ZMP
si:dkey-225d17.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate carbamoyl-phosphate synthetase 1, mitochondrial (CPS1) [Source:U
Human Orthologue:
CPS1
Human Description:
carbamoyl-phosphate synthase 1, mitochondrial [Source:HGNC Symbol;Acc:2323]
Mouse Orthologue:
Cps1
Mouse Description:
carbamoyl-phosphate synthetase 1 Gene [Source:MGI Symbol;Acc:MGI:891996]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41493 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa7635 | Missense | Mutation detected in F1 DNA | Not yet available |
| sa44709 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34714 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa18960 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10807 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41493
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004742 | Essential Splice Site | 68 | 1482 | 2 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40082114)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39220010 |
| GRCz11 | 9 | 39029805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGATCAGTCTGCAGCTGGAGAGCTGGTCTTCAACACAGGACTAGTTGG[G/A]TGAGAAGGCATCCTCTGAATATGGTCATGCATAAATATATTGTTTTGTCA
Long Flanking Sequence:
ACATTTATTTATTCTAAGCTATTCCCCCAAAGCCGACTTGTTAATATATAAACTTGAACATGTAACTTTTTTATAAAACTATATATAAGTTGTCTGTTCAAGACAAGAGTACACACAGCTACTGGAGAAGTCAAGTAGAATATCTAATCTCTAATATAACACTAAGTATACTGTAGGCTTTTCAAATTTTCTTATGTCAGTGTAACTAAAAAACTATGCATGTGTGTAATTGTAAGCATACTTCTGAGATCTACATAAAAAGCAGACTAAAAAGTATACTTACATGTATTTATCAGCATACTTATATATATTGAAAATGATGGGTTATGAAGTGTCACATTGCATCTAAAGAATACATCTGTTGCTTTTAAATTCATTCTACTGTTTTAGGCTCAGACTGCACACCTGGTGCTCGAAGATGGCACAAAGATGAAGGGCTACTCCTTTGGCCATGATCAGTCTGCAGCTGGAGAGCTGGTCTTCAACACAGGACTAGTTGG[G/A]TGAGAAGGCATCCTCTGAATATGGTCATGCATAAATATATTGTTTTGTCAGCAGTGAAAGTGCAGAGGTAACAACTTTCCAGATGACAAATCTTGAGACCAAATATTTCAGCTGGAACTCCTGCTAAGATTTTAAGCCAGTGCTTCAGACTAGCTTCAGTCTACCAGCCATTCTTGCAACGCTCTTGCAAATACAGTTTTTAAACTGAAATCTCTTCTCAAAATTTTAACGACTCCTAAAGCTTTAGTCTTTTAAATCAATATTTATAGTTCCACTCTGTTATTTTTTTGGTTACTATCATACAGGTATTAGCTTTAAGTGTTGTGTGTTATCTCCAGATACCCTGAAGCTCTTACAGACCCCAGTTACAGGGGGCAGATCCTGACCCTCACCTACCCTATCGTGGGAAACTATGGTGTCCCCAATACACAGGAGCTGGATGAGCTGGGACTCAAGAAAAATGTGGAGTCTGATCGGATTCAGGTAATCTATGTAGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7635
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:
T > C
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004742 | Missense | 138 | 1482 | 4 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40083768)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39221664 |
