ZMP
LOC565173
Ensembl ID:
Human Orthologue:
RPS6KA5
Human Description:
ribosomal protein S6 kinase, 90kDa, polypeptide 5 [Source:HGNC Symbol;Acc:10434]
Mouse Orthologue:
Rps6ka5
Mouse Description:
ribosomal protein S6 kinase, polypeptide 5 Gene [Source:MGI Symbol;Acc:MGI:1920336]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6491 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28901 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23140 | Nonsense | Available for shipment | Available now |
sa36479 | Essential Splice Site | Available for shipment | Available now |
sa36478 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15790 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6491
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 |
---|---|---|---|---|---|
ENSDART00000085438 | Essential Splice Site | 193 | 802 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38597159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38482056 |
GRCz11 | 17 | 38429641 |
KASP Assay ID:
554-4927.1 (used for ordering genotyping assays)
KASP Sequence:
AYGGTCACATTGTGTTGACGGATTTTGGTCTAAGTAAGGAATTTCATGAG[G/A]TAAGTTTGCTTGCAGAAATCTTTTGCAATTTTTAGTWACTGACAGCTTTA
Long Flanking Sequence:
CTCCAAATTTCTCGAAGGCTGTGTTTACAAAAAGAGGAAGAGAAGTGTTTTTAATGCACGCTTGTTCTGTGTGCTGCAGCCATTATTCAGAGTTGGCCTGAGGGCACCGCAGTGTTTGGGACCTTGACAGTGAGATTAACATTGTTTTGGTTCGGACTCACTTTTTGTCATCGCCTATTATGTTGTAATTTATTATTTATTAAAGTAGTGCTACATTTTCCAGGTGAATGACTGCATTTTATGATCTCAGACAAAGTGGAGGGTTGTAAACCAGGGAGTTGAGTAAATGCTTTTGGCAAGGACAAAAGAGGAAAAGGAATGTGGTGAACCATTTGAAGTATTTGGGCTAAACATAAAAGCTTATTCATTTCTGTTTTTTTTTATTCCTTTTTTTTCAGCTGGGAATCGTCTACAGAGATCTGAAACTTGAGAATATACTTCTTGATTCAAATGGTCACATTGTGTTGACGGATTTTGGTCTAAGTAAGGAATTTCATGAG[G/A]TAAGTTTGCTTGCAGAAATCTTTTGCAATTTTTAGTTACTGACAGCTTTATACATGTTTCAAAACTTAAAATATAAAGCACATAGTTAGTTAAAATCCTGTCTTATACTGATAAGCTGAGAAGTATTTTAGGCCACTGTTATCGGCCTTATTTAAGCTAACCTAGGATCAGTCTGAAAAAGATTTATTAGAGTTCAGAGTCGAATTAGAAATGTAAATTTAACCAGAGTGTTTAAATAAGGCACATAAAAAATCCAAAGTTAAACACACTCAGAGGCCACTTTATTAGGTACACTTTACTAATATCGGGTTGAATGCACTATTGCCTTCACAGCTGCCTTAATCCTTCGCATAGATTCAACAAGGTAATGGAAATATTCCTCAGAGATTTTGGTCCTTATTGCCATGATAGCATCATGAAGTTGCTGCAGATTTGTCTGCTGCACATCCATGATGTGAATCTCCCATTCCACCATATCCCATAGGTGCTACATTGAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28901
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000085438 | Essential Splice Site | 360 | 802 | 9 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38583769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38468666 |
