Busch Lab

ZMP

oxnad1

Ensembl ID:
ENSDARG00000062664
ZFIN ID:
ZDB-GENE-060503-199
Description:
Oxidoreductase NAD-binding domain-containing protein 1 [Source:UniProtKB/Swiss-Prot;Acc:A3KP77]
Human Orthologue:
OXNAD1
Human Description:
oxidoreductase NAD-binding domain containing 1 [Source:HGNC Symbol;Acc:25128]
Mouse Orthologue:
Oxnad1
Mouse Description:
oxidoreductase NAD-binding domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1916953]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa44913 Nonsense Mutation detected in F1 DNA Not yet available
sa5922 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9257 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44913
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090860 Nonsense 41 306 3 8
ENSDART00000128300 Nonsense 41 306 2 7
Genomic Location (Zv9):
Chromosome 19 (position 20757462)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 20690842
GRCz11 19 20275165
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTATAAACTATACGACCCTAAATGTGTTTCAGAAAAATGACATCCAGG[A/T]GACGGACTGACCATCTAGAGAGAACTGCTAGTGTTCATCGACAAATGGTG
Long Flanking Sequence:
TAAAAATAAAACCAATAATTTAGTTAATAACACTAATTTGCTTGTTTCTCACACGTGTGAATGTCTTTATATATTGGCTGTTAAAAAGAAATTCTGATATTTCAGTGTCGTTGGTTATTATTATTAAAAGACGAACTGCCCTTTCTGTCTGATAATGTTATAAGGTGTTTGACAGAGTTCCTCCCGTCACATCTGACCATGAGTGCCCCGTGCTTTGTACGAACGGTGGCCAGAGGTTTCTCCGGTGGATCAGGACTGTTCAGACCTGCTGTGTTGTGTTCAGACAAAGTCACAGTCACACGGTGAGTATCGTCCAGAATCCACTGCTGTTTCTAGAGGCTTTGGACACTAAGGTTGTGTCCTAAAACCTGGTAAGCAGCCTACCTAGTCGGCATGCTACAAAACATCCACAAAAAAGTATGTAGTATATGAGACAAAGTCATTGTTTTAGTGTATAAACTATACGACCCTAAATGTGTTTCAGAAAAATGACATCCAGG[A/T]GACGGACTGACCATCTAGAGAGAACTGCTAGTGTTCATCGACAAATGGTGAGTTTTCTTAGATTTGTTTTCTGTTTTTTAGATGAAAATCTTGACTTTTTAGTTATAGATTCTTGCTTGGGTCTTTATAAATGGTTAACAAATGTTGGAGCCTTGTAGGTGAAAGTTCAGACACTTGTTTTGTGTTTTAGGTCCACCAGTGTGTCATTTGATTTGTCACAAGACTAAATTCAAGATGATGTAATCGAACGTTAAGTTGTTTCAGTTAGTAACACTTTTCAAAAAGGTTCCATTAGTTAATGTATTTTTACTAGCACGAACAAAGATGCAAAAACACATTTATTACAGTAGTAATTACAGTGTTTATTTTTTGTTAATATTAGTCGGTGGAAAAATCTTTCATTGTTGGTTATTGTTAACCCACTGTGTTGCACTTTACATTAAGGTTCGTTAGTTAACGCTAGTTACTGTATTTACTAACTTGAATTAAGAGTACAATAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5922
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090860 Essential Splice Site 140 306 6 8
ENSDART00000128300 Essential Splice Site 140 306 5 7
Genomic Location (Zv9):
Chromosome 19 (position 20770187)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 20703567
GRCz11 19 20287890
KASP Assay ID:
554-3716.1 (used for ordering genotyping assays)
KASP Sequence:
AGTGTTAGTGTTAGATTAGTCTGTTAAAAATCCTAATCCTCTTCTGTTGC[A/T]GTGCTCTGTGGACTCTCAGGTAGCCGTGAGGGTGGGGGGTAATTTCTACT
