ZMP
rxfp2
Ensembl ID:
ZFIN ID:
Description:
relaxin/insulin-like family peptide receptor 2 [Source:RefSeq peptide;Acc:NP_956737]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34944 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa4378 | Nonsense | F2 line generated | Not yet available |
sa12070 | Nonsense | Available for shipment | Available now |
sa13851 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34944
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 |
---|---|---|---|---|---|
ENSDART00000050328 | Nonsense | 107 | 509 | 4 | 17 |
ENSDART00000147775 | Nonsense | 107 | 723 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 34821356)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33849214 |
GRCz11 | 10 | 33793074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGGACGTGAACCTGCATGTCGTCCCCATCCTCTCTTCCAATGTGACTT[G/A]GTTGTAAGTACAGGGAACTGAAAGCCATCTGCACAGCTTTACTCCATTGC
Long Flanking Sequence:
GGACATGGGAGCATTTGAAAGCTGCATCTGTCAGCTGAACCGTCAGATATATAAATTATCAGCCCACAGATCAGCTGATTAACAGTTTTCAACCACTTCAGTGCACTTTCAGAGCTATAATAAAGTACTTATGAGGGCTTCATATCTGCGATATACATCACTGCATTTTCTAATGGTAATGTCCTCTATGTCATTAACTGTCAAATGCAGTAACATCTTGAATGTCTTGGAAAAAACTCTATTGCGATATACATTGATTTTGAATTATTGCCTAAAAATAAAATAATATTGTGTTACCATTGTAGATAAGTTTTGTTGAAGTTTAGTTATATTTATTACAATGTTTATGTGTATCTAAGTTATGTTTAAGTAATTAAGTTTTTATTGATCTTGTGCAGATCTGCAGCAATACCCGCAAAGCTGTTCGTGCAAAAAGACGGAGGTGGAATGTGTGGACGTGAACCTGCATGTCGTCCCCATCCTCTCTTCCAATGTGACTT[G/A]GTTGTAAGTACAGGGAACTGAAAGCCATCTGCACAGCTTTACTCCATTGCTCCCATGAGAGGTTATTAATCTGGAGCTGGAGAACAGGAGAATAAATGTGACATCAGTGAGCCATGAAGCTTAACGAGATAAAGAGCTGCTTTGCACTAAGCAATTACCAGCACAAAGAAAAGTTACCCACACTACCTGTTTGATTTTGCCTAATCATTTTGCTCACTATGTTTTGATTGTTCCGCATGATGGAGGTAGTAATTGTGGTTTTGAAGATGTTTGATTTATTGTGATCTGCGCTCTGAAGATACTGAGATGTACAGGGTGGATATTTATAGATGATTAATGTCTTTTGGAATGAAGAGTTTGAAGACGATCTTTTGGAGTCTGGGGATGTTTTTGGAAAATGGAGAAATGTAGAATAATTTATATCAGTGGCCACTGAGGTTATATCCAAGAAAATCACATTGTTTCATCCCTGTGGAATGTAAAGACTCCTAAAATAGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa4378
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 |
---|---|---|---|---|---|
ENSDART00000050328 | Nonsense | 308 | 509 | 13 | 17 |
ENSDART00000147775 | Nonsense | 308 | 723 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 34878855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33906713 |
GRCz11 | 10 | 33850573 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTCATGTCATTTTTATTCCATTTGCAGGAACATATCCCACAATCCTT[T/A]GCTCCATATTCACACCGGGCACTTCGATCACCTGGTGCAGCTTCAGTCTC
Long Flanking Sequence:
CAGTATTGTATATCTTTACTGCAAAATATACAATAATTATTACAATTCAACTTTAAAATAAAGTAACATACTGCATAACTGTCCTACTGTAGTAACTTACCGGCCGCAGTTCACCAGTAACTTACTGTAAATCAATTACAACATATATATTGTATTTGCATTTACAGCACCATTTATCTTGCAGTTTATGTATTTACAGTATTGTATATCTTTACTGTAAATATGCAGTAATTTTCATAATGCAACTTTAAAATACAGTAACATACTGCAAAACTCTACTACTGTAAAATAGAGTTCATATTACAGTGTATTATCGTAAATCATTAACAGTTTTGCTGATATTCTAAGTAAATATTTAAAAAGCACTTCTTGACCCCTTTATAAAAAATCAAACAACATTATATTTGGACTATGAAGGTCAAAAAGTATAATTCCACCTTTTACTGATCACATTTCATGTCATTTTTATTCCATTTGCAGGAACATATCCCACAATCCTT[T/A]GCTCCATATTCACACCGGGCACTTCGATCACCTGGTGCAGCTTCAGTCTCTGTAAGTGCCAGCCATGCAGGTTTAAAAAAGAATGCGTTTTAAGAGCCTATTAGTAGGTGTCACATGAAATACAGCCCTCATTTGTGTTTAACAGGAGTCTGGAGGGCATTGAAATTCCTAATATAACCACCAAGATGTTTCTTCCGATGGGGAATCTGTCCCACATGTACGTATTCTCTCACTGGGTGGTTTGTGCATTATCGTGCATACGCCGGATGCTCAGCTTGTAATTCACCATTTGTGTGTGTTTTGTTTAAGTGTTATTATTATTTTTTGTAGATATTTTAAAGACTTTCAGTACTGTTCCTATGCGCCACATGTACGGAAATGCAAACCTAACACCGATGGGATTTCGTCAGTGGAAGACCTGTTAGCCAGCCTGGTTCTGCGGGTGTCTGTGTGGGTTATGGCCTTCATCACATGCTTTGGGAATCTCTTTGTTATCGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12070
