ZMP
foxe1
Ensembl ID:
ZFIN ID:
Human Orthologues:
FOXE1, FOXE3
Human Descriptions:
forkhead box E1 (thyroid transcription factor 2) [Source:HGNC Symbol;Acc:3806]
forkhead box E3 [Source:HGNC Symbol;Acc:3808]
forkhead box E3 [Source:HGNC Symbol;Acc:3808]
Mouse Orthologues:
Foxe1, Foxe3
Mouse Descriptions:
forkhead box E1 Gene [Source:MGI Symbol;Acc:MGI:1353500]
forkhead box E3 Gene [Source:MGI Symbol;Acc:MGI:1353569]
forkhead box E3 Gene [Source:MGI Symbol;Acc:MGI:1353569]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39620 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32687 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39620
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109297 | Nonsense | 33 | 354 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 25668903)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 26009120 |
GRCz11 | 1 | 26702834 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAGTGAATGACAGTCAGAGAGCAGAGCCGCAAAGAGGCCGTCGGAGG[A/T]AGAGGCCCCTTCAGCGAGGCAAACCACCATACAGCTACATCGCTCTGATC
Long Flanking Sequence:
GTGTGGCTAATAACTCTTCAGGTAGTGTGTTCCTTGGTCAGCACAGTCAGTTATTGACTGCTCACTTGTCTCTTCCACATTACGAAGACCACTACCAAAAAAGACTGTTTATGTGAGTGCTTCCATTTTTTATGTTCACTTAGTTTTGCATGAACTCCTCTGAATTAAGGACACTGTGGTGTAAGGATACACTTAACGATACAGATGAAGATCAAAGGAACAGATCTTTCTGCTTGGGGATTTTAAGGTCTGCATTATGACTGGTACTTTTTCACCAGAATACATTCAGCAAGCAAAGACCATTTGCTGCTCCTGACAAAGAACCCGGTGAACCGAATCAGTGACAGTCAGACTATAGTGATTTCCAAGCTGTGCTACCTTTGGGAGCGATTCTAACTAGAGTCATGCCTGTGGTTAAAGTGGAGAGTGATTCTCCCTCTGAAACCACTCTTCCAGTGAATGACAGTCAGAGAGCAGAGCCGCAAAGAGGCCGTCGGAGG[A/T]AGAGGCCCCTTCAGCGAGGCAAACCACCATACAGCTACATCGCTCTGATCTCCATGGCCATCGCTAACTCGCCTGACCGCAAACTCACTCTGGGAGGGATCTACAAGTTTATCACCGAGAGGTTTCCCTTCTATCGAGACAACTCCAAGAAATGGCAGAACTCCATCCGCCATAATTTGACACTCAACGACTGCTTTATCAAGATCCCACGAGAGCCCGGTAGGCCCGGAAAAGGCAACTACTGGGCTCTTGACCCTAACGCCGAAGACATGTTTGAAAGTGGAAGCTTCCTACGACGTCGAAAGCGGTTCAAGCGCAGCGACTTCACTACATATTCATCATATGTGCACGAATCTCCCGTTTTCTCACCGGTCCAGATTGCGCGCTCAGCCTACGCCAACTCCGTCTACTCCAACATGGCTGTGAGTCCGCCATACGCACAACAGCTTCCTTCTGCTTACTACCAGTCCTCCTCTCCAAACTTCACAGCGGGTCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32687
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109297 | Nonsense | 84 | 354 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 1 (position 25668749)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 26008966 |
GRCz11 | 1 | 26702680 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGTTTATCACCGAGAGGTTTCCCTTCTATCGAGACAACTCCAAGAAAT[G/A]GCAGAACTCCATCCGCCATAATTTGACACTCAACGACTGCTTTATCAAGA
Long Flanking Sequence:
CTCCTCTGAATTAAGGACACTGTGGTGTAAGGATACACTTAACGATACAGATGAAGATCAAAGGAACAGATCTTTCTGCTTGGGGATTTTAAGGTCTGCATTATGACTGGTACTTTTTCACCAGAATACATTCAGCAAGCAAAGACCATTTGCTGCTCCTGACAAAGAACCCGGTGAACCGAATCAGTGACAGTCAGACTATAGTGATTTCCAAGCTGTGCTACCTTTGGGAGCGATTCTAACTAGAGTCATGCCTGTGGTTAAAGTGGAGAGTGATTCTCCCTCTGAAACCACTCTTCCAGTGAATGACAGTCAGAGAGCAGAGCCGCAAAGAGGCCGTCGGAGGAAGAGGCCCCTTCAGCGAGGCAAACCACCATACAGCTACATCGCTCTGATCTCCATGGCCATCGCTAACTCGCCTGACCGCAAACTCACTCTGGGAGGGATCTACAAGTTTATCACCGAGAGGTTTCCCTTCTATCGAGACAACTCCAAGAAAT[G/A]GCAGAACTCCATCCGCCATAATTTGACACTCAACGACTGCTTTATCAAGATCCCACGAGAGCCCGGTAGGCCCGGAAAAGGCAACTACTGGGCTCTTGACCCTAACGCCGAAGACATGTTTGAAAGTGGAAGCTTCCTACGACGTCGAAAGCGGTTCAAGCGCAGCGACTTCACTACATATTCATCATATGTGCACGAATCTCCCGTTTTCTCACCGGTCCAGATTGCGCGCTCAGCCTACGCCAACTCCGTCTACTCCAACATGGCTGTGAGTCCGCCATACGCACAACAGCTTCCTTCTGCTTACTACCAGTCCTCCTCTCCAAACTTCACAGCGGGTCAGTCAAGGGTCTTCAGAATCAATTCTCTCATTGGGTCACCAAGCCGGATGGGTCAAAACGCAGAGATGATCCCACAGCAGTCCTGTCGCAGTTTCAGTCCTGAAAGTGGCTCCTGCAGTTTGGGAGGACCGGGCTTCCAGCATCAGTCCTGCAACGGGG
Associated Phenotype:
Not determined