ZMP
flt1
Ensembl ID:
ZFIN ID:
Description:
vascular endothelial growth factor receptor 1 [Source:RefSeq peptide;Acc:NP_001014829]
Human Orthologue:
FLT1
Human Description:
fms-related tyrosine kinase 1 (vascular endothelial growth factor/vascular permeability factor recep
Mouse Orthologue:
Flt1
Mouse Description:
FMS-like tyrosine kinase 1 Gene [Source:MGI Symbol;Acc:MGI:95558]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30092 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1504 | Essential Splice Site | Available for shipment | Available now |
sa15078 | Essential Splice Site | Available for shipment | Available now |
sa301 | Nonsense | F2 line generated | Not yet available |
sa37886 | Nonsense | Available for shipment | Available now |
sa37885 | Nonsense | Available for shipment | Available now |
sa12242 | Essential Splice Site | Available for shipment | Available now |
sa39448 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30092
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Essential Splice Site | 361 | 1272 | 8 | 30 |
ENSDART00000130446 | Essential Splice Site | 361 | 473 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22396803)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21643681 |
GRCz11 | 24 | 21788855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCCTCACTCCGAAATTAAAGGCTTTCCCTGCACCTGAAATCATCTGG[T/G]AAAAAAAGCTGTAATCTGAAGGGATCAAGAATGATGTTTTTGTTCAAAAG
Long Flanking Sequence:
ATGAATAATTCACACCCTGTTGATAACCTTATTTCGATGAGAAATATATTTATTCTGCATAATATATTTGTATTTTAATACTCTACTAATTACGCTTCTATGAACTCATTTTTTTTAGAACTGTTGATTTTATGTACAGTATTATAGGCAAGTACATTATAAGTAACTGTAATGAAATAACCTAAAAATTAAAAGTAATCCATCACTTTTTTTGATAAGCTTAATCTAATTACAGTAACTAGTTACTTTGTAACTGATATCACACAACACAACCAATACATTAAAACACTTAGTCATGGGTGGAAAAATGTGCATACACCATAATAACAAAAGATGGATTCTAATTCAGCATTTCTGACCGTCCTATTTTCATTTTTACAGACCAGCCTTTCATTCGACTCAAGCACAGAAATGGCCCCGTCGTTCAGGCTTTTGCAGGACAGAAATCTTTCCGCCTCACTCCGAAATTAAAGGCTTTCCCTGCACCTGAAATCATCTGG[T/G]AAAAAAAGCTGTAATCTGAAGGGATCAAGAATGATGTTTTTGTTCAAAAGGAAGGGATCTCAACAGCTGAATGTGTTTTTAGGCTGAAGGATGGGATGGTGGCAGCCGAGCGATGCTCCCGTTATCATGTGGATGGGTTTTCTCTGGTTATTCGGGATGTTGCAGAAGAGGATGCAGGAATCTATACTATCCTTACTGGGATCCAGCAGTACGGGCTTTTCCAGAACCTCACCATCACACTGGTGGTAAATGGTGAGAGTCTGCTTTCATTAAACTACTTGATTGTGATTGGTTGAAAAAAAAGGGATGTGATTATTTTTAGGGAAAGACATTATCATTATTTAGTTGTTTTTTTAAAGCAGAAACGTATATAATTATTAATTATTTGTTTAACCTATTTTCTATTAAGCAGATAATATTCAGACATTTTATTAATATTCATTTAACTGATGGTTGTTCAAAGAGGACCATTAAATCAAGTGTTTATTTCGATATTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1504
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Essential Splice Site | 418 | 1272 | 9 | 30 |
