ZMP
LOC558772
Ensembl ID:
Human Orthologue:
NFE2L1
Human Description:
nuclear factor (erythroid-derived 2)-like 1 [Source:HGNC Symbol;Acc:7781]
Mouse Orthologue:
Nfe2l1
Mouse Description:
nuclear factor, erythroid derived 2,-like 1 Gene [Source:MGI Symbol;Acc:MGI:99421]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31880 | Nonsense | Available for shipment | Available now |
sa42051 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11267 | Nonsense | Available for shipment | Available now |
sa10608 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31880
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110934 | Nonsense | 21 | 815 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 30403890)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28740827 |
GRCz11 | 12 | 28855729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGTTGCTTTTTGAGTTTTCTTTTTTGTTCCTTTGCAAAGAAATGCTTTA[C/A]TTGAAAAAGTACTTCACAGAGGGTCTTATTCAGTTCACTATCCTCCTGAG
Long Flanking Sequence:
AAACAAAAATGGTCTGTGACATATAGATTGATATTACTCTGTTTTTGATATTATAATAAAACTTGATTTGTATAGCATGATAAGTCATGCTGCAAGTTGTAAACTTTAATGTTTCTTTCATTTATATCAATCTTTCATTGCAATCATAATCAGCTGTTATTCATGCCAATATAATGGCATTTTGACTATTGTTTCTCTTCTCTATGTTTGCAGGAAAAACTCATGCTTGCAGATATAACCTGGATATTATTTGGGGCGCAAAAGCGTTAATCAAAAACAAAAGTGGATTCAACTTTAGTAGTATTTAATTAAAAGCACATGACTGTGGAACAAAGCGAGCATCATTTTATGTTGTGTCTGCTTTTGATTTTTTATTATATACAAGGTTAAACGTAACCTAATTTGGTTTGACGTTTGTTTGCGTGATTTGTTTTTCTTTTTTTTGCTTTTTAGTTGCTTTTTGAGTTTTCTTTTTTGTTCCTTTGCAAAGAAATGCTTTA[C/A]TTGAAAAAGTACTTCACAGAGGGTCTTATTCAGTTCACTATCCTCCTGAGTCTGATTGGGGTACGAGTGGACTTGGACACTTACTTAAACAATCAGCTCCCCCCGCTCCGTGAGATCATCCTGGGCCCCAGCTCGGCCTACACCCAGACGCAGTTCCACAATCTCCGCAACACCCTGGACGGCTATGGCATCCATCCTAAAAGTGTGGATCTGGACCATTTTTTTGCCACTCGTCGGCTATTGAACCAGGTGCGTTCGCTGGATCATCTGCGTGTGCCTAGCACGGAGCTGAGTGCCTGGCTGGTGCATCGTGACCCTGAGACTGTGGTTTCGGCAACCAGTCAGTCCGGCCCCAGCATTGCCCTGGACAATGGGGGCAGCCTGGAGGACGTGAACAACTCCGAAGCCTCGGCCATGAGAGGGGCTGGCGGTACTTCTGAGACCACTTACAGCCTCAGTGGAGAGGACAGTCTGGGAGCCGTGGCCCCTGAGGACAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42051
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110934 | Nonsense | 317 | 815 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 30408524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28745461 |
GRCz11 | 12 | 28860363 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTCATTTTGCATTGTCTTTTATAGTTCCAGGCCACTGCTCCCACCTCA[C/T]AGCTGAGAGCTACAACTGAAGAAACGCCTTCAACGTCACAAGGGATTCCT
Long Flanking Sequence:
GGCTGATAAACCTAATGAAGAGAACGAAGAGGCAGGTGGAAGAGAGGAAAGCTGGAGAAATGGACTTGATCTCCGAGCAGTGCATAGCCTAACTCATGTTGATGGAGAGACAGGAGAGAGCATACCTGAGGAGGTATGTGCTGTAATGTGATAGGCTTACAGGAAGGTGTGAGGAGCATAGCAAGGTTTTGGTTAAAATTGCTTTTAGATTGTTTTCCTAAAAGGCTGGTAAGCTGTAGACGCATATGAGTTCCTGTCAAGCCTGTAATTACATGGACTTTTCTTGTCTTATTTTCTAGCTTACCAGTCTCGGTGCTCAGACTTCATTATCCCTGCAGGAATGTCTGAGGCTTCTGGAGGCAACTTTTCCATTTGGAGAAGAGCCAGAGGTAGAGTTGATTAAATGTTGTTATGTGGCACATTAAAACAGTTTTTTTTATTATTATTTGATTGTCATTTTGCATTGTCTTTTATAGTTCCAGGCCACTGCTCCCACCTCA[C/T]AGCTGAGAGCTACAACTGAAGAAACGCCTTCAACGTCACAAGGGATTCCTCTACAACCCACACTGTCGCAGACCGATACACCACTAGATCTGGAGCAGCAGTGGCAGGACATTATGTCCATAATGGAACTGCAGGTTTGTTCATTCTTTGCATTCTAGTGATGAATTTGAAGACTTTCTGAATTTATAGGTCAGGTTACAATGATTATAATGAGATTCTCAAGATATGAAGTTTAAGAATCAGTTTAAAAGTATACCTTTTTCACTTCATTGACTTATGGTATATCCTGTCAGTCAAACGTAATAGCACATTACACCGTAATTTTTTACGTTGGTCTTACTTCACATTACGGCTGGGTGTATCGAAATATATATCACTGCTTCAATATCTAAAATTTCTATTGTTAGTGATTTTGCTATATTATTTGGCCTATCACCTGAAGTGTACAGACAAAAAGCACCTTTCTTAGACAGCATGCAATCCTGATTTCAGTTCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11267
