ZMP
zgc:110727
Ensembl ID:
ZFIN ID:
Description:
DNA primase large subunit [Source:RefSeq peptide;Acc:NP_999947]
Human Orthologue:
PRIM2
Human Description:
primase, DNA, polypeptide 2 (58kDa) [Source:HGNC Symbol;Acc:9370]
Mouse Orthologue:
Prim2
Mouse Description:
DNA primase, p58 subunit Gene [Source:MGI Symbol;Acc:MGI:97758]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12346 | Essential Splice Site | Available for shipment | Available now |
| sa15538 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12346
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000005004 | Essential Splice Site | 345 | 508 | 10 | 14 |
| ENSDART00000136406 | Essential Splice Site | 345 | 508 | 9 | 13 |
| ENSDART00000146216 | None | None | 199 | None | 5 |
The following transcripts of ENSDARG00000052721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23765625)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 23411285 |
| GRCz11 | 13 | 23541735 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCAGTTCTGGAGGTCAGAGTTTGTCAAGGGGAAAGTYGATGCAGACAAG[G/T]TAACTCTTCAACTTCAGCTTCTAACTCCCTCACATWGTCCTGGTTTTCCC
Long Flanking Sequence:
CTGTATAACTGTCCATTCAAACCAAGGGTTTAGCGTTTGCATATATAAGAACATGCACATTCTGCTCTGGCCTTGCACATTTCACATCTAAAAAGTTATCCGTTTCATTTGAATTTTACATTTAAATTTAGTCTTTTAAAGCAGCGGAATGGTCAGACAGACTCAGCATTGCTTAATAGACTTTAGCTGTCATGAGCTCAGTGACTGTGTCTTCATGTTTCAGTTGAAGTTTAGTCAACACATTCAGCAAAGCTGCTCATTCCATTGCACTTCAGGGGATCTTTAATAACCTCTCTATTGTTTATTTCCACCAGCTCTCAGGCAAGTCGTTTCCTCTATGTATGAGGCATCTCCACAAGGCACTGAGGGAGAACCACCACCTGCGGCACGGTGGACGCATGCAGTACGGCCTCTTCCTCAAGGGCATTGGTCTTACTCTGGAACAGGCCATGCAGTTCTGGAGGTCAGAGTTTGTCAAGGGGAAAGTTGATGCAGACAAG[G/T]TAACTCTTCAACTTCAGCTTCTAACTCCCTCACATTGTCCTGGTTTTCCCCAAACATACATCCCAAGATGCTTACTTCATATTTTTGTGTTATTAGCAATTCTTTTAATTCTGCTGATGTGATTTTTTTTTCTTCACCCCTCAATAACTCTTGAGAGGGTCACCCACATGAGCAAGAGAATGTATTAGAAGGCCACGTTTAGTTCTAATGCTTGTGATAATTTGCCGCCCTTCCATCTTGTCCTTAATTACAATTCCAGAGGAACACGTGAGATCTTCGTTTTCGCGCATGGTACATTAAACAAGAAAATTACACCCCCAGTCTTAGACCTATGTTTCCCTCCTCCCTGCACTCTGCAAATGATTGCTTATTCTCAAAAGATGCTCAATCAAGGAGAAACAAATGAATTTTATATCCTTACCTGAGAATGACCATTTTGTCAGACAGGCTTATGTAGTGATCTTTAGCCCCACAAGAGCACAGTAGCATCTCAGAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15538
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 |
|---|---|---|---|---|---|
| ENSDART00000005004 | Nonsense | 370 | 508 | 11 | 14 |
| ENSDART00000136406 | Nonsense | 370 | 508 | 10 | 13 |
| ENSDART00000146216 | None | None | 199 | None | 5 |
The following transcripts of ENSDARG00000052721 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23737395)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 23383055 |
| GRCz11 | 13 | 23513505 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCGCCACATGTTTGGGAAGGAAGGCAAGCGCWCTGACTACACCCCCTA[C/A]AGTTGCATGAAGGTGATTTTGTMAAACCCACCCAGCCAAGGCGACTACCA
Long Flanking Sequence:
AAATGTGCATTTCACATATTTGCATACAGTTTGAGTGTTCAGACTGTTTTTATTTTCCTTGGGGTTGCAGCTCTCATGTGTTAATTTTTTTTAATTTGGTTTGATGCTGATGCCTCAGAGACATGAGATTTGTGTGTGGAGAGTGAAACCGAGACGGGGGAGGGGAGAGAGACAGAGAGCAGCCACATTATCCATAATCCAGTCACAGCTGTCTGCGGTTTGGCGACACCGCTACAGCAGGTCCCTGCTAATAGCTCTATATTTCATAGCGGAAAACGCCCTGCCACAACCCACTTGATGTACGACAATGTCTTCGTTTCACCCACAACCTCCCCACCATTCCTACCCCTGTTCTTGCACGCTTTACTGTCCTCTTTCTTAAACTCACCATCACTTTCTCTCTCTCTTCTTTGTCTTGCTCTGCAGTTTGATAAAGCATATGCCTACAGCATCCGCCACATGTTTGGGAAGGAAGGCAAGCGCACTGACTACACCCCCTA[C/A]AGTTGCATGAAGGTGATTTTGTCAAACCCACCCAGCCAAGGCGACTACCATGGTGAGTCATACTGAGTCAGACTGTTGGTTTTCAATGCGATCCGTTCCCCCGAGGCCCATATTTAGTTCTGTAGCGAAGAGAATTAAAAGAGTGCTTAGTACGCAGGTGGTCTTAAATTAGTTCTAAAAAAATTCCCAAGTCCAGGCTGGCTAATTGATAACACCTGCTTTTCGCCATGCATGTAATGGGCAAAATCCATTTGAAAAGAGCATCATTAAAGGTAAGAGAGAGTAAGTGTGTCAAAGATTGAAGAACATTGCTGTCTTATGTGTAGATTTGCTATACTGTTGCAAGGCTTTACAGCACTTCTACTTTAATGTATGTTTTAATAATAGACAAAAATGTCATGCTTTAGGAACACTTATTTCACTTCAAAGGTGCGGTATGTAAGTTTTTGACTTTTCTAAAGCATAAAAATTCCATAATGTGTTTGCAGATATTTAAGAAA
Associated Phenotype:
Not determined