ZMP
LOC566708
Ensembl ID:
Human Orthologue:
FLT3
Human Description:
fms-related tyrosine kinase 3 [Source:HGNC Symbol;Acc:3765]
Mouse Orthologue:
Flt3
Mouse Description:
FMS-like tyrosine kinase 3 Gene [Source:MGI Symbol;Acc:MGI:95559]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15012 | Essential Splice Site | Available for shipment | Available now |
sa24498 | Essential Splice Site | Available for shipment | Available now |
sa37884 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15012
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 |
---|---|---|---|---|---|
ENSDART00000081357 | Essential Splice Site | 35 | 956 | None | 24 |
ENSDART00000147759 | None | None | 439 | None | 12 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 24 (position 22321487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21568365 |
GRCz11 | 24 | 21713539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGGACGGTTTAACTGAAGCTCATCCGCGATGCGACACTGATGGATCGG[T/C]AAAGTTTCTTCTTTCTAATCAGCCCYYAGTACAACTGTCTGTCTGGAACT
Long Flanking Sequence:
GTCCTCTGCAGATGCTGGCCGACTAATACTGAACCTGAAACGTTTAAAGAAGTGTGTGTGTGTGTGTTTGTGTATATGTGTGAGTGTGAGTGTGAGTATGTGTGTCACTTACAGGCTGAAGTGAAAGTCTTCTTGCCTCTGTTCGCTGTCCATCCTATTTCACGGTCTGACAAGAGTCGGGGAACAAACTGTTATGTATTCACGCAATGCATCTTGGAATCAAGCTCTTGCTGGGTAAGTGAGGCAAAACTGTTTATTTACTTGCGGCAAAAACTGCAGTAATTCGTCCGTTTTAATGGCTTGTCTTATGCAGAATATTGTTTGTTATAAATATATTCAAGACTGAAAGTCTAGTCTGTTGAATAGTGTTTTTTGTTTTATTTCTTTCTGTCACATTTGTATTGTTTTCTCTTTTACCGTAGTGCTGCTCGTGCTGCACTGGAGCTCGTTGAAGGACGGTTTAACTGAAGCTCATCCGCGATGCGACACTGATGGATCGG[T/C]AAAGTTTCTTCTTTCTAATCAGCCCTCAGTACAACTGTCTGTCTGGAACTGTGAGACTCATTTACAGCTGGTGTTTAGCGTCACCCACGGAATAAACTGAGATTACAGATGCCTCGTTACATTAAACTAAATGTTACAAGGTGTTTGGTGCCGCCTCAGTTTGAAAACGTGATTTCTAAAGCACCTATTTAAAATATGCTAAACCTAATACATATCCATTTGTTTACTGTATGTGGTATCATGGCTGATAATTTAACAAGCTATAAAGTGCAAGTAGTGAGCATTTGTCAATGAAGAGCTCATAATTTAACATCAAAAAGTCACTTATGTAACTTATTAAGAAAGCACACTTTCAAGGAATAGTTCACTGCAAAATATAAAATTACTCATTTTTTAATCTACTTATGCTTCAAGTCGATATGAATTTTTCTGTCAAACACAAAAGAAGATATTTTGAAGAATGTAATAATAAACTTACTTCTCATCATTTAGCCAGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24498
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 |
---|---|---|---|---|---|
ENSDART00000081357 | Essential Splice Site | 597 | 956 | 15 | 24 |
ENSDART00000147759 | Essential Splice Site | 184 | 439 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 22311485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21558363 |
GRCz11 | 24 | 21703537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATCAGCAAGCCGGGTGTTTCTGTTCAGGTAGCGGTAAAAATGTTAAAGG[G/A]TAAGTAATGACAAATCTGTTATGAATATTTAAATAAGATAAAATAAATAA
Long Flanking Sequence:
ACATTACTATGAGAAATTACCATTTTTATAAAGGGTAATGCGTTATTTTGATGGCTCCTATTGCATGTTTTATTTGCAAAAAGTTGCATTGCAAATGCCAATTACTTCTCATTTGAGTATTAGTAGACTGTCTGCTTAATATAGGTTGATATGCTCCTTCAACAGATATTTAACTGACTATAAGTAACTTTGCAAGTACATGTCAACTTACAACAACCTTAAACCCAACCTAACAGTCTACTTATAATCTAATGAGAATTTGTTGGCATGTAGATGCAATAAACCTTAAAGTCAACAAAATGCGTTAAAGGGACCATCAAAATAAAGTGATACTATAATGTAATCAGTCATTAACTACCATTTTGAAGTAACTTACCCAATACTAATTTCCACAGGGAATGAACTTGGATCTGGTGCTTTTGGGATGGTTGTTCAGGCTACAGCATATGGGATCAGCAAGCCGGGTGTTTCTGTTCAGGTAGCGGTAAAAATGTTAAAGG[G/A]TAAGTAATGACAAATCTGTTATGAATATTTAAATAAGATAAAATAAATAACAACCTGTGCTTTGTATGCTTGGCGGATTAAACAGAGAAGCACCAGGCAGTGGAGAAGGAAGCTCTGATGTCTGAACTGAAAATGCTGACTCATATTGGACACCATGAGAACATTGTCAACCTGCTTGGTGCTTGCACGGGATCAGGTAAGATTTGGAGAGGCCTTGGGTTTGATAATTATATTATCAGTTGGAGACACACACCTATATGCAGATGTAGATAAAAATTAGAGAACCACTTATAAAGGCTTATTTTTTTTCAGACGTAGTGCAATCGACTTCCAATTTTAGAGTTTAGATAAATGTTTTGAAGAAATTTAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAATGAATAGGAAGTGAGCAACTTTAAATGGTGTGATCTTGATCTTGGCCTTTTCCACAGTTCACGGACTGACAAGTTTCTTAGCCAAACCTTGATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37884
