Busch Lab

ZMP

gpr133

Ensembl ID:
ENSDARG00000053344
ZFIN ID:
ZDB-GENE-041212-24
Description:
G protein-coupled receptor 133Novel protein similar to H.sapiens GPR133, G protein-coupled receptor
Human Orthologue:
GPR133
Human Description:
G protein-coupled receptor 133 [Source:HGNC Symbol;Acc:19893]
Mouse Orthologue:
Gpr133
Mouse Description:
G protein-coupled receptor 133 Gene [Source:MGI Symbol;Acc:MGI:3041203]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa41283 Nonsense Mutation detected in F1 DNA Not yet available
sa34472 Nonsense Mutation detected in F1 DNA Not yet available
sa31670 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa41283
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075372 None None 240 None 8
ENSDART00000110688 Nonsense 128 485 5 12
ENSDART00000134073 None None 240 None 9
ENSDART00000146152 Nonsense 27 186 1 3
ENSDART00000148358 None None 359 None 11
Genomic Location (Zv9):
Chromosome 8 (position 46213199)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43930290
GRCz11 8 43923709
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTATCTGAACGGCGATAACGGGGCCACTTTCCTTCACTTTGGCAACTA[T/G]AAGGACTCCTGCATTAGTGATCCTACTCTCTGCGGACCTGCTGGTGAGTT
Long Flanking Sequence:
GGATGAGGGTCGGTCAGTCAATCGGTCGGTCAGCCAGCAGTGGCCTCTGGTGGATTTACGTGAGAACAGCAAGTGCGAATTGCACTTGCAAGAGAAATTTGAGGTCTTAAAAAGCGTACACAACGGCCTCTGGGGGATTAGCGAAAACAAAAACTGCAAAAAACTTAGCTCATGGTACGTATTTGGCGCTCTCCAGAAATGTTTATATCAGTATGTTTTCAGAATGAGCCTGGTTGTTAAAGTGACTCCAGGTGGCTCAATAATATAGCCTAAACTGGTATTTAAACTAAAGTGTTTCCAAAATCATCACTCAAAGGCTTTACATTTCAAAACAACAAAATTAGGCCCTTGCTGTACTGCACTGCTTTCTGAAATGAATTTCAAGTGTTATAATCTTGCTGGTTGCTTTCTCGTAATGTAGACATTGTAGAAGGAATGGTGAATAGAGGCATCTATCTGAACGGCGATAACGGGGCCACTTTCCTTCACTTTGGCAACTA[T/G]AAGGACTCCTGCATTAGTGATCCTACTCTCTGCGGACCTGCTGGTGAGTTTTTATTGTCCTCATTCACCCTTTTGCTGTTGATATAGAAGCACACTGAGATCTTTATATGGTCATAGATTTGTTGCTCAGGTTTATAGGTGACGTAATAAAGGCTAATGATTCAAAATTAAGTTTATATTTCTCAAGAGTAAATATATCAGCTTACATCAAGCGTTTCTGTGCGTGAAAGCTGAAATCATCTGTTATTCATCTGCTCACATCAGCGTTCGTTCCTTTGCTCCCAAAACTGAGAATATGTTGTGTTTATGTTTATTTTCCAGGGCTTGACCAAAGTAAGCCTTGCGATATTGTTTGTGATGGAAGCAGGCTGGATCTAATAAAGACGGTTTTGTTTAAAGATAGATATCTACATATCGGAAAAACTGTTTGGTGATAGCCAGAGGATTATGAAAATCTGATTAAATGTATTGATACATAACACTTTAAGTCATTTATTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34472
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075372 None None 240 None 8
ENSDART00000110688 Nonsense 164 485 6 12
ENSDART00000134073 None None 240 None 9
ENSDART00000146152 Nonsense 63 186 2 3
ENSDART00000148358 None None 359 None 11
Genomic Location (Zv9):
Chromosome 8 (position 46214152)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43929337
GRCz11 8 43922756
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCTTCTGGAAAAACAATGACGACGAGTCTCGTTTTGCGATCGCATCC[G/T]GAGGTAAAGTCATCTCAAGCGGTTTCTCAGTCTACTCAAATCCTTATGGC
