ZMP
pcca
Ensembl ID:
ZFIN ID:
Description:
propionyl-CoA carboxylase alpha chain, mitochondrial [Source:RefSeq peptide;Acc:NP_001002746]
Human Orthologue:
PCCA
Human Description:
propionyl CoA carboxylase, alpha polypeptide [Source:HGNC Symbol;Acc:8653]
Mouse Orthologue:
Pcca
Mouse Description:
propionyl-Coenzyme A carboxylase, alpha polypeptide Gene [Source:MGI Symbol;Acc:MGI:97499]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1201 | Essential Splice Site | F2 line generated | Not yet available |
sa5937 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17977 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1201
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 |
---|---|---|---|---|---|
ENSDART00000034097 | Essential Splice Site | 432 | 709 | 15 | 23 |
ENSDART00000133905 | Essential Splice Site | 444 | 721 | 15 | 23 |
ENSDART00000135252 | None | None | 152 | None | 7 |
ENSDART00000136786 | None | None | 159 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 28854758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 29105587 |
GRCz11 | 1 | 29909518 |
KASP Assay ID:
554-1110.1 (used for ordering genotyping assays)
KASP Sequence:
TTCAAGAAGGAAGCGACATCAGTATTTATTATGACCCTATGATTTCTAAG[G/A]TAATCAATGACCATCATGAAAGTCTAATTTCAATTAAGATGTCAGTTTGT
Long Flanking Sequence:
TTTTTATTTTAGAAATCCACACACATAAAGGGATACAGATGAGCTTTAAATGTCTAAAGAAAGCAAACATCACTGAGGAGATTAACAATGGTCTTTTATTTGTAGGTAGGGCCAAAAAAGATAACATTGTGTGATGTTCTTAGTGGTTATTTATAGTTTTGTGTTGTTTTGAAGGGTTAGTTCACACACAAATAAAAAAAAAATTTGCTCACCATTGACCCTTAAGTGGTAATTTTTTGTGTGTTAAATGCTAAAAATTATTGTTTGAAGAATGTTGGAAACTTACAACTATTGGAATCCATAGTATAAAAAAACTACCATACTATTGAAGTATTTATTAGAACTATCCCTAAGGTGAGGGTTAAAGTATGTAAGTAAATACTTCATGTGTAAGTGTTTTAATTCGATTTTTTTTTTTGCTTCTCCTGTAGGTTCGAGTGGACAGCGGAATTCAAGAAGGAAGCGACATCAGTATTTATTATGACCCTATGATTTCTAAG[G/A]TAATCAATGACCATCATGAAAGTCTAATTTCAATTAAGATGTCAGTTTGTTTCATTTTATATATTGTTTTATAGCTGGTCACGTATGGCAAAACACGGGAGGAAGCTCTGAAGAAAATGGAAGAAGCACTTGATAATTACGTGGTCAGAGGTAAATGGCCTCCGAAAGAATTATGACAAATGAAGGTGAAAACATTTCAGATCATAGACTGCTTCTCTTGTTGGCACAGGTGTAACACATAACATACCTCTACTGAGAGAGATCATTGTTCATCCTCGGTTTGTGTCTGGTGATATCAGTACTAAGTTTCTCCCGGAGGTGTATCCTGATGGGTTCAAAGGTCACATGTTAACAGCAGGAGAAAGACAGGAGCTGCTTGCTACGGCTGCGGCACTCTATACAGCAGCACAGCTCCGCTCTCAGAGGTTCCTGGGGGATCTCAGGTGAGACAAAGATGGAGCAACTTCCAGCTAGGGATATATTTTACACTCTTTTGTCAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa5937
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034097 | Essential Splice Site | 458 | 709 | 16 | 23 |
ENSDART00000133905 | Essential Splice Site | 470 | 721 | 16 | 23 |
ENSDART00000135252 | None | None | 152 | None | 7 |
ENSDART00000136786 | None | None | 159 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 28854910)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 29105739 |
GRCz11 | 1 | 29909670 |
KASP Assay ID:
554-3742.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGCTCTGAAGAAAATGGAAGAAGCACTTGATAATTACGTGGTCAGAGG[T/C]AAATGGCCTCCKAAAGAATTATGACAAATGAAGGTGAAAACATTTCAGAT
Long Flanking Sequence:
ATAGTTTTGTGTTGTTTTGAAGGGTTAGTTCACACACAAATAAAAAAAAAATTTGCTCACCATTGACCCTTAAGTGGTAATTTTTTGTGTGTTAAATGCTAAAAATTATTGTTTGAAGAATGTTGGAAACTTACAACTATTGGAATCCATAGTATAAAAAAACTACCATACTATTGAAGTATTTATTAGAACTATCCCTAAGGTGAGGGTTAAAGTATGTAAGTAAATACTTCATGTGTAAGTGTTTTAATTCGATTTTTTTTTTTGCTTCTCCTGTAGGTTCGAGTGGACAGCGGAATTCAAGAAGGAAGCGACATCAGTATTTATTATGACCCTATGATTTCTAAGGTAATCAATGACCATCATGAAAGTCTAATTTCAATTAAGATGTCAGTTTGTTTCATTTTATATATTGTTTTATAGCTGGTCACGTATGGCAAAACACGGGAGGAAGCTCTGAAGAAAATGGAAGAAGCACTTGATAATTACGTGGTCAGAGG[T/C]AAATGGCCTCCGAAAGAATTATGACAAATGAAGGTGAAAACATTTCAGATCATAGACTGCTTCTCTTGTTGGCACAGGTGTAACACATAACATACCTCTACTGAGAGAGATCATTGTTCATCCTCGGTTTGTGTCTGGTGATATCAGTACTAAGTTTCTCCCGGAGGTGTATCCTGATGGGTTCAAAGGTCACATGTTAACAGCAGGAGAAAGACAGGAGCTGCTTGCTACGGCTGCGGCACTCTATACAGCAGCACAGCTCCGCTCTCAGAGGTTCCTGGGGGATCTCAGGTGAGACAAAGATGGAGCAACTTCCAGCTAGGGATATATTTTACACTCTTTTGTCATTTCGCTAAAGGAATTTGTGCAGCATATTATTACAACTAATGTGACATCGTTGAGAAAACAAAAGTTAAGAAAGCATCTAGCATCAAGTTAATTTACAGACAAAATTATCAACCCTGAAATTTAAATTGTTTTTTTAAAATGTTTTCCAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17977
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 |
---|---|---|---|---|---|
ENSDART00000034097 | Nonsense | 514 | 709 | 17 | 23 |
ENSDART00000133905 | Nonsense | 526 | 721 | 17 | 23 |
ENSDART00000135252 | None | None | 152 | None | 7 |
ENSDART00000136786 | None | None | 159 | None | 7 |
Genomic Location (Zv9):
Chromosome 1 (position 28855157)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 29105986 |
GRCz11 | 1 | 29909917 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTAACAGCAGGAGAAAGACAGGAGCTGCTTGCTACGGCTGCGGCACTCTA[T/A]ACAGCAGCACAGCTCCGCTCTCAGAGGTTCCTGGGGGATCTCAGGTGASA
Long Flanking Sequence:
TAATTCGATTTTTTTTTTTGCTTCTCCTGTAGGTTCGAGTGGACAGCGGAATTCAAGAAGGAAGCGACATCAGTATTTATTATGACCCTATGATTTCTAAGGTAATCAATGACCATCATGAAAGTCTAATTTCAATTAAGATGTCAGTTTGTTTCATTTTATATATTGTTTTATAGCTGGTCACGTATGGCAAAACACGGGAGGAAGCTCTGAAGAAAATGGAAGAAGCACTTGATAATTACGTGGTCAGAGGTAAATGGCCTCCGAAAGAATTATGACAAATGAAGGTGAAAACATTTCAGATCATAGACTGCTTCTCTTGTTGGCACAGGTGTAACACATAACATACCTCTACTGAGAGAGATCATTGTTCATCCTCGGTTTGTGTCTGGTGATATCAGTACTAAGTTTCTCCCGGAGGTGTATCCTGATGGGTTCAAAGGTCACATGTTAACAGCAGGAGAAAGACAGGAGCTGCTTGCTACGGCTGCGGCACTCTA[T/A]ACAGCAGCACAGCTCCGCTCTCAGAGGTTCCTGGGGGATCTCAGGTGAGACAAAGATGGAGCAACTTCCAGCTAGGGATATATTTTACACTCTTTTGTCATTTCGCTAAAGGAATTTGTGCAGCATATTATTACAACTAATGTGACATCGTTGAGAAAACAAAAGTTAAGAAAGCATCTAGCATCAAGTTAATTTACAGACAAAATTATCAACCCTGAAATTTAAATTGTTTTTTTAAAATGTTTTCCAAGTAATGTTTAACTGAACAAGGAATATTTTTCACAGTATTTAGTATTATAATTTTCTTCTAGATATATTCTTATTACTTGTAGTTTGGTTGTAATAAAAAAAAAAAAAACAATATATAATGAACAAGACATTGTCGTCCAATTAATTTAACTTGCCAAGGCAACCTAATTAACGGTAATGTTTAAATTGCCCTTTAAGCTGAATACTAGTGTGTAGCAGTCACTAGTAAATTATTATATACTGTCATCATG
Associated Phenotype:
Not determined