ZMP
PPFIA3
Ensembl ID:
Description:
protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), al
Human Orthologue:
PPFIA3
Human Description:
protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), al
Mouse Orthologue:
Ppfia3
Mouse Description:
protein tyrosine phosphatase, receptor type, f polypeptide (PTPRF), interacting protein (liprin), al
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40081 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30834 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33191 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10550 | Nonsense | Available for shipment | Available now |
sa18755 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20029 | Nonsense | Available for shipment | Available now |
sa20028 | Nonsense | Available for shipment | Available now |
sa40080 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40081
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109953 | Essential Splice Site | 38 | 1063 | 2 | 29 |
ENSDART00000109953 | Essential Splice Site | 38 | 1063 | 2 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30248935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29966974 |
GRCz11 | 3 | 30097816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGACAAGGTCTCCCTGTTGAGTCATAGTCTATTGTTCTTCTCTCCCTC[A/C]GGTTCGTGAGAGATTGCGTGTGGCTTTAGAGAGAGTTGCCGTTCTAGAAG
Long Flanking Sequence:
GACATTTTATTTATATATAAGAAGTGAAAGTTCTATGTTTTTGACAATATTACAAGATCACCAAACAAAGGCTGGAAATTGAAAAAAACTAAATAAAAAAATAATGATGAAATAAATTAATAATAAAAATAAAAATGAAATAAAATTCATTGCAATAAACAAATATGTGTTTATAGGTATGTATATTAACTTATGCATTAAATATATGCTCCAAACTTTTTCCTGATTGAGACGTGTTGAATCGGAACTTGGTATCGGTTGCAAAAGTCCTGATCGGAACATGCCTACTTATAAGTTATCCAACAGTTTTGGCCTTTTTTGTTCAATTCATACTTCTTTTTTTTAAGTCATAATTGTGACTTTGTAAACAAAAAATTTAATGACAGAAACAATTCATATCAAACAACCCGATATCTAGACAATAACTATCTCTTCAAAGAGGGCATGTTTTTGGACAAGGTCTCCCTGTTGAGTCATAGTCTATTGTTCTTCTCTCCCTC[A/C]GGTTCGTGAGAGATTGCGTGTGGCTTTAGAGAGAGTTGCCGTTCTAGAAGAAGAGCTTGAATCATCTACGAACGAGGTGAACATCATATCTTTTTGTACCAGCTTTTTTTTTCTAAGCATGTGGCATGTCAGTCTTGCATGCTTAGATTTGTTCGTTATGCTCAGGTACTGTCTTTGCGGGATCAGATTAAAAGGAGAGAGCGGGGTTTGGACAATGGAAAGGAGGTGAGTCACAACTATTTTGAATCTTGTTTCGAATGTTTTCACTGTTTTTTTTTCCCTCATGTCCCTCTGTTTTTCACACAGCGGCTCCCAAATGGCCCGTCCTCCATCTTGGATGATGGCGAGATTGACAGACAGAGAGAGGGAGAGATAGAGAGACAGAGAGCAGAGCTTTCACAGTTAAAAGAAAGACTGGCGCTCATGTGCAGACAGGTAAGTGTTGCACTGCTGTCTGAAGAGGATGCATCGTAAGGACTGCAGACAAGATTAGCTGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30834
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109953 | Essential Splice Site | 38 | 1063 | 2 | 29 |
