ZMP
si:dkey-100n23.3
Ensembl ID:
ZFIN ID:
Description:
LOC571373 protein [Source:UniProtKB/TrEMBL;Acc:A8WFW9]
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 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17833 | Nonsense | Available for shipment | Available now |
| sa7191 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17833
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089539 | Nonsense | 488 | 991 | 10 | 21 |
| ENSDART00000128876 | Nonsense | 488 | 991 | 9 | 20 |
| ENSDART00000131519 | None | None | 217 | None | 5 |
| ENSDART00000140929 | None | None | 141 | None | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 31262833)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30418779 |
| GRCz11 | 9 | 30229525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTCTTCAGATTCTASAGTGAAAATTTCTTTGTCAGMGATTAATGTGTA[T/G]AAATATAGCTTGTGGGAGGAGCATACATTATGGGGGTGTGATCTGGATAA
Long Flanking Sequence:
AATATTATTGATAATGATAATATAGCTTTTTGAATGTAAATGTTTCATGTTCAATGAAAATGGTTTGAAAATGCAGCAATAAACTGTTTTGCATTTCTAAATAGTAAAACTTATATTTAACATGTTCAAAACACTAATCTGATTCAATAAAAGAGGTGTTAGTAAGACTAATCCCAGTATCAGAATTGGCCTATTCTTTAAATACAAAAATTTTGCATGTAAATAATTAAACAAATTTATGAAGAATGTTTTTGGATGCATGTCTGTTTCAGAGTGTTTTTTATACATTGCTTTTTAGATCACTCCATACAAGATCACATTTTCTTTGAAAGGTAAACGCATATTTTATAAGAACTGAATTACTCCGTATATACATTATAATATAGATTTAAAAAATCTTTACATTTGAGAGTTTTGTAAACTATTTTTTCCTCTTGTGGACTTGCAGGAAACTCTTCAGATTCTACAGTGAAAATTTCTTTGTCAGCGATTAATGTGTA[T/G]AAATATAGCTTGTGGGAGGAGCATACATTATGGGGGTGTGATCTGGATAAGGACAATGAGGCCACACCCACTTCTCTACTCTTCCTTTGGCTATCTGATGCTCAGGCACACAAACTACACGATGATCTCTCTGTCCTTGAGTTAGGCACACGTCCAGGTCAGCTGCTCGTCTACATTATTAATATATTTAAAATGTCTTTTAAAAGCAATATTAGCCATCATTCTACAACATTCTGATCCTTCTTCACAAATGTTTTTTCTTTGTGTGTACACAGCTGAAAGCAGTACTTGTTTGTTGCTGTGTATGGCTGAACCTCTTTCTGGTATTGAGAGTGCGCTTTTGTGCTCTTTGTTGGACATTGTGGTTTCGAATCAGGGCAGCCCTGAACTTTATTGTACCTGCCTCACACAGTCAGACAGCCTGAATCTTCTGCAGAGCTCAGAGGAAACACACCTGCTCCAGCTACTGACACCCAAACCTGATGAGCAAACCAGTACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7191
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000089539 | Nonsense | 888 | 991 | 20 | 21 |
| ENSDART00000128876 | Nonsense | 888 | 991 | 19 | 20 |
| ENSDART00000131519 | None | None | 217 | None | 5 |
| ENSDART00000140929 | Nonsense | 58 | 141 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 9 (position 31251689)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 30407635 |
| GRCz11 | 9 | 30218381 |
KASP Assay ID:
554-5270.1 (used for ordering genotyping assays)
KASP Sequence:
AATTTATGGTCATTATATTTTATTCTTTTTCAGGTACCTTCAGGTTGAAT[G/A]GGAGACAAAGAGAATGGGTACTCGTGACTTTAGTGCTGAACGTATGGTTG
Long Flanking Sequence:
CCCCAGGACACCAGCCCGCCAGGACTGAGTCTGGACACCCCTGCCTTAACCGAACACACCTGATTCAGATCATCAGCTCATTAGCAGAGACTGAAAGACCTGTAATGGGTGTGGCAGACAAAGGAGACGTCCAAAACATGCAGTGTTGGTGGTCCTTTAGGAACATGGTTGAGAAACAGTGTTTCACGGTAAGGTTTTCACTGGGATATTAGTATGTACATGGCAGAAATGTTTGAAAGAACTGTAAATTTTGATGTTTAGATTTGAAAATGAAACCTTGTTTTCAGGCCATGTATTCTCATCATGGATTCTCTGAAGTTGTCCATTCATGAACGCATCTTCAAACTCTTGCGCGAGTGAGTGTTTACACTTTTCTGCTGTTTAGTTATTTTTCTTTCTTCATTTGCTATTAGTTATAGAATGCTAGTACAATAATAAACATATGTTTGTAATTTATGGTCATTATATTTTATTCTTTTTCAGGTACCTTCAGGTTGAAT[G/A]GGAGACAAAGAGAATGGGTACTCGTGACTTTAGTGCTGAACGTATGGTTGGTTCCCATTGTAAAGTTCCTCTACAAGACAACAGCAGTGACTGTGGCCTTTACCTGCTTCAATATGCAGAAAGTTTTTTACAGGTACACTTATGTTTGTTCTTTATTTCAAATACAGGAAGTGTCCATTTTGACTTTAAAGGGAACTCCAGTGCTGTATGTGTGTCTTTCAGGACCCTGTGGTCCACTTTGATTTGCCATTGAGATTGGAGCGCTGGTTTCCTCGACAGCAGGTGCGAGGGAAACGGGACGAAATTCGAGACCTCATCCTGCACCTATACAGATTTCAGAAAGGCTCTCTGGGAAATGATGCTGCAGATGATAGGACAGATTATGGCAATGTCATTAAGTGATATAAAGCCTTTAAGATTACACACTTAATTTACACTAGACATATTTATATTTTAGCTGTTTCTAAACCTTTTTTTATTGTACGCTTTTATATGGACTG
Associated Phenotype:
Not determined