ZMP
nktr
Ensembl ID:
ZFIN ID:
Description:
Nktr protein [Source:UniProtKB/TrEMBL;Acc:Q1JQ26]
Human Orthologue:
NKTR
Human Description:
natural killer-tumor recognition sequence [Source:HGNC Symbol;Acc:7833]
Mouse Orthologue:
Nktr
Mouse Description:
natural killer tumor recognition sequence Gene [Source:MGI Symbol;Acc:MGI:97346]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37874 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24485 | Essential Splice Site | Available for shipment | Available now |
sa37873 | Nonsense | Available for shipment | Available now |
sa37872 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37874
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082112 | Nonsense | 10 | 428 | 2 | 13 |
ENSDART00000123682 | Nonsense | 10 | 1396 | 1 | 16 |
ENSDART00000127923 | Nonsense | 10 | 1396 | 2 | 17 |
ENSDART00000127988 | Nonsense | 10 | 105 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 21265196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20512325 |
GRCz11 | 24 | 20656744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCCCACTCTGTGGAAAAAATGGGGGTGAAAGATCGCCCTCAGTGCTA[T/A]TTTGACGTGGAAATCAACAGAGAACCAGGTAAGATTTGACATTCATTAAT
Long Flanking Sequence:
TCTCTCTTTTTTTAACTTCATAAGTGCCAAGTTCTTGTTTTAATTTGTTTAGTCTCTTTCCTATTCATATTTGTAGCTCCTCCCCTTATGCAAATATCCAAACAAAGCCCAAAGATAGAAAACATCTGGTTTATCCAGGATGAGAGCAAACATTACCGCAACAATGTAATGTTTCATTCATCACAGAAGGGTGGTGTCCGGCACCAGTGACAGACAGAGCACTGCTCAAAAAAGGGGGAGGAAGTTTGGAGGGGCGTGTGTCTCATTGGTTAACTGAAACGCTTCCCCAATCTCACTGTCTGACTTTGTTCACTTACTCTTCATGTCACCTTAAAATCTGAGGAGAAAGAGAATTTTGGAAGAGAACTGAAGTGGAATGTTTTCCTTTCAGCTGTGAGTTATTGGAGAATACAAGATTTAACAGTGTTTTGCTTTGATTGTACACTACAGGAAGCCCACTCTGTGGAAAAAATGGGGGTGAAAGATCGCCCTCAGTGCTA[T/A]TTTGACGTGGAAATCAACAGAGAACCAGGTAAGATTTGACATTCATTAATAGTAAGCTGATCTCTGAACTGTTTTAAAGTGAGCTATAGAAATTAACTTTTGCAAGCATTTTGCTTCAAAGTTGCAAGTGTATAAAAAAGGTTCAGAGTTGCATGATCTGTAATTATCATTTTGTGTGAACTGAAACTTTGAAGTCAAGGAATTTGGATGTAAAATGAATACTCTAACCAGCTAAATATGAATGCATTTAATACGAAAGTGAAACATTATATGTGCTTGTTTTGTAACATGTGAAAGGCTGTTGTGGCAGTCCACAGACTCCACACCCTAACCTGCAGCTCTGTTTTAATGAACCCCAGACATTGTGTGTGCTAAATAATGTCTGCATTTCACCTCAGTCTACCAGTAATGATGTGTTTTAAGAGAGACGTCTGTGCCATAAAGCCAGGAGTGCTTATTTAGTAATTTTACACCTGTAATTTTACTAAGCAAATGTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24485
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 |
---|---|---|---|---|---|
ENSDART00000082112 | Essential Splice Site | 95 | 428 | 5 | 13 |
