ZMP
ptprga
Ensembl ID:
ZFIN ID:
Description:
Protein-tyrosine phosphatase gamma-a [Source:UniProtKB/TrEMBL;Acc:C7U133]
Human Orthologue:
PTPRG
Human Description:
protein tyrosine phosphatase, receptor type, G [Source:HGNC Symbol;Acc:9671]
Mouse Orthologue:
Ptprg
Mouse Description:
protein tyrosine phosphatase, receptor type, G Gene [Source:MGI Symbol;Acc:MGI:97814]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21839 | Nonsense | Available for shipment | Available now |
| sa27719 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21840 | Nonsense | Available for shipment | Available now |
| sa14383 | Nonsense | Available for shipment | Available now |
| sa27721 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10080 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21839
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Nonsense | 104 | 1414 | 3 | 30 |
| ENSDART00000122270 | None | None | 234 | None | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5343919)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5313375 |
| GRCz11 | 11 | 5259681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATAGCCGACCAAGACACTAAGGTCTCGATGGAGTACCAGGAGCTCACAT[T/A]GGACGGGTTTGATGCGGAGTCGTCCAACAAAACGTCAATGAAGAACACAG
Long Flanking Sequence:
AGGTGCCAAAGATCAGATAAGGGTTTATCTGTGAATATTTTGCTTTACAGCAGAATTCAGAGTCTTGCAGTGTCCCTGATTACCTCCGAACACAGTTTTCCTCTACTGAATTCTTGTAGAGTCGGCAGAATTTGAAACAAAGTCGTGTCTGCTTTAGTCTGCGCAGTTCAAAGGTCTCGGATTAAAGTGTGACTAAACTGTCAAATCTGTCAGGTTTTTATACTTTCCATGAAACACGCAGACAGACAGATGGTCGTCTCAGGACAGCTCTAGCGTGTTTTGACTGGCATTTATGAAGAATAAAGTGAGTCTGGGAGCGGTTCGGCTTCTGTTTGCACTGTGATGATCCATTGATTTGCTGTCTTTCTCTTCTGCAGGGACGTACGGACCAGATACAGGCTGGGCGGCAGCTTTTCCTGAGTGCCAGGAGAGAAACCAATCGCCAATCAATATAGCCGACCAAGACACTAAGGTCTCGATGGAGTACCAGGAGCTCACAT[T/A]GGACGGGTTTGATGCGGAGTCGTCCAACAAAACGTCAATGAAGAACACAGGCAAAACGGGTAAATCTGAAGTGGATGGTCTGCCCAAAATAAACATTGATCCAACTTGCTATCCGACGTGAGGTCGTACTGTAATTATCAGGAAATCTAGGCTGTTAAATAAAAGGGAATGTGATTTAAAATGGGCCATAAAATGAAACAAAAAGTCCTTTTATGCAGCAGAGGCTCCAGGATTCTTTTTGTTGGGGTTGCAAATGGGAGGCTTAACACTTTAGAGAGGAGTGCTAAAATTGATTAAACGTATAGCTTAATTATCAAGGAACTTTACTGGCGCACCATGGCTGCACAATGATATTACGCAGCGCTTTTACCTAGCTGGCAAATATTTTCAGGCGCTGTGTAGTAATATTGCGCTAGCTTCAGCCGTAGTAAGCCAGTAAATTCCTTGATTATTATACCAGAATGAAAGTATAGTTCCTAGCCAAACTAGTCTAGAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27719
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Nonsense | 132 | 1414 | 4 | 30 |
| ENSDART00000122270 | None | None | 234 | None | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5350293)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5319749 |
