ZMP
eprs
Ensembl ID:
ZFIN ID:
Description:
LOC562037 protein [Source:UniProtKB/TrEMBL;Acc:A8WG07]
Human Orthologue:
EPRS
Human Description:
glutamyl-prolyl-tRNA synthetase [Source:HGNC Symbol;Acc:3418]
Mouse Orthologue:
Eprs
Mouse Description:
glutamyl-prolyl-tRNA synthetase Gene [Source:MGI Symbol;Acc:MGI:97838]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44876 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23149 | Essential Splice Site | Available for shipment | Available now |
sa36487 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44876
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 |
---|---|---|---|---|---|
ENSDART00000075743 | Nonsense | 663 | 1683 | 16 | 34 |
Genomic Location (Zv9):
Chromosome 17 (position 39886104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 39771001 |
GRCz11 | 17 | 39718586 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTCTCCAGATAGAGGAGAAGATGATAGGAGACCCTTGTTTGAAAGACT[T/A]GAAGAAAGGTGACATCATACAGCTGCAAAGACGGGGTTTCTATATCTGTG
Long Flanking Sequence:
TGTAAAGAAAAAAATATTTTATATATTTTATTTACATTTTTATGCAGTTATTTTAAACATTTCATGTCTTAATTTCCGCTCAGTTTAATTGCTGAACATTTGATCATTTTAATTCTTCCTCACTAATTACACTTTTAGAAAATGGATTTATATGGGGTTTTTGTTCATAAAATCAAGAAGCATTTTCTAGACAAGCAAAAAGTATAGTTGTTTTTAGAAATATTTAGTCAAAAAATCAGTTTTTTTTTTTTTTGCCTGTTTAACCAAAATCTAACTTTTTTCTGAAAACAACACAATATTTTTATGCATGTCTAAAAAATGCTTCTAGATATAAGACTTTTTTGACATTTGAATAAGAAACAAGACAAAAACGAGACATTTTGTACATTTTAAGGGCCACAAGCATTTGAATGGTTGTGTATATTTTGTTCAAATGTATTAAAATATAATGTGTCTCCAGATAGAGGAGAAGATGATAGGAGACCCTTGTTTGAAAGACT[T/A]GAAGAAAGGTGACATCATACAGCTGCAAAGACGGGGTTTCTATATCTGTGATCAGCCTTATGAGCCAATCAGGTAACACCTCTAATCAAGTCTGAATTTTAAATGAACCTGTTTTAACTGTACAAATATACATGTAAACTGTCTGATTTATGCTCTGTTTGTGATTCTGTGCTTCATTTGAATTTCATGTAGCCCTCACAGCTGCAGGGAGAGTCCCTGTGTCCTGCTTTACATCCCAGATGGACACACGAAAGAGATGCCCACTGCTGGCTCCAAAGACAAGAGCAAGAGTCAGCCAGCCAAACCTGTGAGTTCATAACTGGATCTTTTCAGTCTCCGCTTATGTGTCATATTGGACATCCAGTTCATATAATTCAAAGATGTCTATGCTTAATTAACCACTGATAAGGTGTATTGATTTTTTTGTAAAAAAAGAAATAAATAAATAAAACATAACATTTTTTTAAAAAAGCACAATTTTAAAAGCAAAAAACAGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23149
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000075743 | Essential Splice Site | 925 | 1683 | 19 | 34 |
Genomic Location (Zv9):
Chromosome 17 (position 39890940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 39775837 |
GRCz11 | 17 | 39723422 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAACAGGGGGAGCTGGTCAGAAAGCTAAAAGCAGAGAAAGCACCAAAA[G/A]TGAGATCACACTTCTTTTTGATCTGTTGTTTGTTGTGTAATTATTGTTTT
Long Flanking Sequence:
