Busch Lab

ZMP

por

Ensembl ID:
ENSDARG00000055092
ZFIN ID:
ZDB-GENE-050809-121
Description:
NADPH--cytochrome P450 reductase [Source:RefSeq peptide;Acc:NP_001030154]
Human Orthologue:
POR
Human Description:
P450 (cytochrome) oxidoreductase [Source:HGNC Symbol;Acc:9208]
Mouse Orthologue:
Por
Mouse Description:
P450 (cytochrome) oxidoreductase Gene [Source:MGI Symbol;Acc:MGI:97744]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa4381 Nonsense F2 line generated Not yet available
sa21780 Nonsense Available for shipment Available now
sa38807 Nonsense Mutation detected in F1 DNA Not yet available
sa13459 Essential Splice Site Available for shipment Available now
sa41702 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa9088 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa4381
Status:
F2 line generated
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
ENSDART00000077404 Nonsense 150 674 5 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36317802)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35350504
GRCz11 10 35294364
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGCAACCTATGGAGAGGGAGACCCTACAGACAACGCTCAGGAGTTCTA[T/A]GATTGGTTGCAAGGGACAGATGACGATCTGGAGGGGGTTAATTTTGCTGT
Long Flanking Sequence:
ATGGGCCATCTGACCAATCAGAACAGATTATTGCATGATCTGACCAATCAGAATAGCCTGGGCTATGATCTGACGAATCACAGTCAGAATAGAATAATCAGAGCAGAATAGGTTGTCGAAATGTGGGGTTTTGAGAGACCAGATGCTGAAATGAACCATTTCAGACCTTGTGCAGAAAAAAATGATGCTGCAAAGGATATTGCAAGTAATTTAAAGGATTATTAAACCTGCATGAATGTTTAAACTATTCATTATAAACCATCAAAACAAAATTAGGAATCTTTAAAATGGTAAATATGGGGTACATTAAAAATCACTTAAGATAAGAATTGTTCTGTGCTTTTTTACTCTTTTTTACTCTTTTGACTTGTAAATTAATATCTTCAATCCCATTCACAGTCTGAGTTGTCCCGACTGAAAGAGATTCCTAAATCGATGGCTGTGTTCTGCATGGCAACCTATGGAGAGGGAGACCCTACAGACAACGCTCAGGAGTTCTA[T/A]GATTGGTTGCAAGGGACAGATGACGATCTGGAGGGGGTTAATTTTGCTGTGAGTATAACCTCAGAAAAGCCCATAGGAAGCTAGTATTGTCTCTAACCAAACTAAAGAGAATGTATCAGATAAACCATTCGTCTATTTTCAGTCTGACGCCAGGTGTCACCGTTTCTTGGTCCAAATCACATCAGATGTCATACAACAAATGATAATATATGCTCATAATATGCTGTATTATTTTTGAAAATCATGATCATATTGTCTGTCCATGCATCTTAGATGGTCAGATAGGATTTAATCTTTTATAAATCATTGAGAGAGTGGTTTCTGGAATACAGTAAGGTTTAGAGACTGTTTAAACTTTGATTTTTGTAAATGATTCACTTTAATGTGGGATATGCAGTGGTAAAAAAAGAGAATTGAAAAAAAAAACTGAAGTAAAAGTACCATTACTTGCCAATAATAATAATACTGAAAGTAAGAGTAAAAAGTAGTCCTTCAGAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21780
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077404 Nonsense 258 674 8 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36323889)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35356591
