ZMP
aldh7a1
Ensembl ID:
ZFIN ID:
Description:
alpha-aminoadipic semialdehyde dehydrogenase [Source:RefSeq peptide;Acc:NP_997889]
Human Orthologue:
ALDH7A1
Human Description:
aldehyde dehydrogenase 7 family, member A1 [Source:HGNC Symbol;Acc:877]
Mouse Orthologue:
Aldh7a1
Mouse Description:
aldehyde dehydrogenase family 7, member A1 Gene [Source:MGI Symbol;Acc:MGI:108186]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45400 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1371 | Essential Splice Site | Available for shipment | Available now |
sa41611 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45400
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 |
---|---|---|---|---|---|
ENSDART00000122540 | Nonsense | 118 | 541 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 16048649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16061956 |
GRCz11 | 10 | 16020075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTATGTGTTATTTAGGTACCTGCTCCAAAGAGAGGGGAAATTGTTCGA[C/T]AGATTGGAGAGGCTTTAAGGAGGAAGATCAAAGCTCTCGGCAGCTTAGTA
Long Flanking Sequence:
ACACATTTCATTTCATTACTTCAAGTAAAATAATGAAAAGTTACAAGTGTTTTTCTAAGGCTACACAGCTGTTTAGTCCCAGTCCCTTGGGTTCCCATTTCATTGTGTGTAGAAATACTTCTACGTTCACTATTAAAGATGGCTGTAAAGCTTCTTTTTTATCATTCATTCTGGTTCATTCTGCTGTGGTGACCCCTGAAAAATCAGGGACTAATCTGAAGGAAAATTAATGTATGAAACTAATTAACATTTGCTCTATGTTTTGTTTTGACATGATTGTTAAAAAAGACAAGAAGATACTCTGTGTCAGTTAGGATTCTGTTACTTTCTGAAACATAATCATCTATGCAGTAATTACCTAATGGAGGCTCTTACCTATTTGCTTAGTTAAATTCAGGTGGTTACATTCTTTTTTTTGGACTGTGTATATGCAAAAACAATGCTGACTAATGCTATGTGTTATTTAGGTACCTGCTCCAAAGAGAGGGGAAATTGTTCGA[C/T]AGATTGGAGAGGCTTTAAGGAGGAAGATCAAAGCTCTCGGCAGCTTAGTAAGTTTGCATTACAGTAATTGTATTCACAGGATTGAGGAAAAGTGCAGAAGTTTTACAGGAGTTTGCTATGCGTAGGTGTCTCTAGAGATGGGCAAGATCTATGTGGAGGGTGTTGGTGAGGTGCAGGAGTATGTGGATGTGTGTGACTATGCTGTAGGACTGTCCCGTATGATTGGAGGTCCCATTTTGCCATCTGAAAGTGAGCGTACTTTGTTACACTTTCAGAAAAATATGACTGTGGTTGTATTGAGACAAACTTGGAAACTGAGTGTTGTTTACCTGTGATCTAAGGGCCAGGTCATGTGCTGATCGAGCAGTGGAATCCTGTTGGCTTGGTAGGAATCATCACAGCCTTTAACTTTCCTGTGGCTGTATATGGCTGGAACAATGCCATTGCTCTCATCTGTGGAAATGCCTGTCTTTGGTTAGACTTGACTTTTCTCATCGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1371
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122540 | Essential Splice Site | 293 | 541 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 16045925)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16059232 |
GRCz11 | 10 | 16017351 |
KASP Assay ID:
554-1283.1 (used for ordering genotyping assays)
KASP Sequence:
AGCACTCATGTGGGCAAACAAGTGGCAATGATGGTACAAGAACGGTTTGG[T/C]GAGTTTTATGCATTACAATAGAATTTAATCGCAGTCTGTCATAATGTTTT
Long Flanking Sequence:
GCATTTAAAAAAAACTTTTGTCTGAGAATTTATGTATCTACTTTTATTTATTAATCGCTCAAAATGATCTATAGCTAAGCTGGTGTGTTTTTGACTTTTAGGTTTGTATTGTTTTCTGTTATATACTTGACCTTTTTAAATCTCTCATATTCTATTGTAGGATTGTAGCTGAAGTTTTGGAGCAGAATCATCTTCCTGGTGCAATCTGTTCTATGACATGTGGTGGCGCTGACATTGGGTATTTGACAAATATATGAAATTGAGCACTAAAGCATTTGTAGTCTTATGAGTGTTAGTACTCTTTTTGGCAGTTCACAGGTGCATTATAAACGTTTAGACTGCCACCTACTAAACTTGTACTGTACAGAGAAAATTGTTTAGTTGGTTATGCGTGTTTGCAGCATGGCCATGGCTAAAGACGAGCGAGTGGGTCTTCTGTCCTTCACGGGTAGCACTCATGTGGGCAAACAAGTGGCAATGATGGTACAAGAACGGTTTGG[T/C]GAGTTTTATGCATTACAATAGAATTTAATCGCAGTCTGTCATAATGTTTTGATGGCAAACCCAAATCCTCTTTATTGACTGAAAATGAAACAGCATCTTTATATTAGCATTGCTACAATATGTCTCATGCTACCAAACCCACTAAGTTAACACAATAGTGAGTATATATTAAGATATTACCTGCTTTGATATTATTGCATGTGCTGATTTAGTGTATTTTTGATATTTACACAAAAATGACAAAATCATTAGTTATTAGTTTTTATAGCTCAAATTGAAAATGCATAGAGTGAGAACTAAAAACAACACATGTTAGATATTTTTGCTTGCTGCATGTGTGTTCTGTGCACCTTGCATTGTAGAGAGCTGTGAATTAAAAGCTTCTGTCACCGTCAAAACAAACAATCACTTTTAATCATAAGCCTGTCTCACTGCAGGCATTCTCCCGTTGAAACACAAAGTATGATTGTACTGATTCATGTAATTTCCTGTTGTCACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41611
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 |
---|---|---|---|---|---|
ENSDART00000122540 | Essential Splice Site | 498 | 541 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 16038489)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 16051796 |
GRCz11 | 10 | 16009915 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGAACGTTAACATTCCTACTAGCGGTGCTGAGATTGGAGGAGCGTTTG[G/A]TGCGTATATTATACACCACACCATTCTAAAATTAACTAACTAAACTTACA
Long Flanking Sequence:
TTTATTTGACAGATCATGGATCGGCCGGGTAACTATGTGGAACCCACTATTATCACTGGACTACCGCACAATGCTTCTATAGTTCACACTGAGACCTTTGTGCCCATCCTTTATGTGCTGAAATTTAAGGTGGGCTTCTTTACTATGTTGTATTTTGCTAACTTTATCAAATGATTAGTATTTTGCTTGAAATAGTGTTTTCTCTCTGGGTTCAGACAGAGGAAGAGGCATTTTCCTGGAATAACGAAGTTAAACAAGGGCTCTCCAGCAGTATCTTTACTAAAGACATGGGAAGAGTGTTCCGCTGGTTAGGGTATGTGTGCAAAGGCACTTTCTGGATTTGAAGTCACTTGACACAGGTCTTGCTTGATAAACCAAATTGTTTTACTATTGAAAACTCTTTAGTAACACTTATCTGTTGTATAGTCCTAAAGGCTCCGACTGTGGCATTGTGAACGTTAACATTCCTACTAGCGGTGCTGAGATTGGAGGAGCGTTTG[G/A]TGCGTATATTATACACCACACCATTCTAAAATTAACTAACTAAACTTACATTGAACTTTTTTCAGTGATAAGCCTTATTGTTGCTAGTCCTAAAGCCACCTTCAATAATTGGTAACTTCCACCAATTGGAAATATGCTTTTCAGCAATTATGACTTTTTAGTTGCAAAACGCATTGAAATACTAAATGATCTTTAGATGAAGCTTTACAGAAGTTACCAAAAATTTTGTTGAACATTCTTTTTATAGATTTGTGTATTTAAGTTAAAATACCTGGGGCCTGTTTCAGTAAGAAGGTTCAACCTACTTGAAGTTTAAACTTGAACTCAGAGTTTTTAATCTCTCGGTAAGTCAACTCAGAGTTTCCAGTTTCAGCACAGCTAATCTGAGTTTGGTCAATCAACTTTGAGTAGACTAACTCAGAGTTAAGCGCGCACACCACAACTATAAAAAGGCATTATCAATGGAGCACAAATATTACGAGTCACCATGGCAACATCTG
Associated Phenotype:
Not determined