ZMP
ptprfa
Ensembl ID:
ZFIN ID:
Description:
Receptor protein-tyrosine phosphatase LAR [Source:UniProtKB/TrEMBL;Acc:Q90YJ5]
Human Orthologue:
PTPRF
Human Description:
protein tyrosine phosphatase, receptor type, F [Source:HGNC Symbol;Acc:9670]
Mouse Orthologue:
Ptprf
Mouse Description:
protein tyrosine phosphatase, receptor type, F Gene [Source:MGI Symbol;Acc:MGI:102695]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18650 | Essential Splice Site | Available for shipment | Available now |
sa10718 | Nonsense | Available for shipment | Available now |
sa20608 | Nonsense | Available for shipment | Available now |
sa10963 | Nonsense | Available for shipment | Available now |
sa20609 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18650
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026738 | Essential Splice Site | 511 | 1893 | 7 | 31 |
ENSDART00000142544 | None | None | 1186 | None | 21 |
The following transcripts of ENSDARG00000076810 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 2949914)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 2962614 |
GRCz11 | 6 | 3143424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGATGGACCACCTTCCGATATACTGCAGGTTAAAACACAGCAAGGAGG[T/G]GAGATGTGTGCTTATAWATACAGTTGAGGTCASATGCAACAAAAGACAAA
Long Flanking Sequence:
GAACCCGTATCATATTACGTGATCCAGTATCGATCCAAAATCTCTGACAATGGTTTCCAGGAGGTGGACGGCGTGGCATCCACCCGCTACAGCATCGGCGGGTTGAGTCCGTACTCAGAGTATGAGTTTCGAGTAATGGCGGTCAATAACATTGGTCGCGGGCCGCCCAGCGGGATGGTGGAGACTCGTACCAGTGAACAGGCACCGTCATCTCCTCCGCTGCGCGTTCAAGCCCGGATGTTGAGCGCTACGACTATGCTGGTGCAATGGGAACCTCCTGAAGAGCCCAACGGACAGATTCGAGGATATCGAGTGTACTACACGTCTGACCTGCACTTCCCGCTCAGCACATGGCAGAAGCACAACACTGAGGACAGCAGTCTGACCACCATCTCCGGCCTGGTTCCTGACATCACGTATGGGCTCCGTGTGCTGGCCTTCACCTCTGTTGGAGATGGACCACCTTCCGATATACTGCAGGTTAAAACACAGCAAGGAGG[T/G]GAGATGTGTGCTTATATATACAGTTGAGGTCAGATGCAACAAAAGACAAACCATGGCTAATAATGTCAGAATGGGGGATTTTTTTGTGTGTATAGTCAGTCTAAAACTGACTTTTTTTTGCATTTATTCATGCAGTCCCTGCTCAGCCGACTGGTTTTGAAGCTGAAGCCGAGTTGGACACGCGGATCATGCTGTCATGGTTGTGGCCCGTCCAAGATCAGATCACCAAATATGAGCTCACATACTGGGAGGCTGACTCTGACAACAAGGTACACGGCAGATTATTGATACTGATATATCTGGATGACTACAATGCAAATACAATCGTTGTATTTTTTTATTTATCAAATTTTACTTAATTAAAATTGTTATTAATTATTTGAAATTATTTATTATTTAATAATGGAAAAATGCTTATGACATCATGAATAACAGATGGTGAACTCAGGCTTATTTGCAGTATTGGGCTATTAAATAATGAGCACTGTTTCTAATGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10718
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 |
---|---|---|---|---|---|
ENSDART00000026738 | Nonsense | 519 | 1893 | 8 | 31 |
ENSDART00000142544 | None | None | 1186 | None | 21 |
The following transcripts of ENSDARG00000076810 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 2950073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 2962773 |
GRCz11 | 6 | 3143583 |
KASP Assay ID:
2259-7012.1 (used for ordering genotyping assays)
KASP Sequence:
GACNTTTTTTTGCATTTATTCATGCAGTCCCTGCTCAGCCGACTGGTTTT[G/T]AAGCTGAAGCCGAGTTGGACACGCGRATCATGCTGTCATGGTTGTGGCCC
Long Flanking Sequence:
GGGCCGCCCAGCGGGATGGTGGAGACTCGTACCAGTGAACAGGCACCGTCATCTCCTCCGCTGCGCGTTCAAGCCCGGATGTTGAGCGCTACGACTATGCTGGTGCAATGGGAACCTCCTGAAGAGCCCAACGGACAGATTCGAGGATATCGAGTGTACTACACGTCTGACCTGCACTTCCCGCTCAGCACATGGCAGAAGCACAACACTGAGGACAGCAGTCTGACCACCATCTCCGGCCTGGTTCCTGACATCACGTATGGGCTCCGTGTGCTGGCCTTCACCTCTGTTGGAGATGGACCACCTTCCGATATACTGCAGGTTAAAACACAGCAAGGAGGTGAGATGTGTGCTTATATATACAGTTGAGGTCAGATGCAACAAAAGACAAACCATGGCTAATAATGTCAGAATGGGGGATTTTTTTGTGTGTATAGTCAGTCTAAAACTGACTTTTTTTTGCATTTATTCATGCAGTCCCTGCTCAGCCGACTGGTTTT[G/T]AAGCTGAAGCCGAGTTGGACACGCGGATCATGCTGTCATGGTTGTGGCCCGTCCAAGATCAGATCACCAAATATGAGCTCACATACTGGGAGGCTGACTCTGACAACAAGGTACACGGCAGATTATTGATACTGATATATCTGGATGACTACAATGCAAATACAATCGTTGTATTTTTTTATTTATCAAATTTTACTTAATTAAAATTGTTATTAATTATTTGAAATTATTTATTATTTAATAATGGAAAAATGCTTATGACATCATGAATAACAGATGGTGAACTCAGGCTTATTTGCAGTATTGGGCTATTAAATAATGAGCACTGTTTCTAATGGAAAATTGAATGGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGAATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGGTGGGTGTGTGAATGGATGGATGGATGGGTGAATGACTGAATACATGAATAAATTGATTGATTGATTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20608
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 |
---|---|---|---|---|---|
ENSDART00000026738 | Nonsense | 768 | 1893 | 11 | 31 |
ENSDART00000142544 | Nonsense | 63 | 1186 | 1 | 21 |
The following transcripts of ENSDARG00000076810 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 2974063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3006831 |
GRCz11 | 6 | 3167126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATGGAGAGCCGCGCGGACAGCCCATCATTCTGGACGTGGCGCTGCCA[G/T]AGGCACAGGTACACTGCGCAAACACAACACTGTAAATCAGTCCAGACAGT
Long Flanking Sequence:
ATGGTAAAAGCAAACCATTGTGAAATAGCTCTGCCCTCCTGATTTTTCTTTTGCAGTAGTAAACTATTTTCAGGAGTCACTCAGGAATAAATAGCATTGGTTTGTAACAACATGAGGGTCTAACATAACAAAACAACTTTAATTTGTGTAGACTCTGTATTGGCCTTTTTAAAAAAAGTGAATATAAATAAAATTATGGAGTGTAGATAGAAGTGTGTTGGCTGTAGCCTGTGAGCAGGTTTGTACCGGCGTGTGTGTGTTTGTAAGTGATGTGTGTGTGCTGAAGCAGTAAGCTGTGTTTCTCTTCTCTCTCAGTGCCTGGTGCTCCTCCACGCAGGGTTGAGGTGGACAACATCAACTCCACTGCACTGCGTGTGTCCTGGAAGCCGCCTCTGCAGCAGAAACAACACGGCCACATACGTGGATATCAGGTGGTTTACTCACGCCTGGAGAATGGAGAGCCGCGCGGACAGCCCATCATTCTGGACGTGGCGCTGCCA[G/T]AGGCACAGGTACACTGCGCAAACACAACACTGTAAATCAGTCCAGACAGTTATGTAAAACACTCAATATAGGCTCATTCTGAAAACGCAGCCCTATAGACCTTTTTCATGGCTGCTGCATGGTGGGCGCCATAGCGACCAGCGTCTTCCGGTAGAATGCTAAAAACTTCCGTTTACAGCGTTTACAACTGGTAATTTGCGCTCCGAAAATGGGTTTCAATAATGTTTTTAATGGATAACAGAGTGTTTTTGTGACACACAACTTAGAAATGTGTCTGTTAAAGCCGTTATAATCTGTCGATGTGGTTCAAGTGCATCAGAAATACGAGAAAAACGTTCTCCTAGTTCACGTGTCTGCAGTCAGAAATAGCTCAGCAGCTTTTTAACACACACACACACACACACACACACACACACACACAGACACACACAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGCAAACCAGAGTACTGGCGTAAAACTTAACAGGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10963
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 |
---|---|---|---|---|---|
ENSDART00000026738 | Nonsense | 878 | 1893 | 13 | 31 |
ENSDART00000142544 | Nonsense | 171 | 1186 | 3 | 21 |
The following transcripts of ENSDARG00000076810 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3003785)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3036553 |
