ZMP
adhfe1
Ensembl ID:
ZFIN ID:
Description:
hydroxyacid-oxoacid transhydrogenase, mitochondrial [Source:RefSeq peptide;Acc:NP_996969]
Human Orthologue:
ADHFE1
Human Description:
alcohol dehydrogenase, iron containing, 1 [Source:HGNC Symbol;Acc:16354]
Mouse Orthologue:
Adhfe1
Mouse Description:
alcohol dehydrogenase, iron containing, 1 Gene [Source:MGI Symbol;Acc:MGI:1923437]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32995 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa39904 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32994 | Essential Splice Site | Available for shipment | Available now |
sa17509 | Nonsense | Available for shipment | Available now |
sa19835 | Nonsense | Available for shipment | Available now |
sa25118 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32995
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075551 | Essential Splice Site | 128 | 477 | 5 | 14 |
ENSDART00000110177 | Essential Splice Site | 160 | 509 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42208643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42258107 |
GRCz11 | 2 | 42107525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAACACAAGCTCTATGAGGATGTACGAGTAGAACCAACAGACAAAAGG[T/C]GAAAATGCAACAGAAAATGTGTCAAAAACATAAAAAAAACACGCCTGCAT
Long Flanking Sequence:
TGCAACCCATCACTGGGAAACATCCATACACAGTCATTCACACACATACACTACAGACAATTTAGTCTACCCAGTTCACATACAGTACATGTCTTTGGACTTGTGGGGGAAACCGGAGCACCTGGAGGAAACTCATGCAAACATGGGGAAAACATGCAAACAACACAGAAATGCCAACTGGCCCAGCCGAGGCTCGAACCAGCAACCTTCTTGCTTTGAGGCAATTGTGCTACCCACTGCGCCACCGTGCAGCCCTACTTAATGTTTGCATAATACTTTAAAATCTCTGTTCAGTTCAGTTTTGGAGTCGACGGTCATTAGTTGTTATTGTATGATTTGATCAGGATTTGCAGAACATGGGAGCACGTAATGTGTGTCTGATGACTGACAGGACCTTGTCTCAGCTGCCGCCAGTCGCAGCAGTTCTGGACTCACTGATAAAACATGGAGTCAAACACAAGCTCTATGAGGATGTACGAGTAGAACCAACAGACAAAAGG[T/C]GAAAATGCAACAGAAAATGTGTCAAAAACATAAAAAAAACACGCCTGCATTTTCTCACAACACATGCAAATAGAACAGAACACAACAGAAATGTTTCAAAAACCCAAAAACGTGACGGACCTGGCTGGGATTTGCTTAATGGGCTGTGACTAGTTCAAGTTCAAGTTGCTTTATTGGCATGACATTCAGTACAGTATTGCCAAAGCAATTTAAATATGCAATATATTAAAACCATAAAAAAATAAAATAAAAAAAAAATTATAATAGTAATACAGTAGATAAGAAATAATGACAAAAAACAGAATACATTTGATAAATATAACAATAATAATAATAATAATAATAATAACAAGTTTAAATTATTTAAATAAGATACATAAATTTACATTAACCATTTCTTTTGATGTTTAGGGTGTATACATATTTTACAGCAAGTCTAGATGTCAATTCATTCTCTCTGAGTACATGGTAAAGTTTTTCTGAGTCATTAAAATATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39904
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075551 | Essential Splice Site | 194 | 477 | 6 | 14 |
