ZMP
rps6ka3a
Ensembl ID:
ZFIN ID:
Description:
ribosomal protein S6 kinase alpha-1 [Source:RefSeq peptide;Acc:NP_997951]
Human Orthologues:
RPS6KA3, RPS6KA6
Human Descriptions:
ribosomal protein S6 kinase, 90kDa, polypeptide 3 [Source:HGNC Symbol;Acc:10432]
ribosomal protein S6 kinase, 90kDa, polypeptide 6 [Source:HGNC Symbol;Acc:10435]
ribosomal protein S6 kinase, 90kDa, polypeptide 6 [Source:HGNC Symbol;Acc:10435]
Mouse Orthologues:
Rps6ka3, Rps6ka6
Mouse Descriptions:
ribosomal protein S6 kinase polypeptide 3 Gene [Source:MGI Symbol;Acc:MGI:104557]
ribosomal protein S6 kinase polypeptide 6 Gene [Source:MGI Symbol;Acc:MGI:1914321]
ribosomal protein S6 kinase polypeptide 6 Gene [Source:MGI Symbol;Acc:MGI:1914321]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10515 | Nonsense | Available for shipment | Available now |
sa40417 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14662 | Nonsense | Available for shipment | Available now |
sa6974 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10515
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 |
---|---|---|---|---|---|
ENSDART00000051546 | Nonsense | 101 | 732 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 25687339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 23514604 |
GRCz11 | 5 | 24018404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATTTAAGCGTGTTATTGTTYGTTTACAATCTGGTTTGTGGTTTCAGTG[C/T]GAGATCGAGTGCGTACAAAAATGGAGAGGGACATTCTTGTTGAGGTCAAC
Long Flanking Sequence:
TCATGTATAGCTACCCAATCTGGCCATTAACACCTATGCGATCACCATCAATCCATCTTATTAAAACATTTTAATTTAAAAATTGTTTTTGCATTATTGTTTTTTTTTCCTTACAGTAAGATTTGCTTTAAAAGTTCTCCATTTATTTACTAAAGTAATTGACAGTTATGTTTTGTTCTATTTGGTAAGGGTTATTGGGTTTGTAAATGGATATATTTGAAAATTAATAAAAAAAATATTAATACTGAATTATTGTTATTAAATGTATTAAATTAATATTTTTTTGATCGGACAAGTGAAAATCTTTTCTAAATGGGATATTTGAAAAACATACTTTAGCATTTAGCCTTGTACAAGTTGAAAATTTCATACATAATGATCTTAAAAGTCTTAAATCAAACTTGATGAAACATGTAGAAACTCTGTTGAATGCACACACTCGGCTGAAGGAAATTTAAGCGTGTTATTGTTCGTTTACAATCTGGTTTGTGGTTTCAGTG[C/T]GAGATCGAGTGCGTACAAAAATGGAGAGGGACATTCTTGTTGAGGTCAACCACCCATTTATTGTTAAACTGCACTATGGTGAGTCTTTGACATCTTATCGCTGATCAGATTCTCACACTTCATGGTAGTTTTTTTTACTTTAATTTAAACTTGCTATTTATCTACTTAATCTCTGGATTAATTTTATTTATTTATTTGTTTGTTTGTTATCATTTTTGTGTTTCCAATGCCTCGCCCAGTTAACTTTGTTTACGCTTGATATTAAAAGGATAGTTTGCCCTCCCTTATATATTATACATATATTGCGCTCTAAACCCATATACATTTCGTTTTTTTCTGCTGATCACAAAGGAAGATATTTGGAAGAATGTCAGCGATCAAACAGATCTCAACACACTAACTCTGCCGTAGTTGGAAAAATAAATACTATGGGAGTGAGTAGGTGACAAGATCTGTTTGGTTATTGACATGCTTCCAAACAACTTCCTTTGTGTTCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40417