ENSDART00000130446 | Essential Splice Site | 418 | 473 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22396549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21643427 |
GRCz11 | 24 | 21788601 |
KASP Assay ID:
554-1429.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCAGTACGGRCTTTTCCAGAACCTCACCATCACACTGGTGGTAAATGG[T/G]GAGAGTCTGCTTTCATTAAACTACTTGATTGTGATTGGTTGAAAAAAAAG
Long Flanking Sequence:
TGATATCACACAACACAACCAATACATTAAAACACTTAGTCATGGGTGGAAAAATGTGCATACACCATAATAACAAAAGATGGATTCTAATTCAGCATTTCTGACCGTCCTATTTTCATTTTTACAGACCAGCCTTTCATTCGACTCAAGCACAGAAATGGCCCCGTCGTTCAGGCTTTTGCAGGACAGAAATCTTTCCGCCTCACTCCGAAATTAAAGGCTTTCCCTGCACCTGAAATCATCTGGTAAAAAAAGCTGTAATCTGAAGGGATCAAGAATGATGTTTTTGTTCAAAAGGAAGGGATCTCAACAGCTGAATGTGTTTTTAGGCTGAAGGATGGGATGGTGGCAGCCGAGCGATGCTCCCGTTATCATGTGGATGGGTTTTCTCTGGTTATTCGGGATGTTGCAGAAGAGGATGCAGGAATCTATACTATCCTTACTGGGATCCAGCAGTACGGGCTTTTCCAGAACCTCACCATCACACTGGTGGTAAATGG[T/G]GAGAGTCTGCTTTCATTAAACTACTTGATTGTGATTGGTTGAAAAAAAAGGGATGTGATTATTTTTAGGGAAAGACATTATCATTATTTAGTTGTTTTTTTAAAGCAGAAACGTATATAATTATTAATTATTTGTTTAACCTATTTTCTATTAAGCAGATAATATTCAGACATTTTATTAATATTCATTTAACTGATGGTTGTTCAAAGAGGACCATTAAATCAAGTGTTTATTTCGATATTTTATTTATTTTAATATTTTGCATATATTAGGCAAGACTAACGACTAATTTTAAACTAACTCACTACTTTATTAAATGTTTTATTTATTTATTTATTTTTTACAATGACTATGTGATCTGATTGTTATTTCTCTTCTCCCTGAATCCGTTCACAGTGAAGCCCCAGATTGGAGAGAAGAGCGTGTCCTCCCAACAGCCTGGAACAGTCCAGCGGGGCAGCAGACAAGCCCTCCACTGCACCTCTCATGGCGTCCCACCA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa15078
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Essential Splice Site | 507 | 1272 | 11 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22386305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21633183 |
GRCz11 | 24 | 21778357 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATCTTGACWATCAGCCACAGACAGGAAGTGTTAGAAGGGAAGAATAAG[G/A]TGAGTGTTCCAGTGGGTGGACTGATCATAGGGGACATGCCAAAYGATAMA
Long Flanking Sequence:
CTTCGGAAGCAGGGCCTAGGATGGTTTACAGGCAGGAAAGGGAACACATCCAAACCCTACACACTGCTAATTATGGAACACTCCAAACGAGTGTCACTGTATCCTGATAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACTCAGAATTCCAAAAGAAATTCCATAAGATGACTAGAGTGAAAAATGAATTCCCAAGAGACCTGAAATCGGAAGTTTCCCCTTTCGGGCTGCAGCTGCACCACACATCTGTCTTGTGACATCACTTCACTTGTGAACTGAGAGTGCTGTCGTTCTCTCTTCCTCTTTCTCGTTCTCTGTCTTCCTCTCTCTCTCTAAGATGTGAGAAGCCTCCTCCTTCGTCCTGGACTGCAGTCAGAAAGAAGACCGGAGTCACGTCCACCCACAATCCCATCTTGACTATCAGCCACAGACAGGAAGTGTTAGAAGGGAAGAATAAG[G/A]TGAGTGTTCCAGTGGGTGGACTGATCATAGGGGACATGCCAAATGATACACGAGAGGGCACACAAGAACTCCCTCGGGATTCACAAAAGCAGGTCTTCCCGTTTTGTGGAATTATGTGTTCTGCCAAATGCCTCAAGATAACTGCAATCAAGCTGCAGTTGTTTAGCTCTAGAGGTGGATAGGCAGGTGTCCTTCCTCTCTGATTACTGGAACAAGATTAAATGATTTATTATTTGGAGAATATTTAATCTTCATTCTCCCCACTTGTTCCTAAATCTGCATCCTTGTTGGTGTTGGAACAGCAATAAAATAATACAAACAAATGCAACAATAACAAATAATTTTAGAAAAGCATTGTGTTAGAGGCATGGGGGAAACAAACTGATGTCACGAATTTAGGCCCACAGAAAGACACACTGAATTCATGGCTTAAAAGCCGTTGGTTTTATCCTGTTTAGTAAAGGATCTTAACCTTAGATCTTAACCTTGTATGTATTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa301
