ZMP
si:ch211-239j15.4
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100006377 [Source:RefSeq peptide;Acc:NP_001116418]
Human Orthologue:
SENP7
Human Description:
SUMO1/sentrin specific peptidase 7 [Source:HGNC Symbol;Acc:30402]
Mouse Orthologue:
Senp7
Mouse Description:
SUMO1/sentrin specific peptidase 7 Gene [Source:MGI Symbol;Acc:MGI:1913565]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1021 | Nonsense | Available for shipment | Available now |
sa24195 | Nonsense | Available for shipment | Available now |
sa45774 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5008 | Nonsense | F2 line generated | Not yet available |
sa43869 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1021
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 |
---|---|---|---|---|---|
ENSDART00000086868 | Nonsense | 20 | 879 | 2 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30421572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28288996 |
GRCz11 | 22 | 28239117 |
KASP Assay ID:
554-0925.1 (used for ordering genotyping assays)
KASP Sequence:
TTGGACTAACCTTATTGCAGTTACTTTTTTTGCAGATGGCGGTGTCCTTT[C/T]GAATCCCCAAAAAGAAGCAGCCGTCAGATTCCTGCAGTCTTGATATGCAG
Long Flanking Sequence:
ACATTTAACAGATTTTCTTATTATGTTCATTAGTTCTCTTTATTTGATCTTAATAATTTCTTTTAAAAGTTTGTTACCCTTCTATTAAATGCCCTTAATAAACTTATATTAATATTGCTAAAAACCTTTTTAAACATGTGCACGCACACAAAATTCTAAATGAAGTCGATTTTTTTTATATCTTGTTTTAAAAACAAATTTATTATAAGGGCTCTAACATGTTGCACTGGTGCACCTGAAATTACAACCACATCGCATTGAGCATAACGCCCTTCACCATCTCTGACTGGTTTTAGCCAGAACATGATCTAATGTGTGCCTATTCTGTTGAACCACAGTTGTGGAGAAGTTTTAACAAAATCTATTTGCCCTCGATTGGCTGGTAGCAACCTTAGATTATTTTGTTGCACCATTGAGAAATTAAGTCACACTCTAGAACCCTGATTATGCTTGGACTAACCTTATTGCAGTTACTTTTTTTGCAGATGGCGGTGTCCTTT[C/T]GAATCCCCAAAAAGAAGCAGCCGTCAGATTCCTGCAGTCTTGATATGCAGTCTCCGCTTTCTCGATTGCAGGACGATAATTCACAAAAGGTAAGAAATGCCACAAATCACACCGTAGACAACAGGTTATCTGCTTTAAAAGTGAACTGAACCACTGTGGTTTTGTGTAAAGCTGTTTCTTTTGCTTTTTTTAGTCAGTGCATCACGTTTTTTTGTCCGCATCAAAACAAAATGTGCAAAAGTACTATCGTAAAAAGGTTTGTGATGTTACTGTTTTAAAAAAAGCTAGTTTTGCTCACAGAAACAGAATTTTACAATATATAAAAAAAATATATATAAAAGGGAAATGTAATAAAAAAAATAAATGCAAATAAATGCTGCTATTTTGAACTTTTTTTCATCAAGGATAAGCAAAATAATATCAATTTGCTAATAAGCAAATAGTGTCACAGTTTCCACAAAGCATTGAAGCAGGAAAAAAAATTTCAACATTGATAATTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa24195
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 |
---|---|---|---|---|---|
ENSDART00000086868 | Nonsense | 417 | 879 | 11 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30395132)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28315436 |
GRCz11 | 22 | 28265557 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTAGCCATTAGCATTTCATGCTCTCAACTTCAAATGTACGGCATGT[G/A]GGATGGTGGACTGGCCAGTGACGGCAGTCTGTTATCCATCACAGAGGAAC
Long Flanking Sequence:
TTATATATATAGAATTTAAAATGAGTGCATAATATCAAACCATTGTGATGGGTTTATGGCTTTTAGCTATTAACATTGCAACAAATGTGCTTGTGCATATGTAAAAGTAGGATAATGGTCACTTTTGTTAAAAGTAACTAAATAGCTATTCGGTTAACTTTAGCAGTTAGCATGTGAAGTTTAAAATTCAGTTCAGAAACTTTAAACATAATATAAATGGAGCATATTATCAAACCTTTATGATTAGTTTGTTTTTTTGCTCTTAAAAAATCAAAAAGATACTAAGAAATTAGCCCTATAGCGTTTTAAACTACCTTAAAAGCATTAATAACATTTTTTATTACGTTTGTGCTGTGAATGACCCTTTTTGATGAACTGCATTATTATACATCATGACCAAAGTCAAAAATCCTTCTTGTTTGTTTTATTTCTAGATGCAGATGGAGAAGGTGAAGTAGCCATTAGCATTTCATGCTCTCAACTTCAAATGTACGGCATGT[G/A]GGATGGTGGACTGGCCAGTGACGGCAGTCTGTTATCCATCACAGAGGAACCCGCTCCTTCTCTTTTCTTTCTCATGGTGTCAGATGCTCAAGCCAGGCTGCTTCGGAAAGAGCTGTCTTTGCAATACAATACACACACTTCAGGTGAGGCATTTAAAAGGATCCATACTAATAAAATATACAGTTGAAGTCAGAACTATTAGCCCCCCTGAATTATTAGCCCCCCTGTTTATTTTTTTCCCCAATTTCTGTTTAACAGAGAGAAGACTTTTTCAACACATTTCTAAACATAATAGTTTTAATACCCATGTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTTACTGCGTATTTTTCAAGACACTTCTATACAGCTTAAAGTGACATTTAAAGGCTGAACTAGGTTAATTAGGTTAACTAAGCAAGTTATTATAATTAGGCAAGTTATTGTATAACAATGGTTCTGAAGACAGTCAGAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45774
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086868 | Essential Splice Site | 542 | 879 | 12 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30376010)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28334558 |
GRCz11 | 22 | 28284679 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCACTGCTGGGGCAAAACTGCAAGGACACGGGCCAGGACAAAGCAAAG[G/A]TCAGCCTATCAATACAATTTGTTGTTTCATGCTTTCTGTTTGTCAGTCTA
Long Flanking Sequence:
AGTATGTGTGTGTGTATGTGTGTGTATATTTGGACAAAGACAATGAAAGGATTAATTCCTTTATTAAAAGATTCATTCTGTCTTTTTTCATTCTGTTGTTCATTTGTTGGTTGTTTTATTATATGGCGTGACTGTGGCTGTTTTTTTTTTATTGTTCATTTTGGCCACCCATTAAACATCTGATCAGGTTTAAATGCTACAGATAAACAAATAAAACCTGCTCCGTTAACAGTAATAAAAAGTGTGTTTTGTGCTGTGTTTCTCTAGGACAGGCCTGCCCGTTTGTCCTGCTTGTGTTGAGTGGTCAGCTGGATGATCTTCGGGTGGCTCTGTTGGCATCTCTCATGGACGTGATTGGGCTGAGATACGCTCAGGACTCTTTGAGTAACCCTGTGTCCTGGGCTGATGGGCTCAGTCGACTTCTCTGTCACCCGCGGGGAGAACACTTCCTCTCACTGCTGGGGCAAAACTGCAAGGACACGGGCCAGGACAAAGCAAAG[G/A]TCAGCCTATCAATACAATTTGTTGTTTCATGCTTTCTGTTTGTCAGTCTATCCAATTCATTTTTCATGTCAAACCTTTTGTCTATCCACAAGTGTTCCATTATCCATTCATCCATCTTTGTACATCTTTTTTTCTTAGGAGTAACAGAAAATTTATCCATCTTTAGTCCTCAGTGTCTTTGACTTTGCCTCTTTGTTTAGTTTTTCATCTTTATTTAGTATTCTTCTGTTCATCCACTTTTTTATTGTTTTTATTGTCTGTCCATCAAACATCATTCAGTTTATTTGTTCATCCATCCGTCTGTCTGTCTATCCATCTGTCCATCCGTAAGTCCATCCATTCCTCCATCTATCTTTCTCACCATCCATCCATCCATCCATCCATCTTTCTCACTATTCATCAATCCATCCATCTGTTCTTTCATCCATCCATTCTTTGTCTCTCCATCCATCCTTTGTCTCTCCATGCATCCATCCATTTGTCTCTCCATCCATCTATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5008
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086868 | Nonsense | 662 | 879 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30366553)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28344015 |
GRCz11 | 22 | 28294136 |
KASP Assay ID:
554-3600.1 (used for ordering genotyping assays)
KASP Sequence:
TTTCCTGCAGGTCTGCGTACAGACGACATCAGAGAGTGAGAACGTGGACA[C/T]GAYATGTGGACATATTTAGCAAAGACTACCTTTTTATACCAGTTAATCAT
Long Flanking Sequence:
AACTTTTATTAAAGCTGAACCATTGTCTGAGAAGCTGATATTCGGCAAGGATATTAATATTATATGATCATGGTGTTCAATAATATTATAGCACACAGTGAGTGTATATTATGACCATTTGTCATTTGCGTTTGGATCTTGAAACTGTAAAACATTGGATCATATCTAACAAGCAGATACTCTAATACTGAATTCTCTTTCAGGTATCTTCTGTTGGAAAGAGCTGACAAAGATATTGCAGAAAGATCTCACATCTTCAGCAGCTTTTTCTACAAACAACTTACTCGAAAAGACACCAGTGGCCCAGAAGAGACTGGAAGCACGTAAGAAATCATTTAAAATCGCATTTAGAGAATTAAAGAAACAGTAACAGCTGTTTTTTTAGCTGTACTGTTCCATTTAGTATATTATGCTGGAGATTTGAAGCTGATTTGAACGAGTGTGTGATGTTTTCCTGCAGGTCTGCGTACAGACGACATCAGAGAGTGAGAACGTGGACA[C/T]GACATGTGGACATATTTAGCAAAGACTACCTTTTTATACCAGTTAATCATGAGTAAGTGAGGAATTTAAATTGAAACCACACCACAATCAAATGCAAGTTTTAGACCAGGGATGCCCAAACCTTTTCATATGAAGGGCCAAAAACCAAATATCATTGATAGCTGTGAGCTGACAATAAATATAACAAATTATTTTACATTAAAGTTGCCATGGGTAATATTCTAATTTATTTAATAATATTTAAAAATAAATAGAAAACATTACTTTGAGTCGAATTAACTAATGCAGTATAACCTTTTTATTTATAACTTAGTGTGAATAAAATCATAAACAATCACATTTACAGTATAATATAGTGGAGTTCAATGCTGAATACACTAGTAAAGCAGAATCTGCCTTTGACTTCATTTGCTCATCAAAGTCCTCTGTCGGGTGACAGTATGTATGTTTTAAACTAAATCTGATTAAATGACACCATTTGGATTGAAACATTTAATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43869
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 |
---|---|---|---|---|---|
ENSDART00000086868 | Nonsense | 702 | 879 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 22 (position 30362965)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 28347603 |
GRCz11 | 22 | 28297724 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGATCTGTTTTCCTGCTCTGGAAAGGCCTCAGATTGTAGAGTGGAGA[C/T]AAAAAAGCTCAGTGTCCCAGGATGAAAGCCAGACCACCAAAGAGAGACCC
Long Flanking Sequence:
CATTTGCCTGTGATTGAATTTTTATAAACTCTTTATTCTTATTTTTTGTGGTAAAAGATCAACACAATTTTTTTTTTTTTTTTCTAGTTCATTTTGCTTTGCTATTCTTTTGGTGTTCAACCCCATAAAAAGTTTTTGTTTAGTAACATTACATGAAGGAAATGATTACATCTTATGTTTATTTATTTATTTGAGAAACCATAGAAAACATTCACTTTTGTTATATTTAGTTTTAAACCAAACATGCCTTTTATCCACTTTAAAGCAAATCCACATACATTATGTTTACAGTACATATAAAAACCATCCAAAAGCATCATTGTTCAGGTTTTCTGCTTCAGGATGTGTTTGGCAGTGGAAACGAGACTTTATCACAGATCACTGACTTCCACTTCCTCCTCTATCTGTGTTTTCTGCTCTGTTTGTGTATCAGGGCTCACTGGTACCTAGTGCTGATCTGTTTTCCTGCTCTGGAAAGGCCTCAGATTGTAGAGTGGAGA[C/T]AAAAAAGCTCAGTGTCCCAGGATGAAAGCCAGACCACCAAAGAGAGACCCTCTGGAGAATCTCAGCGAGGTATCACACAAACACACACAAACAAATAATAATTGTTTTATTTTTATATTTTGTTTAATAAATTATATATTTTATTTCATTTTCAAATATTTTTTGTTTTGTTTCATTTATTGTATTGTTTTGATTAAATATTTTTTTAATATTATACATGTTTTATTATTTTTTTAATTAGTATTATTTTAACAGTTGCATATTATGTTAAAATTATTTCGCTGTCATTTAGAAACTAGCACATTTAAAACCAATTTTGGTCATGTAGTAATTGAAAATGTAATCTTTTTTTTCTTTTTCTCCTCTAAAAATTTTATATTTCAATATTTTAAGTGTTTTTTATTATTATTTTGTTATTAATAACTATAATAATAATAATAATAATATTAAACTTATTATTTTTTTTAATTTATAGCTATAAGAATAGCATCTCAAGGCAC
Associated Phenotype:
Not determined