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 |
---|---|---|---|---|---|
ENSDART00000051546 | Essential Splice Site | 189 | 732 | 8 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 25685728)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 23512993 |
GRCz11 | 5 | 24016793 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCGCAGTGCACATTTTAATAAGTGCTCAATTTCTTGATTTCTTTTACA[G/A]TATTCTCTTGGATGATGATGGACACATCAAACTTACAGGTATGTGTGCTT
Long Flanking Sequence:
ATCTGTTTTTTTATCACTATTCTCATTTTTTATTAATGTGCCTTTTCTGAGAAAAAATTAATAATATCTTTAAAAATTAAGTTTGAACTGTAATGTATTTGTTAATCTTATTTTAGAGATGTAAATATTTAAATGAGCTTTAAATCATTAAACATAAGGAAATGATGTAAGAATATCTAAACATTCTACCACTCTCTTGTAGGTGATGTTTACAGAGGAGGATGTTAAGTTTTACCTAGCAGAGCTGGCTCTGGCACTAGACCATTTACATGGACTGGGAATCATCTACAGAGATCTCAAACCAGAAAAGTGCGTTTCTCACCCACATATTACATACAAAGTGAGGTGGCCCAGCTCAAAGTACAGCAGCAAACTATATAGTAACCACTACACATTTCCTTATAAAAACTATTTTATCAATCACCATATAGTATATAGATATTAGAAAGCCAGCGCAGTGCACATTTTAATAAGTGCTCAATTTCTTGATTTCTTTTACA[G/A]TATTCTCTTGGATGATGATGGACACATCAAACTTACAGGTATGTGTGCTTTATCTATCCAAGAGAACATATTGCTTTTATTATAATGAGTGAATTTGGGTCATAAATGATAAAAGATTAATGTTATAACTGTTTTTTGTGAGTCACGTCATGATAAGTATGTTAGTATGTCTCAGATTTGGTTTGTCTGCACGTGTTACATAGATTTTGGTTTGAGTAAGGAGTCCATTGACCATGAGAACAAGGCATATTCGTTTTGTGGTACGGTGGAATATATGGCTCCAGAAGTTGTCAACCGCAGAGGTCACACCCAGAGTGCCGACTGGTGGTCTTATGGTGTGCTAATGGTGAGGAGGTTTGGTTTTAGATGTACCAAAGTTAAAAATAATATTTGGGTCACTGTGGGCTAATTATAATGCATTTCTATTACCGCAGTTTGAAATGCTAACTGGAGCACTTCCATTCCAAGGGAAAGACCGAAAGGAGACCATGACAATGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14662
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 |
---|---|---|---|---|---|
ENSDART00000051546 | Nonsense | 500 | 732 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 25682445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 23509710 |
GRCz11 | 5 | 24013510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGTCACAGAGTTGATGAAAGGTGGAGAACTACTGGATAAAATCCTCCGA[C/T]AAAARTTTTTCTCTGAGAGAGAAGCAAGCGCTGTCCTCTACACCATWACA
Long Flanking Sequence:
TTTTAAATAGAAGATACATTTATATTATATTTGAGTTTATAACTGTGTAATATTTTCATAGTTTATGCATTCATAATTATTAATATAGTCTTTATTCTATATTCTGTAGTCATTATTAAACTTAATTTGTCTTAGATCAAATAAATGCAGTACTTTTTCCAAATGAAATGTTAAAATATTTATATTTTATAGAATCATATTAGTATCTTTAGATATGGTTCTAAATAGTTCTGATTGGATTGCAGATCATTAAAAAGGAGAGAAGAGATCCAACAGAGGAGGTTGAGATCCTGCTGCGGTACGGACAACATCCCAACATCATCACCCTGAAGGACGTGAGTGACATTTGTTCTGTAGAAGATCATAACTAGACTGTCTCAGGTGTTGTTTGCTTCTATTTTGAGTCTGTTTGGGATTATTAGGTCTTTGATGATGGCCGATCAGTGTACCTGGTCACAGAGTTGATGAAAGGTGGAGAACTACTGGATAAAATCCTCCGA[C/T]AAAAGTTTTTCTCTGAGAGAGAAGCAAGCGCTGTCCTCTACACCATTACAAAGACTGTTGAATATCTGCATGCCCAAGGGGTAAGAACACTTAACATGGACTAAATTCACTTTTACAACACACTGAAAGTTTGTATATATTAGGGCTGGGCCGATAAACGATATTATATCGAATTGCGATACAATTTATGTCAATAACAATGATAAGCTCTGCACTGTTTTACTCTATTCTGATCTAGAAGCCAATCACACAGCAGAAATGTGTAACAATGAGAATCTAGAAGTGTGTTGGTATTAGAGATGGACCAAACTTTCGGCTACCTAAAATGTTATGCCATTTAATTAACCCTTTAATTTTTGTGGCTTTGGTCATTGTTTGGGGTACTCTTTTAAATCTGGAAGCTTTCACAAATTATATCCAAAAATTTATACCGTTATCGTTTAATATGGACAATAATCATCAGGATTTGCATTTTTGCCATATCGCCCAGCCCTAGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6974
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 |
---|---|---|---|---|---|
ENSDART00000051546 | Nonsense | 684 | 732 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 5 (position 25680703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 23507968 |
GRCz11 | 5 | 24011768 |
KASP Assay ID:
554-5278.1 (used for ordering genotyping assays)
KASP Sequence:
GCCATYCATGGATAATCAACAAGGACCAGTTACCCAAATACCAACTCAAT[C/T]GACAGGATGCTCCTCACCTAGTGAAGGTTTGCTTTGCTRTAATGGWCTCA
Long Flanking Sequence:
GTTGCAATATTTTAAAGCCATAATATATTGCACAGGTCAATGTATACTTTCTGCCTGGATTTTTTAAAACATATATTCCAGGTACATATCATAATTTTTTTAAACTCCCAATACTCGTTTGTTTAGGTTCACTCCATTTGCAAATGGTCCAGAAGACACACCGGAGGAGATTCTGGCTCGCATTGGCAGTGGCAAATTCTCATTGACTGGTGGATACTGGAATTCTGTATCACATGATGCAAAGGTTGTAGGCTCTCTTTTTGTTTAACACCCTTTCTAGCCCAATGAATTTATTAAACACTTTGTTCCTGTTTTCGTCATTGTTGTGGATGAAAACGCTGATGAATGCACATGCTCTGTTTAATCTAACATCTTTAAACTGACAGGACCTTGTATCAAAGATGCTGCATGTTGACCCTCATAAGAGATTAACGGCAGCTCAAGTACTTCGCCATCCATGGATAATCAACAAGGACCAGTTACCCAAATACCAACTCAAT[C/T]GACAGGATGCTCCTCACCTAGTGAAGGTTTGCTTTGCTATAATGGTCTCAGATGTAAAACTGATGATTTTAGAAATGGTTGACTAATTTTATTATCTTCCATGTTTACCCAACTGGCCTAAATATATCTTTACCTAAGCATTATGATAGTTAAACTGATTGTTCACCCCAAAATGACTATTCTTTCCTTATTTACTCATGCTTTTTCATTGCAAAAGACTTTATTCATTTTAGAAACACAAAGTCACATTAGTTGCAAAGTATATTTGTAGGAATGGCCAACATTAAGGTTAAATTATTGTTTTTTCTTTTAAGGCAAAAATGGTTTGAGTTTTAAGTAAAGATATTTAGTAAATTTCCTTCTGTTAATGTATAATAACTTTAGTGGTAACACTTAACAATGAAGTTGTATGAGTTAATGTATTTACTAACATGAATGAACAATGAACAATTGTTTATGTTAGTTAATGAAGTGGTTCATTGTTAGTAATAATGTACAAT
Associated Phenotype:
Not determined