ZMP
ptena
Ensembl ID:
ZFIN ID:
Description:
phosphatase and tensin homolog A [Source:RefSeq peptide;Acc:NP_957002]
Human Orthologue:
PTEN
Human Description:
phosphatase and tensin homolog [Source:HGNC Symbol;Acc:9588]
Mouse Orthologue:
Pten
Mouse Description:
phosphatase and tensin homolog Gene [Source:MGI Symbol;Acc:MGI:109583]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu1864 | Nonsense | Available for shipment | Available now |
sa12727 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
hu1864
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 |
---|---|---|---|---|---|
ENSDART00000104735 | Nonsense | 43 | 431 | 2 | 9 |
ENSDART00000104738 | Nonsense | 43 | 444 | 2 | 9 |
ENSDART00000122209 | Nonsense | 43 | 467 | 2 | 10 |
ENSDART00000128958 | Nonsense | 43 | 454 | 2 | 10 |
The following transcripts of ENSDARG00000071018 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 23498331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23648480 |
GRCz11 | 17 | 23668504 |
KASP Assay ID:
1105-0001.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACATGTCAGACATATACCCTAACATCATTGCCATGGGCTTTCCAGCCGAA[C/T]GATTGGAAGGTGTTTACCGAAACAACATTGATGACGTTGTCCGGTAAGTC
Long Flanking Sequence:
GAATGCCTCTGCTGATTTTAAAATTTTTATTCACTGTTGTCATTTTTCTTGCTTGTCTCTTCTCTCACAATCAGTATTTATTTTCAGCTCTGCTCTAAGGCACTATAGCTTTACTTTTGGGCCTGCTCTAGCCAGTAGCATTGTAAAACCTACTGGGGAGGCAGGTGCACAGAAAGTAAGGTCCCGGTTGATTACTCAAATTTGGGTTAACAACCTATGCTTTTAGCACATAAATATTTGGCACATAAAATATTTTTATTGCACCATTCTGTGAGACATATTTCATTTATTACTATTGTTACGATGATAATGTTTTAATAAGACGCAGCGCTAGTTTCTTGTTTAGATTGTTGAATGTATGTAGTAACATCTTGTAGATTTAATTTTATTGTTTATTTTGCTTAATGTTAACCTGGTGTACAGTGCACATATGATCTTTTTCTTTAACACACATGTCAGACATATACCCTAACATCATTGCCATGGGCTTTCCAGCCGAA[C/T]GATTGGAAGGTGTTTACCGAAACAACATTGATGACGTTGTCCGGTAAGTCAACGTGGTAAAACACACAATTCTTTTTTTTTTTATTTATTTATTTATTTTTATTTCGTCTCACCGTAAATTTGACAAATTATGCATTTTTTTTTGAATGAATAGTCACTAACAAATGTTAGTCAGTTGTTTCATCTAATAGCTTGTTGAAATTCAAAATTGTAACTTCTGTCTTTCTTAATTTTTTTGTCTTTCAGGTTTTTAGATTCCAAGCATAAGAATCATTATAAAATTTATAATCTGTAAGTATTTAATTATATTTGAGTAATGACATACCAAACATAAATTGTTTGTTCGGAGTTTAACTCTCCTGATTTTCTTTTTTAGATGTGCTGAACGACACTACGATGCATCTAAATTCAACTGTAGAGGTGAGTACAACCCCTACTTCATTTTAACAGTGTCTAATTCTGAAACTAGTGTTAAAAAGACTACTTTTTATGGTCTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12727
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104735 | None | None | 431 | None | 9 |
ENSDART00000104738 | None | None | 444 | None | 9 |
ENSDART00000122209 | Essential Splice Site | 237 | 467 | 7 | 10 |
ENSDART00000128958 | Essential Splice Site | 237 | 454 | 7 | 10 |
The following transcripts of ENSDARG00000071018 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 23492591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 23642740 |
GRCz11 | 17 | 23662764 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGTGAGGTGAATCCCCAGGGCTTCAAGAAAGGCAGCTGGCACTGGGG[T/C]AAAACGGCATTACTTTACTACTACTGTTAAAGCAAACGTCTTAAWGTTCA
Long Flanking Sequence:
ACTCATGGGTACACTGTCTTTCTCTGTTCCTTTTTTCTTCTTTTTTTAAAAAGTTTCCCCTGAGGAAGTTTCCCTTCGGTTTCTATATATCGGCTCCTGCAGCCCACCACAGTCTGGCGTTTAATGACATCACAGTTCGTGCCCACCCTCATTCCCTCCCTCCATTCGTACATAGCGTGCTAGTCAGTGTTTTGTTCACGTTTGCCACGCCAACCCAAACTGCACCCTACATGCCATTTTTGGGAAGTTCTTCATTTTTCGAAATTGGAACTAAAAGTGCAGAGTCAGTCTCAGTACTCCCATGTTTCAGACTTTCAGACCTGTGTGTGTGTGTGTGTGTGTGTGTCTTGCCAAGGCCAGTGTGGAGCAGCCAAGCTCCTGGCCAGGCTGATTGTGGTGGTGGTGTTTAACTTCCTTCTCTTTCTCTAAGGGGACAGTACTGTTAAAAACAGGAGTGAGGTGAATCCCCAGGGCTTCAAGAAAGGCAGCTGGCACTGGGG[T/C]AAAACGGCATTACTTTACTACTACTGTTAAAGCAAACGTCTTAATGTTCAGACAGGCCCGGCCCTGTACTGCATTCAGTACAGTTCAGTACAGCGTTTACTGTTGCTCTAGTTTCTCTCAGAAAGAAGTCTCATAACATTAACTACAATGTTTGAAATGTTTTTCACAGATGTTCGGTTTTTCAAAAGAACAAAACAATGTAACCATAATGAACAAGTCACACTGAATAAATGTGAAAGAAAAGAAACAAATAGTATGCTGGGAAATATGACCTAAATTTCATATTAAAGTAGGAGCAATTTTATATTACAGTACTGATGATTGAAATACTTCACTTTTATTATACTTCTAAGAAGTTATATATTGGTTAGGAACACATGTTTAATCTATACATTATTAAAAAGGGGTAGTTCACCCTAAAGTCATCATCATTTACTGGACCTCATGCTCTTTCAAACAAATTTTTCCATGTCTTCCTTTTTTTCATGGAAAATAAATGT
Associated Phenotype:
Not determined