ZMP
paics
Ensembl ID:
ZFIN ID:
Description:
multifunctional protein ADE2 [Source:RefSeq peptide;Acc:NP_955831]
Human Orthologue:
PAICS
Human Description:
phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoimidazole succinocarboxamide synthetase
Mouse Orthologue:
Paics
Mouse Description:
phosphoribosylaminoimidazole carboxylase, phosphoribosylaminoribosylaminoimidazole, succinocarboxami
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa892 | Essential Splice Site | F2 line generated | Not yet available |
| sa4900 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa892
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048164 | Essential Splice Site | 630 | 1050 | 7 | 15 |
| ENSDART00000126716 | Essential Splice Site | 5 | 425 | 2 | 10 |
| ENSDART00000132247 | Essential Splice Site | 5 | 425 | 2 | 10 |
| ENSDART00000136475 | Essential Splice Site | 5 | 425 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 25655527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 25726830 |
| GRCz11 | 20 | 25625920 |
KASP Assay ID:
554-0799.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTATTTTGCAGGAAAAACAAATCCCAGCAAGAATGTCTACTGCAACAG[G/A]TAAGTTAGAGTTTATTCTTCTGCTCGATTGTTTCTGTGTGCACCATGTTT
Long Flanking Sequence:
ACCAAAACACCAGTTTAAAAATCCAAGTTAGAGCAGATGGATAATAAAGTTGTTGTTGTTTTTTTGTCCAAGAAAAGCAATTTTTGTCAAATCGATAACACAAAGTCGAAACTGCTCAATAGCTTGCGTCACGCGCCCAAACTTCAATGCAGTTATAAAGAAGTGTTGTAGGGAGAATGTTTGCGTCTAAACATTATCATTCAATAGATAAAACGTCTATATTCCAAAAGCATGCAGATTAAGATTCTGTCCACGTGGTGAAGATGGCATTACTCTGATTGGTTTTTATGAATCGGCAGAGTGTCGTAACGCTTTACTCTCGTGAAAATAAATGAGTTGAGTCTCACCCCTCACCCTTCTTCTTCGTCGAACTTTATAATAAGCCTTCATCTCAAGCACAGCGCGCGTGTCTTAAACCCGAGCACACCGAATAAAGTTCCTCATCATTTATTTTATTTTGCAGGAAAAACAAATCCCAGCAAGAATGTCTACTGCAACAG[G/A]TAAGTTAGAGTTTATTCTTCTGCTCGATTGTTTCTGTGTGCACCATGTTTAGATCCGTGCAGTTGCGCAGTGAATATAAAATGTTCCCATGTGGCACGATTCATTGTTCGGTTCTTATGTTTTATGGTAGATTCGTAAATCACAATAGTTAATAATACTAGATATACTATTATGGTAGCAATTATTATATGGTAGTGTAATTAGCTATGTAAGATGAGTCATTCTGAGGCCAAATAAATAAATTTTTGTGTAAATAAATCTGTTCTTGGACGTAAAGAAAGAAAAATTCTTGGAAATGTAGCCCTTGTTTGTTTTTGTTTTTTCATCTTCTTCTAAAAAATTATTATGAATTAAAATGTAATTGCTTTAACCCATTACCTGCTCCATCAAGAAAAAAAATTGGATTGCATTAACACCTAATGTCACTAGGTAACACACTCAGTGCATTTTTTCCCCAACATATCCCATAATTTCTAAACAATCAACCTCTACCAAATGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4900
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000048164 | Nonsense | 765 | 1050 | 10 | 15 |
| ENSDART00000126716 | Nonsense | 140 | 425 | 5 | 10 |
| ENSDART00000132247 | Nonsense | 140 | 425 | 5 | 10 |
| ENSDART00000136475 | Nonsense | 140 | 425 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 20 (position 25653217)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 25724520 |
| GRCz11 | 20 | 25623610 |
KASP Assay ID:
554-3511.1 (used for ordering genotyping assays)
KASP Sequence:
TNATCTACTATTATGTTTTGCTCAGGATGATGCCAATAATGACCCTCAAT[G/A]GTCAGAAGAGCAGCTGTTGGCAGCTGGTTTTGACCTGGCTGGACTGACTA
Long Flanking Sequence:
CTCGATAATACACGCATGCTGTGTTGAGGATAGTAGGACTGCTGTTTTAGTTACACCATGTGAAAGTGTATCATTTATCAGAACATTACTATTATCTACTTGAAAGTGCAGCTAATGAACCAGAACATTAAGCGTCTACTAAAATGATGCACCAAGTAATGCGAATAATTTCCTTCAGGGCTTAAGACCGCATTTGTCAGGCAGCATTCTGACACTGCATTTGTGGCATCTCGATGTGAAATGATACCCATTGAATGGGTCTGCAGACGTATCGCCACGGGTTCCTTCCTCAAACGCAACCCTGGGGTTAAAGAGGGCTACCGCTTCACTCCTTTAAAAATGGAGATGTTTTTTAAGGTGAGGATTTGATTTTTAGGAATAAAGTCTTTATCACATATCAAATGTAATTCCATGGCATTTCACATTCTGATCCACTACTCTCTTTTTTTTTTATCTACTATTATGTTTTGCTCAGGATGATGCCAATAATGACCCTCAAT[G/A]GTCAGAAGAGCAGCTGTTGGCAGCTGGTTTTGACCTGGCTGGACTGACTATTGGTCGCTGTGAGGTGGACATCATGAGCAAAAGCACTGTGGCCATTTTTGAAGTCCTGGAGAAGGCTTGGGCCACCCAGGACTGCACGCTGGTGGATATGAAAGTAAGAAACCTGAGTGAAACCATAAATTACAGTAAAGTTATAACAGTAATGACACAAAAGAGAAAACCATGATGTTCCTTATTATTGTAAAGATCAGATCACTTCATTGCAAACATATTTTACACATATACACACCACCTTTTTTACAGGACACTATAAATTGTATAACTGCAGGTTAACTATGTACAGTTGAGGTCAGAATTATCAGCCCCCCTGTTTATTTTTTCCCCAATGTCTGTTTGACGGAGAGATTTCCTCAGCACATTTCTAAACATAATAGTTTTAATAACTCATCTCTAATAACTGATTTATTTTATCTTTAACATGATGCCAATAAATAATATTT
Associated Phenotype:
Not determined