Busch Lab

ZMP

ENSDARG00000061481

Ensembl ID:
ENSDARG00000061481
Human Orthologue:
FRRS1
Human Description:
ferric-chelate reductase 1 [Source:HGNC Symbol;Acc:27622]
Mouse Orthologue:
Frrs1
Mouse Description:
ferric-chelate reductase 1 Gene [Source:MGI Symbol;Acc:MGI:108076]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa30118 Nonsense Mutation detected in F1 DNA Not yet available
sa11026 Nonsense Available for shipment Available now
sa19343 Nonsense Mutation detected in F1 DNA Not yet available
sa44166 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30118
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087724 Nonsense 85 570 2 15
Genomic Location (Zv9):
Chromosome 24 (position 30758927)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 29787742
GRCz11 24 29775893
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAACGCTAAATAGCCAAACGGGATATTACTTTGAAGGCTTTATGTTG[C/T]AAGCACGCCCAGTTGGATCGAGCAGTACCATTGGCACTTTTTCTGTGACG
Long Flanking Sequence:
NNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATATATATATAGACTTTAGAATAAAATACTCATTTTACATAGTAACATTTGACACACACACACACACCATTGAATCCTGACAGATGATTCTTTCATCCCTCTGCATAATATGCATTGTTTATAACATGTTAACACATTGTACATACAGTATAAGCTACGCAATGCTCTATTATTTCTGAACTATTTCTTTCATGCAGATTATGTTGAGTCACTCACTACTGTCAAAATCAGTGAAATGTCATTTACAGCTGGTCACTGTATAACACCTGTACACTTATCAACTCATATCAGTGAGTTAATGGTCTGTCTTTATCTGAGAAGTTACACTGAACAGCTTTTCTTTTCTTTTCTCAGTAACGCTAAATAGCCAAACGGGATATTACTTTGAAGGCTTTATGTTG[C/T]AAGCACGCCCAGTTGGATCGAGCAGTACCATTGGCACTTTTTCTGTGACGGGGAATAATGTGCAGGTCCTCAGTTGTAATGGAATGCCTGTGAGTCTTTCTAACCCATCTCCAGTATATATACTGTATATAAAATGTTACATTAAAAACCCTTAAAGCAATTGCTTACTTACCCAAAAGTGAAAACCCTTTCAGTTGTGTATAAGGTATTGAGAAGAATACTGAGAGCCTGACAGCTGGCGATACTGTATGTTTTGACTTCCATAGTATTTATTGTGTTATTTTTTAAGAATCTCTTTAAGCCTGCTGATATTTCATGTAATGTATATGGGTAAAGATGCTATGTCCTGTTTTGGTGTCTGCAATCAAATTTAAAATGTAAAAAATGTTGATTTAATATACTTTTTAAAATTGCATTATTATTATTATTATTATTATTATTATTATTATTATTGCAGTCTTGAATTAGATACAATATTAATTTTAAATTAATGTTGTTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11026
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087724 Nonsense 459 570 11 15
ENSDART00000087724 Nonsense 459 570 11 15
Genomic Location (Zv9):
Chromosome 24 (position 30745330)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 29774145
GRCz11 24 29762296
KASP Assay ID:
554-6210.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGTTTGGTGATGATCCTCAGTCTCATTCAGCCCATCGTCGCTGCTTTC[C/T]GATGTGAGCCGCAACATGAACGGTGAGAATATAACCANNGCTATGTTTTT
Long Flanking Sequence:
ACTTTTATGCTGATTTCACTCCCTTACAAAATCATCACAATCAGTGTAAATTTATTGTAATTTTTTATTTAATGGAGTTGTGTCATCTTATATTGTGACATAAAAATGTGAAACTATATTCATATCACAATTTATATCACAGAAAAACAAAATACCGTCAATTTTTTTCCAATATCGTGCAGCTCTAATATAACATATATATTTTAAACCAGTATTTAAAGTCTGAAACATGGAACATTTAACACTGATCTACTGTCATTTTCTGCATATAAATGCTCTAATATAAAATCTCTTTTTTGAAATTTTTGAAGACATGTTATCAGTCGTTTATAAGACATAAATGCACATTTTAAGCATGTCCCTAGTATTGGCAAATGCTCTTGATTTTGGTAGTTTAAAGTAAAGTGTGTCTAACTTTAGTCTGTTTTTAGGGGGCTCATCCTGTCCTGGGCTGTTTGGTGATGATCCTCAGTCTCATTCAGCCCATCGTCGCTGCTTTC[C/T]GATGTGAGCCGCAACATGAACGGTGAGAATATAACCATAGCTATGTTTTTTTGTTTAATTAGTGAGGACTGGGGATCAATACAAATGTTCTTTAATAAAGACTACAATTAAAATGTATCATTTCACATAATCCATTAATATGTTAATTCTTGTAATAATGTTAACTAATAGGAATTGGTGTACAAAATATGAATAAGAACTTGGTTAAAGGTCTGTATATCTCGTTAGCTATCTCGTAGTAGCTGACGGTCCTCGCTTAGAGATGATCCTCATCATATTAAATCTGGTGGTTTTCTTTACAGGAGGTTTGTTTTCAACTGGGCTCACTCCTGCAATGCTTTCGCCATCAAATGCCTGGCAGGTATAGTATGATATCATTTCGTCAGTGTCTGCTCTGTTATTGTCCTCGGAAGAAAATAAGGTTTCATTCTGTCCCACAGTTGCTGCGATTTTCACCGGTCTGGCTCTGTTTGAAGAATATGATTCAGATGGGTGGATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19343
