ZMP
psmd4a
Ensembl ID:
ZFIN ID:
Description:
26S proteasome non-ATPase regulatory subunit 4 [Source:RefSeq peptide;Acc:NP_001002112]
Human Orthologue:
PSMD4
Human Description:
proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 [Source:HGNC Symbol;Acc:9561]
Mouse Orthologue:
Psmd4
Mouse Description:
proteasome (prosome, macropain) 26S subunit, non-ATPase, 4 Gene [Source:MGI Symbol;Acc:MGI:1201670]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23470 | Nonsense | Available for shipment | Available now |
sa44908 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23470
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 |
---|---|---|---|---|---|
ENSDART00000104063 | Nonsense | 58 | 372 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 11934629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10960558 |
GRCz11 | 19 | 10879483 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGATGCTGTTTCATGTAATAACAGACATTTTGGTTTTGTTCAGTAATTG[C/A]GAGGTCCTCACCACTTTAACACCAGACACTGGCCGCATCCTTTCAAAGCT
Long Flanking Sequence:
TTGTTGAGCCCTGCTAATACACTTGTTGGTTTTATAATCCCCCATATTTTATTGAGTTGGTTTTATATTCCCCCATTCAGATATAATTTCAGAAAACTGTTATTTGCATATCCTTAACAGGGAAGTCATATTAGCAGCCAATGACTATTAAAACACAACATTGTTCACAGTAAATTAAACAGCGCTAATGTTGTTTTGAAGTCAATCTTGCAAACATTCAGTGTTTGTTTCATAAATATTTGCCTTCATTCTATTATTGTTTTGCAGTGTGGACAACAGTGAGTACATGAGGAATGGAGATTTCCTGCCCACCAGGTTACAGGCGCAGCAGGACGCCGTCAACATTGTCTGCCACTCAAAGACCCGCAGCAACCCAGAGAACAATGTGGGCCTTATCACAATGGCCAAGTAAGTGTCTGTGTTGGTGTTTTTCCTATGTGTATAATCAGTCGGATGCTGTTTCATGTAATAACAGACATTTTGGTTTTGTTCAGTAATTG[C/A]GAGGTCCTCACCACTTTAACACCAGACACTGGCCGCATCCTTTCAAAGCTCCATGCGGTTCAGCCTCTGGGAAAAATCTCCTTCTGCACTGGCATACGAGTGGCACATGTAAGTACATTTATAATCATTTATTTTAATAGATAATGTTTTTTTTTTTATTATTTAAACCAACTGTTTTCTAATTGAATCAGTTTTAACACGCAAGTTATTTGTGATGATAAAGGTTATTTTTCAGCAGAACTACTCATGGTGTCAGATGATCCTTTATAAATCTTTTGAATATGTTGATGTGATTTACATTTTCTTGTTGTTGTTTGCACATCTCATTTGCACATGTGGTGTTTGAGAGACGACCTCTGCAAGCTATGTTGCCAAAAGGGAATACTAGCACACATATTGTCAGGGTGTATAACATCTTTAACCCAGGGTCAATATAGGTGGCAACATGACAAGGTGCTCTTGACCCTTCTGCAAATGAGCAGGAGAGGCACAAGAAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44908
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 |
---|---|---|---|---|---|
ENSDART00000104063 | Nonsense | 131 | 372 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 11937865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10957322 |
GRCz11 | 19 | 10876247 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAACTAATTTCACAAACTCTCTTCCAGCTGGTGAAGATGGCAAAGAGGT[T/A]GAAAAAAGAAAAGGTCAATGTGGATATAATCAATTTCGGAGAAGAGGTGA