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Nonsense | 683 | 1272 | 14 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22376964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21623842 |
GRCz11 | 24 | 21769016 |
KASP Assay ID:
554-3093.1 (used for ordering genotyping assays)
KASP Sequence:
ATCACTCTCCACTGCCCTGCTCGGGGAGTGCCACAGCCACACATAACATG[G/A]TATAAGAACCAAAGGAAGCTCCAGCAGGTGTCTGGTGAGACTAGGAAGTG
Long Flanking Sequence:
CATGTCAAAAGTCCCCGTTAAGTATGTTTTTAAGCATTTTTAACTACACAGACACAAGGCATAAAGCAACGTAATATAGTACAACTAGGTCATAAGCATGTCATTTATTCATTTTATTTTCAGCTTAGTCCCTTTATTAATCTGGGGTCGCCACAGCGGATTGAACCGCCAACTTATCTAGCAAATGTTTTATGCAGAGGAGGCCCTTCCATCTGCAACCCATCACTTGGAAACATACCCATGTCATTATGCAATTTTGTGTCCTCATAAACCACACAAACCTGCACACACTTGTATGCACAAGTGCACACATTTGCTCAGGTGTTCACGAGTTCAGATGTTTAAGAGGATCATGCATAATAACCCCTCTCTCTCTCACACTGTACAGTTCTGCAGGCGCCGGTGCTGCTTGGAAATCTAAGTGATCATACTGTTAATGTAAGCAACTCTATCACTCTCCACTGCCCTGCTCGGGGAGTGCCACAGCCACACATAACATG[G/A]TATAAGAACCAAAGGAAGCTCCAGCAGGTGTCTGGTGAGACTAGGAAGTGTACTTTTTAAATGTTTATTTGCTGTATAAAAATATAATGCATACATGTTCATGTTATTGACAGGAATCATGCTGTTTCCAGAGGAAGGGACTCTTCACATTGACCGAATTACAGTTGAAGACCAGGGATTTTATACCTGTCAAGCCACCAATCAGAGGGGGTCTGTGGAGAGCTCCGCCTACATTTGGGTTCAAAGTAAGTTGGCTTGAGTGTGTGTTCACACTTGGAAAGTTTGGTTGAATTAAAACTCAGGGGAAATTGCTTTGTTAGTGTAGTTCATTTTATTAAAGGTGCCATACACTGCATTGGTTCAATAAGTTAAATTGTTCTCTGATATCTAAATAGTATGCATATGGCTTAGCTAAGCAAAAAAAAGTTTTCATTTATTACTCCATAAAATACCCATAGAATCACAAGATCCATAATTGATCCTCTGTATAAATGTATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37886
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Nonsense | 742 | 1272 | 16 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22374006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21620884 |
GRCz11 | 24 | 21766058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTTTCTTTTGTGACAACACTTATTTATGTGTCCTATAGATTCGTCT[G/T]AATCCCTTTCTCTGGAGATCCCGACCCTAGCATGTACGTGTGTTGTGGCC
Long Flanking Sequence:
CAGAAAGTAAGAAGAATGGCAAATGTTTTTATTCACATAAGTTTTCAAGATGTTATTTCACCAAAAATATGTCTAGAAAAGATCATTATTAACATGTTAGAAAACATGGCACCTTTTTTGTTATCGTTTGATACAAAAGCTTCTTTAAATTACACCATTTTTAGTGTTTTTTCTCACACTCCCCTATTTAGTCTAGTCAGATGCTTCTAAACTGAGTGCTGAGAGGAGACGTTCATGCTGTTCTCTTCCGAAAGGGTCAGGAAGGAAACTGTCTCCCATTTTCATTTCCCACAGATGGCCTTGGCTTTTCAACCCTTAAACTGTTTACCTATTTCTATGTGGGTTCATTTGTTTAGCTATTTCTATAGAGGCTGATGCATAACTCACAACCTCTATAGGGAGTTGTCAAGCTCATGGGGACAAATCTAATCTGGGTCATGTCCCAGTCTCTCTTTTTTCTTTTGTGACAACACTTATTTATGTGTCCTATAGATTCGTCT[G/T]AATCCCTTTCTCTGGAGATCCCGACCCTAGCATGTACGTGTGTTGTGGCCACACTCTTCTGGCTGCTTCTCACACTGCTGATTCGGAAACTCAAACATGTGAGGGCCAATAAAATCATACATTGTATGGCTATATTTCTGTATTGTGTAATATATAACTGTATTGTCTGGCTCATTCTCAGCCAAACTCTGATAATGGCAAAGCAGAGTACCTGCCGATCATCTTGCACCCAGGGGAGGAGCCTCTGGTCGAGCACTGTGATAGGCTACAATATGACCCCGCAAAATGGGAGTTTCCACGGGACCGCCTTAAACTGGGTACATTGTGTGTATGTGTGTGTTTAAGTTGTTTTGATGCTCTTGTGCAGTATACTGATATGCAGTTTATTATGCTGTTTTCCAGAAAAGCCCCTGGGGCGCGGAGCATTTGGGCGAGTGATGCAGGCCTCAGCTGTTGGCATTGGCAATTCAGCCAGCTGCACCACAGTAGCTGTGAAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37885
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 |
---|---|---|---|---|---|
ENSDART00000025621 | Nonsense | 805 | 1272 | 17 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22373732)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21620610 |
GRCz11 | 24 | 21765784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCACCCAGGGGAGGAGCCTCTGGTCGAGCACTGTGATAGGCTACAATA[T/A]GACCCCGCAAAATGGGAGTTTCCACGGGACCGCCTTAAACTGGGTACATT
Long Flanking Sequence:
CCCATTTTCATTTCCCACAGATGGCCTTGGCTTTTCAACCCTTAAACTGTTTACCTATTTCTATGTGGGTTCATTTGTTTAGCTATTTCTATAGAGGCTGATGCATAACTCACAACCTCTATAGGGAGTTGTCAAGCTCATGGGGACAAATCTAATCTGGGTCATGTCCCAGTCTCTCTTTTTTCTTTTGTGACAACACTTATTTATGTGTCCTATAGATTCGTCTGAATCCCTTTCTCTGGAGATCCCGACCCTAGCATGTACGTGTGTTGTGGCCACACTCTTCTGGCTGCTTCTCACACTGCTGATTCGGAAACTCAAACATGTGAGGGCCAATAAAATCATACATTGTATGGCTATATTTCTGTATTGTGTAATATATAACTGTATTGTCTGGCTCATTCTCAGCCAAACTCTGATAATGGCAAAGCAGAGTACCTGCCGATCATCTTGCACCCAGGGGAGGAGCCTCTGGTCGAGCACTGTGATAGGCTACAATA[T/A]GACCCCGCAAAATGGGAGTTTCCACGGGACCGCCTTAAACTGGGTACATTGTGTGTATGTGTGTGTTTAAGTTGTTTTGATGCTCTTGTGCAGTATACTGATATGCAGTTTATTATGCTGTTTTCCAGAAAAGCCCCTGGGGCGCGGAGCATTTGGGCGAGTGATGCAGGCCTCAGCTGTTGGCATTGGCAATTCAGCCAGCTGCACCACAGTAGCTGTGAAAATGCTTAAAGGTATATTCTAAGACATGAAAACAGCTGCTCACACAATCTGATGAAAATACAGGTAGCCTACTGTTTGGCTAGAAGTATGCAAAGAAGACGTCTTTGATGTAAAATCTGACTTTAAACGTGTTTCTTTAGAGCAGGGATGCCCAAACTTCTAAACTGCCTAAACTTGATTGAGGGCTGTGGGTTGTGGGTTGAATATATACCAAAACTTATAACAATAAATTTGCCAAGGGGAATTTCCTAACTAGAAAACGATGCTTTAAATCCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12242
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 |
---|---|---|---|---|---|
ENSDART00000025621 | Essential Splice Site | 922 | 1272 | 20 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22371361)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21618239 |
GRCz11 | 24 | 21763413 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTCTGCWTACCTCAAGAGTAAACGAGAAGTGTTCCTGTTGAATAGGG[T/C]TAGWCTGTTATTCTGTCTGTAATATCTATCTATCTMTCTATCTMTCTATC