Long Flanking Sequence:
AATCTGATTAAATGTATTGATACATAACACTTTAAGTCATTTATTATTGTTTTGAATTTACGATACAATTATATTTAACAAAATAAACTGCATGAAAAAAATTATAAGGAAACTTATTTTGGAAGGATTAATACATTTATTAGAGCATCAAAATGTAGCCTAAATACTGTAAGATTGTGTACTTATTTTATGAAGACTATGCTTCTTGATGTGAACATGTCGTTAGAATATAAAACATGTGAAAAACTCTTTAAGTGATGTGTGCCACATGTGAGTGTACAATACGTGGGACCAGAAGCACACACTTTAAGTCGCTATTCTTGTTTAAAACTAAATTCCCAAGTTTCAAATTCATGTTTCATAATAATTCAATGTTTCATAATTGTGTCAAAATATCTTAGATTCAAAGCTAAAGCTTTGCTTGTACTCTTACACCAGGGATAACGTTCTCCTTCTTCTGGAAAAACAATGACGACGAGTCTCGTTTTGCGATCGCATCC[G/T]GAGGTAAAGTCATCTCAAGCGGTTTCTCAGTCTACTCAAATCCTTATGGCGGATATGTGGAGTTCTACACCAGAGGAGACTTCAAGACATGGAAAGCAAATATCGAACTCCCAGGTACTTTGGGTGTCTGGGGAAATTTCAGTCTGAGTTGTGGAATGTGTGTTTTAAAGCTTCTGAGTATTTTGCTGAGTATCTCTGAGGAAAAGAAAAGATTTCCCATGGTCTTGAAATTTTGTACACATAGACTCATTCTGGTTTGGAATTACAGTTGAAATTCGACCATAAATATTTCAAACATATGTAGTTTTGCGCATAATTACATTGATTACATCCAGATGTCCACAAAGTATGCGAGTCGATAGGCTTCAGAATAAACTTTCTCTGTTGAGCTTGACAGAGTTGTTTACACTTGTATCTGACTGAAAAGAAAAGGAAGCGGGAGTGAAAAGGTGACAAATCATTCAGCTCCCTAGAAAATAATCAATACGGTTTTTCAGTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31670
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000075372 Essential Splice Site 178 240 6 8
ENSDART00000110688 None None 485 None 12
ENSDART00000134073 Essential Splice Site 178 240 7 9
ENSDART00000146152 None None 186 None 3
ENSDART00000148358 Essential Splice Site 297 359 9 11
Genomic Location (Zv9):
Chromosome 8 (position 46314126)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 43829363
GRCz11 8 43822782
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAAGGGGTTCTTCATATTCCTGTTTCACTGTCTGTTAAACTCTGAGG[T/C]AAGTGTGTGTTTGTGCAGCTGTGACTGAAGTCTGTGCTGTGTATCTGGGG
Long Flanking Sequence:
AAAAAAAGCAATCTAGAAAGAAAAGTCACTAGACTTTTTTTCATGCTTATACATGTCTTTGCAGGCTGACGACCAAAGCAGTGGCTGTTCTTTTACCTATTCTGGGCATATCGTGGGTCTTTGGGGTTCTGGCGGTGAATGATCACTCTCTGCTTTTCCAGTACATGTTCGCAGTGTTCAACTCTCTTCAGGTCAGTTATCACTACTGTGTAACAAAACAGAGCTGCACAAATCACCACAGGTTTTACACAAACTGATCGATTTTCACATAGTTAGCGGCCTCCAAAGTCAATAGCATGTTGGCCAAACAATGACAGCTTTAAAAATACGAGACATAACGATGTTTGAAATGACTTTGGACCTGGACTGACTTGTAAGAACTGTTGCAGATGTGAATTGGAGCGCTTTCCACAACATTTAGCGTTATCTTTTGTTTTCTTTTTTTTTTTTCTCTAAGGGGTTCTTCATATTCCTGTTTCACTGTCTGTTAAACTCTGAGG[T/C]AAGTGTGTGTTTGTGCAGCTGTGACTGAAGTCTGTGCTGTGTATCTGGGGAAATGTCTGATGTAGCGAAGCAAACAGCATATGGCAAGCCGTGCTAACATTAACTCTAATAGCAAAACTATTGTATATATATTCATGCTAAAAACATTTTGGGATTTGATTTGTACAAAATAAAACAAACCAACCAAAAATTGTGAGAAAAAAATTATGAATTAAATAGCATAACAATTTAATTGTCTTCAAATAAACTTTACTAATTAAGCTTTACTAATTACTAATTGCTTTTCTAATAAGATCAACAGAATATTTACTTTTCAAGTACTAATAAACATCCAATATCTAAATAATAGGCAGGTAATAAGCCTTTAGTTATTAGTGAGAATTGATACTTAAAGAGCCCCTATCATGCTTCATAAAAGGTAATATTTTGTTTTTTAACAAAAATTAATTTGTTCCAAAACCCCTCCTTAGCATGAGGCTAATCTGCACTGATTGGTCCGA
Associated Phenotype:
Not determined