ENSDART00000109953 | Essential Splice Site | 38 | 1063 | 2 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30248935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29966974 |
GRCz11 | 3 | 30097816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGACAAGGTCTCCCTGTTGAGTCATAGTCTATTGTTCTTCTCTCCCTC[A/C]GGTTCGTGAGAGATTGCGTGTGGCTTTAGAGAGAGTTGCCGTTCTAGAAG
Long Flanking Sequence:
GACATTTTATTTATATATAAGAAGTGAAAGTTCTATGTTTTTGACAATATTACAAGATCACCAAACAAAGGCTGGAAATTGAAAAAAACTAAATAAAAAAATAATGATGAAATAAATTAATAATAAAAATAAAAATGAAATAAAATTCATTGCAATAAACAAATATGTGTTTATAGGTATGTATATTAACTTATGCATTAAATATATGCTCCAAACTTTTTCCTGATTGAGACGTGTTGAATCGGAACTTGGTATCGGTTGCAAAAGTCCTGATCGGAACATGCCTACTTATAAGTTATCCAACAGTTTTGGCCTTTTTTGTTCAATTCATACTTCTTTTTTTTAAGTCATAATTGTGACTTTGTAAACAAAAAATTTAATGACAGAAACAATTCATATCAAACAACCCGATATCTAGACAATAACTATCTCTTCAAAGAGGGCATGTTTTTGGACAAGGTCTCCCTGTTGAGTCATAGTCTATTGTTCTTCTCTCCCTC[A/C]GGTTCGTGAGAGATTGCGTGTGGCTTTAGAGAGAGTTGCCGTTCTAGAAGAAGAGCTTGAATCATCTACGAACGAGGTGAACATCATATCTTTTTGTACCAGCTTTTTTTTTCTAAGCATGTGGCATGTCAGTCTTGCATGCTTAGATTTGTTCGTTATGCTCAGGTACTGTCTTTGCGGGATCAGATTAAAAGGAGAGAGCGGGGTTTGGACAATGGAAAGGAGGTGAGTCACAACTATTTTGAATCTTGTTTCGAATGTTTTCACTGTTTTTTTTTCCCTCATGTCCCTCTGTTTTTCACACAGCGGCTCCCAAATGGCCCGTCCTCCATCTTGGATGATGGCGAGATTGACAGACAGAGAGAGGGAGAGATAGAGAGACAGAGAGCAGAGCTTTCACAGTTAAAAGAAAGACTGGCGCTCATGTGCAGACAGGTAAGTGTTGCACTGCTGTCTGAAGAGGATGCATCGTAAGGACTGCAGACAAGATTAGCTGATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33191
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 |
---|---|---|---|---|---|
ENSDART00000109953 | Essential Splice Site | 490 | 1063 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30226839)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29944878 |
GRCz11 | 3 | 30075720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGCTATCATGTTGCAGGAGCAGCTGGAGGCCATCAACAAAGAAATAAA[G/T]TGAGTTCACTGCAGACAGAGAGACCTTGAGGACGACTTGGAAAAACAAAC
Long Flanking Sequence:
CTCCAAGCAATTGCCTTAACACAAGCTATAATGAAAACTTCACAAACACAAAAGTTACATCTGTGCAATCCTTTTATTTGCTGAGAAACATCACTAAATCGCAGAAGCGTGGAATGAACAAATGTTAAAATTTGTTACATTTATTAAAGTAATACAGAATGCCAAAAAATGGCCAGTTGATGATTGAACATTTTAATCAAAATCCAGCCAATTCTGATTCCTCTGATCTCTACATTTACTAAGAGATGAACAGAATGATTTAATTTGATATTTGAAGAAGTGATGTCTTATGTTGGTCTGCTTCAGTATGGCGATTGGGAAAGCGGAGCGCTGCTGGGCTCTGGTTTCGAGGGCGGTGTGGAGGACAGGTGTTCTGATGATGAAGAGGACCGCGAGACGCTTTTCGGCTCGGAGCTGCTCTCACCGAGCGGCCAGACAGATGTGCAGACCCTCGCTATCATGTTGCAGGAGCAGCTGGAGGCCATCAACAAAGAAATAAA[G/T]TGAGTTCACTGCAGACAGAGAGACCTTGAGGACGACTTGGAAAAACAAACTTTTATTTAATGTGGAAGACAGTTGAAATTGAGAGGGCCTTGAATGGGAGGATGATGGGAAAGTGCAGGAGGAAAGCTCGCACATCATGATTTAGCCAAGTGCGACATCTATGTTGATCCTGGAACATCATTTTTGATGGAAACTGTAATTAATACCTATTCCTCGCCCCTAAACCCAACTATAACTGTAAATCATTCCCTAAATCAGAGGGGGAATAATAGTTTTATAACACTCATGTAGAAATGCATATACCTAACCGTAAGCCTAAACATAACATAAATGATAAACATATCCCCTTAATTCTGATTGGCTGATTGGAATGTTGTTTCAGAATCAACATAGATGTTAATCCAGGAACATGTCCTACTTAGTGAAATCAGGTTGGCAGGAGAGCTCAGTATAGAGGGTAAATTGTAGGAGACTAGTTTTCAAACTGACTTAGGGAAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10550
