Busch Lab

ZMP

psme1

Ensembl ID:
ENSDARG00000002165
ZFIN ID:
ZDB-GENE-991110-17
Description:
proteasome activator complex subunit 1 [Source:RefSeq peptide;Acc:NP_571450]
Human Orthologue:
PSME1
Human Description:
proteasome (prosome, macropain) activator subunit 1 (PA28 alpha) [Source:HGNC Symbol;Acc:9568]
Mouse Orthologue:
Psme1
Mouse Description:
proteasome (prosome, macropain) 28 subunit, alpha Gene [Source:MGI Symbol;Acc:MGI:1096367]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa12220 Essential Splice Site Available for shipment Available now
sa6761 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa14800 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa12220
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000005105 Essential Splice Site 13 248 1 11

The following transcripts of ENSDARG00000002165 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 12850192)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 12801640
GRCz11 24 12946059
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCTGCAGCAATGACTTCCTTAGACATGAGCCCCGCGTCCAAGAAACAGG[T/A]AAGCCGAATATKACAGGCCCAAAAGCTGAYATACACTCATTACATTTCAT
Long Flanking Sequence:
ATATATATATATATATATACTTTTTTAAGTTTAATATATTATAATTGCATACTATTGGTACAAATAAATATATGAAAGCATATTAATAAAATAAATTTTAGAATTCATTGTTCATGATATATATATTTAAAACCACAACTAAACAAACAAAAAATTAAAACAAACGTCGGACTTTTATTCTACTTTTATTCTGTTAAACCTGTTTCCGTAACTCACTGATGTTGTCGCCCCCTTCAGTTCTTATCGAGAATGATTTATTAAACTCACTTTCATTTTCACTTTTTATGCTGACTAACTGCGAGTTCTCGTCGTTTCGTCGGTGACATCTTTATCCAGCCGTCTCTTCTCAACTTAAATGCCACACTATCCAGTGGGATAAGACATTACACGCGTATTTTCCTGCAAACAGGTCTATTAAAGTTTTTGCGAAAAGGTAAATCATTACGACTGTTCTGCAGCAATGACTTCCTTAGACATGAGCCCCGCGTCCAAGAAACAGG[T/A]AAGCCGAATATTACAGGCCCAAAAGCTGATATACACTCATTACATTTCATGTATTGGCCAACAAAAAAGATTTTTAATCGTACTTTGTCAATAAACTGTATTATTTTATAATTTACTCGTTTGTGCTTGTGTGGCGAGTTTGGTAAACACTTCCTATGTAACGTTACCTTGCAGGTGGATGGATTCTCTCAGAAAATCACCAAGGAGGTAATTATACTAAATATTCCTTAATTTTCTTTTATATCCATTACAAATGTGCCACGTGCAAATGCAAATTGTATTTTCTAATAATAATAAATTAAATTTAAATTTAAAATAAATTACACTTATAACAATAACTGCAGTAAAACGTTATTAAATATCTGTTCGTTTTTATCAGGCTGAACAGTTGATCTCGAAGATTTTCCCTGAGAAGATTGCAGAGATGGACAATGTGTTGCAGGTATGAACTCAACCATTTAATATTAAGGCTTTATGAGTACATATTATGCCAATTGTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6761
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000005105 Splice Site, Nonsense 45 248 3 11