GRCz11 10 35300451
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTGAACTGGTGGTTCATAATGACATCAATATGAATCAAGTGTACACC[G/T]GAGAGATGGGCCGCCTCAAAAGCTTTCAGACGCAGAAACCGTAAGTTCAT
Long Flanking Sequence:
GAGGACTTTATATCTTGGAAGGAGCAGTTTTGGCCTGCGGTGTGTGAGTATTTTGGCGTGGAGGCCACTGGAGAGGACAGCAGGTATTACTTTTTATTCTCAAAGTGCTTGTCTTGTCATTTCAATTCAGAATTCTGTTGTTTACTTTAAAAACAGACTGCATTGGTAGGCAGCGTATTTATAAGAGCTGACCATCTGTATCAGATTGTCTAGTTCAAACATGATGTTTATTTGATGGCTGTTTTTGTAGCCATAAAGCGCATTCAGTCTCGCATCTCCATATTAGAAGGACCACATCCATTCATCATGTGCTTTCATAACAAAGACCTCCCCTGTCCTGCTTTGAATAGGTTTTTGCATCTTATTAAACATCATAGGTGTTTTGAATGCTTTAAATGCAGTCTAGTAAATGATCTCCAGTCCTTTTTTTGTGTGCTTTCAGCATTCGGCAGTTTGAACTGGTGGTTCATAATGACATCAATATGAATCAAGTGTACACC[G/T]GAGAGATGGGCCGCCTCAAAAGCTTTCAGACGCAGAAACCGTAAGTTCATCCCTTTCAACTAAGCCATTGATTGGCATTTTAAAAGATCAGCTTTTCATTCTTGATCTAAAATGTCATGCTTCTTTTGTAAGGTAGTCTGTGAAAGTAATGTTTGGTGCAATGTTTTATTTACAACATATTTAGCAAGAGTTTGTAAAAAGATTTTGATCTGATGGATAGATGTGTTGTTGTGTAGACCGTTTGATGCCAAGAACCCTTTCCTTGCATCCGTGGCTGTTAATCGTAAGCTGAACAAAGGAGGAAACCGCCATCTGATGCATATCGAGTTAGACATCACTGAGTCCAAGATCAGGTACATGCACTGATTGGGTTGAGTAAATTGTGAGAATGCATTTACATTAAAATGTGTATTTTATTTTTCTTTTCAGAGGAAAACATTATGGCTATCATACATTTGTACCCATGATTTGGAGAAGACACTAAAATGTCATTCAGTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38807
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
ENSDART00000077404 Nonsense 425 674 12 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36327682)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35360384
GRCz11 10 35304244
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTAGGCTCTCTACCAAAGTTGGGTTCTGGATTCGGAGAGGAACATAT[T/A]GGCTATTCTAGAGGATCTGCCTTCGCTGAATCCTCCTATAGATCACCTGT
Long Flanking Sequence:
CGGTCCTGCTGAGTTTAGCTCCAACTTGCTTCAACACACCTGCCAGGATGTTTCTAGTATATCTAGTAAGAGCTTGATTAGCTGGTTCAGGTGTGTTTGATTAGGGTTGGAGTTAACTCTGCAGGACACCAGCCCTCCAGGACTGAGTTTGGACACTCCTTCTGTTCATAATATAACATGCTTTTGATGTTTCAATTCTGCAGAGGAGTCCAATAAAAAGCACCCTTTCCCCTGTCCCACCACATATCGCACTGCACTGACCCACTACCTCGACATCAACAACATGCCCCGTACGAATGTGCTGTATGAGCTGGCGCAGTATGCCTCGGATCCGCAGGAACAGGAGAACATGCGCAAGATGGCATCTGCGTCGCCTGAAGGAAAGGTCAGGATTGTACCGTAATCACTGCTGTTATGCCCAGAGGAGTCTTTTTTACCTTCTGCTTGGTCTTTTTAGGCTCTCTACCAAAGTTGGGTTCTGGATTCGGAGAGGAACATAT[T/A]GGCTATTCTAGAGGATCTGCCTTCGCTGAATCCTCCTATAGATCACCTGTGTGAGTTGCTGCCTCGGCTTCAGGCTCGGTACTACTCCATCGCCTCCTCCAGCAAGGTAAAAATGACAGTTTGTCATAAACAATCAGAAATTTTGAGTCAGTAGCCCCTTTCACACATACAGACCTTTCCGGAAAATTGCCAGCAATTTTCCCGAAAGGTTGTATGTGTGAACAAGTCCTTTTTGAAAATACCGGTAAATTCGTTCTGGCTATTTTCCGTAAAGAGAAGTTGTAACATTACCGGCAATTTGCCGGAATGCTGCGCTGTGTGAACGCAAAAGGAAGATTGCCGGAATAAGCGTGTGCTGGTCTAGATTGGCTGACGTGAGACGTCTGCTTTAGCCAATCACAACAGTCAGACGCATTTATGTCCGCGCGGTTCATGAGAATAAAAGCCTTTGAATATTTTTCCAGACACATTTAGCTGCTAGAAGTTAGTCAGATCACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13459
