ZMP
kdr
Ensembl ID:
ZFIN ID:
Description:
Vascular endothelial growth factor receptor 2 [Source:UniProtKB/Swiss-Prot;Acc:Q5GIT4]
Human Orthologue:
KDR
Human Description:
kinase insert domain receptor (a type III receptor tyrosine kinase) [Source:HGNC Symbol;Acc:6307]
Mouse Orthologue:
Kdr
Mouse Description:
kinase insert domain protein receptor Gene [Source:MGI Symbol;Acc:MGI:96683]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13239 | Nonsense | Available for shipment | Available now |
sa43425 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43426 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23684 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13239
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 |
---|---|---|---|---|---|
ENSDART00000049204 | Nonsense | 121 | 1357 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 22304991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22333158 |
GRCz11 | 20 | 22232831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTATAAGAGCMTGCCAAAAGAGGATGGGAARACATCTGWAGCTGTATA[T/A]GTCTTCATACAAGGTATCATTGTCATGTCGGAAAAGTTTTAAGACAATTT
Long Flanking Sequence:
GATATGTTTTATTCTTGCAGCGATAGAGCTCAGGTTTGTACCTGATCCTCCAACCTTGAACATCACTGAGAAGACTATCAAAATCAATGCTTCAGATACACTTCAAATCACATGCAGGTAAACTTTCCATCAGTTGTTTAATCCTTATTATAACAAAGTTACTTTGTCTCATATTCTGAATAAGGGATACTGATTTTGTTTATTGCTTTGTTTGGTTTACAATAATAACATATAGTAAACAATGTAATTTTGTTATCAATTTTCTCTATTAATAGTCTTTTTTTAAATCTGTTTCTCAGGGGTCGTCAAATTCTGGAGTGGTCCACACCTCACAACCGGACCAGCTCTGAAACCCGGCTCACTATATCCGACTGTAGTGGCGATGGACTATTCTGCAGCACTCTGACACTTTCCAAAGCTGTAGCCAATGAGACAGGCGAATACCGCTGCTTCTATAAGAGCCTGCCAAAAGAGGATGGGAAAACATCTGTAGCTGTATA[T/A]GTCTTCATACAAGGTATCATTGTCATGTCGGAAAAGTTTTAAGACAATTTTTAAAATACTCCTACTTTCTCTCTTAAGTAAAGTGGGAAAGAGAGTTGGAATGTTGCAAAAAATGTGTCCATCACATACTTCCTTTGTTATCCTTCTGGATAACCCTTTGACCTCTTCATCCTTCATAACCTCTTCACCACTACATTTTACCTCCCATTTCAGCCAGCTGTAAACTCCTCCCTTGTCCAGACAGACAAAATATAGGAAATAGCTTGTTTCGAGTTTTAAATGTGGTTGTGTAAACCTGCATTGCTTTCTGTGCCTGCAGATCCGGACTGGTACATTTGTTGTCCATAAGAAGTGTCATGTCTCTTATACAAGCTAAAAAGAATAGTTTTTGCAAAAATCATTCACCCTGGGTTTTTTTTTTTAATAAAACCTATTTGAATTTCTTTCGTTTGTTGCACCTAAAGGGAAAAAAGCATATTAGGTTTAGTTCCTATAGTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43425
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049204 | Essential Splice Site | 268 | 1357 | 6 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 22309482)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22337649 |
GRCz11 | 20 | 22237322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCTCAATGTTGGAATCGACTTCCAGTGGACCTTCCCTCATGAGAAGG[T/C]CAGTAATGGAGAGAAATGCCCAGAGTTCAGTCATTTTTACCTCTGATTGG
Long Flanking Sequence:
CTTATAAAATATATCAAAATAAAAAACAGTTGTTTTAAATTGAAATAATATTTCACAATACTACTCATTTTATTTTTGAAGAGACTTTTTGAAGAAACATTCCTACTGATCCCAAAGTCTTACTTATAAACTTTTTGATGGTGGTGTAAGCATCTGACATACAGTATGCATTGATTATGCTTACTCAATATCATGTCAAAAGCATGTCAAAAAGTGATAAAGCTTTTGTTTTTGAGGAGACTTGCTTGTTTCAGAATGTTTTGTTGATACTGAGAACAGTGTGGTGTGAGATCAGCTGCCTGGGTCTCAAGAGAACAATGCTCCTCCCGGCACGTCTCTCACACCCCTTCCCTCTTCCGCAGGATACAAGATCTATGACCTCACCCTGAGTCCACAGCATGAGAGGCTGACGGTCGGAGAGAGACTCATACTCAACTGCACCGCGCACACAGAGCTCAATGTTGGAATCGACTTCCAGTGGACCTTCCCTCATGAGAAGG[T/C]CAGTAATGGAGAGAAATGCCCAGAGTTCAGTCATTTTTACCTCTGATTGGTGACATTTGTCACAATTGTGATTACCTCAACATAAAAAGACCAGCCCTTGGAGATTTTTTTTCTGTGGTCTTTTTCCTGTTCCCCTTCAGTATGTGCTGTAAGTTTGCAATGTACGGCGATGAAAAACAGCCAGAAATAGTCTAAACAAAAGCAGTCTGCTTCTTTTTTCTGATTGCAGGTGTCTGACTGCTTATGTCTAAGATACAGTTTCAAATACAATTTCACTAGTGCCGTTTAATGGGGTCAAAATTTTCAAATTGTTTTAATAACTGATTTCTAATAACTATTTTATTCTGTCTTTGACATGATGACAATACACATAATGGGCCCTATAATACACCTGTTGCAATAAGGCGCAAGATGTGTTTGGCGCGATTGGTTGCTATTTTCAGACCAGCACCACCATAATTTACAAGTTTTGCACCACGCAAATCCATTTGCGCCACTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43426
