ZMP
srp54
Ensembl ID:
ZFIN ID:
Description:
signal recognition particle 54 kDa protein [Source:RefSeq peptide;Acc:NP_957282]
Human Orthologue:
SRP54
Human Description:
signal recognition particle 54kDa [Source:HGNC Symbol;Acc:11301]
Mouse Orthologues:
Srp54a, Srp54b, Srp54c
Mouse Descriptions:
signal recognition particle 54A Gene [Source:MGI Symbol;Acc:MGI:1346087]
signal recognition particle 54B Gene [Source:MGI Symbol;Acc:MGI:3714357]
signal recognition particle 54C Gene [Source:MGI Symbol;Acc:MGI:3714359]
signal recognition particle 54B Gene [Source:MGI Symbol;Acc:MGI:3714357]
signal recognition particle 54C Gene [Source:MGI Symbol;Acc:MGI:3714359]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11820 | Nonsense | Available for shipment | Available now |
sa36339 | Nonsense | Available for shipment | Available now |
sa421 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11820
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 |
---|---|---|---|---|---|
ENSDART00000018678 | Nonsense | 14 | 504 | 3 | 18 |
ENSDART00000133424 | Nonsense | 14 | 504 | 3 | 17 |
The following transcripts of ENSDARG00000003813 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 10525136)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 9920188 |
GRCz11 | 17 | 10076222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACCGCAAAAATGGTTTTAGCTGATCTGGGGAGGAAAATAACCTCAGCTT[T/A]GAGGTCTCTCAGCAATGCCACCATCATCAATGAGGAGGTACAGATGYAAT
Long Flanking Sequence:
GAAGTTTTGAAGCTTGTCACTTCAACAAAGATTAAAAGTTTATTTATACAATGAACACTATACGGTGTTAATTTACATTTGATTTTTTTCATTTCTGCACCTCAATGCTGTTTGACTTCACTGAAAACTATGAAGTGCTGTTTTTTTAATATATTTTTTATCCTTGTTCTATTATTTTCATCTGTGCTTTAGATATTTGTTCATATTTTTGTATAGTTTTATATATTTTTTGCAGATGCACTTCTTAAAATTATAAATACTTTCCAAATGGAGTTTACTCAAGTCATCTTGTGAAATTATATTCAAGTCTCAATTTATATTGCAGAAAAACAAATTATCACAATGTCAGTTTTTTTTTCCAATATCGTGCAGCCCTAGTACAGATACTTTCTCTTTAATCTTTACTACCTGATGTAACAAATAGTCCCTGTTGCAGGTTGGCAGCTGATTAACCGCAAAAATGGTTTTAGCTGATCTGGGGAGGAAAATAACCTCAGCTT[T/A]GAGGTCTCTCAGCAATGCCACCATCATCAATGAGGAGGTACAGATGCAATCTTAAAGTCACACTTGATAAGCATTGCCACCATCATAAAATGTTAATTTAATTGCGATCTCCTTAGGTATTAAATGCTATGCTCAAAGAAGTCTGTGCTGCCCTGCTGGAGGCTGATGTGAATATCAAGTTGGTAAAGCAGCTTAGGGAAAATGTCAAGTAAGTAACGAAAGTTAAACAAAACGTCATTGCATGGTATTATTGAATGTCTCTAAAACCACTCTATTATCTCCAGGGCAGCCATTGATTTGGAGGAGATGGCCTCCGGTCTGAACAAGAGACGAATGATCCAACATGCCGTTTTCAAGGAACTTGTCAAGGTAAATGATGCTGTATTATTATTGTCTGTTAAATCTTATTACATCGTTCCTTAGAACTGGGACAAACCAAGCTGATGCCAAACAACTAGCACTGACGAACACTAGATTCAAGCCCTGTTCACACAAACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36339
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018678 | Nonsense | 219 | 504 | 10 | 18 |
ENSDART00000133424 | Nonsense | 219 | 504 | 10 | 17 |
The following transcripts of ENSDARG00000003813 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 10520629)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 9924695 |
