ZMP
ntrk2b
Ensembl ID:
ZFIN ID:
Description:
BDNF/NT-3 growth factors receptor [Source:RefSeq peptide;Acc:NP_001184090]
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 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17771 | Essential Splice Site | Available for shipment | Available now |
| sa17691 | Essential Splice Site | Available for shipment | Available now |
| sa13660 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17771
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 |
|---|---|---|---|---|---|
| ENSDART00000002966 | Essential Splice Site | 376 | 792 | 12 | 21 |
| ENSDART00000108513 | None | None | 238 | None | 6 |
| ENSDART00000135885 | None | None | 854 | None | 18 |
| ENSDART00000002966 | Essential Splice Site | 376 | 792 | 12 | 21 |
| ENSDART00000108513 | None | None | 238 | None | 6 |
| ENSDART00000135885 | None | None | 854 | None | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 57058229)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 54978839 |
| GRCz11 | 5 | 55649056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTATCTGACATACTGTAAAAATTTCCTTGCTCTRTTAAACACCAATA[T/A]AATAATTCTGACACCAACTGTATAATGCAGTTCCTGACACATTCAGTTAT
Long Flanking Sequence:
TGGATGAATCTTTAAAAGGATATATCTTCTGTTTATATACAGCGGAAGTCAGAATTATTAGCCCCTCTGAATTATTAGCCCTCTGTTTATTTTTTGTTTAATTTCTGTTTAACGGAGAGAATATTTTTTTTCAACACTTTTCTAATCATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAATTTATATTTTACTAGATATTTGTTAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGGTAATCAGGCAGGTTAGGGTAATTAGGCCAGTTATTGTATAATGGTGGTTTTTTCTTTAGACCATCGAAAGAAGTTGTTTAAAGGGGCCAAAAATTTTGACCTTAAAATGGGTTTTAAAATTTTTTAAAAACAGATACAACTTTTTCCAAAAGAAAAAAATATTATCTGACATACTGTAAAAATTTCCTTGCTCTATTAAACACCAATA[T/A]AATAATTCTGACACCAACTGTATAATGCAGTTCCTGACACATTCAGTTATAGACGGCAACAACTCACACACCTCTTAGCCTAAAACGCACTAAACTGCTTTTCCTACAAAAATACAGAGCAGGTTATGTTTTCCAGCTCTTTTTTTCTTTTTTTCGCTTGATGTTATGAGAACTACTCCCTCGCAATAGCTGTAAGCAGCATTAGCTACGGATATTTGAATTACATATCAACAGAACAAAACCGAGATGTGAGAACAAACGGAGCACTTGCAATCAATATACTTCACCTGCAGCTGTTTTTCACTCATTTATAAGCCTCATGTCCTTGTCAGAGGTTCAACTCACCGATACTTTTCATTTTAGAGATATAGTCATTGGTGACTGTGTTATATCGGGTTAGTTTCTGCTTATATTTGGGGTCAGATAAATATTTGCTGGTAGGGAAAATGTATTGTTTCACTTCTGCTATTTATACTTTGATTTGCATTTCAGTTTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17691
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 |
|---|---|---|---|---|---|
| ENSDART00000002966 | Essential Splice Site | 376 | 792 | 12 | 21 |
| ENSDART00000108513 | None | None | 238 | None | 6 |
| ENSDART00000135885 | None | None | 854 | None | 18 |
| ENSDART00000002966 | Essential Splice Site | 376 | 792 | 12 | 21 |
| ENSDART00000108513 | None | None | 238 | None | 6 |
| ENSDART00000135885 | None | None | 854 | None | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 57058229)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 54978839 |