Long Flanking Sequence:
CAATTATGTAATTATGTTGTTTGGTTAGATTTATATTATATCTTTTAATCTTTATTTATCAGAATATGCTATTACAAAAAAAATAAGCAAATAGGCATAGTTGACATCAACAAACATTTCTTGATCATCAAATCAACATATTTTATTTTAATATTATCATTTTAATCATTTCTTTGGATAAAATGAAAAAGTTTTATATTAAAAATTTGTTTGTTTTTAGACCTTAAATTTTGAAGAAAGCTTGCATATATTTTAAGCATATTTAATTTTTCAATTTGTGCAAATTATATTTTTTCAGTTTTTTCTTCAAATAAATAATAATATCCTTGTTTAAACATTTGAAGGCACACTACAAACACATGAACCTATTCATTGAAAAAAATATATATTTTTTTTGTTGTTGTTTCCAGGGCCGTTGATGGTCATTGTTGAATACTGCCAGTTTGGCAACCTGTCTGCATACCTCAAGAGTAAACGAGAAGTGTTCCTGTTGAATAGGG[T/C]TAGACTGTTATTCTGTCTGTAATATCTATCTATCTCTCTATCTCTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATATATCTATCTATCTATCTATCTCAGTCTGTTTGATTGTCTGTCTGTCTGTCTGTCTGTCTGTCTCTCTGTCTCTCTAAAACAATATTACTTTTGCAGGAATTTATATTACAGTTTTTCTCAGTGGCTTTGGTGCATTTCTCACAACACTATTATATTTGCACAACAGTTAATGCATTTCTCAAAACTCTAAAAACACTGTTATTACAAACTGCAAAACCTAGTTGATAACCTGCAAAAGTCACTGCGTGTCACTTGCTCAAATTGGATAGCTCATTCCTCAAAAGCAAGTATTGATGTCAATGAAAGTGTAAGTTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39448
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025621 | Nonsense | 1239 | 1272 | 30 | 30 |
ENSDART00000130446 | None | None | 473 | None | 11 |
Genomic Location (Zv9):
Chromosome 24 (position 22359084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21605962 |
GRCz11 | 24 | 21751136 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTGACTTCATTTAAGTGTCAGTGTTTTGTGTGTTGCAGGTTTTTCTCC[A/T]GAGGTCAAAGTCAGCCTCGTCTGAGCAGCGCCCCCTGTTGTTCTGATCAA
Long Flanking Sequence:
ACATTTTTTAATGTTTCTGCTGAGAATCTTGTAAAAAAAAAAAAAAAAAAAAGTGGATTTATTGCGGAATTATTTTGGGAGTATTAAAACAAAAAAAACTTGATATATGAAATAAAAAAAATACCTTATTAACTTGTATTCAATGTTTACAATGGAAATCCAATTAGATTCACTTATTTGGTAATCAAAGCAAGTCTCTAATATATCTACTAAAAGACAGAAAATATTACTTTACAAACTGTACTCTAAATAAATCATATGAACAGTTTCATATGTCAAGAATATTACTAAAATTATTCCAATAAACCGAATAAATATAAATTGACACACATTCACACAAATATGTACATTTTTCACTTCATTAAAAGTGCATTGCTCGTACAGCGTTTGAGTGCTGCTATGGGCTTTTAGTCCTTTAAGTTTCATAGCAGTTCTGACCATATGAAAATATTTTGACTTCATTTAAGTGTCAGTGTTTTGTGTGTTGCAGGTTTTTCTCC[A/T]GAGGTCAAAGTCAGCCTCGTCTGAGCAGCGCCCCCTGTTGTTCTGATCAAACAGCGCTTCCTCCACCACATTATGAAGGCGATCTTCTTTACCCCAGTTTCTAACATTTGCGTATGACAAACCTGCATGTAAACATCCGTTGGCACTGGTAAAAACACCTCTTATCTCAATTCTGCTGCTTTCGGTTCCTCATTAGGCTCAATTTATCACGACAAAGTAGCTTTTCTGAATAGACATCAGCAATAACCACACCATATTAAAGGGACAGTCGCTACAAATAAATGCTCGTTTCTTCGGTTTAACACAAATGTGTTCATTTTGAACAACAAGAAACAAATGTGCAATACCAGGAAAAGAAATGAGAATTTTCATTGTGAACTAACCCTTAACCAAATAATTTGCTGTCACTAATTAATCCTTAACTTTTTATTTCCTAAGATACTTTCTTGAGTGTCGTATTTTGAGATTTTGTTTTAAACTTCTATCTGATGTGTGTATTC
Associated Phenotype:
Not determined