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050328 | Nonsense | 359 | 509 | 15 | 17 |
ENSDART00000147775 | Nonsense | 359 | 723 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 34879216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33907074 |
GRCz11 | 10 | 33850934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTATTATTATTTTTTGTAGATATTTTAAAGACTTTCAGTACTGTTCCTA[T/A]GCGCCACATGTACGGAAATGCAAACCTAACACCGATGGGATTTCGTCAGT
Long Flanking Sequence:
AGCACTTCTTGACCCCTTTATAAAAAATCAAACAACATTATATTTGGACTATGAAGGTCAAAAAGTATAATTCCACCTTTTACTGATCACATTTCATGTCATTTTTATTCCATTTGCAGGAACATATCCCACAATCCTTTGCTCCATATTCACACCGGGCACTTCGATCACCTGGTGCAGCTTCAGTCTCTGTAAGTGCCAGCCATGCAGGTTTAAAAAAGAATGCGTTTTAAGAGCCTATTAGTAGGTGTCACATGAAATACAGCCCTCATTTGTGTTTAACAGGAGTCTGGAGGGCATTGAAATTCCTAATATAACCACCAAGATGTTTCTTCCGATGGGGAATCTGTCCCACATGTACGTATTCTCTCACTGGGTGGTTTGTGCATTATCGTGCATACGCCGGATGCTCAGCTTGTAATTCACCATTTGTGTGTGTTTTGTTTAAGTGTTATTATTATTTTTTGTAGATATTTTAAAGACTTTCAGTACTGTTCCTA[T/A]GCGCCACATGTACGGAAATGCAAACCTAACACCGATGGGATTTCGTCAGTGGAAGACCTGTTAGCCAGCCTGGTTCTGCGGGTGTCTGTGTGGGTTATGGCCTTCATCACATGCTTTGGGAATCTCTTTGTTATCGGGATGCGCTCTTTCATTAGAGCCGAGAACAATCTGCATGCAGCCTGCATCAAAGTCCTCTGCTGTGAGTACTGCTGAAACTATTCTTGATATTCAATTGAGACATACACCGCGTGACCTGAAATATTAATCCTGTGAAATGATCAGAGGTATCAATAGTTATGAAAACAGCTTCAGTAACCAGATTTCATTATGTTTGTTATAAAAATATTGCAGTAGTACTGAGATAAAGAAGGTTCGCAGTGGTGATCAAAATAAAGTAAACTAATAAAATAAAAAGTTAGCTCAACTTAAAATTGGACATCAAATTGCTGCATTGCAATTATATGAGTTGACTCAACTTTTAACCCAAGTACTGAGGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13851
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000050328 | None | None | 509 | None | 17 |
ENSDART00000147775 | Nonsense | 668 | 723 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 10 (position 34894924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 33922782 |
GRCz11 | 10 | 33866642 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGCCCTTAACCCCATCCTCTACACCCTGACCACCAGCTTCTTCAGAGAG[C/T]AGGTGGAGCTGCTCCTTTGCCGCTKGCAGCGKCGCTCTGCCACAAAGAAA
Long Flanking Sequence:
GTGGGGGAAAACGAAGCGCCTGAAGGAAACCCACGCGAACACAGAGAGAACATACAAACTCTACACAGAAATGCCAACTGACCCAGCCGAGGCTCAACCCAGCGAGCTTCTTGCTGTGCTGCGGCAGCACTAACTACTGCGCCACCGTGTTGCCTAAAAGAAATCAGTTATTGTAAATGAGTTATTAAAACTATATAACTTATAAATGTGTTGAAATAAATATTTCCTTTAAACAGAAATTAGGGGAAAATTTATACAGGGGGGCTAATATTTCTGACTTCGACTGTACATCAAATCAACATCTAACATTGGTGTTTTTTGCCTGCCGGGAGGTGTACTCTCCCTTTAAGATAATAAGTGCGTCCGAGCATTGCTGACATCAGTGCATTCTGTTTATCTCTGCAGGGACGATTAACTCCTGGGTGGTGATCTTCATTCTCCCTATAAACAGCGCCCTTAACCCCATCCTCTACACCCTGACCACCAGCTTCTTCAGAGAG[C/T]AGGTGGAGCTGCTCCTTTGCCGCTGGCAGCGTCGCTCTGCCACAAAGAAAGACCGCAAGAGCGTCACCAGCTCCACCATCTACATGGAGACCTCACGAAATCCTGAATACCCTGCAAAGAATTCTTTACCACGACTGTCTTTGGCTGACATGGACAACCAATATGGGTGAAAGAGCCGGAAGGTATCGTAGCGTAGGTCTATCATAATCATTATCTCCATTCAGACCGGAGAATGACAGGCTTTCCTGGAACAATTTAAGTGAAAGGATGGCGCTGTGATTCCTGCCGTTCGGGATCAGAAATGGAGAGCTCTTTGTAGACGCATGACTGTAGCTACACTGTTTTCTCCATTAGGAGAAGCATTTTTATTCACTTAAGCTGAGATAAGAGCCTCAGATCCCTCCAGCGGCCATTACCAACAGCTAAACAGCATGTCTGGCTCACAAATGTTGAGCTCGGCTTGTTGTTTGTCAAAAAAAAAAAAAAACTTCTGGGGAAGT
Associated Phenotype:
Not determined