ZMP

pias1

Ensembl ID:

ENSDARG00000036094

Human Orthologue:

PIAS1

Human Description:

protein inhibitor of activated STAT, 1 [Source:HGNC Symbol;Acc:2752]

Mouse Orthologue:

Pias1

Mouse Description:

protein inhibitor of activated STAT 1 Gene [Source:MGI Symbol;Acc:MGI:1913125]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20991	Nonsense	Available for shipment	Available now
sa1753	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa20991

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000052397	Nonsense	440	653	11	15

Genomic Location (Zv9):

Chromosome 7 (position 35224545)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	33618885
GRCz11	7	33890035

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTGTGCGTGTTTGTTTGTGTGTAATCAGGTGGGTGTCGTACAAGCGTGT[T/A]GGAGCAGAATTCTCAAACAAATGGCAGCAGTGGAGGAGGAAACAGAAAAA

Long Flanking Sequence:

TTAATGAAGGGACTAAGCCAAAAAGGTGGCAAGGGGAGACAATCGAACTTGGGTTTGGTCCAGGCTATTAAACCAAGTGTAAAAGCACCCATATACTCCACCAGTTCCTAACCTATTTGAGTTTCTTTCTTCTGTTGATCACAAAGGAAGATATACTGACTAATGAAAGAAAAAGCAGCCATTGGATATTATTTTTTGTTTTTACTATGGCTGTTTATTTCCAGTATTCTTCACAATATCTTTTTTGTGTTCAAAAGAAGAAATTCATAAAAGTTTCAAACCATTTGAGTGTGAGTAAACAGTGAGATACATTTTCATTTATGGGTGAACTATCCCTTTAAAGCTCCCCCTGAGAAATGTCATCGCACATTTCGTCACACATTCTTATATAAAGTGAGCATGCATCCTGAAACAATTTTATTTACAACCCGCTGTGTGTGTTTATGTCTGTGTGTGCGTGTTTGTTTGTGTGTAATCAGGTGGGTGTCGTACAAGCGTGT[T/A]GGAGCAGAATTCTCAAACAAATGGCAGCAGTGGAGGAGGAAACAGAAAAAAGGTGGAGGTGATTGATTTGACTCTGGACAGCTCATCTGAAGAGGAGGAGGATGAAGAACCTCTCCCGAAGAAGAGCTGTCCGTCACTGTCCAGCCTCTCTCCTCAGATGGATAATGGGTAAATGATCATTTTCATCCACACAAATAGCATTCTAAGGGTCATTTTGGCTGAATGCTCTACTCAAGTTTGTTTGTTTGCATCTGTTCACAGGGTGCTGAATCTCCACAGACAAGCATCTCCAGTGAGTCGAACTCCCAGCATGCCTCAGGTGGACACCAGTTACATTCCCCCACCTCCTCCCCTCATTCAGGACTACCGCCACTACTACTCCACACCCACTGAACTGTCAGGTACAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1753

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000052397	Essential Splice Site	535	653	13	15

Genomic Location (Zv9):

Chromosome 7 (position 35222387)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	33616727
GRCz11	7	33887877

KASP Assay ID:

554-1746.1 (used for ordering genotyping assays)

KASP Sequence:

ATGAYGTCCCACACCCCAATAGGCATCAATTCAAATTGAAATTTTTACTT[A/G]GTTCCAGCTCAAGCTAGAAAATCAAATTAAAATGTAGCTTTATTTTTTNC

Long Flanking Sequence:

TAATTCCCACATCATACACTCTTGATTTTTTTATTTACATAAAACGTGGAAACACTAAAGATGCTTTAATATGTTTTATGTGCTTCTTGTCCATGTGATCACAACTGGAAAAAAACTGAAGTAGTCGACTGTGGCATATCAAAAACTCCACTTTTTTTGTGCCACGTCACATTTGTCTCTCATCAGCTTGCTTTTGTTTTGCGTAGACGGCTTTTGGTCGTTCTTTGCTTCACACTACTCTTATGATGTTTTGAATACTTTAGCTAAGTGGTGATCAACCTATTTATCACAATCGACCGGTAGATCTTAATGACTCTACCCATAGATCCCAAATATCACAGAAGAATAAGTACAAGAAATGCATCTCGAGCGATGTAGGCCTATCTCGCTTTATTTTTCTTGATCCAACTGCTGTGTTAACTGCCGCAATGTCATTACACAGCTCTTCATATGACGTCCCACACCCCAATAGGCATCAATTCAAATTGAAATTTTTACTT[A/G]GTTCCAGCTCAAGCTAGAAAATCAAATTAAAATGTAGCTTTATTTTTTTCTGTCAGCTCTTTAAAGGGTAGATCTTGCCCTTTTGCAAGGTTAGTTATCTTCAGTTAAAAAAGGATTTAGCTCATCCATCAACATGATTTCAAGTCAATTATCATGACAGTCCCATAGAATCTAATGAAGACCACAATTTTCATGATTCCACACTTATGTTTGCTTTTTGTGTGTGCCCTCCAGCAGCAACTATTACATGCTGTGCTTTTAGGAGTACAAAGACAAAAATAGAGTATGTGGTGTCAACTTTTTGTTAGAATATTTGGTCCCACTTTATATTAAGTGGCCTTAACTAATATGTACTTACACAGGATTTAATAGTTTGTTACAATGTACTTATTGTGTAAATACATGTATTTATTGTGTTTGTATGCTTGATTAAATACCTGTATGTAATTACATCTGTAATTAACTTCTGTAATTACATTTGCAAATATACTGTTGACCAT

Associated Phenotype:

Not determined