ZMP
zgc:136377
Ensembl ID:
ZFIN ID:
Description:
POU transcription factor [Source:RefSeq peptide;Acc:NP_001038720]
Human Orthologue:
POU2F3
Human Description:
POU class 2 homeobox 3 [Source:HGNC Symbol;Acc:19864]
Mouse Orthologue:
Pou2f3
Mouse Description:
POU domain, class 2, transcription factor 3 Gene [Source:MGI Symbol;Acc:MGI:102565]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11296 | Essential Splice Site | Available for shipment | Available now |
| sa20549 | Nonsense | Available for shipment | Available now |
| sa38512 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33730 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38513 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11296
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044803 | Essential Splice Site | None | 398 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 60019462)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 57881080 |
| GRCz11 | 5 | 58550789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCATARAGTTGTGATCCTGTAGGAAAATCAGCTGTATTTATCATTWC[A/T]GATATTAAGATGAGCACAGACGCTGTTGAGCWGACAGAATCTCAGCATGA
Long Flanking Sequence:
CTACTAACTAACCCACTTTGCTAAATGAGTTCCTCTGAACATTTTTAAAAAGGCTTCTCTCAGTTTGTGAGTTGAGAAAAAGCAGGAGACATAATTCAACAGACCTTTTAGGTAAGTGGATATTTTTTATACATACTGTATAAATACAAATCTTCTTGGTCTCTCAGATTCCTGCAGTCTTCTCAAGCAGTGACCGTTTTGTGGAATCATATTGTTTTGCATCGTACCTGTTCACAGCTCTCTATATTGACAGATTTAAATGTTTTTGACTAGAAGAGATTAGGGTGGAGAGACAGAGTGATTGTGGTGAATGCTCAACGGGGATACCCTTGCTCTTATGAATATTACAACGAGCCCTTTACATAAAGGAGAGCATTTGAAAGCTGGACACATTAGAATAAACCTCAAGATCATTTTACTGGCAGGGCCATGGCATGAATTGCCCCAGTGTCTGCATAAAGTTGTGATCCTGTAGGAAAATCAGCTGTATTTATCATTAC[A/T]GATATTAAGATGAGCACAGACGCTGTTGAGCAGACAGAATCTCAGCATGAACAAGCTGGTAAGGAGCATTTTCACGCTTTCAGTGTTGCTTTGAAACGGTTTCTTATCTAATGTATGATATTTAGTGGAAACAACACACCTATGTGTGTGTATGTATGTATGTGTGTGTGTGTATTTATATATATACTGTAAAGAAATCTTAAATATTTTTAGTTATAAATTAAGAATTAAACTTAGTAAATTAACAAACCACATTCATTGTCATTAATTTTTGTTGGGCTCATTATTTATTGATCTAAAGTCTTAATGTTAATGAGTTGTAGCTTAAAGTAAAGTGTGAAATTGTTTGTTACAGTGATGACATACACAACATTTATACACATTTCGAAGTATTCTGTGCTATATTGAAAGTATTTGATTAACCTAAACCTAACTATCGCTAACTAACTATTAAAAAGCAGCTAATTAATCGTTTATTGAGCTAAAATCTTAGTTAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20549
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044803 | Nonsense | 225 | 398 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 60042162)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 57903780 |
| GRCz11 | 5 | 58573489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAAGCTCTCAATCTAAGCTTCAAAAACATGTGCAAGCTCAAGCCTT[T/A]ACTGGAAAAGTGGCTAAGTGATGCAGGTAAATGTGCTGCTGCCCTCTGGT
Long Flanking Sequence:
ACCCTAGTTCAAAAACCCCATGTTATTTATGATTTATTCTCATGAATAAAATCACCCTGTATTTATGTGTTTATATTGAATACATTTACGCATATTGACAATTGTGTGTTTGGTATTTTATACATATCAGAAAAATAAATGAGCATACTTATTTACAAAATATAATGTAGGCTACTGCTAAAATTGTATCTATATTGTTTATCATGTTTGGGGACTTTCATTCTTATCATTTTTATAGAAAACTTATAAGTTAAATTTCCCCCCTTTTCAGTGGTCTTTTCTATTTCAAATTTAAACCGACAAGGAACCATTTTATGTATCTTGCACAATGCTTTTGTTAAGCTCATCCAGTTCCCATCCTAACTCTTGTGTGATGTGTCCGCAGGGTGATGTGGGTCTGGCCATGGGAAAGCTGTATGGAAATGACTTCAGTCAGACTACCATCTCACGCTTTGAAGCTCTCAATCTAAGCTTCAAAAACATGTGCAAGCTCAAGCCTT[T/A]ACTGGAAAAGTGGCTAAGTGATGCAGGTAAATGTGCTGCTGCCCTCTGGTGGACACAGCTAACTCTGGTTTTTATGAGAGGGGTCTGGATGCAGACCTGCAGTGCAACCTGAGCTGCATCCAATGCTTTTTAATATGCTCACCTAACCGCACCCTAACCCTACCCGTCACAGTGACGTCACTCAATCCATTGAGTGCATGTGTCTGACATTGCATCACTGAGTGATGCAATTTCAGCTTGCTTCATAAAGGCTGCATCAAGATACTTTTGGTTTTTATCACCTAAACGTGAAAGTCCATTGTTCGATGTGATCAGTTACAAAGGAACTAGTTAGTATAATTAAATTACTTTTCAGGAGAAAGAGTAAAGTAAGATTACTTTTCATTCATGTTGACATGTACTTGCAAAGTTTCTTAGAGTCAGTTAAATGTCTGTTGAAGAAGCATATCAACAGATATTAAGTACAGCCTACCAATACTCAAATCCACCATCAAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38512
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044803 | Nonsense | 286 | 398 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 60048174)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 57909792 |
| GRCz11 | 5 | 58579501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTATAAATGCTTTTTGCCCAATCCAGAACCCAAAACCCAACTCTGAA[G/T]AGATTACGCTGATCTCAGAGCAGCTGGCCATGGAGAAGGAGGTGGTGCGG
Long Flanking Sequence:
GTTATTGCATCATGATGGTTTGTTCTGTAGACTATCAAAAAAGAAATAACTTAAAGGGGCTAATGTTTTTTCCTTAAAATTGTGTTTAAAAATTAAAAACTGCTTTTATTCTAGCCAAAATAAAACAAATAGGACTTTCTCCAGAAGAAAAAAATATTATCAGACCTACTGTGAAAATTTCTTTGCCCTGTTAAACATCATTTGGGAAATATTTAAAAAAAAAAGAAAAAAAAATTAAAAGGGGGGCTAATAATTCTGACTTCAACTGTATGCAGTTGAAAGGGAATCAAAATATTCTCTGCCATTACTGTGAAACACCTTTTCATTATTTCTGTCTATGCTTATATTTTATATATTATTGTATAATTTTGCAGTACTTGCCATGTGCTTTAAGATTCTGGAGACTACTACATTACATGTGGAAAACAGTAAGATAGCAGTACTCATTGAAACTTATAAATGCTTTTTGCCCAATCCAGAACCCAAAACCCAACTCTGAA[G/T]AGATTACGCTGATCTCAGAGCAGCTGGCCATGGAGAAGGAGGTGGTGCGGGTTTGGTTCTGCAACCGGCGGCAGAAGGAGAAGAGGATATACTGCCCAGTTTCCACTTCACCCATAAAACCTCACAACTTCAACCCTCGTCTGGTAAGTCTGACAAATCATTTTTGAATGAGACACATGTCTGTCTGTTCCCTGCACTAATGATTCAATTACTGAGGAAATAATCCACACTCTGGCAACCTAAATGGTGACTGTCATGTCTTATGTCCACCATACACTGAACATCAGTTTAGTTCTAACCCTGCTCCAACACACTTACCTGTAAGTTTTAAACAAACCTTAAGGACTTAATTAGTTTGATCAAGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGATCTGAGGCTCTCCAGGAACTGTTTGACACTTGTGGTGTAGAGGATATTAAAAGAGAAAATCATAGGTGCATCCTAAATTACATACATATGCACTGTTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33730
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044803 | Essential Splice Site | 333 | 398 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 60048318)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 57909936 |
