ZMP
psme4b
Ensembl ID:
ZFIN IDs:
Description:
proteasome (prosome, macropain) activator subunit 4b [Source:RefSeq peptide;Acc:NP_001177949]
Human Orthologue:
PSME4
Human Description:
proteasome (prosome, macropain) activator subunit 4 [Source:HGNC Symbol;Acc:20635]
Mouse Orthologue:
Psme4
Mouse Description:
proteasome (prosome, macropain) activator subunit 4 Gene [Source:MGI Symbol;Acc:MGI:2143994]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18110 | Essential Splice Site | Available for shipment | Available now |
sa22097 | Nonsense | Available for shipment | Available now |
sa13795 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18110
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003143 | None | None | 285 | None | 7 |
ENSDART00000128865 | Essential Splice Site | 115 | 1827 | 2 | 45 |
Genomic Location (Zv9):
Chromosome 12 (position 25505941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 23874617 |
GRCz11 | 12 | 23995836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATCAGCATGATGCAGAGCTTTGCACGACTCCTCGTCAACTTGCTGAAG[T/G]AMGCAAAAGTCTGACATCAACAATCACCAGACCACTGYCAAATATTTGAG
Long Flanking Sequence:
TGGAGCGACTCCTAGGTTTATATGATTTTAAAATGACTTTTTGATCCTGTTGAAGGACTAAGAAGTTACATGGTTGGGACAAAAGTCCTCCCTTAGTTCAAGATAAAGGAAAACCAAGACTTATAACAGCCAACTTTGACTATTAAAACTGAAATGGTCAAATTTAAGTATGGACCATTACACTAAATTTCCAGAGCATTATTTATCTTTTTTGCAAAAACTATTTGAGTGATTGAAATAAACTTTGCCTTTAATGTCTTCTGTGTATGTAAAATCCATTTTGCAACATTTATTAGATGATATGTAAACTGTTTGTCATGTTTCTCTCTTATTGCTGTGATATTTTTCACCTTTAAAGGTACCTTCGGCTGTACGGGAGGAAGTTCAGCAAAGAGGACCATGTGCTCTTTATCAAGCTGCTGTACGAGCTGGTCACCATCCCCAAGCTGGAGATCAGCATGATGCAGAGCTTTGCACGACTCCTCGTCAACTTGCTGAAG[T/G]ACGCAAAAGTCTGACATCAACAATCACCAGACCACTGTCAAATATTTGAGAACGGCACAGCTGATTTGTTGTCGGTCATTTACAGTTTTTATTTATATTATTTACTTGTGTAACACTTTAAAATAATGGTCCATTAGTTAATTTTAGTTCATGTATTTAATAACTTGAACAAAGTGATACATTTATTATGGTATTTATTCATGTTTGTTAACTTTAGTTAATGTTAAGTTAAATAACGTTAGTTCATGTTAACTCACAGTGCATTAACTCCTGTTAACAAGCTCGACTTTGGATTTTAATAATGAGTAGGTAATGTTCAACTATGATTAATAAATGCTTTACAATTGAACGAGGTAAAGTCATTTTTTAATGATTGAATAATACATTATTTTTATTGTTAGGGCACATTTCCACCAAAGTGTTTTTGTTCAGGTGAAAATGCCAGCATTCTTCTAAAAAATCTAAGCTGTGAGCACTTCTTAAACTTTCAAGGCTGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22097
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000003143 | None | None | 285 | None | 7 |
ENSDART00000128865 | Nonsense | 1505 | 1827 | 40 | 45 |
Genomic Location (Zv9):
Chromosome 12 (position 25551307)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 23919983 |
GRCz11 | 12 | 24041202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCAGCGTATTGACATACATCTTCATGATTGATGTGGCTCTGCCCTA[C/A]ACTCTGCCCACTAAATCCCCACACATCGCCGAGTTCACCGAGCGGATCCT
