ZMP
aldh1a2
Ensembl ID:
ZFIN ID:
Description:
retinal dehydrogenase 2 [Source:RefSeq peptide;Acc:NP_571925]
Human Orthologue:
ALDH1A2
Human Description:
aldehyde dehydrogenase 1 family, member A2 [Source:HGNC Symbol;Acc:15472]
Mouse Orthologue:
Aldh1a2
Mouse Description:
aldehyde dehydrogenase family 1, subfamily A2 Gene [Source:MGI Symbol;Acc:MGI:107928]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa16776 | Essential Splice Site | Available for shipment | Available now |
| sa2367 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa16776
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000075519 | Essential Splice Site | 300 | 518 | 8 | 13 |
The following transcripts of ENSDARG00000053493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 31670000)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30062342 |
| GRCz11 | 7 | 30333492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGGAGCTCGGGGGAAAGAGTCCCAACATCATTTTTGCAGATGCTGATT[G/A]TAAGTAWTCWGACACTGTTTTACGGCTGGCCTCCTGTTGTCCCGCTGCAA
Long Flanking Sequence:
ATTCAGTTCGGTTTAGTATAAATGTCACTGCGGTAATTCAGTTCAGATAATCTCAAGTACATGTGTTTTCATTTAGTCACTAACAAAGCCAATAAATGTATTTTTAGGGTCTTGTTTTACTGTTATTTTGTGACAGCGTCGAGCATCCTACACAAACCTGCGGTCAGATCTTCCTGTTCTCCATTAGCCAGCAGATACTGTTGCGTGCGGGACATTCCATCCTCCGCGAGCACTAATAGAAATTTAAGATGTGGGCTGAAGCTCAGGGGTCTGATAATGCTGCTGGTTGTCCAGTCAAAGAGCAGGGGACGATTTATTAATGACAGCGTCCCACAGATAGGGAGATTTAGTAAGGCTCCTCTGCTGTGATTAAGGCTCCTCGTCTCTGTCTCCACAGGTAGGCAAGCTGATCCAAGAAGCAGCAGGAAAGAGCAATCTGAAGAGAGTCACGCTGGAGCTCGGGGGAAAGAGTCCCAACATCATTTTTGCAGATGCTGATT[G/A]TAAGTATTCAGACACTGTTTTACGGCTGGCCTCCTGTTGTCCCGCTGCAACAGTTTGTGCACAGGTGCTGCTTCAGACTGTCACTTCACATCAAAGACCTTCAGGGAGCTTTTAGAGCTGCGTCTGAACCAAAGAAAGAAAAATCTTGAGTTTTGAAGAGGCATACCTGCATGTAAATGAGTCTCACTTCCTAAACTGCTGGACATTAGTGGCTGGATGTAGCCCACCAAACCAAGGCGCACGTCAGTGCTTTAAATGCTTTCAGCAGCCGCAAGCACAGCCCCCCATAAATCAGCTGAATGAACCACATCTCACTAGAACCGTAAATCTGCCTGCTCCATTAACCCGTCAAATGCCAAAGTCTGCCAGTCCAGCCTTTTCCCAGGTGTCTGTTATCTCACCCAGATGTACACATAAGCATGGATCTGTGCATAAACAGCAGACGCACCATAGAAAAACGTATTACAAATGCCTAAGCAGAATTCAATGGCTCCAAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2367
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 |
|---|---|---|---|---|---|
| ENSDART00000075519 | Essential Splice Site | 470 | 518 | 11 | 13 |
The following transcripts of ENSDARG00000053493 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 31666864)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 30059206 |
| GRCz11 | 7 | 30330356 |
KASP Assay ID:
554-2940.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAGCAAGGCCATGACCATCTCTGCAGCAGTGCAGGCYGGCACCGTCTG[G/A]TAAGACAAAAACTTACACAAAAGTCACAAAAAAKATRGATAGCCAAATCA
Long Flanking Sequence:
TGATATTTGTTTAAGTCAAAGTAGGAGTTTTATCAGAATTTGAAGAAAAGCTGTACATTAATAATGATTGACAAATGTGTGTGTGTGTGTTTGTGTCAGGTGAGCGAGGAGCAGCAGAGACGTGTGCTGGAGCTCATCCAGAGTGGCATCACTGAAGGAGCCAAACTGGAGTGTGGAGGCAAAGCTCCTCCTACTAAAGGCTTCTTCGTGGAGCCCACAGTTTTCTCTAATGTGAAGGACCACATGCGCATCGCCAAGGAGGAGGTCTGATTTATTTTTTTTCATCTCTAAATAATCAATCTAAATTCAAATGGTTAACTAAAACAACTACTTTTTTTGTAGATATTTGGGCCAGTGCAGCAAATCATGAAGTTCAAAACAATTGAAGAAGTGATTGAGAGAGCCAACAACACAGAATACGGTCTGGCAGCGGCCGTCTTCACCAGAGATATCAGCAAGGCCATGACCATCTCTGCAGCAGTGCAGGCCGGCACCGTCTG[G/A]TAAGACAAAAACTTACACAAAAGTCACAAAAAAGATGGATAGCCAAATCATTGGCAATATCTTTCAAAAAACTAGATTCCAACCATTTGTCACCAAAAGACTTTAAATGTGTAAAAAAATTAATACAAATACTATGATTGTGGTTTTATTTTTACATTACAGTTTTTTTCAATTGCTTTGGCTCATTTCTTGATAAATTTTATTTTTCAAAACCACATGTTCAGCTCTTTAAACAATTAGCTTATTGTTCACTTCAGATTGTCATTTTTTTTTATTTAAGCACATGTGTGCAAAGAGTAAGCACAGTTGTCTGCAGTTTGGACAAAAACTAATTACATATGGCTTGTTGATCAAAACTGAGTCGATTCTTATTTAAATTGGTAAACTCTTCATAACTTCTCAATAATTTTTCATTGTGTAAGCCATCAAACTCAAAACAATTAACTCAGTTGTCAAACACGTTTACACCACAAATCAACCAAAATGTCGTGGAAGAGCAA
Associated Phenotype:
Not determined