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