Busch Lab

ZMP

aldh3a2

Ensembl ID:
ENSDARG00000028259
ZFIN ID:
ZDB-GENE-040718-74
Description:
fatty aldehyde dehydrogenase [Source:RefSeq peptide;Acc:NP_997814]
Human Orthologues:
ALDH3A1, ALDH3A2
Human Descriptions:
aldehyde dehydrogenase 3 family, member A1 [Source:HGNC Symbol;Acc:405]
aldehyde dehydrogenase 3 family, member A2 [Source:HGNC Symbol;Acc:403]
Mouse Orthologues:
Aldh3a1, Aldh3a2
Mouse Descriptions:
aldehyde dehydrogenase family 3, subfamily A1 Gene [Source:MGI Symbol;Acc:MGI:1353451]
aldehyde dehydrogenase family 3, subfamily A2 Gene [Source:MGI Symbol;Acc:MGI:1353452]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa35869 Nonsense Available for shipment Available now
sa5879 Nonsense Mutation detected in F1 DNA Not yet available
sa18111 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa35869
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031625 Nonsense 29 488 2 11
ENSDART00000133948 Nonsense 29 116 2 3
ENSDART00000141746 Nonsense 29 195 2 5

The following transcripts of ENSDARG00000028259 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 19799933)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 20902559
GRCz11 15 20838291
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGGCGTTCTTGACCGGAAGATCCAAATCCCTGGACTACAGAATCAAA[C/T]AACTTAAAAACCTAAGTCGATTCATTAAAGAAAGAGCAGCAGACATCACT
Long Flanking Sequence:
CTTGTAGTTATCTTAAACCACATATGAACCAAGAGAGTTTAAGTAAAGTTATTTTTTTATTTTTGATCTACAAAGACGTTTAGTATACAGTGGTAATACTGGAGTAAAGAAAAACATTCCCAAACGAATAAAGTATGACAATCACAGTCAACTACTAAAGTACCTCTATTAATTTGTAAAAGTGATGACGTTGAACTTATACAATTCATAGAAACAGCAAATGTTAGCTAAATCATAAACAAGCCAATGCTTCAAAGTGGCAAAGTACATGTTGCGAAATATGCTCGCTGAACTTACTTTGATATTTTTTTTGTTTGTTTCCATTTATATCTCACCCTAGGAATAAAGATTAACTCTTCACCTTTATTTTATTATCTTTCAGCTCATTGAATCACAGACCAGACTGACTCTTAACGATGTCTCGAGAGCAGCTTGCTGTTCAACAGGCCAGAAAGGCGTTCTTGACCGGAAGATCCAAATCCCTGGACTACAGAATCAAA[C/T]AACTTAAAAACCTAAGTCGATTCATTAAAGAAAGAGCAGCAGACATCACTAATGCCCTGAGAAAAGACCTCTATAAGGTGAATCAAAATTGCCAGCTCTGCATATTCTGTTTGGATGATTAACTGGGTTGAACGTAATGTCTGTGTTTTTGTAGAGCGCAAACTCAACACAGTTGTTTGAGATCCTTGGCTTGGAGGGAGAGATCAATCTGGCTGTCAGCAAACTGGCTGAGTGGGCAGCACCTCGTCCTGTGAATAAAAACCTTCTGACCATCTCAGACGATGTGTTCCTACAGCCAGAGCCTCTTGGTGTTGTGCTCATCATTGGGGCGTGGAACTATCCAATAGCAGTTACCCTGCAACCCCTTGTTGGTGCCATTGCTGCAGGTGAAGCATAAACCTACCTTATGTTGACATTATTGTTAGAGTCGTGAGACTACAAGTTTAAAGAAATAAGTCCAAAAAGCGTCATTAAAGTCTGCAAGACATTCAAATTTACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5879
Status:
Mutation detected in F1 DNA
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
ENSDART00000031625 Nonsense 248 488 6 11
ENSDART00000133948 None None 116 None 3
ENSDART00000141746 None None 195 None 5

