ZMP
zgc:112211
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553690 [Source:RefSeq peptide;Acc:NP_001018501]
Human Orthologue:
PTK7
Human Description:
PTK7 protein tyrosine kinase 7 [Source:HGNC Symbol;Acc:9618]
Mouse Orthologue:
Ptk7
Mouse Description:
PTK7 protein tyrosine kinase 7 Gene [Source:MGI Symbol;Acc:MGI:1918711]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10484 | Nonsense | Available for shipment | Available now |
sa37574 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37573 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10484
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 |
---|---|---|---|---|---|
ENSDART00000098461 | Nonsense | 470 | 1061 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 41320533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 38424666 |
GRCz11 | 22 | 38410952 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAAGCTCTTCTCCAATGGGACTCTTCGCATAAATAACGTGGAGGTGTA[C/A]GACGGCCACATGTACAGCTGCGAGAGCAGAACGGAGGCWGGAAGAGTGAA
Long Flanking Sequence:
TGTATTTATTTATTCAAATTAAGCTTTTATAAGTTATTTTATAGAACACAAAAGAAGATATTTTGAAGAATGTTTGAAACCATTGACTTCTGTAGTAGGAACAAAAAATACCATGAAAGTCAATGGTTACAGGTTTCCAGCATTCTTCAAAATATCTTCTTTTGTGTTCTACAAAATAAAATAACTTATAAAAGATTTATAACCTTTATTTAAATAAATAAATACCTATATTATGTATTTTTATTTATTTATTTGTTTATTTATTTATTTATTAAAGTGATAGTTTGCTTGAAAACGAATTTTCACTCAACATTTGCTCTCCATCAAGTTTATTATAAACCTTTATAAGTTTCATAATTCTGAAGACCACAATAGAAGATATTTCGAAGAATGTTTTAAATGCTTGTTGATATTTAATGCACTCTTCTGTGTTTTTGACAGGACGTCCGCTTCAAGCTCTTCTCCAATGGGACTCTTCGCATAAATAACGTGGAGGTGTA[C/A]GACGGCCACATGTACAGCTGCGAGAGCAGAACGGAGGCAGGAAGAGTGAACGCCCAGGCGAGGGTTTTTGTGCTTGGTGAGGAACTTTTGTTGTTTTATTTTTGAGTCTTAAGGGCGCAGTGTGTAACATTCTCCACTAGAGGGTGTGTATTCACAACAAACAAAGGTGTAGTTTGATGAGTGAACACGTATTGAACAGGTCATGTATTTTCCTGGGAGTAACATTTCTAAAGGAGCTGCTGAGATGGAATTGAACCGGATTTTGGTAAAAACCCCAAACAATACACACATAAACATAAAACAAATCAAAACCAATGAGTTTTTTGTAATGATAACAGGTGAATGACAGAATGAGAAAGTGCTGAGCTGCTGAAATGTGTTTAATACTGTATATAAAAGTCTGTTTGGTGCTCTCATATGGATAATGAAGGCACATGCAGTGTTTCACAGACTTCAACAGTTTTAAATCTTGATGCTTCTGTGGGTCTCGTCTATCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37574
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098461 | Essential Splice Site | 872 | 1061 | 17 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 41308146)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 38412279 |
GRCz11 | 22 | 38398565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTCTGAGCTGCATTTATCACTGTTTGATTGTGCTGTGTGTGCTTTTC[A/T]GGGTGATCTGAAGCAGTATCTGAGAGTCTCCAAGAGCAAAGATGAGAAAG
Long Flanking Sequence:
TATCTTTTGACAGATCTTTTGGGAAAATGCTTTGAAAATGTATCCAAAACTCAACAATACACTGTTGGCAAATTGACTACCCTTTCAGTATGTTGGGGGCTGTTTTTGCCCCATTGACTTCCATAATAATTTGATGCAGGTTTTTGCTTTCTAGGGTGTCTGTGGGGTCTTAAAGTCTTAAATTCACAGAAATATTGTGTTGTAGGTCTTAAATCATTTTAAACAAGTCTTGATTTTTTATTTTATCTTAATTTTCCTAAGTCCATGTAAAGCTACCTACATCACTAACAATAAAACTTTAACAAAAGTTTAAATTATTAACTCTGTTTACAAATATTGTAAATTATATATTCTATTTTTTTTTGTTAAGTTGTGTTTATAGCTGTAACAAACACCACAGTAATGAATGTCCTCTTGTGCCTTTGATTTCGGAGTGTTGATTGAAATATCATGTTCTGAGCTGCATTTATCACTGTTTGATTGTGCTGTGTGTGCTTTTC[A/T]GGGTGATCTGAAGCAGTATCTGAGAGTCTCCAAGAGCAAAGATGAGAAAGTCAAAGTCCAGCCGCTCAGCACCAAACAGAAGGTTAGTTCATGGTGTGAGTTACAGGGGGGGCTTGATCTCCCTAATTAATGCTTGATCTACCATGAAGGGGAGTTTGGGGGGGGGGTCCTGATATTGTATCCCACCTGTCAGATTCTGCTACCAACTCTTTATTTGACAGATGTTGAGGTTAGGGATTGGGGTGGGTTAGGGTGATATTAGAATTTTACACACACACACAGGTTTGTTTTTGTGAATTTTGGTGACATAATCCATAGGTTTCCATTGATTTTATACTGTTCAAACTATAATTTCTATTGACCTACAGTGTGCGATTTTACTTTCTGAAAAAATACTCATTCTGTATTATTTATAAGCTTTTTGAGAAATGGAGACATCAGCAATGTCCCCATAATTCATGATCTCCTGTAATTCCTGTGCCATATACATGTCTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37573
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098461 | Essential Splice Site | 1009 | 1061 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 22 (position 41305710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 38409843 |
GRCz11 | 22 | 38396129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGGGGAAATGCCCTACGCTGACCTTGCTGATGATAAAGTGCTGGAAGG[T/C]GAGAAAGAGGATCCAAACATGCTATGACTTTCCAAAAACAATCATTTCTT
Long Flanking Sequence:
TTCACATTCACTTCACTCCCGCTGCTCTCAGCCTCCTGCTGCGCACACACACACACACACACACACACACAATATTTACTCATTTGTCTCATCAAAGTATCCATCCAGAGCAGGACTCGACACTTCTCAGGCCCCGTTTACACTAGTGCGTTTTAGTTTTAAAACGGTGTTTTAGAATGAAAACGATCCGCGTCCACACTAGCGTTTTACCCAGCGTTTCTGAACTTCAGAATGTACACAACATCAGGAATACAAGGAACACCCCCTCTCTCTGCCGCCTCCTGGTGGTGACTGTGTGTTTGTTGTGTTGTTCCACACAGCGAGTATTACCATTACCGGCAGTCCTACATCCCTCTGCGCTGGCTGCCGTCTGAAGCAGTCTTCGAGGATGATTTCTCCACCAAGACAGACGTGTGGTCGTTCGCCGTGCTCATGTGGGAGGTGTTCAGTTTCGGGGAAATGCCCTACGCTGACCTTGCTGATGATAAAGTGCTGGAAGG[T/C]GAGAAAGAGGATCCAAACATGCTATGACTTTCCAAAAACAATCATTTCTTAAGGTGGATAATAATACAGAGTATAACCCTTGTGTAAGGTTCAGATCTACTACTCTTTCATTGTGTTCGGGGCTGTTTTTGCCCCATTGACTTTCATTTTAATCGCATATTTTTGATTGCAAAGCCAAGACGGCAAACAGTATAATCAATATAGAGTACAGTAATTTAATATTTGCTTATTAGATTTGATCTATAGAGTGCTCTAAGTGAATATTTACTATTAAGAATTTGATTTGATTATAAAATGCTCTAATTCAATGTTTACTAGTAAGAATTGAACTATAAAGTGCTCTAATTCAATGTTTACTAGTAAGAATTGAACGATAAAGTGCTCTAATTCAATGTTTACTAGTAAGAATTGAACTATAAAGTGCTCTAATTCAATGTTTACTAGTAAGAATTGAACTATAAAGTGCTCTAATTCAATGTTTACTAGTAAGAATTGAACTA
Associated Phenotype:
Not determined