Busch Lab

ZMP

foxp2

Ensembl ID:
ENSDARG00000005453
ZFIN ID:
ZDB-GENE-041203-2
Description:
forkhead box protein P2 [Source:RefSeq peptide;Acc:NP_001025253]
Human Orthologue:
FOXP2
Human Description:
forkhead box P2 [Source:HGNC Symbol;Acc:13875]
Mouse Orthologue:
Foxp2
Mouse Description:
forkhead box P2 Gene [Source:MGI Symbol;Acc:MGI:2148705]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa152 Nonsense Available for shipment Available now
sa13041 Essential Splice Site Available for shipment Available now
sa11787 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa152
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060861 Nonsense 353 697 8 16
ENSDART00000134820 Nonsense 353 697 13 21

The following transcripts of ENSDARG00000005453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 5833989)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 6436533
GRCz11 4 6445103
KASP Assay ID:
554-0014.1 (used for ordering genotyping assays)
KASP Sequence:
TGGATGACAGGAGTACTGCGCAGTGCCGAGTACAGATGCAGGTGGTACAA[C/T]AGCTAGAGATACAGGTACAGTAGACGCACAATTATCATCCCAAACATACT
Long Flanking Sequence:
TGAAAGGATGAGTAGATACGTTTAATATGTCGTCGGAATAATGCACTCTTCGTAGGAGGCGCTTTTTAAACGTTACTCGAGTTAAATTGCATTTATTGTATTTATTTCTTGATAAATGTACAAGACAAAACCTCTGCGCGAGGCCTTTTGTACGCCAACATCCCTCATAAGCCGTTGTGTTCTGAGCGCTGCCTCTCATTCGCATGACAGCCGCTCTATTGTGATGTTAAACACCGGCTTTCATCAAGCATGGGACACACTTGTTAGATGGCGGCGGTTTGTTAAAAGCTAATGGGATGGACGTCCTGTAATCCAGAAATCATATTCATCAACAACAGTAGTAGTTGATCAACAGGAAGCGGTTATTAGTAGTACATTGTGTAAGTGTGGGGTTAGTTTTTCATCAGATTGTCCTCTTTTCCTACAGGCACCTTAACAATGAACACGCACTGGATGACAGGAGTACTGCGCAGTGCCGAGTACAGATGCAGGTGGTACAA[C/T]AGCTAGAGATACAGGTACAGTAGACGCACAATTATCATCCCAAACATACTCGGTACTCATAGGAACAGTTCACCCAGATTGGACAAGTCTGAGATTGTTGACTTAGCAATTTGAAAACATGCACTGAAAGTTGGTTTATTGTCCATTTGGAGCCCATTTATTGTTTCTCTATAAAAGCTCAAGTGATCATAAAGGAATAGAATGGCATGGCAGAATTGTTGTTTTTGAAAGAGCTTTTTAATATGAAATATGACATTAAACATTCATGTGTGATGTGTTTTCTTTATGAATTGAGAATCGTGTAGGCGTTCCACCAATAAACATTAGTTTATGTAGTCAGTTGGTAATGCTAACATAATATTTGAAGTTATAATTGTAATTATCAAATTTAGCATATTACACAATGCGCTGGCAACTTCTCATTTGCTACTTATTTAACAATTTAACAGCTCTTATAATACTAAAGGGTTTGGTTAATGCTAACCTACACCATTGTGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13041
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060861 None 456 697 None 16
ENSDART00000134820 Essential Splice Site 456 697 None 21

