ZMP
STK31
Ensembl ID:
Description:
serine/threonine kinase 31 [Source:HGNC Symbol;Acc:11407]
Human Orthologue:
STK31
Human Description:
serine/threonine kinase 31 [Source:HGNC Symbol;Acc:11407]
Mouse Orthologue:
Stk31
Mouse Description:
serine threonine kinase 31 Gene [Source:MGI Symbol;Acc:MGI:1924735]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44850 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7421 | Missense | Mutation detected in F1 DNA | Not yet available |
sa36102 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22819 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44850
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 |
---|---|---|---|---|---|
ENSDART00000078790 | Nonsense | 86 | 977 | 5 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 23618574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21728325 |
GRCz11 | 16 | 21533361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACACTGAAAATTGTTTTTGTTTTTTTTGTCTTATTCTGCCTAGTTCTA[T/A]ATTCTCTACATTGACTTTGGAAATATGGAGATTGTCAGTCGATCTGATTT
Long Flanking Sequence:
TGAAACAGGTTGATGAAATAAAAAAAATTAATAATTTTTAAAACAAAAAATGCTAATTAACTATACAAACTAATATACATAAAGTATATTGATGGTTGTTATTGTCCTAGTCCCAGCTGGACCAGGAGCCCAGGAGTTTGCATGTTCTCCCTGTGTCCCTTTGTTTCCTCTGGGTACATTGGTTTCCCCCACAGTCATGCATTGGATAAATTGGATAAACCAAGTTGCCAGTAGTCTGTGAATGAGAGAGTGTGTGGGTATTTCCCAGCATCCACAGCCAAAACATATGCAATAATTGGTGGTTCATTCTGCATGGCGACCCCTGATAAAGAGGGGAATAAGCCAAAGGAAAGTAAGGAAGTGGTTATAGTGCATGAAGTTACTTCAAAATCCCACGAATGACAGTTTTATAAATAATAAAAAAAGAGAAGAGCTGTTTTTTCATGATTAAAACACTGAAAATTGTTTTTGTTTTTTTTGTCTTATTCTGCCTAGTTCTA[T/A]ATTCTCTACATTGACTTTGGAAATATGGAGATTGTCAGTCGATCTGATTTAGTTGAACTGCCAGAGGAACTGCAAACTGCAGGACTTGCAAAAAAGTACAGGTTCTGGGGAATTCATGCGTCAAGCGAACAGGATTCCGCACTTCATCCACAGGTAACTGACAACTAACTCTTTTACTAAATGGACCGTGCACCTAACAATTTACTTTTAAATGCAACTGATATTTGTGTACAATAGCTACATTTCCACTATCGGGCCAGTGCGAGCCAGGACTTTTATCGGGCCGGGCTGGGCCAATCGTCCGGGAGGTTGAGCAGTGAGGCCGAAATCATGTCGCGTTTCCCCTGTCGGGCTGGTAGCTCGCAGCGCGTCATGCCAACCCCGCCCCTAGAACGTCCCCTGAATCAAACGTCACACAAACCTCCTAATTCAGCGGGAATCAGGCAGATAAAGCACACCGTCGCATCATGCCGAAGCGATTTAAAATTGAAGACAACCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7421
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 > C
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078790 | Missense | 493 | 977 | 12 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 23604084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21713835 |
GRCz11 | 16 | 21519084 |
KASP Assay ID:
554-4180.1 (used for ordering genotyping assays)
KASP Sequence:
CTTCATCGTTGACWGCAGTATTTAGCTCTGTTATGCTGCCGGAGCAGATC[G/C]ATGASTACGCGTTTGAAAAATTCTGTGAGTGGAAAAGAMACAAACAACAG
Long Flanking Sequence:
GATTAATTAAATAATAATGTGATTTGAAACGGGTGATATCAACAGGTGATTGTAATTATGGTTTGGTACAAAAGCCGCATCCAAGAAAGGTCTAGTTCTTTAGGAGCAAAGATGGGCAGAAGATCACCAGTTTGCCAACAAATACATGATAAATATATTGTAATGTTTAAAAACAATGTTCCTCAAAGAAAGATCTTGTTAAAAGATTCAAGGAATCTAAAGAAATTTCAGTGCGTAAAGGACAAGGGTGCAAGCCTAAACTTAACTACCATGATCTCAGATCCTGGACTGTTCTGCCCTTTAGTTTCTTGTCTAGTATCTAATAAAAGTGTGAAAACTCTAATAATTCAATAACTCTATAATTCAAAATAAAAACAGCATGAAGAATGTAGTGATTTTTTTTTCTACCAGCTCTTCATAAACTGTATTTTCTGCATCTACAGGAAGTTGCTTCATCGTTGACAGCAGTATTTAGCTCTGTTATGCTGCCGGAGCAGATC[G/C]ATGAGTACGCGTTTGAAAAATTCTGTGAGTGGAAAAGACACAAACAACAGAGAATCAAAACCGTGCAAAAAGCTACAGATGAGGCTCTCCTTGCTCTTAGTGGTTGGGCATCCAGTTTTAGCAAGGTATGTTTGCTAATGTAAACCTCATGACAGTCATGTCTATTTTTACTGGGTATTTATTAACTGGTTATTTGACCATTTCTTTGTAATTTTGTAATTTTTAGTTTTTGTGTTTGATGGAGAAAACATCAGTGACCGAAAAAGATGTTTCTGAAGGTGTGGATGAGATCCTGATGAATGCTGACAATGCCCTGTCTGAAGAACTCGATACCGAATTCTCTGTAAGACTAAATGATTTATTCTGCTCAATACCACCATGGCTGCCTCTCAATGTGAATTCCCTCTCTTTTGATCTGAAATTTTCAAAAAGTACAGACTTCATTACAAGTCAGTATTCAAATTTTAAAGACAAAGTCAATTTCCCACTAACTTGCGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36102
