ZMP
raver1
Ensembl ID:
ZFIN ID:
Description:
ribonucleoprotein, PTB-binding 1 [Source:RefSeq peptide;Acc:NP_001018503]
Human Orthologue:
RAVER1
Human Description:
ribonucleoprotein, PTB-binding 1 [Source:HGNC Symbol;Acc:30296]
Mouse Orthologue:
Raver1
Mouse Description:
ribonucleoprotein, PTB-binding 1 Gene [Source:MGI Symbol;Acc:MGI:1919016]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20124 | Nonsense | Available for shipment | Available now |
| sa9586 | Nonsense | Available for shipment | Available now |
| sa9053 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20124
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 |
|---|---|---|---|---|---|
| ENSDART00000040083 | Nonsense | 112 | 312 | 2 | 4 |
| ENSDART00000127832 | Nonsense | 112 | 725 | 2 | 14 |
| ENSDART00000146189 | Nonsense | 112 | 322 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 46600856)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 48610409 |
| GRCz11 | 3 | 46562743 |
KASP Assay ID:
2259-4020.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGTGACTGAAATCTTGCTGTTTTTTTTGTAGGAGGTTCATGAGCTGT[T/A]GGGCAACTATGATTTAAAGTACTGCTTTGTGGACAAATACAAAGGAACAG
Long Flanking Sequence:
TGTGTGTGTAATATAATATAATAGTTTTTATGCTATTATAGTAGTTCATATAGGTCAGTTGGTTCTTGTTCATTGTGTGTGAGGTTTCTCTTAGGAAAATGCTTGATTCATGGGGAAAACGGGTGTGTGTGTGCGCGCGCACGGCTGTGGTATTGTTCCAGATTGGAATGGGAGCAGTGAGGATGTCAATGGACAGAAGGCGCTGAAACAAAACGCTTTGCTTTCACTGACACTAAAAGAAAATGCTGGTTCATATTATAGTAGCATGTTAGGATGCCTAAAAGCAGAAGAGGCCTTTTTTTGTTGTCTACAGTTAATTGGTGAATCAGTCAGCCTTAACCACTGAAAGAAAGGTATTTGTGAACGTTCAGAATGAGAGTAAATGCAAATGTTACAGGATAGAGCCATTCAAGTGCCAGTCATCATGTAAAATGCAGTATACAAATATTTGTCAGTGACTGAAATCTTGCTGTTTTTTTTGTAGGAGGTTCATGAGCTGT[T/A]GGGCAACTATGATTTAAAGTACTGCTTTGTGGACAAATACAAAGGAACAGGTGTGTACGACTCCTTTATCACATGAATGCGTGTGTTTTTTTTCTGCTGTTGAAGAGTGTAGTGTCTTAATGATAACATCGACTATCATGTGTTAATTTCTAACTTGCTTGCTTTCAACAAACTTTAGAAAGTCTTTTTTTAAAGCATATGTATATGCATTTAATAGAGTTGATGGTCAAGCCATATATATTTTTTTCATTTGTTTTTGTTTGTATTTACATATTTTATTTTATTTAAGGTTTGTGTCAGAATCATGAGAATTGCAATGGTTTCCTCAGAGTAAAGAATGTAAATGCTTTTAACACTTAATTTTTTTCTTAAGCCCTAAATAATAATAATAATAATTATTATTATTATTATTATGTTCCTTAGAGACTGTTTGACCAATTCAAGATTGATCTTTTTTTCCTTGCTATTCAGCTACAGTATGATTTAGGCTAGCCCTGAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9586
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 |
|---|---|---|---|---|---|
| ENSDART00000040083 | Nonsense | 180 | 312 | 3 | 4 |
| ENSDART00000127832 | Nonsense | 180 | 725 | 3 | 14 |
| ENSDART00000146189 | Nonsense | 180 | 322 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 46604520)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 48614073 |
| GRCz11 | 3 | 46566407 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGACGCTCTGCTCTGCATCGCCAACCTTCCCAGGGCGTTCACTCAGCAA[C/T]AGTTCGAGGAGCTAGTTCGGCCCTTCGGAAACATTGAGCGCTGCTTCCTT
