ZMP

foxi3a

Ensembl ID:

ENSDARG00000055926

ZFIN ID:

ZDB-GENE-031126-3

Description:

forkhead box I3a [Source:RefSeq peptide;Acc:NP_944599]

Human Orthologue:

FOXI1

Human Description:

forkhead box I1 [Source:HGNC Symbol;Acc:3815]

Mouse Orthologue:

Foxi1

Mouse Description:

forkhead box I1 Gene [Source:MGI Symbol;Acc:MGI:1096329]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29622	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa29623	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa29622

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078341	Essential Splice Site	184	353	1	2

Genomic Location (Zv9):

Chromosome 21 (position 29095952)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	30315196
GRCz11	21	30351891

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTCGCTCAATGACTGCTTCATGAAAGTGCCCAGAGATGACAGCGATCCAG[G/A]TGAGAACTTGTTCAAACTGTTCGTGTGTATCTGCTTGGGTTGTACTTTAG

Long Flanking Sequence:

GGAGTCCCAAGAGTTCAGCCTGTACGGTGACAACTTCTACAGCGCCCAGCATGTGCCTAGCCCACAACAAACCCTGCCATCCGCTTACGATTTCGGAGAATACGCAGGGCAGACCTCCAACCCTTACCTGTGGTTCAACGGGCCAGGACTCAGTCCAGCTCCTTGCCTCACCACAGGGCCTCAGCACTATGGGATGGCGAAGCAGTATGTGGGCGCAAGTGGAATCGGAGGCTCAGAGGGTGCCTTCAGCTGGTTCTCTCTGCCATCCCAAGAAGATCTGATGAAACTCGTGAGACCTCCCTACTCGTACTCTGCACTTATTGCGATGGCAATACATGGAGCTCCAAACCGCCGGCTCACCCTCAGCCAGATCTACCAGTATGTGGCTGACAACTTTCCTTTCTACAACAAGAGCAAAGCCAGCTGGCAGAACTCAATCCGGCACAATCTCTCGCTCAATGACTGCTTCATGAAAGTGCCCAGAGATGACAGCGATCCAG[G/A]TGAGAACTTGTTCAAACTGTTCGTGTGTATCTGCTTGGGTTGTACTTTAGCCTTAGTTCGATGTTTAATGACAAAATAATCAAGTTTCTTCTTTTTTTAATAGGAAAAGGCAACTATTGGACTCTTGACCCAAACTGTGAGAAGATGTTTGATAATGGAAACTTCCGGCGCAAGAGGAAGAGAAAGTCGGACTCTCAGGCTGAAGAGGAGGGAAAAGGGTACTCTGGATCAGACTCTGCTCTGTCCAGTCCTAAAAACCCCAGCGACTCCTCGGAGAGAGGAAACTCTCCAATCTCCACAGATCAAGCTCCGTGTCTCAACAGCTTCCTAAATCAAATGGGGGATGTGGCTTCAGGATCCAGAGAGGCTCTCCTCCCTTCTCCTCTGGCTGTCCCGCTGAGCCAAAGGTCATCTCCGACTGGGGTCTATGGCTCATACTCACCGAACGCAACCATGCCACAATGGGAAACCCAAATCCCTCAATCCAGCATCTCATCCAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29623

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
ENSDART00000078341	Nonsense	216	353	2	2

Genomic Location (Zv9):

Chromosome 21 (position 29096148)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	30315392
GRCz11	21	30352087

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTTTGATAATGGAAACTTCCGGCGCAAGAGGAAGAGAAAGTCGGACTCT[C/T]AGGCTGAAGAGGAGGGAAAAGGGTACTCTGGATCAGACTCTGCTCTGTCC

Long Flanking Sequence:

GCGAAGCAGTATGTGGGCGCAAGTGGAATCGGAGGCTCAGAGGGTGCCTTCAGCTGGTTCTCTCTGCCATCCCAAGAAGATCTGATGAAACTCGTGAGACCTCCCTACTCGTACTCTGCACTTATTGCGATGGCAATACATGGAGCTCCAAACCGCCGGCTCACCCTCAGCCAGATCTACCAGTATGTGGCTGACAACTTTCCTTTCTACAACAAGAGCAAAGCCAGCTGGCAGAACTCAATCCGGCACAATCTCTCGCTCAATGACTGCTTCATGAAAGTGCCCAGAGATGACAGCGATCCAGGTGAGAACTTGTTCAAACTGTTCGTGTGTATCTGCTTGGGTTGTACTTTAGCCTTAGTTCGATGTTTAATGACAAAATAATCAAGTTTCTTCTTTTTTTAATAGGAAAAGGCAACTATTGGACTCTTGACCCAAACTGTGAGAAGATGTTTGATAATGGAAACTTCCGGCGCAAGAGGAAGAGAAAGTCGGACTCT[C/T]AGGCTGAAGAGGAGGGAAAAGGGTACTCTGGATCAGACTCTGCTCTGTCCAGTCCTAAAAACCCCAGCGACTCCTCGGAGAGAGGAAACTCTCCAATCTCCACAGATCAAGCTCCGTGTCTCAACAGCTTCCTAAATCAAATGGGGGATGTGGCTTCAGGATCCAGAGAGGCTCTCCTCCCTTCTCCTCTGGCTGTCCCGCTGAGCCAAAGGTCATCTCCGACTGGGGTCTATGGCTCATACTCACCGAACGCAACCATGCCACAATGGGAAACCCAAATCCCTCAATCCAGCATCTCATCCACTCCCTACAAAGATGGCTATAGTGACTCAATGCTGAACCCGTACAGCAGCCAGCTCTATCCAGTGCTGGGATCCTCTGATTTGCTGTATCCACGGGAGGGATCTGAGGTGTAATGTGGGACATAGCATTGTCGGGTATGAACCAAGGCCCCAGGCACTTGAGGGAGCGGCCGGCCTGCATGGTGAGCCCAGTTCTCA

Associated Phenotype:

Not determined