ZMP
tnk2b
Ensembl ID:
ZFIN ID:
Description:
tyrosine kinase, non-receptor, 2b [Source:RefSeq peptide;Acc:NP_001073486]
Human Orthologue:
TNK1
Human Description:
tyrosine kinase, non-receptor, 1 [Source:HGNC Symbol;Acc:11940]
Mouse Orthologue:
Tnk1
Mouse Description:
tyrosine kinase, non-receptor, 1 Gene [Source:MGI Symbol;Acc:MGI:1930958]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44662 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40895 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20947 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44662
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 |
---|---|---|---|---|---|
ENSDART00000089856 | Nonsense | 356 | 732 | 8 | 14 |
ENSDART00000135313 | Nonsense | 357 | 733 | 8 | 14 |
ENSDART00000140528 | None | None | 123 | None | 4 |
ENSDART00000141353 | None | None | 183 | None | 4 |
The following transcripts of ENSDARG00000069433 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27681500)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26284439 |
GRCz11 | 7 | 26555632 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTTGTATGCTGTGATGCGCAAATGTTGGGCCTGCAATTCTACTGAA[C/T]GACCGACCTTCGCACAGCTCACCACCATGGTATCAGAGGTCAGTGTTACT
Long Flanking Sequence:
CATGTTTATTAAATCAGCCAAGGTACTAGCACAAAATAAAACTCAACAAAAATACTGTTTATAAAATACTGAAGAAATCGGCAGAAATTTTGAGATATCATTTTTTTTACACTTCTAGCCAATCATCCAATTAAATACAGGACAGTAATTCCAGCATCTTTCTTTCCTTCCACAGGTGTGCTCCTGAGAGTTTGCGTACGGGATCTTTCTCTCATGCTTCAGACGTCTGGATGTTTGGTGTCACGTTGTGGGAAATGTTCACTTACTGTGAGGAACCCTGGTTGGGGCTTTCTGGCAGACAGGTAGCTGGTTTAAAGAGAAAAATGTTAATGAACAGACACTTTAATCAGCACTATATACATAAATGACTGTGTGTTATGTGTTTTGTGCAGATTTTGTATCGTGTCGAGCGGGAAGGTGAGCGTTTGGAAAGGCCTCCTGATTGCCCGCAGGAGTTGTATGCTGTGATGCGCAAATGTTGGGCCTGCAATTCTACTGAA[C/T]GACCGACCTTCGCACAGCTCACCACCATGGTATCAGAGGTCAGTGTTACTCCTCTGCTTCTTATTGAAAAATATCTTAATATACACTACTGTTCTAAATAAGGGCTGAACGGAAAATGAAGTGTGACCTTAATATTCAGCAACCAGAATGTTGTACCAGCAAGGTAGAATGATGAAGAAATTGTGCTTGGCCAACACAGGAATGAATTACATTTTTAAATATATATTACAATCAAAAACGAATATTTTATATTGCAATAATATATGTTTAATAACTTCTTTAAAAAAAAAAATACTGACCCCAAACTTCTTTACTTATTGTGCTAGACTGTAAGTGTTGCAAAGAATGCACTACAGGAAAAAACTGAGAACTCCCCTGAGAAAAAACATTAGAAAAATAATATTGTATCTTATAGTACTCCTGAGAATATTGTATTCTGTCCGACAAAAAGCCCAGCGACTTTGATTATATTTGGGGACATTTACTTGACACATTACCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40895
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089856 | Essential Splice Site | 400 | 732 | 9 | 14 |
ENSDART00000135313 | Essential Splice Site | 401 | 733 | 9 | 14 |
ENSDART00000140528 | None | None | 123 | None | 4 |
ENSDART00000141353 | None | None | 183 | None | 4 |
The following transcripts of ENSDARG00000069433 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27682453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26285392 |
GRCz11 | 7 | 26556585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGACTCTCTCTACAGGCAAATGATCTAGTGACTGTAATAGACCATGGG[T/G]AAGAGTGGGGGTGGAAGGCTGGAAGGATAAAACAAAAAAAATCATGTTTC
