ZMP
pcl
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC553283 [Source:RefSeq peptide;Acc:NP_001032759]
Human Orthologue:
PC
Human Description:
pyruvate carboxylase [Source:HGNC Symbol;Acc:8636]
Mouse Orthologue:
Pcx
Mouse Description:
pyruvate carboxylase Gene [Source:MGI Symbol;Acc:MGI:97520]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16065 | Nonsense | Available for shipment | Available now |
| sa23952 | Nonsense | Available for shipment | Available now |
| sa37328 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16065
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 |
|---|---|---|---|---|---|
| ENSDART00000001098 | Nonsense | 204 | 1181 | 4 | 20 |
| ENSDART00000028401 | Nonsense | 204 | 229 | 5 | 5 |
| ENSDART00000131874 | None | None | 784 | None | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 26151400)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 26720238 |
| GRCz11 | 21 | 26756933 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCTACGGCTTCCCCATTATCTTCAAGGCTGCGTACGGTGGTGGGGGA[C/T]GAGGAATGCGGGTGGTCAGAGAGTATGAGGTACCGTGTCTTAGATTAAAA
Long Flanking Sequence:
ACGTTATCATAGAAGGAAATATTTTGTTCAATTTTGTATGCTTAATTAAAATATGGATGATCTTTATATACTTTTTGGTAATTGTGTAAATTCTTCCAATAAATAAAATAAATGAACTAATGGCTTAAATGCACATATAAACATGATTAACAACCTTTAAGCGTTAAGCTGTCAGATCTTTAACAGTTTACAACTTTCTAAAACTGTAATCCCATATTGCGAAAATTAATACCATTTATTTTAACTTCCAAAACACAATTGTTGCACCCAATTTAAAGTGGAAGCGTTATAAATCATGTTGTAAAATTGACATGATAACCTGACTTAATTTGAAAGGTTGCAGGTTTGATTCCTGGGCAAACAAATTTTCTGTTCATCTTGCAGGAGTGCCGGTGGTTCCTGGGACAGACGCTCCCATCTCCTGTTTGCAGGAAGCTCAAGAGTTCTCCAACAGCTACGGCTTCCCCATTATCTTCAAGGCTGCGTACGGTGGTGGGGGA[C/T]GAGGAATGCGGGTGGTCAGAGAGTATGAGGTACCGTGTCTTAGATTAAAATTATTAGTTGGGGTTCATAATCTTGTTTAATCTCTGTTCAATTCCTTCCAAGTTGAGGTTTGATAAAGGGGGGCTTTTAAATGAGCGCAAAAGTGAGCACCCGTTTGCCCTTTAGATTTGTTTGCTGTTCAGTTACTGGTGCTGTATGAATTAGTGTGTTGGGTATTTGCGCTGGGTGACCCGGTCACTGTGTGTGTGTGCTTGTGATCAGGAACTAGAAGAGAACTATCAGCGGGCGTACTCTGAAGCCCTGGCAGCCTTTGGCAATGGAGCTCTGTTTGTGGAGAAGTTCATTGAGAAACCCAGACACATCGAGGTGCAGATCCTGGGTAAGTGAGGTTGTTGTTGGTGTGTGTTTTTCTGTAGTGGAAAAAAAAGCATTGATATATAAAAAAATAAAAATAAAATAAAAAGCCTAAATATTTTACAGTCTGGGATGATTTACTCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23952
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000001098 | Nonsense | 1015 | 1181 | 18 | 20 |
| ENSDART00000028401 | None | None | 229 | None | 5 |
| ENSDART00000131874 | Nonsense | 618 | 784 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 26355538)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 26924449 |
| GRCz11 | 21 | 26961144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCACGGTGACGAAATCACTCCAGAGGATGTGATGTCAGCAGCCATGTA[T/A]CCCAAAGTATTCCAGGAGTTCAAGGATTTCACCAGAACCTTTGGGCCTGT
