Busch Lab

ZMP

LOC566750

Ensembl ID:
ENSDARG00000022570
Human Orthologue:
NMUR2
Human Description:
neuromedin U receptor 2 [Source:HGNC Symbol;Acc:16454]
Mouse Orthologue:
Nmur2
Mouse Description:
neuromedin U receptor 2 Gene [Source:MGI Symbol;Acc:MGI:2441765]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa13171 Nonsense Available for shipment Available now
sa21931 Nonsense Available for shipment Available now
sa31837 Nonsense Available for shipment Available now
sa41855 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa13171
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028641 Nonsense 35 342 1 2
Genomic Location (Zv9):
Chromosome 11 (position 28986493)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27862479
GRCz11 11 28109653
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTACCTTCAGACCATTGATGAAGTTCWGTTTAAGCTTCTGGGCCCAAGA[C/T]RATCTCCKTTYTTCTTCCCTGTAACCTGTACTTACWTCCTCATCTTCATG
Long Flanking Sequence:
CATTCACACTCATACATAATTCATTCAGTACTACCAACTTTGCCACCCCGTCACCCTAGAGAACATTCAGTTATAAATAAATATATAGTAAAATATACTGTATAATAAATTCAGAACTGCTGAAAAAAATCATAATAAAATGCAAAAAATAAGTTTCCATTTCTGTCTGCTATACCCCCACTGCAGTATATCCTTCATGTCTGTACTTATAGCCTGTACCTCCCTGTACTAATCTGTTTAACACAGGTCTTCCATCATGCAGAAGAAACAATGCAGGAGGTAGCAGTTTCAGCGCTGACTCAAGACAGGCTCATTTAACCTTATTTAATCACCCTTGGATTCCTATGATGGCCCTGATCTGCCTTTGCGAGTCTGTGAATACATCAGACCAGGATTATGAGTTCTGCAACAGCAGTACGTTCAACTTCACTGGAAATGACAGTGCACACTGTTACCTTCAGACCATTGATGAAGTTCTGTTTAAGCTTCTGGGCCCAAGA[C/T]GATCTCCGTTCTTCTTCCCTGTAACCTGTACTTACATCCTCATCTTCATGACCGGGGTCTTAGGAAACCTCCTGACCTGCGCTGTAATCACTAAAGATCGAAAAATGCAAACTCCCACCAACTTGTATCTCTTTAGCCTGGCCATCTCCGATCTTCTAGTGCTACTCTTCGGGATGCCTCTGGAAATCTACGAACTTTGGCAAAACTACCCTTTTCCCTTCGGCGAGAGCATCTGCTGCTTTAAAATCTTCTTGTTCGAAACAGTTTGCTTTGCTTCCGTGTTAAACGTCACAGTGCTAAGTGTGGAGCGATACATAGCTGTGATTCACCCGCTCAAAACCCGTTACGCCATCACCAACAAGCACGCTCGAAGGGTCATCGCTGGGGTTTGGGCTATGTCTCTGCTCTGCGCCGTCCCGAACACCTCCCTCCATGGCCTGCAGTATCAGTATCTGCCGGAGAGGGTTCAGGAATCGGCTACCTGCAACCTGCTCAAGCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21931
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
ENSDART00000028641 Nonsense 158 342 1 2
Genomic Location (Zv9):
Chromosome 11 (position 28986862)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27862848
GRCz11 11 28110022
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGATTCACCCGCTCAAAACCCGTTACGCCATCACCAACAAGCACGCT[C/T]GAAGGGTCATCGCTGGGGTTTGGGCTATGTCTCTGCTCTGCGCCGTCCCG
Long Flanking Sequence:
AGTCTGTGAATACATCAGACCAGGATTATGAGTTCTGCAACAGCAGTACGTTCAACTTCACTGGAAATGACAGTGCACACTGTTACCTTCAGACCATTGATGAAGTTCTGTTTAAGCTTCTGGGCCCAAGACGATCTCCGTTCTTCTTCCCTGTAACCTGTACTTACATCCTCATCTTCATGACCGGGGTCTTAGGAAACCTCCTGACCTGCGCTGTAATCACTAAAGATCGAAAAATGCAAACTCCCACCAACTTGTATCTCTTTAGCCTGGCCATCTCCGATCTTCTAGTGCTACTCTTCGGGATGCCTCTGGAAATCTACGAACTTTGGCAAAACTACCCTTTTCCCTTCGGCGAGAGCATCTGCTGCTTTAAAATCTTCTTGTTCGAAACAGTTTGCTTTGCTTCCGTGTTAAACGTCACAGTGCTAAGTGTGGAGCGATACATAGCTGTGATTCACCCGCTCAAAACCCGTTACGCCATCACCAACAAGCACGCT[C/T]GAAGGGTCATCGCTGGGGTTTGGGCTATGTCTCTGCTCTGCGCCGTCCCGAACACCTCCCTCCATGGCCTGCAGTATCAGTATCTGCCGGAGAGGGTTCAGGAATCGGCTACCTGCAACCTGCTCAAGCCCAAATGGATGTACAACTTGGTGATCCAGATCACAACTGTGCTCTTCTACTTTGTTCCCATGATGATGATCAGCGTGCTGTATCTGATGATCGGTCTGACGCTTGGCAGAGGGCAGAAGCAGAAAAAGGACAAGCTGGGAAGCAATCACAGCAACGACAGCTGGAAAATCCATCTGGACAGCAGACGGAGAAGGCAGGTCACCAAGATGCACTGTAAGTGATGGCCTGCTGTTAGTACAGTGAATATGTAATGCTATTTCAGCAGTATTCAAGCGTGTAAAACTCAAACCCTACTGTAATTGTCAGGATTTTCACCAAATGTGGTTTTTAAATGAGTGTTTTCCCACCATGTTCCTGGAGGCACACCAGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31837