Long Flanking Sequence:
CAATATTATTATCCCCTTTAAGCTATATATTTTTTGATAGTCTACAGAACAAACCACTGTTATACATTCACTTGCCTAATTACCCTAACCTGCCTAATTAACCTAGTTAACCCTTTAAATGTCATTTTAAGCTGAATAGGAGTGTCTTGAAAGATAATATTATTTACTGTCATCATGGCAAAAATAAAATAAATCAGTTATTAAAGATGGGTTATTAAAACTATTGTGTTTAGAAATGTGTTGAAATGTTTCTCTCCATTAAACAGAAATTGGGGGAAAAATATACTGAGGCTAATAATTCAGGGAGGCTAATAAGTCTGATTTTTGACCTAATTCTGATGTTCTGAGACTATTCAATCTAGGTTAATTATTTTTTTATGGCAAATGCTACATTAGTTCCACTTATTTACTTTAACTATCGAGAAGCCTGAAAACTACATTTAATAAAACAGTGTTAGTGTTAGATTAGTCTGTTAAAAATCCTAATCCTCTTCTGTTGC[A/T]GTGCTCTGTGGACTCTCAGGTAGCCGTGAGGGTGGGGGGTAATTTCTACTTTGACCCTCAGCCTTCTAACCCTGTGGTGGACCTGTTGCTGGTGGCTGGAGGTGTTGGAATTAACCCTCTATACTCCATCCTGCTACATGCAGCTGATCTGCACAGACACACTCACAGTCACAGATACACACCAGGACACACACACCTGTGTTACAGCGCCAAGAACACTACAGAGCTGCTCTTCAAGGTAAGTGTTTGTAATCTTGACTTTTAAACACATAAAAGTGAAGCTTGACACTGATTTTGAAACATTTGCTCTCTTCAGGACACCATTATTGACATTTGTCACGAGCGACCAGATAAATTCTCCTGCCATTTCCATGTTACCCAGCAGAGCTCCGACATAGAGCCACAACTTCAGCCTTACACTATACGTGAGTTGCAGATCATCATACAGTGACGATCAAAATTAGAGAACAGTTGTTTTAAACATCTTTAAAAATGTAATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9257
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090860 Nonsense 275 306 8 8
ENSDART00000128300 Nonsense 275 306 7 7
Genomic Location (Zv9):
Chromosome 19 (position 20774598)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 20707978
GRCz11 19 20292301
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGMAGAAGAGCTTCAGCGTTATGTAGWCCCTGAGCGAACGCTGTGTTA[T/A]CTTTGTGGTCCTCCTCCTATGATAGAGAAAGTGASTTCAGATCTGCAGAG
Long Flanking Sequence:
TGTGTAAACACTCATTGCCCAGAGTGACATTTGCTGGAGCATTGGGTGATGAGCGCAGAGAAGGATCTGCATGCTGTTGAAAGAGCTTCTGATCAACATTTGCATTCACTCTGTCTTGTACTGTAACTCTAAACTAGAACACATCCTCAACCACCTATGGCTGACTTTTGAAAGTCATTGAAGTTATAGCTGCAAGTTAGATGGGGATTGTTTAATAATAAAAAAAAGACAGAAAATTCGGAATATATGTAACCCATGAAACATGCTTTAAACATTCCTGTTAGAATAACTTCAAACAGGACTAGCTGTGACATTCAATTTAGGAAATTGAAGATTGTTCTCTAATTTTGATCTCCAATGTATTTTTTGCTTTACGTTACCTGAAGTTTTAAGTATGTTCAGGTTCGATGTGTCACGTGAGCTTCTTATGTCTCTGTAGGTGGAAGGATATCAGCAGAAGAGCTTCAGCGTTATGTAGACCCTGAGCGAACGCTGTGTTA[T/A]CTTTGTGGTCCTCCTCCTATGATAGAGAAAGTGAGTTCAGATCTGCAGAGCACCGGCCTTCCAGAGGATAGAATCCTGTTTGAGAAATGGTGGTAGTTTTACAGCTCCCCCAAGACCTCAGGCTTCAGAAGTGGATGTATCTGTCTCTTTGTCACCGTAGACACTCACTGTTGTGGCAATTTGGACCAGTAATGCACTCGAGTTTTAACGCACAACAGACACCATGTCTGCAGTTCTTCTAGACTTGATATATACTAATGTTCAAAAGTTTGAGTTTGGCATGATTATATTTGTTTTTGAAAGGGCTTTTATGCACACAGCAGTTACATTGCTTTTATTACACACGTATGCAATGCTGTGTATTATTCAAGGTGCAATCTGAAACGAAATAACTGGTTTCTATTGAAATATATTTAAAAGTGTCATTTATTCCTGTGATGGCAAAGCTGAATTTTCAGCATTATTACTTCAGACTTCAGCATCACAGGATCTTTTAATAT
Associated Phenotype:
Not determined