| GRCz11 | 5 | 58579645 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCCAGTTTCCACTTCACCCATAAAACCTCACAACTTCAACCCTCGTCTG[G/A]TAAGTCTGACAAATCATTTTTGAATGAGACACATGTCTGTCTGTTCCCTG
Long Flanking Sequence:
AAGAAAAAAATATTATCAGACCTACTGTGAAAATTTCTTTGCCCTGTTAAACATCATTTGGGAAATATTTAAAAAAAAAAGAAAAAAAAATTAAAAGGGGGGCTAATAATTCTGACTTCAACTGTATGCAGTTGAAAGGGAATCAAAATATTCTCTGCCATTACTGTGAAACACCTTTTCATTATTTCTGTCTATGCTTATATTTTATATATTATTGTATAATTTTGCAGTACTTGCCATGTGCTTTAAGATTCTGGAGACTACTACATTACATGTGGAAAACAGTAAGATAGCAGTACTCATTGAAACTTATAAATGCTTTTTGCCCAATCCAGAACCCAAAACCCAACTCTGAAGAGATTACGCTGATCTCAGAGCAGCTGGCCATGGAGAAGGAGGTGGTGCGGGTTTGGTTCTGCAACCGGCGGCAGAAGGAGAAGAGGATATACTGCCCAGTTTCCACTTCACCCATAAAACCTCACAACTTCAACCCTCGTCTG[G/A]TAAGTCTGACAAATCATTTTTGAATGAGACACATGTCTGTCTGTTCCCTGCACTAATGATTCAATTACTGAGGAAATAATCCACACTCTGGCAACCTAAATGGTGACTGTCATGTCTTATGTCCACCATACACTGAACATCAGTTTAGTTCTAACCCTGCTCCAACACACTTACCTGTAAGTTTTAAACAAACCTTAAGGACTTAATTAGTTTGATCAAGTGTGTTTAATTAGGGTTGGAACTAAACTGTGCAGATCTGAGGCTCTCCAGGAACTGTTTGACACTTGTGGTGTAGAGGATATTAAAAGAGAAAATCATAGGTGCATCCTAAATTACATACATATGCACTGTTCCACTAGTGTAAGTACTGCGTTCACACTAAAAACTAAATACCCGATTGATGCACTTATTCAAACATTAAAATGAAGTGTAGAATGATCAACACTTCATGCAATCCATACACAACTGCTTTGCTCACGTAGCGGAAGGGGCGGAGCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38513
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044803 | Nonsense | 389 | 398 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 5 (position 60070053)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 57931671 |
| GRCz11 | 5 | 58601380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACTAGTAAAACTGATGAAAAAACTGTTCTTTTCCCTCAGATCGTGGTA[T/A]CGCTGGAACACCGCCTCATACCATCACTGAGTCCCTTTGAAGTAGCACAT
Long Flanking Sequence:
TTCAGGATCTCCATCTGCCACAGCCCAGTGTTGTTCGTCCCTACGTGAAGGACGATAGCACGGATGCTCTAGCCAGTGCTCAGGATAGTAAATACCTGGGCAAAAATATTCTTAAAGCGAGCACCAGGGGAGTAGTGAGGTGCGTAAGTTGTTACTTTTAGTGGACGCAGCACGGACGTGGTGAACGATGGAGTCACCAATGATAGCAACATCGGGACCCGTTAAGTTCCATATCCACATCATGCCTGCATGGCTAAAGACTCGTTACCGCGACAATTCATTCGAACCACTAGTCGACTCTTTTATAGATGAATCAATAGTTTGAAACATGGTGCACTTTCAGATTTAAGCCTCAGCTGGATATTTCACTTCACTTAGAGTTGTGTTACACATTGCATTTTTAAAAAAGCCCATTATAGGGGCTCTTTAAAGTATACTGTGCCTTTTGAAGAACTAGTAAAACTGATGAAAAAACTGTTCTTTTCCCTCAGATCGTGGTA[T/A]CGCTGGAACACCGCCTCATACCATCACTGAGTCCCTTTGAAGTAGCACATCCCGAAGCTGCAGCTTAATTTCATATCCTACCAGATGGAAAAAAAAGCACTCATTCTGTAACGTTTACAACCTGCACTAAATCTAGAGGCAGAACACAGAACTACTTCTGCTTCTCCTGGTCTAATGTTCAAGGGCTTGTAAAAAAGAGCTTCACTGCTAATTACTGAAGGGAAAATGCACTAATATGCTACAGTACGCTGTTTAGATATGCAATTTTGCTATAAAGAACATGTTCGGCATTTTCAGCAGAACTTCTAAGGTGTTTGAATCTTTATTTTACTTTCTGAGCAAAAATCTCTGCGCCAGTTTTGTTGGAGATGAAGGTTCAAATCTGGCTTAATGCGTCTAAAACAAAACTGCACACAGCTAAAAACAAAGACCACTCATATTTGTATGCATTGTTTACATGCTTTATTATTGTTTTCACTCTTGCCTTAACTGATGTTATG
Associated Phenotype:
Not determined