Busch Lab

ZMP

gpr137c

Ensembl ID:
ENSDARG00000045289
ZFIN ID:
ZDB-GENE-041114-145
Description:
integral membrane protein GPR137C [Source:RefSeq peptide;Acc:NP_001007434]
Human Orthologue:
GPR137C
Human Description:
G protein-coupled receptor 137C [Source:HGNC Symbol;Acc:25445]
Mouse Orthologue:
Gpr137c
Mouse Description:
G protein-coupled receptor 137C Gene [Source:MGI Symbol;Acc:MGI:1917963]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa23023 Nonsense Available for shipment Available now
sa36358 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15519 Essential Splice Site Available for shipment Available now
sa42893 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23023
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
ENSDART00000066604 Nonsense 79 433 1 7
Genomic Location (Zv9):
Chromosome 17 (position 14807326)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14958154
GRCz11 17 14966087
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACGGACACAAACGCTTCAGCTACCAGAGTGTTTTTCTCTTTCTGTGTT[T/A]GCTCTGGTCTGCTCTGAGGACGACGCTCTTCTCTTTTTACTTTAAAAATG
Long Flanking Sequence:
TGCCTTGCAGAGATTGGGGGCTCTGCTGTTTTTTAATTACTTGTTTTCCCAATTTTTGGTTACAAACATCTGAGAATTGTTTTAAAGTCTGTTCAATACGATAATAACTTAGGGTAGGCTGTAGTTTTATTATTTTCCGCTCATGTGTCATTTGTAATTAAGTTTGACGTTTTTCAGTGTTTGTATCATTTCAAAACATCTCCATGAAAAGTTTTGGACAACTCGTTTTGGATAAGTCGGCGTGATAGCGAGCCATCGTGTCGATATGTTGTTTTTACTAGAAAACCAGGTCAGTGTCAGTGTTTGGACGGACTCATCCTCATCATCCTCCGCCGAACTGATCCAGGCTGCGGTTCCCCCGTCCGTGCAGCTCGGTCTCACTGTTCTCTACACGGTTTTGTATTCGCTCCTCTTCGTGTTTGTTTACCTGCAGCTCTGGTTGATTCTGCACTACGGACACAAACGCTTCAGCTACCAGAGTGTTTTTCTCTTTCTGTGTT[T/A]GCTCTGGTCTGCTCTGAGGACGACGCTCTTCTCTTTTTACTTTAAAAATGTTGTTCAAGCAAACCAGCTCCAGCCTCTGCCGTTCTGGCTGCTGTATTGTTTCCCAGTCTGCCTGCAGTTCTTCACCCTGTGTCTGCTCAACCTTTATTTTGCTCAGGTAAGTGCTGTTTTCCCAATGTGTTTGTGTCTCGCAGTGTGTTGCACAACGTCTTTATGAAAGCAGGTAGTCTAAGTAGCATGTAATCTACCATAGAGAGGAAATGAATAATTGTGCGTTCAGTCTGATAGCCATTTTCATGCAACTCGCATCTAAGTGGGTCCCCTCCCACCAAATGTGTTTACTTCATGTGACTGACTGGAACTTCACGCTGTAATTGCGATTAAAACCAGAGGTGTATTGTTATAAAGTCAAATTATGCTGCTTTAAACAATCAAAGACATTTGACATATCCGTGATAGTGTAATAAGAGCACAGCTGGAGGTCATCAGTTTCTGTCCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36358
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066604 Essential Splice Site 131 433 1 7
Genomic Location (Zv9):
Chromosome 17 (position 14807484)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 14958312
GRCz11 17 14966245
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGCCTGCAGTTCTTCACCCTGTGTCTGCTCAACCTTTATTTTGCTCAG[G/T]TAAGTGCTGTTTTCCCAATGTGTTTGTGTCTCGCAGTGTGTTGCACAACG
Long Flanking Sequence:
TAAGTTTGACGTTTTTCAGTGTTTGTATCATTTCAAAACATCTCCATGAAAAGTTTTGGACAACTCGTTTTGGATAAGTCGGCGTGATAGCGAGCCATCGTGTCGATATGTTGTTTTTACTAGAAAACCAGGTCAGTGTCAGTGTTTGGACGGACTCATCCTCATCATCCTCCGCCGAACTGATCCAGGCTGCGGTTCCCCCGTCCGTGCAGCTCGGTCTCACTGTTCTCTACACGGTTTTGTATTCGCTCCTCTTCGTGTTTGTTTACCTGCAGCTCTGGTTGATTCTGCACTACGGACACAAACGCTTCAGCTACCAGAGTGTTTTTCTCTTTCTGTGTTTGCTCTGGTCTGCTCTGAGGACGACGCTCTTCTCTTTTTACTTTAAAAATGTTGTTCAAGCAAACCAGCTCCAGCCTCTGCCGTTCTGGCTGCTGTATTGTTTCCCAGTCTGCCTGCAGTTCTTCACCCTGTGTCTGCTCAACCTTTATTTTGCTCAG[G/T]TAAGTGCTGTTTTCCCAATGTGTTTGTGTCTCGCAGTGTGTTGCACAACGTCTTTATGAAAGCAGGTAGTCTAAGTAGCATGTAATCTACCATAGAGAGGAAATGAATAATTGTGCGTTCAGTCTGATAGCCATTTTCATGCAACTCGCATCTAAGTGGGTCCCCTCCCACCAAATGTGTTTACTTCATGTGACTGACTGGAACTTCACGCTGTAATTGCGATTAAAACCAGAGGTGTATTGTTATAAAGTCAAATTATGCTGCTTTAAACAATCAAAGACATTTGACATATCCGTGATAGTGTAATAAGAGCACAGCTGGAGGTCATCAGTTTCTGTCCGAGTCCCACAACAGAGCATTTCACAGGACAGTCTGAATGAGGTCTATTATTGACACTTTTTGGTCCATCCTTCCACCCTTTGTGGAGTTTTGGCAGTCTGTGAAAGCATAACCTCATCATACAGGGGATGAAATATTGTTTATCTTCTCAAAAGCTTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15519