GRCz11 | 6 | 3196848 |
KASP Assay ID:
2259-7015.1 (used for ordering genotyping assays)
KASP Sequence:
CGCACTGATGACCACTTCACTGTCACCGGCCTGCACAARGGCGCGACGTA[C/A]ATCTTCAAACTCTGCGCTAAAAACCGCGCCGGGAATGGAGAGGAGTACAG
Long Flanking Sequence:
TTCTTGTTGAATCGCTGAATGCCTTCTCAATTGTAAGTTGCTTTAGACAAAAGCATCTGCTAAATAACTTAATGTAAATTAAACAGTATGACTATTAGCTGTTTTCCCAGAGATGGGTTGCAGCTGGAAGGGCATCTGCTGCGTAAAAAAGTGCTGGATAAGTTGGCGGTTCATTCCACAGTGGCGACCCCGGATTAATAAAGAGACTAAGCCAACAAGAAAATGAATGAATGAATGAATGACTATTAGCTGTGACTACATACAGTAATGACCCTCTCATCTGTGCCTCTGTCAGTTCCAGGAAAGCCCACTATGATCATCAGCACCACCATAGGCAACACGGCTCTGATCCAGTGGCAGCCGCCTAAAGAGATGGTGGGAGAGCTGATGGGCTACAGACTCCGCTATAAGCGTGAAGAAGAGGATATTTACACTGTCCGAGACTTCAGACGCACTGATGACCACTTCACTGTCACCGGCCTGCACAAGGGCGCGACGTA[C/A]ATCTTCAAACTCTGCGCTAAAAACCGCGCCGGGAATGGAGAGGAGTACAGCAAAGAGATCAGCACCCCGGAGGATGTGCCCAGCAGTTACCCACAAAACCTCAAAGTCGTTGGATTGACCACAACCACCACAAAACTAGCCTGGGATCCTCCGCCGCTGCCCGAGAGGAATGGGAAGATCGTACGATATGTGGTGGTTTATCGAGACATTAACAGCCATCAGAATCAGACCAACGGCACAGCGGACACGGAGATGACCATTCAGGGCCTGAAGCCGGACACCACCTATGATATCAGGGTGAGGGCGTTTACAGGGAAAGGTGGAGGTCCCATCAGCCCCAGCATCCAGAGCAGAACCATGTCTACCTCCATGCCTGGTGAGTGCTTCAATGGAAGCATTAGCTTCAGCTCATGCTCACCTTTTCTCCATTACATCAGGTTGAAATGGCTTCTGGAATAATAATGGATGAGGTTGGCTGTTTAAAGTTGCAGAATTTAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20609
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 |
---|---|---|---|---|---|
ENSDART00000026738 | Essential Splice Site | 1443 | 1893 | 22 | 31 |
ENSDART00000142544 | Essential Splice Site | 736 | 1186 | 12 | 21 |
The following transcripts of ENSDARG00000076810 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 3056461)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 3089229 |
GRCz11 | 6 | 3249524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAACCAGCACTATCGTCATGATGACCCGACTGGAGGAGAAGAGCAGG[G/A]TGAGATTATATATAATATCTGCCTGCCTTGCTAACATACACAAACACGTG
Long Flanking Sequence:
TTTTGAATTGATCTGAAATGAATTCATTCGTTACGGCTTAGTCTATGATTCATACGAATTGAACCAGCTGTTTAAAAATACACATAATTTGTTATATTATAAATATTTACAGTCACTTTTAACCACTTCAATGCATCCTAGTTTCTTTCTTTTAAAATCAATTCTTTCCCCAAAAGTAGCTTGACATCTCAAAATCTAAACCTGCATAGTTCACAAGGAAAAACAAAGCAACACTCAGTAGATAATTAGAACAAAAGGAAACAGCACAATCTAGTCGCAGTTATCTGCCTGCACATGTATTAACATGGCTCTGTTGAACCGCAGGTGTTCCCGGAAGTGACTACATCAATGGAAACTACATTGATGGCTACCGTAAGCAGAACGCCTACATCGCCACGCAGGGTCCGCTGCCTGAGACGCTCAGTGACTTCTGGAGGATGGTGTGGGAACAGAGAACCAGCACTATCGTCATGATGACCCGACTGGAGGAGAAGAGCAGG[G/A]TGAGATTATATATAATATCTGCCTGCCTTGCTAACATACACAAACACGTGGGCTGTCTGTGATGTGCATGGAAAAGGAAGTGACCATAAGTGTCCCAATAGGTTTAGTGAAATGGAAGTGGCGTGTGTGTGTGTGTTTGAGAGAGAGATAGAGGAGAGAGGGATGGGTTACATGTTCCCTCACCTGCCGTGTGACCAGATGGTCATTCTTTCTATCCTCCACATGGCCAGTCTTAATATACTGTACAGTACATGCACAGGAAGGCGATCTAAAGTAAGTTTATAGTTTATTCTACTGGAATTTACTTCTTTTTTTAATTTAATGCAATTACATGCAATGCAAAATATATTTATTTAACCAGTTAAACTCTGCGGACCCGGTACCAGGTCTGTGACGTCATTGACTTTCGCCTTAAGATTTAAAGGGCTAGCATTGCACCAGACCCCCTTAAGTGGTTTCATTTGAAAGTGTAGAATCTATATTTTATGCACATATGCATC
Associated Phenotype:
Not determined