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087724 Nonsense 459 570 11 15
ENSDART00000087724 Nonsense 459 570 11 15
Genomic Location (Zv9):
Chromosome 24 (position 30745330)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 29774145
GRCz11 24 29762296
KASP Assay ID:
554-6210.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGTTTGGTGATGATCCTCAGTCTCATTCAGCCCATCGTCGCTGCTTTC[C/T]GATGTGAGCCGCAACATGAACGGTGAGAATATAACCATAGCTATGTTTTT
Long Flanking Sequence:
ACTTTTATGCTGATTTCACTCCCTTACAAAATCATCACAATCAGTGTAAATTTATTGTAATTTTTTATTTAATGGAGTTGTGTCATCTTATATTGTGACATAAAAATGTGAAACTATATTCATATCACAATTTATATCACAGAAAAACAAAATACCGTCAATTTTTTTCCAATATCGTGCAGCTCTAATATAACATATATATTTTAAACCAGTATTTAAAGTCTGAAACATGGAACATTTAACACTGATCTACTGTCATTTTCTGCATATAAATGCTCTAATATAAAATCTCTTTTTTGAAATTTTTGAAGACATGTTATCAGTCGTTTATAAGACATAAATGCACATTTTAAGCATGTCCCTAGTATTGGCAAATGCTCTTGATTTTGGTAGTTTAAAGTAAAGTGTGTCTAACTTTAGTCTGTTTTTAGGGGGCTCATCCTGTCCTGGGCTGTTTGGTGATGATCCTCAGTCTCATTCAGCCCATCGTCGCTGCTTTC[C/T]GATGTGAGCCGCAACATGAACGGTGAGAATATAACCATAGCTATGTTTTTTTGTTTAATTAGTGAGGACTGGGGATCAATACAAATGTTCTTTAATAAAGACTACAATTAAAATGTATCATTTCACATAATCCATTAATATGTTAATTCTTGTAATAATGTTAACTAATAGGAATTGGTGTACAAAATATGAATAAGAACTTGGTTAAAGGTCTGTATATCTCGTTAGCTATCTCGTAGTAGCTGACGGTCCTCGCTTAGAGATGATCCTCATCATATTAAATCTGGTGGTTTTCTTTACAGGAGGTTTGTTTTCAACTGGGCTCACTCCTGCAATGCTTTCGCCATCAAATGCCTGGCAGGTATAGTATGATATCATTTCGTCAGTGTCTGCTCTGTTATTGTCCTCGGAAGAAAATAAGGTTTCATTCTGTCCCACAGTTGCTGCGATTTTCACCGGTCTGGCTCTGTTTGAAGAATATGATTCAGATGGGTGGATGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44166
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087724 Essential Splice Site 486 570 12 15
Genomic Location (Zv9):
Chromosome 24 (position 30744967)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 29773782
GRCz11 24 29761933
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAACTGGGCTCACTCCTGCAATGCTTTCGCCATCAAATGCCTGGCAGG[T/G]ATAGTATGATATCATTTCGTCAGTGTCTGCTCTGTTATTGTCCTCGGAAG
Long Flanking Sequence:
AGTATTGGCAAATGCTCTTGATTTTGGTAGTTTAAAGTAAAGTGTGTCTAACTTTAGTCTGTTTTTAGGGGGCTCATCCTGTCCTGGGCTGTTTGGTGATGATCCTCAGTCTCATTCAGCCCATCGTCGCTGCTTTCCGATGTGAGCCGCAACATGAACGGTGAGAATATAACCATAGCTATGTTTTTTTGTTTAATTAGTGAGGACTGGGGATCAATACAAATGTTCTTTAATAAAGACTACAATTAAAATGTATCATTTCACATAATCCATTAATATGTTAATTCTTGTAATAATGTTAACTAATAGGAATTGGTGTACAAAATATGAATAAGAACTTGGTTAAAGGTCTGTATATCTCGTTAGCTATCTCGTAGTAGCTGACGGTCCTCGCTTAGAGATGATCCTCATCATATTAAATCTGGTGGTTTTCTTTACAGGAGGTTTGTTTTCAACTGGGCTCACTCCTGCAATGCTTTCGCCATCAAATGCCTGGCAGG[T/G]ATAGTATGATATCATTTCGTCAGTGTCTGCTCTGTTATTGTCCTCGGAAGAAAATAAGGTTTCATTCTGTCCCACAGTTGCTGCGATTTTCACCGGTCTGGCTCTGTTTGAAGAATATGATTCAGATGGGTGGATGTTGAAGGTTATGGGAGGTTATTTGGCCTGGGAGGCTCTGATGTACATTCTGCAAGATCTGAACCTGCGTGCCAAGAAAAAAGGTAATCTGATGCAAAATTTTACATTAATCAATGCTGTATCAATGCTGCAGACTGGAAGAAGCATAAAACTACCACTGAATAAATGATTTTTATAGTTCATAATTATAATAATAAAAAAAAAACTACTGTAAAGTTTGGCGTTAGGATATTTGTTTATTTATATTTTTAATATTTATTTTAAAAGAAGTCAGTTGTGGTCACCAAAGCTGCAGTTATTGTTCAGCTATGATTTATTATTGCAATTTAAAGATGACAGTTTTCTGTTGGGATATATATTTAAAA
Associated Phenotype:
Not determined