ZMP
ogfod1
Ensembl ID:
ZFIN ID:
Description:
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 1 [Source:RefSeq peptide;Acc:
Human Orthologue:
OGFOD1
Human Description:
2-oxoglutarate and iron-dependent oxygenase domain containing 1 [Source:HGNC Symbol;Acc:25585]
Mouse Orthologue:
Ogfod1
Mouse Description:
2-oxoglutarate and iron-dependent oxygenase domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2442
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17956 | Essential Splice Site | Available for shipment | Available now |
sa34084 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa10828 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17956
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052349 | Essential Splice Site | 285 | 543 | 7 | 13 |
ENSDART00000129699 | Essential Splice Site | 263 | 521 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30440339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28832681 |
GRCz11 | 7 | 29103831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYGCTACATTGAGCCCTCAGCTCCCCGAYACGCTCACATCCCCAGAGAYG[T/G]AAGTCAACTTGGCCTGACAGCACANTTTTTAGTGTGTGTCATGACCAAAT
Long Flanking Sequence:
ATGTCGCGGCTGGGCCAGTTGCCGTTTCTGTGTGAAGTTTGCATGTTCTCCCTGTAATGGCGTGGATTTCCTCCGGTGCTCCGGTTTCCCCCACAGACCAAAGACATGCGCTATAGGTAAATTGGATAAACTAAATTGACATTAGTGTATGTGTGTGAATGAGTGTGTTTGGGTGTTTCCCAATACTGGGTTGCGACTGTTTGGGCATCCGCTGCATAAAATATATGCTAGAATAGTTGGTGGTTCATTTCGATGTGGCGAGCTCTGAAATAGAGACTAAGCTAAAAATTAAAATTCTTGTTGTTTTTAGTATGATTATTTGCAAGTATTTACATGCGTGGGAATGATCTGACCTGTGAGCTTGACCTAGGTGGCGGAGGTGCTTTCAGAGGAGAAGTGTCGTTTATCTCTGAGCGGCTGGTTTCATGGCCCTTCCTTACCAAGACCCTCACGCTACATTGAGCCCTCAGCTCCCCGACACGCTCACATCCCCAGAGACG[T/G]AAGTCAACTTGGCCTGACAGCACATTTTTTAGTGTGTGTCATGACCAAATGGCCATAACCTGACCTGCGTATTTATGTGTTTTATACAGGAGACTTTGCTTTTCGAATGGGTGAACGAGATGTACCTGGATCCTCGCTATCAGGCGCGGGTACAACAGGAATTCGAGGACAGTTCAGAGATTTGCTTGCCTAGTTTCTTACAGGTTAGTCATCATTATTATCTTTTACACTGTGCTTAATGTACACACAGTAGTATACCAACAATGTGCATTTTTGCATGTTGTTATAAAGCGCAGGGTCACAATTGGAAGGATTTGTACTTGGATAAAATAAACTCTGCCAGAAGAGGCTTTTTCTGTCTGCGCTGTTGTGGAGCTTCATCTATAATTGATGCAAAGGAGAAATTCCTGTAGATGTGAAATTTAGTGACATGTCCCATGCCCACAGTAGAGGCATGTAGTCCGGGTATGTGGTAAATAATTAATTGTCCAAGTTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34084
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 |
---|---|---|---|---|---|
ENSDART00000052349 | Essential Splice Site | 323 | 543 | 8 | 13 |
ENSDART00000129699 | Essential Splice Site | 301 | 521 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30440543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28832885 |
GRCz11 | 7 | 29104035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAGGAATTCGAGGACAGTTCAGAGATTTGCTTGCCTAGTTTCTTACAG[G/A]TTAGTCATCATTATTATCTTTTACACTGTGCTTAATGTACACACAGTAGT
