ZMP
aldoab
Ensembl ID:
ZFIN ID:
Description:
aldolase a, fructose-bisphosphate, b [Source:RefSeq peptide;Acc:NP_998380]
Human Orthologue:
ALDOA
Human Description:
aldolase A, fructose-bisphosphate [Source:HGNC Symbol;Acc:414]
Mouse Orthologues:
Aldoa, Aldoart1, Aldoart2
Mouse Descriptions:
aldolase 1 A retrogene 1 Gene [Source:MGI Symbol;Acc:MGI:2447811]
aldolase 1 A retrogene 2 Gene [Source:MGI Symbol;Acc:MGI:1931052]
aldolase A, fructose-bisphosphate Gene [Source:MGI Symbol;Acc:MGI:87994]
aldolase 1 A retrogene 2 Gene [Source:MGI Symbol;Acc:MGI:1931052]
aldolase A, fructose-bisphosphate Gene [Source:MGI Symbol;Acc:MGI:87994]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22002 | Essential Splice Site | Available for shipment | Available now |
sa22001 | Nonsense | Available for shipment | Available now |
sa19021 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22002
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042200 | Essential Splice Site | 181 | 364 | 5 | 7 |
ENSDART00000042200 | Essential Splice Site | 181 | 364 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 4738451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4021173 |
GRCz11 | 12 | 4057938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACAGTGTGTCAGATGAATCATTTATATTCATTTCTGTTGCTGTGGTC[A/G]GCATGGTATTGTACCCATCGTGGAGCCTGAGATCCTGCCTGATGGTGATC
Long Flanking Sequence:
CGGAAAAGCGCAATATAAAAATGTAAGGAATTATTATTATTATTATTTTACTGTCTTTTCTTTATTACAAGTACGCACTGTTTTAAATACGTTTTAGTTTGAAGTTGTGAAAGTCATTCTTGATGTGCAGCTGATCACAGAGGGTTGGAACAGATCTTTTAATCCTAGTTTCTTTGCAAATCCTGTTCTGTGGATATGTTCATATGCGTTACTATGGAGACATGTTATCACGTGCCTGTCAATCAATTCGGTGGGCGGGGAAAACTGCACTCCTACATCACTTTGCGGTGAGCCTCAAAATCTCTAGGATTAGGATCCTATTTGGTCAGAAAATTGACTTATTGTGTTTATATCACACCAATATGACAGTGGACACACTATACCTACACACAGTCCTGTCTAAACAGCTTCCTAAAGTTGTTTTTCACATCATAGGTGGCCTTTAACATATGCACAGTGTGTCAGATGAATCATTTATATTCATTTCTGTTGCTGTGGTC[A/G]GCATGGTATTGTACCCATCGTGGAGCCTGAGATCCTGCCTGATGGTGATCATGACCTGAAGAGATGCCAGTACGTGACGGAGAAGGTTCTGGCAGCGGTGTACAAGGCTCTTTCAGACCATCATGTGTATCTGGAGGGAACCCTGCTGAAGCCCAACATGGTGACGGCCGGTCACTCCTGCTCCCATAAATACTCACCTCAGGAGATCGCCATGGCTACTGTCACAGCCCTGCGCCGCACCGTTCCACCTGCTGTCCCCGGTGAGCCCAAAAACACCCACAGTCACGCTTAAAGGGATAGTTCACCCAAAAATCCACCTTCTGTCATCATTTATTCACACTTATAAACTCGTTTCAAACCTTTATGAGTTTCTTTCTTTTGTTAAACACTAAATAAGATACTTTGAAGAATGCTGGGGGAAGCCATTGATTTCAATAGTATTTGTTTTTTCGACTATGGAAGTCAGTGGTTACAGGTTTTCAGCTTTCTTCAAAATATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22001
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042200 | Nonsense | 223 | 364 | 5 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 4738321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4021043 |
