ZMP
PTK2B (1 of 2)
Ensembl ID:
Description:
PTK2B protein tyrosine kinase 2 beta [Source:HGNC Symbol;Acc:9612]
Human Orthologue:
PTK2B
Human Description:
PTK2B protein tyrosine kinase 2 beta [Source:HGNC Symbol;Acc:9612]
Mouse Orthologue:
Ptk2b
Mouse Description:
PTK2 protein tyrosine kinase 2 beta Gene [Source:MGI Symbol;Acc:MGI:104908]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22987 | Nonsense | Available for shipment | Available now |
sa36298 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13889 | Nonsense | Available for shipment | Available now |
sa2896 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa22987
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 |
---|---|---|---|---|---|
ENSDART00000028407 | Nonsense | 301 | 933 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 5925475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 6004411 |
GRCz11 | 17 | 6161641 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAATTCGAAGTATTAAATGCACACATCAGAACGATGGAAAGGCACTGT[T/A]ACATATCAATATAGAAGGAGCTAAACAGGTAAATGCATCTGTCTTTAACT
Long Flanking Sequence:
ATTATTTAATTGTAAATTAGATGGCATTTGTCTTTATTCATATTTAGTATAATGCATTGATTAATGTTTTAATTTGTATATTTTTTTTAAATGTTAGTTTTAATGTCTTTGGCGTCATTTAGATCATTTTAATTAATATTTATATGTATTTAATACTTTATTTTAAAATGTTTTTGTCTGTCTTTTTTTGTTATTTTTTTAACAGTGCACACCATTTATAAAAAAATTTATTTCAACGTTACTGTAACTTTTTTACCTCAGGTAAAATTAAATAAAAATTAGTATGTTACATTTTAAAGTACTTGAATATATTGTGTAATTGTTTTATTTCAGTAAAAGTTTGAAAATTAACTATTTTATTCATTTATTTATTTATTCATTTTAACTAAATATTGAATTAATGCTGGTCTTTTTGTTTCCTCATTAGCCGGTATCTCTTGCCACATTTTCACAAATTCGAAGTATTAAATGCACACATCAGAACGATGGAAAGGCACTGT[T/A]ACATATCAATATAGAAGGAGCTAAACAGGTAAATGCATCTGTCTTTAACTTGTTTTAGATTTGCGGGTCAGTTTCAGGCTGTTTCTCTTTGTATTCTTTAAACTGGTATTACATACGACAAATGTATAATTTACAGTAACCTGAATCCATTGATAATGTTCAAGGCTAAATGCCTGAATGTGATAGGGAACATTTGATTGTAAAACTATTTCTTTTGAAATTTTTTGTTAAACTTTTTAAGGCAAAAGATTTGACAATTTCAAAATTGACACTGACAGAGTTAACAACGACAGAGTTGACAAATAACAGAATTGACAAAAATAGTTGACAAATAGCAGAGTTGACAACGACAGTTGACAAATAGCAGAATTGACAATGACAGAGTTGACAATGACAGAATTGACAATGACAGAGTTGACAATGACAGAGTTGACAATGACAGAATTGACAATGACAGAGTTGACAATGACAGAGTTGACAATGACAGAATTGACAATGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36298
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028407 | Nonsense | 384 | 933 | 13 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 5918223)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5997159 |
GRCz11 | 17 | 6154389 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATCTCTCGTTGTTTTTTGCAGATTCAGATATTTATGCAGAGATACCC[G/T]AAGAAAAACCACTTGCAGGTAAGAACCAAATAATGATTTATGCTTTAATT
Long Flanking Sequence:
AATCACGCCAAACATGTCTTGCACCCTTTTACGCAGAGTGTATGATAGGGCCCAAAATGTGAATTGTGTTTATGATTTATTTGTTTATTTATTATTTAATGTTTGCTTGTGTTTAATAGACAGAGAATCCAGAAACTCTCTACCTCCATTACCCGGCAGGTGAACACTGATGCTTTTCTTTTTCTGTATTTTGTCCTTTTATATATTTTAATTGCATATGATTTTATGTATATGATATCATTATATGTAACTCCACCCATTTGTTTTTAATCTCAATGTCTCAAATCATATATTGGAAATTAGCAAGGAGAATACCACATCTCACAAGGAAGGCAAAAGTATGTAAACCCAGATAAATTCAGTGTATATGTTTACTGTTTATAATATAATTATTTATTATTAAAGCCAAATTTTTCAATATCTAATAATGTCTTTAATATTCTAAATTATTTCATCTCTCGTTGTTTTTTGCAGATTCAGATATTTATGCAGAGATACCC[G/T]AAGAAAAACCACTTGCAGGTAAGAACCAAATAATGATTTATGCTTTAATTGTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCAATTAATTATTAATTCAATGATTAATTCATTCAATTATTTATTCATTCATTCAATGATCCATTTATTCATTCATACTATCATTTTTAGATTCATTCATTCATATAATCAACCTTTAATTTTTTAATGAGTTAATTTATTCAAGGATTCACTCATTTATCAATCAATCCAAAGATTCATTCATTAATTCATTCATGTAATTATTCATTCAACCATGAGTTTATTCATTCAATCAATTATTTATTCATTCAATCAGTGAGTAATTAATTTATTCAGGGATTTTTACATTTAATTATTCACTGATTTAAGGATTTATTCATTCAATCATTCATTTATTCAATCATTCATTCGATGATTTATTTATTAACTCAGTGATTAATTAATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13889
