ZMP
LOC557981
Ensembl ID:
Human Orthologues:
AC053481.2, USP32
Human Description:
ubiquitin specific peptidase 32 [Source:HGNC Symbol;Acc:19143]
Mouse Orthologue:
Usp32
Mouse Description:
ubiquitin specific peptidase 32 Gene [Source:MGI Symbol;Acc:MGI:2144475]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa30684 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1084 | Essential Splice Site | F2 line generated | Not yet available |
sa35888 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2801 | Nonsense | Available for shipment | Available now |
sa35887 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30684
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 |
---|---|---|---|---|---|
ENSDART00000088808 | Nonsense | 261 | 1585 | 7 | 34 |
Genomic Location (Zv9):
Chromosome 15 (position 23217394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23928581 |
GRCz11 | 15 | 23863846 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAATCATATTGACTTTAAGGAGATATCCTGTGGGCTCTCAGCTTGCTG[T/A]CGCGGCCCAGTAGCGGAGAGGCAGAAGTGTAAGCTTTTTATTATTGCTTA
Long Flanking Sequence:
AGAGAATCAGATTTCTCGTGTTTCCTTTCTTGCAGTAGAAGAATCAGACATTATCGACTTGGAAAAACGCTACTGGCTGCTGAAAGCTCAATCAAGGACAGGCCGCTTTGATTTGGAAACCTTTGTCCCGCTGGTCTCGCCCCCTATTCATGCATCGCTGAGTGAAGGTAAGACCGAATTCATTATGCCAATTTTAAAAGCTTCTCAAATGGATTGAGACACACATACGCACCCATCCACACACTCCTTGTATGCTTTGAAAACATTTGCGGTACCCAGGAAAGTCACGCTTCATCTTATTTTAGTAGAAGTGCTTTTCCGCTTTTGAAATGTATTGGATCATTTGTGATAAAAGATCTCCAAAGAATCCAATTACTCATTCTGGCTAATCTAAACACTGACATTTTCTCCCATTTGCCAGGCTTGTTTCACGCCTTTGATGAGAATCGGGACAATCATATTGACTTTAAGGAGATATCCTGTGGGCTCTCAGCTTGCTG[T/A]CGCGGCCCAGTAGCGGAGAGGCAGAAGTGTAAGCTTTTTATTATTGCTTATCATCCTCTCTTAGCTGTTCACCCTATTTCAAGGCAGATGCAGGATTATTGTGGATGTTAGAGGACTTTTTTAATGTGCATAAATAGTCTTTAAAATTTGTATTTAAGCTTAGTTATAAATGGAGAGCACAGAGAAAATATAAAAGATTTATATATGTTTTTTTTTTTTATTTCTTCCTTTTTTAATAGATCTATTTTCTTACTGCTGTACCTTTTGCATATTTGTATTTATTTTATCTGTATTGCTGTTAATGGAGGTGTGAACCTATACTGGTCTCACGGTTTGGTTCGGTTCGGTTACCATTATCATGCCTTTGATTCGGTTCAATTCGATTTCTCGGTGCATCACAGTGCAATGACGATGCTTTCCATATACAGTGTTATATTTTAGGGGGGAGGCTATAACAAGCTCTCTGTATAAACACACAGACACACAGCACCACACTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1084
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088808 | Essential Splice Site | 1140 | 1585 | 27 | 34 |
Genomic Location (Zv9):
Chromosome 15 (position 23183907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23895094 |
GRCz11 | 15 | 23830359 |
KASP Assay ID:
554-0986.1 (used for ordering genotyping assays)
KASP Sequence:
CTTGCAAGTCCACTGCCGCCGCAGGAAGCCAGYAACCATGCTCAAGACTG[G/A]TCAGTGGCRTCATGTTTGTTTGTTTGTTTGTTTTTTATTTTGTTGTTTAT
Long Flanking Sequence:
CACTCTTTTTGTTGTTGACCCATCCATGTTGTCATTAGAAAAACCACCTATTGCCAATGGGACAGCAGGAAACAATCATATTGGAAAGTCTGGCCTGATTCCTAATGGTATGCCCAGTACAGTGGTCCCCTGCACCCTTGAGAAACCCCTCGCCAATGGTATCCCCAATGGCCATGCTGTGCCAGTGCAGGACAGCCCATTCATTGGCTACATTATTGCCATGCACAGAAAGATGGTGAGCATTCACTGATATATTCACTGTTGGACTTCACAAGATGGTCGTAAGCATCCTAAATGTGAGGTCTGTCCCTGCAGATGCGGACGGAACTGTACTTCCTGTCCTCTCAGAAGAACAGGCCCAGTCTGTTTGGTATGCCTCTGATTGTGCCATGCACAGTGCACACGAGTAAGAAGGACCTGTATGATGCTGTGTGGATTCAAGTGTCCCGACTTGCAAGTCCACTGCCGCCGCAGGAAGCCAGCAACCATGCTCAAGACTG[G/A]TCAGTGGCATCATGTTTGTTTGTTTGTTTGTTTTTTATTTTGTTGTTTATGTTTTTTTTATTTAAATAGATAGTATCAACTTAAGTGCATAAAAAAAAAAAAGATAACAAAAACAAAAAAGGTAAATACAATACACACAATACACTTTACTTTGAACTTGCGAAAGAAAATGTTTCAATTTTGTTGTGGAGCAAGGACTTGGTCTATATTTGACAATAAAACATGTTCTTGGATATATTTCTCAGTGGCATCATGTTGAGGATTGGTTTGGAATGTTTGGTTTTTGTCAGAATATGTTTGACTTGCACCCAAAGATGTATTTATAAAAATATATACATGTGAAGTGTTATTGATGTTTAAAATTAATATTTAAGGTTTTTAAATAGTTATGAGTAAGTCATTTATTTCATTTTTTAATTATTTATTTATTTATTTATTTAAGGATGAGCTCTGAATATTAATCTGGAGATCATAATTTTAGTTTTCTTTAAATAGACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35888
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088808 | Essential Splice Site | 1273 | 1585 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 15 (position 23181701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23892888 |
GRCz11 | 15 | 23828153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCCTGGCCACTAAGAAGCTGGACCTCTGGAGGCTGCCTCCTGTACTGG[T/C]AAGAACAATAAATCCTTTGCAGGAACTGTATTAAAAATCCCACATTTCTC
Long Flanking Sequence:
TACTACTTGGCACTTTCTAAGCTGAAAGAGCTTTTGCAAATGCAAAGCAATTGCAAATTAGCTGTTTACAATTTGGAGATAACAAAATAAAATTTGCACCTTCTTTTATAGTGCATTTCAGACCAGATTTGTCCATTTTACCATCCATCTTACTAGAATGCATATAATGTTTAATTGTACATTAAAAATAAATAGTATTCTTAAAATCTAACCACATTCAGATTTAATTGAATCGTTACATAGTCCACAGCTCTGTTTCTAAGTAATTGTCATTCTGTTAATGTGGGTCCATTCATTGCTAATACAGATAGTTGAAGAGCATCCCAGTGTTGAGCAGAGTCGACGCGCTCAAGCAGAGCCCATCAGTCTGGACAGCTGTCTGAAAGCCTTCACCAGTGAAGAAGAGCTGGGAGAGGACGAGCTCTATTACTGCTCCAAGTGTAAAACACACCGCCTGGCCACTAAGAAGCTGGACCTCTGGAGGCTGCCTCCTGTACTGG[T/C]AAGAACAATAAATCCTTTGCAGGAACTGTATTAAAAATCCCACATTTCTCTTAAAAAGCCAACCTCTATTTTTATTAACAGTAGAAAGCTCATGCTGGTTAATTCCCAGAAGTAAACTTGCTATGTGCATTTGTGCATAGATTTGTTTTTCTGACCAAATGCACATTGTATGTGGTGAATCGGGGTGAATGAGCTTTCAGCTACTACGCACCTTACTGCTGGAATCAGCTTTCAGAAATGATCAGATGTGTTCCAACTTTTGGCACATTCAAATCAAGACTGAAAACACATCTGTTTAGCTGTGCCTTTACTGAATGAGCACTGTGCTACATCTGACAGATTGCACTGTTATATTTTTCTCTTCTGTTTCATTATTTTATAACACATTTTATCTGTTTTTATGTTTTTTACTCATTTTTATTATTTGTTTTAATTTTCTTATACTTGCTTCTTTTATTTTTGTTTATGTAAAGCACTTTGAATTGCCATTGTGTATGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2801
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088808 | Nonsense | 1287 | 1585 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 15 (position 23180305)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23891492 |
GRCz11 | 15 | 23826757 |
KASP Assay ID:
554-2881.1 (used for ordering genotyping assays)
KASP Sequence:
TCATTTCAGATYGTTCATTTGAAACGCTTCCAATTTGTAAATGGTCGATG[G/A]ATCAAGTCTCAGAAGATTGTGAAGTTTCCACGCGAGAGCTTCGACCCCAG
Long Flanking Sequence:
AATAACTAGAGTATCATTATAGAATATCATTAAATAACTAGAGTATTAAGTATTTTTATTTGACAAGTCTCATACATCCTGATCCTCAAGCAGTATGAATAAAACTTTCAAAAAACATAAAATAGGTTTTAATAGGAAATAGGAAAATTATCCTGTAAAGTTCTATTCTGTAATGAATTATTTTTATTAAATATATATTTAAGAATATTTGAATACCATAAAGTGTGTATTTAAATTGATCAAATGTATTTAAAAATATATTAAATTATTATTATTAAATAATTATTAAATTATTTTGCTTTAGACAAAATCATTTTTAACTGAAATCTTTTCTCCGTTAATATTTATGATAAGCCAGATATTTGTATTTATCACAAAAAAACTTGAACTGTATGTCGTAGCAAGCTTCTCCTTCGAACATTAAGTGTCAATATCTTTATTTTCTGTGTTTCATTTCAGATTGTTCATTTGAAACGCTTCCAATTTGTAAATGGTCGATG[G/A]ATCAAGTCTCAGAAGATTGTGAAGTTTCCACGCGAGAGCTTCGACCCCAGTGCGTTCCTTGCCCCACGGGAGGTGTCTCAGAGCCTTGGCAGCCTGCAGAGCCTGCAGAGCGAGTGCCTGGTGGAGGAGCTCCAGAGGCTGGAGAGAGGAGACTCCTCTGTGTCCTCCATCTCCACCACCACCTTGGCCAGTCCTCCCATATCTGGCAGAGGTCTGTCTCACTTCCTTTGCTTCTTGCATGACATTGGGGGAAATTATTCTGTGAAATTTTATTCTGCAATATACAGTTGAAGTCAGAATTATTAGCCCTCCTCTATCTTTGCCTCAATTTCTGTTTAATAAAGAGAAGATATTTTTAAACGCATTTCTAAACATAATAGTTTCAATAACTCATCTCTAATAACGGATTTATTTTATCTCTGCCATGGTGACAGTTCATAATATTTGACTAGATATTTTTCTGGACACACAAGGGTTAATAATTTTCACTTCAGCTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35887
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088808 | Nonsense | 1405 | 1585 | 32 | 34 |
Genomic Location (Zv9):
Chromosome 15 (position 23177211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 23888398 |
GRCz11 | 15 | 23823663 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGCTTGCGTCTTCCCCAGCTGGGCAGCAGACATCGACTCTGCAACAGC[A/T]AAGAAAACCTGGAAGCCTGTAGCACCAACAAGGAGAGCGAGAGCGAGGCC
Long Flanking Sequence:
TAAGTATGCCTAGGCCCTGCCATTAAAAGGAGCATCTAGCTTGGCTGCTGGAAAAAGATGATTATTACATATGGTTTCTAAAAAAAAAAAAAAGTTTGTGTATTAAAATGCTTGTCTAAATCCACTGGACCTGAGGAATATTGTGATGGTAAGAAAGGTGACTTCAATGTAATTAGTGCTGGTAGTGAAGTTGATTTGCAAGACTTAGCCTCTGCTTCACACCATGCCATATGTAGGAACTGTAACCAATAAATGATTTTCTGTATATTTGCTGCCCAATAGTAATTTAACAGATTTGGAAGAGCCAGTTCTCCATCTCCTTTGGGTCTTGACAAAATTTGTCTAAACGTTGTCTTTTAGCCACCCCGTGCTCCATCAGGAGGGTCGGCAGTCCCCTGAGCAGAAACAGCAGTCCCGGCAGCAGCCCCAGAAACACAGGCCGAAAACAGGGCCGCTTGCGTCTTCCCCAGCTGGGCAGCAGACATCGACTCTGCAACAGC[A/T]AAGAAAACCTGGAAGCCTGTAGCACCAACAAGGAGAGCGAGAGCGAGGCCGAGCAAAGCGCAGTGACGGACGGGGAGAATCTGACCCCTGATGCCAACACACAAGACACCTGGTCACTAGACGCCTCCAGCAACGACTGCGATGTCATTATGGTGAATGGACTAGGACAGGACAGCAGTCAGAGCAATGGACATTCAGAGGTCAGCGCCGATCTGGACACCCCTCACCAAAGAAATGACATCTGCCTGGAGTCCCTGTATAATTTATATGCAATCTCAGTAAGTGATTCTTGTGTTGCGCGTTTCATTATGGAAGATGTGCCTTGGCAAATTGGTAAACAAGCCTCTCTGTTTTGCTTTCAGTGCCATTCGGGAATAATGGGAGGGGGGCACTATGTGACTTATGCCAAAAACCCCAACGAAAAATGGTACTGTTACAATGACAGCAGCTGCAAGGTGAGATCTCAGCTTCTGTGACACTTTACACGTTTCCATTATTTG
Associated Phenotype:
Not determined