTTATTTTTTTTTTTTTTGCTGTGTTTCTTCAGCAAGCCCAAGGAAAACTGCTCCAAATATCCGAGTGCGTTTTCCCGCTGAGACATACGCTTTATCAGGGCAAACCGCACAGCTGGAATG[C/A]TTTGCCTATGGCAAGTAAGTCCCCCTTAACTCCTAGAGATCACTGCAGCATCGCTTTAACATAATCCATATCGCAGTCAGCTATAAAAATGTAACCATTTTTTCCATCATGCTCTCACTTTTACTTTTCCTCCTTTAGTCCGATTCCTAAAATCCGCTGGAGGAAGGTGGATGGAATTTTACCCCCTAAGGTTGGAACAAGTGTGGATGGGCCCATCTTGATTATTCCTGAACTGAATTTCGATGACGAGGGCATGTATGAGTGTGAGGTTTACAACTCAGAAGGCCGTGAGACGCATCAGGGACGTGTTTCTGTGCAAGGTAGGCATAGTATTAGAAATAGACAGAAATATAAATATTTTTCTCATGAACATTAAGTAGGGCAACACGGTGGCTCAGGGGTTAGCACTGTCACCTCACAGCAAGAAGGTTCAAGCCCCGACTGGGTCAGCTGGCATTTCATTTCCTCCAGGTGCTCTGGTTTCCAAAGGCATGCGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35078
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 311 | 853 | 7 | 18 |
ENSDART00000103800 | None | None | 412 | None | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24889700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23728999 |
GRCz11 | 11 | 23966856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTGAACTGAATTTCGATGACGAGGGCATGTATGAGTGTGAGGTTTA[C/A]AACTCAGAAGGCCGTGAGACGCATCAGGGACGTGTTTCTGTGCAAGGTAG
Long Flanking Sequence:
GTCAGCACCAAGAGCATCTTCAGCAAAGCTGTCCAGCTCACAGTTCACCCTGATGGTTAGTTCAAAGCCTTATATTTCCTTCAGCAACAAGCTCAAAAACTGAATCTTATTTTTTTTTTTTTTGCTGTGTTTCTTCAGCAAGCCCAAGGAAAACTGCTCCAAATATCCGAGTGCGTTTTCCCGCTGAGACATACGCTTTATCAGGGCAAACCGCACAGCTGGAATGCTTTGCCTATGGCAAGTAAGTCCCCCTTAACTCCTAGAGATCACTGCAGCATCGCTTTAACATAATCCATATCGCAGTCAGCTATAAAAATGTAACCATTTTTTCCATCATGCTCTCACTTTTACTTTTCCTCCTTTAGTCCGATTCCTAAAATCCGCTGGAGGAAGGTGGATGGAATTTTACCCCCTAAGGTTGGAACAAGTGTGGATGGGCCCATCTTGATTATTCCTGAACTGAATTTCGATGACGAGGGCATGTATGAGTGTGAGGTTTA[C/A]AACTCAGAAGGCCGTGAGACGCATCAGGGACGTGTTTCTGTGCAAGGTAGGCATAGTATTAGAAATAGACAGAAATATAAATATTTTTCTCATGAACATTAAGTAGGGCAACACGGTGGCTCAGGGGTTAGCACTGTCACCTCACAGCAAGAAGGTTCAAGCCCCGACTGGGTCAGCTGGCATTTCATTTCCTCCAGGTGCTCTGGTTTCCAAAGGCATGCGCTATAGGTAAATTGAATACACTAAAGTGTCCATAGTGTATGTGTGTGAATGAGTGTCTAATGATGTTTCCCAGTACTGGGTTGTGGCTGGAAGGGCATCCGTTGCATAAAACATATGCGAGATAAGTTGATGGTTCATTCCTCTGTGGCACCCCCAAATTAATTAAGGGATAAGCCAAAGGAAAATGAATGAATGAATGAATGAACATTAAGTCGAAGCTTGATGCAATATAAACTTTGCGAGCAAGTGTGTTGTTGTTGTAGACAAAACTAAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41831
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 524 | 853 | 12 | 18 |