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 |
---|---|---|---|---|---|
ENSDART00000109953 | Nonsense | 594 | 1063 | 16 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30224201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29942240 |
GRCz11 | 3 | 30073082 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTCTCTGGCCYTACTGGACTCCACCCCTCCTCCCACCCCTCGTGCGCTA[C/T]GATTGGACAGGATGACACACACTCACCCTGGTGCATTGCTGGATGACAGT
Long Flanking Sequence:
AAAAAAAAAAGAATGGATGTAAATTCCATTTAGGTGGTCTTAGAAAAGGTTTCTTGATACCTTCGTCTCACACTCCTTTTATGTTTCCTTCAGGCTGATTCAGGAAGAGAAGGAGAGCACAGAGCTTCGTGCTGAAGAAATCGAGAGCAGAGTCAGCAGCGTGGCTCTGGACGGGCCTCCCATTCCACCGACCTCTCTGGGACGGGACAGCACAGGACGGGGCTTCATCCCCCCATCCCTCACATCCTCCACCCTGGCTTCACCCTCTCCGCCCAGCTCTGGGCACTCCACACCCCGCCTGCCCCATTCCCCCGCACGCGAGACAGACAGACAGGCAAGAGCGAGCGTGTGCTGGATTATTAACAAGTCCTGCTGTTACACTTAAATATCATCATGTTAAAAGCTGATGGTGTTTATCTTCTGCTCTTCAGAACAACAAAGAGGACGACAGGTCTCTGGCCTTACTGGACTCCACCCCTCCTCCCACCCCTCGTGCGCTA[C/T]GATTGGACAGGATGACACACACTCACCCTGGTGCATTGCTGGATGACAGTCGCGAGTTTCGCAGGTGTGTTTATCAACCCGGCCCATTATAAAGCAGTGGTCAAACGTTTGAGATCAATACGATTTTTTTTTTAATTTGCAATGAAATTGAAATTTACACTTCTTGTTTTTGTGTTCATAAACTTTTTATAAACTGTGCACTTCATTATTTTAGTGCAAATATTTTTGCCCTCATAAACTTTAATCAAATACAATAATCTTCCCTCCTTTTCAAAATGACTTTGTTCACTTTCTGGTCACATGGATTTACATTAGGTCAGGAATGTAATTGGTGTCTTGTTTCTGCCCTGAATTCGTCCATTTGTCAATCTTCCTTCATTTTGTTGGCAATGACTATCTTTCAACAGTTCAATCAGTTCCCAACGAATGAAATCATGCACTGCTCTACGTTTTTTATTTATTTCAAGATTGTTTTAAGTGCATTTAAGTCATGATAATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18755
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109953 | Nonsense | 849 | 1063 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30213012)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29931051 |
GRCz11 | 3 | 30061893 |
KASP Assay ID:
2259-3556.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGGCAATGACTGGCTGCCCAGTCTGGGTTTGCCCCAGTACAGAAGCTA[C/G]TTCATGGAGTCTCTTGTGGATGCCCGCATGTTGGACCATCTGACCAAGAA
Long Flanking Sequence:
