ZMP
ptpn20
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens PTPN13, protein tyrosine phosphatase, non-receptor type 13 (APO-1
Human Orthologues:
PTPN20A, PTPN20B, PTPN20C
Human Descriptions:
protein tyrosine phosphatase, non-receptor type 20A [Source:HGNC Symbol;Acc:23422]
protein tyrosine phosphatase, non-receptor type 20B [Source:HGNC Symbol;Acc:23423]
protein tyrosine phosphatase, non-receptor type 20C [Source:HGNC Symbol;Acc:23424]
protein tyrosine phosphatase, non-receptor type 20B [Source:HGNC Symbol;Acc:23423]
protein tyrosine phosphatase, non-receptor type 20C [Source:HGNC Symbol;Acc:23424]
Mouse Orthologue:
Ptpn20
Mouse Description:
protein tyrosine phosphatase, non-receptor type 20 Gene [Source:MGI Symbol;Acc:MGI:1196295]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13082 | Nonsense | Available for shipment | Available now |
sa7227 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42230 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28137 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16981 | Essential Splice Site | Available for shipment | Available now |
sa17567 | Essential Splice Site | Available for shipment | Available now |
sa17079 | Essential Splice Site | Available for shipment | Available now |
sa35525 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42229
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 |
---|---|---|---|---|---|
ENSDART00000111705 | Nonsense | 664 | 1925 | 19 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31407531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31053479 |
GRCz11 | 13 | 31183929 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAACATTCTATGTGACTTCAGTGATTTGACTGTAATCATCCGAAGCTA[C/T]AAGAACACCTTTGTGCACCAAAAATTGTAAATACGACTTTATTTGCCATT
Long Flanking Sequence:
TCATCCAGGGCGTTATGGTGGCGTAGTGAGTAGAACAGTCACCTCACAGCAAGAAGGTTGCTGGTTCTAGTCTCGGCTGGGTCAGTTTGCATTTCTGTGTGGAGTTTGCATGTCTCCCCGTGTTGGCGTGGGTTTCCACAGGGTGTTCCGGTTTCCCCCACAAGTCCAAAGACATGTGGTATAGGTGAATTGGGTAAGCTAAATTGTCCGTAGTGTTTGTGTGTGCTTGAGTGTGTATGGATGTTTCTCAGTGATGGGTTGTAGCTGGAAGGGCATCTGCTGCGTAAAACATAAGCTGAATAAGTTGGCGGTTCATTCCGCTGTGGCAACCCCAGATTAATAAAGGGACTAAGCTGAAAAGAAAATCAATGAATGAATGAGCTCCCTCATCCTCCATGCACAGCAACTGTCCACAGATATTCAAAGTCCAAAAAAGCTATCAAAACATGGCTAAACATTCTATGTGACTTCAGTGATTTGACTGTAATCATCCGAAGCTA[C/T]AAGAACACCTTTGTGCACCAAAAATTGTAAATACGACTTTATTTGCCATTTTTTTCTCTTCCTCATCTGGTTGCCAAAGTGCGTCTTTACTAAGAGCATAACATACTGCCATTAGAGTCAGCAGCGAAACACATAAGCAATGTTTTGCTTAGAGTAAATGCTAAGCCTGATCTAATGTGGGAGACATAAGTGAACAAAGTCCTTTTTACCATTTTTGGCGCAAAATATTGTTCGGGGAGCTTTGCATGATTGCAGTCGAGCAACTGAAGTCAAATAGACTGTTTTGATATATTTATTTTTAGTTTCTTTTGTGGGCTTTGAACATCTCAGTTCTATAAAGTATGAGGGAACTCTCTGATTTTACATAAAATATCCTTATTTGTAATTTAATGTTGATCAAATGTCTCAGACGATTGAAACAACATTAGGGTGAGTAATTAATTACTAACAGAACTTTTCATTTTGGGTGAAACTAATCCTTTAAACCTAAAACAACTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13082
