ZMP
ca16b
Ensembl ID:
ZFIN ID:
Description:
Protein turosine phosphatase gamma B [Source:UniProtKB/TrEMBL;Acc:D2U7Y3]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33951 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33950 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12018 | Nonsense | Available for shipment | Available now |
sa7588 | Missense | Mutation detected in F1 DNA | Not yet available |
sa9647 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33951
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 |
---|---|---|---|---|---|
ENSDART00000017309 | Nonsense | 10 | 1382 | 1 | 29 |
ENSDART00000122241 | None | None | 217 | None | 7 |
ENSDART00000126246 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 46099235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46160169 |
GRCz11 | 6 | 46162051 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCTAATTGCGCATTTAGACATGTGGAGATTGCGAGGACCGTGTCGTT[T/A]AGGGATGTTGTGTTTGACTTTATCAGCCCTTCTCATCCAACCCATCAGCT
Long Flanking Sequence:
GTCTTCAGCGGGCGCTCAGAAGCTCAGCCTTCGGCGCTAGGATCCAGAGGGCAGGGCTTTGATTTCTCAACTAATTCCTCTGGCAAAACACGAAAGGCTCATATGCACAACTTCCTGGATAGAGAAGCGGATTCAAGCGACTGACTTTGTAGATGCGCGCGCTCGAGATAGAGAGAGAGAGAGCCGCTGTACAGAACAGACGAGGACGAGCATCTGAAAGTGCGTCCGGCTGGGATTAATAACTACTTGATAATGTAAAGAGAATGTAAAAAAGGACGCCACAGACAAGAGAAGTGTGCGCGGATTGTGGGCTGTCCGAAATGTCCCACCAAACAGGCGCAAGATTCGTCGCCGGTCATTAAACATCGCCTCGACCACTTGTCATTATTTTGGTTCGTCAAGTTTGTGGTGTTTTTTCTTCACTGACGCTCAATTTTGATCCGCCATTCTGGCTCTAATTGCGCATTTAGACATGTGGAGATTGCGAGGACCGTGTCGTT[T/A]AGGGATGTTGTGTTTGACTTTATCAGCCCTTCTCATCCAACCCATCAGCTGTCATCCCGGTAAGAGAGGCCTTTGTGCTTAATATTTTATCATCGGAATCATATTTTTTCTCCTCTGAAAAGTTGTGTTCGGCGTGCAGGTGCATCCGTGTCGATCAGCGCCAGAGATCATGAGGCATTAAGAGTGATGGTGTGTGTTTAGAGCACGTAACTGTAGGGTGCAAAGCGAAATGATCGTAACTGTAGCTGATGAATTTTAGCATTTAAAAAGGTGGATATGATTCATCACCGATTGTCAGTTTTGAAGTGTTCAGTGACAGGATTTAGCTAAGAGATCGAATGGTCTCGCGGACTTGATTGTTCCCAAGGTGATGTCATGCAGGCTGCGTGAAGGGTATCCAGAAACTCATAGATTTGACTTGAGTTAATTAAGTATTTTATTTAATTTCCCTCGTTTTAAAGTGTAATTAATAAAAAAGTAATAAAACATATTTTAATTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33950
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 |
---|---|---|---|---|---|
ENSDART00000017309 | Nonsense | 311 | 1382 | 8 | 29 |
ENSDART00000122241 | None | None | 217 | None | 7 |
ENSDART00000126246 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 45966033)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46026967 |
GRCz11 | 6 | 46028849 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATTACCTGAGGAATAACCATCGGCCCATTCAAGATCTCGACAGCCGG[C/T]GAATCTTCAAATCGGCTCTAATGGATGCCTGGATGCCTGAGACCATGGCC
Long Flanking Sequence:
TAGTGACCCTCTAGTGACCCCTAACCGAAGCACTAAAAAATTAACTGTAAAATTGAAGCACAAATAATTGTACATTTTTATATCCAGGAATGACTTTACTCTCTCTGAATAAATCAACCTCACTCCTAAATCTTACTCTGGATGTGTACACAGCTAGCACGGATTAACTAATCCTTTTCAATCTTTCAGTTTTTACCGCCTGCTTTATTCATCGTCACACAAAATAAAGCCATTAATTCCCATCATGCACGTCTCTATCACCTTTTTTTTTCACCTCCTTTCCAAAAGTAACGTGGCATCATACGCGTGTTTCTCCTGCATGAAATAATGAAACGAAATGGAAAATCATGATCAAACCAGTGGATAATAACATGACTCTCTCTCTGTCTCTCTAGCTCGAGGCGTTTTATTCCATCTTCACCACAGAGCAGCAGGATCATGTGAAGTCTGTGGATTACCTGAGGAATAACCATCGGCCCATTCAAGATCTCGACAGCCGG[C/T]GAATCTTCAAATCGGCTCTAATGGATGCCTGGATGCCTGAGACCATGGCCAGCGCCGCAGACACAGAAACATCTCGAGGTATGAGTCTGACTGATTGAGGAGAAAGGCAGATTTGATTTCTATTCATATGATAATTGTACCAATACAAAAGTGATGGTGATTAAATAGAGAGGTTGCCCCAAAATGCAAAAAAGAAATGCTGTTGATTTGCTCACCCTTTAGACCATCCATGTAGGCGACTTTTTTCTTTTGTCCCCAATCTTTTTATCAAAGCTTGACTAATTTAGTGAGTGTACATAGATTGCTAGGTGACCATCAACCGTCAAAGACCCAATATGTGAACGAACCCTAAAAGGCCATCTTCATTTGTGATCTCCAGCAGTTGATCTTCTTCAAACGTGTTGTAGATCCATTCCTTGGCAGTCCTTCACTGGGCCTTTAAAATAGTATTATTTTTTATTTTAAATATTAAGTTTTTAGTTACTCCCAAAATCTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12018
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 |
---|---|---|---|---|---|
ENSDART00000017309 | Nonsense | 584 | 1382 | 12 | 29 |
ENSDART00000122241 | None | None | 217 | None | 7 |
ENSDART00000126246 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 45944685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46005619 |
GRCz11 | 6 | 46007501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATAAAAAAGAGGACGATGAAGAGGAGGANNNNNNAGAGGAAGAAGAARAA[C/T]AGAGAGATGAGGAGAAGAAGAAGAAGGGGAAAGATGTGACRGTCAAGGAT
Long Flanking Sequence:
ATGGGTGTTTAAATCATTTAGGATTAATCATGCAGCTCAGCATCTAATCATTTTTAAACCTATGTATGCACTTATTTATTCACACTTCTTCCATCTGATTTCAGCCTACAGTTTCTCCGGCCTCTTCAGCAGACATGGCCCCCATCAGCTCAGGCTCTTCAACCTGGACGTCGGCTGGCCTCCCCTTCTCCTTCGTCTCTATGGCCACAGGAATGGGTCCACCATCCAGTGGAGGACAGGCCACCGTCGCTTCTGTGGTGACCAGCACATTATTAGCCGGCCTGGGCTTCAGCGGCAGTGTCATTTCATCCCTTCCTGGATCCTTCTGGCCAACGCATTCAACAAATACAGGCCCGTCGCCTACTCAACATCCAGCCACTCCAACAGCCGAAAACAGCCCATCTGAAGACAGCACCGACACTCAGAACAAACTCGAAGAAGAAGAAGAGCATAAAAAAGAGGACGATGAAGAGGAGGAGGAGGAAGAGGAAGAAGAAGAA[C/T]AGAGAGATGAGGAGAAGAAGAAGAAGGGGAAAGATGTGACGGTCAAGGATAAAAAGCAGACAGTGCAAAAGCCCACCGCTCCAATCCCGACATCTAAACACAGAGATCGAGAGAGACCGGATGCTGAGAGTTCTACACTGACCCCTGCTGAAGTGGAGGAGCAGGTTTCTGGAGCCACTGAGAGGCCGGATGCTGAGGATTCGTCAAAAGCGACATGGCAGGATGATAATGATATGCAGATTCCCTCCAGCTCTACAGAAAGCAGCAAACTGAGTGACGAGGAGAAAGCAAACTGGCCATACTACATTAACACTGGTAAGGGAGCTGTGAAGCTGCTGTGAAAAATAATATCTGTGGAGAAGAGCGAATAATTGCTAATAATTTTGACCTTGCAATATTTTTTGCCTTAAAATGTTTTTTATTTTTTTTATTAACAACTGGTTTTATTCTAGCCAAAATAAAACAACTGGATAAGACTAAAATAAGACTTTATACAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7588
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 > T
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000017309 | Missense | 671 | 1382 | 12 | 29 |
ENSDART00000122241 | None | None | 217 | None | 7 |
ENSDART00000126246 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 45944424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 46005358 |
GRCz11 | 6 | 46007240 |
KASP Assay ID:
554-4252.1 (used for ordering genotyping assays)
KASP Sequence:
CGACATGGCAGGAYGATAATGATATGCAGATTCCCTCCAGCTYTACAGAA[A/T]GCAGCAAACTGAGTGACGAGGAGAAAGCAAACTGGCCATACTACATTAAC
Long Flanking Sequence:
CCAGCACATTATTAGCCGGCCTGGGCTTCAGCGGCAGTGTCATTTCATCCCTTCCTGGATCCTTCTGGCCAACGCATTCAACAAATACAGGCCCGTCGCCTACTCAACATCCAGCCACTCCAACAGCCGAAAACAGCCCATCTGAAGACAGCACCGACACTCAGAACAAACTCGAAGAAGAAGAAGAGCATAAAAAAGAGGACGATGAAGAGGAGGAGGAGGAAGAGGAAGAAGAAGAACAGAGAGATGAGGAGAAGAAGAAGAAGGGGAAAGATGTGACGGTCAAGGATAAAAAGCAGACAGTGCAAAAGCCCACCGCTCCAATCCCGACATCTAAACACAGAGATCGAGAGAGACCGGATGCTGAGAGTTCTACACTGACCCCTGCTGAAGTGGAGGAGCAGGTTTCTGGAGCCACTGAGAGGCCGGATGCTGAGGATTCGTCAAAAGCGACATGGCAGGATGATAATGATATGCAGATTCCCTCCAGCTCTACAGAA[A/T]GCAGCAAACTGAGTGACGAGGAGAAAGCAAACTGGCCATACTACATTAACACTGGTAAGGGAGCTGTGAAGCTGCTGTGAAAAATAATATCTGTGGAGAAGAGCGAATAATTGCTAATAATTTTGACCTTGCAATATTTTTTGCCTTAAAATGTTTTTTATTTTTTTTATTAACAACTGGTTTTATTCTAGCCAAAATAAAACAACTGGATAAGACTAAAATAAGACTTTATACAGAAGAAAAAAATAGCAAATACTATGAAAAATGCCTGGCTCTGTTAAACACCATTTGAGAAGATTTTAAATAAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTAAAGTCAGAATTATTAGCCAATTTTTTTCTTCTTTTTAAAATATTTTCCAAATGGTGTTTAACAGAGAGTGTTTAAATGTCACCTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9647
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 |
---|---|---|---|---|---|
ENSDART00000017309 | Nonsense | 935 | 1382 | 19 | 29 |
ENSDART00000122241 | None | None | 217 | None | 7 |
ENSDART00000126246 | None | None | 253 | None | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 45909571)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45970505 |
GRCz11 | 6 | 45972387 |
KASP Assay ID:
2259-8057.1 (used for ordering genotyping assays)
KASP Sequence:
ACATAATGGTGACTCTGAAGARCACTAAAGTTTATGCTTACTATACACTM[C/T]GACATTTCATCRTACGCAACAGCAAACTGAAAAAGGTGCGTTAAAGCATT
Long Flanking Sequence:
GGTTCATTAGACAAGTTAGAGTAATTAAGCAAATCGTTGTATAACAGTGGTTTGTTTTGTAGAAAATTGAGAAAAAATATTGCTTGAAGGGGCTAATAATTTTGACCTTAAAAGTTTTTTTTTTTTTTTTTTATTTAAACTGCTTTCATTCTAGCCTAAATAAAACAAATAAGACTTTTTTCTAGAAGAAAACATAGGATCAAACATACTGTGAAAATTTCCTTGCTCATCAACATCATTTGGGAAATATTTGAAAAAAAAAGAAGAAACTCACAGGAGGGCTAATAATTTTGACTTTCAATGTACATAGTCTGAAATGCATTTAAGAACTGCTCTGTGTGGCTGTCATTTGTTGAGTTATTGTGCTAATGTAGATTTTGATGTCTTTGTTGTGTTTCCAGAGGAAATGTGATCAGTACTGGCCGTCGGAGAACAGCGAGGTGTATGGTAACATAATGGTGACTCTGAAGAGCACTAAAGTTTATGCTTACTATACACTC[C/T]GACATTTCATCGTACGCAACAGCAAACTGAAAAAGGTGCGTTAAAGCATTCATAGTTTAAAGAGACGGCTTCATAATATTTCTATATTACTTCAATACTTCTATAATACATAAAAGAACAAAGAGCAAAGAAACAGATCCAGGATGTTTCTTAATTTTTATTTAATTCACATTATTTTAACTTTCAACAACTCTGTTAATAAACAGAGCACTTCTGTTTGGTAGCTTGAACAATCAAGTAATAAATAACTTAAATTATTCACTTCTGGACTTTGTAAATATATTTTTAAAAATCTAATATAAAAACAAATAGCACCTCAACTTAAAATACCTGGCAGGCATTCCTAGATTTACATATCTCACAGTTTGCTATGGCAATGTTGTCGTCATCAACTTTATAATACCTCCAGGCCGCAGACATACTCACGCTTTCCGCTCCATGCTGCTTCTGTGTTCTACTTTGCCGGCATTTAACCAATAGTTTCTCAGCAACAAAAAGTG
Associated Phenotype:
Not determined