ZMP
si:ch211-124k10.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate leucine-rich repeat-containing G protein-coupled receptor family
Human Orthologue:
RXFP2
Human Description:
relaxin/insulin-like family peptide receptor 2 [Source:HGNC Symbol;Acc:17318]
Mouse Orthologue:
Rxfp2
Mouse Description:
relaxin/insulin-like family peptide receptor 2 Gene [Source:MGI Symbol;Acc:MGI:2153463]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38488 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40494 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa13404 | Nonsense | Available for shipment | Available now |
| sa2221 | Nonsense | F2 line generated | Not yet available |
| sa40493 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38488
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 |
|---|---|---|---|---|---|
| ENSDART00000113765 | Nonsense | 166 | 393 | 6 | 15 |
| ENSDART00000143448 | Nonsense | 96 | 622 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 37524862)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35306811 |
| GRCz11 | 5 | 35906964 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGTATAGAAACGATCTCCAAGAGGGCATTTTCAGGACTGGTCGCTT[T/A]GCGTAAACTGTGAGTAATCTGTGAATGAATGACTCACTTAATGTGTGCAA
Long Flanking Sequence:
TCCACTGGCGACCCCTGATTAATAAGGAGACTAAGCCGAAAAGAAAATGAATAAATGAATGAATGAAAGTATTACATTTTTTGAAAAGTCATTCTAACTCTAAACTTATGAATAGTAATTAGCATAAAAATTTAAAATTTCACTGTGATAAAGCCTCATTCAATTATTATGCCGACATAAACAGTGATGGAGAGAATGTGTCTTCACAGAAGCCCTATGTAATCCTTGAAGGTTTATTTTTTGTAATGACTGGTTAACCAAGCAGTGCTCCATCATGAAACAGTGTGGACTTGGTTTGCAGGCATTGCTTTATTATACAAAAACTTGGGATGCTCTGATTGATTATGCTGTTATTTAAGGGCCAGAGCATGTTTTAATAAGGTGAAAAATACACCGTGCATGAAAAAACCACTGTGAATATTTTTCCTGTCTCTGCAGACATTTGGAAAGCAACAGTATAGAAACGATCTCCAAGAGGGCATTTTCAGGACTGGTCGCTT[T/A]GCGTAAACTGTGAGTAATCTGTGAATGAATGACTCACTTAATGTGTGCAATTATATTAATGCCACGTGGCATCAATCCTTCTCAAAGCTCCAGCTGAATGTGTAACACTGATTATCTGTCTGCGCAATTATGAGCATCAGACACCTTTTTGTGCCATCAGTCAGTCTAAGGCTTTCATCATCTACGCATTCATCCTGTAAAAGAAAGCAATGTTGAAATGGATATAACAATGACAATGGTGGATTAGGCTTGGTTCAGGCAGAACGGATATCCATGATCAAAGAATGCATTTTAATGCATCCAAATGATGTTGTGTGTTCATGTGTACATACAGTAGGTACTTATTTCCAGAGGTCTGCCTCGATACGTACATAACTGTTGGTCTAATCAGCGTCATACTTACAATAATCAACCATATTGAACTTATTCTAAAATGCGGAAGTGCGCCTGTTTTCGGGATTGTCTTAGAACTTCCGTTTCAGTCGCCTATGGGAGAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40494
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 |
|---|---|---|---|---|---|
| ENSDART00000113765 | Nonsense | 372 | 393 | 15 | 15 |
| ENSDART00000143448 | Nonsense | 302 | 622 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 37506308)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35288257 |
| GRCz11 | 5 | 35888410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTGTTGAACAATTTCAGTTATTTCAAGCGTTTTGAATTCTGTGGATA[T/A]TCTCCAAATGTGCGGAGCTGCAAACCAAACACAGACGGAATCTCATCCTT
Long Flanking Sequence:
ATTACTTGACTGAGTTCACAAAACTCATCTGAATGGTCTGAAGTGTGATCTAGTTTTCAGATATTGTCCACAGCTGATCAAAGTGAAGATGATTTTCAGATTTAAATTTCAGTCTGTTCCAAACAACGGCATATATGACTGACAGTTGCCTGGACTATTCTAGACATATTTTTATGACATGCTTTTGACATTCTGAAACCTGACATCCTCAGTCTTCATGCACTTCATGATGCTAAAATAAAATGGTTAGGATACGCTTTTAAATCCACACGAATGACACAAGGATGAAAAAAAAAAATTATGACCAATTTTCACTTATGCATGAGCAAATCTAACCAATTGCAATTAAACGAACATTTATGAAGTTACATGTGATGATTAAGCTTTATATGATTGCTTTCTGTTATGTGTAAAACAATTGAGCTTTTCTGTTTGTCTTTTTCTGTCATTTTTGTGTTGAACAATTTCAGTTATTTCAAGCGTTTTGAATTCTGTGGATA[T/A]TCTCCAAATGTGCGGAGCTGCAAACCAAACACAGACGGAATCTCATCCTTTGAGAATCTGCTCGCAAACATCATTCTGCGGGTGTTTGTCTGGGTTGTCGCCTTCATCATTTGCTTCGGAAACATCTTCGTCATCTGTCTGCGGTCCTGTATTGCTTCAGAGAATCAACATCACACCATGGCCATCAAATCCCTTTGCTGTGAGTCTATTATACATCAAACATGAGCATGACACGGCCAATATCCAGCTCATATTCAACCCCAAACTCAAAAGATCAATCAGTCAGTCAAAACATTAAACTAAAGCACTTCACACACAAAAAATGCCATTCGCGATCTTCAGACATTTCAGATTGAAACAAGATTTTCAGCATCAAAAAAATCAGACTTGTTTTTATTCCATCATGAGCTCACTAGATTATAAAGTTGGACTTTGTAGGAAGGTTTAGAAATGTATTTTAATAAATATTGTTTTAGATACTAGTATAGTTCAGTTTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13404
Status:
Available for shipment
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:
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113765 | None | None | 393 | None | 15 |
| ENSDART00000143448 | Nonsense | 342 | 622 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 37506190)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35288139 |
| GRCz11 | 5 | 35888292 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACATCATTCTGCGGGTGTTTGTCTGGGTWGTCGCCTTCATCATTTGCTTC[G/T]GAAACATCTTCGTCATCTGTCTGCGGTCCTGTATTKCTTCAGAGAATYAA
Long Flanking Sequence:
CCAAACAACGGCATATATGACTGACAGTTGCCTGGACTATTCTAGACATATTTTTATGACATGCTTTTGACATTCTGAAACCTGACATCCTCAGTCTTCATGCACTTCATGATGCTAAAATAAAATGGTTAGGATACGCTTTTAAATCCACACGAATGACACAAGGATGAAAAAAAAAAATTATGACCAATTTTCACTTATGCATGAGCAAATCTAACCAATTGCAATTAAACGAACATTTATGAAGTTACATGTGATGATTAAGCTTTATATGATTGCTTTCTGTTATGTGTAAAACAATTGAGCTTTTCTGTTTGTCTTTTTCTGTCATTTTTGTGTTGAACAATTTCAGTTATTTCAAGCGTTTTGAATTCTGTGGATATTCTCCAAATGTGCGGAGCTGCAAACCAAACACAGACGGAATCTCATCCTTTGAGAATCTGCTCGCAAACATCATTCTGCGGGTGTTTGTCTGGGTTGTCGCCTTCATCATTTGCTTC[G/T]GAAACATCTTCGTCATCTGTCTGCGGTCCTGTATTGCTTCAGAGAATCAACATCACACCATGGCCATCAAATCCCTTTGCTGTGAGTCTATTATACATCAAACATGAGCATGACACGGCCAATATCCAGCTCATATTCAACCCCAAACTCAAAAGATCAATCAGTCAGTCAAAACATTAAACTAAAGCACTTCACACACAAAAAATGCCATTCGCGATCTTCAGACATTTCAGATTGAAACAAGATTTTCAGCATCAAAAAAATCAGACTTGTTTTTATTCCATCATGAGCTCACTAGATTATAAAGTTGGACTTTGTAGGAAGGTTTAGAAATGTATTTTAATAAATATTGTTTTAGATACTAGTATAGTTCAGTTTTGTCATTAAAGGTGCCATACTGCAGTGGTTTAATAAATTCAATAGTTCTTTGATATCTACATAGTGGGTTCATGGCAAGGGTAAGTTAATAAAATCTCTAGAAATGGTTTTATACATTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2221
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113765 | None | None | 393 | None | 15 |
| ENSDART00000143448 | Nonsense | 358 | 622 | 13 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 37506142)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35288091 |