The following transcripts of ENSDARG00000002165 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 12850632)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 12802080
GRCz11 24 12946499
KASP Assay ID:
554-5462.1 (used for ordering genotyping assays)
KASP Sequence:
TGATCTCGAAGATTTTCCCTGAGAAGATTGCAGAGATGGACAATGTGTTG[C/T]AGGTATGAAMTCAACCATTTAATATTAAGGCTTTATGAGTACATATTATG
Long Flanking Sequence:
ATTACGACTGTTCTGCAGCAATGACTTCCTTAGACATGAGCCCCGCGTCCAAGAAACAGGTAAGCCGAATATTACAGGCCCAAAAGCTGATATACACTCATTACATTTCATGTATTGGCCAACAAAAAAGATTTTTAATCGTACTTTGTCAATAAACTGTATTATTTTATAATTTACTCGTTTGTGCTTGTGTGGCGAGTTTGGTAAACACTTCCTATGTAACGTTACCTTGCAGGTGGATGGATTCTCTCAGAAAATCACCAAGGAGGTAATTATACTAAATATTCCTTAATTTTCTTTTATATCCATTACAAATGTGCCACGTGCAAATGCAAATTGTATTTTCTAATAATAATAAATTAAATTTAAATTTAAAATAAATTACACTTATAACAATAACTGCAGTAAAACGTTATTAAATATCTGTTCGTTTTTATCAGGCTGAACAGTTGATCTCGAAGATTTTCCCTGAGAAGATTGCAGAGATGGACAATGTGTTG[C/T]AGGTATGAACTCAACCATTTAATATTAAGGCTTTATGAGTACATATTATGCCAATTGTGTTTGTATTCATGTTGCTGCTGCTATTGTTATATTTATCACCAATTAATAGTTTTTAATTTGTATTTTTTTAGGGTTCCTGTAGTCTGAAGGATCTTTCTGTGATCAAGGCTCCTCTGGACATCCCAATTCCAGACCCGGTTAAGGAGGAGCTCAAGAGGAAGAAAAAAGAGGAGGTCATTATAACACAATTTATTATTAACAAGCCTGAGGATTAACATTCCATGACTTTGTAATTGAACATATACATTGCTCAGCATAAATGAGTTGTACACCCCTCACAGATCTCTCTTTTATATTGCTATTATTATTATTATTATTATTATTATTATTATTATGTTTCTTTACAATTATTTATTCATGCACATGTATTAGATTAGTCAGCTTTTTTTTTTTGCAATAACTTGTTTGAATTTAAGTGGATTATCTTTCTATTTCTAAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14800
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
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000005105 Essential Splice Site 173 248 8 11

The following transcripts of ENSDARG00000002165 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 24 (position 12854041)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 12805489
GRCz11 24 12949908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGACCAACACCCGCACCAAGATCGAAGGATTCCAGAYACAGATATCCAA[G/A]TAAGAGACCAGACTACATGACAACCACAGTCCAACACTAACCTTATGATG
Long Flanking Sequence:
ATAATATTAATTACTATATGTTAAATAAATTAATAAACTAAATTACATTGGAGCCAGCAATCTGATAAAAGAGAAGTAATGACACTTTATTACAATAGCATTCTATTTAACCTTCTATTCATAAAAGAAAAATTATATTATTGTTTTTACAAAACATTTAAGCAGCACAACTTTTGAACAACATTAAAAATAATCAACAATGTTTCTTGAGCTTTGAATTAGATGAATAGAATGACATCTGAAGGATTTTTAGACTGGAGAACATCACAAACACCATGTTTAAACAGTGGTGTGTATCCTAAATAATTACATTGATAAAACATTACACATACTAATGTGGCTGTGGTATAAAAGTAAAGCAATGGAAATGCAATTTTTATTGTATTGTGTTGTGAGAATTTCGCTTGAATATATGCAAAATTTATCTCATAGGAAAAGGTTTTTGAACTGATGACCAACACCCGCACCAAGATCGAAGGATTCCAGACACAGATATCCAA[G/A]TAAGAGACCAGACTACATGACAACCACAGTCCAACACTAACCTTATGATGACTCTATTATAAACAACGATTATGTTTTTTTGTATTTATTTCATTTTGGCTCATGTAAATATGCAGTTGTGACAGAGCTTTTCACAGAACGCATTACACTGGCTTACTGTCATCCTAAACACCGCTTTTCACCCTGAATATATGAGGAATTCACATTTTTATTTTAGAAACGCAGGATTATCCTGTGTATTCTGACACAATATGTTAGTTACTTCCAAACCAAATCCAACCAAGAGCCAATCACATGTGTCATTTTTAGGTGCACCGTCAGACTCACCATTACTTCTGACTTATACTGATTATAAAGTTGCCTAGCATTAAAATAGAACATTAAAACAAAATCAGCATACAAATATCGGTGTGAAAATAAAGGTAACATGTTGGTAGGTTTGACAAGCTAACTCACTCTAATACCATTGGTATAAATGTGTAAAGTGGGATTTAAATCTA
Associated Phenotype:
Not determined