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066604 Essential Splice Site 358 433 6 7
Genomic Location (Zv9):
Chromosome 17 (position 14852595)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15003423
GRCz11 17 15011356
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCGATGACGACCTGACTAGAAACGCATCKTCCAGAGGAGAGAGATGCAG[G/A]TGTGTTCTCTATTTTTTGTCTTTTCAGTGATGYGAGTGCTATTGTTTTAT
Long Flanking Sequence:
GCCTATAGGCAGATGCAGAGAAGATCTATGGTGAAGCCTATGTGGTGTTCGGGATCATCCTGTTCTTCTGGGAGCTGCTGCCCACCAGTCTAGTGGTGCTGTTCTTCAGAGTCCAGCGGCCCAATCAGAACCTGGTAAAAGTCTAATCCAGTCTCACTTCTCTAAATCCCCCCATCAATATCACAGCCAGACACTTACTCAATGAAGAGAGCCTGCAATTGGCATTTTTAGCCCCAGTAGAGAGCGGCTTTCCAGTCAGATACAATTAATTACTCGCGTCTAAAAAAAAACACATCCCATGCTGTTGTGCTGGTCACGTATGTTCCTGTCTATGTTGGGCCAAATAAGACAGATTAATTTTGACTTTGTATGCAGACGCCAGGCGGGATGATCAACAGCCACAGCTTCAGCTCCAGGGCGTATTTTTTTGACAACCCACGGCGGTACGATAGCGATGACGACCTGACTAGAAACGCATCGTCCAGAGGAGAGAGATGCAG[G/A]TGTGTTCTCTATTTTTTGTCTTTTCAGTGATGTGAGTGCTATTGTTTTATTGTATTTTGTATGTATATTGTGTTATTTATTTTCTTTTAAACCTCTAGCTCTATCTTTTAAAAACATTTTCCAAGTGCCGTTTAACCGAGAGATTTGTTTTCAACACATTTTAAACTGTAATAGTTTGAATTACTTATTTCTAGGGCCAGACAGAATCTGTAGACATTTTTGGCTATTTCTGTGCAGAATTTTGTAAAAAACCTTTTGCAAAGATTTCAATGATGTCAAAGGCTCAAGAAAAGATTGGTTTTCTGAATCGACGGCAGCTTAAACTCACATGATTGATGTTCTGTTTTCCAGCAGTATCCTGTCATCCACACCACAAACGGGCCAAAGTTGGTACGGCTCCATCCAGAGAAACAGCAGCCTCTCAGCCATCCCATACCTGAGCAATGGCCCCCAAACATCCACCGCACCGCTTCTCTTCGCTTACGGCACCAACCAAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42893
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000066604 Nonsense 372 433 7 7
Genomic Location (Zv9):
Chromosome 17 (position 14852989)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 15003817
GRCz11 17 15011750
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCAGCAGTATCCTGTCATCCACACCACAAACGGGCCAAAGTTGGTA[C/A]GGCTCCATCCAGAGAAACAGCAGCCTCTCAGCCATCCCATACCTGAGCAA
Long Flanking Sequence:
ACAGCCACAGCTTCAGCTCCAGGGCGTATTTTTTTGACAACCCACGGCGGTACGATAGCGATGACGACCTGACTAGAAACGCATCGTCCAGAGGAGAGAGATGCAGGTGTGTTCTCTATTTTTTGTCTTTTCAGTGATGTGAGTGCTATTGTTTTATTGTATTTTGTATGTATATTGTGTTATTTATTTTCTTTTAAACCTCTAGCTCTATCTTTTAAAAACATTTTCCAAGTGCCGTTTAACCGAGAGATTTGTTTTCAACACATTTTAAACTGTAATAGTTTGAATTACTTATTTCTAGGGCCAGACAGAATCTGTAGACATTTTTGGCTATTTCTGTGCAGAATTTTGTAAAAAACCTTTTGCAAAGATTTCAATGATGTCAAAGGCTCAAGAAAAGATTGGTTTTCTGAATCGACGGCAGCTTAAACTCACATGATTGATGTTCTGTTTTCCAGCAGTATCCTGTCATCCACACCACAAACGGGCCAAAGTTGGTA[C/A]GGCTCCATCCAGAGAAACAGCAGCCTCTCAGCCATCCCATACCTGAGCAATGGCCCCCAAACATCCACCGCACCGCTTCTCTTCGCTTACGGCACCAACCAAACCAACCAGCACCACAACTACTACTCGACACCCCAGAACTACTACTCCAGCTCTCAGACACACTACTCCACCCCTCAGAACTAATGGATCATCAAGACTGAGGTTTGGCTTTACTGTTGTCTTCCCCCTCAGCCATTTCATCCTCCGACATCAGTGTTGAAGGATTCAAAAGGGACCATATGAAGGTAATCTGGGGGAGGGGTGTTTGTTAGGACCAAAAGGAGTAGCTTTTTCCTCTTATTTGATGTTCTAATTTCCCAAAATAAAATAAAAAACATCAATCCTATCGCCTCTCCAGTGGCGCATTGAGAGCCTTCAGCACATGGACTCCACTCTGTGAGTTGGGATGTGCTTTTTGCACTTATTATGGGCCTGCGTTTCATATTTCGGGTCAACTG
Associated Phenotype:
Not determined