ZMP
gpr107
Ensembl ID:
ZFIN ID:
Description:
protein GPR107 [Source:RefSeq peptide;Acc:NP_001073515]
Human Orthologue:
GPR107
Human Description:
G protein-coupled receptor 107 [Source:HGNC Symbol;Acc:17830]
Mouse Orthologue:
Gpr107
Mouse Description:
G protein-coupled receptor 107 Gene [Source:MGI Symbol;Acc:MGI:2139054]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33644 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2241 | Nonsense | F2 line generated | Not yet available |
| sa40480 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33643 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa40479 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33644
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000098036 | Nonsense | 7 | 543 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 34107656)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31889605 |
| GRCz11 | 5 | 32489758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTCTTGTTTGTTGAAGCGGTTTTAAAAATGGCGTCCGGAAAGATGTG[T/A]ATGTTTACAGTTATTAATGTGATTATTATAGTGCTTGTCATAGAAAGTCA
Long Flanking Sequence:
ACGCCGGTAGCATGTGATGTTGTCACGAAGCGCTTTACGGCAGAATTTAAACATTTTCCGATTGGTTCGTTCCAATATTATTTTACGACAGTTTCACGCAACATTTTTTTTAAAGCTGTTTATTCATATCGCATTTTAATTTTGTGTGTAAAAACGGAATGTGACGAAAACAAAAATAAATATTTGAAAAAAAAAACATTTTTATATATTTGTGAGACGGTTTTAATTTGGTATGAACGAAACTTTTCTTTGTTTTACCCTTTGGAAGACAAAAACAAAGACACATTTTACAGTCTATACATTATACGCAGGTACACAAACCCAAGTTCACCACACAAACCCGTTTTCTTTTATGTTGTTCGTACTACGTGGTTTCACAACTTTTCCTTTCTTCCATTAGAGGTCGTTCTTCATTTGAATGCGTGAACCGGAAATAATAGTGAAAGTGACCTGCTCTTGTTTGTTGAAGCGGTTTTAAAAATGGCGTCCGGAAAGATGTG[T/A]ATGTTTACAGTTATTAATGTGATTATTATAGTGCTTGTCATAGAAAGTCAGTGTCGAATCCATCATCTTGTACTCAAGGTATGTGTCTAGCGTGCTTTGGTTGTTTTGTAGGACGTTTGTATTGTCGCTGTATTGTCATGACTGCTCAATGCAGAAACAGATGCTCTCTTGTGATTATCAGTCACTCGCTGTGTTGTGAGATAATGCAAATGATGTGAATCAGATTATTAAAGCTGATTTCATCAGCTTCTGATCAATTGTTCTGTCGCAGGATGACATCCGTCAGCGGGTCCACCTGAACACTTTCGGCTTTTATAAAGATGGTTACATGAGTATGAACATGAGCCACCTCAGCTTCACTGGTGGCAAGATGGACAACATTGACAGCTCCACGGTCAGACTTTCACCTCTGTCAAATCAATCACACGCTGAAATATATAAATACGATAGAAACAACGCAATATGAAAATTGAAATAAGAAATATAAAAAAGTTTCATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2241
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
|---|---|---|---|---|---|
| ENSDART00000098036 | Nonsense | 183 | 543 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 34103011)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31884960 |
| GRCz11 | 5 | 32485113 |
KASP Assay ID:
554-3162.1 (used for ordering genotyping assays)
KASP Sequence:
GAACAGATATAGATTTTTCCCTTTCCCTAGAACAAGGCAGAAGATACCTA[T/A]CCTCTTCAGTACGAAGATAACGGCTACTCCTTCCAGGTAGGASRTGCATG
Long Flanking Sequence:
TATATATATATATATATAAATGTGTAGTGTATTTAATCATAAAACACAAGTTCCAGGAAAAGTAAAAGTTATTTCTGTAAAGAACACTTTCTTTCCTATTAATTATAATAAAATATTGATATTGTATGATATGAGAAAAGAAATAAATGTCTCTGGTGCCCAGCCCTAGTACCAGAAATTAAATGCACTTTAAACCCTTTGCAGTGTTAATTATATCAGCTTTGTTATCACAAAATAAATGGCATTTTAAAACTTTTAGCAAGTGTTAATGTGTTAAGTTTGTCTTCATACACAGCCAGTGTTTTGATTTATTTTTGTCCTCTTTATTTCCAGCAGCTTCTAAATCCAAGCGTGATGCTGAGGTGAGATCTGCTTAAACTTCAACATTTTTTAAAATTGTTTGACTCTGCGTAATAATAATAATATCCTCTTAATATCTTAATTCTACATGAACAGATATAGATTTTTCCCTTTCCCTAGAACAAGGCAGAAGATACCTA[T/A]CCTCTTCAGTACGAAGATAACGGCTACTCCTTCCAGGTAGGACGTGCATGAACTAGTATTGTTAAGAGCTCATGGGGCTATGAAGGCAAACAGGCCATTTCTGATCAGAACTGGAGTCTGTAGATTTATTTATTTATTTTTTATTTTTTGAAGTCTTCCCAGTTCTACATCCACTGACTGACCTCTTTTTGTTTTAGTTTTACTTCAATGTCACTACCGATGAGCAGCAGGGCCTTTATAACTTTTACTTCTACAACTGCTACTCTTTGCCAATGAACCAGGAGAGCTCTGTGTCAGACATGCTGCCTTTCAGCATTGAAGCAAGTGGTTTTCTGCATATTATCCATCAGTACAATTAATGCATTTGTTCAGGTTATAATCAGGCAATGATTCTTATTTCAGATTACAATCAAGGAGAAGAATCCAGAGAGCTTCCTCTCTGCAGGAGAGATCCCTTTGCCTAAGCTTTACATCTGCATGTCCATCTTCTTCTTCCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40480
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098036 | Essential Splice Site | 281 | 543 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 34102473)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31884422 |
| GRCz11 | 5 | 32484575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTTCCTCATTGGCATACTGTGGGTTCATGTTTTGCGGACACATAGG[T/C]AAGTCTTGTGCGTTATATCTGACTTCACGCACACATGCTATAAATGACCA
Long Flanking Sequence:
TAGGACGTGCATGAACTAGTATTGTTAAGAGCTCATGGGGCTATGAAGGCAAACAGGCCATTTCTGATCAGAACTGGAGTCTGTAGATTTATTTATTTATTTTTTATTTTTTGAAGTCTTCCCAGTTCTACATCCACTGACTGACCTCTTTTTGTTTTAGTTTTACTTCAATGTCACTACCGATGAGCAGCAGGGCCTTTATAACTTTTACTTCTACAACTGCTACTCTTTGCCAATGAACCAGGAGAGCTCTGTGTCAGACATGCTGCCTTTCAGCATTGAAGCAAGTGGTTTTCTGCATATTATCCATCAGTACAATTAATGCATTTGTTCAGGTTATAATCAGGCAATGATTCTTATTTCAGATTACAATCAAGGAGAAGAATCCAGAGAGCTTCCTCTCTGCAGGAGAGATCCCTTTGCCTAAGCTTTACATCTGCATGTCCATCTTCTTCTTCCTCATTGGCATACTGTGGGTTCATGTTTTGCGGACACATAGG[T/C]AAGTCTTGTGCGTTATATCTGACTTCACGCACACATGCTATAAATGACCAGTAGAGAGCAGCAAAATCATGTCTTTGACTGTTTATTATAAAATTGGTAATGCAGATTTCTAAATGTGCTTCTCTTTTGTGTTCTAGTGCTGATGTTTACAAGATTCACTGGTTGATGGCTGCTCTTCCATTTACAAAGTCGCTTTCCCTTATTTTCCATGCTGTGAGTTTAATCGTGCTTGTTTATTTGTCAGTCTTGAAAGATGGTTTTTTTATGTGTAACAAAATTCAGCAAATTAGTGGAAATATGATTAATATATAGTTTCATTTTTGTCTTTGAACAACTACGGTTATAGCATTACATTGTTCTTGTTTTAACAATTCTGTTCCTATATTACAGATTGATTACTACTACATTTCCAATCAGGGATCTCCTATTGAAGCCTGGGCTGTGGTCTATTACATTACTCATTTGTAAGTTCTAATCGGTTCAGCCAGTGTTTCTAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33643
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098036 | Essential Splice Site | 445 | 543 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 34090490)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31872439 |
