ZMP
stat4
Ensembl ID:
ZFIN ID:
Description:
signal transducer and activator of transcription 4 [Source:RefSeq peptide;Acc:NP_001004510]
Human Orthologue:
STAT4
Human Description:
signal transducer and activator of transcription 4 [Source:HGNC Symbol;Acc:11365]
Mouse Orthologue:
Stat4
Mouse Description:
signal transducer and activator of transcription 4 Gene [Source:MGI Symbol;Acc:MGI:103062]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa25434 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21554 | Essential Splice Site | Available for shipment | Available now |
| sa34719 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25434
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 |
|---|---|---|---|---|---|
| ENSDART00000105764 | Nonsense | 3 | 742 | 1 | 23 |
| ENSDART00000147052 | Nonsense | 3 | 731 | 2 | 24 |
Genomic Location (Zv9):
Chromosome 9 (position 42233411)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41358581 |
| GRCz11 | 9 | 41160368 |
KASP Assay ID:
554-7355.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTATGACTACAATATAGTATGTTTCTTTTCCAGCATCACCATGAGT[C/T]AGTGGAAGCAAGTTCAGCAACTGGATATTAAGTTCCTCGAACAGGTGGAT
Long Flanking Sequence:
ATGACTCCCAGCCATCTACAAGCCTGGATTGCTGCTGGTGATTGTGACAATAATGCAATTCATATGACCACTTATAATTTTATGTATTTTAATATAAGAGGGATATTACACTGAATGATGATGGACCATTTATACTTCACACGTATTTTGATATTTTATTTAAAAAAGACTTTTAAAACAATTTAAAACAATAAATTAGACACTTTTACTTGCATTTGTTTTGTATAATAATCATCTCTATTTTGCTTTTAGAATTATTAGAGTAGGCCAGTTCTGTCATTTCACAAACACATCCAAAAAGAACGGTTTAATTTTGCACGGTCAACCTAAAAAAAGATTGTAACCTCAACAAGACTGTAACCTCAAGAAGGTTAAGGTGGATGATGCTCATGTATGATAGTGGTTTGGTTATTTCTTATCACATAACTGACTCTCTGAAGGCACTGTTGCTTTGTTATGACTACAATATAGTATGTTTCTTTTCCAGCATCACCATGAGT[C/T]AGTGGAAGCAAGTTCAGCAACTGGATATTAAGTTCCTCGAACAGGTGGATTATTTTTACGATGACAATTTTCCAATGGAGCTGAGACAAGTGCTGGCTAACTGGATTGAAAGCCAGGATTGGTATGTGGTTTATTGATCATAATTTGCACGTTTATCAAATCTCACTTTCAATTTGTGGCCCTATAAAATGATAGAAAATACACAAATCTCACACTTTTAACAATTGTCTGTATAATTTACAGTAACTTACTGGCACAGTTTGCCAACAATTTACTGTAAACCAAACTTACAGCAAAAATACTGTATTAATATTTATAGTACCGTTTGTTTTTCTGTACATGTTTTTACAGTATTTTACAGTATATCTTTACTTCTTCAGGCTTCTCATATTTTTTTACTGTTATATTTTCTAATATTTTGTTTAACAGCAAATTAAAAATAATGTTTTAATGGCAATAATTTTCTTATATTTTTTACAATGCAACTTTGAGATACAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21554
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105764 | Essential Splice Site | 343 | 742 | 10 | 23 |
| ENSDART00000147052 | Essential Splice Site | 342 | 731 | 10 | 24 |
Genomic Location (Zv9):
Chromosome 9 (position 42261446)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41386616 |
| GRCz11 | 9 | 41188403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAACCCCTCATCATCAAAACACAGGTGCAGTTCACCACCAAGGTCAG[G/A]TATGAACCACCGCTGAATCTTCCTGTAACTCTAAGTAAACAAGTCTGAAG
