ZMP
psmb7
Ensembl ID:
ZFIN ID:
Description:
proteasome subunit beta type-7 [Source:RefSeq peptide;Acc:NP_001039029]
Human Orthologue:
PSMB7
Human Description:
proteasome (prosome, macropain) subunit, beta type, 7 [Source:HGNC Symbol;Acc:9544]
Mouse Orthologue:
Psmb7
Mouse Description:
proteasome (prosome, macropain) subunit, beta type 7 Gene [Source:MGI Symbol;Acc:MGI:107637]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23856 | Nonsense | Available for shipment | Available now |
| sa29521 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23856
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 |
|---|---|---|---|---|---|
| ENSDART00000055325 | Nonsense | 118 | 286 | 4 | 9 |
| ENSDART00000129749 | Nonsense | 118 | 277 | 4 | 8 |
| ENSDART00000133804 | Nonsense | 52 | 211 | 3 | 7 |
The following transcripts of ENSDARG00000037962 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 7844246)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 8251797 |
| GRCz11 | 21 | 8344336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATCTCCTCCAACCTGGAGCTTCATTCTCTGTCCACCGGTCGTCTGCCA[C/T]GAGTCGCCACAGCAAACCGCATGCTCAAACAGATGCTCTTCAGGTGACAA
Long Flanking Sequence:
AATAGCAGAGATTAAATAACAAAATAAAACCTTTGTGCTATTTTAGAAATGCTCTTCTGGAGGCAGACATCACTAAACTGGGTTTCAGCTCTCCTGCTGCCCGTAAAACCGGAACCACTATCTGTGGGATTGTTTATAAGGTAAGAAAAAAAAACAGTTGAATTTAATGTGTGAAATCCAAGGTTTGACTAGATACTCACGTCTCACTTCTGTCTCAGGATGGTGTTGTTTTAGGTGCAGACACTCGTGCAACTGAAGGAATGATCGTCGCTGATAAGAACTGCTCTAAAATTCACTACATCTCTCCCAACATTTAGTGAGTATAAACTCACGTCATGCATGCTTGTAGTTTTTGATCCCTGACATCAAATGACACTGCATGTTTTTCTGATTTGTTGCATAGCTGTTGTGGAGCAGGTACAGCGGCGGACACTGAGATGACCACACAGATCATCTCCTCCAACCTGGAGCTTCATTCTCTGTCCACCGGTCGTCTGCCA[C/T]GAGTCGCCACAGCAAACCGCATGCTCAAACAGATGCTCTTCAGGTGACAAACACCTATTCTGCGTGTGCAATATAGATCTTAAATGTAGAATTCTGATGTTTAAATGAAGAGTTTAAAAGCAAAAACCTCTTAGTGCCTTCTGATTTGTATTTTTTTTTTGTCTAAAACGAGCATTTTGTGTGTAGGTTCAGTAATTTCACTTTAATGGAAAGTATACGTGTTCTTTTTATGGCCTTTAAACTGAAATGACTGAACACAAACATAGGAAGCTGAGATAAATGCTAATTTTTGAAGAAAATATTTAGATTGCACTTAGAGGTATTTGCATCTAAACTCTTCAAATGTTTCTGAAAAAAGTCCCTTGTATTGTATGAATACAGTACATAAAAAAAAATCAACATTTTATTCAGATTTTTCTATATGTTTTAAAATGTAATTTATTGCTGTGATTCAATGATAAATTTCAGCATCCTTACTCCTGATCACGTGACACTGAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29521
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 |
|---|---|---|---|---|---|
| ENSDART00000055325 | Nonsense | 133 | 286 | 5 | 9 |
| ENSDART00000129749 | Nonsense | 133 | 277 | 5 | 8 |
| ENSDART00000133804 | Nonsense | 67 | 211 | 4 | 7 |
The following transcripts of ENSDARG00000037962 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 7846005)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 8253556 |
| GRCz11 | 21 | 8346095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAAATATGTATTATTGATGAGTCTACCATGTGTTCATGTATGCAGGTA[T/A]CAGGGTTACATCGGTGCTGCATTAGTTCTTGGAGGTGTCGATTGCACCGG
Long Flanking Sequence:
TGAAAGATCATGTGACATTGAGTGAAAGAATGATGCTGAAAATTTATCTTTGCATTATAGAAATAAATATAATTATAATATAAATATAATACAAGTTTTCATGTTCTCCCTGTGTTCGCGTGGGTTTCCTCCGGGTGCTCAGGTTTCCCTCAGTCCAAAGACATGTTATAGGTGAATTGGGTAAGCTAAATTGTTCGTAGTGTATGTGTGTGAATAAGTGCGTATGGGTGTTTCCCAGTGATTGGTTGTAACTGTAAGGGCATCCACTGCGTAAAATAAATAAAGGGACTAAGCCGAAAAGAAATTGAATGAATAATACAAGTTTAATATATCATTGAAAATATTTTTTTAAAAGTGTTTATATTTTTCAAAATCACATTATTAAACTTTTTACTCTATAATTCTGATCAAATAAACAGCCTACATGGACAGAAGCTCTTTTCAAAAACATTGAAATATGTATTATTGATGAGTCTACCATGTGTTCATGTATGCAGGTA[T/A]CAGGGTTACATCGGTGCTGCATTAGTTCTTGGAGGTGTCGATTGCACCGGCCCACACTTATACAGCATCTATCCACACGGATCAACAGACAAGCTGCCCTACGTCACCATGGGTGAGTCACACTAGCGTACATACACATGCACATGAAGCGTTTTCCATATCTACCAAAAGGGGGAGATAGTGTGTTTCAGAAATGCTTTTGTTGGTGCCAAGAAATGAAAGATGTTGGACTGCCTGCTTTACAAGTTTTGATATCAGACTGACTGGCTTTACAAGACTTTTAATACAAACATTCATTTAAAACCGTTAATGCAAAATATGCTGGTTTATTGTTAACCCTTTTATGCACAGGTTAAAAAAAATACTCCAGCTGACTCAACTTTGAGTTTTTTTTTAATGGTGACCGTTATTTAGAACGCTTCTCTTTAAAATTCCCAAAGTGACATGTCAAGATTGTCATGTGACATCACAGCACCATTGATTCTTGCATATATCCCTTT
Associated Phenotype:
Not determined