ZMP
psma5
Ensembl ID:
ZFIN ID:
Description:
proteasome subunit alpha type-5 [Source:RefSeq peptide;Acc:NP_991271]
Human Orthologue:
PSMA5
Human Description:
proteasome (prosome, macropain) subunit, alpha type, 5 [Source:HGNC Symbol;Acc:9534]
Mouse Orthologues:
Gm8394, Psma5
Mouse Descriptions:
predicted gene 8394 Gene [Source:MGI Symbol;Acc:MGI:3647964]
proteasome (prosome, macropain) subunit, alpha type 5 Gene [Source:MGI Symbol;Acc:MGI:1347009]
proteasome (prosome, macropain) subunit, alpha type 5 Gene [Source:MGI Symbol;Acc:MGI:1347009]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10901 | Essential Splice Site | Available for shipment | Available now |
| sa19010 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30952 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21956 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10901
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020655 | Essential Splice Site | None | 241 | None | 10 |
| ENSDART00000141477 | None | None | 240 | None | 9 |
| ENSDART00000146495 | None | None | 195 | 1 | 8 |
| ENSDART00000020655 | Essential Splice Site | None | 241 | None | 10 |
| ENSDART00000141477 | None | None | 240 | None | 9 |
| ENSDART00000146495 | None | None | 195 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37191663)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 36088891 |
| GRCz11 | 11 | 36350874 |
KASP Assay ID:
2261-7168.1 (used for ordering genotyping assays)
KASP Sequence:
ACACTTCCTGTACTGTTGAAACTAGCAAACTCACCCTCCACWGCWGAAGG[T/A]AAGAAATTCACRACATACTTCTATYATGCTGTGYTTWACTGCAGTAAATT
Long Flanking Sequence:
GCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAACAGGGTTGGCCACCCCTGAACTAAATGAACGCCAAAGTCTATTTAAATGATTATATTTTAATTACATTACAACATCAATGCTGTAAAAGGAACCATATAAAATTGAAAAAGTCATATTAACCGTTCACCTGATGTTTATCAGCATGGAAAGAAACAGTAGCTGTGCATGTACCCTACTGAAAGACGAATATAAATATAAATATGCATAAAGAAGAAACAGACTGTGGCGATTAATAATTAAAGTAGTGTAAAAATGCATCTCGAACAAAAGACTACAAGTAGCGATCGCCATATGTCACAATAAACCGTGACGAGCAACCATAGCCAGTGTCCTGTAGTACACTGCTGATGAATTCAGCGGGGTAGGAACCCAAAGTTGACTTGCAGTGTTTTTTGTCGAGCGGGGATGAATGAACACTTCCTGTACTGTTGAAACTAGCAAACTCACCCTCCACTGCAGAAGG[T/A]AAGAAATTCACAACATACTTCTATTATGCTGTGCTTTACTGCAGTAAATTGCAGCTTTGGAGGCAAAAGCATTTTAAAATAACACACGTTATAATGTAAAGTTATTTTAGCGGCCCCTGTGCTGTTTATTGAGTAGTAAACCGGTTTGCTAACGGCAGATGCTCATGTGTATATGTTCCCACATGGTTTGTATCATAATAAAGAACAAAATTATTTTAAAAAGTCCAAACTGATTATTGAGGACTTTATGCGTTTTTAAAAGTACATAAATGAACGTAAATATGTTTGGAAATATCTTACATATGAATGACTTGGTTGAAATGAAACATGCCTTGTCATTGAGTGAAGGGTGCTTCGGCCAATCAAAATGACAGTTGATTCTTAGTCCCGCCTTTTATCTCAAAACTGTCCAATCAGTGGAACCGGAGTCGCTGTCTGATTGGATATGAACTCCAATGCAAACATCGCGTTGCTACATAGCAAGCAAGCAAGCGAGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19010