Long Flanking Sequence:
CATTTCAACTAGAATGAAAGGAGCTTTTAATAAAAATACAATATTATTAGCCCCCTAAGCAATATTTTTTTTTCAATTGACTACAGAACAAACCACTGGTATGCCTAATTATCCTAACTTGCCTAATTAACCTAAGGAAGCCTTTAAATGTCACTTTAGGCTGAATATTAGTATCTTGAAAAATATCTAGTACAATATTATTTACTGTCATTATGGCAAATAGCAAAGAAATCAGTTTATACTATTGAAACTATTATTTAGAAATGTGTTGAAAAAAATCTTCTCACCGTTAAACAGAAATTGGGGAAAAAATATAGAAGAGGGCTAATAATTCAGACTTTAACTGTAACACAAAACCCAGAAACGGTGCACAACAAATAAAGTCTCTCTTTGGTCAATGTTTGCAGCTCCTTTGTGGTGGAGAAGCAGCCCTGTATGCCAACACACCTCCAGAAACCCCTCATCATCAAAACACAGGTGCAGTTCACCACCAAGGTCAG[G/A]TATGAACCACCGCTGAATCTTCCTGTAACTCTAAGTAAACAAGTCTGAAGCCTTATTGAACTGACTGCCTGAAGTCCAACGCAAACTTTTCATTTCACTTGTTTTTTCTTTTTTTTTCCAGGTTGCTGGTTAAGTTACCTGAGGTGGATTATCAACTCAAAGTCAAGACAACATTTGATAAGTATGTTTCCTAAATATGGTTTACATTATTAATATTTTTTTCTTTACCCTCTATTCTTTATTTTTATAACCTGGGTCATTCATATTACGCAAAACATTTTCAGCTCATTAACTTATTAAAATGCAATAAATACAGTTGTGGGCAAAATGATTAGCCCTCCTGTGATTTTTTTTTTCCTTTTTAAATATTTCCCAAATGATGTTTAACAAAGCAAGGAATTGTTCAAAGTATTTCCTTTAATATTTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAAAAAAAGGAGTTTTACATTTTTCAAAAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34719
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 |
|---|---|---|---|---|---|
| ENSDART00000105764 | Nonsense | 495 | 742 | 17 | 23 |
| ENSDART00000147052 | Nonsense | 489 | 731 | 17 | 24 |
Genomic Location (Zv9):
Chromosome 9 (position 42271486)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 41396656 |
| GRCz11 | 9 | 41198443 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGTAGAACCTGGCCTTCTTCAGTAACCCGCTGCGGGCGAGCTGGAGT[C/T]AGCTCTCTGAGGTGCTCAGCTGGCAGTTCTCGAGTTTCGCAGGCCGAGGG
Long Flanking Sequence:
TGTAGTGTCTCTTTGCTTGTTGCTGGCTGCATGTGGGCGGAGTAATACACAGAGGTGAAGGGTGAAGAGGCCTTTGTGTGATGTTACTGGCAAAATATTGCACGGCTATCAGCCAATCAGATTCAAGAACCAGACAGAACTGTTGTATAAATATATTTATTATGTTAGAAATTAAACCTAATACAGCTTACAGTGTTTATATTTTCTCCTGTCTAGACTTGCTCTCTGCCGCTGGTGGTCATCTCTAATGTCAGTCAGCTCCCAGGAGGCTGGGCTTCAGTCATGTGGTACAACCTGCTCACGGATGACCCAAAGGTCAGATTCTCACACCTCTGATACAGATATCAGAGAATGCATGTCTAGCATAATATCTAGTATCTAGAAATGATGCTTAAGATCTACATTTTACTGAATTCGACAGGCAGTTAGTTATATGTGACCTTGTCTGTCTTGTGTAGAACCTGGCCTTCTTCAGTAACCCGCTGCGGGCGAGCTGGAGT[C/T]AGCTCTCTGAGGTGCTCAGCTGGCAGTTCTCGAGTTTCGCAGGCCGAGGGCTCAACAAGGAGCAGCTAAACATGCTGGGAGATAAACTTCTGGGTATGTTTTCTATTCTGACACAAAAGAGTTAAAAGCAGAGTTTGGAAAAAGTGCTGCAAAAGTGGGCGTGGTCAATTCAGATTATTAAATTTCACTCTTATTAGTATTACATAAAACCTGCTTAATGGAAACGCCAAGATGTGCATAAACTAAAAGAATGTGAATAGAAACAAACTATGAGTAGGATAAAGGTTTTATTTGGTATGACAAAAATGAGCATAAACTGCAATGGAAACACAGTTAATGAATAAATTCCAGCATGTACATCAAAAGTGGTTTTGTTTTAACAGATCACGATGTGATAACAAAAACGAGCATGATGGGACAGCATTAGTTGACAATCCAGCAGACTGACCACAATGTAAAACATCTTAAATGTTGTTTTGATCATAGTGAAATCTCTTAAT
Associated Phenotype:
Not determined