Long Flanking Sequence:
GCATCCGCTGCATAAAATATATGCTAGAATAGTTGGTGGTTCATTTCGATGTGGCGAGCTCTGAAATAGAGACTAAGCTAAAAATTAAAATTCTTGTTGTTTTTAGTATGATTATTTGCAAGTATTTACATGCGTGGGAATGATCTGACCTGTGAGCTTGACCTAGGTGGCGGAGGTGCTTTCAGAGGAGAAGTGTCGTTTATCTCTGAGCGGCTGGTTTCATGGCCCTTCCTTACCAAGACCCTCACGCTACATTGAGCCCTCAGCTCCCCGACACGCTCACATCCCCAGAGACGTAAGTCAACTTGGCCTGACAGCACATTTTTTAGTGTGTGTCATGACCAAATGGCCATAACCTGACCTGCGTATTTATGTGTTTTATACAGGAGACTTTGCTTTTCGAATGGGTGAACGAGATGTACCTGGATCCTCGCTATCAGGCGCGGGTACAACAGGAATTCGAGGACAGTTCAGAGATTTGCTTGCCTAGTTTCTTACAG[G/A]TTAGTCATCATTATTATCTTTTACACTGTGCTTAATGTACACACAGTAGTATACCAACAATGTGCATTTTTGCATGTTGTTATAAAGCGCAGGGTCACAATTGGAAGGATTTGTACTTGGATAAAATAAACTCTGCCAGAAGAGGCTTTTTCTGTCTGCGCTGTTGTGGAGCTTCATCTATAATTGATGCAAAGGAGAAATTCCTGTAGATGTGAAATTTAGTGACATGTCCCATGCCCACAGTAGAGGCATGTAGTCCGGGTATGTGGTAAATAATTAATTGTCCAAGTTATTTATTTATCATTTTTGCGCATAAAAGAGTCACGTTTGCTGACTTCACATGCAAGAATATGCTGTTGTCTTGCTGTATGATCAATAACATGACATAAGAATTACAGTCAATATGCTGAAACACTTTTTATTTATGCATTTATGTGTTCTGTTAAATACTATTTTTATTCTGAATATTTGATTTACTTGCAGTGCTCAGCATATATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10828
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052349 | Splice Site, Nonsense | 437 | 543 | 10 | 13 |
ENSDART00000129699 | Splice Site, Nonsense | 415 | 521 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 30443426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 28835768 |
GRCz11 | 7 | 29106918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCCAGCACTGAAGCTGATGCTTCCTCACGTGAGAACAAGAAAGACAAA[G/T]GTGAGTACATGTGTGTATGGGTGRTGTGCTTTCAGATCAGTTCTTANATT
Long Flanking Sequence:
TTGTGTCTTTTTGCTGTCAGGAGGAGAAACTGAGGCAGGTGCGCAGCGCACTGCAGTCCTCTGAGATCCAGTGGGAGAAGAGAGGGCCGCCAAATAAGAGGTCAGATCCGAACATCTGTCATGTGGTTTGATCATTTTCAGCTGTTAATCTCTTCCTGCACTTGCATGTTTTTCCTCATTCTGTTAATTGTCATCTGATTTGTTTATGCTCTGGTGTGTTAAAGATTATCATTGTGTTTAGGTGTTATAGCTGTGCAGATCTGCAGAGCATCCCGTCTTGTGTTCAGGAGTGCTGGGAACTCCTCTCGTCTGAGGCATTCTTCATCCTCTTATCTAACCTGACCGGCCTCAGTCTGCACTATCTGTGCACCAACGAGGATGACGGCGAGAATGAAGAGGGAAAGAGCGAGACGGAGAATAGAGACACAGAGGGAGATGCTCAAGCTGGGGGCTCCAGCACTGAAGCTGATGCTTCCTCACGTGAGAACAAGAAAGACAAA[G/T]GTGAGTACATGTGTGTATGGGTGGTGTGCTTTCAGATCAGTTCTTACATTTACAATCATTAAATTTGAATTCTTGCAGGACCTCCTAGTTGTGTTGGAGAAGTGCGTCGCTGGGCGCATGGGGACTATACACTGCTGCATGACTCCGTCAAAAGAGAGTATGCATTAGATCTGCAGCTCCACATGGGCTGTGCGGGTATGTCATTTGAAATTGATGTTACTGAATTAGGGCTTTTGCACAGGAGAACCTTTTTTTTTTTGGTTCCTAGAACTATACGCTTGTTAAGTCGTGATGTATGGAATACTGTTTCTGGGTCAAGGACGCTACTCATTTGAATTGAGAAAATATTTGTTTAGGACCATTTTTTTAGTCACACATTCTATATAAAATATGAATTCTATATAAAATCAGGCAGTACACATCAGTCTCTGGACTTGCTGCATCACAGACATCAATATTTTAACAATTTATACAAAATTCACTTTCTGGCCATTGGATAT
Associated Phenotype:
Not determined