Long Flanking Sequence:
TGATTGAGAATCCTTGATGGCAAGTTTTTGCCTAAGAACCCATCATAGTCAGTGAACTGTGGAAGAGACAGAAAAAGAGTGGAAGAAGATCACTGCAGAGCAGTGTGATGTCCACGAATGTGCTCAATTCATTCAAAGCAGTGGCCCCTTTAGAAATATTAGTTTCAATCATTCTTCATGCTACAATCATTGCGGTTCTCTCATGTTTCCACAAGGTAAAGGCTTTTTATTAAAGTTATTTTGCAAAACTATATAGTGCAACTAAAATTCCCTCCATTTTCTAACCATGAAGACTGTTATTTCTGAGAAAATGTGTTTATTAATTGTTCTTTAAGTTTCTCTTTTGTTTTTATTGTTTAGGTTTTGAAGTCACTTCCCCGTGTCGAAGGACGTCCTGGAGCCTCTCTGCCTGCCATGGATTTCCAGGCCTTGGAGAAGCAACTGAAAGATGCTCACGGTGACGAAATCACTCCAGAGGATGTGATGTCAGCAGCCATGTA[T/A]CCCAAAGTATTCCAGGAGTTCAAGGATTTCACCAGAACCTTTGGGCCTGTGGATTGTTTGGATACCAGACTCTTCCTAGACGGACCAAAAATTGCTGAAGAGTTTGAGGTGGGAGTATTTCAGTCTTTCAATTATTTAACGGAAGTGGCATCAAATTTTTATTCTCAGTTGCCCTGTCATAAATCTTCCTGTCAGCCATGATTGTACATGTCATTCCTACATTCCAGGCATCAGTTGTGTATTTCCTCTGCTCATATCTGTGCTGTCTGTCTCAGGTGGAGCTGGAGCGAGGAAAGACACTTCACATCAAGGCTCTGGCTCTGGGAGATCTTAATAAAGCGGGGCAGAGAGAGGTGTTCTTTGAGCTCAACGGTCAGCTGAGATCTGTTCTGGTCAAAGACACCGTGGCCATGAAGGTGGGTTTCTGAATTTCACTTACAGCTTTTAGGGAAGTTTTCCCCTTTTTTTAGTGACAGTTAGTGAAATGTCTCCTGACCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37328
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 |
|---|---|---|---|---|---|
| ENSDART00000001098 | Nonsense | 1137 | 1181 | 20 | 20 |
| ENSDART00000028401 | None | None | 229 | None | 5 |
| ENSDART00000131874 | Nonsense | 740 | 784 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 21 (position 26360097)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 26929008 |
| GRCz11 | 21 | 26965703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTAAGGTGGTGGAGGTGAAAGTGAAGCAAGGGCAGCAAGTGGAGAAAGGA[C/T]AGCCGCTCTGCGTGCTCAGCGCCATGAAGATGGAAACGGTGGTCAACTCT
Long Flanking Sequence:
ATTTTTCTGTCTTTCAATCTGTCTATCTATCTGTCTGTCTATTCGTTTTTTGTTTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGGTTTTATTATATTCTGATATACTGTTTTCAATGATCCTCTAATGATCAACATGTATGCATTTCTTTTTAAAGAGTTTCTGAAGGTCGAATGCAAATTGTAAATGAACCGGACACCCCTGCTGACCTAAATCAATTTTCTTGGATTTGCAGGAGATGCATTTCCACCCTAAAGCCCTGAAGGACGTTCGTGGTCAGATCGGAGCTCCTATGCCCGGTAAGGTGGTGGAGGTGAAAGTGAAGCAAGGGCAGCAAGTGGAGAAAGGA[C/T]AGCCGCTCTGCGTGCTCAGCGCCATGAAGATGGAAACGGTGGTCAACTCTCCCATCTCCGGCACCGTGGCCAAGATCTACGTGACCGCCGACAGCACACTTGAAGGAGATGATCTTATTCTGGAGATCACCGAGTAGATATCACGAAAGCCAACAGCAGGGAACATAACACATCACCACTGCCAATCCCTGCACGGCTAAACACACATACACGCACACATGGAGGCTGACAGTAGAAGCTGTAGCACTAGTACAAGCACAGATTACAAATTACAGATATTTTTACAGGATCTCAAAGAACAACACATCACAAATCTGCAAATGTCAAGCGTGAATTCTTTGGCATTAGTGTCATGTGCTTTTGTGATCTTCAATCACATTTGTTATATTAATATGTGACGAGAATTTGTTCTAGTGTTGTTTTGTTAACAGAAATCTATCATTAGTATTAATGAATGTAGTGGAAACTAAACGATTGACATTGAAAACAAATAGATAGCA
Associated Phenotype:
Not determined