GRCz11 | 17 | 38416251 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACATACTCGCCAGCAGCACTTCCAAACAACTGTGACCGCATCTTCCAGG[T/C]AGTGCAATTAATGGATAATATTATTGTGTAATATGAGTTGTGTAATGGAA
Long Flanking Sequence:
GCAAGGATCATATTTTTATTAATCTTTATCTCTCTCTTTTCCTAATAGGAGAATTATGAAAAAAGATCCTCCATTCCCCAAAGACATGGGGCCTCTGGCCAAAGACATCATCCAGCGACTGCTTATTAAAGACCCAAAGAAGAGACTGGGCTCTGGCCCTTCAGGAGCCCAGAATGTAAAAAAACATCCATTCTATCAGGTAAGACAATATAAAAAACAAACTAATTCCCTCTTAAAATGAATTCTCCTGTAATTTTGTTTGTCTGTTATAGATAAGTCAGATTCATTCAGTATTTGAGGGATCAGCAACAAAAATGTTTGACTCTTGTTGTTTCAGAAATTAAACTGGGAGGATTTGGCTGCTAAGAAAGTTCGGGCTCCGTTTAAGCCTGTGATTCGGGATGAGCTGGATGTGAGCAACTTTGCGGAGGAGTTTACTGAGATGGACCCGACATACTCGCCAGCAGCACTTCCAAACAACTGTGACCGCATCTTCCAGG[T/C]AGTGCAATTAATGGATAATATTATTGTGTAATATGAGTTGTGTAATGGAAGACATGTTTGGTCACTGCAGGTTATAACTTCCTGAAATGTTTTAATATTGTGCAATATTCCAATATTTAGCTGCAGTAATAGCCATAATCCATGTTAGTTTTGATGTTGGCTGCATTCCAGAAAAACAAAAGTGTGAATGAACAGTGGACTGAATTGAATTCAAATATATTTAAATATTTTTTTATATTTTAGTATTACTATTAATAGATAAGATAATAACTATTACAATAATTGTGTTTCTTTTTACTCCTGTTTAATATTTTTTGCAAAGCCTTTACTAGTTTAATTTAATATTATTGAAATTTAATTTAAATTAATTTAATTTGATTTAAATTTTACTTTTTTTATTTAATTAAATTTTATTATATTTGGATTTTGATTTAATTTTGAGTTAAGATGTTTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23140
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 |
---|---|---|---|---|---|
ENSDART00000085438 | Nonsense | 362 | 802 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38581821)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38466718 |
GRCz11 | 17 | 38414303 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTTTCTGTTTGCCAGTGTGTTTATAGATGTTTGTGTCTGCAGGGCTA[T/G]TCCTTCATGGCTCCCTCTATCCTGTTCAAGAGGAACGCGGTGATGGATGA
Long Flanking Sequence:
AATTCTCGGGCGGTACAATTGCAGCGACGTCTGCAATGATAACTTTGCGAAGCGCTCCAGCACACACACACACACACATGCATAGCCGCATATAAACCCAGCCACCCCCTCACAAACTCCTCACAAACTGAAATTAAGCTGCATTAGAGGACTGTGATAATTTGAAAAGCAGGGCAATCAAATACCTTGGCTTATCAATTAAAAGCATTTCAACCATTCATCTCCTCATCCTTCCGTCCAGCAATCCTCTCATCCCGCCAGCCACTCCTCCACCCATGTACCACACAGCTGCAGTCTGGCCGCGTAAGTGGGACATGGGCTTTATTTAGATGATGCAGTCGCATGCAAACAATGTGACTGGAGTCCCTTAACATGAAGGATTCGCAGAAATGCGAAAGGTTACGCTGTTTGAGTTCCATCGGTGACCCTGAAACTTCATCCGCATTAGTTCCTTTTTCTGTTTGCCAGTGTGTTTATAGATGTTTGTGTCTGCAGGGCTA[T/G]TCCTTCATGGCTCCCTCTATCCTGTTCAAGAGGAACGCGGTGATGGATGACCCGGCTCAGCTGTGTGGTGGGTCAGAAAGGCCGGGCTCTGCTGCTGTTGCCCGTAGCGCTATGATGAAGGTCAGTCTGCATAATCCTGTGTTGTAAGAAAAAACAAAACATTGCAACATTTAAAAGCTGTCGCGTGTCCATTTTATATATATAAAAGAATTCTTAAGAAGGTCATGATTCACACTCATTAAATAATTACTTTGTATAGCTTTTATTTTACATTCTTAGGTGATACAAAAGACAAACATTTCAACACAATGCCTTTCTCAGTGTGTGACGCAATCCTCTCATTCCACCCTTTTATCCCACAGTCAATCACATTACGTCATTAGTAAGATGGCCACTTAATAATTGAAAACAATCTCATTTTTATTTCAAAATGCTGTAATTAACCACACAAGAAATATTTACCTTCACCTTTAAAAAACATTTTTTCCACTGCACAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36479
