ZMP
kdrl
Ensembl ID:
ZFIN ID:
Description:
Vascular endothelial growth factor receptor kdr-like [Source:UniProtKB/Swiss-Prot;Acc:Q8AXB3]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa28333 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19086 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9469 | Essential Splice Site | Available for shipment | Available now |
sa45520 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44811 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15912 | Nonsense | Available for shipment | Available now |
sa44810 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa28333
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Nonsense | 411 | 1301 | 9 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33878842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32683455 |
GRCz11 | 14 | 33023769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATCGCTCTGTCAAACCAGGAGAGGGGTCTCTACAGAAACATCAGTTA[C/A]AAGCTTGAAGTCAGAGGTAATGCCGTGAAAAACAATAAGAACAGCACATC
Long Flanking Sequence:
TGTTTATGGTGAGGATGTTGTGACACTGCAATAACACACTGTTGCTATCAGTTTAAATTGATTTAATAGATTTTTCTCTCTACAGAACATCCATTCCTCAATGTTACTCATAATAAACGTAAATTCACCTCTACTGTAGAAGGTAGAAGGGTGCAGTTTGAGCCTCGGGTCAATGCTGTTCCTGCGCCCGACAGAGTCTTGTGGTAAGTTTGTGCTTTGCATTATAAGAGCAAAAGATATGACTAAGAAACCACAACAAGGATTCATGCTAAATATGTTGTCATGCATAAGCAGCTAACAGTAATCGATTTAGATTTATCATATCATTTTGCTGTCAATTTGTATAGGTACAAAGATGGAGTGGCCATTTCTGAAAATTCCACATGTTACGAAACTGCAGGCTACAACCTGACCATAAAACAAGTGAGGCAGAAGGATGCTGGGATTTTCACTATCGCTCTGTCAAACCAGGAGAGGGGTCTCTACAGAAACATCAGTTA[C/A]AAGCTTGAAGTCAGAGGTAATGCCGTGAAAAACAATAAGAACAGCACATCATGGAATATAGATTACCAGTCTCTTGTGTCAAAAACAGTTCCTGGAGGGCCAAGCTCTGCATAGTTTAGTTTGTACCCTGCTTTACCACACTTACCTGTAGCCTTCAAACAAGCCTGAAGGATTCATTTGATCAGGTGTGTTTAAGGTTAAAGCTAAATCATGCAGCTCTGCAGGAATTGGATTTAACACATGTAGGTTTAATAGAGATGCCATAGCTAAACACAAATAATCATTAATGGATTTCTGAAATGTTCAACTATTGTTTGTTTGCTCTTTGAATTTTGTTTTATACTTTAAAAACCATGACATATTCGTTTATCTGTGCTTCAGTTTGTATTTTATATCTTAAAGCTATATATTTCAATATTTCCTTCCATCAGCAAACTTTCATATTGCTTTAAATTTGTACACAGTTTTAAGCAAATATGCAGACTATAATCATTTGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19086
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Essential Splice Site | 469 | 1301 | 10 | 30 |
ENSDART00000007819 | Essential Splice Site | 469 | 1301 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33876491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32681104 |
GRCz11 | 14 | 33021418 |
KASP Assay ID:
2260-7725.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATTACCTGGTTTTGGCAGCCATGTGACCCCAGTGCTAATCTTACAGAG[T/C]AGGTCAATCAATGTTCACATTTACTGTTTATTTTCTGATTTCATATGCTA
Long Flanking Sequence:
TCCAGTAAATGACATCATTACAGACCCAAAAGCAAAACCAAGGTCAAAAACAACAGAAACAGCATTCAGAGATTTCTGGTTGCAATTAAGAAACTATTTTAGGCATCATTCATCGAATGCTGAAATATTCAAACTTGATGTTTCATGAGAACAGATGCACTGCTTTAATGGTCAGTAAAAGCAATAGTGCTCTTATTCTTCTTAAAGTTTGTGTAAACATGAATATTCTTACTCATCCTAATTGGAGTTATAAGGTGATTTTTTTTAAATCATGTGTGAATGATCTGTATTATTACCTGAGACTGACTATTTAAAAGACTAATGTTCTGTATATGCACACAGTGAAGCCAAAGATCTTTGAAGAGGATGTGGCTCCAGCAGGTCCCCAGACCTTCAGATATGACCAGAGGCACAAGCTCACCTGCACTGCATTTGGTATTCCCATGCCGAACATTACCTGGTTTTGGCAGCCATGTGACCCCAGTGCTAATCTTACAGAG[T/C]AGGTCAATCAATGTTCACATTTACTGTTTATTTTCTGATTTCATATGCTAGATCTAATTGGTATTCTAACAGATAAAGATTGTACAACTTATAAACAAAGGAAATTGTGTCAACGCAGAAATATGGGGTGTTTATTCTTGTAATTTCCACAAATTTGGGTTTGTGGCTCCATAAACAGTTGTCGTACTCCTGCATAGCAGATGTCATTTCTTGCTGAGGTGTTAACATAAATGATGAAGGCTGGCTTTTACCCACAGCTCTCATTATTCAAGTGATCTGCATCCGTTTCCTTGACACGGGTCCAAAATAAAGTATGCTTATCGATGAAAAATAGCCCCAGAGCTACGTTTTGCAGTTATTGGCTCTGTAAATGCAAGGACAATTTATTAGTTTCATTCCCCAAGCTTGGATTGTGCTGAAAGCAAGAGTATCCCTGCGTAAATGCCAGGCTTTTAGTGAACTTTTATGACCGCTGCAGATGTCCCCTAAACTAGTGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9469
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Essential Splice Site | 469 | 1301 | 10 | 30 |
ENSDART00000007819 | Essential Splice Site | 469 | 1301 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33876491)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32681104 |
GRCz11 | 14 | 33021418 |
KASP Assay ID:
2260-7725.1 (used for ordering genotyping assays)
KASP Sequence:
ACATTACCTGGTTTTGGCAGCCRTGTGACCCCAGTGCTAATCTTACAGAG[T/C]AGGTCAATCAATGTTCACATTTACTGTTTATTTTCTGATTTCATATGCTA
Long Flanking Sequence:
TCCAGTAAATGACATCATTACAGACCCAAAAGCAAAACCAAGGTCAAAAACAACAGAAACAGCATTCAGAGATTTCTGGTTGCAATTAAGAAACTATTTTAGGCATCATTCATCGAATGCTGAAATATTCAAACTTGATGTTTCATGAGAACAGATGCACTGCTTTAATGGTCAGTAAAAGCAATAGTGCTCTTATTCTTCTTAAAGTTTGTGTAAACATGAATATTCTTACTCATCCTAATTGGAGTTATAAGGTGATTTTTTTTAAATCATGTGTGAATGATCTGTATTATTACCTGAGACTGACTATTTAAAAGACTAATGTTCTGTATATGCACACAGTGAAGCCAAAGATCTTTGAAGAGGATGTGGCTCCAGCAGGTCCCCAGACCTTCAGATATGACCAGAGGCACAAGCTCACCTGCACTGCATTTGGTATTCCCATGCCGAACATTACCTGGTTTTGGCAGCCATGTGACCCCAGTGCTAATCTTACAGAG[T/C]AGGTCAATCAATGTTCACATTTACTGTTTATTTTCTGATTTCATATGCTAGATCTAATTGGTATTCTAACAGATAAAGATTGTACAACTTATAAACAAAGGAAATTGTGTCAACGCAGAAATATGGGGTGTTTATTCTTGTAATTTCCACAAATTTGGGTTTGTGGCTCCATAAACAGTTGTCGTACTCCTGCATAGCAGATGTCATTTCTTGCTGAGGTGTTAACATAAATGATGAAGGCTGGCTTTTACCCACAGCTCTCATTATTCAAGTGATCTGCATCCGTTTCCTTGACACGGGTCCAAAATAAAGTATGCTTATCGATGAAAAATAGCCCCAGAGCTACGTTTTGCAGTTATTGGCTCTGTAAATGCAAGGACAATTTATTAGTTTCATTCCCCAAGCTTGGATTGTGCTGAAAGCAAGAGTATCCCTGCGTAAATGCCAGGCTTTTAGTGAACTTTTATGACCGCTGCAGATGTCCCCTAAACTAGTGTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45520
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000007819 | Nonsense | 582 | 1301 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33869404)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32674017 |
GRCz11 | 14 | 33014331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCACAAGATACCTCTACGATAGGCTGACTTGGTATGATCCTCTGGGCTA[T/G]AAGGTGCCCAAAGATGAAACCACTCTGCGGATTGAGCCCTACACTATATC
