Busch Lab

ZMP

GPR112 (2 of 2)

Ensembl ID:
ENSDARG00000087813
Description:
G protein-coupled receptor 112 [Source:HGNC Symbol;Acc:18992]
Human Orthologue:
GPR112
Human Description:
G protein-coupled receptor 112 [Source:HGNC Symbol;Acc:18992]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa35712 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44809 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa28329 Nonsense Mutation detected in F1 DNA Not yet available
sa22507 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa35712
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128379 Essential Splice Site 467 1201 12 26
Genomic Location (Zv9):
Chromosome 14 (position 32601665)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 31391472
GRCz11 14 31731786
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACATGCAATTAAAAAAAGCTGCATTGTTACTCAAATGACATCTTTTTC[A/T]GGTACAAGACTACTTTTCAGGTCCAAGCATTGGCACCAGTGAATGAAACT
Long Flanking Sequence:
TTTGCACTTTGTACAAATAAAATAAAAAAAGACTGATAGTATCTCGGCAAGGAAGATGTTTTTTGGATTTAATTATATTAACTTTGCAATCACTGCACAATTCACATGTTTTCAGCAGTGGCTGCTGGTGAACTATAATCCCGACAATCTCAACATTGCAGATCATCTAATGTGACTTTTGTGGGTAAACATTGCGATACTGATGCTGATATGATATATTGTGCAGCCCTAGTACAATTATTGTATTTATTATTAGTTCATGTTACTAAAATACATTAACTCACATTAACTAATGAAACCTAATTGTAAAGTGTGACCAAATTTAGAGCCTTTGCATTTGATTTTCTTCTTTACTTCAGCTTCAGGAAACACTGCAGAGATGCAGAATGGATGTTTGGAATATTGTGATAAAAGGAGAACCAAAGTAAGTGTCCCAACATGAAAAAAATGTAACATGCAATTAAAAAAAGCTGCATTGTTACTCAAATGACATCTTTTTC[A/T]GGTACAAGACTACTTTTCAGGTCCAAGCATTGGCACCAGTGAATGAAACTGCAACAGAGAGGCTGATTTTTGAGCTCTTAACACAAGGATACATTAATGCTTCCATAGCAATCAGTGTCCCGACTGGTGAAGTCAACATTACCCAAATAGGTACCGCCTGGTTTTTACCTTTCATTGATGACCTGTCAAAATAAATCATAGAAATGTATTTTAATAAATCACAAACTGTAAAACAGAAAGTTAAAATGTGTTGTGTCTAAATGAAAGCTATTTACTGCTGCAGATCCAGGCCTTTGTCCAGAAGAAGCTATGCTCACAGTTTATGGTATGTACATGTGGCCCAGCATGACAGCTCAAAGCCAGTACGAACTCACGTGTGTGAAAGGGAATGAAAGTGCTACGAGATTTTGGTAAGTACTACACTTTGTATTTATCACTGATGCAAACAACACTGGTTGATTTTGTTTCTTCAGAGAAGTTTTTTTCTCCTCATGTTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44809
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000128379 Splice Site, Nonsense 559 1201 14 26
Genomic Location (Zv9):
Chromosome 14 (position 32604150)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 31393957
GRCz11 14 31734271
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTGATGGATTTGCATTAATACATTGTGATGTTTTCTCATTCCATTCAG[T/A]AAATTAAACGGGGCAACTGACAAAGCTATTTGGGAGGCGCCAGATATGAG
Long Flanking Sequence:
TCGCTGATTCGAATCTCAGATCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCTCTGCTAATATGTTGAGTGCATGTTCTCCCTGCATTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCTACAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCCATAGTGTATGTGTGTGTATGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCATAAAAATGAGCTGGATAAGTTGCTGGTTCATTCTGCTGTGGCGACCCGGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAGTGTATAGTGGTCAAAAACACTGCTATTTATAATATAAATTACTAAAGTAATTTTTTATATAAAATGAAGTAGAATTAGATTTAAAACCCTGTTGTCCATTTCCTTCATTACCATGGGAAAGTGATGGATTTGCATTAATACATTGTGATGTTTTCTCATTCCATTCAG[T/A]AAATTAAACGGGGCAACTGACAAAGCTATTTGGGAGGCGCCAGATATGAGCAAGTGTTTAAAGACTGTATCAGATTTTGGTGATTTGGAAAACATTACAGTCACACCTGGTAAGTTATCAGTGTGTGCTTTTATTGGCTTAAATGTTTAAAGAAGGATTAAATTAATCTTTTATGACCTTCATTGGTTTTTAGGTAACTCAGAATACATTGTGGACATGATTGAGGATTTGTTAAATGAACAAACTGGTCTGAGTAATGCTCAGCTGGACATCATGCTGGAAAAACTCTCCGAGGTCACTGAGGTGGGAACCCTGACCCCAGATCTGTCCAGCAGCATCACTAACATAGTTTCAGAAATCTGTCACATTACAACTAATCTCACCCAGGTCACCAACAAGTAAGTATGAATGTATTTCAGGAAATTCTGTGCCATTGAAATACATAATCAATAATTGATTTTAAAATTAATATTCTATCATCATTTACTCAAATACATGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28329