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077404 Essential Splice Site 598 674 14 16
ENSDART00000077404 Essential Splice Site 598 674 14 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36332962)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35365664
GRCz11 10 35309524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGTGCTGACGCAGCTTAACGTGGCCTTTTCCAGAGACCAGGAGCAAAAGG[T/G]RAACYAATTCATGGAAAATAATGATACAAATRTTATTGTGTTATTGCTGC
Long Flanking Sequence:
AATCCAATTCACCAATAGTGAAAGTCTTTGGACCGTAGGGGAAACTGGAGCACCTGGAGGAAACCCACACCAACACAGGGAGAACATGCAAACTCCACACCGACTCGAACCAGCGACCTCCTTGCTGTGTGTGACAGTGCTAACCACTGACCCACCGTGCCACCCTATTTAAGATACATATCAAAGCAAACTATTTCTGACTGTTTTAAGGCCTAACACTTGACACATCTTGTTTTGACAACCTTCAGGGGCGATCAAGCATTAATTATGGGTATCCAACCTCTTAAACCCCCCTGTAAATCACACACTTGTAGTATTGAAAAGGTATGACTTACTTTTGCTCTTTGTTGCAGGAAAGGATGTTGGTGAGACGATACTTTACTTTGGCTGTCGCCATAGCAACGAAGACTTCCTGTACCAGCAGGAACTGGAGGAATTTGAGAGGGCAGGCGTGCTGACGCAGCTTAACGTGGCCTTTTCCAGAGACCAGGAGCAAAAGG[T/G]GAACCAATTCATGGAAAATAATGATACAAATGTTATTGTGTTATTGCTGCCATAGGTATTTGTTTACTTCCTGTATTAAATATGCAATATGTTATACCACTTATATACAGTCTGGGTATAAACACAAGCCCCAGGATTCCAAAGGCATTTGAAAATATATTTTTAAAGTTATTATTTTACTCAAGAAGGATGCATTAAATTCATCTAAAGTGACAGTAAAGATATGTATATTATTACTAAATATGTGCTGCTCCTTTAAACTTCAAAAACTGCTCCCCAATAATGCGAAGCAGTTTTCAACATAACGATGATCAGAAATTTGAGTCCTTTTATGTACTGGGCTGTTTTTCGCAGGTCTATGTGCAGCATCTTCTGAAGAAAAACAAGCAGCAGTTGTGGAAGCTCATCCATACAGATAATGCTCATATCTACGTTTGTGGGTAAGAACCAGAAGTTGCTTCTATTCAGTCTGTCAATGCAGAAAACACACTATAAATTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41702
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077404 Essential Splice Site 598 674 14 16
ENSDART00000077404 Essential Splice Site 598 674 14 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36332962)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35365664
GRCz11 10 35309524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGCTGACGCAGCTTAACGTGGCCTTTTCCAGAGACCAGGAGCAAAAGG[T/C]GAACCAATTCATGGAAAATAATGATACAAATGTTATTGTGTTATTGCTGC
Long Flanking Sequence:
AATCCAATTCACCAATAGTGAAAGTCTTTGGACCGTAGGGGAAACTGGAGCACCTGGAGGAAACCCACACCAACACAGGGAGAACATGCAAACTCCACACCGACTCGAACCAGCGACCTCCTTGCTGTGTGTGACAGTGCTAACCACTGACCCACCGTGCCACCCTATTTAAGATACATATCAAAGCAAACTATTTCTGACTGTTTTAAGGCCTAACACTTGACACATCTTGTTTTGACAACCTTCAGGGGCGATCAAGCATTAATTATGGGTATCCAACCTCTTAAACCCCCCTGTAAATCACACACTTGTAGTATTGAAAAGGTATGACTTACTTTTGCTCTTTGTTGCAGGAAAGGATGTTGGTGAGACGATACTTTACTTTGGCTGTCGCCATAGCAACGAAGACTTCCTGTACCAGCAGGAACTGGAGGAATTTGAGAGGGCAGGCGTGCTGACGCAGCTTAACGTGGCCTTTTCCAGAGACCAGGAGCAAAAGG[T/C]GAACCAATTCATGGAAAATAATGATACAAATGTTATTGTGTTATTGCTGCCATAGGTATTTGTTTACTTCCTGTATTAAATATGCAATATGTTATACCACTTATATACAGTCTGGGTATAAACACAAGCCCCAGGATTCCAAAGGCATTTGAAAATATATTTTTAAAGTTATTATTTTACTCAAGAAGGATGCATTAAATTCATCTAAAGTGACAGTAAAGATATGTATATTATTACTAAATATGTGCTGCTCCTTTAAACTTCAAAAACTGCTCCCCAATAATGCGAAGCAGTTTTCAACATAACGATGATCAGAAATTTGAGTCCTTTTATGTACTGGGCTGTTTTTCGCAGGTCTATGTGCAGCATCTTCTGAAGAAAAACAAGCAGCAGTTGTGGAAGCTCATCCATACAGATAATGCTCATATCTACGTTTGTGGGTAAGAACCAGAAGTTGCTTCTATTCAGTCTGTCAATGCAGAAAACACACTATAAATTGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9088
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
ENSDART00000077404 Nonsense 600 674 15 16

The following transcripts of ENSDARG00000055092 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 10 (position 36333322)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 35366024
GRCz11 10 35309884
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATCAGAAATTTGAGTCCTTTTATGTACTGGGCTGTTTTTCGCAGGTCTA[T/A]GTGCAGCATCTTCTGAAGAAAAACAAGCAGCAGTTGTGGAAGCTCATCCA
Long Flanking Sequence:
TGTTGGTGAGACGATACTTTACTTTGGCTGTCGCCATAGCAACGAAGACTTCCTGTACCAGCAGGAACTGGAGGAATTTGAGAGGGCAGGCGTGCTGACGCAGCTTAACGTGGCCTTTTCCAGAGACCAGGAGCAAAAGGTGAACCAATTCATGGAAAATAATGATACAAATGTTATTGTGTTATTGCTGCCATAGGTATTTGTTTACTTCCTGTATTAAATATGCAATATGTTATACCACTTATATACAGTCTGGGTATAAACACAAGCCCCAGGATTCCAAAGGCATTTGAAAATATATTTTTAAAGTTATTATTTTACTCAAGAAGGATGCATTAAATTCATCTAAAGTGACAGTAAAGATATGTATATTATTACTAAATATGTGCTGCTCCTTTAAACTTCAAAAACTGCTCCCCAATAATGCGAAGCAGTTTTCAACATAACGATGATCAGAAATTTGAGTCCTTTTATGTACTGGGCTGTTTTTCGCAGGTCTA[T/A]GTGCAGCATCTTCTGAAGAAAAACAAGCAGCAGTTGTGGAAGCTCATCCATACAGATAATGCTCATATCTACGTTTGTGGGTAAGAACCAGAAGTTGCTTCTATTCAGTCTGTCAATGCAGAAAACACACTATAAATTGGCAGCATAATGCAGAATGACATGAAATCTGGCAAATTTTACAGTGATTGATCAAATCAGCGGCGCGGTGGCTCAGTGGTTAGCACTGTCGTCTCAACGGCAAGAAGGTCGCTGGTTCGAGCTCGAGCACAGAAAGTTGACATTTCTGTGTGAAGTTTGCATGTTGTCCCCTTGATGAATTGTTCTCCCCCGGGGTGATCCGGTTACCCCCACAGTCCAAAGATATGCAATATGGGTGAATTGGATTAAAAAAAGATGACTGTAGTGTATGAGTGTGTCTGTGAAGAAGTGTGTATGTGTGCTTCCCAGTACTGGGTTGCGGCTGGAAGGACATCTGCTGCGTAAAATCTGCTGGTGGTTCA
Associated Phenotype:
Not determined