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000049204 | Nonsense | 586 | 1357 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 22326174)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22354341 |
GRCz11 | 20 | 22254014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGAAGGACAGGATGTTATAATGCGTTGTGTAGCAGACCGGCTGCTGTA[C/A]TATAACTTGCGCTGGTATCGGGTAGCAAATGTAGCCAACCATGATCCACC
Long Flanking Sequence:
CATTTTACGGTATTTATCTCATTAAATCAAAGTGGATAAACCAGATTCAAAGACTTTCTTGAAATTCATGTACTTTTTTTATCCTAACATTTAATTTTGAAAATGCAAAAGATGAGCTTTTTAATTTATGCACCAAGTTTCTGTATTGAGGGTTAATCTTGATAAATCTGGTAAAAATGCATTTTATACACAATGTGCCTTTCTGCAGACCATCAGCACTCTGAAGATCCAGAAAGCAGTGGATCATGCCCTATACAGGTGCATCGCTACCAATAAGATGGGTCAAGATCAGCGAGTCATTGTGTTTCAAGTAACTCGTAAGTGCCTCCAAACCTATGACAATCCCAAATTAAATTGGATTTAAGTAAAGATATAATCAAGTTCAACCTTCATATATTTGTCTTATTCACAGGTTTTCTCAACCTAAGCGTCCTCCCCTCCAGCAGCCCTATTGAAGGACAGGATGTTATAATGCGTTGTGTAGCAGACCGGCTGCTGTA[C/A]TATAACTTGCGCTGGTATCGGGTAGCAAATGTAGCCAACCATGATCCACCTCCAGCAGCTGTGCCGTGTGATACTCTCACACTGTCACACTTACACCAGCCCAACGTCACTGTTTCAGGCCTGCAGGGGACCAATGTCACACTGGACATGCCCATACCCAATGCCACAATGATGGACCAAGGCTTGTACGCTTGCCAGGTGGAGATTGTGGGCACCAATGAGAAAACCTGCTTACTTCACAATCTCAGACTCAGAGGTAGGTCCTTAGTTTACATTGAGTGGAAACCTGTTTGAAAACAGTCATTATTTTTAGTATTTCAATTGTTGGAGATGCTAAAGTGTGGTATGTGTGGTGGATACACTAGGGTATGGCTAATTTCAGACTTGACTGTAATTATCTCAGTGTGCTTTCACATCTGTTGTTCAATTCATTTGGTCCAGCCCAAGGGCAACATTGTCGCAATTTTCTGCCATTTTGGGTCCTTTTCACACCACACTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23684
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 |
---|---|---|---|---|---|
ENSDART00000049204 | Nonsense | 1131 | 1357 | 25 | 30 |
Genomic Location (Zv9):
Chromosome 20 (position 22344186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 22372353 |
GRCz11 | 20 | 22272026 |
KASP Assay ID:
2261-4232.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTCCATATCCAGGTGTGTGCATTGATGAGTCTTTCTGCAGGCGACTT[A/T]AAGAGGGAACCAGAATGAGAGCTCCAGATTACGCCACGCCTGAAATGTAC
Long Flanking Sequence:
TCTCACAGATTATTTTCTCTTTATTTTTCAATACTTGGAATACAGTACTAATAAACTCATCCATAATATTACAGTGGAAAGACTCTTTTCAAGTTTTTTTTTTTGGTTATTCTAGGTCTGCTGAAAGTAATTTGTTCATTCTAATAAGTCGACTTTTAATATCCAATAGGTAAACTGTAAGGAGAATAATGACACCTCATAGTATGTTGTTTTTTATAGCACATTACTGATTGATTATAATTTAATAGAAGCTCCTTAATAATTCACGCAAAAGCATTGTGGTTGGAAAAGGGCAGATTCTGTGCTCTAACAAAGATCCATAGAAGGATCTTTACTGAACCATTAATATCAGTAAAGAAGCTTTATATAAACAATACTACTGGAAATAGTTTAAACCTACAGTATTTGCTTGACATGTCCCGTTGACCATTTTTTTCTTTGGTGCAGGTGCATCTCCATATCCAGGTGTGTGCATTGATGAGTCTTTCTGCAGGCGACTT[A/T]AAGAGGGAACCAGAATGAGAGCTCCAGATTACGCCACGCCTGAAATGTACATAAATATATTTCACATTTTTAAAATGTCCCCATTATTCTACATTTTTAAGGTTTCTAGATTTGTTTAGTAGGTCTCCTACAGTGACTTTGATGTGATTTCTTTTTTTTTGTCAGATACCAGACCATGCTGGACTGCTGGCTTGATCGACCTTTAGACAGGCCAACTTTTACTCAGTTAGTTGAGCATCTGGGTAATCTGCTACAAGCTAGTGCTCAACAGGTTAGACTTCATTCCAAGTATATTTTTCTTGCAATTTTTAATTTTATTTATTATTTTATTTAATTTTATTTTATTTTATTTTATTTTATTTTATTTTATTTCATTTTTTAGAAGTAGAAATTGATTCTTGATATAGATAAAATTGACCAGGGTTTAAAAAAACATATATATTTTTTTATTTAATTTAGTAATTTTTTCATGTTTTGGTGAGCCTAAATGACTGTTGTTT
Associated Phenotype:
Not determined