ENSDART00000103800 | Nonsense | 83 | 412 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24895113)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23734412 |
GRCz11 | 11 | 23972269 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGATGCCACAAAAATCACACTAGCGCCCTCTAATGCTGATATCAAT[C/T]AGGGTGAAAATGCCACTTTGCAGTGCCATGCATCACATGACCCTACCATG
Long Flanking Sequence:
TCGATTACATGGACTCTAATACACTGATAACTCACAAGATCACCTCACTTAAATAACATGTTGTGCTAGATTACATGCAAACCAATAAGTAAAACCTGTTTGATATATTTTATTAATTTATCAGTTTGATTTCCCCACAGTGATTTTGAAAACAAATCATTTGTATATCTAACAGTTGAGAATTTAATTTGTTATGTTGGTTGTCAAGATAAATAAATATTTACAAACTGAAGAAAAGTACTGTAACACTGGAAAACTTACATCTCATATTCCATCACATTTTGATTGTATCTTCTTGTGCTGCATGTGATAAGAACATGTTTATAAAAAAAGAGTCAAGTAATCATGAAAGAGTCTGCATGTAAACAAATTAAGACCTCTAAAATTATCATTTTAAGTAGTCATCAGCAAGTCATTGATGATACACATTGTTTTTAATTTTGTTCATTCAAACAGATGCCACAAAAATCACACTAGCGCCCTCTAATGCTGATATCAAT[C/T]AGGGTGAAAATGCCACTTTGCAGTGCCATGCATCACATGACCCTACCATGGACCTCACCTTCACCTGGTCACTCAACGGAGTTCCGCTGGACCTAGAGGAACCAAATGGACACTATCGGCGAATGGAGGGGGTGAGCACTTCTTGTCATTTCTCCAGGTGTTGTCCTGAAGAATAGATACAAAAGAAGTTTAAAAGGCTTATTGAACCCCTCTATAGTGTCATTTTTCACCATCAAATTAAAATGACATAATATTTCTGATTCAGCATGTCATGTTTTTTCCATGTTCATACAGGTCAATTTGTTGCAGATGTTTTTTATTTAGACTTATATTTAAACATATCATTTAAGCAGTATTTTTATTATGATTACTATTACATTCAGACTCAAATAATGTTTATTTAGTGTGATTGTAGTATGTGTTCAATGTGTTATTAGTTTAATATCAGCTGACAATGATTTAATAATCATAATGTTTATCCCATTCTTGTGGTCACCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21903
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 693 | 853 | 15 | 18 |
ENSDART00000103800 | Nonsense | 252 | 412 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24899036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23738335 |
GRCz11 | 11 | 23976192 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCGGCCCTGGATGGATTATGAGTTCCAGGTCATTGCCAGCAACATCT[T/A]GGGCAGCGGAGAACCAAGCATGCCTTCCCCGCGTGCACAAACCAAAGAAG
Long Flanking Sequence:
TAATTAATGTATTTAATGTATAATATAATATTATTATAATATAATATAGTATAATATAATAGTATTATTATTATTTTATATTTCTTTCTATTTTAATATGGTAATAATATATTAAGATATATTTTATTAATTCTTTTTTTATTCTCTTTTGTTTTGGTATCTTTATATTTTTCTAGTCTATTTTTCATTTATTCACTGTTACAGCCACTTTTCTGAATGATTGAACTAATCATACAATTACATGCATACATGTATTTGCTTGCTTACTTTACCCCATAAACTGCCTAAAGAAAAGCTGCCCAGGACACTTGTTTGAAAAATATAGTAGTATTATGACATCATATATAATGTTACCCTTAGTAATCGAATGCATACCTTTCATTTTGTGCTAATGCTTCCTCCAGACCCTGCAAACATAGAAGGAAATGCTGAATCTGCACGTGTGATAGATCTTCGGCCCTGGATGGATTATGAGTTCCAGGTCATTGCCAGCAACATCT[T/A]GGGCAGCGGAGAACCAAGCATGCCTTCCCCGCGTGCACAAACCAAAGAAGCAGGTCAGGACCGTTACACTTTTATTAGTGCTAAATAAAAATCCAAACAAACCGATGATAAACTATTATTGTGGTTCCAAACAATAACAAACTTGATTGATAGAAGGGTAATATTTTGTGTTACAGCACCAACTGTGGCTCCCAGTGGACTCGGTGGAGGTGGAGGAAACCGTAATGAACTTATTATTACATGGACTGTAAGTTCTATTTGTGTAATTTGATGTTAGAAATGCTTAATACTTTTTACTCTGTCCAGTATTTACACATTTTTCCTTGTGCCCCATGATGCCTAGCATGAATTATAGTTTCAACAATGTTTTAAACAACTGGTTTCAATGAGCTGTCATTTTTCCCCTCAAAGTCCTTCCATTGATTATTAAACTTATTAGAATGAACAAATTGCTTTCAAACCTGAAAAAAAAGTCTTTCTGCAAAAATATTACAGTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12173
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 |
---|---|---|---|---|---|
ENSDART00000000486 | Nonsense | 775 | 853 | 17 | 18 |
ENSDART00000103800 | Nonsense | 334 | 412 | 9 | 10 |
Genomic Location (Zv9):
Chromosome 11 (position 24900509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 23739808 |
GRCz11 | 11 | 23977665 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATGGACGGTGGTGAAGGTGCCAAATGTGGAGTCATCTCGATATGTGTA[C/A]AGCAATGACAGTCTGACAGCATACTGCCCGTTCGAGGTCCGAATCAAGGC
Long Flanking Sequence:
GTAGGGAATACAAAGAGAAAATAATCCAGAGAAACAAATACAGTGAACTCAAAACAGCTTTGTCCACAGATAAGTTTGTTACATTAATGTCACATTCAAATAGCAAGCGTAATATTGTTTTCATGACTGTAAGATTAGACTTCGTGCTTTATATTTATCAGAGTATATTGATTATTTTTTGCACAAACTTAATGTTTCAAATGATTTGTTTTAATTCATTTAAATATACGTTCCTCAACCTGGAAGTGCAACCAGTAATTTGAAACACAGTATTCACATTTGGGAAAAAGATGTGTAGAATTGCAAACAGAAGGTCAATAGATGTGTCTTTATTACCCTCAACAAAGAAATTAACATTTCTGCTGGTATGCATCACAGCCCATGGCCAGAGAGTATCAGAATGGAGACAGTTTTGGTTATATCCTGGCATTCAGAAAGCAAGGCATACCAACATGGACGGTGGTGAAGGTGCCAAATGTGGAGTCATCTCGATATGTGTA[C/A]AGCAATGACAGTCTGACAGCATACTGCCCGTTCGAGGTCCGAATCAAGGCCTACAACAAGAAAGGAGAAGGGCCCTTCAGCCAGATTGCTGTAGTACACTCTGCGGAGGAGGGTGAGGGTTATTACTGAGGATTTTATTTTTATGGATATAATTATAGAATTTATTATATTCTGATTGAATGTTACTTAACCCCTAAAGGGCAGACATAGGAGATTACCTAATTAAAAGCTTAAATTGTTTCAAGAAAGCAAAATTATCACATTTATTTAAATGATGTTATTTCTTTTATACTATGAAATGCCATAAAGGTCTATCAATTGACTGGTTAATTTACATTAACTAGATCATTTAAAAAAAAAACACGCACACAAATTTTGATTTAAATGAAATGTTAATGAAATTGTTTTCATTTAAATTGAGAGATTTCTGTATTTCCATTGAAATTATGTTGACCAAAAATGCATGAATCAAGCAACTATTTTTTAAATAATTAAAACAG
Associated Phenotype:
Not determined