| GRCz11 | 5 | 55649056 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTATCTGACATACTGTAAAAATTTCCTTGCTCTRTTAAACACCAATA[T/A]AATAATTCTGACACCAACTGTATAATGCAGTTCCTGACACATTCAGTTAT
Long Flanking Sequence:
TGGATGAATCTTTAAAAGGATATATCTTCTGTTTATATACAGCGGAAGTCAGAATTATTAGCCCCTCTGAATTATTAGCCCTCTGTTTATTTTTTGTTTAATTTCTGTTTAACGGAGAGAATATTTTTTTTCAACACTTTTCTAATCATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAATTTATATTTTACTAGATATTTGTTAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGGTAATCAGGCAGGTTAGGGTAATTAGGCCAGTTATTGTATAATGGTGGTTTTTTCTTTAGACCATCGAAAGAAGTTGTTTAAAGGGGCCAAAAATTTTGACCTTAAAATGGGTTTTAAAATTTTTTAAAAACAGATACAACTTTTTCCAAAAGAAAAAAATATTATCTGACATACTGTAAAAATTTCCTTGCTCTATTAAACACCAATA[T/A]AATAATTCTGACACCAACTGTATAATGCAGTTCCTGACACATTCAGTTATAGACGGCAACAACTCACACACCTCTTAGCCTAAAACGCACTAAACTGCTTTTCCTACAAAAATACAGAGCAGGTTATGTTTTCCAGCTCTTTTTTTCTTTTTTTCGCTTGATGTTATGAGAACTACTCCCTCGCAATAGCTGTAAGCAGCATTAGCTACGGATATTTGAATTACATATCAACAGAACAAAACCGAGATGTGAGAACAAACGGAGCACTTGCAATCAATATACTTCACCTGCAGCTGTTTTTCACTCATTTATAAGCCTCATGTCCTTGTCAGAGGTTCAACTCACCGATACTTTTCATTTTAGAGATATAGTCATTGGTGACTGTGTTATATCGGGTTAGTTTCTGCTTATATTTGGGGTCAGATAAATATTTGCTGGTAGGGAAAATGTATTGTTTCACTTCTGCTATTTATACTTTGATTTGCATTTCAGTTTATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13660
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 |
|---|---|---|---|---|---|
| ENSDART00000002966 | Nonsense | 725 | 792 | 20 | 21 |
| ENSDART00000108513 | None | None | 238 | None | 6 |
| ENSDART00000135885 | Nonsense | 787 | 854 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 57095848)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 55016447 |
| GRCz11 | 5 | 55686664 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGGTGTAGTACTCTGGGAAATCTTCACCTATGGCAAGCAACCCTGGTA[T/A]CAGCTCTCAAACAATGAGGTAAGATGCTACCCAATCAATCATTTGTCTGA
Long Flanking Sequence:
ATTTCTGTTTGGAGTTTGCATGTTCTCCTCAAGTTCGCATGGGTTTCCTCCAGGTGCACAGTCCAAAGACATGCACTATAGGTGAATTAAATAAACTAAATTGGACGTAGTGTATGAGTGTGTGTGAATGAGGGTGTATGGGTGTTTCCCAGTAATGGATTAAAGCTGGAGGGGCATCCACTGCATAAAACATATGCCAGAGTAGTTGGCAGTTCACTCCACTGTTGTGACCCCTGATAAGTAAGGGACTAAGCCAAAGAAAAATGAATGAATGAATATTATTAAATGGTAAGAGCATAATAAGTGCATGTGCTTTCATTAATCAGTGCACCCCCTGTCAATTTATGTCTCACATCGCAGGTGGGTGGTCACACCATGCTGCCCATCCGATGGATGCCCCCAGAGAGCATTATGTACAGAAGATTCACCACAGAGAGTGACGTGTGGAGTTTGGGTGTAGTACTCTGGGAAATCTTCACCTATGGCAAGCAACCCTGGTA[T/A]CAGCTCTCAAACAATGAGGTAAGATGCTACCCAATCAATCATTTGTCTGAAAATAAAGAACTTTCATCATTTAGTCACAGAAATTAGTTATTCCCAATGTTCGTATGGATGCTGTAAATCCTTGAACATGCTTGAAAATTAATCTAGTGGTTTCAAGGTTTAAAGAATAGCTTGAAACTGCTTGAAAATTTGTTAATTATTCACTAAAAAGTTAATCAGTTAAATGTTGAAATAAAATAAATAGTTTTGCTTTTGCATAAATGAAAACCATAGTTTTAAATAATGACTGTTACTGTTAAATAAATAACTGTTTTAAATAATGGTTTACACTGCATTGTTGATTTCATTGTTGGAAAAAAATCAATCAAGCATAATCCTGTGCTTTTGATTTTGTTATTAAAAAAACTAAAGAAAAACAAGCAACCATGTATAATGAGAATCTGAAATATTTGATGGCATACTTGTGTTCAAAAATGTTTTATTTTTATTTAGTTTTTAAG
Associated Phenotype:
Not determined