Long Flanking Sequence:
GTATAGCTTCCTATTAAAATATATTAATTTAAAAGAGAGATTTTTGATGGGTGTACTAATATATGCTGAGCACTGTATGTGTTGTATTTGTTATGAGCATAAAAGCAGGTACCAATTAATAATTGAAAATGGGTAATTGACCACCAAATCAGGATATTGTTACTAACAGATCATTTGACACTGAAGACTGGGGGAATTGCAGATGAAATTCAGCCTTCGGATTTTAGTACAAAAAAAAGTTGTTGTTTTTTAATACACTGACGTTTCCAATTTTGCATGCCTGCATCTAGCTGGCACTGAAGCATAGACAAGGCAAGAACCACAAGATGAGGATTGTCGCTTTTGTGGGCAGCCCAGTAGAGGACAATGAAAAAGATGTATGTTGTTTTATTATATTATTATTATTATTCAGAAATGGCACTTTTCAGCATTCTGTGTAGATCAAACTGGTAAACTAATTTCACAAACTCTCTTCCAGCTGGTGAAGATGGCAAAGAGGT[T/A]GAAAAAAGAAAAGGTCAATGTGGATATAATCAATTTCGGAGAAGAGGTGATTGGCATTGCTGACATTTCTTATCTTTTAAGCAATTATATATATATATATATATTGTGTGTGTTTGTGTGTGTGTGCGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTATATATATATATGTATGTATATATATATATGTATGTATGTAGTGTATACAAACACACACTACTCGTTTTCAATTCTTTTGTTTGATTAATCTGTTCAGGAGATGAACACAGAGAAACTGACTGCATTTGTCAACACTCTCAATGGAAAAGAGGGCACAGGTTCTCATCTGGTCACTGTGCCTCCTGGGCCGAGTCTTGCTGATGCCCTGCTGTCTTCTCCTATCCTGGCTGGTGAAGGTGGCACCATGATTGGTCTGGGTGCAAGTGACTTTGAGTTTGGGGTGGACCCCAGTGCAGACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39237
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104063 | Nonsense | 292 | 372 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 19 (position 11941806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10953381 |
GRCz11 | 19 | 10872306 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAGACTTCAGCAGCATGACGGAGGAGGAGCAGATTGCGTATGCCATG[C/T]AGATGTCCCTGGCAGGGGGAGGTTCGTCCATACAACTTGTTCAATGTAGA
Long Flanking Sequence:
ACAGACGTCCAGTCTGCACGCTGGAATACACGCTATTATGTCATGACCGTGACGCAGCTTCAAAAATTCGTTTCAAACCGGAAGTACGAATTTGCTTGAAATAACGCAAAAACAACCAATTTACACTTTTTAGTGAAATATAGGTGTCTTAATAGTGTTTTTAGCAGTGTGGGACACATATACGACTGTCAACAGCTCAAAAAATGTGTTTTGGTGTTTCGTGACCCTTTAACTTTTTTGCAATAATGTGCACCTTTTTAAAAGCTGCTTTAAAACCATAATTATTGTGAAAGCACTATGTTCTTGTTTATATAAAGCACTTTGAATTGCCACTGTGTATGAAATGTGCAATACAAATAAACTTGAGTTGAATTTTATTTTTGGCTTCAGAATCAGAGGAAGCTCTTTTGAAGATGTCTGCATCTCAGCCTGAGAGTGGTGTAGCTGCACTTCCAGACTTCAGCAGCATGACGGAGGAGGAGCAGATTGCGTATGCCATG[C/T]AGATGTCCCTGGCAGGGGGAGGTTCGTCCATACAACTTGTTCAATGTAGAGCTAACATGCATGGGTTGTAAAGTTGACCCATTATCTCTTTTATGTCAGAATTTGGAGAATCAATGGATACGGGAGCTCCCATCGACACTGCAGAATCTAAGGTAATTAATCTATTGTCTGTTTGCCTTTAACAATCTTAGTGTACTAAATGAAATACAATTATCAAAATATTTTTTTCTCTTATAAATGTTTTGCACTTGACACAACATTATTTGTTCCCTTAATGCTGAATTTTCCCCCTCACATATTTCAACTACAGGAAGAGGATGATTATGATGTGATGCAGGACCCAGAATTCCTGCAAAGTGTCCTGGAGAATCTACCTGGTGTTGACCCCAACAATGAGGCCATCCGCAATGCAATGGGATCTCTGGCCTCTCAGAGTGGTAACAAACCAGAGGGGAAAAAAGATGATGAGAAGAAGAAATAACTGTTTCTGTTTGTGACCG
Associated Phenotype:
Not determined