ZMP
pim2
Ensembl ID:
ZFIN ID:
Description:
Serine/threonine-protein kinase pim-2 [Source:UniProtKB/Swiss-Prot;Acc:Q9YHZ5]
Human Orthologue:
PIM2
Human Description:
pim-2 oncogene [Source:HGNC Symbol;Acc:8987]
Mouse Orthologue:
Pim2
Mouse Description:
proviral integration site 2 Gene [Source:MGI Symbol;Acc:MGI:97587]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12616 | Nonsense | Available for shipment | Available now |
| sa9268 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12616
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 |
|---|---|---|---|---|---|
| ENSDART00000081985 | Nonsense | 60 | 310 | 3 | 7 |
The following transcripts of ENSDARG00000059001 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 9473407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 8889989 |
| GRCz11 | 8 | 8928574 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TRCATTCCTCTTCTAAATTATGGTTATTATTATTTTAGGTTGCTATCAAA[C/T]AAATATCMCGAGACAGAATCCAACAGTGGWCAAAAATGGTGAGTATTCGC
Long Flanking Sequence:
GTGCGTTTGGATCAGCTGGAAATCCTGAAAGCCAAAAATGGTAAGTTTATTATTATTTGTACGCGGGCTAACTAACTGTTAGCTAATAAATCTATATTGTTATTTTTTTGTTTGTTTTGTTTGTTTCTGCATTGTATTTTTGTGCAATTTGTTTAACATTCAAAAGTATTTAACTATTAAGTAAAGCAAAAATGTGTTTGTTTTTAATTTAATTTGTTATTAACGTAATTCAGATGCATAATTTACGTTACAATTAGCTACTTGGTTGTTATGTTTTTTGTTTAATATTGTTGTTTTTATTATTCAGGCAAAGAGCATTTTGAGAAGCAGTATACTATGGGAAATCTTCTGGGAAGCGGTGGTTTCGGTTCAGTTTACTCCGGGCATCGGATTTCAGACGGACAAAAGGTAAGAATGATTAAAAAACAAGAAAAAAGATGCTAATGTGTATGCATTCCTCTTCTAAATTATGGTTATTATTATTTTAGGTTGCTATCAAA[C/T]AAATATCCCGAGACAGAATCCAACAGTGGTCAAAAATGGTGAGTATTCGCGTTTATCTAACGTTACTTGTTTTGATCTGTGATGTGTTTTAATGTAAAATATACTTGGTATCAGTTAAACATATTTAAAAACTCGTCAGGACTTTGAATGTGCACGGACAGCGAATAAGCATTAACACTAGCGCCCTCTATTGATTATTTTGGTTCTTACTGGAAGCTCGTCGCGCTTAACAGAAAGTGACGTAGGCGTGACGTTTCGGATTTTTCAAAACATCTTAAAAAGGAAACTGAATGAACGGGCTTTCCATGTTGTGTCAGAATTAGTTTTAGACCTGCGCGGTGAGATATATTTGGATTAAAAACAAGAAGTGCGTTTCAACGTGTCGTAAAAATGTAGTTTCCCTTTTTAATACCCACGAGAGAGCCCCTGGATATCACCTCAGGGAATTTTCTTTACATAACTTAACCAGAATCGGTAACTCTGGGTTGTATTAGTTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9268
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081985 | Nonsense | 226 | 310 | 6 | 7 |
The following transcripts of ENSDARG00000059001 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 9475849)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 8892431 |
| GRCz11 | 8 | 8931016 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGAGTGGATCCTTTACCACAAATACCACGCTCTTCCGCTCACTGTGTG[G/A]TCATTGGGTGTSCTCCTGTACGATATGGTKTGTGGAGACATTCCCTTTGA
Long Flanking Sequence:
ACTTCAACATCTATATGTTTTGTGTTTAACACAACAAAGAAACTCATAAAGGTTTGAAACAGCTTTGTAAATAGTGAGTAAATGTTCATGTTCACCCAATACCTGTTGTATAATGACTTGTCTGATTACCCTAATTAAACTAATTAAGCCTTTAAATTGTACTTTAAACTGAACACTAAATATCTTGCGTATTAACTAGTGAAGTATTATGTACTGTCATCATGGCAAAGACAAAAGAAATCAGTTATTATAAATTAGTCATTAAAGCATTTATGTGTAGACTATTAAATTAAGTCTTTAAATACTAGATCAAATAGACTATTAAATCTCTCCGTTAACCAGCACTTGGGAAATATTAAAAAACATAATAATTCAACTGTATTTAAATAAGTGTGGATGTGTTTCTAACAGACCCCTTTTTTCTCTTTAGGTACCAGAGTCTACAGTCCACCTGAGTGGATCCTTTACCACAAATACCACGCTCTTCCGCTCACTGTGTG[G/A]TCATTGGGTGTCCTCCTGTACGATATGGTGTGTGGAGACATTCCCTTTGAGCAGGACACTGACATTGTAAAGGCCAAACCAAGCTTCAATAAACGCATCTCCAATGGTGAGCCCCCAAGCGGTCTTAAAATTAAAAAAATTCAATCATTATTTACTCACTTGTTCCAAACTTGTTTGAGTTTCCTCCAGGGCTGGGCTGATAAACTATATTATATCGGATCGCTATAAAATTAATGTCAATAACAATAAGTTCTGGATTTTTTTTTACTCTATATATTAATCTAGGAACCAAATTTTTGGCCACTGAAAATTTGCTGGACGAAAATGTAATGCCATTTAATGGACCCTCTAATATTTGTGGCTTCAGTCATTGTTGGGTACTCTTTTAAATCTGGAAGCATTAACAACTTATATCAAAATGTATATCGTTATCATTTAATAATTATCGAAATAACATTAATTGCCATATCACCCAGTCCTAGTTTCTTCTGCTAAACACA
Associated Phenotype:
Not determined