ZMP
mink1
Ensembl ID:
ZFIN ID:
Description:
misshapen-like kinase 1 [Source:RefSeq peptide;Acc:NP_001083048]
Human Orthologue:
MINK1
Human Description:
misshapen-like kinase 1 [Source:HGNC Symbol;Acc:17565]
Mouse Orthologue:
Mink1
Mouse Description:
misshapen-like kinase 1 (zebrafish) Gene [Source:MGI Symbol;Acc:MGI:1355329]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20489 | Nonsense | Available for shipment | Available now |
sa20488 | Nonsense | Available for shipment | Available now |
sa20487 | Essential Splice Site | Available for shipment | Available now |
sa11333 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20489
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051233 | None | None | 149 | None | 5 |
ENSDART00000051236 | Nonsense | 451 | 1287 | 14 | 31 |
ENSDART00000082408 | None | None | 156 | None | 4 |
ENSDART00000135260 | Nonsense | 449 | 1270 | 13 | 31 |
ENSDART00000140337 | Nonsense | 88 | 208 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 39931523)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37730913 |
GRCz11 | 5 | 38331066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTA[T/G]AAGCGTAAACAGCTGGAGGAGCAGAGACAGTCAGAGAGGCTTCAGAGGCA
Long Flanking Sequence:
TTACTGTATACCCACTACACTGAAGAAGAATCGTACAGCTAAGACAAATGTTTTGCTTTTGTCGTTCAGTTGTACAATAAACACTGCTCAGACTCTTCAGTAAATGTGAGCTATGATCTTATATATATATAATGTAAAACTCAAATAATTACGTTTTCTGTGTGTGTAATAATTCACTAAAGGGATAGTTCACCCAAAAATGACAATTTCCTCATTTACTCACTCTCAAGCAATTCTAAAAACTTAAGATATTCTAAAGATTTTGGAAAAAAATAATATTATGGATGACAATGGCTTCAGTCTATCTTCCTTTGTGAACTATTCCTTTAATACACAATTGTTCGATTGCATGTTGTGAAGGGGTACGTTCTACGTTTATGTGTATATATGTGTATGCATGTTGACTGTGCAGTCCTTTTTTCCACCTGCAAACAACACAGTGCAGTGTATCTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTA[T/G]AAGCGTAAACAGCTGGAGGAGCAGAGACAGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTCTCTCTACAGCAACAGCAGCAGCAGCAAGACAAGAAACCACAGATGTATCACTACAGCAAGAACCTAGAGAACAACAAACCAGCCTGGGCTAGAGAGGTACGCTCTCACCCCACTGAGGGTAAAAGCGCTCTAATAGTCCATTTCCACTAAGTGGTATAGTACAGTACGGGTGACCTTTATTAGGCTTGCATATCCACTGCCAAAATGGTACCAATGGTATGATTTTAATTGCAGATCAATGATAAATAGCTAAATAGCCTACTGCAATATCAGCAATTATATGAACAAAAATAAGTAAATGCAACATATACAGACCCTTACAGTCTGCGATATGTTACCAATTACAGTAAACTACACACATTTATTTCGTTTTTATTTGGGTTCAAAAACAAGACGAAATATAGCACAGTCAGTGCAAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20488
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 |
---|---|---|---|---|---|
ENSDART00000051233 | None | None | 149 | None | 5 |
ENSDART00000051236 | Nonsense | 461 | 1287 | 14 | 31 |
