ZMP
si:dkey-76k16.7
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC553448 [Source:RefSeq peptide;Acc:NP_001139027]
Human Orthologue:
RRBP1
Human Description:
ribosome binding protein 1 homolog 180kDa (dog) [Source:HGNC Symbol;Acc:10448]
Mouse Orthologue:
Rrbp1
Mouse Description:
ribosome binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:1932395]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10197 | Nonsense | Available for shipment | Available now |
sa14359 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10197
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 |
---|---|---|---|---|---|
ENSDART00000017523 | Nonsense | 737 | 1336 | 7 | 28 |
ENSDART00000075764 | None | None | 373 | None | 4 |
ENSDART00000124034 | None | None | 363 | None | 2 |
ENSDART00000130986 | None | None | 353 | None | 2 |
ENSDART00000133073 | Nonsense | 737 | 1336 | 8 | 29 |
ENSDART00000138181 | None | None | 391 | None | 9 |
The following transcripts of ENSDARG00000013763 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 33849628)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33515608 |
GRCz11 | 13 | 33625153 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGWGTTCTTATGTTTTGTCYGCTGCAGGCGAGCAGGGCGAAYGCTGAA[C/T]AAGCTCTGCAGAAGCGTCTGGAGGAAGTGAGTGAGGAGCTCAGACAGACM
Long Flanking Sequence:
GGCAGAATCAACAAATGTTCAATGAAATCTAATTTCTTTTGGCTCAAATATTTTTGTTGTTGTAATTTTAGGGTCAATATCAATCGCCCCCTTATTTTTTTTTCCCATTGTCTACTTAACAAACTACTGTTGTCCAATTAACCAAACTTGCCTAGTTGACCTAATTAAGCCTTAGGTTGTACTTTAAGCTGAATACTAGTATCTTGCAAAATAGCTAATAAAGTATCATGGCAAAGACAAAAGATATTATTTATTAAGTTATTGTGTTTAAAATGTGTTGAAATCTTTTCTGTGAAATATCACTTTGTAAATATTTGGAAAAGAGTTCACTGGAAGGCTAATAACTTTTGTTTTCAACTGTATGTTTGATTGTGTATTATGATCAAACCTGCTTGCTTCATAAACACTCTGACATCGGTGGTATTGTGTGACCAAACCTGACCTGTGTTTTCTGTGTTCTTATGTTTTGTCCGCTGCAGGCGAGCAGGGCGAATGCTGAA[C/T]AAGCTCTGCAGAAGCGTCTGGAGGAAGTGAGTGAGGAGCTCAGACAGACCCAGAGCAACAGAAACAACCTTCAGGCACAACTTGAACAAGCTCAGAAAGATGCTGCTGCTCTTGCAGGTCAGCACCCACTTGGTGTCTCAGAATATAAACAGCTTGCAGAACAAATAAGATACAACCAGAATGTTTCGGAAATCTTTTAGAAAAGTATTGTAATAATTAAATCTGGGCTTCAAGTCCTGCAAAGTATGATTTCTTGCAGTATCGCCAATGTGTCCTTGTACGCAACACTTGAGTATGGTGTACTGCAGCTTTAGGCAGACGCATTATGAATTAGTAATTTAAAGTAAGTGTTTTGTTCCACACTGCACTGTTTTAGAGGCTAAAGCTCGTGTGGCCAGTGTGGAGGTGGAAATGAAAGAGCGGACTGGACATTTGGAGAGTCTGCAGAGCCAGCTGAAACAGACGCAGACAGAGAGAGAGCAGCAGCTGAAAGAACAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14359
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 |
---|---|---|---|---|---|
ENSDART00000017523 | Nonsense | 965 | 1336 | 16 | 28 |
ENSDART00000075764 | None | None | 373 | None | 4 |
ENSDART00000124034 | None | None | 363 | None | 2 |
ENSDART00000130986 | None | None | 353 | None | 2 |
ENSDART00000133073 | Nonsense | 965 | 1336 | 17 | 29 |
ENSDART00000138181 | None | None | 391 | None | 9 |
The following transcripts of ENSDARG00000013763 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 33846337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 33512317 |
GRCz11 | 13 | 33621862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYNNNNNNNNATGGTGTTTTTCAGMATATCTGAAAAAGAGAGCTTGATGACAACACTA[C/T]AACAGGAAGTACAGCAGCTCAAGGAACTAAACCAGTCACAAAGCAAGAGT
Long Flanking Sequence:
AAACCAAGAAATGCTGGAACAATTACAAAAGAGGTACGCGTCATTTGTAATCCACACAAGATTTCACATATATAATCTGTTATTAAAATGATTCCTGTTTCTGTAGTTTGAAAGAAAAGGAGTCTCGTGAGAAGTTGTTTGAAGAACAGATAAGGCAATGTAAGGAACAGTGTAGCACTAAAGTAAGTGAGATTTTACTGTTATTATTATATGTTTGACCTTCAAAGATAAAGTGTATATTTATGGTAAAAATAGCTTTGAACTGTGTCCAATAACACACTCTTCATTTACAGCTGGCAGACAGCACAGCCCAACTAGATTCACTACATAAAAGGTACATAATCAGACCCACTGAAGGCCACTGCATGTTTATGTGCCTCCCTAGCCACCCACGTTAGCATCATTCTTTGATTAAATGCCTTCCTACACGTTGAGTGTTTTTTTTTTTCTTTATGGTGTTTTTCAGAATATCTGAAAAAGAGAGCTTGATGACAACACTA[C/T]AACAGGAAGTACAGCAGCTCAAGGAACTAAACCAGTCACAAAGCAAGAGTTTTGTAAGTAGCTGGGACAATTGTGGACGTGCATGTCATTATCTTGCGTGTACACAGTGATTCATAAAAATATGCGCAGACACATGTTATCATATCTTGTCGACAGGGTTTATGGCCTTACTGCGTAAATGAGATTGTCACAGTACTCTTACATTTCCATTTCAGGAGTGTTGACGTTAAAAGCACTATACGCAGGTCTTTCTGTGTGTAAAATGTAACCGGTATAACTGGTATTGAAAAGAGTGACATCAAGAAAGGAAGTTTTGAGCGTCATCATGTTACTCAGCAGTTTTTAGTTTCGGATTAAATCCATTTGTTACAATTTATTTTGCTTAGAAATGTGCTAAGAGATACAAAACATGCCTTTTTGTTGAATATAAGTGCTTAAGTTAGAATTTTTGTTTAAGCTGTTGCGTTCGGTTATTAATAAGCTTATAATTGTATTACAGG
Associated Phenotype:
Not determined