ZMP
pou3f3a
Ensembl ID:
ZFIN ID:
Description:
POU domain, class 3, transcription factor 3-A [Source:UniProtKB/Swiss-Prot;Acc:P56224]
Human Orthologues:
POU3F1, POU3F3
Human Descriptions:
POU class 3 homeobox 1 [Source:HGNC Symbol;Acc:9214]
POU class 3 homeobox 3 [Source:HGNC Symbol;Acc:9216]
POU class 3 homeobox 3 [Source:HGNC Symbol;Acc:9216]
Mouse Orthologues:
Pou3f1, Pou3f3
Mouse Descriptions:
POU domain, class 3, transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:101896]
POU domain, class 3, transcription factor 3 Gene [Source:MGI Symbol;Acc:MGI:102564]
POU domain, class 3, transcription factor 3 Gene [Source:MGI Symbol;Acc:MGI:102564]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38722 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38722
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 |
---|---|---|---|---|---|
ENSDART00000061593 | Nonsense | 140 | 446 | 1 | 2 |
ENSDART00000113914 | Nonsense | 140 | 438 | 1 | 2 |
ENSDART00000133178 | Nonsense | 140 | 429 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 9 (position 6701713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 6682669 |
GRCz11 | 9 | 6660654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAACAGGGAAGACCTACACTCGGGCACCGCTTTGCACCACAGACCCT[C/A]GCATTTAGGGGCTCACCAGTCGCACCAAAGCGCATGGGGTGGCACCACAG
Long Flanking Sequence:
GCCTTCAAGACTTGGAAACAAAGTTACAACAATTCGGGGAGGGGGAATAATAAGTAGAAATTGTTCAAAGTGGTGAGGAGGGATGGCCACAGCGGCTTCCAACCCTTACCTGGCCAGCAGCACCATTCTCTCATCAGCCTCGCTCGTGCACTCGGAGTCCGGAGGTGGTGGCATGCAGCCGGGAAGTGGTGCAGTAACATCGGTGTCGGGGGGTTACAGAGGAGACCCCACAGTCAAGATGGTGCAGAGCGACTTCATGCAAGGAGCCATGGCGGCCAGTAACGGGGGTCACATGCTGAGCCATGCGCATCAGTGGGTCACCTCACTGCCCCACGCGGCTGCCGCAGCCGCCGCCGCCGCAGCCGCCGCAGCAGCGGAAGCCGGCTCACCTTGGAGCTCCAGCCCAGTTGGTATGGCCGGGAGCCCACAGCAACAAGACGTCAAGAGCAGTTCAAACAGGGAAGACCTACACTCGGGCACCGCTTTGCACCACAGACCCT[C/A]GCATTTAGGGGCTCACCAGTCGCACCAAAGCGCATGGGGTGGCACCACAGCCTCCCACATCTCCACCATCACCGGAGGACAGCAGCAGTCCCAGCAGTCTCTCATCTATTCCCAGCCTGGTGGTTTCACAGTCAACGGCATGTTAAACCCTCCCGGGAGTTTAGTGCACCCTGGGCTGATGCGGGGAGAGTCTCCAGAAATGGATCACCATCATCATCACCACCACCATCAGCAGCAGCACCCCCATCACCACCACCACCACCAGCACCACGCGGGAGTGAACAGCCACGACTCGCACTCAGACGAGGACACGCCGACCTCCGACGACCTGGAGCAGTTCGCCAAACAATTTAAGCAGCGTCGGATCAAACTGGGCTTTACTCAGGCCGACGTCGGGTTAGCGCTGGGAACTCTTTACGGAAATGTTTTCTCTCAGACCACCATTTGCAGGTTCGAGGCTCTCCAGCTGAGCTTCAAGAACATGTGCAAACTTAAGCCAC
Associated Phenotype:
Not determined