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 |
---|---|---|---|---|---|
ENSDART00000111705 | Nonsense | 692 | 1925 | 20 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31408064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31054012 |
GRCz11 | 13 | 31184462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCTAAAACAACTSTCAGTCAATATCTTCATGCTTTTTTTCATGAGTW[G/T]AGGATCTTCGGGGCAGCAAGACTTCACTGGCTCCAAGTAATTTAGGAATG
Long Flanking Sequence:
ACGACTTTATTTGCCATTTTTTTCTCTTCCTCATCTGGTTGCCAAAGTGCGTCTTTACTAAGAGCATAACATACTGCCATTAGAGTCAGCAGCGAAACACATAAGCAATGTTTTGCTTAGAGTAAATGCTAAGCCTGATCTAATGTGGGAGACATAAGTGAACAAAGTCCTTTTTACCATTTTTGGCGCAAAATATTGTTCGGGGAGCTTTGCATGATTGCAGTCGAGCAACTGAAGTCAAATAGACTGTTTTGATATATTTATTTTTAGTTTCTTTTGTGGGCTTTGAACATCTCAGTTCTATAAAGTATGAGGGAACTCTCTGATTTTACATAAAATATCCTTATTTGTAATTTAATGTTGATCAAATGTCTCAGACGATTGAAACAACATTAGGGTGAGTAATTAATTACTAACAGAACTTTTCATTTTGGGTGAAACTAATCCTTTAAACCTAAAACAACTGTCAGTCAATATCTTCATGCTTTTTTTCATGAGTA[G/T]AGGATCTTCGGGGCAGCAAGACTTCACTGGCTCCAAGTAATTTAGGAATGATGCTAGAAAGAAGCTTTGGCTCCCAAAGCACACTGAGCGCCGAGTACAGACCTGTGATGGAGGAGCTGGAGGAGACCCTCTCCAACATCATGGCCCCTAAAATCAACAAACGGATGCACATACCTGTGGTCCGCATTCTGGATATTCAGGTGATTTATAGTAATGCAGTTAACTTCTGGAATGTATCAAAACTAATCACTTTTTTAATGTGAAGACCCTCTTGGCAAAGCTTTGTTAATTTTTTTTTATTCTTCATCCTTTCCAGGACGAGATGTCTAAAAGTTCTTCTGGCTTCAGTTTGAAACCAGGTGAAATAATCTACATGGAGCTCCGAAAGATCAACGGCAGTTTGGGAATCAGTGTTGCTGTGAGTTTTCACTCTGAATGGCATTCATGTGAGTTCTGAAATATTGAAACATGGAGAGTGATACCATTATTTTGATTTCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7227
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 765 | 1925 | 21 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31408328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31054276 |
GRCz11 | 13 | 31184726 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCAGTTAACTTCTKKAATGTATCAAAACTAAYCACTTTTTTAATKTGA[A/G]GACCYTCTTGGCAAAGCTTTGTTAATTTTTTTTTATTCTTCATCCTTTCC
Long Flanking Sequence:
TTTTAGTTTCTTTTGTGGGCTTTGAACATCTCAGTTCTATAAAGTATGAGGGAACTCTCTGATTTTACATAAAATATCCTTATTTGTAATTTAATGTTGATCAAATGTCTCAGACGATTGAAACAACATTAGGGTGAGTAATTAATTACTAACAGAACTTTTCATTTTGGGTGAAACTAATCCTTTAAACCTAAAACAACTGTCAGTCAATATCTTCATGCTTTTTTTCATGAGTAGAGGATCTTCGGGGCAGCAAGACTTCACTGGCTCCAAGTAATTTAGGAATGATGCTAGAAAGAAGCTTTGGCTCCCAAAGCACACTGAGCGCCGAGTACAGACCTGTGATGGAGGAGCTGGAGGAGACCCTCTCCAACATCATGGCCCCTAAAATCAACAAACGGATGCACATACCTGTGGTCCGCATTCTGGATATTCAGGTGATTTATAGTAATGCAGTTAACTTCTGGAATGTATCAAAACTAATCACTTTTTTAATGTGA[A/G]GACCCTCTTGGCAAAGCTTTGTTAATTTTTTTTTATTCTTCATCCTTTCCAGGACGAGATGTCTAAAAGTTCTTCTGGCTTCAGTTTGAAACCAGGTGAAATAATCTACATGGAGCTCCGAAAGATCAACGGCAGTTTGGGAATCAGTGTTGCTGTGAGTTTTCACTCTGAATGGCATTCATGTGAGTTCTGAAATATTGAAACATGGAGAGTGATACCATTATTTTGATTTCTAGGGTGGGATCAACACTAATGTACATCATGGAGGAATCTACATCAAAAGTGTGATAGCAGGAGGAGCGGCAGATCAAGATGGAAGAATACAGATAGGTTAAGATCCATCATTATTTATAAGACAAAGATGCTCAGTGTTCTGAACTCAAACTAATCTGCTGGTCACACTTTTTTGGAATAATGTTACATTTTGTTTTTGTAAGTAAATCAACATTTTATTCTTGATTACCAAGGCTGTTTATTTGTTCCAAAATGCATGAAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42230
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 |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 1030 | 1925 | 27 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | Essential Splice Site | 82 | 286 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31416983)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31062931 |
GRCz11 | 13 | 31193381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATCTGCAGACCTTCACAGGATGAGCATACAGATATTGAGACCTTTCTG[G/A]TAACATCCTCTTCCTTCATGTTTGCAAACAATTTTAAAATTTGACGTCTC
Long Flanking Sequence:
TAAAATATATATTGTAGTAACACAAATGAATAAAGTGATACATAACCACAGTAAACGTGTATTTTTAATGTTTTCTTTCTATTTTCTTTCGTTTAGACTTTCCAAAAACATTATAAGGACCAATTTTTCAGATTTTTAACTGCAATGTTTAGTCTTGAACAGCACAACTGGTTTTAACAGCACAACTGGTTTTAACATTGACAACAACATCCAATGAATCTTAAGCACATATTCAGCATATTAGAATGACTTATGAAGGAACACATGACACTTAAGGCTAATGTTTATAATCATAATGCTGTACTGTATAAATGCAGCCGAGCAATAAATGAGAGAATTCATTTTAAAACAATCTTACAACCCCAAATATCTTTACTATAATGTACAACTTTCTTTTCACACAGGAGGTTCTGCATCTCCTCCAAAAATCTCCATCTGAGATCAGACTGTCAATCTGCAGACCTTCACAGGATGAGCATACAGATATTGAGACCTTTCTG[G/A]TAACATCCTCTTCCTTCATGTTTGCAAACAATTTTAAAATTTGACGTCTCAAACTGACATCCCTTTTTGACAGGTTCCAAACCGTGAACTGAGATCCAGATCTCTCGACCTACAAGCGAGGTCTGTGGCTCCAGATTTCAGTGAGCTCCTCTTGAGGCGGGCGATAGAGATGGGGCTTAAAAAAGAAGCTTCACCTGAGGAAACCCAGGAGAGTGAGCTGCTGGAAACAGATAAATCAATTCCTCCACCTCTACCTCCACGTCCATCTTCTGCTGAAGGTGGAGAAAGAAAACCTCATGTCATTCTAGTGGAGGAGTATGAGAAGAAAGACCCGCCTCCTCCTCCGACTCCTCCTCCAACACCAGGCATTCTTAAAGCGTCAACAACCAACACTGTGCAAACCCCAGCAGCACCTAAAACTGCAATTAAAGCCCATCAGCAAGAGTCACTCGAACCAACTGTCTCTAGAAGCAACCATGTCTCAGCATGTACGAGGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28137
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 |
---|---|---|---|---|---|