GRCz11 | 17 | 10080729 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGCTTCATAAGTCATGTGTGTCCCACAGCAACCTGACAATATAGTGTA[C/G]GTGATGGACGCCTCCATTGGTCAGGCTTGCGAGGCTCAAGCTAAGGCCTT
Long Flanking Sequence:
TGCTGACACATTCAGAGCAGGTAAAGTTTGTACATGGTGATTATATATTTGCATACTTTATGCACTTTGGTCAAAAAATAATAACTATGTCCATTTTTATAGGTGCCTTTGACCAACTCAAGCAAAATGCAACAAAAGCCAGAATACCCTTTTACGGCAGGTAATAAATGTGCCGTTCTCCACTTGAACTATCCTATATATTTAACTCCTCACACTCAGCCATTGATTCATGTTGGTGTGATTGAACAGTTACACAGAAATGGACCCGGTGATCATAGCTGCAGAAGGTGTAGAAAAATTCAAGTCGGAAAACTTTGAAATAATCATCGTGGACACAAGTGGTAGACATAAACAGGAAGACTCGCTTTTTGAAGAAATGCTTCAGGTGTCAAATGCTGTGGTAAGTCCTGTTTCGATGAAATATCAAACAGAAAGACTGATGTAAAGCTTGATGCTTCATAAGTCATGTGTGTCCCACAGCAACCTGACAATATAGTGTA[C/G]GTGATGGACGCCTCCATTGGTCAGGCTTGCGAGGCTCAAGCTAAGGCCTTTAAAGACAAGGTAGATGTGGCTTCTGTTATTGTCACCAAACTGGACGGCCATGCCAAGGGTGGTGGTGCGCTCAGTGCGTAAGTACACACTTTCTGCTTCGTACTTTCAGCTCTTAAGTAAATAAATACAGGGGGTTGACTGTAAATTTATGTTTACAGTGTGGCTGCCACAAAGAGTCCCATCATTTTTATCGGCACAGGCGAGCACATTGATGACTTTGAGCCTTTCAAAACTCAGCCCTTCATAAGCAAACTACTTGGTAAGATATTGCTGAGCTGCTGGGTCCATTAAAGGTCCCATGAAGTGCTTTGAAATGTGCAGTTTTCTATTTGATGTTTGACGTAATCTCAACTGAAAAAGGAAGAGAGGGCAGGACATATAGTAGCTCCTCCCTTTTAAAAACAGCCTAGAGGATTTTGTTTTTATCACAGCCCTGCCAGTGAGAGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa421
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000018678 | Essential Splice Site | None | 504 | 18 | 18 |
ENSDART00000133424 | None | None | 504 | 17 | 17 |
The following transcripts of ENSDARG00000003813 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 17 (position 10511645)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 9933679 |
GRCz11 | 17 | 10089713 |
KASP Assay ID:
554-0318.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAAGTGATCAGCTTGGCAAATACACACACACACACACACACACACACA[C/T]ACACACACACACACACACACACACACACAGAGACGTCTGGATCTGAGTGC
Long Flanking Sequence:
ACAGCATCTGAACCAACTGAAAACACTTGTATAATAATTTGTGCACATGTATTTTTGTGGTAAAGTCTTACTTACAGGGGTTTCTCTTGGTTTCTTGTAAGGTGGCATGGCCGGACTGCAGTCTATGATGAGGCAGTTTCAACAGGGAGCTGCTGGCAACATGAAAGGCATGATGGGATTTAACAACATGTGAACCTGCAAACAGAGGACACTAAAAGAATCTGATGGTTTTGGCAAGCAAAACGGGCCGATGAAGATAGTTTGATTTGTATGTCTTGTATGCCACAAGTAATTTAATTCTTTAAAAGGTGTAAAACATTAAATGGAGGCACATTTACATGTAAAAGCCCAATGTGTCTTCTTTGGAGCAGGATTGATATGGGGGACTATTAGAAGAAATTATGCTTCCTGAGATCAAGTCCAGCGACGTTCAAAATGTCACGTGAGGTTGGAAAGTGATCAGCTTGGCAAATACACACACACACACACACACACACACA[C/T]ACACACACACACACACACACACACACACAGAGACGTCTGGATCTGAGTGCTTTACGATACTGCCAGACTTGTCGACAGCTGATTTCTTTCGGTTATATGATTTTACCGTAATTGCTATGACCGTCTTCATAGCAAAGGATATTCATAAGTAGAAAATCATGGTTTATTGTATAATTGACTGTTTCTGATTTATTAATCTGCCATAGAGAAGCTCCAGCTTTGTATCAGAGATGAATACAGTAGTTGCAAAAGAGTATGTGGCAATATTTTGTCATAATATTATAATAAAGTTTATATGGCAACATTTTAACAATATTTGTCTCTCTTTTTTTAAATCTTTGGTTTGTTTGTACTGAAATTATGTCTTCAAATATTGAATCTGTGTGAGTGAAGTGACTGTATTATTTGCATTGTTTATGATGTATGTAATCCAGGCTGTGCAAAGAAAGAGCTAGACAAATTTACACTGAGATTAGTTGGTAATCTTTGTTTTATCCCTT
Associated Phenotype:
Not determined