ZMP
ptprfb
Ensembl ID:
ZFIN ID:
Description:
Receptor-type tyrosine-protein phosphatase F [Source:UniProtKB/Swiss-Prot;Acc:A4IFW2]
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12334 | Nonsense | Available for shipment | Available now |
sa19723 | Nonsense | Available for shipment | Available now |
sa19722 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12334
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 |
---|---|---|---|---|---|
ENSDART00000083314 | Nonsense | 187 | 1909 | 5 | 33 |
ENSDART00000090341 | Nonsense | 154 | 1870 | 3 | 31 |
ENSDART00000126665 | None | None | 92 | None | 4 |
ENSDART00000133709 | None | None | 148 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 17499642)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 18056971 |
GRCz11 | 2 | 17728140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTTAAAGACTTCCTGCCWGTAGACATCAAYGGCAACGGGCGAATCAAA[C/T]AGCTTCGYTCAGGTAGACTTYCTTACATCCCTACAATCWCTGGAACAAYA
Long Flanking Sequence:
AAGCTTGCAGCTTAAAACTTAAAGCTTGCAGTCCATATGGTGTTACATGTTAGCATAACGGTATACACAAACATCCAGTGGATTAGCCTTGCCACGCTTTGATCTTAATAATGCACAGGGAGGCCTTTTTTCTGGGAAGTGAATTGATTTAGTGCTCTAATGAGACTTCTCCTGGATTTGCTTTTGCAGGACAATTACGCCTGGCTTGCATCTCTAACCCTTGATTCACAGCAATCAGGGTTCTTTAAGATCATTACCCTTATTAAGTAAATGGTGCTCCTTTAGGCTCCTGACTTGACCTGCTTTTTTCTTTCTTTCTTTCTGCAGAAAATCAGATTCCGCATGGTTTCCCCACCATAGACATGGGTCCTCAGCTGAAAGTGGTGGAGCGAACAAGAACAACTACAATGCTCTGTGCTGCCAGTGGGAACCCTGACCCGGAGATCACTTGGTTTAAAGACTTCCTGCCTGTAGACATCAACGGCAACGGGCGAATCAAA[C/T]AGCTTCGCTCAGGTAGACTTTCTTACATCCCTACAATCACTGGAACAATATCCACTCTATTGCTGGAACACCTTTGTTTTGACAATAGCCTGGAGTTAAACAGTTTAGTTTTGCCATTTTTTAATCCATTCAGTTTATCACCAGATCAGGGGGGAGCAAGTTTAGCCTAGCTTAGCATAGATCATTGAATCAGATTAGACCATTAGCATCTGCTCAAAATTACTTAGAATTTTTTTTTATAATTAAAGATTGACAATAAATTTTGAAGTAAGACTGAAGAAAAAAAAAGTTGCTTTTTAAATTTTTTTGTCGGCATGATTAGGAACTATACTTTTTTTCTGGCATAATTGGCACCAAGTACCAAGCCCTACACCTGCACTACAGATTGTAATCTGTGTTATGTCGTTCTCTATCAAGTCTTTTTTTCTCAAGGTCATTTTTGAGTGAGATGCTAATGGTCTAATCCGATTCAGTAGCCGCGTTTCCACTATCGCGCCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19723
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 |
---|---|---|---|---|---|
ENSDART00000083314 | Nonsense | 208 | 1909 | 6 | 33 |
ENSDART00000090341 | Nonsense | 176 | 1870 | 4 | 31 |
ENSDART00000126665 | None | None | 92 | None | 4 |
ENSDART00000133709 | None | None | 148 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 17488555)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 18045884 |
GRCz11 | 2 | 17717053 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTGCAGATTGAAAACAGCGAGGAATCAGACCAGGGCAAGTACGAATG[T/A]GTGGCTACGAATAGCGCCGGGACGCGTTATTCAGCTCCGGCTAATCTCTA
Long Flanking Sequence:
