ZMP
zgc:113028
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC565041 [Source:RefSeq peptide;Acc:NP_001030150]
Human Orthologue:
PIM3
Human Description:
pim-3 oncogene [Source:HGNC Symbol;Acc:19310]
Mouse Orthologue:
Pim3
Mouse Description:
proviral integration site 3 Gene [Source:MGI Symbol;Acc:MGI:1355297]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25231 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38107 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25231
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077445 | Essential Splice Site | 67 | 320 | 3 | 6 |
| ENSDART00000108692 | Essential Splice Site | 67 | 141 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 25 (position 30652880)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 29220241 |
| GRCz11 | 25 | 29663248 |
KASP Assay ID:
554-7807.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGCCACGATCACATATTCATATGCGCGTTTTTCTCTTTTTGTCTGTA[G/C]GTTGCAATAAAACACGTCGCCAAGGAGAGAGTGACCGAATGGGGTACTAT
Long Flanking Sequence:
TATTTGTAACACGACCAACATCGACCACTTACCGGTGAAAATTCAACTCCAAGCAGGTAGATATCGTTTTTTAGATTCATCGCGCTAGTTATTTGCCTTTTCTCACATAACATCTTATTTTAAATTCAATGTTTACTACTAATATTCTATAAGCGACAAATTTAGCCTCTTTAATCGGCACGCGCCTGTCTGTGACCTGAGCGTGGAGCCATTTTGTTGCCAACCGCGCGTTATACACACTCGGATTTATGTCACGTTATTACATTAACACTGTTTATTCCCCTTCTTCATTCCACAGCCAAGACCGAAAGGGAGCCATTTGAGAAGGTTTACCATGTGGGTTCGGTGCTGGGAAGCGGTGGGTTTGGTACAGTGTACGCCGGTACTCGTATCTCAGACGCGTTGCCGGTAAGCGCTCGCTTTGTTTTGGTGGCAGCACATGGCCGCGTTTGGCGCCACGATCACATATTCATATGCGCGTTTTTCTCTTTTTGTCTGTA[G/C]GTTGCAATAAAACACGTCGCCAAGGAGAGAGTGACCGAATGGGGTACTATTGTAAGTAAACTATCATACTCTTTATTAATATTAACAGTATAAACGATTTATTTCTAACCAGTGCGGTTTTATTTGTATTCCAGAACGGGTCGCTGATTCCACTCGAGATTGTTTTGTTGAAGAAAGTGGGAAGCACGTTTCAGGGGGTCATTAAACTCATAGATTGGTATGAGAGACCCGACGGATGGTTGATTATAATGGAGCGGCCGGAGATGGTGAAGGATTTATTCGACTACATCACGGAGAAAGGCGCGCTGGATGAAGACACCGCCCGGGGCTTCTTCAGACAGGTTTTGGAGGCGGTTCGCCACTGCTACAGCTGCGGGGTGGTTCACCGAGATATCAAAGACGAAAACCTCCTGGTGGATTTACGCACGGGGGACCTGAAGCTCATTGACTTCGGCTCCGGGGCCATCCTGAAGGACACCGTGTACACAGACTTTGATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38107
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000077445 | Essential Splice Site | 84 | 320 | None | 6 |
| ENSDART00000108692 | Essential Splice Site | 84 | 141 | None | 7 |
Genomic Location (Zv9):
Chromosome 25 (position 30653013)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 29220374 |
| GRCz11 | 25 | 29663381 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACAGTATAAACGATTTATTTCTAACCAGTGCGGTTTTATTTGTATTCC[A/T]GAACGGGTCGCTGATTCCACTCGAGATTGTTTTGTTGAAGAAAGTGGGAA
Long Flanking Sequence:
TACTACTAATATTCTATAAGCGACAAATTTAGCCTCTTTAATCGGCACGCGCCTGTCTGTGACCTGAGCGTGGAGCCATTTTGTTGCCAACCGCGCGTTATACACACTCGGATTTATGTCACGTTATTACATTAACACTGTTTATTCCCCTTCTTCATTCCACAGCCAAGACCGAAAGGGAGCCATTTGAGAAGGTTTACCATGTGGGTTCGGTGCTGGGAAGCGGTGGGTTTGGTACAGTGTACGCCGGTACTCGTATCTCAGACGCGTTGCCGGTAAGCGCTCGCTTTGTTTTGGTGGCAGCACATGGCCGCGTTTGGCGCCACGATCACATATTCATATGCGCGTTTTTCTCTTTTTGTCTGTAGGTTGCAATAAAACACGTCGCCAAGGAGAGAGTGACCGAATGGGGTACTATTGTAAGTAAACTATCATACTCTTTATTAATATTAACAGTATAAACGATTTATTTCTAACCAGTGCGGTTTTATTTGTATTCC[A/T]GAACGGGTCGCTGATTCCACTCGAGATTGTTTTGTTGAAGAAAGTGGGAAGCACGTTTCAGGGGGTCATTAAACTCATAGATTGGTATGAGAGACCCGACGGATGGTTGATTATAATGGAGCGGCCGGAGATGGTGAAGGATTTATTCGACTACATCACGGAGAAAGGCGCGCTGGATGAAGACACCGCCCGGGGCTTCTTCAGACAGGTTTTGGAGGCGGTTCGCCACTGCTACAGCTGCGGGGTGGTTCACCGAGATATCAAAGACGAAAACCTCCTGGTGGATTTACGCACGGGGGACCTGAAGCTCATTGACTTCGGCTCCGGGGCCATCCTGAAGGACACCGTGTACACAGACTTTGATGGTGCGTCCTTCACTTTTACCCATCCTGCTTTGCTACGGCTTAACGTTGCGTGTGCACCTGCCGCGCTGAGCTTAATGTTTTGGAAAAACTGTCAATTCATGGTTTAAGTAATTTTACTTACAATTTTGATTTTTA
Associated Phenotype:
Not determined