ZMP
sgk3
Ensembl ID:
ZFIN ID:
Description:
serine/threonine-protein kinase Sgk3 [Source:RefSeq peptide;Acc:NP_001103937]
Human Orthologue:
SGK3
Human Description:
serum/glucocorticoid regulated kinase family, member 3 [Source:HGNC Symbol;Acc:10812]
Mouse Orthologue:
Sgk3
Mouse Description:
serum/glucocorticoid regulated kinase 3 Gene [Source:MGI Symbol;Acc:MGI:2182368]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24502 | Nonsense | Available for shipment | Available now |
sa37892 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37891 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24502
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090368 | Nonsense | 52 | 486 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 24 (position 24385791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 23632669 |
GRCz11 | 24 | 23777843 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATGAGTGGTTTGTGTTCCGGAGATATGCAGAATTTGACAAATTGTA[C/A]AACACGGTGAGTAAATGAATTTGTAAGTCCTTTGCATTTTTAGTCCAGTA
Long Flanking Sequence:
CTCAGTGGCCTTCCTGTCCTGTCATGCAAGGCCCAAAAGAGCCCTCTGGAGCTAAAGTGGACGCTGGACTCTGCTGAAAAGAGTGTTTGGCGGAGGTAGAGCCTCTCGCTTATGTTGTGTTACGTTTATTTTCTGCGCAGGAGCCAGAATGGAAAGTTCCCATCAGAATCAGGTGTGCCAAAGAAGCAGGAAAGCTTTCTGAGGACCTGTTACGTTTATGAACGGTCACTTTTGAGATTCTGAGAGGATGGAAGAGCAACCTAGCTGTCCCAATGTTAGCATTCCATGCTATAATGAGCAGAGGGACAAGAAGAAACGCTATACTGTGAGTCACGTGAGCTTTGATGGGTCTTTTCATTTACAATTTGGATTAGTGTGTTTTAAATGTTTAAATTGTAATGTGTGACCACTTTTATTCATCAGGTTTACAAAGTTATGGTCAGTGTTGGAAGGCATGAGTGGTTTGTGTTCCGGAGATATGCAGAATTTGACAAATTGTA[C/A]AACACGGTGAGTAAATGAATTTGTAAGTCCTTTGCATTTTTAGTCCAGTAAACATAAAACCATGCAAATGTGAAAAGATAACAAGAAGTACTTCACTATCTGGTAACATGTCTTCAAAAAGAATACAGTCTTAAGCTCGTTAAAGGGATAGTTCACTCAAAAATGAAAATTCTGTCACCATTTGCTTGCTCTCCACTTGTTCCAAAACTTGTTATACACAAATTAAAATATTTTAAGGAATGTTCGGAAAGCAGCAGCCATTGACTTTCATAGTATTTTTTGTTCCTACTATGGATGGCTGCTGGTTTTCAACATTCTTCAGAATATCTTGTTTTTTGTTCGACAGAAGAAAAAATATTAGTACTACCTGAGTGTAAGAAAATTGTGTGGAAAGTTTTATTTTTGGCTGAATTATTAGGCTGTATTTATTTGAGTGAAAAAATACAATAAAACTGTATTATTCTGAAATATTGTTAGGATTTAAAATAGTTTTTTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37892
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 |
---|---|---|---|---|---|
ENSDART00000090368 | Essential Splice Site | 146 | 486 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 24 (position 24377360)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 23624238 |
GRCz11 | 24 | 23769412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGGAAATTACTTTTGCACATGCCTTCATGCTCATGTGTTTTTCCTTA[G/A]TGCAAAGCCCACTGACTTTGACTTTCTTAAAGTCATAGGAAAGGGAAGCT
Long Flanking Sequence:
AGGTAGTGTAGTTTTTCCTGCTGTATCCTTTGAAATTGAAAATGATGTATGTATCTTTTTGTAATTTGTTTTATTTACTGGTGTTACTTGTTTTTTTGTTGTTGTTTTTTTTGTTTTTAAACCGCTGTCACTGAATTTTTTTGTTCTGTAAAATGTTTTAATGTATAAAAATAAAAAAATAAAATCACTATAACTAAGATCAGAACAAATTATTAATACTAAATGGCAAGTATGCTTTACTACATCACTGAATTGAATCATCACTGTTTTTGTCATATCTTTTATAGAGTAACTCTACCTCTAGAAACATTAACCTGGGGCCATCTGCAAATCCACAGTAAGTGTTCCTAATTATTTTAAATAGCTTTGTAGACTTCATTTATTTCTTTATATATTGACTCATTATGTGTTATGTAACAGATCAGGTAGAAATTCATATAAATATTCAAATGATGGAAATTACTTTTGCACATGCCTTCATGCTCATGTGTTTTTCCTTA[G/A]TGCAAAGCCCACTGACTTTGACTTTCTTAAAGTCATAGGAAAGGGAAGCTTTGGGAAGGTAGGTTCTTTTTAAATGAAATGACTTGATGAAAGCAAAAGCTCTTTATTAAAATCTATTTATGGCTGCCACTAATTGTAAAAGTTTGTGTAAATTTTGTATCAGTTACTGAAAGTTCTAAATGTCACCGAGCCTTTATAATCTCTCAGTTTTGTTTGGTGTATGGTTAGCACTGGTGTTTGTTTCTGAGCCGTGGACTCTCCATTCAGGAAGTGAAAGTCCCTCAGTTTTAAAGACAGACTTGTATTTTTGTTTTGGCTAATGGGCAGCCGTAGTGGAAGGTGAAACTGTTACTAACCCACCATGTCCTCTCTCACACAAAGGTTCTCCTTGCAAAGAGGAAACGGGATGGGAAGTGTTATGCCATCAAAGTCTTGCAAAAAAAGGTCATTCTAAACAGGAGAGAGGTAACCATTTTCCTTTGTTTCAAAAGCAAAACATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37891
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 |
---|---|---|---|---|---|
ENSDART00000090368 | Nonsense | 486 | 486 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 24 (position 24367601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 23614479 |
GRCz11 | 24 | 23759653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGATGCCTTTCTGGGATTTTCTTACGCTCCGCCATCAGAAGATTCTTTCT[T/A]GTAAGGTTGGCGCTGCTAATGGCGATTTAAAGAGAGCTGCATAAAAATAA
Long Flanking Sequence:
GAGTAAATATTATAATTATTCATTATTTAGTAATTAATTAATAATTATTAAGTAAACAAACTACATGCATAATTATAAAGTTAATTCAATGGGTTTACCCACTTTTTAGAAGTAAAGTAACTAATCGCTTTTTACAGTGCACACGATTAAATGATATTTTAAAATACATTCTTTTAAATTGTAATCATATTTCACAATATTACTGTTTTAGTGCATTTTGATCAGATAAATCCAGCCTATGTGAGCAAAAACAGTAAATTCTTGTTAACTTTTGACAGCTACTGAAACTGAAAAGAAATGTATTAATATGATTAACTCTAATGTTGTCTTGCAGGAATCCCAGTATGACATCTCAAACTTTGATCCAGAGTTTACAGAGGAAACCGTGCCAAACTCTGTGTGCTTCTCATCAGGGCCGTCGATCGTCAATGCGAGTGTCATGGAAGCGGACGATGCCTTTCTGGGATTTTCTTACGCTCCGCCATCAGAAGATTCTTTCT[T/A]GTAAGGTTGGCGCTGCTAATGGCGATTTAAAGAGAGCTGCATAAAAATAAATATCTGTGATCGCACTCTCTGACGAAAGGGAAGAATCTGCCTAGCATCATGTTTCCATCAGATGGTGTGGACCCTTGTGTTTCTTGACAGAAGCAGTGCATAAAGCTTTTGGGATGCAGGGTGTTTCAAACTTTATTTTTACATGTAAATAACATATCTTGTGTCACATTGAACGCCTTAAACTGAGAGTTTAGCTCAGGAGCTAAAGTGCTGATGTATTTTTCTTTGCTATGAATTATTTTCAAGGGCTGATGAGAAGAAAAAAAACAAACATCCACTTTGACAACATTCCTTTTTTGTGCCCCAACTTGTACACTTGATTGCTTATAATACTGTGCAGTATGTGACCAATTATGTCATTGTAGTTTAGTCTTATTAGAAATTTGCTATGGAAAAATGTTTATATATTGTCAGCACAAGCAAATACTTTTGTTGCTTGACACTTTAAA
Associated Phenotype:
Not determined