| GRCz11 | 11 | 5266055 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCTCTTTCTTTTTTCCTCACAGTGGCGATCTTTCTGAAGGACGATTA[T/A]TTCGTGAGAGGAGCCGGGCTACCGGGCCGTTTCAAAGCCGAGAAGGTGGA
Long Flanking Sequence:
CATTTTATTTAATGCTTGGCGTAATCTCAATCTAAACATAAAGAGAAGTTGGGGCAGTGTAGCTCCTCCCCTTTTTTAAAAACAGCCAACAGCGTTTTGTTTTACCAATTGTTTTATGCACTGCTAGTGAGGATGGTTGAACTCCAGTGCATCAAAAATGGGGGGAGAGGGGTACTGTTTTGGTGCACACTAACTTACACTGTGGATATCCTAAGGAACAATACTAGTCCTAACTTCTAAAAAACTTTTATTTAATTTCATGGTACCTCTAAGGTAACTAACTTTTCACTCCCTTTTTCATTTTGACTAAATTAATTCTTAAAAAAACTGAATGTTTTGCATATATAGAGAATGCTTCTTGGTTTAAGAATGTTGAGATATTTGGACTAGAAAAATCTAAGTAAGAACACTTTTTTGCAGTGAATGTATTTGTTTTATTTACATGAAATGAAAGCTCTTTCTTTTTTCCTCACAGTGGCGATCTTTCTGAAGGACGATTA[T/A]TTCGTGAGAGGAGCCGGGCTACCGGGCCGTTTCAAAGCCGAGAAGGTGGAGTTCCACTGGGGCCAGAGCAATGGTTCCGACGGCTCGGAGCACAGCATCAATGGCAGGAGATTCCCTGTGGAGGTGAGCTTCAGCTAATCTTTCTCCAGCGTCTGTCCCATATCTAAACAACCCAGCTCCGAAAAACCCTGGCCCACTTGATTTATTTTGCAGGGTTATGCCAAATTTTGAAAATGAGACTTTTTCTTGAGGCTTTGTTTCGAAAACATTCGAGCAATGCTTTATATATGCATATATAACCATCTGAACTAAACTTGCCGTGTCGTTTCATGTTTCATGACTCATAGCAAGTAGGTTGCTGGTTTGAGTCACGACTGGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGGTTACGTGGATTTCCTCTGGGTGCTCTGGTTTTAGTCCAAAGATATGTGGTATAGGTAAACCGAATAAGCTCAATTGGCGGTAGTGTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21840
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Nonsense | 323 | 1414 | 8 | 30 |
| ENSDART00000122270 | None | None | 234 | None | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5446991)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5416447 |
| GRCz11 | 11 | 5362753 |
KASP Assay ID:
2260-3871.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGGCCACTCCAGAGTCTGGACAACCGAGAGGTCTTCAAATCCGCTGTC[A/T]AAGACGCGTGGCTGCCTGATTTGACTTACCCCCCGGGGAACCCGTACGGT
Long Flanking Sequence:
AACACATTCCCCACACACAAACACAACCTGTGGCTCCTCTTACAGCGTGCTTTAGTTCAAGTGCCCCATCAAATGACTCCAGATTTCTTCGGATTTAGTTTTTGGCTTTTGGCTTTCTGAGCATTCAGTGTTTTATGAAAGCGAGAGCGGGAACGATGCAGGAGGTTAGTGAGGCATGGCAGAGGCGAAAATAAGACAGACAGTCGGTCATGTTTTTGGTCTTTGATCAGTCCGTGAGCTGAAATAACATTCCTCCGAGTCGCCAGTTTGGAAGGAGTGAAAAAAAAAGACATCTTGAGGGATGACTTACTGAAAAATAAGAGATGGATGTGAAAACATACTAAATTCTCTCTCTCTCTCTCTCTTTTTCTCAGCTGGAGGCGTTCTACTCCATCTTCACCACGGAGCAGCAGGATCATGTTAAATCTGTGGAATACCTACGTAACAACTTCCGGCCACTCCAGAGTCTGGACAACCGAGAGGTCTTCAAATCCGCTGTC[A/T]AAGACGCGTGGCTGCCTGATTTGACTTACCCCCCGGGGAACCCGTACGGTACCGAGGCTTCTAAAGGTGAGCGGGCTCTTCTCACAGCTGATTGGCTGTCTTCTACCAAGCCAGATGTTTTTACAACATTCTGCACTGACATCACAAAAAAGTTCACAGATTCTGTCTGGCCCTGATAATACAGTAAGTTACATGTAATTAGGGTTGTAACGGTATGAATTTTTCACGGTATGATAATCGTCTAAAACAATACCACGGTTTGACGGTTTCGCGGTATACGGTATGTTACAAATGTTACAAAATAATAGAACAGTAAAGCAAATTTGACTTTTTCCAAATAATATATTTTTAGTTACTATAAACAACACCACTTACAATGAACAAATAAAAAAATAAGAAAATAATAAATAATGTGTCAAAGTCCAAATAAAGTCCAAATAAACATGGTGCAAATCCTCAGTAAAAATAGATATAAATATTTACTATACTATAAATAGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14383
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Nonsense | 562 | 1414 | 12 | 30 |
| ENSDART00000122270 | None | None | 234 | None | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5480273)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5449729 |
| GRCz11 | 11 | 5396035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCCTCCACCCACCAGAGCCCRGCCAAACCTGTGGTGACCACTGCAGAA[C/T]AGGCCTCTGACRCAGACACCACCMCAGCCACTGAYAACGACAGGTCATTC
Long Flanking Sequence:
AATATATTCAGGAATTACATTATTTAAATATATTTTTATTATTTTTATGGAAATTACAGAAATGCATTTGTATAATACTTTTCAAATAATAAAAAAATGACATTATTTATGCATATGCATATTTTTTAAAATATTTCATGTATACAGTAATTCACTAATAGACTCATGTTTTTATTTTGTTTTTTAACTTTTAGCCAACAGTTTCTCCTGCATCGTCAGCAGACATGGCCCCCATCAGCTCCGGCTCCTCCACATGGACCTCCTCCGGTCTTCCCTTCTCCTTTGTTTCGATGGCCACCGGAATCGGCCCATCCTCCAGTGGCAGCCAGGCCACCGTGGCATCCGTGGTGACCAGTACACTCCTGGCAGGACTGGGCTTCAGCGGAGGCGTCATCTCCTCCTTCCCTAGCTCCGTGTGGCCCACCAGACCACCACCCTCCAGCCCTGCTCCAGCCTCCACCCACCAGAGCCCAGCCAAACCTGTGGTGACCACTGCAGAA[C/T]AGGCCTCTGACGCAGACACCACCACAGCCACTGACAACGACAGGTCATTCCTCCTTCTGTCACTCCAGTGTTTTAACACATAACAGTTTAGGGCTGCACGATCACAGAAAAAATGCTAATCACGATTATTTTATTATATATATATATATACACAACAGTTCTGTCTGGTTCTTAAATCTGATTGGCTGATACCTGTGCAATATTCTGCAATATCAGAACTTTATTATAAATTATTATATTATAAATATCGGTTTATGTGAAATAGGTCTGTACTTACATAAACATACATTTTGTGTGATCCCTCTTATTTAGGCAAAATAATTAAATAATTAATAATAAATAAAGAAAAACTTCAGATTAATCTTATAACTTTTGACCTCAACTGTACTGTATGTATGATTTGACAGTTTTATTTTGATAAAAATTGTAAAAAAAAAATCTAAAGTTACATTTACATGAACACTTTACACTTGGCTCTGCGACTGCATGTTATTGTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27721
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Essential Splice Site | 1030 | 1414 | 21 | 30 |
| ENSDART00000122270 | None | None | 234 | None | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5524646)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5494102 |
| GRCz11 | 11 | 5440408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTGCCGCACAGACCCCAGACATGGGCCCCATGCTTGTACACTGCAG[G/A]TAAAACCCACACACATTTGAGTATTGTTTATAGTTTACATTTGTATTTTA
Long Flanking Sequence:
AAAGTGTTCTCGCTAGGCTTGGAGATCAGCTAGTTATGGATTCAAAAAATGGTAAAACTCTGCAGTTTAACTTTAGGGAAGCTGTACAATGAGCCAAATTTTCCTCCAAAAAAAGGTGAAGTGTTCCTTAATGGAAAGATATATAAAAAATATATATTTAGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATATATAGTATATAAATATATTTGTTATATTGAAGAACATTTGGATGTTCAAGGGTCATGTGGTTTGTTTGTTTGCAGGGTCAAAAGGGGAACACTAAGGGCCGTCAGAGTGAGAGAACGGTTCTGCAGTATCACTACACCCAGTGGCCGGACATGGGTGTCCCAGAATACACTTTACCCGTGCTCACATTCGTCAGGAAGTCTTCTGCCGCACAGACCCCAGACATGGGCCCCATGCTTGTACACTGCAG[G/A]TAAAACCCACACACATTTGAGTATTGTTTATAGTTTACATTTGTATTTTATTTTTGTATCTTTATTGGAATGACATCTGGTTAGGGGACCACCAATGAAAACTTGTCTTTGGGATATTTGGCTATATTTACCTTCTTGGAGAATGCTGATTAGAGTATACTGTCCTTTGTTGTGAAATCAAATAAGCAAACATTCCTACATCTGATTTAATGGCTGAACAGAGTAATAAATGCACTGACTCGTATGATATCCATGTGTTTTTTTTTTCCTCAGTGCCGGTGTGGGAAGAACAGGAACATACATTGTGATTGACAGCATGCTACAGCAGCTAAAGGATAAAGGCGCTGTCAATGTGCTCGGCTTCCTCAAACATATACGAACTCAGAGAAACTACCTGGTCCAAACGGAGGTGAGTCAGCTGACATGGGGTCTGATTTATACAATTTGAGTAGAAATTGAACGTATACCAGAACGTATTTACATTTCTTGATTATTGATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10080
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 |
|---|---|---|---|---|---|
| ENSDART00000092552 | Essential Splice Site | 1124 | 1414 | 23 | 30 |
| ENSDART00000122270 | Essential Splice Site | 6 | 234 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 5528329)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 5497785 |
| GRCz11 | 11 | 5444091 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCTGACGCCGGGCCCAGGGGGCAAAAMACGACTAGAGAAGCAGTTYAAG[G/A]TGGGCACCGTCTCTTTCTTTATGCAAAGTATATTCAACAAGCAATTTATC
Long Flanking Sequence:
CCTGCATTTGTGTGGGGTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGCGGTACAGGTGAATTGGGTTGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGGATGTTTCCCAGAGATGTGTTGCGGCTGGAAGGGCATCCGCTGTGTAAAAACTTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGAATTAATAAAGGGACTAAGCCAAAAAAATGAATGAATGAATAATATTATTAAGTGACGTAATTGCATAGGAAATATTCAGCAGTAGCTAATTAGACGTATTACAGTACTTCTGAATAAACAAGGCCTCTGCCTTTGTGCATTTAGGAGCAGTATATCTTCATCCACGATGCCTTGATGGAAGCCATTCTTGGGAAAGAAACAGAGGTGCCCTCGAGTCAGCTGCACAGTTACGTCAACAGCATCCTGACGCCGGGCCCAGGGGGCAAAACACGACTAGAGAAGCAGTTCAAG[G/A]TGGGCACCGTCTCTTTCTTTATGCAAAGTATATTCAACAAGCAATTTATCGGTGGAAACTGTTTGCAGAACTGCCCTGCATGACATACACTTAGCATATCACAACACTCATGCTCACACGCAGTTCATTTTTAATGCATATTTATGCTGGTCGGAATTTTGCTTTTATCACTTCATACTTTATCGTTTCACACCTGCGACTTACAAGCCAAGCCTGACAGGTTCTGTGCGGGTAAAATGTGTGATATGTGGTTTGCTGGAGTTTCATGAGTTCATGAAATGTTTTATTAGGCCAGATAGTCCAGCTTTTTAGAGTCCCTTTTGGTTCAGTCTCAGTGGCTGAATATAAATCACATTTTATTTGGGATGCTACATATCAAGACAAAGGTTGGAGTGGCAGTGCCTAATATAATTTTCGCATATGCGCCCGAAAATTAATCTATGCGACCTCACAATATATCTGGGAGCATTAGTGCGACTGCAGATAATGATTGTAGTGCG
Associated Phenotype:
Not determined