ZMP
foxq1l
Ensembl ID:
ZFIN ID:
Description:
Zgc:162905 protein [Source:UniProtKB/TrEMBL;Acc:Q566W3]
Human Orthologue:
FOXQ1
Human Description:
forkhead box Q1 [Source:HGNC Symbol;Acc:20951]
Mouse Orthologue:
Foxq1
Mouse Description:
forkhead box Q1 Gene [Source:MGI Symbol;Acc:MGI:1298228]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32819 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18716 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9415 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32819
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045770 | Nonsense | 34 | 310 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 903396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 849688 |
GRCz11 | 2 | 722054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCTGAAGCTCTGCCAATGAAACTGGAGGTTTTCTGCGGGAGTCACTA[C/A]GACTCCAAGCCTGCGGAGTTGTGCAGCGATGCTGAGGGGAGCATCCCATC
Long Flanking Sequence:
GTGAATCACACAAATGTTGATTAACAGATATTTTTACAGTGTAGAGCATCAGCAGCGGAGGTTTCGCTCATCGCAGGTGTGTTGTCTGATAAACGCACGCCACCTGCTTTCCTCAGGTGAAATTCTTCTGCGAGCAAAGGTGAGCAAGCGCGCAGGTGAACCAACAAACACACTGTGACGAAACCCGTCTGCAATCAACAAACCCATTCATCATCATCATCTCAGATCTCAGATGTTTGTCCATATGCGCGCGACCGCTTTATTATTTCAAAACAGGGTGTGCATGATCCCGGTGTTTTTGTGACTTGATTTTAAGACTTAAAGACAGGCCCCGCCCCTGTAGGCTTTCCCCGGAGGTGAGCGCCTATATTAGCCTGCCGACAGCCGCTCGGGATGTCAATGCACTCATCATCTGCAACAGGTAGCTACACCGCCCTGTCACTCTTCGAACTTTCTGAAGCTCTGCCAATGAAACTGGAGGTTTTCTGCGGGAGTCACTA[C/A]GACTCCAAGCCTGCGGAGTTGTGCAGCGATGCTGAGGGGAGCATCCCATCGCCGGTGTCCGCAGAGGAGGAGCTGGGCTCGGATGGAGACTGCGTGGCGCACAGTCCGGCACCTGTCGCCGACACCAAAGGCAAACCCTACACTCGGAGACCCAAACCTCCATACTCTTACATCGCACTTATCGCCATGGCCATCCGAGACTCCAACTCCGGCCGACTCACTCTAGCCGAAATCAACGACTACCTCATGAAGAAGTTCCCGTTTTTTAGAGGCAGCTACACCGGCTGGAGGAACTCAGTGCGCCATAATCTGTCTCTAAACGACTGCTTTCTTAAGGTCTTAAGGGATCCTTCGAGACCGTGGGGAAAGGACAATTACTGGATGCTGAACCCGCACAGCGAGTACACCTTCGCGGACGGAGTGTTTCGCAGAAGGAGAAAGCGCATTAGTAAAAAAACCGGCAGGGAGCCAGAGGGGCCGGTGCAAACCCACGCATTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18716
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045770 | Nonsense | 270 | 310 | 1 | 1 |
ENSDART00000045770 | Nonsense | 270 | 310 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 902690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 848982 |
GRCz11 | 2 | 721348 |
KASP Assay ID:
2259-1433.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGCTTCGATCCTATGGTGCCCTGGAGGACCCTTCCATGAGCCGCCGA[C/T]AGCGCGACTTTTTCGCATTCCAGCTGCCGCCTGAGTGCCTCTCAATCCCG
Long Flanking Sequence:
ACTCCGGCCGACTCACTCTAGCCGAAATCAACGACTACCTCATGAAGAAGTTCCCGTTTTTTAGAGGCAGCTACACCGGCTGGAGGAACTCAGTGCGCCATAATCTGTCTCTAAACGACTGCTTTCTTAAGGTCTTAAGGGATCCTTCGAGACCGTGGGGAAAGGACAATTACTGGATGCTGAACCCGCACAGCGAGTACACCTTCGCGGACGGAGTGTTTCGCAGAAGGAGAAAGCGCATTAGTAAAAAAACCGGCAGGGAGCCAGAGGGGCCGGTGCAAACCCACGCATTGGACAGCAATGACTCCATCGCTACGCCTCCTTCGAGCGGAAAGTTCACCAGTTCTTTCGCCATTGAGAGCATCCTCAGTCGACCCTTCAGAAGGGAGGACCGCCCCGTGCTCAGCCCTGACACCTGGCCGGGGGGAGTGGACACTGTGCTGCCGTATGTCATGCTTCGATCCTATGGTGCCCTGGAGGACCCTTCCATGAGCCGCCGA[C/T]AGCGCGACTTTTTCGCATTCCAGCTGCCGCCTGAGTGCCTCTCAATCCCGCATACGAGCGCGGCGGTGCCCGCGCCTGCAACCGCGGGATATCACCCGTTCAAAATTGACTATTTGTTGTCGTAACATTGGGTACTTTGTGATGGGGAACTTCGGCACTTTCTACAGCACTCGTGACTTGAAAGAGACATTGTGCAAGATACATTTCATTCGACTGCATTTTTAAGAATCGTTCTGAACCTTTAATATGCACCACGAAAACAAGTGAACTCAAAGTTGTGAACTATTTAAGTCTATTCTATTTTGTACTGTCCTACTGAATGATTAAGTCGTTTCCGTGTATTTATTTGTCATATTTTGTGTTTGTTCTGTGTTAAACCAGCGGTGCCTCAAACGATGATGCCTTCATTTCAGATTTAATACTCAAGATGAACTATATGAGAGGCGAGCTCAGTTTGTGAGGCTCCTGCATCAAACTTGTAAACTGGAATTGTTTAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9415
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 |
---|---|---|---|---|---|
ENSDART00000045770 | Nonsense | 270 | 310 | 1 | 1 |
ENSDART00000045770 | Nonsense | 270 | 310 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 2 (position 902690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 848982 |
GRCz11 | 2 | 721348 |
KASP Assay ID:
2259-1433.1 (used for ordering genotyping assays)
KASP Sequence:
TCATGCTTCGATCCTATGGTGCCCTRGAGGACCCTTCCRTGAGCCGCCGA[C/T]AGCGCGACTTTTTCGCATTCCAGCTGCCRCCTGAGTGCCTCTCAATCCCG
Long Flanking Sequence:
ACTCCGGCCGACTCACTCTAGCCGAAATCAACGACTACCTCATGAAGAAGTTCCCGTTTTTTAGAGGCAGCTACACCGGCTGGAGGAACTCAGTGCGCCATAATCTGTCTCTAAACGACTGCTTTCTTAAGGTCTTAAGGGATCCTTCGAGACCGTGGGGAAAGGACAATTACTGGATGCTGAACCCGCACAGCGAGTACACCTTCGCGGACGGAGTGTTTCGCAGAAGGAGAAAGCGCATTAGTAAAAAAACCGGCAGGGAGCCAGAGGGGCCGGTGCAAACCCACGCATTGGACAGCAATGACTCCATCGCTACGCCTCCTTCGAGCGGAAAGTTCACCAGTTCTTTCGCCATTGAGAGCATCCTCAGTCGACCCTTCAGAAGGGAGGACCGCCCCGTGCTCAGCCCTGACACCTGGCCGGGGGGAGTGGACACTGTGCTGCCGTATGTCATGCTTCGATCCTATGGTGCCCTGGAGGACCCTTCCATGAGCCGCCGA[C/T]AGCGCGACTTTTTCGCATTCCAGCTGCCGCCTGAGTGCCTCTCAATCCCGCATACGAGCGCGGCGGTGCCCGCGCCTGCAACCGCGGGATATCACCCGTTCAAAATTGACTATTTGTTGTCGTAACATTGGGTACTTTGTGATGGGGAACTTCGGCACTTTCTACAGCACTCGTGACTTGAAAGAGACATTGTGCAAGATACATTTCATTCGACTGCATTTTTAAGAATCGTTCTGAACCTTTAATATGCACCACGAAAACAAGTGAACTCAAAGTTGTGAACTATTTAAGTCTATTCTATTTTGTACTGTCCTACTGAATGATTAAGTCGTTTCCGTGTATTTATTTGTCATATTTTGTGTTTGTTCTGTGTTAAACCAGCGGTGCCTCAAACGATGATGCCTTCATTTCAGATTTAATACTCAAGATGAACTATATGAGAGGCGAGCTCAGTTTGTGAGGCTCCTGCATCAAACTTGTAAACTGGAATTGTTTAAGCA
Associated Phenotype:
Not determined