ZMP
ntrk3b
Ensembl ID:
ZFIN ID:
Human Orthologue:
NTRK3
Human Description:
neurotrophic tyrosine kinase, receptor, type 3 [Source:HGNC Symbol;Acc:8033]
Mouse Orthologue:
Ntrk3
Mouse Description:
neurotrophic tyrosine kinase, receptor, type 3 Gene [Source:MGI Symbol;Acc:MGI:97385]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38019 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24620 | Nonsense | Available for shipment | Available now |
sa13864 | Essential Splice Site | Available for shipment | Available now |
sa38018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30214 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38019
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091727 | Essential Splice Site | 259 | 684 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 12338860)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 11902299 |
GRCz11 | 25 | 11998804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGCCGTCAAAACTGTGTACGCCCACTTTCTACACCCGCCTTTTGAAGG[T/A]ACGTAATTTTTATTGTTACTGTTGTTTTCTTATCGTCTCAACTTACATTA
Long Flanking Sequence:
ATTTACTTTCACTCTTGAACAATTTGTTGTGTTGAATAAAATTAAGAAGTTTTTATAGTATTTTCTATTTAAAAAATGGAGCCTTCGTGAGCAGAATAACCTTCTTATAAAACATAAGAAAAATTGTACTGATTCTAATACTTTGACTGGCACTGTGTGTTGGAACAAAGCAGCAAAAAACTCTTTTGTTTCTCTCTTGCAGTCCCTCCTGCCATCATTAACTTCGAGGAGCCGCAGAAGAGGCACGACACATGTATGATGTTCACGGTACGGGCCAATCCCCTGCCAACCCTGCACTGGAGCTTCAAGGGTGAGGAGATCAAGGCGACCGAGTACGTCCACCCAGAGATGGAGGTCTATCAGGACAATCTGGAGGGTTGCCTCTTGTTTAAAAACCCTACACAACACAACAATGGAAATTACACACTGGAGGCCAGAAACTATCTGGGCGTGGCCGTCAAAACTGTGTACGCCCACTTTCTACACCCGCCTTTTGAAGG[T/A]ACGTAATTTTTATTGTTACTGTTGTTTTCTTATCGTCTCAACTTACATTAATCAAAATTACTAAAATGATCAAGTTAAGCTTTGTATAACTTAAAAATATGTAGTTGAAACCTTATTAAATTAGTTAAAGCAACATAAAACATTACAAAGTGTTATTTTCTATTTAATTAACTGACAAATACATATAAATTACACATAAAGGTGGAGGAATTAAGCAATGAAATACATTGCTGCAGTAGCTTACTAGTACATGCTAGCCACTGAATCTCAAATGTGTTAGCATCATGCTAAAATGTTAGAAAAGTTGTAACATGCTAGTAACTGAGCAATCAAACTCCAGAATAATCACAAATAAATGAAGCAGATTGAGGTATTATTGTAGCATTCATAAATAGTTTAAATAATAAAAAAAAAAGCTATAAACTTGTTAAAATGCAAGAAACAATACTGGAACTTGCTAAATGATGTTAACAACTGAGTATTTAAGCTATATGCTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24620
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 |
---|---|---|---|---|---|
ENSDART00000091727 | Nonsense | 314 | 684 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 12330323)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 11893762 |
GRCz11 | 25 | 11990267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTGGCTTCGCCTGCGTTCTCCTCGTCGTTATGTTTGTGCTAATCAAC[A/T]AATATGGCAGACGCTCAAAGTTTGGCATGAAAGGTAAGCAAGTGTAAACT
Long Flanking Sequence:
TCATACAAAAATATCAGATAACAATTAGTTGAAAGTTGCACATTCCATAATGAATTGTTCACTGATTTCACTCTCAAAACCAATTATGTAAGCAGAATTCCACAAATGATCACATATTTTGCAGACATTTTGATTATAAATCAAAATAGCTACACATAGCTACTATTTGGAGATTTTTCACTCCTAAAATGGCTGACATACGCTGTTTTATCCTACCATGTTAAGCAGTGTCACACATATTAATGTCTTTTAATTACTTGGCAGAAACAGTTTTAGGCAGTAAACAATGTGCTAGCATTCCAAACATAATCCTGTAACACTGCTAACATGCTAAAGCTAAGCGCTAACTTGACTGCAATCTTAAATCCTGTTCTCATTTTACATTTGGGTTTCTCAGTTCAAACTAAATGTTGTCTCTCCTCGTTCTCTAGGTGTCGATTGCGGTTGGCTTGGCTGGCTTCGCCTGCGTTCTCCTCGTCGTTATGTTTGTGCTAATCAAC[A/T]AATATGGCAGACGCTCAAAGTTTGGCATGAAAGGTAAGCAAGTGTAAACTTTTCAGCGGGAAACTTGGCACTTAGCATTATTAGTGAATAAGTGTGATATCAACCGACTTATACCAGCGACTGTGTTTTGTAGGATGATGGAAAGCAATAGAGTATTCATTATGCTATCTTTATAGCAGTTTGTTTTGGGAAAATGTGATGGATTTAATTGGAACTTACTATTATTGTATTGATGCCTTCTTTAAACCAATCCTAAAGGAATTCTAAAGGAATATGTCTCAAAACACACTAGAAACCATTGAGTTAATCTGGTTTTAATGGGTAATATTTGATGGTTTACAAAGTTTTTAATAAAGTTGACTATTGATTTTATCAGCAGGTTGAGTTCTTGTTGAGCTTCTTGGATATTTATACATTGTAAATGTTTTTCGCAAGGCAATAATCCAGTTGGATTTTGGAAATATTTCTTTGTTGGAGTTTGAACGTGTTTGCACATCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13864
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091727 | Essential Splice Site | 325 | 684 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 12330288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 11893727 |
GRCz11 | 25 | 11990232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTGCTAATCAACAAATATGGCAGACGCTCAAAGTTTGGCATGAAAGG[T/A]AAGCAAGTGTAAACTTTTCAGCGGGAAACTTGGCACTTAGCATTATTAGY
Long Flanking Sequence:
TTGCACATTCCATAATGAATTGTTCACTGATTTCACTCTCAAAACCAATTATGTAAGCAGAATTCCACAAATGATCACATATTTTGCAGACATTTTGATTATAAATCAAAATAGCTACACATAGCTACTATTTGGAGATTTTTCACTCCTAAAATGGCTGACATACGCTGTTTTATCCTACCATGTTAAGCAGTGTCACACATATTAATGTCTTTTAATTACTTGGCAGAAACAGTTTTAGGCAGTAAACAATGTGCTAGCATTCCAAACATAATCCTGTAACACTGCTAACATGCTAAAGCTAAGCGCTAACTTGACTGCAATCTTAAATCCTGTTCTCATTTTACATTTGGGTTTCTCAGTTCAAACTAAATGTTGTCTCTCCTCGTTCTCTAGGTGTCGATTGCGGTTGGCTTGGCTGGCTTCGCCTGCGTTCTCCTCGTCGTTATGTTTGTGCTAATCAACAAATATGGCAGACGCTCAAAGTTTGGCATGAAAGG[T/A]AAGCAAGTGTAAACTTTTCAGCGGGAAACTTGGCACTTAGCATTATTAGTGAATAAGTGTGATATCAACCGACTTATACCAGCGACTGTGTTTTGTAGGATGATGGAAAGCAATAGAGTATTCATTATGCTATCTTTATAGCAGTTTGTTTTGGGAAAATGTGATGGATTTAATTGGAACTTACTATTATTGTATTGATGCCTTCTTTAAACCAATCCTAAAGGAATTCTAAAGGAATATGTCTCAAAACACACTAGAAACCATTGAGTTAATCTGGTTTTAATGGGTAATATTTGATGGTTTACAAAGTTTTTAATAAAGTTGACTATTGATTTTATCAGCAGGTTGAGTTCTTGTTGAGCTTCTTGGATATTTATACATTGTAAATGTTTTTCGCAAGGCAATAATCCAGTTGGATTTTGGAAATATTTCTTTGTTGGAGTTTGAACGTGTTTGCACATCTTTAGCCATTCATTAAACTCAATCATAATGGGTGTCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38018
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 |
---|---|---|---|---|---|
ENSDART00000091727 | Nonsense | 645 | 684 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 12146425)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 11709864 |
