Busch Lab

ZMP

GLP2R

Ensembl ID:
ENSDARG00000078548
Description:
glucagon-like peptide 2 receptor [Source:HGNC Symbol;Acc:4325]
Human Orthologue:
GLP2R
Human Description:
glucagon-like peptide 2 receptor [Source:HGNC Symbol;Acc:4325]
Mouse Orthologue:
Glp2r
Mouse Description:
glucagon-like peptide 2 receptor Gene [Source:MGI Symbol;Acc:MGI:2136733]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa13102 Nonsense Available for shipment Available now
sa10676 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa13102
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109713 Nonsense 95 493 3 13
Genomic Location (Zv9):
Chromosome 12 (position 340237)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 322601
GRCz11 12 328542
KASP Assay ID:
2260-4757.1 (used for ordering genotyping assays)
KASP Sequence:
GCACCGTCAACGGCACTTGGWAAACTGAGGAGAACTCCTCCASCGTATGG[A/T]GAAATCAGTCAGAGTGCGAAAACCATTAWTTTTTCAAGTCCGAGGTGAAT
Long Flanking Sequence:
ACTTTGCCAACATCTTAAAACTGAAGACTCTTGCATCCAATAGATTTTGTGTATTTAAAGTCTTGTTTGTGCATTTAAAGGGATAGTTCATACAAAAATTAATTTACTCACACTTTACCTTCATTCATTTCTTCTGTTGAACTCAAAGGATGATATCTTGAAGAATGTTTGAAACCGGTAACCATTGACTTCCATTCTATATGTTTCCTACTGTGAAAGTCAATAGTTACCAGTTTCCAACATTCTTCAAAACATCGTCCTTTGTGTTCTACTCATATAGGATTGGAACCTCTTAAGAGAGAGCAAAAATACATTTGTGTGAACTAACCCTATAATTTGATGCAAACACCAAAACCACATTTCCTCCTTGACTCATTTTTGAATTAAATGCACACAAAACATTGACGATGTTGTAATTTTCAGGTGCTACTGGAAACGTCTATAAGGAATGCACCGTCAACGGCACTTGGAAAACTGAGGAGAACTCCTCCAGCGTATGG[A/T]GAAATCAGTCAGAGTGCGAAAACCATTATTTTTTCAAGTCCGAGGTGAATATTGCAGCCATACAGTGACGTATGGTGTCCGTCATGGTGTTATTCTTATGCTGATGTCTCTCTGCACGCAGGAGGAAGAGGTGTTCCGGCAGTCTGTGCTGAGAGTGCTGTCCATTGTTGGATATTCGCTGTCGTTTTCTTCTCTGTGTTTGGCTGTTCTGATCATGAGTCTGCTGAGGTGAGGGGAGTTCTGCAGGGCTCGCTCTCGGGTCCGCTTCAGTTTCATTTCAACAAGAAAATGCACAATTGGAGAGAAAGCGACAGAATTAAGAGAGGGGGTGTAAACTTTTGCACAGAAATCAGAGATCAACATTTGCATAAATTAATAAATATATAGACAACGTTTGAAGTGAGTGAAAGTATTTTGAATTTGTCTTAAGACATGGTTGTTTCATCGTTTTACGACAACTTTAATGAAAGGTTTTTGATGTTGACTATATGCTAATATAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10676
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109713 Nonsense 104 493 3 13
Genomic Location (Zv9):
Chromosome 12 (position 340208)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 322572
GRCz11 12 328513
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAACTCCTCCASCGTATGGAGAAATCAGTCAGAGTGCGAAAACCATTA[T/A]TTTTTCAAGTCCGAGGTGAATATTGCAGCCATACAGTGACGTATGGTGTC
Long Flanking Sequence:
CTTGCATCCAATAGATTTTGTGTATTTAAAGTCTTGTTTGTGCATTTAAAGGGATAGTTCATACAAAAATTAATTTACTCACACTTTACCTTCATTCATTTCTTCTGTTGAACTCAAAGGATGATATCTTGAAGAATGTTTGAAACCGGTAACCATTGACTTCCATTCTATATGTTTCCTACTGTGAAAGTCAATAGTTACCAGTTTCCAACATTCTTCAAAACATCGTCCTTTGTGTTCTACTCATATAGGATTGGAACCTCTTAAGAGAGAGCAAAAATACATTTGTGTGAACTAACCCTATAATTTGATGCAAACACCAAAACCACATTTCCTCCTTGACTCATTTTTGAATTAAATGCACACAAAACATTGACGATGTTGTAATTTTCAGGTGCTACTGGAAACGTCTATAAGGAATGCACCGTCAACGGCACTTGGAAAACTGAGGAGAACTCCTCCAGCGTATGGAGAAATCAGTCAGAGTGCGAAAACCATTA[T/A]TTTTTCAAGTCCGAGGTGAATATTGCAGCCATACAGTGACGTATGGTGTCCGTCATGGTGTTATTCTTATGCTGATGTCTCTCTGCACGCAGGAGGAAGAGGTGTTCCGGCAGTCTGTGCTGAGAGTGCTGTCCATTGTTGGATATTCGCTGTCGTTTTCTTCTCTGTGTTTGGCTGTTCTGATCATGAGTCTGCTGAGGTGAGGGGAGTTCTGCAGGGCTCGCTCTCGGGTCCGCTTCAGTTTCATTTCAACAAGAAAATGCACAATTGGAGAGAAAGCGACAGAATTAAGAGAGGGGGTGTAAACTTTTGCACAGAAATCAGAGATCAACATTTGCATAAATTAATAAATATATAGACAACGTTTGAAGTGAGTGAAAGTATTTTGAATTTGTCTTAAGACATGGTTGTTTCATCGTTTTACGACAACTTTAATGAAAGGTTTTTGATGTTGACTATATGCTAATATATTAATATGCTAATTATTCAGCAAACATAAG
Associated Phenotype:
Not determined