ENSDART00000123682 | Essential Splice Site | 95 | 1396 | 4 | 16 |
ENSDART00000127923 | Essential Splice Site | 95 | 1396 | 5 | 17 |
ENSDART00000127988 | Essential Splice Site | 95 | 105 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 21260646)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20507775 |
GRCz11 | 24 | 20652194 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAGGCAATGGAAGAGGGGGAGAATCTATATTTGGTGGTTTCTTTGAAG[G/A]TAAGCCATCTTCAGATCGGGTTTGGTTTGAATCAAGCACTCTGTAACCTT
Long Flanking Sequence:
GATGGGTTTGATTAGAGTTGTAGCTTAACTCTCCAGGACCCCAACCCTCCAGGATTTTAGACACCCCTGCTTTAGTAGGTGTCTTCAATATATCACAGTCAAAATGTCTAAGACGATCAAAATGAACAGGACACATTCTAATGCATTGGGAAAAAACTAAATATGAAATATTTATAGTTTGATGCTTGAAAATCACCTTTGACCCAAAATAATCAGAAATTATGTGTTCTTTTGGGTTTCTTGCAGGCGAGAAAGGCAGTGGCAAAGCTACAGGGAAAAAATTATGCTATAAAGGTTCAACTTTCCATCGAGTTGTAAAGAACTTCATGATCCAGGGGGGTGATTTTACTGAGGGTATGCACAATTATGCTTATAACTAAACCAGTTTGGTTTGGGTTGTGTGTTTGTTATTCTCACTATTCTTGTTAAAGAATTTTTTTTTTTTTTTTGCTTAGGCAATGGAAGAGGGGGAGAATCTATATTTGGTGGTTTCTTTGAAG[G/A]TAAGCCATCTTCAGATCGGGTTTGGTTTGAATCAAGCACTCTGTAACCTTAGCAAAGTCACTTAATTTGTGTTTTAACAGCTTTTGCATGACATTTTTGATTGAGGATCTCAGTTCTGTGCATGAATTTCATTCATTCAGTTCTTTATCCTGATCTCACTGCAGCTGTAAATGTTGGCTCTGTTTTATTCCTGTGATCATATAATGGTCTTCTTTTTGAGTCAGCATGGAGAATAAGGGCTATTTATTTATTTAAAGGTCCAGTCTTCTTGCCTAAAATTTTCAACATATTCTTTTATTTATAGAGATTGTGGTCTTTTGCAAAATGAAAAGGTAAGAGATGTACACAGTGCAGTAACACAATGTAGACTAAACATTTCCCATTCCAATCCCTTATGCCAACATTGACAAAAACGTCCACACCGCAGAGTGTGCTCATGGATATGTGGACCTTGAAATTGATTTGGTTGACTGACTTTTGTTTTCATTCCTTTGTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37873
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 |
---|---|---|---|---|---|
ENSDART00000082112 | None | None | 428 | None | 13 |
ENSDART00000123682 | Nonsense | 513 | 1396 | 12 | 16 |
ENSDART00000127923 | Nonsense | 513 | 1396 | 13 | 17 |
ENSDART00000127988 | None | None | 105 | None | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 21255658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20502787 |
GRCz11 | 24 | 20647206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCTTCTAGAGATTCACGGTCTTATTCGAGATCTAGGAGCAGATCATA[T/A]TCTAGAAGTGACTCAAGGTCAGAGAGGCGGGCTCGATCATCCAAGAGGTC
Long Flanking Sequence:
GTTATATCTTATTTGAATAAGCTAAAATTGGAAGTTTACTTCTGTTTTTTTTTTTTTTTTTCATTTCATGAGTTTTTACATCACTTTCACTTTGACTATTGTTCAAACAGATGGGATGACAGAAGTGACACCCCAAGGTCCAGGTCAGAATCCAGAGAACATTCCTTGGGTGAGGCCTCTGTGTACTCAAGCCAACATAGATCTAAAAAAGAAAAAAAGAAAGCCAAACAAAAGAAGAAATCTAAGAAACGGAAGCATGCTAAAAAACATAAAAAGACCAAGACCAAGGAAACATCTCTGACGGATGGTGAGGTGTCTGTGTCCTCAGGTAAGAGGACAAAACACTCAAGCCGTGCTGAAAGGAGACGTTCTCGTTCTTATTCTCGCTCATCCTCACGTCACTCACATAGATCGTATAAATCGGAGTCAGAAAGGAGACATTACTTATCGAGCTCTTCTAGAGATTCACGGTCTTATTCGAGATCTAGGAGCAGATCATA[T/A]TCTAGAAGTGACTCAAGGTCAGAGAGGCGGGCTCGATCATCCAAGAGGTCAAGTCGAAGCCGATCAGGGAGGTCTGTTACACATTCTAGGTCACGGTCTCGTTCTAGATACAGGACAAGGTCAAGAACCAGATCAAACTCTAGGTATAGTTCAGAAACCCCAACACGTTCCAAGAAAAGAAATGAATTGAGATCCCCTCGAAAGTCCAAGCCTACAGAGGGTGGTATTTCCAGATTAGATAAGTCTGTCCCTAAATCGATTAAAGGTGAAGAAGCTAAAGTTCAACCTTCAGCGTCTTCAGAGAGTGTCTCTGCATTGCCTATGAGTGACAGTCCACCACCTTCTCGATGGAAACCAGGCCTGAAACCCTGGAAACCTTCTTATGTCCGTATCCCAGACACTGATGTAAAATCAGCTCTGGCTTCCAATGCACTAACAAGCTCATCGTCAAATGCACCTCTGGAGACAATGTCCTCTTTAAAGCAAGATATAGCTGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37872
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000082112 | None | None | 428 | None | 13 |
ENSDART00000123682 | Nonsense | 630 | 1396 | 12 | 16 |
ENSDART00000127923 | Nonsense | 630 | 1396 | 13 | 17 |
ENSDART00000127988 | None | None | 105 | None | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 21255308)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 20502437 |
GRCz11 | 24 | 20646856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAGTGTCTCTGCATTGCCTATGAGTGACAGTCCACCACCTTCTCGAT[G/A]GAAACCAGGCCTGAAACCCTGGAAACCTTCTTATGTCCGTATCCCAGACA
Long Flanking Sequence:
CCGTGCTGAAAGGAGACGTTCTCGTTCTTATTCTCGCTCATCCTCACGTCACTCACATAGATCGTATAAATCGGAGTCAGAAAGGAGACATTACTTATCGAGCTCTTCTAGAGATTCACGGTCTTATTCGAGATCTAGGAGCAGATCATATTCTAGAAGTGACTCAAGGTCAGAGAGGCGGGCTCGATCATCCAAGAGGTCAAGTCGAAGCCGATCAGGGAGGTCTGTTACACATTCTAGGTCACGGTCTCGTTCTAGATACAGGACAAGGTCAAGAACCAGATCAAACTCTAGGTATAGTTCAGAAACCCCAACACGTTCCAAGAAAAGAAATGAATTGAGATCCCCTCGAAAGTCCAAGCCTACAGAGGGTGGTATTTCCAGATTAGATAAGTCTGTCCCTAAATCGATTAAAGGTGAAGAAGCTAAAGTTCAACCTTCAGCGTCTTCAGAGAGTGTCTCTGCATTGCCTATGAGTGACAGTCCACCACCTTCTCGAT[G/A]GAAACCAGGCCTGAAACCCTGGAAACCTTCTTATGTCCGTATCCCAGACACTGATGTAAAATCAGCTCTGGCTTCCAATGCACTAACAAGCTCATCGTCAAATGCACCTCTGGAGACAATGTCCTCTTTAAAGCAAGATATAGCTGTTAGTCAAAGGGATCCAAGCAGTGGTAACAGTAACATTCCTGATAGGCTCTTGGAAAGAAGTTTATCCAGGAGCAGGTCTTGTAGTCAATCAGGAAGCTGCAGCAAATCACCAACTCATTATGGCAATAGATCGTCCTCCTGCAGTAGGTCAGAATCTTATAGTTCATACAAAGAAAGATCCACTGTGAAGAAGAGAAAACATTTCAGTTCTCATAGAAATGCTCAAAAGAGAGACAACCATGCAAATCGTCATGATGGTGGCCACAAAGATACATCTCCCTCCTCAGAGGATGTATCAGATAATCCATACAGCCCATTACACGTGCAAAGTGACATCTTGGTACAGAAAAACA
Associated Phenotype:
Not determined