ZMP
cad
Ensembl ID:
ZFIN ID:
Description:
CAD protein [Source:RefSeq peptide;Acc:NP_001009884]
Human Orthologue:
CAD
Human Description:
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase [Source:HGNC Symbol
Mouse Orthologue:
Cad
Mouse Description:
carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase Gene [Source:MGI Sy
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11882 | Essential Splice Site | Available for shipment | Available now |
sa23778 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11882
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061361 | Essential Splice Site | None | 513 | None | 44 |
ENSDART00000061365 | Essential Splice Site | 165 | 2230 | None | 43 |
ENSDART00000075262 | Essential Splice Site | 169 | 2154 | None | 41 |
ENSDART00000122056 | Essential Splice Site | 165 | 261 | None | 9 |
ENSDART00000125333 | None | None | 485 | None | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 38847528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38919940 |
GRCz11 | 20 | 38822819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTGACAATCCAGAYGCCCGAAACCTTGTTAAAGAAGTTTCYATGAAAG[T/A]AGGTGTCTAGCTTCAGTGTTTTTTAGATGGATGATGTTGTGTAATGCAGT
Long Flanking Sequence:
AAATATATCTAGTAAAATATTATTTACTGTGGTCATGGCAAAGATAAAATAAATCAGTTCTTAGAAATGAGTTATTAAAACTAATTTGCTTAAAAATGTGTTGAAAAAAATCTTATTTCCTCTAAACAGAAATTGGGGGGAAAATATGCAGGGGGGCTAATAATTAAGGAGGGCTAATAATTCTGACTGCAACTGTATCTGCTATCCGATAAATCTTGTATAGCAATAAACAAACAGCACTACTACTCTTGCTTGACAAATATTTGCTTTTATTCATACAAAGTAAAAGCAAGAATTTTAATCCCATTGTACTATGGTTCAAAAAACTAAAACATAATTTATCCTGTGAAAATCAGGTGTTGACACTCGATGCTTGACCAAAAAGATCAGAGAGAAGGGAACCATGTTGGGAAAACTTGTGGTGGAAGGAACTCCAGCCGACAATATTCCGTTTGACAATCCAGATGCCCGAAACCTTGTTAAAGAAGTTTCCATGAAAG[T/A]AGGTGTCTAGCTTCAGTGTTTTTTAGATGGATGATGTTGTGTAATGCAGTGAAATTTATTTTTTGTGTTCTGTATTGCCCATTCAACAGGCACCAAAAGTGTTTAATCCAGAGGGCACAGTGAGAATCACTGCTATAGACTGTGGCATCAAGTACAACCAGATACGTTGCTTGTGCCAGAGAGGCGCCCGGGTCACTGTTGTCCCCTGGGATCAACCTCTGGACAGCAATGGTAAACAATAACACTATTGTTGAGGGTTGTCTTCTGGGAAAATGGCAAATGAAATGAATGTATAAACAACTGGTGTATTGTGTGTAAACTTTGTGAATCCCCAAAAATGATTACATAAATTGATAAGTAATAATTTGTATCAATATTTCACTCCCCTAGTAAATGCATATTGAAAATGTTATCACTGGGCATGTTGCCTCTGTTTTTTCTAGACTTTGATGGGTTGTTTATCAGCAACGGTCCTGGCAATCCTGAGTACTGTAAGGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23778
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 |
---|---|---|---|---|---|
ENSDART00000061361 | None | None | 513 | 27 | 44 |
ENSDART00000061365 | Nonsense | 1465 | 2230 | 27 | 43 |
ENSDART00000075262 | Nonsense | 1465 | 2154 | 27 | 41 |
ENSDART00000122056 | None | None | 261 | None | 9 |
ENSDART00000125333 | None | None | 485 | None | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 38828264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38900676 |
GRCz11 | 20 | 38803555 |
KASP Assay ID:
2261-4751.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTGGACAGGCTCCTCGCGTGAAGACACATGTAGACAGCATGACCTCA[C/T]AGAAACTCATCCGTTTGCCAGGTAAGTGTGGTCTCTTGCATCCTTTCAGT
Long Flanking Sequence:
TAATAATTATAATATTAATAGAAAATCATTCTAAAATTATTAATTATTATTAATATTATTGTATTTGTAACAATAATTAATATTTATTAGTAGATAAAAATAAATGTATAGAAAGAACAAAATAAAGCATAATTATAAATAACAACAACTATTATGATTATTATTATTTTAAACTTTATTTTCTATAGCGCTTTTAATGGTATATCCCAAAGCCATTCACAGGTTTTTTTTAAGGTAAAGATTCAAAGGAAAAAAGACCTAAAAAATATGATTATAAAAGGTAAATTTAACATCCTACATAAGACACCAAGAAATCACCTAAAAGCCATTCTGAAAAGTTTTAAGACCAGATTTTAAAACAATAAATGCTAAACACTAGAACGCAGTTTTATTGTATCACCCCTAAAACTAAAGATTGAAATGTATGTGGGTTTTGGCAGGCACTGAAGCAAATTGGACAGGCTCCTCGCGTGAAGACACATGTAGACAGCATGACCTCA[C/T]AGAAACTCATCCGTTTGCCAGGTAAGTGTGGTCTCTTGCATCCTTTCAGTTATTCAATACAATTTTTGTCAAAACAAATGAGTGTCCCTGCTGATTACCTTACCTGTAATGTAGCTGTTTGTGAATGTTAAAGTCTATGATGTTTTAAAAATCAAAGTGCTCGATAAATACAGTATCATTTTACAATAAGGTTGTATTATGTTAACTAACATAAACAAACAACTAACCACAAATTTATTACATCGTTTATTCATCTTTGTTAAGGTTAATAAATAGAATTTGTTTGTTGTTGGTTCATTTACTTAGTGCATTAACTAATGATAACAAACATTAGTTGGGTTGTAATAATGCATTAGTAAGTGTTGTGAGCAATGATTAACTGATTAATAAATGCTGTACAGTTATTTTTCATTTTTAGTTCATGTTAGTAAATACATTAATGAATCCTTATCTTAAAGTCCAAAATAAAAGCAATTCTTCCTGCAGTTTTGTGTTGTGAA
Associated Phenotype:
Not determined