Long Flanking Sequence:
CTGTTGTATAAATATTTATAACCACTTCAGAGAATATTTGAGGTCGCGAGTCACTGGCATTGGTAATTTGGGGGTCACAGGCTGAAAAGCCCCTGCCCTACATTACAGTAATATTCAACACTTCACTAATTTTACCCCATAGAGACTTGTTTTGAATTATATTTTGGGTTATTCACGGTCTGCTGAAAGTAATTGAGTTAGTTAATTCTAATAAGTTGTCTTTAAATATTCAGTGGATGGACTGTTATGAAAATAAAGCCACTTCATTGTACCCAGAATAAAGTAAAATAAAAAAGCTGTACTAATTGTTTAACACATTGTTACTCTAATAGTTCACGCAAAGCATCATGGGGGCATAGGAAACATTGGATTGGACAAACAGTTTAAACGTGGCTACTATAATCCAAAAATACACCAGCACTCGCTTTCATCCTCTTGTCGTGATTAATTCCTTTCAGCGTATTGACATACATCTTCATGATTGATGTGGCTCTGCCCTA[C/A]ACTCTGCCCACTAAATCCCCACACATCGCCGAGTTCACCGAGCGGATCCTGTCTCAGCTGAAACCCCTGATCGAAGGTGACGAGGAGATCCAAAACCACGTGGTGGAGGAGAATGGAGTTGGTGAGCAGGACGAAAGGACCCAGGCCATCAAACTGCTGAAAACAGTGTTGAAGTGGCTGATGGCCAGTGCGGGACGCTCGTTCTCCACTCCAGTCCCTCAGCAACTCCAGCTGCTGCCGCTGCTCTTTAAGGTCTCGTGTGCTTCTGTGTCTCATCTTTTATCCATTTGTGCGGAGTGCTCTTAAGTGGATTGCTGACTTGTTTTTCTCTCTGTCTGCAGATCGCGCCTGTTGAAAATGATGACAGCTATGATGAGCTGAAGAGAGACGCCAAGACATGTCTATCTCTTATGTCTCAGGGGCTTCTGTATCCTGAGCAGATCCCGATGGTACTCGCTGTGCTACATGAGGTGAGGATTCAGCCACGCCAGACTTAACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13795
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 |
---|---|---|---|---|---|
ENSDART00000003143 | Nonsense | 140 | 285 | 3 | 7 |
ENSDART00000128865 | Nonsense | 1682 | 1827 | 42 | 45 |
Genomic Location (Zv9):
Chromosome 12 (position 25553875)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 23922551 |
GRCz11 | 12 | 24043770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGTGTTCARGGCGTCAGAGCTCTGGTCATCAGGCTCCTGGAGGACGAG[C/T]AGCTGGAGGTACATCTGGGCCACAATCATTTATTTATTCGCTTTCATGCA
Long Flanking Sequence:
AGCAGAACATGAACCTACATTGTAAACTGGAAATATAAAAATAAATATTAATATTAAAAAATTGTTGACAGTAATTTAAGTAATTTAAACTAATATTATAGTAAGAATAATATGAATGTAAAAAATACATTTTGTGATATCAGTATTATTATATTAACTAAAATAATAAGTTATTACTACCATTATTGTTTCTGTAATACTCATCTTGTATGCAGATAATAATTTAAATTGTAGAAAATAATTATTAATTGTCCAAAATAATTAATTGTCTTATTTATTACCAACCAACACGTATCACCTTGTCCTTATTTCTACAGTTGTGAAACCATAAGCTTCTTTTTCTACATTTACAGATTGCCGGTAGCAGCTCTTGGCATGCCAGATACTCAGTGTTAACGTATCTCCAGACAATGGTGTTTTATAATCTGTTCACCATCCTGAGCAGCGAGCAGTGTGTTCAAGGCGTCAGAGCTCTGGTCATCAGGCTCCTGGAGGACGAG[C/T]AGCTGGAGGTACATCTGGGCCACAATCATTTATTTATTCGCTTTCATGCACCCTTTTCATTAAAGCTTCATCTCTGTGCGTGTCTCTGCTGTAGGTGAGAGAAATGGCTGCCACCACACTTAGCGGCTTCCTGCAGTGCAATTTTTTGGCAATGGATTCCTCCATGCAGACCCACTTTGAGGCTCTATGCAAAACCAGATTGCCCAAAAAGAGGAAAAGAGATGTGGGTTCTGTGATGGACACCATTCCTTCTGTTGGTATGATCACACTTTAATCAAACGCAGTGCTGTGCTCTGTGGACCGGAGAAGTAGGGCAGTAGAAACATTCCAAAAATTCAACAGCAAATGTCATTTAAGTTCAAGTTTAATACCAGCTCTTTTAAATTATCCTGTCATAAAAAGGTACAAAAAGAGGTTCATATTTTTAAGGATGTTTGTATGTGCATATTTTGTGGTTAATAAACAAAAATATTCAATGTACTGTCACACTGACTTTTAAT
Associated Phenotype:
Not determined