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 |
---|---|---|---|---|---|
ENSDART00000081357 | Nonsense | 613 | 956 | 16 | 24 |
ENSDART00000147759 | Nonsense | 200 | 439 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 22311355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21558233 |
GRCz11 | 24 | 21703407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGAGAAGCACCAGGCAGTGGAGAAGGAAGCTCTGATGTCTGAACTG[A/T]AAATGCTGACTCATATTGGACACCATGAGAACATTGTCAACCTGCTTGGT
Long Flanking Sequence:
TCTGCTTAATATAGGTTGATATGCTCCTTCAACAGATATTTAACTGACTATAAGTAACTTTGCAAGTACATGTCAACTTACAACAACCTTAAACCCAACCTAACAGTCTACTTATAATCTAATGAGAATTTGTTGGCATGTAGATGCAATAAACCTTAAAGTCAACAAAATGCGTTAAAGGGACCATCAAAATAAAGTGATACTATAATGTAATCAGTCATTAACTACCATTTTGAAGTAACTTACCCAATACTAATTTCCACAGGGAATGAACTTGGATCTGGTGCTTTTGGGATGGTTGTTCAGGCTACAGCATATGGGATCAGCAAGCCGGGTGTTTCTGTTCAGGTAGCGGTAAAAATGTTAAAGGGTAAGTAATGACAAATCTGTTATGAATATTTAAATAAGATAAAATAAATAACAACCTGTGCTTTGTATGCTTGGCGGATTAAACAGAGAAGCACCAGGCAGTGGAGAAGGAAGCTCTGATGTCTGAACTG[A/T]AAATGCTGACTCATATTGGACACCATGAGAACATTGTCAACCTGCTTGGTGCTTGCACGGGATCAGGTAAGATTTGGAGAGGCCTTGGGTTTGATAATTATATTATCAGTTGGAGACACACACCTATATGCAGATGTAGATAAAAATTAGAGAACCACTTATAAAGGCTTATTTTTTTTCAGACGTAGTGCAATCGACTTCCAATTTTAGAGTTTAGATAAATGTTTTGAAGAAATTTAAGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTAAATGAATAGGAAGTGAGCAACTTTAAATGGTGTGATCTTGATCTTGGCCTTTTCCACAGTTCACGGACTGACAAGTTTCTTAGCCAAACCTTGATGAAATGGATTTTCACTTTAGGTTTAGGTCAGGAATCTGGGCTGGCTATTTTATCTTTTCAATTATTTCAGCTTTAAAGAAATGATTTACCATTTGTTTCGTGGATCTTGAATGAGTGAGCGACTTTAGCCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44134
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 |
---|---|---|---|---|---|
ENSDART00000081357 | Nonsense | 870 | 956 | 22 | 24 |
ENSDART00000147759 | Nonsense | 396 | 439 | 11 | 12 |
Genomic Location (Zv9):
Chromosome 24 (position 22303836)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 21550714 |
GRCz11 | 24 | 21695888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGAACAACACTTTCTACAGAATGATTGAAAGTGGATATCACTTGGAG[C/T]AGCCCTATTATGCAGCAGAATCTGTGTAAGTGCCTCTAGTTTTTTTTTAT
Long Flanking Sequence:
ACAGCATGCCAAACCTGCTGTTATTATCAAGCTATATTTAAGTGAGAACTCTTGAAGTAAAAGTTTTTTTTCAGTTTGATGTAGAGAAAACATCAGAATGCACTTTTTTGTGTACTATTTTGTAACTCATTCTTGATTTCAGTCAGTATATTACACAATATATATTTTTCAAGGTTGTGTCTTCACAATGCGTGTTTTCTCCTGTACTGAACTGTAAATCTCCTCTTCAGCAGCTTGTATATCAAAATTGATTGTGGAAATGTAAAGAGATGCCCTAAATCTGCTCTGTAAAAACAATTGAATCTAATATTGAAAAAATAAAGAGTTAAACAAGATTTTTGTTGCTGATCCGATCCAACCTTCAGACAACTATGAATGTTTTTTTTTATTATTATTTTGTATTCATTAGACATTCATCTCTTTCAGGAGTCACCCCATATCCTGGTGTGACTGTGAACAACACTTTCTACAGAATGATTGAAAGTGGATATCACTTGGAG[C/T]AGCCCTATTATGCAGCAGAATCTGTGTAAGTGCCTCTAGTTTTTTTTTATTTTTAAAAAATGAATGAGTAGTAGTGCTACCCACGGTGTCGCCCATAATCAAATACTAATACACTGTAAAAACTATTAGTAACTTTACATTAAAAATATTGAGTAAATCATTTGTAACTCAGAACTGTTAGATTGGCTTAACTTCGATTTTATAATTATGCTCCTACACTGTAAAAAGTGATTAGTTACTTAAAGCAAGTAAACCGATTGCTTTAAAAGAAACAAGTTGACTTTACAAAAATAAAGTTAACCTATTGTAACTTGGAACTGTAAAGTTGACTTAATTTTTATATATATGCTTGTAATTACTTTTTTTAAGTCAACTAATGCGTTTGTACAATGTCAGACTATTTTAGCACGTCTGTTTTCAAATATTTGGTGCTTCATTAAGTCTATAAAATCTACAATTATTGCCTGTATTAACTTAGGAGACACACTGAAGTCTAGAAG
Associated Phenotype:
Not determined