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078790 | Essential Splice Site | 574 | 977 | 14 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 23600273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21710024 |
GRCz11 | 16 | 21515271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTACTGTTACTCAATTGGAAAAATATGTTTTACACTTTTGCTTTCACA[G/A]AAACAAAACAACCAAGACAGGAAAATAGTGTTTAATGCCTTTCTCAAAGC
Long Flanking Sequence:
CCCGACATCTCTCTGGCTGAAACATGAATGGCTGTGGTAGCCTAGCAATCCATTCTGGAGATATATAATCCTATAGGCACAGAATGCATGTTGTTGTTTCAGTTCACTGTAATCTGTTTAGTGTGTTTTTGCTCAAAACCTTGGTCCAGATGGGACTATTTAGTTTGGTGTTTGCTGGCGTTTAAACACTGCTAATTAGCCATTGTGTTCATAGGCTCAGCAGATACCTGTGATTTAGCTCCAGTAATCATCGCTTTATGCTCTGCCCCAAGCATTTACACAGATGCTGATATATACAGATGCATATATAAGCATCATCAGATAACAAATTCAGTACCGTTTGGTAGTAAAATTGCTACATTTGACAAGCCTATTTTAAAGTGTAAAAATCTTTGTTTTTTATTATTCTGTAAAATTTCTGATTTGTGTTTGCATAAATGTAAAATGCAACTTTACTGTTACTCAATTGGAAAAATATGTTTTACACTTTTGCTTTCACA[G/A]AAACAAAACAACCAAGACAGGAAAATAGTGTTTAATGCCTTTCTCAAAGCTATGCAAGACATCCAGAAAGAACAAAGTTTGTTGGAGGACATAAAGAAAATGTACGACCTCAACTCTAAGGTAAAGGATTAAATAGCTGCTGTTTTTAGAATAATAGATGAACAAATTTAGGGAATAATTATATGTTTACGGATTATTTATGAGCCTGGCTACAAAAAGGCAAAAACATCGAGTGGACAATGTTTTCTGATTTGAGGATCTGCAAAAAATGGATTAAAGCATCAAAAATAAGCATTTATTGAGCTATGTCAATATGACAGTATGATTATGCTTACCAAGACTGCTTTAACTTGATCAAAAATAAAGTAAAAACCTTTTAAATGTTATGAAATTGTTGACTTATGTTTTTTCTACTTTATAATATATTAAAATTTACTCATGTGATGGAACCACTGTATATTCTGCAGTCTTGATTGTCATGTGTTTCAGAAATGATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22819
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078790 | Essential Splice Site | 719 | 977 | 18 | 24 |
Genomic Location (Zv9):
Chromosome 16 (position 23595056)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 21704807 |
GRCz11 | 16 | 21510016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAGGACAGAGATATTTGTTTTTTATTTTACTACATGTGTTTGCTTTC[A/T]GAGCTCTGCAGGGCTGTTAGTGAAGAGCTTGGACAGAGACATGTTTGACG
Long Flanking Sequence:
CTAAAAACGGCTGCAAATCATTAGCAATTAGGACTCACACTGCCTTTGTTATTTTTATGTGTCTCTCGGAACCAGTTGGGTATGTCTGCTTGAAAGATTCAGCGAGGGATTGTTGCTATTTGGAGGACTTTATTACCTTCTCTGCTATCCTGCCTTCAGACAGTGATATTTCTTGGTGATGGCACTGCAGATGTGCAGTCATGGTTATATGTGTAAAACAATGCTTGCACACAGTTATTTTTTGTTCACCATTTTTTCTTTTATTGGCATTATGCTTGCCAGCAAAATCGAAATGTCCTCACAGCGCAGATTTGAAAGACTCCGGAAAGACTGTTAATAGCTCAAAAAATGTGTTTTAGTGTTTCGTGACCCTTTAAAGTTTCATTAATTGTCATAAAAGTGTCTTAAAAAGTCTTAAATTTGACTTGATGAAGCTTGCAGAAACCCTGGCATTAGGACAGAGATATTTGTTTTTTATTTTACTACATGTGTTTGCTTTC[A/T]GAGCTCTGCAGGGCTGTTAGTGAAGAGCTTGGACAGAGACATGTTTGACGCAGAGCCGATGAAAGAGCTGAGCGGAAAGAGACCTCTTCTTAGTACAGATTTCCAGGGGCAGAAGGTGGTCCTGAAGGTCAGAGATATTGCATATAATCTTAATTTGCTTCACTTAAGTTTATGTATGGTTTACTTAATATATATTATAGCTATATTGTCATTTTCAAAACAAACTATTTAGAATATTGACGTTAATACATATATGATTTAAAGAGCTGTTCAGGGGTTTATTGTTAGTTGGGTTTTTTAATGCTTTTAAAAGATGTTTCACCAATGGTACATTTTATTAGATTTATGTAATATGGTGTATATTAATATACATATACTGAAGTGTTATTATAATTTAAAATAAATTTTATTGTCTGATTAATTTTATGAATTATTCAAGTCTTAAGCAACACGTTATCTTTTAAAACTCTTTATAATATGCTGATTTGGTGTGTGTGTGT
Associated Phenotype:
Not determined