ZMP
pou2f1b
Ensembl ID:
ZFIN ID:
Description:
POU domain, class 2, transcription factor 1 [Source:RefSeq peptide;Acc:NP_001082798]
Human Orthologue:
POU2F1
Human Description:
POU class 2 homeobox 1 [Source:HGNC Symbol;Acc:9212]
Mouse Orthologue:
Pou2f1
Mouse Description:
POU domain, class 2, transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:101898]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41470 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34687 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41470
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000035522 | Nonsense | 366 | 676 | 9 | 13 |
| ENSDART00000144272 | Nonsense | 316 | 626 | 7 | 11 |
| ENSDART00000146480 | Nonsense | 366 | 676 | 9 | 13 |
| ENSDART00000147913 | None | None | 284 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35315243)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34534754 |
| GRCz11 | 9 | 34343939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATGATTGCAGACCAGCTCAATATGGAGAAGGAGGTGATCCGAGTGTG[G/A]TTCTGTAACCGCAGACAGAAGGAGAAGAGGATCAACCCGCCCAACAACGG
Long Flanking Sequence:
TCCTAAATCTTGTAAAATATCTAAAAGTTTTTGTTTAATTGAGTAAGTCAGTCTTTCCATTGCTATACAAGAAGACATTTCCTTAATCTAGAGTGACAAAGATGGACCATGGATAATTTTCCAGTGAATGACAGTCAGGTGCTTCGCATTCAATAGACACAGGTTAATAAACTTCTGTTCATTTGTGTTCAAAGATAAGGCAGATGGGATAAGACCAAGAAGTCATGTTTTATCTTTTAATACACCATAAACAAACATTAAGAAACACTGATGCAACACTGTAAGACCCTTTCTTAATAGAGTGTCATCCTCAATTTTTTTCTGGAGGGTTGTCTACTTGAACATTGGACTGCAGCATTGCAGATCTTTGTGATTGGTTTTTGCCGTAAGGGCGTTTCTTGTGCCTTTGCCATTTTCAAGCAGAACCAAAAACCTACCTCTGAGGAGATCACCATGATTGCAGACCAGCTCAATATGGAGAAGGAGGTGATCCGAGTGTG[G/A]TTCTGTAACCGCAGACAGAAGGAGAAGAGGATCAACCCGCCCAACAACGGCAGCGCTGCCAGCACCCCTATCAAAGCAATCTTCTCTCCCACCACAACTCTGGTATGAGATGTCAAAACATAAAAACTGCCTTCCATCATTCAGCCCAGCAGCTCAAATCATGCTGAACCTCTTCTTTTCTGTTTAGGTGCCGAGTACAGCCAGTCTTATTACCAGTAACACACCGACTACAATGACTGTAAACCCAGTTTTGCCTCTCACCAGCACTAGTGTCTCCGGCATCAGTTTCACTGGTAGGCAAGAGTTAAAAGGGTAGATCACTCAAATACATGAATGCTGTTAATTCATTTACTCACCTTTAGGCCATTCTGTAGATAAAATCTGTTAATTAACAGTTTCCATATCTTGTAATTCACAGGTGTTTTTAGTTTATTTACAGTTGTGAGTTACATCACGGGACATTTATGTCTGCTCTGACTTTAAACGTGGAAAGTTCAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34687
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 |
|---|---|---|---|---|---|
| ENSDART00000035522 | Nonsense | 546 | 676 | 11 | 13 |
| ENSDART00000144272 | Nonsense | 496 | 626 | 9 | 11 |
| ENSDART00000146480 | Nonsense | 546 | 676 | 11 | 13 |
| ENSDART00000147913 | None | None | 284 | None | 8 |
Genomic Location (Zv9):
Chromosome 9 (position 35317826)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 34537337 |
| GRCz11 | 9 | 34346522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCCATGGCTGCCGCCGCGGGCCTTAATCCTGGGCTCATGGCGTCCTCA[C/T]AGTTCGCCCCTGGGTGAGTGCTCTTTTAGACCTTCTGACCTCAGGTTTGT
Long Flanking Sequence:
AATCTTCTTTAATTCCTCTTGAGGAAAAAAACCTCATTACCTTTGAATGGCTTTAATGGGTGTAATTGAACAGCATTTTCCCACATTTCGGTGAGCTATCTCTTAAAAACATCAAACTTTCATATTGTTGACAGACCTCTCAACAATTAACATCTTCTCTTCCTCTTGAAGGCACAACTCTGGGCTCGGCCATCAATAACACTGCATCGGTCATCTCCACTGCACCCGCGGCCACCACCGCCTCGTCCTCTCCCTCCCTCAGCCCTTCTCCCACTGCAGTGCAGACGTCCTCCTCAGAGCAGGCTTCAGCTCAGGAGACGCTCACGGCCGTCAGTCAGGCACCTTCCTCCCTGGCGTCTACCCTGGGCACTGGGCAGGTGATGGTGGCGGCACCCAGCCTCTCAGCCGCTCTACAGGGAGCTGCTCAGCTGCCCACCAGCGCCAGCATCGCCGCCATGGCTGCCGCCGCGGGCCTTAATCCTGGGCTCATGGCGTCCTCA[C/T]AGTTCGCCCCTGGGTGAGTGCTCTTTTAGACCTTCTGACCTCAGGTTTGTTGTGGACGCCTAGATGTTTATTATATTATGTATTTTCTGGTATTTCCTGCACAGCGGGGCTCTTCTGAGTTTGGCACCCGGTGGTCTCGGAAGCGCTTTGAGTCCGGCATTGATGAGCAACAGCACCTTGGCCACAATCCAAGGTGTGTGGAGCGGCAAGTACACTTATATTTACATTATGGCTTTGCATGCGCTTGTTAATCTTGGTGCCAGCAGCAATATTATTATATGTAAAATGATGTATTAAGCCAAAAATGAACATTTACTTGCACACAAGTGGTTCCAAACTTTTATGATTTTTCTTTTTGTTGTACACAAAAGAAGATGTTTGACAAATGTTAGAAACCTGTAACTATTAAATTCCACAGTAGAAAACAAGAAATACTATGGGATAGGGATGTCCAGATCTGACCAATCGATCGGAAATCTGGCCCGTTCATGTGGTTTCAG
Associated Phenotype:
Not determined