ZMP
rps6ka3b
Ensembl ID:
ZFIN ID:
Description:
ribosomal protein S6 kinase alpha-3 [Source:RefSeq peptide;Acc:NP_001076495]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24507 | Nonsense | Available for shipment | Available now |
sa960 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa24507
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066648 | Nonsense | 108 | 688 | 6 | 22 |
ENSDART00000130057 | Nonsense | 139 | 739 | 6 | 22 |
ENSDART00000135060 | Nonsense | 139 | 709 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 24818698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 24065576 |
GRCz11 | 24 | 24210750 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGTTTACCAGTGAACGCATTCGCTTTTCTCTCACAGCATTCCAGACC[G/T]AAGGAAAGCTTTATCTGATTCTGGACTTCTTAAGAGGAGGCGATCTCTTT
Long Flanking Sequence:
TGAAAAAAAAGAAAAACCTGTAGTGTCTCGCCTTAAAACTCTAAATCCATGTCCCTCCTGATGATCAACATCTTCATCCACATGAGTAAATGGATTCTCCTCTCCCTTCAGCTCTCAGCTTCTCTTGTCTCTCTCCTGCGCTGCATTTTCCCCCTCTTTTATTTAATTAGTCATCCATTGCCATCTGCGTAATTGTGTTGTGCCAGATTCCTGGACGTAGGGAGGATTGGGGGCTGTTAAAGTGGAGAGAAAACATTGTTAGTGAACTTAATAGAAGTAAACTCAAGTGTTGTTATTTATGCATGTGTTTTCAGTACGGGATCAGGTCCGGACTAAGATGGAGCGGGACATCCTGGTGGAGGTTAATCATCCCTTTATTGTTAAGCTACACTATGGTGAGCGCTGGTCATCATTAGCCAATCTGAATGAAGAGCAGCTGCTGATTTAATGTTGTGTTTACCAGTGAACGCATTCGCTTTTCTCTCACAGCATTCCAGACC[G/T]AAGGAAAGCTTTATCTGATTCTGGACTTCTTAAGAGGAGGCGATCTCTTTACTCGACTGTCAAAAGAGGTATTTAATGAATGGTTTAGGGTAATAATGATACACAAAATTGACAAATCACTTTTTAAATTTTTGACCAGTGTTGAAGTGTTAAAGTTGTGTTCTGGCTGATTAAGATGTGAAGCATATTCTATACTTTTTTCTGTTCTTTTTTTTCCTCTGCTCAGGTGATGTTCACTGAAGAGGATGTGAAGTTTTATTTGGCCGAACTGGCTTTGGCTCTGGATCATCTGCATGGACTGGGCATCATTTACAGAGATCTGAAACCAGAGAAGTACTGAATGTTCTCTAAATAAGCCTATATACAGTGGAGCAAAAAAGGTATTTAGTCAGCCACCAGTTGTCCAAGTTTTCCTACTTAAAAAAGATGAGAGAGGCCTGTAATTTACATCATATGTCTCAATTATGAGAGACAAAATGAGAATATAATCCAGAAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa960
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000066648 | Nonsense | 348 | 688 | 14 | 22 |
ENSDART00000130057 | Nonsense | 379 | 739 | 14 | 22 |
ENSDART00000135060 | Nonsense | 379 | 709 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 24802526)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 24049404 |
GRCz11 | 24 | 24194578 |
KASP Assay ID:
554-0865.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTNTTTTNNNNNNAGATTCTCCAGGTGTACCTCCTAGTGCCAATGCCAAT[C/T]GACTTTTTAGAGGGTTTAGTTTTGTGGCCATCACTTCAGAAGAAGAATCT
Long Flanking Sequence:
GAAATAAGTAGATTTATGGACACTAGACACAATAGGTATTAGAGGTACTACTGTACATGCCATGACTGATAATGAGTCTGGTATCCTAGGTGAGTGTTGTATCCTGTGTAGGCTCAGACTAAAAAAATAATTTTAGTACTCTACACTGTTAAAAAATACAGGTTGCCTTACATGTTTAAGCTGAATCAAATTAATCTTATGAGTCATTTTAACTTATATTACATTAAACTTAAGCTTGCTTAACTTATAAAATTAAGTTAGAACCCAACCAACTTAGTTTAATAAGTTACAATTAACTAAAAAGAAATGTTGTCATGACTAATTGATCATATCATCTTTTACAGTGTAGAGTGTAGTCATTATCTTGTGATGTCCACGGAAAAAATGTTACCTTCTGGTGGTTCTAGTGTTAAAGACTAGATCAAAACATTGGTGTGTATTGGTTTATGTTTTTTTTTATTTTAGATTCTCCAGGTGTACCTCCTAGTGCCAATGCCAAT[C/T]GACTTTTTAGAGGGTTTAGTTTTGTGGCCATCACTTCAGAAGAAGAATCTCAATCCCTGCCGAGCAACAGCATGTCATCTATAGTTCAGGTATGTGCACTTGCATAACACGTTTCCTCCAAATTAAACCTGTTTCTTCATTTTAATGACTGCATTTACATCTTGGTTGTATTGTGTATTTATAGCAGCTCCACCGAAACGTGTCTCAGTTTAGTGACGCATATGAGGTGAAGGAGGATATCGGCATTGGTGCTTATTCCATCTGCAAACGCTGCATTCAGAAAAGCACAATGATGGAGTATGCAGTGAAGGTGAGGAAAGAATTATATTAGAACACCACAATACCAGATATAACCGTATATTAGCAGCAAATCAACCCTTTAAAAAAAAGCACTTGAACTTCTTTAGCTAATAGATTTTAAAACTTTATATTATTAACTAATGTAGGTAAATATTGGATATGTTATACATTTATAAATATTAGTGCCGTGCAAAGATTAA
Associated Phenotype:
Not determined