ZMP
aldh1l1
Ensembl ID:
ZFIN ID:
Description:
aldehyde dehydrogenase 1 family, member L1 [Source:RefSeq peptide;Acc:NP_001185701]
Human Orthologue:
ALDH1L1
Human Description:
aldehyde dehydrogenase 1 family, member L1 [Source:HGNC Symbol;Acc:3978]
Mouse Orthologue:
Aldh1l1
Mouse Description:
aldehyde dehydrogenase 1 family, member L1 Gene [Source:MGI Symbol;Acc:MGI:1340024]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20698 | Essential Splice Site | Available for shipment | Available now |
sa18221 | Splice Site, Nonsense | Available for shipment | Available now |
sa40691 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12463 | Nonsense | Available for shipment | Available now |
sa20699 | Nonsense | Available for shipment | Available now |
sa20700 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20698
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 |
---|---|---|---|---|---|
ENSDART00000112636 | Essential Splice Site | 240 | 904 | 5 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23763619)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20019065 |
GRCz11 | 6 | 22079287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGAGGAAATGACAGAGTACCTGGAGCCTGGGCAGAGATAGATGGCAAA[G/A]TGAGTGTTTTTCCTCTTAACAACAACAATACACCAAACATGCTCTCTTAA
Long Flanking Sequence:
TGGACACAGGACCAATTCTTTTGCAAAGAGAATGTGATGTTGAGCCAAATGACAACGTAAACAGCATCTACAAGCGCTTCCTGTTTCCAGAGGGAGTCAAGGGCATGGTGTGGATTATTGCAGTAATCAGAACTAGCATAGCATATTTGCATATGATCATTCAAAGTCCAGGAAGTAGTCTGATTTAGTTGTTAAGAATGACTTCACCCATGGATTTAATTTTGTGTGCATGTAGGTAGAGGCAGTCAGGTTGATTGCAACAGGGAAAGCTCCAAGAATCAAGCAACCAGAAGAAGGAGCCACATATGAGTGTATTCAGAAGAAAGAAAATTCAAAGGTGATATATTGATATATAGTTTGTCTAATTCTAATTGTTGTTTCACAATAACCATTTGTGGTTGTTTGCATAGATTGACTGGAATCAACCAGCAGAAGCCATTCATAACTGGATCAGAGGAAATGACAGAGTACCTGGAGCCTGGGCAGAGATAGATGGCAAA[G/A]TGAGTGTTTTTCCTCTTAACAACAACAATACACCAAACATGCTCTCTTAAAGGGCACCTATGATGAAAATCATCTTTTGGAAGCTGTTTGGACAGAACTGTGTGTAGGTAGGACCACAGTCATACTGGGGTGATACAAAGACAATAAGTCTTGGAACCATGAATTCTGCTGTGTGCCAAAATATTCTGTATGAGAATGTTCGACCATCTGTTAGTGACCTCAAGCTGAAGCGAACTTGGGTTCTGTAGCTGGACAATGATCCTAAGCACAACAGCAAGTCCACTTCTGAATGATTGAAGAAAAACAAAATAAAGACTTTGGTGTGACCGAGTCAGAGTACTGACCTGAATCCAATTGAGATGCTGTTGCATGACCTTAAAAAGACAATTCATGCTCACAAACCCTCCAATGGGCTGAATCGGAACAATTCTACAAAGATGAGTGTGCCAAAATTCCTCCACAGTACTGTAACAGACTCATTGCAAGTTATCGAAAATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18221