GRCz11 | 12 | 4057808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAAGGTTCTGGCAGCGGTGTACAAGGCTCTTTCAGACCATCATGTGTA[T/G]CTGGAGGGAACCCTGCTGAAGCCCAACATGGTGACGGCCGGTCACTCCTG
Long Flanking Sequence:
CTGATCACAGAGGGTTGGAACAGATCTTTTAATCCTAGTTTCTTTGCAAATCCTGTTCTGTGGATATGTTCATATGCGTTACTATGGAGACATGTTATCACGTGCCTGTCAATCAATTCGGTGGGCGGGGAAAACTGCACTCCTACATCACTTTGCGGTGAGCCTCAAAATCTCTAGGATTAGGATCCTATTTGGTCAGAAAATTGACTTATTGTGTTTATATCACACCAATATGACAGTGGACACACTATACCTACACACAGTCCTGTCTAAACAGCTTCCTAAAGTTGTTTTTCACATCATAGGTGGCCTTTAACATATGCACAGTGTGTCAGATGAATCATTTATATTCATTTCTGTTGCTGTGGTCAGCATGGTATTGTACCCATCGTGGAGCCTGAGATCCTGCCTGATGGTGATCATGACCTGAAGAGATGCCAGTACGTGACGGAGAAGGTTCTGGCAGCGGTGTACAAGGCTCTTTCAGACCATCATGTGTA[T/G]CTGGAGGGAACCCTGCTGAAGCCCAACATGGTGACGGCCGGTCACTCCTGCTCCCATAAATACTCACCTCAGGAGATCGCCATGGCTACTGTCACAGCCCTGCGCCGCACCGTTCCACCTGCTGTCCCCGGTGAGCCCAAAAACACCCACAGTCACGCTTAAAGGGATAGTTCACCCAAAAATCCACCTTCTGTCATCATTTATTCACACTTATAAACTCGTTTCAAACCTTTATGAGTTTCTTTCTTTTGTTAAACACTAAATAAGATACTTTGAAGAATGCTGGGGGAAGCCATTGATTTCAATAGTATTTGTTTTTTCGACTATGGAAGTCAGTGGTTACAGGTTTTCAGCTTTCTTCAAAATATTGTATTATTACGTATAAGTCAAGTCTCGCTTTCAGTTTCAGGCTCTGGCGCGTTTTGCACTCATACACAAGCGTACCGCGCCAAAGCCCAAGTGAACCGCTCGATTCAGCGCACTCACACTTCTCAAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19021
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000042200 | Nonsense | 302 | 364 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 12 (position 4737620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4020342 |
GRCz11 | 12 | 4057107 |
KASP Assay ID:
2260-4843.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCAACCAGTGTCCGCTGAGCAAACCCTGGGCCCTCACCTTCTCCTA[C/A]GGACGGGCCCTGCAGGCCTCCGCTCTTAAAGCCTGGGGAGGAAAGAAGGA
Long Flanking Sequence:
TTATTCACACTTATAAACTCGTTTCAAACCTTTATGAGTTTCTTTCTTTTGTTAAACACTAAATAAGATACTTTGAAGAATGCTGGGGGAAGCCATTGATTTCAATAGTATTTGTTTTTTCGACTATGGAAGTCAGTGGTTACAGGTTTTCAGCTTTCTTCAAAATATTGTATTATTACGTATAAGTCAAGTCTCGCTTTCAGTTTCAGGCTCTGGCGCGTTTTGCACTCATACACAAGCGTACCGCGCCAAAGCCCAAGTGAACCGCTCGATTCAGCGCACTCACACTTCTCAAATGATGTGGGAAACGGGCCTGGGCACAGTTCGCATAGCATAGTGTGAGAGAATCGTCCTAACTCCCCTTAATATTATCATCATCATCATCTTCCCAAAGGCATCACCTTCCTTTCTGGAGGCCAGAGCGAGGAGGAAGCTTCAATCAACCTGAGCACCATCAACCAGTGTCCGCTGAGCAAACCCTGGGCCCTCACCTTCTCCTA[C/A]GGACGGGCCCTGCAGGCCTCCGCTCTTAAAGCCTGGGGAGGAAAGAAGGAGAATGGCAAGGCCTGCCAGGAGGAATTCGTCAAGAGAGCCGTGGTATGTGAACTTGCATGAATTATTAGCCCTCCTGTACATTTCCTCCCCAATTTAGGCAAGTTAAGGTAATTAGGCAAGTCATTGTATAATGATGGTTTGTTCTGTAGATAATTGAAAATAAATACTGCTTAAGGGGGTTAATAATATTGACCTTAAATTGTTTTTTTTTTAAATAAAACTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTGTCTCCAGAAGAAAAAAATACTATAGGAAATACTGTGAAAAATTCCTTACTCTGTTGAACAATGATAATACATTTTTTTTAAATCACAGGATGGCATTTTGACTTCAATTAAGTATTTATACCCAATTAAAAGAGTACTATAGTAATTACAGCGAATACTATAGAATACTATAGAAAAGTAAAATAAAATGT
Associated Phenotype:
Not determined