TTTTCTTTTTTTTTTTCTTTCTTTTTTTTTTTGCAACATTAGTTAATTGTGTAACATTGCATAGAATTTTCATTCAAGTAAAGTAGCTTTCTCTTGGCCTTACACAGAAGTCCTGATTACACATATTTTTATTGAAATTACTGAATTTCACCAGTTAAAAAAAAGAAATTCTGCCGCTTTAGATCATAGCTGCATGTTAAAATGTAGTATGCAATCAGCTTACTAAATTATGAATAAAAGAATGAATTTTAAGTGAAGTGATTGATTGATTGTTCTTTATTTTGTAGGAGCAAATAGATGCCGCAGTGAAACAGCTCCTGGCATTCAAAGCTGAGTTTAAACAGCTCACTGGTCAAGATTACAAACCAGGCATGGCTCCTCCCACAGCATCTCCCCCAGAGCCCGCCCCTTCATCGAACTCCTCTCCTGCTGGCATTTATGAGCGTGTGTCTGAACAGGGGGAGCTGGTCAGAAAGCTAAAAGCAGAGAAAGCACCAAAA[G/A]TGAGATCACACTTCTTTTTGATCTGTTGTTTGTTGTGTAATTATTGTTTTGTTTGGGGGGATTTTTTTGCTTCCATGCAAGCCCGGATTGGCTAATCGGGAGAACCGGGAGAATTCCCGGTGGGCCGGTCCGTTTTTTTGGCCACGAGGGCCGGTGTCCCTAGCTGCTTGCACTCTCAGCAATTGCACTTTTTTTTCATTTATTTATTTATTTGACCATAGCCTCACTCTTTTTATTCATTATTTTGCCGCAGCTCCGCTCTTTTTATTTTTTTTCTCACAGCCCCGTAAACAAAATGCAGCCTGCAGATTATTAATGATGTAACTATCATCATTCGACTCTAAACAGCGGCACCTTAGTGAATGTAAGAATTTGAATAATTAATATTGATTAGTAAATCAGATGATTCACTATATTAATAAATCTCACATAACTTGATCAGAAATCTAAAAAGGAGAGAAAAAGATTGAGCCATCAATAAATGTCTTGCAAGTCATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36487
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 |
---|---|---|---|---|---|
ENSDART00000075743 | Nonsense | 1033 | 1683 | 21 | 34 |
Genomic Location (Zv9):
Chromosome 17 (position 39896135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 39781032 |
GRCz11 | 17 | 39728617 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTAAAACAGTTGCTGAACCTTAAAGCTGAATACAAACAGCAAACTGGA[C/T]AGGAGTACAAACCAGGTGCACCTCCTTCATCTGGTTCTGCCACTGCACAG
Long Flanking Sequence:
TGCTACAGATATTTTAGGCAGCACAGCATATTGGTTGGCTTATTAGTTTGTAAAGCTACTTGATATCCTTTTTTCCCCCTCTACAGGACCAGGTTGATGCCGCAGTGAAGCAGCTTTTGGCTCTGAAGGCTGAATATAAGCAGGGGACAGGGCAGGACTACAAACCTGGAGTTCCTACTGCTAAGGCTTCTCCGGCATCATCGTCATCTCCAGCTCAGCTTACTGTTGCCTCCACCCCTGCAGCGTCTGCCCCATCAGACAGCTCTCCTCAAGCCATTTATGACCGTGTCTCGCAACAAGGAGACCTAGTGAGGAAACTGAAAACAGAAAAGGCACCCAAGGTTTCTGAATAATCTTATTTTGGTCAAATCTTTAAAATATCTTTATTAAAACAAGCTTCAAAACTGATTAATATCACTTTCACAATTTTACAGGATCAAGTTGATGCAGCTGTAAAACAGTTGCTGAACCTTAAAGCTGAATACAAACAGCAAACTGGA[C/T]AGGAGTACAAACCAGGTGCACCTCCTTCATCTGGTTCTGCCACTGCACAGTCTAACCCCACCCCACCTCAATCTAGCTCCTCCCAGCCCCAGTCCAGCTCCTCCCCTCAGGCTCAAGCACTGTTTTCAGACATAGCCCAGCAGGGGGAGCAAGTGAGACGACTTAAAACCGAGAAAGCACCTAAGGTTTGTTTGTGAACACATTCTGATAATTGCCAATTTTTTAGTCCTTAACGCTCATTAGCACTTATGTAAAATGTTTTTAGGAGCAGGTCGATAAAGCAGTAAAAACTCTACTTGAGCTGAAGGGTCAGTATAAAGCTCTCACAGGGGAAGAGTACAAGCCTGTGACCACTCCTGGAAATTCTGGAGGAGAAGACAAGAGCCGCAAAGAGCGGGAGAATAAGTCTGAGAAGCAGGGAGGAGGAGGTGGAGGAGGACGCAAGCAGCAGAAAGGAGGAGAGAAACCTCAACAAGGTCAAGAGTCTGGAGCAGGTGGAG
Associated Phenotype:
Not determined