ZMP
grhprb
Ensembl ID:
ZFIN ID:
Description:
glyoxylate reductase/hydroxypyruvate reductase b [Source:RefSeq peptide;Acc:NP_991248]
Human Orthologue:
GRHPR
Human Description:
glyoxylate reductase/hydroxypyruvate reductase [Source:HGNC Symbol;Acc:4570]
Mouse Orthologue:
Grhpr
Mouse Description:
glyoxylate reductase/hydroxypyruvate reductase Gene [Source:MGI Symbol;Acc:MGI:1923488]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19472 | Nonsense | Available for shipment | Available now |
| sa17209 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19472
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 |
|---|---|---|---|---|---|
| ENSDART00000009457 | Nonsense | 8 | 336 | 1 | 9 |
| ENSDART00000132958 | Nonsense | 33 | 361 | 1 | 9 |
| ENSDART00000139314 | Nonsense | 33 | 228 | 1 | 6 |
| ENSDART00000147502 | Nonsense | 33 | 351 | 1 | 9 |
The following transcripts of ENSDARG00000019986 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18587128)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19152296 |
| GRCz11 | 1 | 19845233 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACCGTGACCGGACATCACCGCGCGATGTCCGCGTTACCGAAAGTGTA[T/A]GTGACCCGCAGGATTCCACCAGATGGACTGGACATTCTGCGAAAATCCGG
Long Flanking Sequence:
GACACGCACAAATAGTAATGCCTGTTGTCTAAATCTTTTTTCCATATGTTGTTTTTATATGATAGTGTAAAGTGTTGGCCTATTTCAATATTCATTGTTTTTCATACAGCTTGTTTACACATCTTGAGCCCCTGATTAATGATTGAAACAAAATCAATGCCAATAGCCTATCAGAAATCGAGACACATCCATGCCTTTTGTGATTAGTTGTGGTACTTTGGAATGTTAAAACAAATAAACAAAATATATTAATCTTACATATTTGCTCTCTTGGCTCGTGGACTGGACAAAGACCACCCATTCGTCTCCTCCCTCGAAACTGAGCACAAAGACGCACACACACAGCACCTGCCGCGTCTGTCCTCCTCAGCTCAGACTCCCTGACTGATCCAGTTGTTAGTAATGTGGTGCAGCAGAACAGCGCTCGGGAGACTACAGAGAATCGCCCCCTGTACCGTGACCGGACATCACCGCGCGATGTCCGCGTTACCGAAAGTGTA[T/A]GTGACCCGCAGGATTCCACCAGATGGACTGGACATTCTGCGAAAATCCGGACAGTAGGTTGAAGCACTCAGCAACTTAAAAAAAACATTTGTGCGTTGTGTTTGTTTGTTTGTTTGTTTGTTTGTGTGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGAAATGCATTATTTTTCCTGATTCCAATGTTTATAAGCGATACAATTTGGCTTCTCATAAATAAGCAGACAATGTGAAGAAATGATTAATTGTTGCTTTATTATTAAATTGACAACACTTTACAGTAAGGCTCATTTGGTTTGGTACATCAGACTGTACCATTTATTCAACTTAAGATATGACTGTGTTTAAGAATTTTATTAGCCTCTAAATTAAATTAACTGTTTATTATGCAGGCTATGTATTTTTTTTATTGCCAATGTCAGTGTGGGTAATTTGTTTTACAAAATCAGACCCTTTGATTCTAGGCCATAAGGTCTCTATAAAAAGCCTGTAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17209
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 |
|---|---|---|---|---|---|
| ENSDART00000009457 | Nonsense | 307 | 336 | 9 | 9 |
| ENSDART00000132958 | Nonsense | 332 | 361 | 9 | 9 |
| ENSDART00000139314 | None | None | 228 | None | 6 |
| ENSDART00000147502 | Nonsense | 322 | 351 | 9 | 9 |
The following transcripts of ENSDARG00000019986 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 18578978)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 19144146 |
| GRCz11 | 1 | 19837083 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTMTGTTTGTATTTGCAGTGATTCTTCCTCACATTGCCAGTGCGTCCTA[T/A]ACCACACGAAACGCCATGTCWGCCCTCGCTGCCAACAACCTGCTGGCAGG
Long Flanking Sequence:
AATCTGTTTTTAATCATTTTTATTCTTTGTTGTGTTTATTTCTTATACTTGTTTCTTTCATTCTTGTTTATGTAAAGAATTATGATTGTGTATGAAATGTGCTATATAAATAAACTTACCTTGCCTTGCCAAATAAACACAATCACAGCAGTTATGTACAAATAATATCTACAAAGATTCACAGAAGCAGATTCTCAAAGAATAAAAATAAAACAGAGTCTTGACCTCTTGCCTGTAATGGTGTTGTTGTAAAGAGGTGGCGTGGTGAACCAGGAGGATCTGTATGAAGCTCTGTCGACGGGTCTGATTGCTGGCGCAGGGCTGGACGTCACCACTCCTGAACCGCTGCCAACACACCATCCGCTCTACACCCTCAAAAACTGCGGTAAGAACGCCTCGCATGGCTTAGATTGAAACCTTTGATTGGTTTCCTGCTAAAACATTCTGTGTGTTATGTTTGTATTTGCAGTGATTCTTCCTCACATTGCCAGTGCGTCCTA[T/A]ACCACACGAAACGCCATGTCAGCCCTCGCTGCCAACAACCTGCTGGCAGGACTCAGAGGTGAAGCCATGCCCAAAGAGCTGAAACTGTAGAGGGGAAAAGTACTGGTGAAATTAAAACAATCTGTAATGATTCCTTCAACTTTTGTTGTTTCAAACCTGTATGCTGTTGTTGTATTTGCATAAAAGACATAAAGATGAACGTTTGAAAAATCTCCACAGCATGTCTCTGCACAACAAACAACTTGATGCTACTGAAAAATGTTACACTTGGAGAATTAGTATGAATAAATCACATTCAGATGCAAAAAGTAAAAAAATTTAAGGGATCCTTCACCCTGAAATTAAAATTGCTTGTAAATAAAAAGTTGCTTCTAAAACTTTAGGTTTTTTTCTTCTGTTGAACACAAAAGAAGATAATTTGAAGAATGTTCGAAACTGGTAGCCACTGACATCCAGTTGAATTCAGAATTATATGTATATTTTATTCCTCAATTTCTGTT
Associated Phenotype:
Not determined