ZMP
ntrk3a
Ensembl ID:
ZFIN ID:
Description:
Tyrosine-protein kinase receptor [Source:UniProtKB/TrEMBL;Acc:B8JLJ1]
Human Orthologue:
NTRK2
Human Description:
neurotrophic tyrosine kinase, receptor, type 2 [Source:HGNC Symbol;Acc:8032]
Mouse Orthologue:
Ntrk2
Mouse Description:
neurotrophic tyrosine kinase, receptor, type 2 Gene [Source:MGI Symbol;Acc:MGI:97384]
Alleles
There are 11 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12452 | Essential Splice Site | Available for shipment | Available now |
sa34500 | Nonsense | Available for shipment | Available now |
sa15536 | Nonsense | Available for shipment | Available now |
sa13707 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12452
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 |
---|---|---|---|---|---|
ENSDART00000083790 | Essential Splice Site | 56 | 806 | None | 19 |
ENSDART00000131732 | None | None | 392 | None | 7 |
The following transcripts of ENSDARG00000059897 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 52039792)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49790179 |
GRCz11 | 8 | 49778948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCCCCAAGCTGGAGTCCGAGGCGGACATGGAGAACGTCACTGACATG[T/A]AAGTCATGCTGGGGGTCATATACACTGAAACAAAAGCGATACATTGGATT
Long Flanking Sequence:
TGATACACTATAAAGAAAGCCTTGATCAGTGTAAGGATGTTGTCAGGCGGTCAATAACGCGTGTGAGTGAGTGAAGGATTGATTGATGTGTCCTGCTGGTCTCCTCCCCTCAGACGCGCGCATCATCCAGCGCGTCTCCAGAGCGCGTCTTCAGTCCGCATCCGAGCGTCATTCAGCGCAGCATCTCGGGCATTCGTTCTGTAGGAATATACGGTCACTCGCTGTTGCTTTTTCTGCTCCGGCTCTGCGCGTCTCCAGACTCCGGGTTTTTTTCGGGGGTCGTTAAATCTGGAGGTGAGGACCCGGGGATGAGCTTCGGCATGACGGGCTGCGGGTTCGGTTGGGCGGTGATGCTGCTCGCGCTCTGGAGGCCCGCGACCGCTTGTCCGGAGCTCTGCACGTGCACGGGTTTGCGGATCTCCTGCGTGGACGCGGAGCGCAGTATTATGGCTTTCCCCAAGCTGGAGTCCGAGGCGGACATGGAGAACGTCACTGACATG[T/A]AAGTCATGCTGGGGGTCATATACACTGAAACAAAAGCGATACATTGGATTTACTCCGGTTTTTTAACCGCGGTAAAGTTTGACATTCATTAGAAATTCGATTTCAAACCAATTAAATTATTTGCCCCTGCTATAGTTTGAGCCAAAAATATCTCAGATAGGTATAATTATGTGTCCTTTATGTTGCACAAGGCTTAATCGATAAAAAAGACCAATTAAACAATTCAACGAAATTATACAATAAAACCAGTAGCAAAATGTTCAGAAAAACACCCTGCTTATTGCACAAGACTCTGTTTTTTGCAATTAGCACTTTATTTATTTTATTATATTTTTAAAATAACTTTTAATGTAAAAATGGTAAAAGTTTTGTTTTTCACAGTTATGCCTTTGTTGATTTTATATACAGTACTGAATCCATATTTTCAGTAATTCGGATACACTGTAAACACTTAAATGAATTAAACACTGACACCATTTGAGATAAAAATATACAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34500
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 |