| GRCz11 | 9 | 39031459 |
KASP Assay ID:
554-4361.1 (used for ordering genotyping assays)
KASP Sequence:
GGTTCAGGATTATAGTGCTGAGTACAGCCACTGGAACTCTGTGAAATCCT[T/C]AGCACAGTGGCTTCAAGAGGAGAAGGTGTGTTTATCTTAATAAATGTTCC
Long Flanking Sequence:
ATATAATGTATAGTAAGAATAATGTCATGTAGTGATTGTTATAAATTTAAAACAACCAGTTTCTATTTTAATATATTTCAAAATATTTTTACTCATGTGATGGTAAAGACATCTAAATTGTTCTAAAACTACTACTAAAAGACCTTGTAAAGTGCATCCCAGTTTTCTACATATACTGTATGATAATCTTTTTAACGCCATATCATTATTATCAATTGTATATTATCATTTCTTGATTTAATTTCTTAATAAGTTTTAATATTTCACAAAATATTTTACAAATTTGATACTGTATTTTGAGTTAAATAAATGTAGCTTTGCTGGTCATAAGATCGTGTAGAACATTACAACATTGAAAATATTCAAAACAGTTGATTGTGTATGTTTATCCCTTATCTCCAGTAATAATTTGTTTCAATATATTCGTTTTTGGAAGGTGTCAGGATTGCTGGTTCAGGATTATAGTGCTGAGTACAGCCACTGGAACTCTGTGAAATCCT[T/C]AGCACAGTGGCTTCAAGAGGAGAAGGTGTGTTTATCTTAATAAATGTTCCTAATTTCATTTACTTTTACAGTAAGTATTAAACAATTTGTTTTCTTGTGCCTGCAGGTGCCAGCACTTTTTGGCATAGATACCAGGATGCTGACAAAGATCATTAGAGATAAGGTTTGCATTGACACTACTTTTAAGTATGTACAATGTATCCTAAATGTATCATAAATGTATTAATTTGTTTCAAATAAGGGTACTGTTTTGGGGAAGATTGAATTTGATGGACAGCCAGTGGAGATCACAGACCCAAACCAGAGAAATCTTGTTTCTGAGGTCTCAACCAAGGTAACCAGCATACTTTATTATCAGCAGTGTTCATTGCTGTGCATTGCAGTTTCAGTGAGTGTTCACCCTCTTTCCCCTTGATTAAGGATATTCAAGTGTTTGGGAAAGGTAACCCCGTCAAAGTGGTTGCTGTTGACTGTGGAATCAAACACAACATTATAAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44709
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004742 | Nonsense | 959 | 1482 | 24 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40116404)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39254300 |
| GRCz11 | 9 | 39064095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTAATTATCCAATTTTTCTTTTTGTCCTTGTCGACAGGAGCATGATT[T/A]GGATTTTAAGGACCATGGCACCATGGTTGTTGGTTGCGGTCCATATCACA
Long Flanking Sequence:
TATAACAATGGTTTGTTCTGCAGACTATTGAAAAAAAATATAGCTTAAAAAGGGATAATAATTTTGACCTTAAAATGGATTAAAAAAATACTGCTTTTATTCTAGCTAAAATAAATCAAATAAGACTTTCTCCAGAAAAAAAAAATATATATTATCAGACTTACCGGAAAATTTCCTTGCTCTGTTAAACATCATTTAGGAATTATAAAAAAAATTAAAAATAATAAATAAATAAATAAATAAATAAATAAATAAAATCAAAGGGGGGGGGGGGGGGGTTGTTAATTTTGACTTCAACTGTATGTGTGGGAAGCACTGAGTTTTATAATTCTATTTTAAAAAAAATTATTGGATAATAAAGTAGAAAAAAATAGTAATTGTGAGCTAATAAAAAATCTAAATAAAAAATACAAGTCAAAAATAAAATAAAAGATAAGCATAAGAATAAACCCAGTAATTATCCAATTTTTCTTTTTGTCCTTGTCGACAGGAGCATGATT[T/A]GGATTTTAAGGACCATGGCACCATGGTTGTTGGTTGCGGTCCATATCACATCGGTGAGCTGAAATCTATTTTTTTTAACCCTAATAATCCTGTGATTTTTCAATTCACACCAACCCGTTAATGTACTGTCTTCATTAGTTTTAATGAGCAATTAGTGCAGGAGTGTGTCAGGCTAGCGTTTGGCTTCTCTCCCCCACAGGCAGCAGTGTGGAGTTTGACTGGTGTGCCGTGTCAAGCATTCGTGCCCTCAGACAGATGGGCAAGCGTACAGTGGTGGTGAACCATAACCCGGAGACGGTCAGTACGGACTTTGATGAGTGTGACCGTCTGTACTTTGAGGAATTAACCCTGGAGCGCATCCTGGACATCACACAGCAGGAGGTGAGAGGTCAAAGCTCAGTCTGGGCATCTGGTGCGTTTACTTTAACTGAAAGGTGTTATTGACTTTCATGTTTGACAAGGGCATTGTTACCATGCGGTCAGATTTCTGAAAATTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34714
