ZMP
foxq2
Ensembl ID:
ZFIN ID:
Description:
forkhead box Q2 [Source:RefSeq peptide;Acc:NP_001098411]
Human Orthologues:
FOXF1, FOXF2, FOXG1, FOXK1, FOXK2, FOXQ1
Human Descriptions:
forkhead box F1 [Source:HGNC Symbol;Acc:3809]
forkhead box F2 [Source:HGNC Symbol;Acc:3810]
forkhead box G1 [Source:HGNC Symbol;Acc:3811]
forkhead box K1 [Source:HGNC Symbol;Acc:23480]
forkhead box K2 [Source:HGNC Symbol;Acc:6036]
forkhead box Q1 [Source:HGNC Symbol;Acc:20951]
forkhead box F2 [Source:HGNC Symbol;Acc:3810]
forkhead box G1 [Source:HGNC Symbol;Acc:3811]
forkhead box K1 [Source:HGNC Symbol;Acc:23480]
forkhead box K2 [Source:HGNC Symbol;Acc:6036]
forkhead box Q1 [Source:HGNC Symbol;Acc:20951]
Mouse Orthologues:
3110039M20Rik, Foxf1a, Foxf2, Foxg1, Foxk1, Foxk2, Foxq1
Mouse Descriptions:
RIKEN cDNA 3110039M20 gene Gene [Source:MGI Symbol;Acc:MGI:1914543]
forkhead box F1a Gene [Source:MGI Symbol;Acc:MGI:1347470]
forkhead box F2 Gene [Source:MGI Symbol;Acc:MGI:1347479]
forkhead box G1 Gene [Source:MGI Symbol;Acc:MGI:1347464]
forkhead box K1 Gene [Source:MGI Symbol;Acc:MGI:1347488]
forkhead box K2 Gene [Source:MGI Symbol;Acc:MGI:1916087]
forkhead box Q1 Gene [Source:MGI Symbol;Acc:MGI:1298228]
forkhead box F1a Gene [Source:MGI Symbol;Acc:MGI:1347470]
forkhead box F2 Gene [Source:MGI Symbol;Acc:MGI:1347479]
forkhead box G1 Gene [Source:MGI Symbol;Acc:MGI:1347464]
forkhead box K1 Gene [Source:MGI Symbol;Acc:MGI:1347488]
forkhead box K2 Gene [Source:MGI Symbol;Acc:MGI:1916087]
forkhead box Q1 Gene [Source:MGI Symbol;Acc:MGI:1298228]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37499 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37499
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000105519 | Nonsense | 159 | 244 | 2 | 2 |
ENSDART00000136744 | Nonsense | 78 | 104 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 20749344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 20404020 |
GRCz11 | 22 | 20428998 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAGTGCTTCATCAAAGCTGGTCGCAGTGACAATGGCAAGGGTCATTTCT[G/A]GGCAATTCACCCGGCCAACTTTCAAGACTTCTCAAACGGGGACTACCATC
Long Flanking Sequence:
ATAATACACAAAAGTAAAAAGGTTTCAAGGTAAGGAAAGGGGTTTTGCAATAAAGACATGCAAAATACCAAAAACCCAAAAATGTTTTGGTTCCCTGTAGAACTCTTTAGTTCTTAAAAGAACCATTTTTTCTTTGAACTAAGCAAGAAGTGTAGATCTAAAGAACACTTTTCCACTATAAAGAATCTCTTGTGGAATGGAAAGGCTCTTTGGATAATAAGATTATTCACAGAACCTTCAATGCTAATAAAGAACTTTTTATTTTTAAGAGTGCACATAATTATGAACCTTCACAAACAATAGATCTATAACATTATATAGATCTTTAATACTCAGATTCATTACTAGATGTCAAACTTTTGACCTTTATAGGAGTCATAATTGCTAATCTCTGCTCTTCAAACAGGACAAGAACTGGAGAAACAGCGTCAGACACAATCTGTCTTTAAACGAGTGCTTCATCAAAGCTGGTCGCAGTGACAATGGCAAGGGTCATTTCT[G/A]GGCAATTCACCCGGCCAACTTTCAAGACTTCTCAAACGGGGACTACCATCGGCGGAGAGCTCGGAGAAGGATCCGCAGGGTAACAGGGCAGCTGCCCTACGCTCTGCCTGCACATTACCAAACCCTGGGCCGCCTGAAACGGACACCGTGCTGGTGTTGCCCACCGTCCCATCCGTTATTGTGCTTCCCGCCTAGAGTCTACTGGAGCTGGGCTGCACTTCAGACACAACGCACACCGGCCCTTCATGGACTCATATAACAAGATCTGCTCTGAAATTATTTCTGCATGTGCTGGAAATGAATTTGTACATATATTTAAGCCATATTTTAAATATGCACATTTGTTTGTAAAATGAAAACCAATAAATATAGATAAGAATTACTGTCTTCATTCATTTTCTTTCGGCTTAGTCCCTTATTTATCAGGGATCACCACAGCAGAATGAACCACCAACTATTTCAGCAATCCAGCATTTACGCAGCGGATGCCCTTCCAGACT
Associated Phenotype:
Not determined