ENSDART00000110177 | Essential Splice Site | 226 | 509 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42206887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42256351 |
GRCz11 | 2 | 42105769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGGAAAAGGAAAACCCATCACAGCCACCCTGAAGCCACTAATCGCTGG[T/C]ACAAACGCATACATAGAGAAATCCTCATTGTTACTTTCTTTTTTGCCTTC
Long Flanking Sequence:
AAATAGTCGTGTCCGTCACATTTTAGGGTCCCCTTAAAACATTTGTGTTGTACTCCATGCTATTTGCATGTTTTGTAAGAAAGTGCAGGTGTTTTCTTAATTTGTTTGCGTTGTTGGGAAAATGCAGTGTGTTTTTATGTGTTTGCAACATGTCAAACTGATGAGGATCTTTTAATAATATGCTGGCGTTTTTTGTAATTGCATCTGTTTTCTTAAATTGCAGAACGGTAAGCTCTCGAGGAAGTTGATTAGTAAAGTAGTGTGTGATTATTATATATTTTTTTGTATTATTTTGTGTTCAGCTTTAAAGCAGCAATCGATTTTGCCAAAAAAGGGCATTTTGATGTGTATGTTGCTGTGGGCGGCGGCTCTGTGATTGACACCTGTAAAGCAGCCAATCTTTATGCATCTCATCCGGAGGCAGAGTTTCTAGACTTCGTCAATGCACCAATCGGAAAAGGAAAACCCATCACAGCCACCCTGAAGCCACTAATCGCTGG[T/C]ACAAACGCATACATAGAGAAATCCTCATTGTTACTTTCTTTTTTGCCTTCCTTTCTCTCGGCCCAGTTACTTTTACTGACCATCTGCATAAACAGATGAAGAGTCCAAACAATTGAAACATAGCACAGATACTGTATGCTGATTAATGATAGTTGTTTGTGTATATTTTTTGTGTCTGCATATTTAAGTTCCCACTACAGCTGGAACGGGGAGTGAAACCACAGGAGTGGCGATCTTTGACTTGGAGGACATGAAGGCCAAAACTGGTCCGTGAAACGAATTACTCATTAATATTTCAGCACTGTTCTTTGAATATCAAGAACTCAGTATTGTTAAGCATTTGTTTTGTATAAAAAAAGATCAAAGTAGAATTGAAGGCAAAATTATTAGCCCTCCTGTGAAATGTTAAATCTTCCTCAGATATTCCCTGTTTAATAAAGAGAAAAACTTTTTAACACATTTTTAAATATAATAGTTTTAGTAACTAATGTTTAATAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32994
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075551 | Essential Splice Site | 220 | 477 | 7 | 14 |
ENSDART00000110177 | Essential Splice Site | 252 | 509 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42206619)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42256083 |
GRCz11 | 2 | 42105501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCACAGGAGTGGCGATCTTTGACTTGGAGGACATGAAGGCCAAAACTGG[T/A]CCGTGAAACGAATTACTCATTAATATTTCAGCACTGTTCTTTGAATATCA
Long Flanking Sequence:
TATTATATATTTTTTTGTATTATTTTGTGTTCAGCTTTAAAGCAGCAATCGATTTTGCCAAAAAAGGGCATTTTGATGTGTATGTTGCTGTGGGCGGCGGCTCTGTGATTGACACCTGTAAAGCAGCCAATCTTTATGCATCTCATCCGGAGGCAGAGTTTCTAGACTTCGTCAATGCACCAATCGGAAAAGGAAAACCCATCACAGCCACCCTGAAGCCACTAATCGCTGGTACAAACGCATACATAGAGAAATCCTCATTGTTACTTTCTTTTTTGCCTTCCTTTCTCTCGGCCCAGTTACTTTTACTGACCATCTGCATAAACAGATGAAGAGTCCAAACAATTGAAACATAGCACAGATACTGTATGCTGATTAATGATAGTTGTTTGTGTATATTTTTTGTGTCTGCATATTTAAGTTCCCACTACAGCTGGAACGGGGAGTGAAACCACAGGAGTGGCGATCTTTGACTTGGAGGACATGAAGGCCAAAACTGG[T/A]CCGTGAAACGAATTACTCATTAATATTTCAGCACTGTTCTTTGAATATCAAGAACTCAGTATTGTTAAGCATTTGTTTTGTATAAAAAAAGATCAAAGTAGAATTGAAGGCAAAATTATTAGCCCTCCTGTGAAATGTTAAATCTTCCTCAGATATTCCCTGTTTAATAAAGAGAAAAACTTTTTAACACATTTTTAAATATAATAGTTTTAGTAACTAATGTTTAATAACTATTTTTTTTTGTCTTTGCCATGTTGACAGTACATAATATTTTACTAGTCATTTTGCAAGACACTAGTATTAAGCTTAAAGTGACATTTAAAGGCTAAACTAGACTAGTGGTTTGTTCCAAATGAAAAAAATAATATTGACTATAAAAACTATAAGAAAATATATGTAAAAACTGCTTTTATACCTGCCAAACAAACAAAAATTTCTCCATAAATAAAATATAACAGAGTTTAACAGAATTTTTTTTATTTGCTTTGTTTAACAGTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17509
