ZMP
foxp1b
Ensembl ID:
ZFIN ID:
Description:
Forkhead box protein P1-B [Source:UniProtKB/Swiss-Prot;Acc:Q2LE08]
Human Orthologue:
FOXP1
Human Description:
forkhead box P1 [Source:HGNC Symbol;Acc:3823]
Mouse Orthologue:
Foxp1
Mouse Description:
forkhead box P1 Gene [Source:MGI Symbol;Acc:MGI:1914004]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16567 | Nonsense | Available for shipment | Available now |
sa40774 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20798 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16567
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 |
---|---|---|---|---|---|
ENSDART00000064938 | Nonsense | 124 | 659 | 7 | 20 |
ENSDART00000128174 | Nonsense | 124 | 660 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 6 (position 43594561)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 43665725 |
GRCz11 | 6 | 43663261 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACACCAAGTCCTGAGCCCTCAGCAGCTCCAGCTGTTACTGCAGCAACAA[C/T]AAGCACTGATGTTACAGCAGGTATACTCGCTCTCGTTCTGCTTTACACTA
Long Flanking Sequence:
AACATGTAGCACACAAATTCTCTGTGGCTTTGCATTACTCTCAAATAGTCTCCTTGCGTGTTTGAGTCAGATATTCTGCACATTTATTGATTAATAGTGCGCTCGCTGTACTGTCAAGACTCACTCAGTCAGTCTGTTTAAGAGTATACAAGTGAAAATAGATCTCAATCACTGGCCAATTAGATCTAACAGTTTATCAGCTCATGCCTTCCATCGCATAATGCATAACATTTGGTGACAAATATGAGTGATTTGAGGGTTGGTCTCATAGGACGTTCATGTGGAGACAGGCTACTGATACTGTAGGATGTGTGGCATGTTATCTTTAGCATACGGGAGTATTATAGTATTCACACGGACTTCCTCTTTCTGTGTTTGTGTAGGTGCCAGTTTCTGTTGCTATGATGACACCACAGGTCATAACTCCTCAGCAGATGCAGCAAATCCTCCAACACCAAGTCCTGAGCCCTCAGCAGCTCCAGCTGTTACTGCAGCAACAA[C/T]AAGCACTGATGTTACAGCAGGTATACTCGCTCTCGTTCTGCTTTACACTACATACTGAATGTATCACGACGACTAGACTATTGCCCATCGCCAGAGAGTTACATCATTAGAATTTAACAGGTTCAGAGTAATACTGCTATCATATCATGCACACACACAAACACAAATAAGTAAATGGTAACCCTTTACAATAATTTTGTATTTACTAATAGGAATAAACAACGAACAATACATTTATTACACAATTTATCCATCTTTGCTAGGTATTTAAAATTGTTGTTCATTATTGGTGTTAACTCAAAGTGCATTAACTAATGTTCGCAAGCATAACTTTGGGTTTTATTCAAGCAGTAAATGTTAACCTATGATTAATAAGTCTAATTTTAAGTCTAGATTAATAATAATAATAAGTCAAGATTAAGAAGTAGTGTTCATTCATGATAGTTTCTGTTAGAAAATACATTAATTAATGTAACCTTATTGTAAAATGTGACCAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40774
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064938 | Essential Splice Site | 208 | 659 | 9 | 20 |
ENSDART00000128174 | Essential Splice Site | 209 | 660 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 6 (position 43586882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 43658046 |
GRCz11 | 6 | 43655582 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCCATCCAGCCCAACCAGACTCTGCCTCTGCACACCCTTACTCAGGG[T/A]AAGAGCAGGCACAGCCGTCGACTTTTATTCACACACACACACACACATAC
Long Flanking Sequence:
TAGACTAGTTACTTTGTTAGCTAGTTACTCCACACTCCCCATTTACCCAAAGGAATCAACGGTTGGCTCCTTCGTCTCTGAATATTAAGCAGCTCTTTTCAGTCAACGGCTGTTTGCGGAGTTATGAATGGCCATAATTAAAATCCTGTGGCTCTTATTAGGAATGATTAACAACATTTCATTATTTGTCACGAGCCTCCCAGACTTCTTGTTAATTAAGGAGGTTACATGAATACAGGAATGTACCTGTGTGTGTGTTTATCAGCCCTCAGTGTATACGTATATTTGTGCATGTGTTGACAGAATAGTTTGTGAGTGTGAGGATGATATGTAGTTTGTCTCTTTCTCTCTCGGCAGGTGTCCGCACAGCAGTTGGCGTTTCAGCAGCAGCTGCTCCAGGTCCAGCAGCTCCAGCAGCAGCATCTCCTGAGTCTGCAGAGACAAGGCCTGCTGTCCATCCAGCCCAACCAGACTCTGCCTCTGCACACCCTTACTCAGGG[T/A]AAGAGCAGGCACAGCCGTCGACTTTTATTCACACACACACACACACATACAGCTACAGAATGGAAATCAAAAGTAAAAGACAATCATTCAAAAAATTCATCACACTCCAAAGCAAATGTCTCTTTCTTTCACACTGGATGGCTGATGTGGCCTTTTTAATGTGTCATTGTTGTTTGTATTTATTTCTTTATTTAGATGATTCATTTGGTTTCATATTCTGAAAAAACTGCTGCAGAATTATACAGATTGCAACATGATTTTTGTGTTTGCTTTCAAGATAATTTTTTAACGCTGGACTAATTTGGCTTTATTATTTTTCTGATACATAAAGAAGGATAGATGGTTTTAAAAATATAATGTTTAACATGTTTAAACAATTTTATAAAACATCTCAGAAAGAGCTTATAATAATACATTAAGTACATTGCATATTGTGTGTTATTATGAAATATTTCATAGGATTTTCTGTAGTATTAAATAAAAGTTGTTGTATATACGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20798
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064938 | Essential Splice Site | 493 | 659 | 16 | 20 |
ENSDART00000128174 | Essential Splice Site | 494 | 660 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 6 (position 43546073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 43617237 |
GRCz11 | 6 | 43614773 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTCACGCGAATGTTTGCATATTTCAGACGCAACGCAGCAACGTGGAAG[G/A]TGAGCTCACGATTATGGTTTTATATGTATATTTGTAATTATATCCAATGA
Long Flanking Sequence:
AGTAGGAACGAGGCTTTTTTTGAGATGCCCAGTCAATTATCAGGCCTGAACCGGTAATCTGTGATCACACGGGCATTAATCTGGGCCTGCAATAATTGCCGCTTTATAATCTGCCTCTATAAAATAGTGTGTTTTTTTTTTTTTTTTCTCCTCTTCTTGTTCTGGTCGTTTAGCGGAAAAGGATGTACTCAAATTGGCACATTTGCATAAGGAAGCGTTCAGTAAACAAAGTAGCTCCCATTTGAGAACGGAAAAGCGTGGAGCTGTTTTACATGCAGCCTCTGATCAACTTTAACATGACATTACTATGTGCATCTCACTTTGTTTTTGCTCCAGGTTTGAACGGAAACGAAATAGCTTTTTTGCTTATCAGCATTTGTGTGTGTGTGTTTTTCCAGGCAATACTAGAGTCGCCAGAAAAACAGCTAACACTAAACGAGATATACAACTGGTTCACGCGAATGTTTGCATATTTCAGACGCAACGCAGCAACGTGGAAG[G/A]TGAGCTCACGATTATGGTTTTATATGTATATTTGTAATTATATCCAATGAAGTTTGAATTGACTGAATAAAAGGCACTGAATGAAGCAGAAATAATATAGATAGTTTATATGTAAGTTTTTAATTATTTAAAATATAATAATGGCTCATTTCCACTGACTGGTACAGTATGGTACGGTATGGGTCGGTACGGGTCACCTTTATCAGGCTTGCGTTTCCACTGCCAAAGGGGTACTAATAGTATAACAGAAAGTTTCAGCGACAACATTCTCACTTGAGGAAGTCTTGCTCAAAGTAAAGCTCTACAGGTCATTTAAATATCATATGAGAAGCACTTCTCACAAAACAGATGCACACATATATACACATAAATACTTGTATATAAATGTTCATTACTAACCTTGAACATGATTATATAAAAAATAAATAAATAAAAGCAACATATATGAGCGCACAGACCCTTACAGTCTCAGATATGTTATCAATTACAGAAAAAATACA
Associated Phenotype:
Not determined