TCACCTTATGATGCACTGTTTTTATCAGTAGTGACCAGACAGTCCTTCTAGTTTTGTACAGCACTGGCGTTTCGTTCATTTTGGCGGGTATAAATATGCCACCGCAATAATAAAGTCATGTGCTGTAGCATAATTGGCCCCAAGTCAATGACATTAATATCCCGAAAGCTTTTTTCTAATGACAGTGAAAGGCAAATGTGTTGAGCTGTAGACTCTCACAACCTGCAAAATCAGCTTTATGCATATGTCTTAGGCAGCATTCTCAGCCAATAAAGCATACACACAGCGGAACAGCTCTGACATTTAAACAGGGAGTGTTTACTGATTGTTCTCCGTGAAAGTTTGTGGTTTGGTGTGGGGAAAGTTGCGGCAGGGGATTCATAATCGTGTTCGTAAATCAAAGAGGTGACTTTTCCCCTTGTTTTATTTTTCTTTTTTTTTTCTTCAGGAGCTCTGCAGATTGAAAACAGCGAGGAATCAGACCAGGGCAAGTACGAATG[T/A]GTGGCTACGAATAGCGCCGGGACGCGTTATTCAGCTCCGGCTAATCTCTACGTGAGAGGTAAGAAACATGCTGCAGGTGCCGCCCCTATCAAAACAACTTCCTCCACAATGCTTCACACTTTTATTTTGACCGTGTTGCAATTTTGTTTTGACTTCCACATGCGTTGAACTTTGTCTGACATTTCAGAGCCAAGATAAACTAAAAGTTGTTGTCCTAATCTAGCCGGAAAACAAAACATTCCAGGCTCTGTTTTGATTTCGTAGCAACAGAGGCACAAGTAAACATGCATATTTCTTAAAGCATTTGTTATGAGAGTGAGAAGACAAAAGGGTTTAACTGAAGGTTAGTGCCACCGAGGACACCTGCGGTATTAATATGTGGATTTACAGGTATAAGGGTGTCAAGGCATTGTGTGTGAAACAGAACTCTGGGAGCGCTCTTGTTATGAGTGTCAACCCCTTTAGCTCTTTCCATGCAGGTAATAACAGGGAGCTTATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19722
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083314 | Essential Splice Site | 556 | 1909 | 9 | 33 |
ENSDART00000090341 | Essential Splice Site | 524 | 1870 | 7 | 31 |
ENSDART00000126665 | None | None | 92 | None | 4 |
ENSDART00000133709 | None | None | 148 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 17472534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 18029863 |
GRCz11 | 2 | 17701032 |
KASP Assay ID:
2259-1828.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCATCAAATACGAGCTGCAATATTGGGAGGCTGACTCAGACAACAAGG[T/A]ATCATGCCAGTGCTTGTTTCTGCCCTATTCATTGAGAATTGCAAGCAGAC
Long Flanking Sequence:
TGGGTCGTTTTTCCCCACGAAATAAACAAAATCAATACTTTTCAATTACAATGTACTTAATATTACCAAGTTTATTTGCAATGATCAAAAACATTTAAATATCATTATCAAGTACATTAATAATACTATTTGACTTTAATGTTTTTGTAAATATTAAAAATATTTATACTTAGGAAATTGTAGTTATTTTAACATTTAACATTGCACTTTTAAAATTATTTATTCGCACCAAAAAGTGAAAAATTATTGTTATGGATCATGTATTAAAATGTGCATCAAAACCCAGAATTTTAATGTCAGTAGTAGATATAGATAGGAATCGAGAAATGCTCTTTTGAACATGTTTGTTTCTGTTTTACTTCAAGTTCCTGCTCAGCCATCCAGCTTCGAAGCTGAAGCAGAGCTAGATACAAGGATCCTACTAACTTGGCTGTGGCCCGTGCAGGACCCCATCATCAAATACGAGCTGCAATATTGGGAGGCTGACTCAGACAACAAGG[T/A]ATCATGCCAGTGCTTGTTTCTGCCCTATTCATTGAGAATTGCAAGCAGACCAGATATTGAATGCGTACAGCTGCTGCGGTGGGCCATGGATGCAAGTGAAAGATAGCCAAAATTGACATTTCACAAAATGACTCCAGGCAAAAAGTCTGCAGTCAGATGATAGAATTAGATTGTGCATTTGGCTTCAAAAACAGAAAGGTACTTATCAATGCTCAGCGCTTGACAGCATTCCAGCTGAGGCCAGAGTGGGCTGTTTGGATGGCTTTTCTTGATGTCAGTTCATCTACATTGAGATCAGATGTCTTACGTGCACTCTCATCACGATACACATCAGTGTCTGTATGCTAATATAGTGGTTCTCTGTGGAAAGAGATAAAACCTCTGCAGCTGCCCTTTAAACTTTAATTGTTAAATGGATAATAAGAAAATGTACTAATGAATTAATTTAGCTAATAGTTATGAAGGGGAATGAAATAGAGGTCTGTTTTCATCTGATGAAT
Associated Phenotype:
Not determined