ZMP
si:ch211-195b13.1
Ensembl ID:
ZFIN ID:
Description:
serum/glucocorticoid regulated kinase 1-like [Source:RefSeq peptide;Acc:NP_001070770]
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 |
|---|---|---|---|
| sa45673 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43285 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45673
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 |
|---|---|---|---|---|---|
| ENSDART00000010580 | Essential Splice Site | 132 | 423 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 25370896)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 25301008 |
| GRCz11 | 19 | 24885231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTATGCTGTGAAGGTGCTTCAGAAGAAAATCATTATGAAAAAGAAAGAG[G/A]TAAGAGCTAATGCAATGCTCACATTGATGTGGAAACATTTTCTGACAAAT
Long Flanking Sequence:
TTTCTGCATAACTGACAATGCGGAATTGTTTTCTTTTTCTTTTTCTTAGTGCTGATGTTGGTTCCTTTCTAAAAATTGATGAGAACCAGAATGAGGAACTGGATGAGAATCTTCTGTGTTTGACCCATCCTAGGAGCTCTTTGGCTGAGGAGACTCAGTACGTTCATTTTTTTCTTCCCTCCTTTGATTTTCAAGCTTTTGTTTGTTATTTTGGATTTCAGCCATTAAGGCCGCTTGGTGTTTACATTACTAATGTTATTTAATTTCCTTAACAGGATCAAACCCTCAGATTTTGACTACTTAAAGATCATCGGCAAGGGGAGCTTTGGGAAGGTGTGTATAAGTATTATTCTTACAGTGAAGATGTCAACATTCAATGTTATAATCAAGAGTGCTAATGGCATCTTATGCCACAGGTTCTGCTTGCGCGGCACAAGGAAAACGAACTCTACTATGCTGTGAAGGTGCTTCAGAAGAAAATCATTATGAAAAAGAAAGAG[G/A]TAAGAGCTAATGCAATGCTCACATTGATGTGGAAACATTTTCTGACAAATATTATAACATTCAAACTCAAAACTGTTTTTCAGCAAAAGCATATCATGGCAGAAAGGAGTGTACTAATGAAAAATATCAAACATCCATTCCTGGTGGGTCTGCACTACTCTTTCCAAACCACAGACAAACTGTATTTCGTGCTAGACTACGTCAATGGAGGCGAGGTTAGTATACAATCCATTCACACTCTTAAATAGCCCAAAAGAGATCACTCCCACCTCTGACTGCATTCATGAACTCATGATATGTTTATCTCCAACAGCTGTTTTACCACCTCCAGCGTGAGAGAGTGTTTTTGGAGCCCAGAGCGAGGTTTTATGCTGCTGAAATCGCTAGTGCACTTGGTTACCTCCACTCACTGCACATAGTTTACAGGTATGTGATTGCCAGCAGTGACCCCTAGTGGAGAAGTTGTTGAAGTGCACCCTCATTTTGGTTTATTATGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43285
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 |
|---|---|---|---|---|---|
| ENSDART00000010580 | Nonsense | 182 | 423 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 19 (position 25371225)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 19 | 25301337 |
| GRCz11 | 19 | 24885560 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCATGAACTCATGATATGTTTATCTCCAACAGCTGTTTTACCACCTC[C/T]AGCGTGAGAGAGTGTTTTTGGAGCCCAGAGCGAGGTTTTATGCTGCTGAA
Long Flanking Sequence:
GAAGGTGTGTATAAGTATTATTCTTACAGTGAAGATGTCAACATTCAATGTTATAATCAAGAGTGCTAATGGCATCTTATGCCACAGGTTCTGCTTGCGCGGCACAAGGAAAACGAACTCTACTATGCTGTGAAGGTGCTTCAGAAGAAAATCATTATGAAAAAGAAAGAGGTAAGAGCTAATGCAATGCTCACATTGATGTGGAAACATTTTCTGACAAATATTATAACATTCAAACTCAAAACTGTTTTTCAGCAAAAGCATATCATGGCAGAAAGGAGTGTACTAATGAAAAATATCAAACATCCATTCCTGGTGGGTCTGCACTACTCTTTCCAAACCACAGACAAACTGTATTTCGTGCTAGACTACGTCAATGGAGGCGAGGTTAGTATACAATCCATTCACACTCTTAAATAGCCCAAAAGAGATCACTCCCACCTCTGACTGCATTCATGAACTCATGATATGTTTATCTCCAACAGCTGTTTTACCACCTC[C/T]AGCGTGAGAGAGTGTTTTTGGAGCCCAGAGCGAGGTTTTATGCTGCTGAAATCGCTAGTGCACTTGGTTACCTCCACTCACTGCACATAGTTTACAGGTATGTGATTGCCAGCAGTGACCCCTAGTGGAGAAGTTGTTGAAGTGCACCCTCATTTTGGTTTATTATGAATTGTAACCATGATTTCTATCTTTATCACAGAGACTTGAAGCCAGAGAACATCCTCTTGGACTCTCAGGGCCACATTGTGCTGACAGATTTCGGTCTATGCAAAGAGGGACTGGATCCCAACGGCACAACCACAACATTTTGTGGAACTCCTGAGGTAAGCCATTCCCATTCATGAAAAACACTTATAGACTGAAGTTGATTGTGCTGAATGTGCCCTGCTAGTGAGCTACTAATAAAAAGGCAACTTCAAAGTCCCTTTACACTTTAATGTTTATTTTCTTATTATTTTAATAATGTAGTTTGAAAGTACTTTTAATTATATTTATCTAAT
Associated Phenotype:
Not determined