ZMP
patl1
Ensembl ID:
ZFIN ID:
Description:
Protein PAT1 homolog 1 [Source:UniProtKB/Swiss-Prot;Acc:A2RRV3]
Human Orthologue:
PATL1
Human Description:
protein associated with topoisomerase II homolog 1 (yeast) [Source:HGNC Symbol;Acc:26721]
Mouse Orthologue:
Patl1
Mouse Description:
protein associated with topoisomerase II homolog 1 (yeast) Gene [Source:MGI Symbol;Acc:MGI:2147679]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11013 | Nonsense | Available for shipment | Available now |
sa18712 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11013
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 |
---|---|---|---|---|---|
ENSDART00000100937 | Nonsense | 745 | 765 | 17 | 18 |
ENSDART00000139577 | Nonsense | 745 | 758 | 17 | 17 |
ENSDART00000100937 | Nonsense | 745 | 765 | 17 | 18 |
ENSDART00000139577 | Nonsense | 745 | 758 | 17 | 17 |
The following transcripts of ENSDARG00000017423 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 53264201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 52133772 |
GRCz11 | 1 | 52768510 |
KASP Assay ID:
2259-1169.1 (used for ordering genotyping assays)
KASP Sequence:
TCATCACCGCTGTTCACTCCTCCAAACCTGGTGTCTCTGTTCTCTCGATA[T/A]GTGGACCGCCAGAGACTTGAACTCTTACAGGAGAAACTACAGTGAGTTTG
Long Flanking Sequence:
ATCCAACTGATATTTTTGTTTTTAAGTGAACTAACCCTTTAATTCTGAGTAATGATAATTGATCATAATAGAGCTGCAAATCATCATCATATTAGAGTGATTCCTGAGGGATCATGTGAAACTGAAGAGTGGAGTAATAATGCTTAAAATCAGCTTTGACTCACAGGAATAAATTACATTTTATACCATATTCAATACGAAGACCTATTTCACAAATTGACTGTTTTCACTGTAATGTTGATATACTAAAGAGCCGGTTACTTTTAAACTGTATAAACAAGAACAAAAGGCTTTACAGTGGCTAGCGTAGCAGTATTTCATTCATTCTGGTTTTGTCAGTGGTGTTTAATGCATCTGATAATGTTTTATCCTGTATTTATTCTTTTGTCCAGGACTGAATTGGTGTTCTCTGTGACCCGGGAGTTGCTGAAGGTCCCATCCTCTGCTCTCTCATCACCGCTGTTCACTCCTCCAAACCTGGTGTCTCTGTTCTCTCGATA[T/A]GTGGACCGCCAGAGACTTGAACTCTTACAGGAGAAACTACAGTGAGTTTGTGCTCCAAAACATACTGTCGCCGCTGTTTTCTTACTGGCACTCTCTTAGGAGCATGAGAGTGTGTGGATATGTTTGGAGAAAAAGTGAAAAAAAATTTTTTTTTAAATAAGTCAAGCAAAGCAAGTCTAAAATGGCCACCTAAGTTTCAATTTAGTTTACACCAATTCTCGGTTATTCTATACAGGGATATACATAATTGTAGTCAACAATAATAATACACACTACATGACAAAACTCTTGTCGTCAATCCCAGTTGTAAAAGCAGCAAATAATAACTTGACTTCTAGTTGATCACTGGATAAGGTGGCAGAAGGTCGATTTTTATTTATTTATTTATTTTGATTTTTTTCTTGAATCATCTGCATCCCAGTCATAACAATTACTGCAGAAGACTTATTGGAACCAGCATGGACCCAAGATTTTCATAGAAATCAGTCAAGTTTGGTGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18712
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 |
---|---|---|---|---|---|
ENSDART00000100937 | Nonsense | 745 | 765 | 17 | 18 |
ENSDART00000139577 | Nonsense | 745 | 758 | 17 | 17 |
ENSDART00000100937 | Nonsense | 745 | 765 | 17 | 18 |
ENSDART00000139577 | Nonsense | 745 | 758 | 17 | 17 |
The following transcripts of ENSDARG00000017423 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 53264201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 52133772 |
GRCz11 | 1 | 52768510 |
KASP Assay ID:
2259-1169.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCACCGCTGTTCACTCCTCCAAACCTGGTGTCTCTGTTCTCTCGATA[T/A]GTGGACCGCCAGAGACTTGAACTCTTACAGGAGAAACTACAGTGAGTTTG
Long Flanking Sequence:
ATCCAACTGATATTTTTGTTTTTAAGTGAACTAACCCTTTAATTCTGAGTAATGATAATTGATCATAATAGAGCTGCAAATCATCATCATATTAGAGTGATTCCTGAGGGATCATGTGAAACTGAAGAGTGGAGTAATAATGCTTAAAATCAGCTTTGACTCACAGGAATAAATTACATTTTATACCATATTCAATACGAAGACCTATTTCACAAATTGACTGTTTTCACTGTAATGTTGATATACTAAAGAGCCGGTTACTTTTAAACTGTATAAACAAGAACAAAAGGCTTTACAGTGGCTAGCGTAGCAGTATTTCATTCATTCTGGTTTTGTCAGTGGTGTTTAATGCATCTGATAATGTTTTATCCTGTATTTATTCTTTTGTCCAGGACTGAATTGGTGTTCTCTGTGACCCGGGAGTTGCTGAAGGTCCCATCCTCTGCTCTCTCATCACCGCTGTTCACTCCTCCAAACCTGGTGTCTCTGTTCTCTCGATA[T/A]GTGGACCGCCAGAGACTTGAACTCTTACAGGAGAAACTACAGTGAGTTTGTGCTCCAAAACATACTGTCGCCGCTGTTTTCTTACTGGCACTCTCTTAGGAGCATGAGAGTGTGTGGATATGTTTGGAGAAAAAGTGAAAAAAAATTTTTTTTTAAATAAGTCAAGCAAAGCAAGTCTAAAATGGCCACCTAAGTTTCAATTTAGTTTACACCAATTCTCGGTTATTCTATACAGGGATATACATAATTGTAGTCAACAATAATAATACACACTACATGACAAAACTCTTGTCGTCAATCCCAGTTGTAAAAGCAGCAAATAATAACTTGACTTCTAGTTGATCACTGGATAAGGTGGCAGAAGGTCGATTTTTATTTATTTATTTATTTTGATTTTTTTCTTGAATCATCTGCATCCCAGTCATAACAATTACTGCAGAAGACTTATTGGAACCAGCATGGACCCAAGATTTTCATAGAAATCAGTCAAGTTTGGTGAA
Associated Phenotype:
Not determined