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028641 Nonsense 183 342 1 2
Genomic Location (Zv9):
Chromosome 11 (position 28986939)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27862925
GRCz11 11 28110099
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTCTCTGCTCTGCGCCGTCCCGAACACCTCCCTCCATGGCCTGCAGTA[T/A]CAGTATCTGCCGGAGAGGGTTCAGGAATCGGCTACCTGCAACCTGCTCAA
Long Flanking Sequence:
CACTGTTACCTTCAGACCATTGATGAAGTTCTGTTTAAGCTTCTGGGCCCAAGACGATCTCCGTTCTTCTTCCCTGTAACCTGTACTTACATCCTCATCTTCATGACCGGGGTCTTAGGAAACCTCCTGACCTGCGCTGTAATCACTAAAGATCGAAAAATGCAAACTCCCACCAACTTGTATCTCTTTAGCCTGGCCATCTCCGATCTTCTAGTGCTACTCTTCGGGATGCCTCTGGAAATCTACGAACTTTGGCAAAACTACCCTTTTCCCTTCGGCGAGAGCATCTGCTGCTTTAAAATCTTCTTGTTCGAAACAGTTTGCTTTGCTTCCGTGTTAAACGTCACAGTGCTAAGTGTGGAGCGATACATAGCTGTGATTCACCCGCTCAAAACCCGTTACGCCATCACCAACAAGCACGCTCGAAGGGTCATCGCTGGGGTTTGGGCTATGTCTCTGCTCTGCGCCGTCCCGAACACCTCCCTCCATGGCCTGCAGTA[T/A]CAGTATCTGCCGGAGAGGGTTCAGGAATCGGCTACCTGCAACCTGCTCAAGCCCAAATGGATGTACAACTTGGTGATCCAGATCACAACTGTGCTCTTCTACTTTGTTCCCATGATGATGATCAGCGTGCTGTATCTGATGATCGGTCTGACGCTTGGCAGAGGGCAGAAGCAGAAAAAGGACAAGCTGGGAAGCAATCACAGCAACGACAGCTGGAAAATCCATCTGGACAGCAGACGGAGAAGGCAGGTCACCAAGATGCACTGTAAGTGATGGCCTGCTGTTAGTACAGTGAATATGTAATGCTATTTCAGCAGTATTCAAGCGTGTAAAACTCAAACCCTACTGTAATTGTCAGGATTTTCACCAAATGTGGTTTTTAAATGAGTGTTTTCCCACCATGTTCCTGGAGGCACACCAGCAGTAAATATTTTGGAGGTCTCACTTATCTCAATCATTAACTTCAGGTTTTGGTCTCTTCTTATGTTCTGATGAGTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41855
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000028641 Nonsense 228 342 1 2
Genomic Location (Zv9):
Chromosome 11 (position 28987074)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 27863060
GRCz11 11 28110234
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAACTGTGCTCTTCTACTTTGTTCCCATGATGATGATCAGCGTGCTGTA[T/A]CTGATGATCGGTCTGACGCTTGGCAGAGGGCAGAAGCAGAAAAAGGACAA
Long Flanking Sequence:
GCTGTAATCACTAAAGATCGAAAAATGCAAACTCCCACCAACTTGTATCTCTTTAGCCTGGCCATCTCCGATCTTCTAGTGCTACTCTTCGGGATGCCTCTGGAAATCTACGAACTTTGGCAAAACTACCCTTTTCCCTTCGGCGAGAGCATCTGCTGCTTTAAAATCTTCTTGTTCGAAACAGTTTGCTTTGCTTCCGTGTTAAACGTCACAGTGCTAAGTGTGGAGCGATACATAGCTGTGATTCACCCGCTCAAAACCCGTTACGCCATCACCAACAAGCACGCTCGAAGGGTCATCGCTGGGGTTTGGGCTATGTCTCTGCTCTGCGCCGTCCCGAACACCTCCCTCCATGGCCTGCAGTATCAGTATCTGCCGGAGAGGGTTCAGGAATCGGCTACCTGCAACCTGCTCAAGCCCAAATGGATGTACAACTTGGTGATCCAGATCACAACTGTGCTCTTCTACTTTGTTCCCATGATGATGATCAGCGTGCTGTA[T/A]CTGATGATCGGTCTGACGCTTGGCAGAGGGCAGAAGCAGAAAAAGGACAAGCTGGGAAGCAATCACAGCAACGACAGCTGGAAAATCCATCTGGACAGCAGACGGAGAAGGCAGGTCACCAAGATGCACTGTAAGTGATGGCCTGCTGTTAGTACAGTGAATATGTAATGCTATTTCAGCAGTATTCAAGCGTGTAAAACTCAAACCCTACTGTAATTGTCAGGATTTTCACCAAATGTGGTTTTTAAATGAGTGTTTTCCCACCATGTTCCTGGAGGCACACCAGCAGTAAATATTTTGGAGGTCTCACTTATCTCAATCATTAACTTCAGGTTTTGGTCTCTTCTTATGTTCTGATGAGTTCATTTAGGTGTGTTTGATTTAAGTAGGTATCGCTGCAGCCCGGAGACCTCCAAGTGGGAGGTATTTACACGGCAAGCAGGTTGGGTAACCTCAGAGTAAGAGGGACTTAAACCACAAGTAGGTTGATAAATAAAACA
Associated Phenotype:
Not determined