Long Flanking Sequence:
GGTTCCCTTGAGGTCTGGCCTTAGCCTGGTTCCTATTGTAATGCTCCAGGTCAGCCATCGCTGCCGCCATTCGCCAACAACGTGCTTCCAATTAGGAGTGATGAAACAGGAAATAACTGCAAATTTGACATTCCTGGCATTGCAGTGTGCGCAGCTTGGCGTTTGTAGTGTGGGCCAGAGAACGACATTGTCTTTCAACAGTACGTCTATAGTGTAGTTTCAGGTCTCTTATGAGCCATATGTTTTGTGAGTTAGTCATGCTTTGTCTGCTTGCCGATTGCAGATTATGCATGAATAGTACACAGTGAATATATTGTGTGTAATGACATGTCAATTCATCTCCTTCCTTAATTGTCTTATTCTCTTTTATCTTTACTAGATCACCCACAGCCTTTTGAGATTGAGCCCTCCACTGCGGTTGCTGGAGATGACATTACATTGACTTGCAGAGGCACAAGATACCTCTACGATAGGCTGACTTGGTATGATCCTCTGGGCTA[T/G]AAGGTGCCCAAAGATGAAACCACTCTGCGGATTGAGCCCTACACTATATCTTTGTCAATCAAGCTGCCCAATGTTTCCAGAAACCATACACTCGGCTATGAGTGCCAGGCTTTAAACATCAACACCAATAAAGTGGTCAATGTAACATCTGCTTTGACTATTGATGGTGAGTTTTATATATCAAGCGCCAAACAGATTTGTAAACAGAGTTGTCTTTATTTAAGCAGCAATCTAAATCATATGACATGACCTAGGACTGATCAGTGAATATGTACATATTTCACTGCATTATTATTATTAGTAGTAGTAGTGGTAGTAGTAGTAGTATTGTTATTGTTGTCGTTATACTTGTAGTATTATATCAGTAGCCTGTAGTTTCTTTATAGCTAGCATTATTCGAATAAAGCAAGGCAATACTAAAGACGATTATTACCTTATATTTATTTATAATAAATTAAAAACATTTTCTAATCCAAGACACATGTCTAATAATTTCTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44811
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Essential Splice Site | 638 | 1301 | 13 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33869236)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32673849 |
GRCz11 | 14 | 33014163 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAACACCAATAAAGTGGTCAATGTAACATCTGCTTTGACTATTGATGG[T/C]GAGTTTTATATATCAAGCGCCAAACAGATTTGTAAACAGAGTTGTCTTTA
Long Flanking Sequence:
TGTGGGCCAGAGAACGACATTGTCTTTCAACAGTACGTCTATAGTGTAGTTTCAGGTCTCTTATGAGCCATATGTTTTGTGAGTTAGTCATGCTTTGTCTGCTTGCCGATTGCAGATTATGCATGAATAGTACACAGTGAATATATTGTGTGTAATGACATGTCAATTCATCTCCTTCCTTAATTGTCTTATTCTCTTTTATCTTTACTAGATCACCCACAGCCTTTTGAGATTGAGCCCTCCACTGCGGTTGCTGGAGATGACATTACATTGACTTGCAGAGGCACAAGATACCTCTACGATAGGCTGACTTGGTATGATCCTCTGGGCTATAAGGTGCCCAAAGATGAAACCACTCTGCGGATTGAGCCCTACACTATATCTTTGTCAATCAAGCTGCCCAATGTTTCCAGAAACCATACACTCGGCTATGAGTGCCAGGCTTTAAACATCAACACCAATAAAGTGGTCAATGTAACATCTGCTTTGACTATTGATGG[T/C]GAGTTTTATATATCAAGCGCCAAACAGATTTGTAAACAGAGTTGTCTTTATTTAAGCAGCAATCTAAATCATATGACATGACCTAGGACTGATCAGTGAATATGTACATATTTCACTGCATTATTATTATTAGTAGTAGTAGTGGTAGTAGTAGTAGTATTGTTATTGTTGTCGTTATACTTGTAGTATTATATCAGTAGCCTGTAGTTTCTTTATAGCTAGCATTATTCGAATAAAGCAAGGCAATACTAAAGACGATTATTACCTTATATTTATTTATAATAAATTAAAAACATTTTCTAATCCAAGACACATGTCTAATAATTTCTGAAATATTTGATTGAAATATTTTGGCAGCATGGACTAAAACAATGTACTAGTTGTCATGAAATTCTCCCTGGTACATCAATTACTCACATTTATTGTGTGAACAATGTGCAACTATCCGTTTTCTGACTCAGAGAGGCAAGGGCCCTGGTTAATGCAGAATCTGACCAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15912
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Nonsense | 784 | 1301 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33866464)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32671077 |