| GRCz11 | 5 | 35888244 |
KASP Assay ID:
554-2779.1 (used for ordering genotyping assays)
KASP Sequence:
TCGGAAACATCTTCGTCATCTGTCTGCGGTCCTGTATTGCTTCAGAGAAT[C/T]AACATCACACCATGGCCATCAAATCCCTTTGCTGTGAGTCTATTATACAT
Long Flanking Sequence:
TATTTTTATGACATGCTTTTGACATTCTGAAACCTGACATCCTCAGTCTTCATGCACTTCATGATGCTAAAATAAAATGGTTAGGATACGCTTTTAAATCCACACGAATGACACAAGGATGAAAAAAAAAAATTATGACCAATTTTCACTTATGCATGAGCAAATCTAACCAATTGCAATTAAACGAACATTTATGAAGTTACATGTGATGATTAAGCTTTATATGATTGCTTTCTGTTATGTGTAAAACAATTGAGCTTTTCTGTTTGTCTTTTTCTGTCATTTTTGTGTTGAACAATTTCAGTTATTTCAAGCGTTTTGAATTCTGTGGATATTCTCCAAATGTGCGGAGCTGCAAACCAAACACAGACGGAATCTCATCCTTTGAGAATCTGCTCGCAAACATCATTCTGCGGGTGTTTGTCTGGGTTGTCGCCTTCATCATTTGCTTCGGAAACATCTTCGTCATCTGTCTGCGGTCCTGTATTGCTTCAGAGAAT[C/T]AACATCACACCATGGCCATCAAATCCCTTTGCTGTGAGTCTATTATACATCAAACATGAGCATGACACGGCCAATATCCAGCTCATATTCAACCCCAAACTCAAAAGATCAATCAGTCAGTCAAAACATTAAACTAAAGCACTTCACACACAAAAAATGCCATTCGCGATCTTCAGACATTTCAGATTGAAACAAGATTTTCAGCATCAAAAAAATCAGACTTGTTTTTATTCCATCATGAGCTCACTAGATTATAAAGTTGGACTTTGTAGGAAGGTTTAGAAATGTATTTTAATAAATATTGTTTTAGATACTAGTATAGTTCAGTTTTGTCATTAAAGGTGCCATACTGCAGTGGTTTAATAAATTCAATAGTTCTTTGATATCTACATAGTGGGTTCATGGCAAGGGTAAGTTAATAAAATCTCTAGAAATGGTTTTATACATTTTATTACTCCATAAAATACCAATAAAATCAGAAAGTCCATGATTGACCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40493
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113765 | None | None | 393 | None | 15 |
| ENSDART00000143448 | Nonsense | 612 | 622 | 16 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 37493018)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 35274967 |
| GRCz11 | 5 | 35875120 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCATCCTGTACACAATCACAACCAGCGCGTTTCAGCAGCGACTTAAA[C/T]AGTGTCTGAAATATCGCTGCCAGCAGACTAACTGACACAAACACACACTA
Long Flanking Sequence:
ATTTGGTGAGAATAACAATTTGTTTTATGTTCTTCTTCTTCTACCAAATACACATTCCTTAACTTTTATATAAAAATTATATACTATAAAAAGTATATATTATTTTTATTAAAAGGATTACATCTCTTTGTTGATTTTATTTTTTCCTTCAAGCTGAATTTTTAAGGCAAACACAACAGACAAGCAAGTAGCCAGTCTAAGCTGAGAGGTGCATTTTGATTAGCAGATGTCTGAGACCTGAAGCCTCGGGTACAACAAAGATTAGACATTCAACCACCATGAGCACACGCGTACACTTATCAGCTAGAATGGATTTGCAGTTCTTCCCTTGGACAATGCAATTTAATCTGCAAGCTCTTCTCTCTCTCTCTCGTTCTGTCTGTCTCTCTTCTCCAGGTACTATCATTCTGTGGGTGGTGATTTTTATCCTTCCTATAAACAGTGCCCTGAACCCCATCCTGTACACAATCACAACCAGCGCGTTTCAGCAGCGACTTAAA[C/T]AGTGTCTGAAATATCGCTGCCAGCAGACTAACTGACACAAACACACACTATGCATCTGCTCTGAGATTAATATTCCATGTGGATTAAAAAGTGAATAGATGACAGGATAATGACCCCACACACATACAGTACACACACGCACAAACACTCAAGATGCTCTCCTCCTCTGCACAAGTTAATAAGGCTTAGAGAAGCCTGCAGGGTTGAAGAAATGAGAGCGCACACAGCCACATTAACCAGCAGACCATCATCAACAATATATGCTTATGCAATTAATATGTAAAACCAGCCTTATATGGAAAAGCAAAGAAAGCACATACCGTAAACCTAAGAAACTGCAACTGCCATAAAGACCTGGAGCAGCGCATGTGTACCAGGAGAAAGCCAAACTCTGTGGCTGTCAGAGGAGCAGATAGGAGACTGTTCGGGACGGACCCGGCGGGATGAGGATTGGAATGCTTCCGACTGATTTAATTGCATTTTTGTTTGCTTGTGTGGAT
Associated Phenotype:
Not determined