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000004742 | Essential Splice Site | 1150 | 1482 | 28 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40150386)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39288282 |
| GRCz11 | 9 | 39098077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAGGATGAGATGAAACGTTTCCTGGAGGAAGCCACACAGGTTTCACAG[G/A]TGAGCTCTGAAGATTTAGCCATTTGGACCTTTGCCACAAAAAAAAAAAAA
Long Flanking Sequence:
TTGTTCATAATTAGTTTATGTTAGTAAATACCTTGACTAATGAAACCTTTTTGTAAAGTGAGACAGAATCATTGTTTGATGATTTGTCTATTTATTTTAAGACTTACTGTCAGTCATAGACATCTAGTGATACCACCAATGTGAGCTGCAGGGCTGATGCCTTTAGAATCACCCACAAAATCAGTAAAAAAAAAAAAAAAATCCCCTCTCTTAATATGAAAAAATTCATTGCTGATCGCCTAGAGGAGCAGCTGACCCAAATATAATTCTCTTGTCGGCTTTTTGCCTCTTTCTTTCTGCATATCTTCCTTTCTTTTCTATTTGACTCTACAACCATTGAAGCATGTTTTTTGTTTTATATTATTTCCTGATGGGTTCATTTAAGTGTCAACGTGATGAATGATGAGACTTTCTCCTTTTTCAGTGGCTCAGCTATGAATGTGGTTTACGGTGAGGATGAGATGAAACGTTTCCTGGAGGAAGCCACACAGGTTTCACAG[G/A]TGAGCTCTGAAGATTTAGCCATTTGGACCTTTGCCACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACTTGAGTGAAGAGCTTTGGGTTTGTCATATGAATCAAGCAATGGATTAGGCAAGAATATGCACCAATTTTTGCTCATTAACTCACATGAATGCTCTTGAAATGATTCCTCAAATATATCCTGTGGAAATAAATACTCCAAAGCACTTACAATTTTTTAAAGGCAAACAAAGCACATTTGCAGCAGCTCCAGTTATCATGTATCTCAGGGCCAGTATTGATTTTCATCCTGTGTTCCTGTTGCCCCTTACAGTATTTTATTTAAGAAAGTTCAGTAGTTTCCAGCAAAATCACTTTATCATCATGTTTTCCATGAATGGGCCAATATTGAGTGCATAAGCCAAAATTGACAGTAATCTAGTTTTAACTTTATGTACAGTGCATCTGGAAATTATTCATAGTGCTTCACTTTTTGCACATTTTTATGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18960
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 |
|---|---|---|---|---|---|
| ENSDART00000004742 | Nonsense | 1161 | 1482 | 29 | 38 |
| ENSDART00000004742 | Nonsense | 1161 | 1482 | 29 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40152210)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39290106 |
| GRCz11 | 9 | 39099901 |
KASP Assay ID:
2260-2234.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCATTTTCTCTAAAACAGGATCATCCTGTGGTCATCACCAAATTCATC[C/T]GAGGTGCCAGAGAGGTGGAGGTTGATGCGGTGGCCAGGATGGGCAAGGTA
Long Flanking Sequence:
TTGCAGCAATTTCAAAAAAATCTTTTTTTACATTGTCATTATGGGGTATTGTGTGTAGAATTTTGATGAAATAAATTAATTTAATCCATTTTGGAAAAAGGCTGTAACATAAAAAATGTGGAAAAAGTGAAGTGATATGAATACTTTCCAGATGCACTGTACAGTAGTCAAACCTCTTGTTTGGCTGTCATAAGACTGAGAAACAGAATACAGTAAAACATTAGTTCTGCAAAACATTATATTTATGTTTGTTAAAGTAACAGGATGAGCCTGTTAGTCAGGCTTTAAGAGACGGTTAGATATTCAGCAAAGCACTTCAGAAACTCTATCCTTTTTAATTTACAGCTTAACAAGGGGGCTTAACTAGAATGAATCTTTGATTTAGATTTCAATGTAGTGCTTTTAGTGTCATTGCAGTATTCTTAGGAAACATTTCTTAGCCAGCATTTACAGCATTTTCTCTAAAACAGGATCATCCTGTGGTCATCACCAAATTCATC[C/T]GAGGTGCCAGAGAGGTGGAGGTTGATGCGGTGGCCAGGATGGGCAAGGTAAGAGAGATGCTAGAACTGTTTTTCAACAGTTATTGAACAGAAATCTGTCTAAAACTGAAAAGCGGAATGTGGAAAGTTTGATTTAACTTTGAAATAGTCTAAAATTGTTTTGCTAAATAAAAAAAAAATATAAAAAATCCATGTTGCTATTTGCTATATCGTGGATTTGATAGTGTAGAGGACGCAGTTTATTGCATGAGAGTTTTTAGAACATTATTCTATTCCACACACCCACACATAATAAAAATAAAATAAGAGATGGCTCAGGCTGCTTCCATCTGGAAAATTGCTTGCAATATGTTCTGGCTCTTTTGTTTCATCCATTATTTCTCACCTAATCTCTGTGCAGAGTACAATTAAAAGTATGAAGTCATGTTTATTTTGCATTTCACTGGGTATAATCTTAAATGTTGGCTGTTTTGCTTTGAACTACACTAATAGAAAAATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10807
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 |
|---|---|---|---|---|---|
| ENSDART00000004742 | Nonsense | 1161 | 1482 | 29 | 38 |
| ENSDART00000004742 | Nonsense | 1161 | 1482 | 29 | 38 |
Genomic Location (Zv9):
Chromosome 9 (position 40152210)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 39290106 |
| GRCz11 | 9 | 39099901 |
KASP Assay ID:
2260-2234.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCATTTTCTCTAAAACAGGATCATCCWGTGGTCATCACCAAATTCATC[C/T]GAGGTGCCAGAGAGGTGGAGGTTGATGCGGTGGCCAGGATGGGCAAGGTA
Long Flanking Sequence:
TTGCAGCAATTTCAAAAAAATCTTTTTTTACATTGTCATTATGGGGTATTGTGTGTAGAATTTTGATGAAATAAATTAATTTAATCCATTTTGGAAAAAGGCTGTAACATAAAAAATGTGGAAAAAGTGAAGTGATATGAATACTTTCCAGATGCACTGTACAGTAGTCAAACCTCTTGTTTGGCTGTCATAAGACTGAGAAACAGAATACAGTAAAACATTAGTTCTGCAAAACATTATATTTATGTTTGTTAAAGTAACAGGATGAGCCTGTTAGTCAGGCTTTAAGAGACGGTTAGATATTCAGCAAAGCACTTCAGAAACTCTATCCTTTTTAATTTACAGCTTAACAAGGGGGCTTAACTAGAATGAATCTTTGATTTAGATTTCAATGTAGTGCTTTTAGTGTCATTGCAGTATTCTTAGGAAACATTTCTTAGCCAGCATTTACAGCATTTTCTCTAAAACAGGATCATCCTGTGGTCATCACCAAATTCATC[C/T]GAGGTGCCAGAGAGGTGGAGGTTGATGCGGTGGCCAGGATGGGCAAGGTAAGAGAGATGCTAGAACTGTTTTTCAACAGTTATTGAACAGAAATCTGTCTAAAACTGAAAAGCGGAATGTGGAAAGTTTGATTTAACTTTGAAATAGTCTAAAATTGTTTTGCTAAATAAAAAAAAAATATAAAAAATCCATGTTGCTATTTGCTATATCGTGGATTTGATAGTGTAGAGGACGCAGTTTATTGCATGAGAGTTTTTAGAACATTATTCTATTCCACACACCCACACATAATAAAAATAAAATAAGAGATGGCTCAGGCTGCTTCCATCTGGAAAATTGCTTGCAATATGTTCTGGCTCTTTTGTTTCATCCATTATTTCTCACCTAATCTCTGTGCAGAGTACAATTAAAAGTATGAAGTCATGTTTATTTTGCATTTCACTGGGTATAATCTTAAATGTTGGCTGTTTTGCTTTGAACTACACTAATAGAAAAATGTG
Associated Phenotype:
Not determined