---|---|---|---|---|---|
ENSDART00000083790 | Nonsense | 347 | 806 | 9 | 19 |
ENSDART00000131732 | None | None | 392 | None | 7 |
The following transcripts of ENSDARG00000059897 do not overlap with this mutation:
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 52059439)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49809826 |
GRCz11 | 8 | 49798595 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGTCCCACGCACATCAACAACGGCATGTACACGCTGCTGGCCAGAAAT[C/T]AATTCGGAGAGGACAGCAAGGCCGTATCTGCTCATTTCATGCATGAGCCA
Long Flanking Sequence:
CATGCTATGATGTTTTAATTCATAGAATAATGAATTGTTGGTCAATAAATAAAAGTAATCCTACTATTTCTGTCATGTCAACTCTCGAAATTGAGATTTAGAGTTGTAATAAATATGGTCTTGGTGACATAAAGCTGCTACACCGCTGCTGCTAATTCTTTAATAGTCAAATAATCCATTTTAGCAATACCATAATGCTACCATAAATAATGAAGTTACATCTGTGCTTGTTGATTCTTGTGTTATTTGGGATGCCAGTTCCACCTGTAATCAGCAAGCTGACAGATGCCATTCCGGACCACCACTGGTGTATTCCCTTCAGCGTGTCTGGCAACCCGAAACCCAAACTCAGATGGTTATTAGACGAGCAACCCATTCAAGAGGGCAAGTTCATCCATACCATGATCCACGATTACTCGGAGGGCGAATACCACGGTTGTCTACAGCTGGACAGTCCCACGCACATCAACAACGGCATGTACACGCTGCTGGCCAGAAAT[C/T]AATTCGGAGAGGACAGCAAGGCCGTATCTGCTCATTTCATGCATGAGCCATGGAACGGTGAGTTGAAATTAGCATGCATTCAAGTTAAAATTGTCAGGTTATACTTTTGCGTCGAGTGCATGGGGTAGATTCGATGGAGCGTTTGAGCAGTCACACACATTTCGCCGTATCCTGACGCGCACCCCTCAAAAAATAATGACAATATGTTTTGCCGACGTGGAGCGCAGGATCTGTCAGATTGGTAGTGGTCAGGGGCATCACTAGACCCCATTTATTAGGGCACGTGCCTCAGTAAAAATCGTCAGTGCCCTAATAAATGCTTTGAGATAAGATTGATATTTATTAGGAGTGGTAATCCCAAAATAAAGATGTCATTCATTATGCAACCCAACCAACGCTGATGAAAGCAATGTAGTGTGATCAAAAGGCAAACTGGGCATGCGCACAGAAAAAAAACCATACCCGCACGCCTCACACACCGCTCCTGCTGACTCACTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15536
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083790 | Nonsense | 721 | 806 | 18 | 19 |
ENSDART00000131732 | Nonsense | 307 | 392 | 6 | 7 |
The following transcripts of ENSDARG00000059897 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 52121583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49871970 |
GRCz11 | 8 | 49860739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACCRGAGAGTATCATGTATCGGAAGTTYACAACAGMGAGTGATGTCTG[G/A]AGTCTGGGAGTGGTGCTGTGGGAGATCTTTACCTATGGAAAACAGCCCTG
Long Flanking Sequence:
GAGCTGGAAATACTGTCAGCGTTTGCCTGAGAGCTATTTGGATTGAACAATGCCCCGATTGCAAAAACAAACAAACAAACAAAAAAAACTGTCTACTCTTTACTCTTGCTCTAAAAGTCTGTAAAATTCTTGTCCATTAGCGCCTATCAGATCCTGAGATATTTGTTTAAGGAACTTGATTTTACGTAACCTGCTGTTGTTGATTTGCGTAAACTTGGACATGTTAATGTCAGTTCAACATAAATCAAATGTTCAGTGCTGTGCTGTATTTGTTTGTAATAATAGTAATAATATTGCTACGAGTTATATACATTATAACTTATATTAATTTCACAGAATCAAACTTATGTCTCCTACATCATGACTCAAAATATCAGTTGAGGTAATGTGCGCTTATTGTTTTCACATGTTAAGGTTGGAGGTCACACCATGCTGCCAATCCGCTGGATGCCACCGGAGAGTATCATGTATCGGAAGTTCACAACAGAGAGTGATGTCTG[G/A]AGTCTGGGAGTGGTGCTGTGGGAGATCTTTACCTATGGAAAACAGCCCTGGTACCAACTGTCAAATAATGAGGTACTCATACAATAACATGTACAGACATGTGTCATCTCCATGCAGTGAAATAACTTTGATTGGTAAATCTACACAACTTGTTTCATTTTTTTCTAAGTCAAAAAAATATATACTCCTAAATACTCGATGCACCCTACATTTGAAGTCCACCTAGTAATGTGCTAGAAACGACAATGAACAGCTTAGCAACTAGAAGTCAGTGGTGTCCATCCCTGTTCCCTGTATTTCAGAGGCAGCGCATTATGGAGAAAGCTAATAAACAAAATAATTGGTTTTAAGGTTGAGCTTCAGGCAATACCAACTCCCGAGCTTACAGCATCAAAATCTTGAGAGGCACAACTTACGGCACCATCTGAGGTTCTGAACTGAAAACGCTGTCAGCATTTGCCTGAGAGCTATTTTGATTAAACAATGCCCCGACAGCGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13707
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 |
---|---|---|---|---|---|
ENSDART00000083790 | Nonsense | 785 | 806 | 19 | 19 |
ENSDART00000131732 | Nonsense | 371 | 392 | 7 | 7 |
The following transcripts of ENSDARG00000059897 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 52125041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 49875428 |
GRCz11 | 8 | 49864197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTGATGCTGGGATGTTRGCAGAGAGAGCCGCACACCCGACTCAATATT[A/T]AAGAGATCCATAACYTACTTCTCAACCTAGCCAARGCATCACCAGTCTAT
Long Flanking Sequence:
CATCAAATTGAAGGGTCATTCCAAACTGAAGTGCTGAAGTTTTGAAGGATACAACTGATGGACATTTCAGGCCTTGATCAGTAGAGAAGGGAATTTGTTTGGTGTATCACTGCGTTCGATTTGGAGAACCTCAACCCTATGCTCCGATCCCTTTAGACCCTAGGATTAGGGCATAGGGATGAGCCTCTCAGAATGGAACCCAAAGTAAGTCCAACATTCCTTCAAATTTTTTTTCAAATAGATGAGGTATTCAAACACTTATGGCTACACTATATAAACTTTATCATGTTTTATTTTACTAAAAAGTCCTGTCAAAATGCAGTTTGTCCCACACATTTCTGACCATTTATTTGGTTGACCTTTTATTCCTTGCTCTTTTGTAGGTGATCGAGTGCATCACCCAAGGTCGTGTACTGCAGCGACCCCGGACCTGTCCCAAGGAGGTGTATGACTTGATGCTGGGATGTTGGCAGAGAGAGCCGCACACCCGACTCAATATT[A/T]AAGAGATCCATAACCTACTTCTCAACCTAGCCAAGGCATCACCAGTCTATCTGGACATCCTGGGATAAACATAAGGAACGTGTGGGACTTCAAGTGTATTCCTGAATCTCCGACCCCCCCCTCCTCCTCTATCCCATCTAAAACCTTTTCTTCTGCAGCTTTAACTCTGTTGTCCTGCTCCTCTTCTCCATGTAAACATCTAGACACACTGGCAGGGATTCGTGTCCGTGTACGCTGACTATGACTGATGTTTTTCTGAACATTGAATTGAAAGAAGTGACTACTGTTTAGTTTACCAAGAACAAAATCCCAGAATGGTTGACCACCCTAAACGTCTGGACCAAGTTCACAGCTGGATATTTAAGTACACCGATCTTAACAACAAATAGGAATCAGCAGCTTCACGAAAAACGAACAAAAACGACTATGAGGAGGAAAATAAGTACTTTTCTGGACAGATTTGGTCCTGTCATCTGATACAAAGCACAGAACGTGAAGCT
Associated Phenotype:
Not determined