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 |
---|---|---|---|---|---|
ENSDART00000028407 | Nonsense | 602 | 933 | 20 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 5907705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5986641 |
GRCz11 | 17 | 6143871 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGTGTGTATGTGGGAGATCATGAGCGGAGGTCAGCAGCCGYTCTTCTG[G/A]CTGGAGAATAAAGATGTGAWCAACCAATTGGAGCAGGGCATGCGTCTGCC
Long Flanking Sequence:
AGACTGCGTATAAAAAAGGTTTATTCTTCTAAATTTCCCAACAAGCTGACTTTAGAGGCAGATATGTAACAAATATTGCTGTAAATTTTAAACAAACATGTCATAAAAGCTCTTATATTCTCATACCTCTTCATTTGTAGCATTGTTATGAAAGATCTCAGTTTGAAGGGCTGTCTGACCCCTACATATCCAACAAAAGTAAATAAATATTTGAACATCATTTAAATTCTGATAACCTTACTTCATGACTTGACAGAATAAGCCAGTCTGTCAGAAAGTGGCTGATGGCTGTGAAAAGCATTGTCTGGTAAAATGTTAATGTTGTATTCGTGTGGTTACACCAATAAATAAAGGCACATTAAACACAAAGTATAGTTCTGTCCATCTTGCAACACTCAGAGGCTCGTACTTGTTCATATGTTTGCTGATGGTGTGTGTGTTGTGTTTCCAGCTGTGTGTATGTGGGAGATCATGAGCGGAGGTCAGCAGCCGTTCTTCTG[G/A]CTGGAGAATAAAGATGTGATCAACCAATTGGAGCAGGGCATGCGTCTGCCCAAACCTGAGCGCTGCCCGCCGACGCTCTACTCTCTGATGACCCGCTGCTGGAGCTACAGCCCGAGAGACAGACCCAGCTTCACTGAGCTTGTCTGTAAACTCAGGTGAGTCACCTGAGGGAAACCTGCAGCAGAGACTGAAATTTGATTAGTTAGCATACATTTATGCTATAGCTCAGTTGGGAGAGAGTTAGACTGAAGATCTAAAGGTCCCTTGTTCGATCCCGGGTTTCGGCAAAACAGTGCTGACGTTCTGGGGCGAAGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCAAAGCAAGAACGTCGCTGGGTCACTGGTTTGAGCCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCATTCGCATGCGTTTCCTCCGGGTGCTCCAGTTTCCCCCACAGTTCAAAGACATGCAGTACAGGTGAATTGGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2896
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000028407 | Essential Splice Site | 755 | 933 | 24 | 29 |
Genomic Location (Zv9):
Chromosome 17 (position 5894204)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 5973140 |
GRCz11 | 17 | 6130370 |
KASP Assay ID:
554-2539.1 (used for ordering genotyping assays)
KASP Sequence:
TTAATTCTGACTTCATCTGTAGCAAGTCACCTTTTCTTGTTTCTCGTTTA[G/A]GTTCCGTTTGCTAATGAAGACATGAAAACGAAAGCGGTAAAGCTTATCTA
Long Flanking Sequence:
TTGCATAATATTGCACGGCTATCAGCCAACAATCAGATTGGAGTACCAGACAGAACTGTTTGTTGTAATATTTGACTAGAAATTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTAGGCAGGTTAGAATAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTAGACTATTGAAAAAAATAGCTTAAAGGGGCTAATAATTTTGACCTTATAATGGTATTTAAAAAAATAAAAACTAAAAATATAAAAAAAATAAAAATAAAAAGCTTTTATTCAAGCCGAAATGAAACAAATAAGACTTTCTCCAGAAGAAAAAACATATGATCAGACATACTGTGAGAATTTCCTCACTCTGTTAAACATCATTTGAGAAATATTTAAAAAATAAATAAATAAATAAAAAGGGGAGCTATTAATTCTGACTTCATCTGTAGCAAGTCACCTTTTCTTGTTTCTCGTTTA[G/A]GTTCCGTTTGCTAATGAAGACATGAAAACGAAAGCGGTAAAGCTTATCTACTTTTTACTGTCATGCCTTTTTTCTGCTGTTGTTTTACACTGTCTTGATTTTATGTTTTTTTTTGTTTCAGACCACAGAAAATGACACTGGCCAAGGTTGTTTTTTTATGTTTGTGTTGTTTAGCTTTCATTTATATTTCATTTATTTTTTAATCATTTTAATGCTTCAAACTAAATGCAATACTGTTATTTTTATATTTATGTCATTTATATAAGTTTTTATTATCAATTTCATGTTGAAATTTATCAACAAGAATTTCATGTTGTTCAATAACAAAGATATATACATTAGATGTCGCCTACCCTGTTGTTGTCTATTGGAAGGAATGCGTCAATAGAGCCGCCATTTTGGAACAGGGTAGCGCTCCATTGAAATGAATGCGAGACCAAGGTACAGTGGAGGACTGTGGCCATCCAAAGCCAGAGATATACACATATACAAATATATCT
Associated Phenotype:
Not determined