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 |
---|---|---|---|---|---|
ENSDART00000085438 | Essential Splice Site | 402 | 802 | 10 | 17 |
ENSDART00000085438 | Essential Splice Site | 402 | 802 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38581699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38466596 |
GRCz11 | 17 | 38414181 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGAAAGGCCGGGCTCTGCTGCTGTTGCCCGTAGCGCTATGATGAAGG[T/C]CAGTCTGCATAATCCTGTGTTGTAAGAAAAAACAAAACATTGCAACATTT
Long Flanking Sequence:
ACAAACTGAAATTAAGCTGCATTAGAGGACTGTGATAATTTGAAAAGCAGGGCAATCAAATACCTTGGCTTATCAATTAAAAGCATTTCAACCATTCATCTCCTCATCCTTCCGTCCAGCAATCCTCTCATCCCGCCAGCCACTCCTCCACCCATGTACCACACAGCTGCAGTCTGGCCGCGTAAGTGGGACATGGGCTTTATTTAGATGATGCAGTCGCATGCAAACAATGTGACTGGAGTCCCTTAACATGAAGGATTCGCAGAAATGCGAAAGGTTACGCTGTTTGAGTTCCATCGGTGACCCTGAAACTTCATCCGCATTAGTTCCTTTTTCTGTTTGCCAGTGTGTTTATAGATGTTTGTGTCTGCAGGGCTATTCCTTCATGGCTCCCTCTATCCTGTTCAAGAGGAACGCGGTGATGGATGACCCGGCTCAGCTGTGTGGTGGGTCAGAAAGGCCGGGCTCTGCTGCTGTTGCCCGTAGCGCTATGATGAAGG[T/C]CAGTCTGCATAATCCTGTGTTGTAAGAAAAAACAAAACATTGCAACATTTAAAAGCTGTCGCGTGTCCATTTTATATATATAAAAGAATTCTTAAGAAGGTCATGATTCACACTCATTAAATAATTACTTTGTATAGCTTTTATTTTACATTCTTAGGTGATACAAAAGACAAACATTTCAACACAATGCCTTTCTCAGTGTGTGACGCAATCCTCTCATTCCACCCTTTTATCCCACAGTCAATCACATTACGTCATTAGTAAGATGGCCACTTAATAATTGAAAACAATCTCATTTTTATTTCAAAATGCTGTAATTAACCACACAAGAAATATTTACCTTCACCTTTAAAAAACATTTTTTCCACTGCACAGGAAAATAACATCAATTATCATCATTCACTTATCCATGTCTACATCAATGCAATGAATTTCCGACAGTCCAAAACATTAAAAATACATTTTCATCTCATTATTTGTATCATAACATACTCAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36478
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 |
---|---|---|---|---|---|
ENSDART00000085438 | Nonsense | 482 | 802 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38569306)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38454203 |
GRCz11 | 17 | 38401788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTAGACCCTCTAACGGGGTGATTTTCTGTTTGTTTAGCTGCACACATA[T/A]CTTGTCCTGGAACTCTTGCGAGGTGGTGAGCTTCTGGAGCGGATCAGAAG
Long Flanking Sequence:
GCGCGAGATAATCAGGAAGTGACGATTTTATTCGGTTTGACTCGTTGGATGGAAACGCTGCTTCATTCGCACATTTTTTTTTATAATTCAGTTTTGTGCATACAGTTAATTCAGATTTATGGAGAGAAACATAGCTATTGTGTGCCGTGTAAATGCAGACAGTCAAATACGAGTCACCTTTATAAGATGATATAAGTGGGTCATCAAAAACATCAGATACAGTCACAAAATCGGAATTGACCTTCAAGATCTGCAGTGTAAATGTAGCCTTTTAGTACAAATATTGGTGCCAACTTAGCCTCAAGGAGTAATTCTGTAGAAAGTGTCTGCAATTCATAGTAAAAATTTGATGTGTTCAAATCAGGATGTGTTTGAGTCTAGACTCTAACCCATAATGCTCACTTGAGCATCAAGCTCAAAGGATCTGCGCACTGAGTCATAACACTAAGTGACTAGACCCTCTAACGGGGTGATTTTCTGTTTGTTTAGCTGCACACATA[T/A]CTTGTCCTGGAACTCTTGCGAGGTGGTGAGCTTCTGGAGCGGATCAGAAGGAAGCAACTCTTCAGCGAGACCGAGGCCAGTCGCATCATGCGCAGACTGGTGTCTGCCGTCAGCCACATGCATGACGTCGGCGTGGTGCACAGGGACCTCAAACCAGAGGTACAACACACTCCACTGTAATTATCATAGATATACAGCCCAGATGTCACAGCACTCCAGACCAAGGGGCCCCAGACTACAAGTTGGACAGGATTCTACCTAGTAGTTAGGCTTCAGGATTGACAGCTCTTGCTTAATTACAAAGAAACATTTGCAAGAAACATCTGCCTATATTTGTTATAGCTTCTTGTGTTTCAGCCTGGTGAATACTGAATTTAGATTAGATTAGATAAGATTAGATTCAAATTTATTGTCGTTAGAAATGTACAAGTACAAGGCAATGGAATGCAGGTTAGGTCTAACCAGGAGTGCAATAGCAGCAAGTGCAGGATACAGGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15790
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 |
---|---|---|---|---|---|
ENSDART00000085438 | Nonsense | 575 | 802 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 17 (position 38567919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 38452816 |
GRCz11 | 17 | 38400401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCTCCTGACAATCAGCTCCTGAAGACCCCCTGCTTCACTCTTCAGTA[T/A]GCCGCACCAGAAATCCTCAAATACAGTGGTTAYGACGAGTCCTGCGACCT
Long Flanking Sequence:
TTTCACCACCCACTGCAGTGCCTTATGCTCAGCAAAAGAGCAGCATCAATAACAGACTGTGACACAGTTGGTTAGGATGCTCTCTATTGCGCAGCGATAGAAGCTCACCAAGACGGCTGATGACAGCTGGTTCTTCATAAGTTGCCTTAAGAAAATGAGGCGCTAGTGAGCTTTCTTGACAAGGCTGGAGATGTTGGTGGTCCAGGACAGGTCTTTTGAGATGTGAGTCTCCAGGAACTTGAAGGATGAGACCAGCTCAACTGCCATCCCATTGATCTGAATTTGATGTGAATTTTATTGAATTTATCATGGCTTACTTATGACTTTTACTTCTTCATAGTGTATTGGAAATGTTCTTTAGTCTCACTTTCCTCCTCCTAGAATTTGCTCTTCACTGATGACACTGAGAATTCGGAGATCAAAATTATTGACTTTGGTTTTGCACGGCTCAAACCTCCTGACAATCAGCTCCTGAAGACCCCCTGCTTCACTCTTCAGTA[T/A]GCCGCACCAGAAATCCTCAAATACAGTGGTTACGACGAGTCCTGCGACCTCTGGAGTTTAGGAGTCATTTTGGTAAGGTCTATACTCATGTTGTTCCTGTAATCCTTACATAGTTGTAAAAGGCAGTAGGGTTGCTGAATGCTTAGAGTTTGCCTAAACTCAGATTGACTTAAGTCTTAAAAAAGCAGCTTTCTAGAATTTAGCAATAATGTTTTCCAGTAGAGTTTCAGTTAGGCTGCTACTTTAGAAGACATCTGGATGTAAAGTCAGTTGTCAGTTATAATGCTTGATCAATAAGTTGATGTTTGTTTCCTTTTATAATATTATGTAATGCATGTTGTAACAAATATTTTACAGATTTAGGGTAGGACTGTTCAATGTTTGGATAAAGAGTGACTGAAAATTATAATCTTGAGTTTTTCTGCTATATATACAGCAGGGAAAATAAGTACACGTCACCATTTTTCTCAGAAGGTGCCGTTGACTTTTTCCCAGATGCA
Associated Phenotype:
Not determined