ZMP
psen1
Ensembl ID:
ZFIN ID:
Description:
Presenilin-1 [Source:UniProtKB/Swiss-Prot;Acc:Q9W6T7]
Human Orthologue:
PSEN1
Human Description:
presenilin 1 [Source:HGNC Symbol;Acc:9508]
Mouse Orthologue:
Psen1
Mouse Description:
presenilin 1 Gene [Source:MGI Symbol;Acc:MGI:1202717]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30700 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43013 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
hu2548 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30700
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033514 | Essential Splice Site | 12 | 456 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 51747276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51133386 |
GRCz11 | 17 | 51222421 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCACAGTTCCGATGGCTGATTTAGTGCAGAATGCTGCCAATAATGTGG[T/A]AAGTTTGCTTATTCCGACCAGGGTTATTGTAGTTCACGAAACCATAAACG
Long Flanking Sequence:
CGAATGTGCGAATATAAAATCAACTTTACCTCTATATTGTTTACCATGTTACCTTGAATATTAGATCAGAGTTAGCATGCAAGTATGACTTCTAAACAACATTAACACTAATTCACTGTGAACAATGCTGTGCTTTGGTAGTCATTTGCTGCTAATATGATTTCTCTATTTACAATTTGCTAACAATACTTTTCTAAATTTATAATATTAAGGAGGATGTCTGAATATCCCAATATAAAACCAACTTCACCTCTATGACTAAGACTGGGATATAACATAATCTTCAAATGGTTTACTGTAAAAATGTACATTAGCCTAATCTCGACCTAGCCAGAGATAACAAGTTTATTACTTATGGGAAGGGACATTGTTTTGTTGTTACTGATGATTATTTGTGGTCTCAATCCTGACAGATCTAGAGTTCCCGCTGTTTCTATGATCCCGGGGTCACATCACAGTTCCGATGGCTGATTTAGTGCAGAATGCTGCCAATAATGTGG[T/A]AAGTTTGCTTATTCCGACCAGGGTTATTGTAGTTCACGAAACCATAAACGTGTAATTGTTGCTTGGAAGGGAACAAACATTACCTGGAATAGTTTCCGGCCATAAAATGTGTTTGTGTACCTGTTTTTGTGACATATCAGGACACAAATCTGTATAATGACATGGGTATAACACAGGTATTACAAAAAGGAGGTGAAATATTAGGACATTGGTGTCATCCTCATTTCTCAAAAAGCTTATAAATTCCACTGGATGAGTTTAATCAGAGTAAAGCTGCACACAGTCTCCTGTGATGGTTGGGTTTAGGGGTGAGGGCAATACAATATACGGTTTGGATAGTATAAAATGAATGGAAACCTATGTAATGCCCCCACTTTTCACAAAAACAAGCGTGTGTGTGTGTGTGTAATGAACATATTCCACAGTTTAGACTTTCGATTTTAAGACATTTGAGTTGTGTTTGGGGGAAATCGTTACCTGAGAATTTCACAATTACAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43013
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000033514 | Essential Splice Site | 279 | 456 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 51738734)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51124844 |
GRCz11 | 17 | 51213879 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGCTCAAGAGAGGAATGAGGCCATTTTCCCAGCGCTCATCTACTCCTG[T/C]AAGAAAAACCCCTCAGCACTTCCATCTTCTCAGACTGTGAATGTCCATCT
Long Flanking Sequence:
CTTAACGATGTTTCTGTTCCCTCCAGGGAAGTGTTCAAGACGTATAACGTGGCGATGGATTACTTCACGCTGGCGTTGATCATCTGGAACTTCGGTGTGGTGGGAATGATCTGCATCCACTGGAAGGGGCCGCTGCGGCTCCAGCAGGCCTATCTGATCATGATCAGCGCTCTCATGGCTCTGGTCTTCATCAAGTATCTCCCCGAGTGGACCGCATGGCTCATCCTCGCTGCTATTTCAGTCTACGGTCAGTCAGTCTGCAAACAGAGCAACACATTCACTTCTGTGTACTGATAGGTTTATTGTTCTGTAATGCTGCTTTGGAACAATAATTAGCCTGAAATGAATTGAATAATTTCAAAAACACAGCCCCTTAAATGTCTTTCCTGCTCCTGTGTAGATCTTCTGGCAGTGTTGTGTCCGAAAGGCCCTCTGCGAATCCTTGTGGAAACAGCTCAAGAGAGGAATGAGGCCATTTTCCCAGCGCTCATCTACTCCTG[T/C]AAGAAAAACCCCTCAGCACTTCCATCTTCTCAGACTGTGAATGTCCATCTGTTTAATTGTGTTATCGTCACGTTTCTATGAAATTTCTCCTTCGATTTGTCAGCTACGATGGTGTGGCTCTTCAATATGGCGGACAGTGCTGAAACCAGGAATAATTCCAGTCATCCAGTCCCTCAGCAGGAGAACCAGGGTGAGTGCTGTTGCTGAATTACACGTCTGCGTCAGCTGCCCTGCATGTAGCCGTGCGTTCATTCTTCTGCGTTCTGTTAGTGTTGCTCTGACAATAACACTTCCCAAATGGGTTTCTATTTATTTGTTTATTTGGCAGGGACAGTGTACATTATTTAGCATTTGTGCCAATGCACCAGAATTAGCCCGAAGGCTATTTTTCATCTGTCGTTCCGCTGTGTCGAGTTGTTTCCTGGGTGTTTTGTTTACACTGGATTGCTAACTTTCTGTACACGTAGCTTAACCAGACGTGCAACAACTTTAGTCATAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2548
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 |
---|---|---|---|---|---|
ENSDART00000033514 | Nonsense | 408 | 456 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 17 (position 51732154)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 51118264 |
GRCz11 | 17 | 51207299 |
KASP Assay ID:
554-0034.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACAATCAACTCAAAACCCTCTTGGCTTTGTTTCTCCTCAGGGTTTATG[T/A]CTGACTCTCCTCCTGCTGGCCATCTTCAAGAAGGCTCTTCCCGCACTCCC
Long Flanking Sequence:
TGGACAGACAGACAGACTGATAGACAGACAGACAGACAGATAGATAGATAGATAGATAGATAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGACAGACAGACAGATAGTTATTGATTTTTTTTATTTCAATAATATATTACTTGTTAATTTCTTTGGACTCTGATTTAATGGCTAAATTTAAAAACTGAAATACACTATTTTTTTCTCAACCTCTGTGAATAATAAAAAATAAAAAAAAGATGATCTGACTAACACATCTGCTATTCAGAATCACTATTCTGAGCAAATGCTTCAGTTTTGCTGCACAGTCCGTCAGACAATCAACTCAAAACCCTCTTGGCTTTGTTTCTCCTCAGGGTTTATG[T/A]CTGACTCTCCTCCTGCTGGCCATCTTCAAGAAGGCTCTTCCCGCACTCCCCATCTCCATAACCTTCGGCCTGGTGTTTTACTTTGCCACTGATAACCTCGTGCGGCCGTTCATGGACCAGCTGGCCGTCCATCAGTTCTACATATAGAGAGGTCGCCTCTCACACACTCCACTTTCATGCTCTTCAGGGAAACGTGAGCCCTGCAGACGAGCACACCTTTCCTCTTTTCTGGACATGTGACTGGATTCACACTAGTTTTTTTTATTTTGGCATTAAATGACTGGTTATTAATTACAGTGCCTCTCCATCTGATCCTGATATATGCTTTAGTAGCAGCATTGATCGGAACATTTGTTTTCGGAGAGAACGCAGAGCACATCTCAAGTCACACGTATGTATGAATGCATTAGCGTAGGGCAGGGGTGTCAAACTCAGTTGCTGGCGTTTAGCTCCAACCCTGCTTCAACACACTCACCTATAGGTTTCAAACAAGCCTGAAG
Associated Phenotype:
Not determined