Long Flanking Sequence:
TCTGACAGCAATGAATATTAATGAAGTTGCACAATAGAGCGCGCTGATTGGTTTGAACCAAGCCTTACTCATGCATTAATGCAACACACTGTAAGACGTAATAAGACTCACTCTGGCACAGACGCCCAGTCTGCACGCTGGAATACACGCTATTATGTCATGGCCGTGACGCAGCTTCAAAAAATCGTTTCAAACCGGAAGTATGAACAACCAATTTACACTTTTTATTAAAATATATGTGTCTTAATAGTGTTTTTAGCAGTGTGGGACACATATACGACTGTCAACAGCTCAAAATGTGTTTTGGTGCTGTCACTTACAGTCATTCTTTTTTCCTTCCTGTTCAAGCCTTTGTGACGCTACTGAATGGTGAGCAGGCCCAGTTTGCCATAAAGGAGTTTCACCAGTATGTTCTCCGTGACCGTGAGATCTCTGTGCAGCTGCAGCCGACGGACGCTCTGCTCTGCATCGCCAACCTTCCCAGGGCGTTCACTCAGCAA[C/T]AGTTCGAGGAGCTAGTTCGGCCCTTCGGAAACATTGAGCGCTGCTTCCTTGTGCACAGCGCCACCACGGGCCACTCCAAGGGATATGGCTTTGTGGAGTACATGAAGAAGGATTCTGCAGCCAGGGCCAAGTCAGAGCTCCTGGGGAAGCAGCTGGGATCACGTATGCTGTATGTGCACTGGACGGAAGTTGGCTCACTCACGTTTACAATGCTGCACTCGCGCTGCCTCTGTGTGGACCGACTACCTCAACACATCCTCACTGCTCAGGATCTCCGCAATGTGCTGACTGACACACATGCTCCCGTATTCTGCCAGGTTGGTGCATTTGACCCGTTTGATTACACAGAACATATTTTTTTACGCTCCATTCATTGCTCTTCCTTTGTGTCAGGTCTCACTGAGCCATTCAGTAGCTGCACCTCTTTTTAAAAATGGCTAATTAGATTTTTTTTTATATCCGTGCTCCAGTAGGAGTCAAGTATGTATCACGGCAGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9053
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000040083 | None | None | 312 | None | 4 |
| ENSDART00000127832 | Splice Site, Nonsense | 421 | 725 | 6 | 14 |
| ENSDART00000146189 | None | None | 322 | None | 3 |
Genomic Location (Zv9):
Chromosome 3 (position 46618339)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 3 | 48627892 |
| GRCz11 | 3 | 46580226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCTCTCTCTGCTGCCCTGATGCAGATGCTGCTTCAGAACCAAGTCCAA[C/T]AGGTACAATGCTGACCTCTCTTTCCACCTCTTATAAACTGCCACTCTCCC
Long Flanking Sequence:
AGTGAAAGGAAAAAAAAAAACTTGAGAGAAACCAGACTCAGTTGGGCTTAACCATATTACCTCGGGCCAAACTTCTCGTGCAGAACTGCAGTCTAAGTGCCGGAGACTTGAGAACACTGAATGTCCAATGTGGTGTCTGAACACTTCCAGTGCTAATTGATTGTAGATCAACATGCTTGTGTAAATGTCATCTGTGTTTCTGCAGGCCTTGAACAGAGGGAAAGGTCTCCTACCCGAACCCAACGCCATGCAGATCCTTACTGGCCTCAATAACCCTGCCACACTGAAGATGTTAATGGCATCTCTCAACCCAGCACATAAACAAGGTGATTCATCAAAGCATTCTTCGTGTGCAAGCTTTCGCACATTGAGATGGTAGATTTGATTTGTGGCTCTTTTGATGTGCAGGGCTTCTGGGAGCTGCGCCTGCTGTACCCCTCCTGGCGAACCCTGCTCTCTCTGCTGCCCTGATGCAGATGCTGCTTCAGAACCAAGTCCAA[C/T]AGGTACAATGCTGACCTCTCTTTCCACCTCTTATAAACTGCCACTCTCCCAGCAGCATCTGTTTTAGCGCTCACTCTCTTCTCTCCCCTCAGCAAGCTCTTTTAGGCAATCCTCTTCTTTGGGCTCATATTCTGCACAATAAAGAGTACAGTCTTCTCCCTTGTGTGAGTGCTTCGCGTGTGTGGTTGTATGTATGTATGTGTGGTTGTGTGTGTGTGTGTGTGTGTGCTGCTGCGGTTTTGTCGTTTTATATTATGAAAATGTATGTGACAAGACTTTGTGGCAAGTCCAGGTAAATATGGTAATGTGTCTCTGCTGAAGCCAAAGCAATTTAGTAATTGATCATCTGTTTCTGTTTGGCATCTGTTAGAACAGTATTTCTCAACCATGTTGCTGAGTGATCCAGCACTGCATGTTTCGGATGTCCCCTTTGTCTGTTACACCCATCTGTCAGGCTCTGCTAATGAGCTGATAATCTTGTCTTTGGTTATGGAGACATG
Associated Phenotype:
Not determined