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112636 | Splice Site, Nonsense | 450 | 904 | 11 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23772498)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20027944 |
GRCz11 | 6 | 22088166 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGKATGCGGAAGGRGGAAARACCTATAAGAGCATTAACCCTACTGACGGA[C/T]AAGTACATACTGGGCACACATCTCTTTTTCTATTCATANTTTTTCCTCAA
Long Flanking Sequence:
GAATAATATTTGTGTAGTGTCAGGAAATAATTATGCCAATCTAACATTTTTACATGATTTAGAGAAGAATAAAGTAATGATATATGGATACGTCTACTTGTATGTCTTTTCAAACATATTTAAAACATTATAAAATTTAGCCCCAAAATATGAATTTAATATAACGTATAGAATAAATATATTGTTTACATATATTACAAAAAATTGACAGTAGAATATTATTTCCTCAACCTTAACATGTATTGCTGATATTAAAAAGCCGGAATGCATATAAAAAAAGTCAGTTATTTCAATTGATTCACTCTAATGCTCTAATTGATTCATTTTTTTATTTTTATCTATATCTATTTATTTTTAATTATGTGTTTGCATGTCTGTTGTAGGTAGAAAAGAAACTGAACAATATGACAATTCACATCCCCCACCAGCTTTTCATAAATGGGGAATTTGTGGATGCGGAAGGGGGAAAGACCTATAAGAGCATTAACCCTACTGACGGA[C/T]AAGTACATACTGGGCACACATCTCTTTTTCTATTCATATTTTTTCCTCAACTTCCATATGCTCAATATCAACTTCTGTTTGTGTGTAGGTAATCTGCGACGTGTCTTTAGCTCAGATCTCTGATGTGGAAAAAGCAGTCGCTGCAGCTAAAGAAGCTTTTGAGGAAGGAGAGTGGGGAAAGATGAACCCCAGAGACAGAGGCAAGCTGCTTTACAAGTATGTTAATGATTTATTTTACCTAACATTTAAAGTATATATGAAATCAAAACTAAACATATTTATTTTGTAACTATGAAAACACTATGAAAACAAACAGATCTGATGTTAGGTTGTAATTTGGGGATAACACACAGTTTGAACCCAAAGAATGACCAGTCTGTCAAATGAAGAAGAGCCGGAGACAGTTTGCAGTTTTATCAGCAGAAGCCAGCTTTAACACTCGCAATGAGTTCCCAGGCCTCTCTTCTTACAATCACAAATCAATAACAATTATACTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40691
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 |
---|---|---|---|---|---|
ENSDART00000112636 | Essential Splice Site | 451 | 904 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23772586)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20028032 |
GRCz11 | 6 | 22088254 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTTTCCTCAACTTCCATATGCTCAATATCAACTTCTGTTTGTGTGTA[G/A]GTAATCTGCGACGTGTCTTTAGCTCAGATCTCTGATGTGGAAAAAGCAGT
Long Flanking Sequence:
TACGTCTACTTGTATGTCTTTTCAAACATATTTAAAACATTATAAAATTTAGCCCCAAAATATGAATTTAATATAACGTATAGAATAAATATATTGTTTACATATATTACAAAAAATTGACAGTAGAATATTATTTCCTCAACCTTAACATGTATTGCTGATATTAAAAAGCCGGAATGCATATAAAAAAAGTCAGTTATTTCAATTGATTCACTCTAATGCTCTAATTGATTCATTTTTTTATTTTTATCTATATCTATTTATTTTTAATTATGTGTTTGCATGTCTGTTGTAGGTAGAAAAGAAACTGAACAATATGACAATTCACATCCCCCACCAGCTTTTCATAAATGGGGAATTTGTGGATGCGGAAGGGGGAAAGACCTATAAGAGCATTAACCCTACTGACGGACAAGTACATACTGGGCACACATCTCTTTTTCTATTCATATTTTTTCCTCAACTTCCATATGCTCAATATCAACTTCTGTTTGTGTGTA[G/A]GTAATCTGCGACGTGTCTTTAGCTCAGATCTCTGATGTGGAAAAAGCAGTCGCTGCAGCTAAAGAAGCTTTTGAGGAAGGAGAGTGGGGAAAGATGAACCCCAGAGACAGAGGCAAGCTGCTTTACAAGTATGTTAATGATTTATTTTACCTAACATTTAAAGTATATATGAAATCAAAACTAAACATATTTATTTTGTAACTATGAAAACACTATGAAAACAAACAGATCTGATGTTAGGTTGTAATTTGGGGATAACACACAGTTTGAACCCAAAGAATGACCAGTCTGTCAAATGAAGAAGAGCCGGAGACAGTTTGCAGTTTTATCAGCAGAAGCCAGCTTTAACACTCGCAATGAGTTCCCAGGCCTCTCTTCTTACAATCACAAATCAATAACAATTATACTCTCTACACAAGACCAGAAAGAGTGTGATTCAGGTAACAGGTTTTCATTGGTTAAAACAAAGATAGACAGCCCTAAATAGGTACGTCGATGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12463
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 |
---|---|---|---|---|---|
ENSDART00000112636 | Nonsense | 457 | 904 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23772606)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20028052 |
GRCz11 | 6 | 22088274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGCTCAATATCAACTTCTGTTTGYGTGTAGGYAATCTGYGACGTGTCTT[T/A]AGCTCAGATCTCTGATGTGGAAAAAGCAGTCGCTGCAGCTAAAGAAGCTT
Long Flanking Sequence:
TTCAAACATATTTAAAACATTATAAAATTTAGCCCCAAAATATGAATTTAATATAACGTATAGAATAAATATATTGTTTACATATATTACAAAAAATTGACAGTAGAATATTATTTCCTCAACCTTAACATGTATTGCTGATATTAAAAAGCCGGAATGCATATAAAAAAAGTCAGTTATTTCAATTGATTCACTCTAATGCTCTAATTGATTCATTTTTTTATTTTTATCTATATCTATTTATTTTTAATTATGTGTTTGCATGTCTGTTGTAGGTAGAAAAGAAACTGAACAATATGACAATTCACATCCCCCACCAGCTTTTCATAAATGGGGAATTTGTGGATGCGGAAGGGGGAAAGACCTATAAGAGCATTAACCCTACTGACGGACAAGTACATACTGGGCACACATCTCTTTTTCTATTCATATTTTTTCCTCAACTTCCATATGCTCAATATCAACTTCTGTTTGTGTGTAGGTAATCTGCGACGTGTCTT[T/A]AGCTCAGATCTCTGATGTGGAAAAAGCAGTCGCTGCAGCTAAAGAAGCTTTTGAGGAAGGAGAGTGGGGAAAGATGAACCCCAGAGACAGAGGCAAGCTGCTTTACAAGTATGTTAATGATTTATTTTACCTAACATTTAAAGTATATATGAAATCAAAACTAAACATATTTATTTTGTAACTATGAAAACACTATGAAAACAAACAGATCTGATGTTAGGTTGTAATTTGGGGATAACACACAGTTTGAACCCAAAGAATGACCAGTCTGTCAAATGAAGAAGAGCCGGAGACAGTTTGCAGTTTTATCAGCAGAAGCCAGCTTTAACACTCGCAATGAGTTCCCAGGCCTCTCTTCTTACAATCACAAATCAATAACAATTATACTCTCTACACAAGACCAGAAAGAGTGTGATTCAGGTAACAGGTTTTCATTGGTTAAAACAAAGATAGACAGCCCTAAATAGGTACGTCGATGCGGGGTCGTATCTGAATCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20699
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112636 | Nonsense | 553 | 904 | 14 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23777592)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20033038 |
GRCz11 | 6 | 22093260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTCTAATATTATTTTCCACAGGGCTGCACTATTCCCATAAACCAGGCT[C/T]GACCTAATCGAAACCTTACCTTTACCAAGAAAGAGCCCATTGGGTAAAAT
Long Flanking Sequence:
GCAGAGGAACAATTTTGAGTATGGATAAAACCATAGCCTTCACTTGAGCATTTGTGGCAAAGTTGATTGAGACCAAAATAATTATATTTTTTTTACATTGAAATACTTAGAAGGGAATCAATCCAATCTCTAAACATATAGTTTAAAAATGTAATGTAAATGATTTTAACATAATATAGTGTGGAAAATAGTGGCTTGCCAACATTTTCAGGATGAAGTTATGTCTAATTGTTTTACATTTTAAATTTAACATAGTAAAGTCCTCAAATTATTATTTTTTTCAATTCATGCTCCTAATGACCCTAAATATTATTCAGCCCAGAATATTCTTTTAAAGGTTATTTTACTACATTATATTCCAAAACAATACTGTCACTCTTAATAGTAGAGTGACTAATGATTTTGTTATATATGACTGGAAACTGTGGTTTTACTAAAATCTGTCTTTGTGTTTCTAATATTATTTTCCACAGGGCTGCACTATTCCCATAAACCAGGCT[C/T]GACCTAATCGAAACCTTACCTTTACCAAGAAAGAGCCCATTGGGTAAAATTAAGCCTCTCTTTAATAAAACGTTTTCTTCCAGTCTTGTCATAATGAAACAAAATAATCTTGATGAACTCAAATCAAGTATTTGGTGCATGTGGAACGAGCAATGATAACATTTGGCTCTTTTTGTTTGGGTAAAGTGTGTGCGGCATTGTAATTCCATGGAATTATCCACTGATGATGCTGGCTTGGAAAACTGCGGCCTGCCTGGCTGCTGGAAATACTGTAGTTCTTAAACCTGCCCAGGTAAACACCTGCAGTTACAGCTCAATCTAACATGCGACATATAAAAACATACAACATAAGGACTGAGTAAGTGTTTCTTTGTTGATTTTTAGGTCACACCTTTGACTGCTCTCAAATTTGCTGAATTAACTGCTCTGGCAAAATTTCCAAAAGGAGTGGTGAACATACTACCTGGATCAGGTATAAATAAAACATTCACAGAACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20700
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 |
---|---|---|---|---|---|
ENSDART00000112636 | Nonsense | 899 | 904 | 23 | 23 |
Genomic Location (Zv9):
Chromosome 6 (position 23786126)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 20041572 |
GRCz11 | 6 | 22101794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTCCATACAGGTCAAGAAGCTCTGAATGAGTATCTGAAGACTAAATG[T/A]GTCACAGTGGAATACTAACTGACAAAACACTGGACGTATAGTAAAGATTA
Long Flanking Sequence:
TTCAGAGAACTTCAGCTGTATATAAAGCCAGCAATTTAAATGTGTACATTGCAATGATTTTTTTGAATTGTTACAATTTAGTAAGAATCTAAATCGGATATTTCTCATTTTTCTTGATTCAGAGAAGTTGACAAGGTGCTGCAGAGGGCTAATGCTACAGAATTTGGCTTAGCATCAGGTGTGTTTACACGTGACATTAGTAAGGCTCTCTATGTGAGTGAAAAGCTTCAGGCTGGCACTGTGTTCATCAACACGTACAACAAGACGGATGTAGCAGCTCCTTTTGGTGGCTTCAAACAATCTGGCTTTGGCAAAGATTTGGGTAAGACATAATACCTGGTGAATTCATTTAAATGCACATACATCTAACAGTTCAATGTGTGGTTACTAAACTAGATTTCAGTCATTTGTTAACTTGTAAGAAAGGAGTTTTTGTATAACACGGGGTGTCTTTTCCATACAGGTCAAGAAGCTCTGAATGAGTATCTGAAGACTAAATG[T/A]GTCACAGTGGAATACTAACTGACAAAACACTGGACGTATAGTAAAGATTACGGTATTTTAATGCTCTGAAGTGGCACTTCAGCTTGACCTTCAATAAATTGTCAAGTAAACTTAATCATTACATATATCTATGAATGAATGAACGAATTCCATTTCTTGAGACAATTAAAAAAATGAAATCTTGTGTTTTTCTAGTTTTGCATCATACCTGTAAATGTCTTGCTGTTTATAATATTGGAGAAATTCAAGGACCATGCATGAGACTTTATCAGTTATAATGGATGTTGTTTCACTTTATATCGTTTGCAGATCACTTGCTTAAGTTAAGAGACTGTGAAAAAGTTTTGGGTAAACCTGATTGACCCGTTGTCCTTCACTGCACTGATATTTTTGGATTGAACTGTAATAACTGAACTGTATTTTATACAGTTTTTAGAAACCAGAACTTTTTTAATTTCTTCCTTGTAAACAGATGAACATATTCCAAGGAAGTGCAAAAA
Associated Phenotype:
Not determined