ZMP
tyro3
Ensembl ID:
ZFIN ID:
Description:
Tyrosine-protein kinase receptor TYRO3 [Source:UniProtKB/Swiss-Prot;Acc:Q9YI66]
Human Orthologue:
TYRO3
Human Description:
TYRO3 protein tyrosine kinase [Source:HGNC Symbol;Acc:12446]
Mouse Orthologue:
Tyro3
Mouse Description:
TYRO3 protein tyrosine kinase 3 Gene [Source:MGI Symbol;Acc:MGI:104294]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5899 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28813 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36334 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5899
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 |
---|---|---|---|---|---|
ENSDART00000040431 | Nonsense | 722 | 868 | 18 | 19 |
ENSDART00000081659 | None | None | 691 | 19 | 20 |
ENSDART00000140391 | Nonsense | 722 | 868 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 10049211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10396113 |
GRCz11 | 17 | 10552147 |
KASP Assay ID:
554-3877.1 (used for ordering genotyping assays)
KASP Sequence:
CTTACCCAGGAGTGGAGAACTCWGAGATCTACGAGTATCTTATCAAGGGA[G/T]AAAGACTAAAGCAGCCGCCGGACTGCCCTSCTGACATGTACGTTTTAATT
Long Flanking Sequence:
TTCAAACCCTGCAATTTTTACAGCGTATAAGAGACTTTCTGTAGCTTTGTTTACCAAACAAGTGGTTCGAATTGGATTTTGATTGTAAACCTTTAATAAAAATGTACCTAGTTTTCTATTTTATGTGTTAGGATTTCAACTTCTTCAAAATCTCTCTGTAAATTTACAGATTTTATTTATTTATATATTTATTTATTTGTTTTACAAAATTATGTGTAGAAATACCAAAAAAGTCTGAGATTCTGTTTGGTCCTAGTCATTACATTACATTACATTACAATTTTTGACAACAGAATCTAGTATATTAGACAGCTATGTAATAGTCTATTATACTAGGTTTTGTAATATGTTTAGCCTTTGTTACTGACCTGTCTTGTGTTTTTTTTTTTTTTTGTTTAAAGTGGGCGTTTGGTGTGACTATGTGGGAGATCATGACTAGAGGTCAAACACCTTACCCAGGAGTGGAGAACTCTGAGATCTACGAGTATCTTATCAAGGGA[G/T]AAAGACTAAAGCAGCCGCCGGACTGCCCTGCTGACATGTACGTTTTAATTGTTGGGGTTTGTAAAATATCCCAAATTTTTTTTTAAGAGTTTTTTTTTTGGGTTTAACTTAATTGTTTTATGTTCAATTCACTTAATTTAGTAAAAGCTAATAAGTTAACTTGGTTCCTTCATGTTACACCAACACAAATCGATTGTGTGGAACCCCACATTTTTACAGTGGTCCTTAAAACCACAAAATATTTTGATGCTCATTGATCCACTTGACCAACTATCCCACATTTTCTCCCTTTCAGTTACGAAATCATGCACAGCTGTTGGTCTCCAGTGCCTAAATGCCGCCCCAGTTTCCAGCACCTCATTGACCAATTGGAGCTCCTGTGGGCGAAGTTGAATCCTGCTCCTGTAAAAGAGCCATTGCTGTATGTCAACCTTGAGGAGGAAGATGGAGAACAGGCTAATAGCGGGACCCGGAGCAGTGAGGAGCCCTCATGGGGCGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28813
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 |
---|---|---|---|---|---|
ENSDART00000040431 | Nonsense | 766 | 868 | 19 | 19 |
ENSDART00000081659 | None | None | 691 | 20 | 20 |
ENSDART00000140391 | Nonsense | 766 | 868 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 10048820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10396504 |
GRCz11 | 17 | 10552538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCAGTTTCCAGCACCTCATTGACCAATTGGAGCTCCTGTGGGCGAAGT[T/A]GAATCCTGCTCCTGTAAAAGAGCCATTGCTGTATGTCAACCTTGAGGAGG