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 |
---|---|---|---|---|---|
ENSDART00000075551 | Nonsense | 224 | 477 | 8 | 14 |
ENSDART00000110177 | Nonsense | 256 | 509 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42205816)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42255280 |
GRCz11 | 2 | 42104698 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTTTATATTTAGCCCATTGATGTGTRTGTTTTTCAGGCATCGCAAAT[C/T]GAGCCTTAAAACCTACATTGGGAATGGTGGATCCTCTACATACTCTTCAC
Long Flanking Sequence:
AAGCTTAAAGTGACATTTAAAGGCTAAACTAGACTAGTGGTTTGTTCCAAATGAAAAAAATAATATTGACTATAAAAACTATAAGAAAATATATGTAAAAACTGCTTTTATACCTGCCAAACAAACAAAAATTTCTCCATAAATAAAATATAACAGAGTTTAACAGAATTTTTTTTATTTGCTTTGTTTAACAGTTCTTAGGAAATATATATAAAAAAAAAGAAAAATATCACAGGAGGGCTAAACCAAAAGGTCTTCAACAGGTGAAAAATCAAAAACATCAAAAAAGACAAAAAAAATTGTTTGCACACTCGTATTTTTATTTTATTAGCAATGATTTATTAACACAAGCAATGTCTTGTGTAAGTCTGGTAAAGATCTTTGAAAAATTTCTATAATTAAGTTATTAAAGATCATGCATATTAGTAAATGTTCACTATTAATGTTATTTGTGTTTATATTTAGCCCATTGATGTGTGTGTTTTTCAGGCATCGCAAAT[C/T]GAGCCTTAAAACCTACATTGGGAATGGTGGATCCTCTACATACTCTTCACATGCCATCCAGAGTGGCAGCTAACAGCGGGTTTGATGTGCTCTGGTGTGTATTTTTTACATTCACATTTTAATTATTAACTACATTATGTGGATCAAAGATATTGCAACAATAATGTAACAACTTTAAATGTTTTTTTTTTAATCTCTGTGAATCCTTTTGCATCCTGTTAATGGCATAATGACTATTACACATTTTACCATGATTTAAATTTGTCCATCTGCCCCACACTGACTCATTTGCCCACTTCATGCAAACTTACACTCCCCATAACTATAGGGTATATGCCGAGCTAGTGCTGTTCCCATGCTGATACACTTCCGGTGACCTGTTATTGTGTACTTTTTTCCATTTTATACGGTTTCTTATACAGCATCGATGTTGTAATGTCATTAAAATACATTCAGTTAAATAAACTTTAGCATTTATTTAGTTGCTCAAGCGTAAAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19835
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 |
---|---|---|---|---|---|
ENSDART00000075551 | Nonsense | 272 | 477 | 9 | 14 |
ENSDART00000110177 | Nonsense | 304 | 509 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42204115)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42253579 |
GRCz11 | 2 | 42102997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCATTAGAGTCATTCACAGCATTGCCGTATAACCTGCGTAGCCCCTG[T/A]CCGCCAAACCCCATCAGCCGGCCCGCTTACCAGGGGAGCAATCCAATCAG
Long Flanking Sequence:
