Busch Lab

ZMP

foxn1

Ensembl ID:
ENSDARG00000011879
ZFIN ID:
ZDB-GENE-021008-1
Description:
forkhead box protein N1 [Source:RefSeq peptide;Acc:NP_997738]
Human Orthologue:
FOXN1
Human Description:
forkhead box N1 [Source:HGNC Symbol;Acc:12765]
Mouse Orthologue:
Foxn1
Mouse Description:
forkhead box N1 Gene [Source:MGI Symbol;Acc:MGI:102949]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa45541 Nonsense Mutation detected in F1 DNA Not yet available
sa35901 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45541
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
ENSDART00000026567 Nonsense 184 565 3 8
Genomic Location (Zv9):
Chromosome 15 (position 27493318)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 28211558
GRCz11 15 28144434
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCTACACAACAGTAAACCATCAGGCATACAGTGCCATCAGTCCTCTA[C/T]AACACCAGGTACAAACATTGTACACAATGACAGTGGAGAGTTTTTGTCAT
Long Flanking Sequence:
GGTAAATAGAAATCGGGGAAAAATAAACAACAGAGGGGCTGATAATTCATTATGCATTCATAGTGCATTTTCATTCTTTCTTATATTTTCATACTTATTCTCCATTCATCTGATCACAATTCCCTATTTCCATCCACTTTTTTGTCTGAACTTTGAGACATACTGTATGTATGGAATTATATATAAATCATTTATAATATACCTCCATCATTTATAATAATTTTTACGGCATGAAGGCTCTTTAAATTCTTGCCAGCACATTTAGCCCAGAGGCAAAAGACATGGAAACAAGAAGACCTGACAGGCAGATGTGCAAGCAGATGTCCTTATTACACTTTCTAAAGAGGCTTGAACATATGAAATTTTAGCACTAAGTAGATGTTGCTCTATATTGTGGGCAGGGAACTCGGCGACCTTACAGTGAGCCTCAGGAGAGCTCTGAAGAACCTCCTGGCTACACAACAGTAAACCATCAGGCATACAGTGCCATCAGTCCTCTA[C/T]AACACCAGGTACAAACATTGTACACAATGACAGTGGAGAGTTTTTGTCATATACTGATTATACAAGATGCAGTTTAAATATCTGAGTGAATATCTTTAATGTTTTTTGAATGTCTCTTATTCAACATTCAACATTCAACTTTCTTTAACAAGGCTGCATTTACTGGGTCAAAAATCGCACAAAACAGTAAATAGTGAAATTATAAATTATATTATATATTTCTTTTTTAATATATTTCAAAGTTACAGTTAATCTGTCGTGTTTGTAAAACTGAATTTTCATGATCATTAATAAACAAAGAATTACAATTTCTGACAAGGGCTGATATATAAATTAATTTAAGTTTTAGTTTTGGTCATTTACACATGCGCACACACACACACACACACACACACACACACACACACACACACACACACACACACGATTTTTATACTGTACGTTCTATACCCCTACATCTAAACCCATCCCTCACAGGAAACAATCTGCATTGTTACATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35901
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
ENSDART00000026567 Nonsense 385 565 7 8
Genomic Location (Zv9):
Chromosome 15 (position 27483787)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 28202027
GRCz11 15 28134903
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTGTCCACGAGAATAGGATCCTGAATCAGAAGGCTCTCTACAACCCTT[T/A]AACATCTCAAAATGCTGTCCTGCCTCCTCCTTACATTTCTCCAGACCCTT
Long Flanking Sequence:
AGCCGCAACCCATTTCTGGGAAACATCCACACACACATTCACACACACACACTCATACACTACGGACAGTTTAGCCCACCCAATTCACCTGTACCACGTGTCTTTGGACTGTGGGGGAAAACAGAGCACTCGGAGAAAACCCAGGCGAACGCAAGGAGAACATGTACACTCCACACAGAAACACCAACTGAGCCAAGGTTCGAACCAGCGACCTTCTTGCTTTGAGGCGACAGCACTACCTGCTGCGCCACTGCGTTGCCTTAAAAAAAAATACAATCAAAAGTAATATATTTATTTGTTCATACTCTCCATTATGCTGATTGTTTTAGAGGAGCTGGAACGTCTTCTTGGTGAGAGACCTGAAAAATTGAAGAGTCACTTCAGTCTGCCCAGCAGCCACACACATTCCCAGCCCTTCAGAGTTAACATGCATCCTGCCTACGGACACCAGCCTGTCCACGAGAATAGGATCCTGAATCAGAAGGCTCTCTACAACCCTT[T/A]AACATCTCAAAATGCTGTCCTGCCTCCTCCTTACATTTCTCCAGACCCTTTAGCCTTCCAATACTACTCTCCAGCCACTCATCAGCCCAGCGTCGGCCATCCCTCCAGTCCCAGGACAGGCAGTTTGGATTCACCTCTACCAGCACACACTCCACCAAGCTACAGCACCGCCCTGCAGGCTGGTCACAGCGGGACAGCGAGCATGCAGGAGCTTCTGCTGGATGGAGAAATCAACAATGATGTTGATGCTTTAAATCCCAGCCTTACAGATCTGCAACTACATGGTAAGACATTATTATTTAATTATATTATCATATAGTTATTATATTAATTTCAGATGTATTACTGAAAAATATAAAAATGTTTATATGATTTATTCACAATACAGTTTGTAAAGTAATATTTTCTGTTATGTGGTTGATATATTATATGAGAGACTTGCTACGTTTACCAAATATTAATTCATTTTCCTTTGGTTAGTTCCTTTATTAATCAGGGGT
Associated Phenotype:
Not determined