GRCz11 | 14 | 33011391 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCAGCAGATTTRAAGACAGGGTACCTGTCCATCAWCATGGATCCTGAA[C/T]AGATGCCTCTCGATGAGCAGTGTGACCGTCTACCATATGACAGCAACAAA
Long Flanking Sequence:
AACAGCAGTGTGAAGTAGTAGTATAATAAATAAAATAATTGTATGCATATATACATTTAAAATGGATTTCTATGACAGCAAATCTGAATGGTCAGTATCATTGCACCAGTGTCTTTGATTTGTTGCTTAAGAAACATTTCTTCTTAGTGTCAGTGTTAAAAATAACTGGTTTAAATTTTGTACATTTTTTCATTTCATAGTTCTTAAGCGTCTTTTTCTAAATAAAAGTATTATTAATCTGTTAAAAATACAAATCTGTCCGACTTCAAACATTTGAATGAGGACTTTATGTGCTTCTGTCCTCTAGTGCTTATGTAACCGACATTCTTGAGTTGCTCTGCTGTTTTATTTTTCTTGCTCTGACAGTAGGAATTATCAGCATCGGAACAGCCGTGTACCTACGTAGGAAGAATGACAAAATGCCAATTTTTTTATTATTCTACCAGCCAAGTTCAGCAGATTTGAAGACAGGGTACCTGTCCATCATCATGGATCCTGAA[C/T]AGATGCCTCTCGATGAGCAGTGTGACCGTCTACCATATGACAGCAACAAATGGGAGTTTCCTCAAGATCGCCTCAGACTCGGTGAGTTCAAAGATCCTTTATATTCAAACTGTTTTTTTTTTCTCATTTCAGACCAAAGTTTCTCTTAAAATGCTTTTAACTAATAAAACACACACACATACACACACACACAAATACAAAGATGCTGCCAAGAGTAAATAACTATAAAATATGTAAATATTTGATGAGAAATTGAAGTTTCTCTTCTGTGGGACTCAATGTGTAAAGTGTGTACCAAAGCATACAAAGGCAAACTTATCCATACATAGTTCAACACAATTGGCTCTTTCTGATTTTTAATTGGCTTAATCCTCAGGTCTATTGTTTGAAACGGTGGGCATAAGGGTTGTCTAAGTTTTCAGAAGAAAATGTTATGCCTTTAGATATCAGCTTCTGTCGTTCAGTCTTAACTGCTCCATGAATTCTCAGTAGAGGGTCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44810
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 |
---|---|---|---|---|---|
ENSDART00000007819 | Essential Splice Site | 884 | 1301 | 19 | 30 |
Genomic Location (Zv9):
Chromosome 14 (position 33862532)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 32667145 |
GRCz11 | 14 | 33007459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCATCTCAATGTGGTTAACCTGCTAGGAGCCTGCACAAAGCGTGGCGG[T/C]AAGAGGAGGATGATAAGATTAGACATTCAACTTTTTCTCTGCTCAGTTTT
Long Flanking Sequence:
ATACAACTAGAGTTTTCTTGTGTTGACACCTTAAAACATGTGGCTAAGAAATAGCTACATTTGATTTTTGTGGCAGGCAAAAAAAATGAAAAATTTAATTGTCCCAACTGGTCCATTATCAAAAATCCTTAATGTTTAGCCTTGTAAAATTCTTAAATTTAATTTATAATGGTCTTAAAAGGGGGTATTAAAGCGTCTTCAGTATTGATAAACCTGCAGAAACCCCGAGTAAATGATGGTCAGCCTTGCATGCTTGAGACACACCACAATGTAATCAAACATTTTTCTAACAATCCAAACAAAAATCCTTTCCGACCACGCAGGACATTGCAATAATTAGTTTTTTCCTTTTATCCTCTCCTCCAACTTCCTCTACGCTTAACAGTGGGAGCAACAAATAACGAATGGAGAGCCTTAATGTCTGAACTGAAGATACTGATCCATATTGGGCATCATCTCAATGTGGTTAACCTGCTAGGAGCCTGCACAAAGCGTGGCGG[T/C]AAGAGGAGGATGATAAGATTAGACATTCAACTTTTTCTCTGCTCAGTTTTAACAATTGGTTTGATTTACACTTAGGCCCCCTAATGATAATCGTGGAATTCTGCAAGTATGGAAATCTTTCCAACTACCTGAGAAGTAAGAGAGGTGACTTTGTGGTTTACAAGGTAAGCAGTGACGCCTCCTGTTCATTTCAGCAGTGATTTGACATGCTAAAAATAACATTGACAAGAGTGTGTTCCCCTCAGTCTCAGGACGGTAAGGCTGTGCGTTCCAGCTCAGGCTGTGATCTGAGCGAGCTCATCAAGCGCAGGTTGGAGAGCGTGGCGAGCACCGGAAGTTCAGCCAGCTCCGGCTTCATTGAAGATAAGAGCTACTGCGACTCGGAGGAAGAGGAGGAAGGTAGCGACTGAGTGTCTTCCTTCCCTTCTCCCCTCCTCCCTCCCAACCTCTGCCTCACCTCCGCCCCTCCCTCTCTCCTCTCAAGGCTCCGCTGATTGTTT
Associated Phenotype:
Not determined