ENSDART00000111705 | Nonsense | 1161 | 1925 | 30 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31420319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31066267 |
GRCz11 | 13 | 31196717 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGATGACGAAGAGGATGATGAAGATCCCAGAAGGGTGAAGCCTGATTG[T/A]ATTTCCTGTAGACATGTGGAATACTCTTTAATTAGAGATGCCTAATTTGT
Long Flanking Sequence:
TAAAGAGATTTCAGAAGCTGCATAGCTACTTTTTGTATGTGTAAATAGATAACCGACAAAATCCTGTTTCACCTTTTGCATGTGCTTTATAAGATTTTTTCTTTGCTTCATTCAAAAAATAGTCATGATCAATTATTCAAATACATTGGCACGGAAAAACATGACTTCACATTATCTCTTCACAGTCACGTGAAAGATGAAGGAGTGGAAGAGAACGTGATAAGTTTCACAGCTAATGGTCTGACCGTCACTGCTGGTGAAGAATACCTGACCATCAGCACTACGGCTCCATCTCCCCCGAGCGGCAGCACTGCAGTCTCCTCTGAAGCTCCTCCTCCTGTGCCTGCACTTTCTCCATCACTGCTGAACACACCTCCAACATACCAGCAGGCCATTCAAGCAGCATCTCCAGCAGAGCCTCCTGCCCAGCCCAGCAACAACGGCTGGGATGATGATGACGAAGAGGATGATGAAGATCCCAGAAGGGTGAAGCCTGATTG[T/A]ATTTCCTGTAGACATGTGGAATACTCTTTAATTAGAGATGCCTAATTTGTCTCTTAGTTTTTTTTTTTAATCTAACTTTGGAGCAAGTAGATTTTATAAGAGGTTGTTTAGAGAAAAAAAAATTTAAGTATAAAAAATAAAAATATTAACGAATAATTTAACAGGCATTAGGAGAAAATAAACAAATTCAATTGAAATAGTTGTAATTATAAAAAAAAAGAAAATTAAATAATATTCAAAGAAATTATCTAAATTGGTTTTATTAGATTAAAATTTATAATAGAATTTGAGTTAAATGAATAAATGTATAAAATTATGCTAAATGTAAAAAAAAATAAACAAATGTACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGTAAGTTTCTAATTAGCCAATCACATGGCAGCAACTCAACTCAATGCATTTAGGCATGTAGATATGGCACACATTCCTGGCACACTTTCAGCCCATTAGTACTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16981
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31420389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31066337 |
GRCz11 | 13 | 31196787 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAYTCTTTAATTAGAGATGCYTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGRTTTTATAAGAGGTTGTTTAGAGAAAAAAA
Long Flanking Sequence:
ACCTTTTGCATGTGCTTTATAAGATTTTTTCTTTGCTTCATTCAAAAAATAGTCATGATCAATTATTCAAATACATTGGCACGGAAAAACATGACTTCACATTATCTCTTCACAGTCACGTGAAAGATGAAGGAGTGGAAGAGAACGTGATAAGTTTCACAGCTAATGGTCTGACCGTCACTGCTGGTGAAGAATACCTGACCATCAGCACTACGGCTCCATCTCCCCCGAGCGGCAGCACTGCAGTCTCCTCTGAAGCTCCTCCTCCTGTGCCTGCACTTTCTCCATCACTGCTGAACACACCTCCAACATACCAGCAGGCCATTCAAGCAGCATCTCCAGCAGAGCCTCCTGCCCAGCCCAGCAACAACGGCTGGGATGATGATGACGAAGAGGATGATGAAGATCCCAGAAGGGTGAAGCCTGATTGTATTTCCTGTAGACATGTGGAATACTCTTTAATTAGAGATGCCTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGATTTTATAAGAGGTTGTTTAGAGAAAAAAAAATTTAAGTATAAAAAATAAAAATATTAACGAATAATTTAACAGGCATTAGGAGAAAATAAACAAATTCAATTGAAATAGTTGTAATTATAAAAAAAAAGAAAATTAAATAATATTCAAAGAAATTATCTAAATTGGTTTTATTAGATTAAAATTTATAATAGAATTTGAGTTAAATGAATAAATGTATAAAATTATGCTAAATGTAAAAAAAAATAAACAAATGTACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGTAAGTTTCTAATTAGCCAATCACATGGCAGCAACTCAACTCAATGCATTTAGGCATGTAGATATGGCACACATTCCTGGCACACTTTCAGCCCATTAGTACTAATTGGGCATCATGTAAATGCAACAGCCTACCTCAGGATTGTTGACGACCATGTCTATCTATGACCACAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17567