The following transcripts of ENSDARG00000005453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 5825554)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 6428098
GRCz11 4 6436668
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCATGCGKAGACGCCACACCGACAAATACTCCATGGCCTTGTCCTCAGG[T/C]TCGAASATGTTTTTCTTTTTATTCAGAYGATGCTAAAATCAAACCATCAA
Long Flanking Sequence:
CAGGTTATGGCAGCAAGCCAGGTGATCACTTCTCACAGCGTGCATGTGTGTGTGTTTTGCATCCAGGGAGCTCTTACGGGATAGAGATGGGGCCGGGATAACTCACAGCCTGATCATTAGATAATCTTTAACAGCGTGCTCTAATTAGAATTCTTATGATACAATTTCATCCTGTAATTAGTGCAGATTGGCTGCTTCCTCCTTTGCTTATTAGGGGAAACACAGCTGTAGGAAAGAGCCAGCACTCATTACAATCTCTCTCTCTCTCTCTTTCTTCCTCTCCTCTAGTTGAATCTGGTCTCCAGTGTCACCATGTCAAAGAACCTCCCGTCCATCTCACCCCCAAATTTACCTCAGACGCCAACCACGCCCACTGCTCCAGTCACACCTCTTTCCCAGATGCCCCAGGTGCCCAACGTTCTCAGTCCCGCCAATGTGCCCAGCATGGGTGCCATGCGTAGACGCCACACCGACAAATACTCCATGGCCTTGTCCTCAGG[T/C]TCGAACATGTTTTTCTTTTTATTCAGACGATGCTAAAATCAAACCATCAATATTCAACGCATTTTAATTACAGACAAATATCAACTAATGCAATATTCAAGAAAGCATGTTCTTGTTTGATGTTTATATTTACTGGTCTTCTGCAAGTGTTGGAAGCAGCAGGGAGGGCATGAATTATTCAGACACATACAAAATATCGACGCAGGCTCTAATTTCACCAGCGTGTTAATGTTTAAGATTTCTCCAGAGAGAGATTAATTAAAAATGTATTTAGTTGGACATGTAAAATGCTGATTTGAGGTGTCCCCCCTCCCTCTAAACTCCGTCTCCCGTTTTAATTTGATAAAACTCTGAATGAATTCCTGGCGGAGACGCGTTTAGCAATCATCCCAGGTGGCGACACTGTTATTTATTTCTTATGTATTTATTTATCTGCTGCTTACTTCTTCCTTATTTGTTTGCCTTTTTACAGAAATCGCCCCAAACTACGAGTTTTACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa11787
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000060861 None 506 697 12 16
ENSDART00000134820 Nonsense 506 697 17 21

The following transcripts of ENSDARG00000005453 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 5824802)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 6427346
GRCz11 4 6435916
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGCTARCGCTCAACGAAATCTACAGCTGGTTCACGCGCACCTTCGCCTA[C/A]TTCCGACGYAACGCCGCCACCTGGAAGGTAATGTCCTTGCAAGGCTTGAA
Long Flanking Sequence:
AGATTAATTAAAAATGTATTTAGTTGGACATGTAAAATGCTGATTTGAGGTGTCCCCCCTCCCTCTAAACTCCGTCTCCCGTTTTAATTTGATAAAACTCTGAATGAATTCCTGGCGGAGACGCGTTTAGCAATCATCCCAGGTGGCGACACTGTTATTTATTTCTTATGTATTTATTTATCTGCTGCTTACTTCTTCCTTATTTGTTTGCCTTTTTACAGAAATCGCCCCAAACTACGAGTTTTACAAGAACGCCGACGTCAGGCCGCCGTTTACTTATGCAACCCTCATCAGGCAGGTGAGTGGGAAATAAATTAGCTTTAGCCTGATTAGATTGTAATTAATTGGCGCTTGAATTAAGTCTGGGTGAGAGCGCCTTGACGCACTCCAGTCTCTAACGCAGCGCTTAATGGCATCTCATCGCAGGCTATCATGGAGTCAAGTGACATGCAGCTAACGCTCAACGAAATCTACAGCTGGTTCACGCGCACCTTCGCCTA[C/A]TTCCGACGCAACGCCGCCACCTGGAAGGTAATGTCCTTGCAAGGCTTGAAAGTGACTTGGGGGGTGATTAGCAGTGATCGTCCCCCCCCCTTTTTTTTTTTACTACCTCCTGAAAAGCAAGAATTTTCTCTTTATCTCGCTCGCTCTCTGTGACAAGTGAAAGAATAATTCAGCCTCTGATATCGTTTTCTAATTCGGTGCAATTAATAGGCGAGTCTTGATGGGGAGGTGTGCGCTCTGACGCGCTAATTACTAACCAGCCACTCAATCATCAGCACCTTTTGTTAGACGTGGCGTATTACTGCTTTCTCAGTGTCTCCTTTTCATCCCCCCCTTCTACCCTGCATATTATTGGTTAATTACGTTGAAATATGGCTGTTTGCCTTGTAGACGCTCGCCGATACATCCCTTTTCCTTGTTGTTGTTGATGTCGGGCCGAGCCTTTCGTATATACACTATAACTCAAACGCCAAGACAAAAACTCAAGGAGAACAAGACAA
Associated Phenotype:
Not determined