Busch Lab

ZMP

QSER1

Ensembl ID:
ENSDARG00000074750
Description:
glutamine and serine rich 1 [Source:HGNC Symbol;Acc:26154]
Human Orthologue:
QSER1
Human Description:
glutamine and serine rich 1 [Source:HGNC Symbol;Acc:26154]
Mouse Orthologue:
Qser1
Mouse Description:
glutamine and serine rich 1 Gene [Source:MGI Symbol;Acc:MGI:2138986]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa23375 Nonsense Available for shipment Available now
sa29095 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23375
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
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109948 Nonsense 724 1708 4 13
Genomic Location (Zv9):
Chromosome 18 (position 44099469)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 45688524
GRCz11 18 45685350
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTAATGCACTCCTCCACCCTTGCACCCTTGAGTGCTGATCAGCTGAAA[C/T]AGCATACTTTACTTCTGAAAGGGTCCAGTTCTCAGCAGCAGAACCATCAC
Long Flanking Sequence:
ACTACGTCTTAATGCAGTCCTCTCCTGGTAGTAAGACAGACAATGCTCTGTTACAGCAGAAGTACTTGTTATCTGTCCAGTCGTCAACCTCTTCTGCTGCCACTTACACCAAGGTCTTACCAAAGGATCAGTCCTCAGTTGAGATTAAACCACGCCAAGAAGATGAGCAAATGTTTCTTCCCTCAAAAGCAAGCTCTGGAGAGCTTCCTCTTGAGGATGTGCAGGCATTGCAAAAAGGCTCTTTGGTAACCTCCCCTCAAAACATTTCAACCAGTGAAATTGGAGAACAAAATAGTGCAAAAAATGATATTTATGTAGTTTCGAAGATGGAAGACAGGCACAACACCCCAAGTGTTATTCGTAGTAACTCTCGAACAGAGGAGCAGACCCTTTCACAGATGGAAAACACTAAAGAACTCACTACCAATGCCAATGCTAAGAGTATTCCTTTGTTAATGCACTCCTCCACCCTTGCACCCTTGAGTGCTGATCAGCTGAAA[C/T]AGCATACTTTACTTCTGAAAGGGTCCAGTTCTCAGCAGCAGAACCATCACGAACAGATAATACAAGTTCAAACGACAGATCCCAGACAGCTGTCTGAGGGGCAAGCACAGTTCATCCGGGTTCCCAGCACTACCCAAGTTCTTCTCGATCCCTCCCACATGATCGTTCTGCAACAGCCTGTGCTCACCACAGCACAGAATCAGCCCAAGCAGACTATGTACATGCAGTCTGTACCAGTCCAGTATGTCCATATGAACAGCGACACTGTTAATTTGACAATTAATGGGCGTCACAACCAGCAATTTGTCTCTCACCAAGTGCCCAACTCAACAGGGTCCACTAAAGAAGACCCAACACTAAAGGACCAGTCAAGTCCTCATGACATAAAGCAAAACTTTTCCCTCAATTCTGTATGCTTTTCAGACTCCATGCTTTTGGCAGATGAGAGAAACATACTCTCAAATGTTGATGACATCCTTGCTGCTACTGCAGCTGCCTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa29095
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109948 Nonsense 1072 1708 4 13
Genomic Location (Zv9):
Chromosome 18 (position 44100513)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 45689568
GRCz11 18 45686394
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAATGATAGTATCATTGAAAATTCAACTGATGGCCTTGCAAAAAAA[C/T]GATCCAGATCAAAGGGTTCATCCAAGCAGACTGCTGAAGATGAAAATGGT
Long Flanking Sequence:
GTGACATGTCATCAGTAGCCAACCCTGTAGACTCCAAGTGCAATTTTCAGTCACCTGAAAACCGACACAATAGTTTCCCATCTCAGCATATGATAATTAACCCACAAGCCATGACTGTAATTGGTGCTCAAACAACATACTCCAAAGAAGAAACTGAGGGACATCAAGTGTTTACACTTTCACACTCTAACAACCAACCTGAAGAAAGATGCAAATCTGCACAAGATATATCTGATAAGGTTGCAAATGCCCATGAGAAAAGTGATGTGTTATCCAAAGGACGTTTTGTAAACTCTAGCAATGGCTCTTTGAATACTAATGGACTTGCTATAAGTAATACAACCTCAAATGATTTTAATTTGGCTAATCAGCAGCAAAGCCAGTCACCACATCATATTACTGAAAATGTTTCAAGTAATCTAAGCCAACAAAAAGAATTGAAAGGTTTTAAAACCAATGATAGTATCATTGAAAATTCAACTGATGGCCTTGCAAAAAAA[C/T]GATCCAGATCAAAGGGTTCATCCAAGCAGACTGCTGAAGATGAAAATGGTCAGCCTAAATTTCAGAAGAAAAGCATACAAGTTAAGCGACAAAATTCCCGTGCCAATGAGACTAGTACAACCTCCGCCTCAGAGGTTTCCCATGATAACTTTCAGCAGCAGGAGAAGATGCGTCAGAAGTTAAAAGAGGTTGAGGAAAAACAGCCAGAGGTTAAAACTGGATTCCTGGGCTCCTTTCTGGACTTTCTGAAATCTGGATCCAGACAAAACTTATCATCTCCACCAATACGGTCACCCAATCGCACAAGGAAGTCTTCAGCCTCCAAGAGGCCTCCTAATCCATTACTTATTCCCTTTAAACCTCCACCTCCTGTAACCCCATTGATATCCCCGGAACCTCAAAGTGTCATTTCTACAAAGCGACTTGATGAAGAGCTCCAGAGGAATCTGGAAACCCTACCATCATTTTCCTCTGATGAAGAAGATTCGGTGGGGAAAAAC
Associated Phenotype:
Not determined