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
ENSDART00000128379 Nonsense 904 1201 22 26
Genomic Location (Zv9):
Chromosome 14 (position 32615528)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 31405335
GRCz11 14 31745649
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTTCTGTATTTTTCCTCACACATGTTGTTTTACCACAGGAAACTGAGA[C/T]GAGACTACCCTTCCAAGATCCTTATTAACCTCTGCATGGCCCTGCTAGGG
Long Flanking Sequence:
ATGATTTCAACGCAAGTCTTCGTACATGAGGCCCCAGGTGCGAATGGCACTCGCGAGAGAAATTAGAGATCTGATAAAGCATACAAAGCTACTTTCGCAAAATCAAAAACTGGAAAAAAACGTATCTCTTGGGACATATTTGGCGCTTTCCAGAAATGCATATAGGGCTACGTTTTCAGAATAAGTCTGGGTTGCAACCATAGTAGGAAAAAAATACCACAGAAGTCCGTTTCCAGCATTCTTCAAAATATCTTATTTTTTGAGCAAAAAAGACCAACAAGTTCAGTAAACAATGACATCATTTTCATTTTTGTGTAAACTATCTCTTTAAGCAGCTTAAATAGATAAGTATCAGCTTTCATAAAAATGCTATTACTGATCAAACAGTTGAGAAACTAAAAGACTTCAAATATTACTGGATGTAATACCACAGAAAATGCATGTTTCGCTGTGTTCTGTATTTTTCCTCACACATGTTGTTTTACCACAGGAAACTGAGA[C/T]GAGACTACCCTTCCAAGATCCTTATTAACCTCTGCATGGCCCTGCTAGGGTTGAACATGTTGTTCCTGGTGAACTCCTGGTTTGCCTCTTTTAACAGCAATGCCCTTTGTATCACCGTAGCAGCCTTTCAACATTACTTCTTTCTGGCTACCTTTACTTGGATGGGACTTGGTGCAATCAACATGTATCTGGCCTTGGTCAAGGTCTTCAACTCATATGTGCCGTCTTACATCCTCAAGTTCTGTGCAGTTGGATGGGGTGAGACAGCAAGTTTTGTAATCACGTACACTTTAGGTGTGGTCACATTTATCCTGCTATGCGAACTTTTGTGGGGAAAATCCAATAATGATGTGTGCAATCATGAGTTTTGCATGAGCTTGAGAAAGTTTGTTGTGCAGACTCTGTTTCAAATTGACCTGAAATGCTTTAAGCACTGAAATCATTATGTTGACTAGCAGAAAAGATCCTTTTGTTTGAGTAATTCTTATCTATCTCCATTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22507
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
ENSDART00000128379 Nonsense 1056 1201 24 26
Genomic Location (Zv9):
Chromosome 14 (position 32618054)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 31407861
GRCz11 14 31748175
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCCTGATCATGGTCTGTAATATCATCGTGTTTGTCGTGGTACTGGTA[C/T]AAATCCACAAAATGCGGGTCAACAAGCCTTCCAGCAGCAGAAAAGGGTTC
Long Flanking Sequence:
CTTTGGACTGTGGGGGGAAAACTGGAGCGGCACAAACACGGGGAGAACTCCACACAGTATTGCCAACTGGCCCAGACAGGATTCAAACCAGTGACCTTTTTGCTGTGAGGCGATAGTGTAAACCACTGAGCCACCATGCTGCCCAATTTCCAATTTGTTGGAGTCAAAGCTCTGTTAGTTCAGCTAATGAATAAGCAATAAAAACACAAGCTCATTCTCACAGGAAAACCACACATGCATCCCATTGCTTTACATGTTAAAAATCCCATGTGAAAGATTTATGATTTTAACGTGAAGCTCATGTGATGTTTTTCTGTATGGATTATTATAGTTAGTTCTTATTATTAGTGTTCTTTCTTGAACATTGTCGTCATATACCATCTCTTTTCATCCTTTTCAGCTGCTGGTTTAAGAATGACGTGACCTTTTATGTGACGGTGGTTTCGTTCGCCATCCTGATCATGGTCTGTAATATCATCGTGTTTGTCGTGGTACTGGTA[C/T]AAATCCACAAAATGCGGGTCAACAAGCCTTCCAGCAGCAGAAAAGGGTTCCTGCATGACCTTCGAGTGGTGGCCAGCCTAACCTTCCTGCTGGGACTTACCTGGATACTAGTCTTCTTCGGTTGGGGCCCAGCCAAAACACCCCTGATGTACCTGTTCTCCATCCTCAACAGTCTTCAAGGTAACAAGAGCTTCTAATGCTCAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAATAAAAGCCACAAAATTGTATGTATTAGCACATTTGTGATTATAAAGGATCATATGGGAACATAAGCAGAAAAAGCATATATTAATCTACACTATCTGACAAAAGTCTAGTGGTTGATCCCAGTTGTAAAACCAACATATGATAACTTGACTTCGAGTTGATCATTTGGAAAAGTGGCAGAAGACAGATTTTTTAGATGAATCATCTGCTGCATCCCAATCATCACAAATACTGCAGAAGAACTA
Associated Phenotype:
Not determined