ENSDART00000082408 | None | None | 156 | None | 4 |
ENSDART00000135260 | Nonsense | 459 | 1270 | 13 | 31 |
ENSDART00000140337 | Nonsense | 98 | 208 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 39931495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37730885 |
GRCz11 | 5 | 38331038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTCATGTGTGTGTAGGAGTATAAGCGTAAACAGCTGGAGGAGCAGAGA[C/T]AGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTC
Long Flanking Sequence:
AATCGTACAGCTAAGACAAATGTTTTGCTTTTGTCGTTCAGTTGTACAATAAACACTGCTCAGACTCTTCAGTAAATGTGAGCTATGATCTTATATATATATAATGTAAAACTCAAATAATTACGTTTTCTGTGTGTGTAATAATTCACTAAAGGGATAGTTCACCCAAAAATGACAATTTCCTCATTTACTCACTCTCAAGCAATTCTAAAAACTTAAGATATTCTAAAGATTTTGGAAAAAAATAATATTATGGATGACAATGGCTTCAGTCTATCTTCCTTTGTGAACTATTCCTTTAATACACAATTGTTCGATTGCATGTTGTGAAGGGGTACGTTCTACGTTTATGTGTATATATGTGTATGCATGTTGACTGTGCAGTCCTTTTTTCCACCTGCAAACAACACAGTGCAGTGTATCTCGCTGCTTAATGACTTATTAATTGTTTGTTCATGTGTGTGTAGGAGTATAAGCGTAAACAGCTGGAGGAGCAGAGA[C/T]AGTCAGAGAGGCTTCAGAGGCAGTTACAGCAGGAACATGCGTATCTGGTCTCTCTACAGCAACAGCAGCAGCAGCAAGACAAGAAACCACAGATGTATCACTACAGCAAGAACCTAGAGAACAACAAACCAGCCTGGGCTAGAGAGGTACGCTCTCACCCCACTGAGGGTAAAAGCGCTCTAATAGTCCATTTCCACTAAGTGGTATAGTACAGTACGGGTGACCTTTATTAGGCTTGCATATCCACTGCCAAAATGGTACCAATGGTATGATTTTAATTGCAGATCAATGATAAATAGCTAAATAGCCTACTGCAATATCAGCAATTATATGAACAAAAATAAGTAAATGCAACATATACAGACCCTTACAGTCTGCGATATGTTACCAATTACAGTAAACTACACACATTTATTTCGTTTTTATTTGGGTTCAAAAACAAGACGAAATATAGCACAGTCAGTGCAAACCTCTCATCTGTGTCTTTAATCTTCACCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20487
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000051233 | None | None | 149 | None | 5 |
ENSDART00000051236 | None | 926 | 1287 | 23 | 31 |
ENSDART00000082408 | None | None | 156 | None | 4 |
ENSDART00000135260 | Essential Splice Site | 916 | 1270 | None | 31 |
ENSDART00000140337 | None | None | 208 | None | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 39915693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37715083 |
GRCz11 | 5 | 38315236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAATGTACCAGCCATCAGGGGGTAGTGGAGATAACATTTCTGTTGGAGG[T/C]AAAGTGGTTAGTTTGGGTACGGAGATTTTAAGGGGATTTTTAACACAAAA
Long Flanking Sequence:
ATTAGTGTCCCACTATGCCTCAGAAGGATAAAGCCTTTATGTGCATGCTAGAAGCCAATATCATAGCACCAGTGTCAGCCCGAGTTTGTTTGTGTGTTTGTTTCTGTCAGACTCCAGAGAAGCGCAGTCATAATGGATACACCAACCTGCCTGATGTGGTTCAGCCTTCTCACTCTCCCACAGACTCGGCCTCCCACTCCTCCCCCGGGAAAGACTCTACTTATGATGTGAGTCTCTGCCCACTTCTGGAGCTTCAGTTACTCCACCGTTTATCATTTCATCAGCATGCCATCCAGCTTTTTTTTTTTGTAATTGATTCTTTATCTGATGTACTGGACAACAAGTGTGTGTTCAATTGGCTGACCGTGATCATGCTATTCATTTCAGTATCAGTCCAGGGGATTGGTCAAGGCCTCTGGAAAATCCTCTTTTACTACCTTTGTGGACCTTGGAATGTACCAGCCATCAGGGGGTAGTGGAGATAACATTTCTGTTGGAGG[T/C]AAAGTGGTTAGTTTGGGTACGGAGATTTTAAGGGGATTTTTAACACAAAAATGTAAATTCCTGTTTAAGTTTCTGTTTTGTTGAACCTAAATGAAGATATTTTGAAGCTTGTTGGAAATGGGTAACCATTGTCTTCCATAGTATTTGTTTTTCATACAACACATGTTAATGTTTACTAGTTTCCAACATTCTTTAGAATCTCTTTTTATGTGTTCAAAACAACAAAAAACTCCCAACTGGTTTAAAAACAAGTCAAAGATGAGTAATAGATGACAGAATTTTTGTTGAATTTTTTAGAATCATTTGTGGGTGAACTACCCCTTTAAGATACACTATTGTTCAACAACACAGGGTGTACTCTGTTCACTGCATTTACAATTACAGGAAAAACAAAAATATTAGCAAACATTAATTTTTAAGATAAATTTTATGATGTAAACTAATGTGAAAGATTTTTAAGTATAATTATTGTCTCATTAAGTAATTAGTGTCATTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11333
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 |
---|---|---|---|---|---|
ENSDART00000051233 | None | None | 149 | None | 5 |
ENSDART00000051236 | Nonsense | 1191 | 1287 | 29 | 31 |
ENSDART00000082408 | None | None | 156 | None | 4 |
ENSDART00000135260 | Nonsense | 1174 | 1270 | 29 | 31 |
ENSDART00000140337 | None | None | 208 | None | 5 |
Genomic Location (Zv9):
Chromosome 5 (position 39910543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37709933 |
GRCz11 | 5 | 38310086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCAGATGGGATGGAGATGCTGTTGTGTTATGAGGACGAAGGTGTTWA[T/A]GTCAACACGTACGGACGYATCATTAAAGATGTGGTGCTGCAGTGGGGAGA
Long Flanking Sequence:
ATCGTGGATGAAATGTGCTACATAAACTTGCCTTGCCTTAAAATTCTTTTAATTTACAATCTTATTATGTTTTTGTTGTTGTTAAAAATAATTAATATCATGCTTTTATTGATGTTTCTTAGTCATTTGGAGACCTGCCGCACAGACCTGTGTTGGTTGACCTCACAGTGGAAGAGGGTCAGAGGTTAAAGGTCATCTATGGCTCCTTGGCTGGCTTCCATGCCATTGATGTTGACTCTGGAAACAACTACGACATCTACATTCCTGTACATGTGAGTTATGTTGTCATGTGACACACCAAGAATACACTGGGTCAGTCAATTGGAAAATGCAGAGGAGAGTTTGATAGTGATTTATTTCTCCTATAAATCCATGTTCCTCTCTCTTGCTCTCGGTCTGCTGCTGTAGATCCAGTCACAGATCACTCCTCACGCCATCGTGTTCCTGCCCAACTCAGATGGGATGGAGATGCTGTTGTGTTATGAGGACGAAGGTGTTTA[T/A]GTCAACACGTACGGACGCATCATTAAAGATGTGGTGCTGCAGTGGGGAGAAATGCCCACATCAGTAGGTGAGTGTGTATACTAGATTAGAATAGATTCAACTTTATTATCATTACAAGTACAAGGCAACGGAATGGAGTTTAGATCTAACCAGCAGTGCAATAGCAACAAGTGCAGGATATAGCTATAAGCTATAAAGTGCAATTATAGAAAAACTATGGTAACATTAGAGCTAAAAAGGGCTTCGTCGCTGCCTATTTTTAAGTCCAAATTAAAGACGCATTTATTTTCTAAGTCTTTTTGAAGCATAAGTCCTTCCCTTTCAGAAGGGGGGGGGTGTTGGGAGTGGGGAGGGGGATAAAAACGGTCATGTTCTCTATCGTGTTTAGTGTTGGTCAACTGTGGTAGCATATTTTAATTAGGAAAAATATTGTATTATTATTATTACGATTTTTTATTTTTATTTACATTTTTGCTCTTTTATTGATAATTTTTCTATGT
Associated Phenotype:
Not determined