GTGTAATGACAAAGTTGAATCTAATCTCTAAAATGCAATTCACTGTACAAATATGTTCATCTGTTTCAAAGATTTTTGACTGCCATATTTGCAACCAGTATAATTTGATGACATTAAAATACTCTTTAAAGATAACAGTGCAGCACCAACACACTCGTTTGTTATCTACAAACTTTATACTTTGCTATATACTTTGCTGTTATACCACAAACCTTTTTACCAGCAATACAGTTTTATTCATTTTAAATACAATCAAATGAAATATGATCACTTTCATTTATTTGAACAAGAACAGGTCATCATGCTACTATATTTGTACAGCTCAGTTATGCAGAATGATGATTGAACATATTCATATATTATCACTGTTCATTTGTAATCTGTAAGGATGCCTTTTTCTATCATAGTTTTATTAGATTGATTTTTTAATTTGATCTTTCTTTTTCTAGTCATGCATTAGAGTCATTCACAGCATTGCCGTATAACCTGCGTAGCCCCTG[T/A]CCGCCAAACCCCATCAGCCGGCCCGCTTACCAGGGGAGCAATCCAATCAGTGATGTTTGGGCAAAGCACGCTCTCCGGATCGTCGCTAAATACTTGAAACGGTATGTTTTTGGGATGTGAAAGGATGTGCATTATATGTTTTAGTGAGACATTAGATTTGATACATTTTATAAGTACAATATTTAAATATACAGTTGAAGACCAAATGATTCGCCCTCCTGTGAATCTTTGCTTCTTTTTCAAATATTTCCCAAGTGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGTCCAGGATAAAAGCAGTTTGAAAATTTTTCAAATCCATTTTTTGAAAATTTTATTAGCCCTCTTAAGCTATATATTTATTTCAGATTGTCTACAGAACAAACCATCAAAATGATTTGCCTATTTATCCTAACTTGCCTAATTAACCTAGTTAAACCTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25118
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 |
---|---|---|---|---|---|
ENSDART00000075551 | Essential Splice Site | 306 | 477 | 9 | 14 |
ENSDART00000110177 | Essential Splice Site | 338 | 509 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 2 (position 42204013)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42253477 |
GRCz11 | 2 | 42102895 |
KASP Assay ID:
554-7303.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTTTGGGCAAAGCACGCTCTCCGGATCGTCGCTAAATACTTGAAACG[G/A]TATGTTTTTGGGATGTGAAAGGATGTGCATTATATGTTTTAGTGAGACAT
Long Flanking Sequence:
ATTTGATGACATTAAAATACTCTTTAAAGATAACAGTGCAGCACCAACACACTCGTTTGTTATCTACAAACTTTATACTTTGCTATATACTTTGCTGTTATACCACAAACCTTTTTACCAGCAATACAGTTTTATTCATTTTAAATACAATCAAATGAAATATGATCACTTTCATTTATTTGAACAAGAACAGGTCATCATGCTACTATATTTGTACAGCTCAGTTATGCAGAATGATGATTGAACATATTCATATATTATCACTGTTCATTTGTAATCTGTAAGGATGCCTTTTTCTATCATAGTTTTATTAGATTGATTTTTTAATTTGATCTTTCTTTTTCTAGTCATGCATTAGAGTCATTCACAGCATTGCCGTATAACCTGCGTAGCCCCTGTCCGCCAAACCCCATCAGCCGGCCCGCTTACCAGGGGAGCAATCCAATCAGTGATGTTTGGGCAAAGCACGCTCTCCGGATCGTCGCTAAATACTTGAAACG[G/A]TATGTTTTTGGGATGTGAAAGGATGTGCATTATATGTTTTAGTGAGACATTAGATTTGATACATTTTATAAGTACAATATTTAAATATACAGTTGAAGACCAAATGATTCGCCCTCCTGTGAATCTTTGCTTCTTTTTCAAATATTTCCCAAGTGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTATAATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGTCCAGGATAAAAGCAGTTTGAAAATTTTTCAAATCCATTTTTTGAAAATTTTATTAGCCCTCTTAAGCTATATATTTATTTCAGATTGTCTACAGAACAAACCATCAAAATGATTTGCCTATTTATCCTAACTTGCCTAATTAACCTAGTTAAACCTTTTAATGTCACTTTAACTTGAAAACTAGCATCTTAAAAAATATCTAGTAAAATATTATGTACTGTCATCTATGCAAATATAAAAGAAATCAGTTATTAGAAAACTA
Associated Phenotype:
Not determined