Long Flanking Sequence:
TTGTTTAAAGTGGGCGTTTGGTGTGACTATGTGGGAGATCATGACTAGAGGTCAAACACCTTACCCAGGAGTGGAGAACTCTGAGATCTACGAGTATCTTATCAAGGGAGAAAGACTAAAGCAGCCGCCGGACTGCCCTGCTGACATGTACGTTTTAATTGTTGGGGTTTGTAAAATATCCCAAATTTTTTTTTAAGAGTTTTTTTTTTGGGTTTAACTTAATTGTTTTATGTTCAATTCACTTAATTTAGTAAAAGCTAATAAGTTAACTTGGTTCCTTCATGTTACACCAACACAAATCGATTGTGTGGAACCCCACATTTTTACAGTGGTCCTTAAAACCACAAAATATTTTGATGCTCATTGATCCACTTGACCAACTATCCCACATTTTCTCCCTTTCAGTTACGAAATCATGCACAGCTGTTGGTCTCCAGTGCCTAAATGCCGCCCCAGTTTCCAGCACCTCATTGACCAATTGGAGCTCCTGTGGGCGAAGT[T/A]GAATCCTGCTCCTGTAAAAGAGCCATTGCTGTATGTCAACCTTGAGGAGGAAGATGGAGAACAGGCTAATAGCGGGACCCGGAGCAGTGAGGAGCCCTCATGGGGCGTCCCGTGGCAGTGTGCAGGTATTGAGGAAGACGAAAAAGATTGGTTAATGGTGTCATCGGGAGCTGCTCTTGCTATTGGTGGAGATTACCGGTACATCATTGGCCCGTCTGTTAGCGCCATTGATGAAGAGAGCAGACATTCTGACGACGGACTATCGGAGGATATCAGGGAAGAAGAAGAGGATGTTATTATTAATGTGTGATTTATACTGTTGAAGTCTGAATTATTAGCCCACCTGTTTATTTTTCCCCTAATTTCTGTTTAACAGAGAGGAGATTTCTACAACACATTTCTAAATATGATAGTTTTAATAACTGATTTCTTTTATCTTTGCCATGATGACAGTACATCATATTTGACTAGATATTTTTCAGGATACTAGTATTCAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36334
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 |
---|---|---|---|---|---|
ENSDART00000040431 | Nonsense | 787 | 868 | 19 | 19 |
ENSDART00000081659 | None | None | 691 | 20 | 20 |
ENSDART00000140391 | Nonsense | 787 | 868 | 19 | 19 |
Genomic Location (Zv9):
Chromosome 17 (position 10048758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 10396566 |
GRCz11 | 17 | 10552600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAAAAGAGCCATTGCTGTATGTCAACCTTGAGGAGGAAGATGGAGAA[C/T]AGGCTAATAGCGGGACCCGGAGCAGTGAGGAGCCCTCATGGGGCGTCCCG
Long Flanking Sequence:
ACCCAGGAGTGGAGAACTCTGAGATCTACGAGTATCTTATCAAGGGAGAAAGACTAAAGCAGCCGCCGGACTGCCCTGCTGACATGTACGTTTTAATTGTTGGGGTTTGTAAAATATCCCAAATTTTTTTTTAAGAGTTTTTTTTTTGGGTTTAACTTAATTGTTTTATGTTCAATTCACTTAATTTAGTAAAAGCTAATAAGTTAACTTGGTTCCTTCATGTTACACCAACACAAATCGATTGTGTGGAACCCCACATTTTTACAGTGGTCCTTAAAACCACAAAATATTTTGATGCTCATTGATCCACTTGACCAACTATCCCACATTTTCTCCCTTTCAGTTACGAAATCATGCACAGCTGTTGGTCTCCAGTGCCTAAATGCCGCCCCAGTTTCCAGCACCTCATTGACCAATTGGAGCTCCTGTGGGCGAAGTTGAATCCTGCTCCTGTAAAAGAGCCATTGCTGTATGTCAACCTTGAGGAGGAAGATGGAGAA[C/T]AGGCTAATAGCGGGACCCGGAGCAGTGAGGAGCCCTCATGGGGCGTCCCGTGGCAGTGTGCAGGTATTGAGGAAGACGAAAAAGATTGGTTAATGGTGTCATCGGGAGCTGCTCTTGCTATTGGTGGAGATTACCGGTACATCATTGGCCCGTCTGTTAGCGCCATTGATGAAGAGAGCAGACATTCTGACGACGGACTATCGGAGGATATCAGGGAAGAAGAAGAGGATGTTATTATTAATGTGTGATTTATACTGTTGAAGTCTGAATTATTAGCCCACCTGTTTATTTTTCCCCTAATTTCTGTTTAACAGAGAGGAGATTTCTACAACACATTTCTAAATATGATAGTTTTAATAACTGATTTCTTTTATCTTTGCCATGATGACAGTACATCATATTTGACTAGATATTTTTCAGGATACTAGTATTCAGCTTAAAGTGCATTTAGGGGGCTTTCACACCTGCCTTATTTAGTTCGATTGAATCGCACTAGAGTT
Associated Phenotype:
Not determined