Long Flanking Sequence:
CCAGCGACTTTGATTATATTTGGGGACATTTACTTGACACATTACCTCTGTTAGACTTTAATAATTCATTTTTATTTTCATATAATTATTGTTAGTTTTGATAGTCTTTTTGTTGTTGTTGTTGTTGCTCCAACTTTCTCTTATTTTATGTTGTTGTTTTAATTTTGTTTTTATCATATATGTAAATGTAATTTATTTGTGCATCATTTCTAGACATTATTGTTTTTATTTATTATTACCATCAGGCATTTCAATTATCTTTATGCAACATCAAAATGAGAAATGTTTTGACAAAATTTGTGACAATTATACCTTGTATGGATAGGGTTGGCAGGGTGGGTTGTATTTATAATGATAAAAACTAAATTTTCCCACTGATTTGTCTTTTTTAATGTATTTTTCAGGCACAGCCTATGGAGGTTCGTTCGGTGAAAGACATTGCAGAGCCCAGGAGACTCTCTCTACAGGCAAATGATCTAGTGACTGTAATAGACCATGGG[T/G]AAGAGTGGGGGTGGAAGGCTGGAAGGATAAAACAAAAAAAATCATGTTTCTTTTTCTTGTACTCTTTGGCTGAGTGGTTAACAGTACTTAATAAGTTGTTCCAATAAATCTTTGCTGACTGCAACTCTAATAAAAGCAGTGTGTAATTTTTAACTTCCCTCCTCTCCTTAATTTAATTACATTCCATTCATAGTTCAGCCTTTTCTTTCATATAACCGCATGCAACCATATGCAAACACCCAGGGGTACAGATGTAAGACTTTCTCACACCAAAAACAGTAACTATAAAGATATATAATAACAACTGTATTAGCATCCGCACTGATAGACAATACAGTTTGTAAGCAAGCTGCAGTTTTATCATCAATGTAACTTCTTTAGGTGCTGCTCTGTGTTTGTATTGTTATATTTGTGTATGCTCTTTGCTTTTTTTTTACCTGTAGACTTGTTTTTACTTTATTTTTTGAAGAACTTTTTACTTTGTGTGAATAAGCCTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20947
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 |
---|---|---|---|---|---|
ENSDART00000089856 | Nonsense | 409 | 732 | 10 | 14 |
ENSDART00000135313 | Nonsense | 410 | 733 | 10 | 14 |
ENSDART00000140528 | None | None | 123 | None | 4 |
ENSDART00000141353 | None | None | 183 | None | 4 |
The following transcripts of ENSDARG00000069433 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 27683493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 26286432 |
GRCz11 | 7 | 26557625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACTTGGCTGTGCTTTTATGTAGGTTGGATATGTGCGAGTGGAAGGGA[C/T]AGAACCAGAGGACTCTGAGTGTTGGCTGGTTTCCCCCTGCGTTAACAGCC
Long Flanking Sequence:
GATCAGAACTACATAAGTGACAAACTTTGATGTTAGCATGATATTAGCAAACTGCTTGCATTTATTAAAATGTTTTTAACATTAATTAGCTTAAATTTGGCTTTTGCTGGGATGTTTCTGTCATGAATTAGCATGTTGCTAAAAACAATCATTATTTTGCTAACATGTAGCATGGCTTTAACGATGATAGGTTGATGCAAATCTATAGATAAATGTCTGAATGTTGTTAACTGTATGGTTGAAGTTGAAATGCTCTGAGATTTACTGTTTGTGAGAAAGTTTTGACCCCTTTGTGATTTTTTTCTAAGTCATTTTAGCATAAAGCTTAAGTTCAGGATCTGACATGGGTTTTGTGGTTGTAGCTTGAATGCTGCAAGCACTCCTTAATTGCTAGAAAATGAAAGGTGCTTTATTCCCCTAAATGTATTTGTGAATTAAAAAAAATGACTTTCAACTTGGCTGTGCTTTTATGTAGGTTGGATATGTGCGAGTGGAAGGGA[C/T]AGAACCAGAGGACTCTGAGTGTTGGCTGGTTTCCCCCTGCGTTAACAGCCCCGGCTCTCACAGCAGTAGTTCCTGCGTCTGGTCCCACACTGATCTCCTCTCCTGTTAGAGGGTCTCTACACCACACGGGACATGGAGACACTGACCCAGGACGCAGCTGGGGCACCCCTGAACGCATAGATGAGTAAGTTGATGATTAAGTTACGAACTGTATAGGCTAAATTTGCTAAAGGATTGGATGTTACTCTAAGTGGGCTGTTTGATATGAACTTTCCAGCAACAGACGTTGGAGGGTCCCATTAGCAAAAGAGAAGGAAGGCTCCAATTTGAAGAAAATGGCAGGTAAGAGCCTACATTATTACTGCAGTGAACTGCATAATATTTACTTATAATTTAAATAAGTTATAATATATAATTTATCATTTTAATCAAATGAGAATCCACTTGATTTTGAAGAGCTCTACCTTGTTTTAAGTGACTGAAACATGTTCAAAAAATAG
Associated Phenotype:
Not determined