ZMP
sgk1
Ensembl ID:
ZFIN ID:
Description:
Serine/threonine-protein kinase Sgk1 [Source:UniProtKB/Swiss-Prot;Acc:Q7ZTW4]
Human Orthologue:
SGK1
Human Description:
serum/glucocorticoid regulated kinase 1 [Source:HGNC Symbol;Acc:10810]
Mouse Orthologue:
Sgk1
Mouse Description:
serum/glucocorticoid regulated kinase 1 Gene [Source:MGI Symbol;Acc:MGI:1340062]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa3228 | Nonsense | F2 line generated | Not yet available |
| sa24374 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa3228
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 |
|---|---|---|---|---|---|
| ENSDART00000035031 | Nonsense | 66 | 433 | 3 | 10 |
| ENSDART00000133569 | Nonsense | 48 | 264 | 3 | 7 |
| ENSDART00000145621 | Nonsense | 47 | 229 | 3 | 6 |
| ENSDART00000146327 | Nonsense | 231 | 305 | 7 | 8 |
The following transcripts of ENSDARG00000025522 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31883462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 31718352 |
| GRCz11 | 23 | 31644883 |
KASP Assay ID:
554-3092.1 (used for ordering genotyping assays)
KASP Sequence:
GTTGTTCTTGCAGTCCTGAGGTTCAGTCCATCCTAAACCTGACACCACCA[C/T]AAGATGTGGAGCTAATGAACAGCAACCCTTCCCCTCCGGTAAATCTGCTT
Long Flanking Sequence:
TGTAGAACAAATCAGTAAAAATAACATATCTGTATCGATTTTTTTGTAATTTTATACTTGAAATACATTTGTAAACATGCACATTATTTGTAACTTATTGCATGTTTACAAATGTATTTCAGCTATAAAATTACAATAAATAGAATACATGTATATTATTATTATTACTGATATGTCATTTCATTCAAATTGTTTTATTAAAACATGCAGTTATAATTTATTATATTTAAACTATTCTCATTTATTTAAAAACAAGCAATTATACATCTTTTTGATTTAAACATCTATTTAAAACAATAATTGTTTTAAATAACTTTTTTAACTATTATTCAAACTGTGTATTTCTTGTTTATTTTAATTATTATATTTATTGATTTATTTATTTTAACTTCCAGTTGTCTTGTTTATAGATTTATCCTCGTTTGTTTTCTCACTGTGCATCTCTGATTTGTTGTTCTTGCAGTCCTGAGGTTCAGTCCATCCTAAACCTGACACCACCA[C/T]AAGATGTGGAGCTAATGAACAGCAACCCTTCCCCTCCGGTAAATCTGCTTGTGTTTATGTTGTGTTTATAGCAGCAGAAAACATGTTTATATGCAGCCTGCATCTCACTCCAAAACAATGTCTGAATCCTATTAATCCAATGATATCTCTCTGCTCCTCAGCCAAGTCCCTCTCAGCAGATCAACCTCGGCCCTTCCTCAAACCCCACCGCCAAACCATCAGACTTCGACTTTCTGAAAGTCATCGGAAAGGGTAGCTTCGGCAAGGTTCTCCTGGCACGACACCGGAGCGATGAGAAGTTTTATGCTGTGAAGGTGCTTCAGAAGAAAGCCATCTTAAAGAAAAAAGAGGTATGAGATCACACACGCACACAGCTATTCACTTAAGCTTTTTGTCAATCAGTAAGTATGCATGACCTCTTAACCTCTGACCCTTAGGAGAAACACATTATGTCAGAGCGCAATGTGTTACTGAAGAATGTCAAGCATCCATTCCTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24374
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 |
|---|---|---|---|---|---|
| ENSDART00000035031 | Nonsense | 180 | 433 | 5 | 10 |
| ENSDART00000133569 | Nonsense | 162 | 264 | 5 | 7 |
| ENSDART00000145621 | Nonsense | 161 | 229 | 5 | 6 |
| ENSDART00000146327 | None | None | 305 | None | 8 |
The following transcripts of ENSDARG00000025522 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 31882908)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 31717798 |
| GRCz11 | 23 | 31644329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATTACTCTTTCCAGACCACTGATAAACTCTACTTCGTACTGGACTA[C/A]ATCAATGGAGGAGAGGTGTGTACTTTAATAAGCAAGACATTACAAACAAT
Long Flanking Sequence:
TTTATGTTGTGTTTATAGCAGCAGAAAACATGTTTATATGCAGCCTGCATCTCACTCCAAAACAATGTCTGAATCCTATTAATCCAATGATATCTCTCTGCTCCTCAGCCAAGTCCCTCTCAGCAGATCAACCTCGGCCCTTCCTCAAACCCCACCGCCAAACCATCAGACTTCGACTTTCTGAAAGTCATCGGAAAGGGTAGCTTCGGCAAGGTTCTCCTGGCACGACACCGGAGCGATGAGAAGTTTTATGCTGTGAAGGTGCTTCAGAAGAAAGCCATCTTAAAGAAAAAAGAGGTATGAGATCACACACGCACACAGCTATTCACTTAAGCTTTTTGTCAATCAGTAAGTATGCATGACCTCTTAACCTCTGACCCTTAGGAGAAACACATTATGTCAGAGCGCAATGTGTTACTGAAGAATGTCAAGCATCCATTCCTTGTGGGCCTGCATTACTCTTTCCAGACCACTGATAAACTCTACTTCGTACTGGACTA[C/A]ATCAATGGAGGAGAGGTGTGTACTTTAATAAGCAAGACATTACAAACAATCAGGATTGAGGAGAGAGAGTGACAGAAAATAGAGACAGCGAGGTAGATGCAGACAGAAAAAAGGAAATCCTGTCATGAGAGGAGCGCCTGGGCTCTGAATAGGAAACTCTCATCAGGAAATGGCTGGGAGGGGAAAGTGTGTGAGGTGGGAGAGCCAGATTTAGCAGCTGCGGTGGTTTAGACTGGGTCTAACCCAACAGACGTCTCTGAGGGGCCGGGGGGGGTGACGTTCTCATTTCCTGCCATTGTTCGGGATCGTAGAGAGTCTAGAAAGCTTTGATTAAGTATGCCATTCAGGATGTGGAACTCACAGTCTAATCTGTCTCCTCTTTCTCCCTGTGCTTCCATAGCTGTTTTATCACTTGCAAAGAGAGCGATGCTTTCTGGAGCCGCGCGCTCGCTTCTATGCAGCAGAGATTGCCAGTGCTTTGGGTTACCTGCATTCACTGA
Associated Phenotype:
Not determined