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 |
---|---|---|---|---|---|
ENSDART00000110934 | Nonsense | 330 | 815 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 30408563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28745500 |
GRCz11 | 12 | 28860402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCCACCTCACAGCTGAGAGCTACAACTGAAGAAACGCCTTCAACGTCA[C/T]AAGGGATTCCTCTACAACCCACACTGTCGCAGACCGATACRCCACTAGAT
Long Flanking Sequence:
AAGAGAGGAAAGCTGGAGAAATGGACTTGATCTCCGAGCAGTGCATAGCCTAACTCATGTTGATGGAGAGACAGGAGAGAGCATACCTGAGGAGGTATGTGCTGTAATGTGATAGGCTTACAGGAAGGTGTGAGGAGCATAGCAAGGTTTTGGTTAAAATTGCTTTTAGATTGTTTTCCTAAAAGGCTGGTAAGCTGTAGACGCATATGAGTTCCTGTCAAGCCTGTAATTACATGGACTTTTCTTGTCTTATTTTCTAGCTTACCAGTCTCGGTGCTCAGACTTCATTATCCCTGCAGGAATGTCTGAGGCTTCTGGAGGCAACTTTTCCATTTGGAGAAGAGCCAGAGGTAGAGTTGATTAAATGTTGTTATGTGGCACATTAAAACAGTTTTTTTTATTATTATTTGATTGTCATTTTGCATTGTCTTTTATAGTTCCAGGCCACTGCTCCCACCTCACAGCTGAGAGCTACAACTGAAGAAACGCCTTCAACGTCA[C/T]AAGGGATTCCTCTACAACCCACACTGTCGCAGACCGATACACCACTAGATCTGGAGCAGCAGTGGCAGGACATTATGTCCATAATGGAACTGCAGGTTTGTTCATTCTTTGCATTCTAGTGATGAATTTGAAGACTTTCTGAATTTATAGGTCAGGTTACAATGATTATAATGAGATTCTCAAGATATGAAGTTTAAGAATCAGTTTAAAAGTATACCTTTTTCACTTCATTGACTTATGGTATATCCTGTCAGTCAAACGTAATAGCACATTACACCGTAATTTTTTACGTTGGTCTTACTTCACATTACGGCTGGGTGTATCGAAATATATATCACTGCTTCAATATCTAAAATTTCTATTGTTAGTGATTTTGCTATATTATTTGGCCTATCACCTGAAGTGTACAGACAAAAAGCACCTTTCTTAGACAGCATGCAATCCTGATTTCAGTTCTTTTTTTGCAGCTTATTGCATTTGAATGTTCAATTACTCACAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10608
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110934 | Nonsense | 519 | 815 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 30410745)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 28747682 |
GRCz11 | 12 | 28862584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCAGCCAAGCCCAGGCTTCTCAGCTCGAGGATGAGCTTGATTCAGACT[C/A]AGGTCTTTCTTTGGATTCCAGCCATAGTCCAGCATCTCCCAGCAACTCGG
Long Flanking Sequence:
TGTCTAACTTTCATTATGTCTTTTTTAGGACATGGAGGTGAACAATACGGCAGTAAATGCCACCATAAATAATGACCCCAATAACAACAATGCCAGCACTACAGAATCAGCAACAGTAGGAAATTTTGGGCTCCCACGATCCACTCTCATTAACCAGGATGTTAGTCTCCAGCAGGCATTACTTCCCAGCTGTGGCCAGGACTTTCCCACACTCTTTAACCCAGAGTTGGGCGGACAGCAGCCTACCTTAGTCAGGCTCTCTTCCAGCAACTCCTCCAACATCAATTCAACATTTGGAGCAACTAACTTGACAGGAATCTTTTTCCCACCACCTCTAAACAGTACAACCAACGTAACCACTACTCCGGTGCTGCCAGATCCATTCTCTAGCCTGCTGGAAGAGTCGATGCTTGATGAAATTAGCTTGCTAGACCTTGCGATGGAAGAGGGTTTCAGCCAAGCCCAGGCTTCTCAGCTCGAGGATGAGCTTGATTCAGACT[C/A]AGGTCTTTCTTTGGATTCCAGCCATAGTCCAGCATCTCCCAGCAACTCGGAGACGTCCTGCTCATCAGCTGCATCATCTTCATCCACCTCTGCTACATTTTCTGAAGAAGGAGCCGTGGGCTACAGCACCGATTCTGAAGCAGCCACAGCAGAAACGGAGGAAGGAGCCGTCGGAGGATACCAGCCAGAGTATAGCAAACTATGCCGCATGAGCTACCAAGACCCTTCTCAATTTCATGGCGTACCACAGTTGGAAAGCGTCAATCACAATCACACCTACAATCTACCGCTGGCATCGTCCTTCTCAGAGCGTTCTCAGCTGTCCACATCCAGCAGCAAGAAAGGCAGAGACAAGCAAATGCAGCAGACGAAACTCCAGCCCCCACAAGACTGCATTGACAGGCAGTCGAGCCGCGATGAGCGTAGGGCAAGGGCCATGGACATCCCATTCTCTAATGAAAAAATCATCAACCTCCCTGTTGAGGAGTTCAACGAGCTTC
Associated Phenotype:
Not determined