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31420389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31066337 |
GRCz11 | 13 | 31196787 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAYTCTTTAATTAGAGATGCYTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGRTTTTATAAGAGGTTGTTTAGAGAAAAAAA
Long Flanking Sequence:
ACCTTTTGCATGTGCTTTATAAGATTTTTTCTTTGCTTCATTCAAAAAATAGTCATGATCAATTATTCAAATACATTGGCACGGAAAAACATGACTTCACATTATCTCTTCACAGTCACGTGAAAGATGAAGGAGTGGAAGAGAACGTGATAAGTTTCACAGCTAATGGTCTGACCGTCACTGCTGGTGAAGAATACCTGACCATCAGCACTACGGCTCCATCTCCCCCGAGCGGCAGCACTGCAGTCTCCTCTGAAGCTCCTCCTCCTGTGCCTGCACTTTCTCCATCACTGCTGAACACACCTCCAACATACCAGCAGGCCATTCAAGCAGCATCTCCAGCAGAGCCTCCTGCCCAGCCCAGCAACAACGGCTGGGATGATGATGACGAAGAGGATGATGAAGATCCCAGAAGGGTGAAGCCTGATTGTATTTCCTGTAGACATGTGGAATACTCTTTAATTAGAGATGCCTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGATTTTATAAGAGGTTGTTTAGAGAAAAAAAAATTTAAGTATAAAAAATAAAAATATTAACGAATAATTTAACAGGCATTAGGAGAAAATAAACAAATTCAATTGAAATAGTTGTAATTATAAAAAAAAAGAAAATTAAATAATATTCAAAGAAATTATCTAAATTGGTTTTATTAGATTAAAATTTATAATAGAATTTGAGTTAAATGAATAAATGTATAAAATTATGCTAAATGTAAAAAAAAATAAACAAATGTACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGTAAGTTTCTAATTAGCCAATCACATGGCAGCAACTCAACTCAATGCATTTAGGCATGTAGATATGGCACACATTCCTGGCACACTTTCAGCCCATTAGTACTAATTGGGCATCATGTAAATGCAACAGCCTACCTCAGGATTGTTGACGACCATGTCTATCTATGACCACAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17079
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
ENSDART00000111705 | Essential Splice Site | 1167 | 1925 | 31 | 50 |
ENSDART00000132326 | None | None | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31420389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31066337 |
GRCz11 | 13 | 31196787 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAYTCTTTAATTAGAGATGCYTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGRTTTTATAAGAGGTTGTTTAGAGAAAAAAA
Long Flanking Sequence:
ACCTTTTGCATGTGCTTTATAAGATTTTTTCTTTGCTTCATTCAAAAAATAGTCATGATCAATTATTCAAATACATTGGCACGGAAAAACATGACTTCACATTATCTCTTCACAGTCACGTGAAAGATGAAGGAGTGGAAGAGAACGTGATAAGTTTCACAGCTAATGGTCTGACCGTCACTGCTGGTGAAGAATACCTGACCATCAGCACTACGGCTCCATCTCCCCCGAGCGGCAGCACTGCAGTCTCCTCTGAAGCTCCTCCTCCTGTGCCTGCACTTTCTCCATCACTGCTGAACACACCTCCAACATACCAGCAGGCCATTCAAGCAGCATCTCCAGCAGAGCCTCCTGCCCAGCCCAGCAACAACGGCTGGGATGATGATGACGAAGAGGATGATGAAGATCCCAGAAGGGTGAAGCCTGATTGTATTTCCTGTAGACATGTGGAATACTCTTTAATTAGAGATGCCTAATTTGTCTCTTAGTTTTTTTTTTTA[A/C]TCTAACTTTGGAGCAAGTAGATTTTATAAGAGGTTGTTTAGAGAAAAAAAAATTTAAGTATAAAAAATAAAAATATTAACGAATAATTTAACAGGCATTAGGAGAAAATAAACAAATTCAATTGAAATAGTTGTAATTATAAAAAAAAAGAAAATTAAATAATATTCAAAGAAATTATCTAAATTGGTTTTATTAGATTAAAATTTATAATAGAATTTGAGTTAAATGAATAAATGTATAAAATTATGCTAAATGTAAAAAAAAATAAACAAATGTACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGTAAGTTTCTAATTAGCCAATCACATGGCAGCAACTCAACTCAATGCATTTAGGCATGTAGATATGGCACACATTCCTGGCACACTTTCAGCCCATTAGTACTAATTGGGCATCATGTAAATGCAACAGCCTACCTCAGGATTGTTGACGACCATGTCTATCTATGACCACAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35525
Status:
Mutation detected in F1 DNA
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111705 | Essential Splice Site | 1673 | 1925 | None | 50 |
ENSDART00000132326 | Essential Splice Site | 287 | 373 | None | 10 |
ENSDART00000133774 | None | None | 205 | None | 4 |
ENSDART00000137664 | None | None | 94 | None | 3 |
ENSDART00000144568 | None | None | 128 | None | 3 |
ENSDART00000147085 | None | None | 89 | None | 3 |
ENSDART00000147936 | None | None | 286 | None | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 31437143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 31083091 |
GRCz11 | 13 | 31213541 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGCCCTCGAGCAGCTAGAAAAGCAAGATCTGGTCAAAGAGTTTATGG[T/A]AAGTTCTGGTCAGCATCAGTATAATGTATATATAAAGCATATAGCACATT
Long Flanking Sequence:
AGAGATGTTCTCTCTCAGGTGTGGTTAATGACCTATGAGTGGTTACTGTTACTGTCACAACAGAGTTACGCTTGTCTTTCTGTTAGCTTAACCAGTCTCAACAAGTCATTTATGTAGCTCCCACAGCCATATTTCTCCTTTTTGAACAATTTTCTGTAAAATGTAGAAATAGTTGAACTGTATGTGATCTTTTTCTATTTAAATCAGCATGTCTGACAAAGTTACTGAAATTAAAAAGTTACTTACAAAGTCACTTAAATCACCCTTTCCACCATTCTAGCCACCCATCCATCTATATATGCAGTTAAGATCAATCATGTCATCTAAACTAAAACAATCTGCAATACATCCAGGTCGGCCAATCGTGTCAGAAGAGGAGCTTTCCAGTCTTGCAGTGATTTCTCCTCCTAAGAATGGGCAGTACACCGGCTCCAGGGTCAAAGCCCTCATCCAGGCCCTCGAGCAGCTAGAAAAGCAAGATCTGGTCAAAGAGTTTATGG[T/A]AAGTTCTGGTCAGCATCAGTATAATGTATATATAAAGCATATAGCACATTACTTAAAGCAATAGTTTACCCACAAATAACACATTTACTGACCCTCAATTGAGTGAATGAGTGAATTTTTGTTGTTGTTGTTGTTGAACATGATTGAAGGTATTTTGTTGAATGTTGATAACATGTAGCCATTCTACAGTGGTGGGAAATGGAACTTAATGGCTTCCAGTTTCCAACATTCATTAAAATGCATTCAAAAGAAAACTTAAATGTGTTTGAAACGAGTACATTATGACATAATTTTTAATTCTGTGTGAACTGGCCCTTTAAATATATTGAATGTTATGGTTTTATAGAAGCAGACACATCTATATATAGTTTTCAGAAATATTATTTTGGTTTATCGTTTTGAAGGTAACTTAATGTCTGACATTTAATGATACTATGGCTGTTTTTATAGGCTTTGGAGCATTTAAACCCTTCAGACAACTGCCTGGTTGGAAAAGCACC
Associated Phenotype:
Not determined