Busch Lab

ZMP

LOC559077

Ensembl ID:
ENSDARG00000079992
Human Orthologue:
SENP6
Human Description:
SUMO1/sentrin specific peptidase 6 [Source:HGNC Symbol;Acc:20944]
Mouse Orthologue:
Senp6
Mouse Description:
SUMO/sentrin specific peptidase 6 Gene [Source:MGI Symbol;Acc:MGI:1922075]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa42977 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa23133 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa42977
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112257 Essential Splice Site 284 565 8 16
Genomic Location (Zv9):
Chromosome 17 (position 37022919)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 36907816
GRCz11 17 36855401
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGATGAAGGGGAATTTTTAAACGATGTGATAGTAGATTTCTATCTAAGG[T/G]TAGATTTGTAGAAGTGGCTATATATTTTAGTCTGTTGTTTCTGTAATGAC
Long Flanking Sequence:
GTTTAAAAAAAAATAGTGTACCTGCTCCTTTACTATCCATTTCCTATCCTAATTTTCATTTCCTTTTTACTGTACTTTTTTCTTTTCGAAAGTTGAGTCTGTGAGCAACAAAAGCAAAAAAAAAAGTGCCTCCAGCATCATTTTCAGTTGTTTTCCTCTTTCTCTCAATGTTCAGCGAGCCTTGATGCCATTTCCACCTTCTCCTGATGCTCCCCGACATGAAATTGCAACCCTCAGCATCTCAGACAGTGATGAGAATGATTTGATGGAGGGCCATTCATCACCTGTACAGGATCTCAAAAAGTCAGTTCACAGACCTAAATGAATGATCAAGTGTTGCGATATTAGATCTAGAAAACCTCATCTCTCTATGTTTTTGCAGACTGCTCGTGTATCCCCCTTCTCCAGCAAAGGGTGGTATAACTGTCACGGAAGAAGACTTTTACTGCCTTGATGAAGGGGAATTTTTAAACGATGTGATAGTAGATTTCTATCTAAGG[T/G]TAGATTTGTAGAAGTGGCTATATATTTTAGTCTGTTGTTTCTGTAATGACATGCATGTTTTATAATGAGCAGGTATTTGGTCTGCAAGCAGCAGGAAAAAAAGGATACTACCCAGTACCATGTGTTCAGCTCTTTCTTCTTCAAGCACCTCACTCAGGGAAATCAAAAAAGGCATTCAGGAGCTACAAGTTTATCGTATGTATAAAATATAGACTTTAACAAATGTATTTTAACTATGATTAAATTAACTATGTTAACGCTGTTCCGCAGCCCTCAAGAGTGTCGACACGACAGGGTGAAAACTTGGACCAGGAATGTAAACCTTTTTGAGAAGGACTTTGTGTTTGTCCCCATTAATCAAATGTGAGTCTTTTCACTAAGCTACACATCTTGGATTTCTGGCTGGGGTATGCAGTATTTGCGATCTATAATTCTGTAATTTCTTTTGTGTTTCCATCCTGTTTCAATTCACTAAAAAATATGCTAGGTTACACTCAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23133
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000112257 Nonsense 541 565 16 16
Genomic Location (Zv9):
Chromosome 17 (position 37017869)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 36902766
GRCz11 17 36850351
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGGACCCACCTCAAGCTTTTCATCACAACATGGACTTGAAAGGCTG[G/A]TTTTCACAAAGAACAGTAAAAAGGAAGAGGTTGCAAATCAAAGAGCTCAT
Long Flanking Sequence:
TCAATGAAACTGTTAATCTTTAAAAGTGTTAATACAATACAATATTTATTTATAAAGCGCATTTAAAAAAAAAAAAAAAAAAACACTGAAGTTGACAATGCATTCTCACGCACACAAATGAAACTCAACACAAGGCAATGTTGTCATTCTAGTCACTTTATTTTTGATTCCTTTAAATCTAAGGTACTTGCAAGAGGAATGGAGGGTGAAAATGGGCTCTCAACAGAGTTTTGAAAAGATGCATGGATGGAGTCCCATCGTCCCAAAGCAGGATAACTATACAGACTGCGGTATCTACCTGCTGCAGTATGTGGAGAGCTTCCTGAAGGTATTTTACAATGGGGGAATCTAATTATTGTCTGTTTTGTTGTAAATGGTTACATATTTCAACGTTGTTGTTGCTTTTGGTTTTGTGTGTGCGCTTTTGTGTGTGTTTGTGTGTTTTTGTTTATTCAGGACCCACCTCAAGCTTTTCATCACAACATGGACTTGAAAGGCTG[G/A]TTTTCACAAAGAACAGTAAAAAGGAAGAGGTTGCAAATCAAAGAGCTCATTCTCAAACTACACAGACAACAATAAGATTTTTTTTTTCATCTCCAACTTATTATTACCACCTGTAATTCAGAAATAGGGTTATTCTTTACTGTATTTTTGAAAGCTAGAAGGTTAACTCGCATTACCTGCATGTCATTCTCCGCCTTGTCATCTGAAAGTATGCAGAAGCTCTTGTCTAAGTCATCTAAGAGGGACAAAATAAGGCATACTGTGGCTTTAATTACTGTAAAAGATTAATAATCTCCTAGAAATGTTTTAAGCAGCAGAACTGTTTCTCACAATGAAATTAGGAAATGTTTCTTGGAGAACCAAATCAGTATATTAGAGATTCACCCAAAAATGAACTGTCATCTTTGACTGCCTTGGTATCCCAGCTGTACTCTCCGTATTATACAGTTATTATTTATTATTATTATTTAAACTCTTGCTGATTTTTCTTGCTGCTTTAA
Associated Phenotype:
Not determined