GRCz11 | 25 | 11806369 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACAAGGACGGGTGCTAGAAAGGCCACGGCTCTGTCCCAAGGAAGTGTA[C/A]GACATTATGCTGGGGTGCTGGCAGAGGGAACCACAACAGAGGTTAAACAT
Long Flanking Sequence:
CCATATGGCGTGGGCATATGGGAAAAAGAAGTTCATACTCACATCCAACATCTTGTTTGTCATAGGGGGCATGCAAGAAATATTCCCGAATTAAATTGAAATTGGAAAACTACAGTCAAAGTGGACAAATAAAAAAGTGAAACACCCGAAATTACATGAAACTTCTGAGAAAATGTGGATAGCGTGGTGACGCAATGACATTAATCAAATTATGTGCTATAACATGTAAAATAAAAGGAACATTCTAAAAGCAGCTCATGTAAACACCTTAATCACATTATTGTCTTATTCAGATTAAGGCAAATAATTTGATAACTGATGTCCATGTAAACAGAGTCACTGAGTTTTACATATATGACATGTCTTTGGTTTGTAAAAGGTTGAAGACCATGCTATAGTAAGTAATTCCATTCTCCTTCCTGACTCTCCTTACAGGTAATCGAATGCATCACACAAGGACGGGTGCTAGAAAGGCCACGGCTCTGTCCCAAGGAAGTGTA[C/A]GACATTATGCTGGGGTGCTGGCAGAGGGAACCACAACAGAGGTTAAACATCAAAGACATCCAGAAAATTCTTTTTGCCTTGGGCAAAGCCACACCTGTCTACCTGGATATCCTGGGCTAGTGTTTGTTGGGAATATGTGTGGATGTCTGTCTGTCTGCGTCCGTCCAACAGAGGAACGAACAACATGGGATTAACCCAAAACTACATGTACCTTACTGCGCCACTGTCAGACACCTACAACATGGGGATGGACTTAAGTGCCTGCTACTCCTTTCGATACACTGGATAACAGTCTTTAAAAGCACTTTTACATTTTGTTTACCTGCATATAAAGATGTACAGTTCTACTGCAAGACGAGGAGTGTCCTTTCATGATTTGATTTCCTTTCGTCTTTTTCGTTTGGTAACAGCAGCCTACTTTTAAACTCCAAAAAAGGAATAACGGAACCATCTGCTCCCTCTCTAAAAATGGAAAATGGAAAAAAAACTAAAGTGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30214
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 |
---|---|---|---|---|---|
ENSDART00000091727 | Nonsense | 658 | 684 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 25 (position 12146388)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 11709827 |
GRCz11 | 25 | 11806332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGGAAGTGTACGACATTATGCTGGGGTGCTGGCAGAGGGAACCACAA[C/T]AGAGGTTAAACATCAAAGACATCCAGAAAATTCTTTTTGCCTTGGGCAAA
Long Flanking Sequence:
CTCACATCCAACATCTTGTTTGTCATAGGGGGCATGCAAGAAATATTCCCGAATTAAATTGAAATTGGAAAACTACAGTCAAAGTGGACAAATAAAAAAGTGAAACACCCGAAATTACATGAAACTTCTGAGAAAATGTGGATAGCGTGGTGACGCAATGACATTAATCAAATTATGTGCTATAACATGTAAAATAAAAGGAACATTCTAAAAGCAGCTCATGTAAACACCTTAATCACATTATTGTCTTATTCAGATTAAGGCAAATAATTTGATAACTGATGTCCATGTAAACAGAGTCACTGAGTTTTACATATATGACATGTCTTTGGTTTGTAAAAGGTTGAAGACCATGCTATAGTAAGTAATTCCATTCTCCTTCCTGACTCTCCTTACAGGTAATCGAATGCATCACACAAGGACGGGTGCTAGAAAGGCCACGGCTCTGTCCCAAGGAAGTGTACGACATTATGCTGGGGTGCTGGCAGAGGGAACCACAA[C/T]AGAGGTTAAACATCAAAGACATCCAGAAAATTCTTTTTGCCTTGGGCAAAGCCACACCTGTCTACCTGGATATCCTGGGCTAGTGTTTGTTGGGAATATGTGTGGATGTCTGTCTGTCTGCGTCCGTCCAACAGAGGAACGAACAACATGGGATTAACCCAAAACTACATGTACCTTACTGCGCCACTGTCAGACACCTACAACATGGGGATGGACTTAAGTGCCTGCTACTCCTTTCGATACACTGGATAACAGTCTTTAAAAGCACTTTTACATTTTGTTTACCTGCATATAAAGATGTACAGTTCTACTGCAAGACGAGGAGTGTCCTTTCATGATTTGATTTCCTTTCGTCTTTTTCGTTTGGTAACAGCAGCCTACTTTTAAACTCCAAAAAAGGAATAACGGAACCATCTGCTCCCTCTCTAAAAATGGAAAATGGAAAAAAAACTAAAGTGGAGGAGGTTCCTGACTGCTTGACAACTCTCTGTGTTATTACT
Associated Phenotype:
Not determined