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 |
|---|---|---|---|---|---|
| ENSDART00000020655 | Essential Splice Site | None | 241 | None | 10 |
| ENSDART00000141477 | None | None | 240 | None | 9 |
| ENSDART00000146495 | None | None | 195 | 1 | 8 |
| ENSDART00000020655 | Essential Splice Site | None | 241 | None | 10 |
| ENSDART00000141477 | None | None | 240 | None | 9 |
| ENSDART00000146495 | None | None | 195 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37191663)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 36088891 |
| GRCz11 | 11 | 36350874 |
KASP Assay ID:
2261-7168.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTTCCTGTACTGTTGAAACTAGCAAACTCACCCTCCACTGCAGAAGG[T/A]AAGAAATTCACAACATACTTCTATTATGCTGTGCTTTACTGCAGTAAATT
Long Flanking Sequence:
GCAACTGAAATCTGCAGGAAGGTGGCTCTCCAGGAACAGGGTTGGCCACCCCTGAACTAAATGAACGCCAAAGTCTATTTAAATGATTATATTTTAATTACATTACAACATCAATGCTGTAAAAGGAACCATATAAAATTGAAAAAGTCATATTAACCGTTCACCTGATGTTTATCAGCATGGAAAGAAACAGTAGCTGTGCATGTACCCTACTGAAAGACGAATATAAATATAAATATGCATAAAGAAGAAACAGACTGTGGCGATTAATAATTAAAGTAGTGTAAAAATGCATCTCGAACAAAAGACTACAAGTAGCGATCGCCATATGTCACAATAAACCGTGACGAGCAACCATAGCCAGTGTCCTGTAGTACACTGCTGATGAATTCAGCGGGGTAGGAACCCAAAGTTGACTTGCAGTGTTTTTTGTCGAGCGGGGATGAATGAACACTTCCTGTACTGTTGAAACTAGCAAACTCACCCTCCACTGCAGAAGG[T/A]AAGAAATTCACAACATACTTCTATTATGCTGTGCTTTACTGCAGTAAATTGCAGCTTTGGAGGCAAAAGCATTTTAAAATAACACACGTTATAATGTAAAGTTATTTTAGCGGCCCCTGTGCTGTTTATTGAGTAGTAAACCGGTTTGCTAACGGCAGATGCTCATGTGTATATGTTCCCACATGGTTTGTATCATAATAAAGAACAAAATTATTTTAAAAAGTCCAAACTGATTATTGAGGACTTTATGCGTTTTTAAAAGTACATAAATGAACGTAAATATGTTTGGAAATATCTTACATATGAATGACTTGGTTGAAATGAAACATGCCTTGTCATTGAGTGAAGGGTGCTTCGGCCAATCAAAATGACAGTTGATTCTTAGTCCCGCCTTTTATCTCAAAACTGTCCAATCAGTGGAACCGGAGTCGCTGTCTGATTGGATATGAACTCCAATGCAAACATCGCGTTGCTACATAGCAAGCAAGCAAGCGAGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30952
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020655 | Nonsense | 8 | 241 | 2 | 10 |
| ENSDART00000141477 | Nonsense | 8 | 240 | 1 | 9 |
| ENSDART00000146495 | Nonsense | 17 | 195 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37191047)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 36088275 |
| GRCz11 | 11 | 36350258 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTTACATAGATTTGCGTTTCAACATGTTCCTGACAAGATCAGAATA[T/G]GACAGGTGAGATATCAATGATATTTGTGCCGTGTAATTTAACTGCTTTGA
Long Flanking Sequence:
CCTGTGCTGTTTATTGAGTAGTAAACCGGTTTGCTAACGGCAGATGCTCATGTGTATATGTTCCCACATGGTTTGTATCATAATAAAGAACAAAATTATTTTAAAAAGTCCAAACTGATTATTGAGGACTTTATGCGTTTTTAAAAGTACATAAATGAACGTAAATATGTTTGGAAATATCTTACATATGAATGACTTGGTTGAAATGAAACATGCCTTGTCATTGAGTGAAGGGTGCTTCGGCCAATCAAAATGACAGTTGATTCTTAGTCCCGCCTTTTATCTCAAAACTGTCCAATCAGTGGAACCGGAGTCGCTGTCTGATTGGATATGAACTCCAATGCAAACATCGCGTTGCTACATAGCAAGCAAGCAAGCGAGCTGTTGTGCTTTATGCTACTTCACTACATTTGAAGTTGGCTAATTCAGATCTCATTTAACACTTCTCTTTGTTTTTACATAGATTTGCGTTTCAACATGTTCCTGACAAGATCAGAATA[T/G]GACAGGTGAGATATCAATGATATTTGTGCCGTGTAATTTAACTGCTTTGAAAGTCTTTCATTCACTTGTTTCAAGTTGTTTCGTAAGCTTAGCTATCGCTTATTTACAATTATATTTAAACACATCTATTAAAGAAATAAAAGAAATCCACAGCATGTTTTTCAACTATCTTGTCTTAGAACTTTCACTTTCAGTTTTGTTTTGCCAAATAAAATACTCACTGGATTAACTATTTAAGTAATTACAAAGAGTGAATGACATTGTAAATATAGGGTTTATATCATATTAACATTTCTGTTTCCATTCTCAGAGGAGTAAACACTTTCTCACCAGAAGGAAGGCTTTTTCAGGTTGAATATGCCATTGAAGCCATCAAGGTGAGCCAAGATTTACTAACTAACGTTACTATAATAAGTTGTAATAGGTGCCAATATGACTGGGCTCGAAATTAACCTTTTTACTTGGTAGCACCAGTGCTCCCATATTAAAAAATGTAGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21956
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020655 | Essential Splice Site | 97 | 241 | 5 | 10 |
| ENSDART00000141477 | Essential Splice Site | 97 | 240 | 4 | 9 |
| ENSDART00000146495 | Essential Splice Site | 106 | 195 | 5 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 37188042)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 36085270 |
| GRCz11 | 11 | 36347253 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATAGCTGATGCCAAAACTCTTATTGACAAAGCAAGAGTAGAAACACAG[G/T]TTGGTGAAAGTCTGTCACTTAAGTACAAGGTTACTTCAAATGTTTATTAT
Long Flanking Sequence:
AAGAGAATAACCTCTCCTCTGATGGAGCCCAGCAGCATTGAAAAGATTGTAGAGATCGACTCTCACATTGGTGAGACAGAGGCTGAAATAACATTGTCATAAGCTATGAATATTAACATATTGCTATACTTCCATCCACCTATTTTTATGCACCGTTTGGATATGTGCATAAAATATCAGTAGATGTAAACGCCATGATGCACATAAGTTTTGAAAATGCGCATAAAAAAACTTACGAATAATTGAGTAGGATAAACTTTTTATTCGATAAGAAAAAATACTTCTTATTGGATGGAAATGCTGCATTATTTGCATGTCTTTTATGCAATATTGCAGTTTTGTGCATGAATTTAATTTGCATCTTTGGATGGAAACAGCAATTGTGGATAATTGTAGTGAAATATGAATAATCATGTTTCATTCTCAATATAGGCTGTGCCATGAGTGGCTTGATAGCTGATGCCAAAACTCTTATTGACAAAGCAAGAGTAGAAACACAG[G/T]TTGGTGAAAGTCTGTCACTTAAGTACAAGGTTACTTCAAATGTTTATTATGATGTTGTAAGCCTCCGTGTGTTTTTGCAGAACCATTGGTTTACCTACAATGAGACGATGACTGTGGAGAGCGTAACACAAGCCGTTTCTAATCTTGCTCTGCAGTTTGGAGAGGAGGATGCTGACCCCGGCGCTATGGTAAGACATGTCTGGGTTAAGTTTTCTTCAGTACATAAGTGCTCAGAGGCCATGCATTCAGATAATATTTATCTAATTTTCTCGTGATCATGGCCCTGCAAACCAAGAGAGATGCAGACGCACATTCGTGCAACACGCGTTAAGGGCGTTCAGAACAGCCAATTGCATCGCGCTCATGATTATCGTACATTCGTGATTATTTGCATGTATATGAATATATATTCCCATTTTAGAGTGTAGGTTCTAGTCGGCTCAAAAAGTTGTTGCATGTTTGAATTAGATTCTGAAGAATGTTTTTGTTTCATTTTAAGT
Associated Phenotype:
Not determined