CTTGAAAAGTAATGCTTCAATTAATGATCGTCCAGATAAAACTTTATAATTCCAATCGTAATATGATTTTTTAGATTTATAAGCTTCTATCTGCATTTTGCCCTGTTATTTTTTTACCCCAATCTGCAAATTTAAGAGAATTTTGAAACATTTTGAGTACACTTTGAACTGTTACACACATATTGTTCACTGTATGGAATGCAAACACTCTGAAGCTCAATATCTCAAACGCATTTAGAACACAGATAGAGCCTTATAATTCCAAGGTGATGATTTTTCGTCTTGACTTTTTGTCAGTACATTTTTTTTTACAGTAAAGCCCTGAACTTCGATTTTTGCATGCATAAGCTCCACACTACAGTGAACAAACGTAAATACAGCTGCAAAAAAAGATGATTTTCCTTTCCTCCATGTTAGATCCTGGCCTATGGAGACATGAACCATGAGTGGGTGGGCAATGACTGGCTGCCCAGTCTGGGTTTGCCCCAGTACAGAAGCTA[C/G]TTCATGGAGTCTCTTGTGGATGCCCGCATGTTGGACCATCTGACCAAGAAAGAGCTGCGTGGCCAGCTGAAAATGGTGGACAGTTTCCACAGGTAATGTCTGTTTTTCTCTCCCCATCAGTTAAATGCCGCCACACGCTTCATTACTCCTTCTCTTCATCAGTCTTAATCTCATGCTCACCTGATGCTCATCAGTTACTCTCAGGGTGCAGGTGTGTGTCTTTGGGCCTTTGCTAATCTCCAGTGTGCCTGGGGTCGGTTTTTGTAACACTTTTTTTCTTGGGGTGGAGGTCTTTAATGAATTTAGATAACCCTGTGACCTCTTTCTTTATCTGTGTGCTCTTTTGACCCACAGGGTGAGCATGCATTATGGCATCATGTGCCTGAAGCGCCTCAATTATGACCGCAAGGAGCTGGAGAGGAGGAGAGATGAGAGCCAGCACCAGAATAAAGGTTTTTAGCTTACTTGATTTTTTGTTTGCTAACAAATATGCCCAACTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20029
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109953 | Nonsense | 865 | 1063 | 23 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30212966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29931005 |
GRCz11 | 3 | 30061847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTACTTCATGGAGTCTCTTGTGGATGCCCGCATGTTGGACCATCTGACC[A/T]AGAAAGAGCTGCGTGGCCAGCTGAAAATGGTGGACAGTTTCCACAGGTAA
Long Flanking Sequence:
TAATTCCAATCGTAATATGATTTTTTAGATTTATAAGCTTCTATCTGCATTTTGCCCTGTTATTTTTTTACCCCAATCTGCAAATTTAAGAGAATTTTGAAACATTTTGAGTACACTTTGAACTGTTACACACATATTGTTCACTGTATGGAATGCAAACACTCTGAAGCTCAATATCTCAAACGCATTTAGAACACAGATAGAGCCTTATAATTCCAAGGTGATGATTTTTCGTCTTGACTTTTTGTCAGTACATTTTTTTTTACAGTAAAGCCCTGAACTTCGATTTTTGCATGCATAAGCTCCACACTACAGTGAACAAACGTAAATACAGCTGCAAAAAAAGATGATTTTCCTTTCCTCCATGTTAGATCCTGGCCTATGGAGACATGAACCATGAGTGGGTGGGCAATGACTGGCTGCCCAGTCTGGGTTTGCCCCAGTACAGAAGCTACTTCATGGAGTCTCTTGTGGATGCCCGCATGTTGGACCATCTGACC[A/T]AGAAAGAGCTGCGTGGCCAGCTGAAAATGGTGGACAGTTTCCACAGGTAATGTCTGTTTTTCTCTCCCCATCAGTTAAATGCCGCCACACGCTTCATTACTCCTTCTCTTCATCAGTCTTAATCTCATGCTCACCTGATGCTCATCAGTTACTCTCAGGGTGCAGGTGTGTGTCTTTGGGCCTTTGCTAATCTCCAGTGTGCCTGGGGTCGGTTTTTGTAACACTTTTTTTCTTGGGGTGGAGGTCTTTAATGAATTTAGATAACCCTGTGACCTCTTTCTTTATCTGTGTGCTCTTTTGACCCACAGGGTGAGCATGCATTATGGCATCATGTGCCTGAAGCGCCTCAATTATGACCGCAAGGAGCTGGAGAGGAGGAGAGATGAGAGCCAGCACCAGAATAAAGGTTTTTAGCTTACTTGATTTTTTGTTTGCTAACAAATATGCCCAACTTTAAGTAGTATTAAGAAGTCCTTTTATGGGATTTATGTGCGCACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20028
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109953 | Nonsense | 917 | 1063 | 25 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30206838)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29924877 |
GRCz11 | 3 | 30055719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTGTTCACTGTCTGGTGTTTGTGTTTCTGCTGTAGATGTGATGGTGT[G/A]GTCGAACGAGCGTGTGATGTGCTGGGTTCAGTCCATCGGCTTGAAGGAGT