The following transcripts of ENSDARG00000028259 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 19797614)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 20900240
GRCz11 15 20835972
KASP Assay ID:
554-3665.1 (used for ordering genotyping assays)
KASP Sequence:
ACTTGGGGAAAGTATTTGAACTGCGGTCAGACCTGCATTGCTCCTGATTA[C/A]ATCCTCTGTGAATCCAGCATCCAAGACAGAGTCATCGATGAGATCCAGAA
Long Flanking Sequence:
AGCGTTATGGAGCTCATGTCTCTCTATCTGGATTCTGTAAGAATTCATTCAGTGAAACTGATTATAAATTATTTTACCTGTTTAATTAATCTAAAGTAGTTCTTAATGTGTACAGGAGATGTATCAGGTGGTGACAGGAGGGGTTCCAGAGACTCAGGAGCTGCTGAAGCAGCGTTTTGACCACATCTTCTACACTGGAAACAGCACAGTGGGCAAACTGGTTATGGAAGCAGCTTCTCATCACCTCACACCAGTCACTTTAGAACTGGGTGGAAAAAGCCCCTGTTATATTGACAAGAACTGTGACATTAGAATTGCTTGCCGGTGAGTTTGCCATCATCAGCTTGAATCTAAATAAACACAGATCATTTGGGTTAAATGTTAATATTAATCAATCAATTTCATCAATATAATGCTGTCCATCATTGTTCTTAAATTCTCAGTCGGATTACTTGGGGAAAGTATTTGAACTGCGGTCAGACCTGCATTGCTCCTGATTA[C/A]ATCCTCTGTGAATCCAGCATCCAAGACAGAGTCATCGATGAGATCCAGAAATGCATCAAGGTGGGAATTTAGATGTAGTTTGACAGTGGACTTTTTGTCTTGATTAGGTTTATTTGCATGCAATTATTTTCCTCAGTCTTGAAGGTATTCAGTAAGTTTTTGGATTCTAAAAGCTTCATTTATGCATCCTATCTCTGCGTAAAGAGTATTTTTTTTCTCCTCTTCCTATTATTTATATCTCATTAGCAGTTTTTCTGCAAAACAACAATTCATTCTAATATATAACAGGTAGAAGAATGTCCACACTTTTTACTTTATTACATGTATTGAACTTCACATATGTGCCCAGTTAGGTTCTGAAATAAATAAAAGTCACCAAAATAATGTTACTGCCAGAGCTACAACGCAACATAATTGATATTCTTAAAGCCTGCAATGGCATGTATGTGTGAGGGTAGTGTTTATGTTTGTCCAAATCCTACATAATACGAATGCAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18111
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000031625 Nonsense 439 488 10 11
ENSDART00000133948 None None 116 None 3
ENSDART00000141746 None None 195 None 5

The following transcripts of ENSDARG00000028259 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 15 (position 19794451)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 20897077
GRCz11 15 20832809
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCACCTTCGCAGCTGTCTTATTAAGAARCTGAACATGGAGGCAGTGAAT[C/T]AGATGCGCTACCCGCCCCATACAACTGAGAAGTTACGCTGGGCCCGTGTT
Long Flanking Sequence:
TAAGAGATGTGAAGCCAGCATCAAAAGTGATGCAGGAAGAGATCTTTGGGCCAATTCTGCCTATCGTCACTGTCAATGGCTTAAAAGAAGCCATTGAGTTCATCAACGATCGAGAAAAGCCACTAGCTCTCTATGTCTTCTCTTCTAGTAAAAAGGTAGAGCGCTACATCATTTCCACCTCCATTCAAACGGCAATTTAACAACTTGCATTTTCTCACAGGTCATTAAACAGATGATATCAGAGACGTCTAGCGGTGCGCTCTTAGCCAATGACTGCATGGTGCATTTCACTCTAAGTGATTTGCCTTTTGGAGGGGTTGGTGAGTATCGTTCATATTCATGGCTTTCTGATTCAGGAAAAGAACTGTCAGACAATGATTTGTTGTATTATTTTAACAGGGTATAGTGGAACCGGTCGTTACCATGGTAAATACAGTTTTGATCAGGTCAGTCACCTTCGCAGCTGTCTTATTAAGAAGCTGAACATGGAGGCAGTGAAT[C/T]AGATGCGCTACCCGCCCCATACAACTGAGAAGTTACGCTGGGCCCGTGTTCTTCTCTTGAAGCAAATAAATGTGACTCGGTGGCGTCAGATGGCACAGGTTGCTGTACTTGCAGCACTTGCTGCTTTTGTGGTGAAGGTGAGATTTTTCTTCTGTTACTTGTGTAAATGTACTTGGGTAAATGTATTAATTAGGATTTAAACATTTAATTAAAGATATTTAATAACACCTGCTAATTGATAAACTGTATATGAGCAGTTGCTTAAAGTAGTGTGTAAGCAAGTATTTTACAGTACTTTAAAGACTCATGTCTCTGTAAATGTTTTCAAACTATTATATTTCATTTACCAAAGTCACACAAGTGGCAATTTCACATCTGTCACATCCATAACAAAGCTTTTTCCTCACAAATGCAAAAATGTAAAGTAAAATACAATCAATAATTTTTGATCTATATGGAGCCAACTCTTATCCTTTTGATTAGTATTGTTTCTTTGGGGT
Associated Phenotype:
Not determined