ZMP
stat5.1
Ensembl ID:
ZFIN ID:
Description:
signal transducer and activator of transcription 5.1 [Source:RefSeq peptide;Acc:NP_919368]
Human Orthologues:
STAT5A, STAT5B
Human Descriptions:
signal transducer and activator of transcription 5A [Source:HGNC Symbol;Acc:11366]
signal transducer and activator of transcription 5B [Source:HGNC Symbol;Acc:11367]
signal transducer and activator of transcription 5B [Source:HGNC Symbol;Acc:11367]
Mouse Orthologues:
Stat5a, Stat5b
Mouse Descriptions:
signal transducer and activator of transcription 5A Gene [Source:MGI Symbol;Acc:MGI:103036]
signal transducer and activator of transcription 5B Gene [Source:MGI Symbol;Acc:MGI:103035]
signal transducer and activator of transcription 5B Gene [Source:MGI Symbol;Acc:MGI:103035]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10709 | Nonsense | Available for shipment | Available now |
sa19972 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10709
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 |
---|---|---|---|---|---|
ENSDART00000024832 | Nonsense | 474 | 785 | 12 | 19 |
ENSDART00000132256 | Nonsense | 474 | 785 | 14 | 21 |
ENSDART00000139763 | Nonsense | 474 | 785 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 16939485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17145818 |
GRCz11 | 3 | 17295618 |
KASP Assay ID:
2259-3235.1 (used for ordering genotyping assays)
KASP Sequence:
CCCCCNNCCAGACTCTTTCTCTTCCTGTKGTGGTAATTGTTCATGGAAGT[C/T]AAGATAACAATGCCACGGCCACCGTTCTATGGGACAATGCCTTTGCTGAA
Long Flanking Sequence:
TTGGGCAGCCCTGTCTTAAAGCATCTAAAACAGGTCTTAATTTTCCAACGACCATGTAACGCAACCCAATGCAATCATCAATAATCCATCTAAAAAAAAAAGCTTTCAGCAAAACTCTATTTACCAATATTTTTCCTTTTGTTGGTGCTTTTGGAAAGAGAAGAAGAAGAAAAGTTATGTTGAAATAAACGTGAATGTACATTAATTAACTTGTGTATGCTTGCTTCAGCAAATTATTTAAAATATGTGGCTAAGAAATAACTTATCAGAATTTTTTTGGATAGAGCAAGTAAACTTCTATTCCATGGAACCAACTCGGATATTAGAAAATATTCTGTATAAGTACTGTATAAGTCTGAAATTTCATTCATAATGGTCTTAAAAATGTTTTAAATAAACCTGCTGAAACCCTGAGTTCATTTATTTGTCTCATTCACATATTTATTGTTTCCCCCCTCCAGACTCTTTCTCTTCCTGTGGTGGTAATTGTTCATGGAAGT[C/T]AAGATAACAATGCCACGGCCACCGTTCTATGGGACAATGCCTTTGCTGAACCGGTTAGTTCCTGATAACATCACTTTATGTTTGATTGTGCATCTTACAGTATAACTGTTCAGTTTCAGGCTGTCATTATTGTGCCTTAAAGTATAGCTCACCCAAAAATGAAAATCCTGTCATCATTTATCAACCCTTTACTTGTTCCAAAAATATTTAACTTTTTTTGCTTTTGTTTTACACAAAAGAACATATTTTGAAAAATGATGCAAACCTGTAACCATTTACTTCTATAGTATTTGTTTTTCCTAATATGTAAGTAGTCAACAGAAGAAACTCCTAAAGGTTTGGAACCACTTGAGGATGAGTAACTTCCAATTTTTGAGTGAACTATCCCTTTAAGCTCAAAAGCAGGGTGTCATCTACAATAAACTCATGAGGTCGCGACATCACATGAAAAGGCATGCAAACAATTTCCTCGAGTCATGTGGTGATAAATAAGATCCTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19972
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 |
---|---|---|---|---|---|
ENSDART00000024832 | Nonsense | 617 | 785 | 15 | 19 |
ENSDART00000132256 | Nonsense | 617 | 785 | 17 | 21 |
ENSDART00000139763 | Nonsense | 617 | 785 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 3 (position 16961991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 17168324 |
GRCz11 | 3 | 17318124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCAAGCTCAGGATATGCTGATGTCCAAACCCAACGGGACCTTCCTGT[T/A]GCGATTCAGCGACTCAGAAATCGGCGGCATCACTATAGCCTGGGTGGCGG
Long Flanking Sequence:
CATTTCACCTGGCTGCTCTGCAAGGAAACATTATTCATAATGGTTCACATTCTTTTTAGATTCTGGTTCTTTTGTTCCGTTTTACCTTTTTTTCTACAATGGACAGGCTATATTCATAATGAAGTGCTTCTTTGCCATGGCAACTGCCTGATTGAGAGATAGTGCAGGTTAAAACTATACATCAAGACATTAAAGCATGCACGGATTAACACAGGAGGGAGATCTGAGAGACCACTTGAGAGTTTGATATGATCTTGTGCGTTTTTTGTTGTTGTTATTTTCTTATCTTTATCCTGTTCAAGCCCCAGTTGGCCATGACTTGTAATGCTTTGTACAGAAATCATGATAAAACTGAACCGTACACACTCTCTGCCTTTGTGATTACAAATGCACTGGTGTTTGTGTTTGTGTTTTTGTGTGTCTCAGGGCAATTCTTGGCTTTGTGAATAAACAGCAAGCTCAGGATATGCTGATGTCCAAACCCAACGGGACCTTCCTGT[T/A]GCGATTCAGCGACTCAGAAATCGGCGGCATCACTATAGCCTGGGTGGCGGAGAACCCTAACAAAGCAGGTATAACTATTTGTTTCCTGTTTTATCTATTTAATTGAATGATGTTTAAAACAGTTTACTTTGCTCTTTCTATTTTATTCAAGCAGCAAGTTTAGATTTAGTTTAAAAATTTAGACTTTAATTTTAGACTTTTGATTAAAACGGCATCTAGTTTTAGTCATATTTAAAGAAACACTTCACTTATTTTGTAATTGAACTCATTTTACAAATCATCTAGAGCTAAACAGTGACGTTTTACCATGTATTTTTAAATTTATTTAGCCGATCTTCAGGTCATCAGGAGCACTTTTAGCTTAGCTTAGCATAGCTCATTGAGTCGGATTAGACCGTTAGCATCTCACTCAAAAATTAGTTTTTATAATGAGACTATAGTTCCCAATAATATATGGATGCAAACTTTGATTTGCAAGTGGAGATTTCATATCTCAGAGA
Associated Phenotype:
Not determined