Long Flanking Sequence:
TTTATTTTAACAAATAGTTAACAACGCTGCCTAAACCAGACCCTTAATTCATGACACACTAACATCTATTGCTCTTCTGCCAGCAGACAGAAGTCTACAGAATATGTCATTACCTGCAGCTGTGTGGGCTGTTTTATATTTACCAAACGGTATTAACACTGTAAATGATTCAAGAAGAACAGTTTGACTGTTTGCCATGATTTCATTCCTTCCTTTCAACTTGGGTTTGGAGAAGCTGAGTCAACAAAACCAATTCAAAGCCCACGGAATCCTCTGGAAATACAAAGCAGAGACAAAGACTTTGGCTAAAAACAAAAACACGTGTGTTCAAATGCGCATTGGCTATAATAGGTCCATCTATGAGATCAGATGCTACTGACACAAAAGATGAAATCCAGAGTCATCACTCAAGATGCTGTGCTGCCGTTGAGTGGTGAACAGCCTCCTGGAAGTCTGTTCACTGTCTGGTGTTTGTGTTTCTGCTGTAGATGTGATGGTGT[G/A]GTCGAACGAGCGTGTGATGTGCTGGGTTCAGTCCATCGGCTTGAAGGAGTACGCAGATAACCTGACTGAGAGCGGTGTTCATGGAGCGCTGTTGGCCCTGGATGACACCTTCGATTACACTGACCTCGCACTGCTCCTGCAGATTCCCAATCAAAACACACAGGTACAGAGACAAGACTGTGCACTAACACTCATTTATTAAAACATGACCTCAAAGCAATGGTTCTCAACCACCACTCCCCTCCCCCCAACCCACTCCTTAAGGCTGAGTTATACTTTCGCCTGGTGCCGCGTTGCGCAACTCTGCTGACTGCGATTACGCCTCACGAAACAAACGAGGCTTTTATACTTGACACATTCGCTGAAATTCTTTAAAACAACAGAGGGCGATCAAAAGAAACTGAACGTAAAACAGAATAACATCATATCATTAAAATTGTTGAATTTATTTATTTTTATTTATTATTTTTATAAGATTTTTATAACCATTTAAGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40080
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 |
---|---|---|---|---|---|
ENSDART00000109953 | Nonsense | 956 | 1063 | 25 | 29 |
Genomic Location (Zv9):
Chromosome 3 (position 30206720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 29924759 |
GRCz11 | 3 | 30055601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGCGGTGTTCATGGAGCGCTGTTGGCCCTGGATGACACCTTCGATTA[C/A]ACTGACCTCGCACTGCTCCTGCAGATTCCCAATCAAAACACACAGGTACA
Long Flanking Sequence:
GCTGTGTGGGCTGTTTTATATTTACCAAACGGTATTAACACTGTAAATGATTCAAGAAGAACAGTTTGACTGTTTGCCATGATTTCATTCCTTCCTTTCAACTTGGGTTTGGAGAAGCTGAGTCAACAAAACCAATTCAAAGCCCACGGAATCCTCTGGAAATACAAAGCAGAGACAAAGACTTTGGCTAAAAACAAAAACACGTGTGTTCAAATGCGCATTGGCTATAATAGGTCCATCTATGAGATCAGATGCTACTGACACAAAAGATGAAATCCAGAGTCATCACTCAAGATGCTGTGCTGCCGTTGAGTGGTGAACAGCCTCCTGGAAGTCTGTTCACTGTCTGGTGTTTGTGTTTCTGCTGTAGATGTGATGGTGTGGTCGAACGAGCGTGTGATGTGCTGGGTTCAGTCCATCGGCTTGAAGGAGTACGCAGATAACCTGACTGAGAGCGGTGTTCATGGAGCGCTGTTGGCCCTGGATGACACCTTCGATTA[C/A]ACTGACCTCGCACTGCTCCTGCAGATTCCCAATCAAAACACACAGGTACAGAGACAAGACTGTGCACTAACACTCATTTATTAAAACATGACCTCAAAGCAATGGTTCTCAACCACCACTCCCCTCCCCCCAACCCACTCCTTAAGGCTGAGTTATACTTTCGCCTGGTGCCGCGTTGCGCAACTCTGCTGACTGCGATTACGCCTCACGAAACAAACGAGGCTTTTATACTTGACACATTCGCTGAAATTCTTTAAAACAACAGAGGGCGATCAAAAGAAACTGAACGTAAAACAGAATAACATCATATCATTAAAATTGTTGAATTTATTTATTTTTATTTATTATTTTTATAAGATTTTTATAACCATTTAAGTTTTTTTTTAATCAAACTTTAATGCATCACTTGCTTTTGTTCATATCTCGGCCAGTTTGACCTATTAAAGTTTATTGAAATGTTAATTCCCACAGAACATGGGTTGCTCTACAAATATTTTTTT
Associated Phenotype:
Not determined