| GRCz11 | 5 | 32472592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCATCAATCTGGCTCAACTGAAACTATTTAGGCACTACTATGTGATGG[T/A]AAGTATTCACCAGAACACGCCCCTGATGCTCAGATCTAAACAGGCCAGAA
Long Flanking Sequence:
TGCAGCTATGGTGAGCAGAGTAGGTCTCTTCTATAATATTCTAAAATATAAAATAAATATCTCCAAAAAAAAAAATCTTACTGACCCCTAACATTTGACCAGTATATAGTGTATACTTTAGCACCATTATATGTTGCGTTGGTGAATAATTATGACTTCATATGATCTTACGTGGGATAGCAAATATTCCCTCCAGACAATCACCATTCTTTTTTCCCTCTCAAATAATCACTGTTTTATTGCTGCCTATCACATTTCATCTTTTCATCTTCTGGCCGTCCCTCGCAGGGTGAGAAGATATAGACTTTGATTGCTTTCTGATTTTTAACAATTTTCACAGCAGGAGCGAGAAGCACAGTAATTGAAGCATGAAAGGTAAAAGGACAGCTCATCCCCTCTCCCGCTCTGTTTTAATCCTAATGTCTGGCCTTTTTTTTCCTTTTTTTTAGCTGCCATCAATCTGGCTCAACTGAAACTATTTAGGCACTACTATGTGATGG[T/A]AAGTATTCACCAGAACACGCCCCTGATGCTCAGATCTAAACAGGCCAGAATACTATGACTTTTTAATTAGGTTTATTAATTCCATGGTTACACTTTCTCTTCAAGTGCATGTAATTATGATGGTCTAGATATTATTATGAATAGTGTTTTTGTTTTTTTACTCTCAATTTAAAAAGAAAAGAAGTACTTACTACATCACAATTGCAGGGAAATATTGAGAATTCTGATAAAAAAAAGATTATGAAGTATAAACTCAGAATTGAGAGATGAAAAGTTGTAAACTCCGAGTTGGATGAAAAAGCTCAGGTCTTAATTTTTTCTTAATCTCCGTGATTGTTTCACATATTGCTTTTTTGGGTTATTTCACATAACTGATTTGTATATCTTGCAACTCTGATCTTATAAGAGATTTTCTGTGATATGAACTCGAGATAAAAAGTCAAAATTGTTGAGTTAATAAAGTTAATAAAGTGTTTTTACTGCGATGACGACAGTTCAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40479
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098036 | Nonsense | 470 | 543 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 5 (position 34089579)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 31871528 |
| GRCz11 | 5 | 32471681 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCATCATTGCCAGTCTCATCAAGGTCATTGTTCCTTTCCAGTGGAAGTG[G/A]CTTTACCAGGTGAGTGACATACAGAAAAGACCTGTTTTATAAGCATGAAT
Long Flanking Sequence:
TTTCTGTGATATGAACTCGAGATAAAAAGTCAAAATTGTTGAGTTAATAAAGTTAATAAAGTGTTTTTACTGCGATGACGACAGTTCAGTTTTATCATTTGTTTAATTGTTGTAGAAACATTTTAATTCATTGATTTGTACTTGCATGCATATCAGCAGTATTTTTTAATAATGCTTTTATGGAAGCAAGTTCAGAAAATCAATGTCACATTTACATAGAATTATTTAATTAGTGACTTAAATAGTCTTCATTTTTATATAAAAAAATAATTTTTTATAATAAAGCTTAATTTTTGTTAGTTTTGTCTATTTATTGATTGATTGATTGATTGATTGATTGATTAATGGATTGATTGATTTTATTTATTTGATATGATCAAATGATCTCACTTTTATTTCTTCTTAATATGTTTTTCTGGGTTGCAGATTGTATGCTATATTTATTTCACCCGCATCATTGCCAGTCTCATCAAGGTCATTGTTCCTTTCCAGTGGAAGTG[G/A]CTTTACCAGGTGAGTGACATACAGAAAAGACCTGTTTTATAAGCATGAATATACTGTACCTATCAATCTCTTCAGATAGAAAATAATTACGCTCTATTGGTAACGTATAACTGTTTTACAATGAAACCGAGGCTGAAAACGTGACATTTGCTTTTTTCTACCAACTGATGTCCGGTTTAGTTCTCTTTTTACGAGTCCACCTGCATCTGAATTGGCCAGTGTTCTTGTACCATGAAGGAAAAACTTTTTTAAAATTGTGTATTAGGCCAATTGTGTATTTATTTTTTCTTATTTATTTTTTTTTTCCAGTAGTTCACTTCATAAATAAAGCCTTGAGCAGACTAGTAACATGCTCTAGTAAGCATGCTTAAATATGCTCTTGTAAGAGTCATAGATTTATTTTGTAGCTAAATGTAGCAGTCTTCATACTCTGGATAACAAATTACCTTTTCAAGTGTGTACACTTTCGTGTTGTCCCGGGAGAGAACCCTGAGCTCGGA
Associated Phenotype:
Not determined