ZMP
grpel1
Ensembl ID:
ZFIN ID:
Description:
grpE protein homolog 1, mitochondrial [Source:RefSeq peptide;Acc:NP_001032461]
Human Orthologue:
GRPEL1
Human Description:
GrpE-like 1, mitochondrial (E. coli) [Source:HGNC Symbol;Acc:19696]
Mouse Orthologue:
Grpel1
Mouse Description:
GrpE-like 1, mitochondrial Gene [Source:MGI Symbol;Acc:MGI:1334417]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21037 | Nonsense | Available for shipment | Available now |
| sa2354 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa21037
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 |
|---|---|---|---|---|---|
| ENSDART00000016803 | Nonsense | 16 | 217 | 1 | 4 |
The following transcripts of ENSDARG00000010021 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 41144185)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39480442 |
| GRCz11 | 7 | 39751459 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGATGGCGAACTGGTGCGTGCGCGCGATCAGACACAGCTCTTCAATCT[T/A]AGCGTCCCCTTCACTAGTAAGGTATGTTTCAGCTTTGCTAAGGCGTGTTG
Long Flanking Sequence:
ATAGATTCCATCATTCGTGTTACTTATGTCAGTGCATCTCTTTTAACATTCGCTATTAATATTTAATAGCCTATATCATGGCTGCATCTACATTTTACATTATTCAGAGAGCAAACACGTGGGATCCAGTCCAGTTAATTACAATTCCTTAATCATATTATAGATTTATTCATGTGTGTTTTCTTAATAATCGAACATAGAGTGATGTAAAATCCTCATGTTAGTTGAGTAATGGCAGTATGCGGTAACCTTCAGTGGGCCAGGCAAATACCCCGTCCTGTGTCACGTGTAAAATGTTTCGACCTTCCTCTCAACCAAACTACAGAATTGCGTCAGTTTAGACTGGGACGATTATTGGTCCTGCCCGACAGTCGTGAAAGAACTGCACATGTGATTGGTTGAATGAGACGACGTTCCGTGCGTGTGTCTCATCTTGGACAGTCAGTGAGTAAAGATGGCGAACTGGTGCGTGCGCGCGATCAGACACAGCTCTTCAATCT[T/A]AGCGTCCCCTTCACTAGTAAGGTATGTTTCAGCTTTGCTAAGGCGTGTTGTTGATGTCAAAGCTTGGGTAATTTTTTGGGTTTTAAGGAACAAATGAATGAATGTTCTTGCTGTTGCGTAAGCTGTTCAGAATTGAATGATTCGTGCTGATGTTCAATGACCATCAGTTTACCTTACTTTCATTTTAATGACAGTTTGTGACAGTCTTGCGTGTTGCCCTGCCAAATACACTTACGTTTTTTTTATTAGTCAGAAGTGATCATTGATAACGCAGTGAAGTTTGCTTTACTGGTCTTTCAGGTCTGTCCTATTGCATATCTTTCTTTACAAAAAAGTATGTGACCTGAGTTTAGGATGTAGGTTTCAGTTGTATTATGCTTTTTTATTGTAAAAGAAAATAGTTTTCCCTCCTTGGCATGTCAGTGACAGACTTGTTTCCGACACGTGCTTGTGTCAAAGCTAGATCTGAAGACTTACTGGTGTACAGTACTGCCAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2354
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000016803 | Nonsense | 66 | 217 | 2 | 4 |
The following transcripts of ENSDARG00000010021 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 41141587)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39477844 |
| GRCz11 | 7 | 39748861 |
KASP Assay ID:
554-2669.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAGCAAGAGCCTGGCACAGCTGAAAAAGCCTTCTTAGAAGAAAAGACA[C/T]AACTGGAGGAGCAACTAAAAGATGTTACGGTAAAGCTGCATTCAATTCTG
Long Flanking Sequence:
CCTGGCTCACACTTTTTACTTGCTGTTCACTTTCTGTAAATGTTAATTTCTCTTTCTGCATTTACGAGTGCAACTAACACTTGTCAAAATCTATTCAACAGCTGATGGACAGAAACAAGTCCCTGCACTACTCTTTTTGTCCCCTCAATTCAATACCCTGTTACTCTTCTATTAATGCCACAATTTAGAAAAAATGTTATAAATTCCGTTTTATTGATTGAGCTTCTAAAAAAGGATAAAATACCTTTGCGCCTTTCAAATAGACTTAAAGAAAGAAAATGCTATTTGAGTCTTTTACATTAGACCAGTTGCATAAACATTGTGTAAAGCATAATCTTGTGAATGAACATTCTGTCAAATTTGAACTTCTCAGGGCGACTCCACGTCTGCTTTGCACAGCAGCCCAACAGAAAAGCTCAGGAGCAGGTACTGAAGAGGAGAGTGGAGCTCAGAAGCAAGAGCCTGGCACAGCTGAAAAAGCCTTCTTAGAAGAAAAGACA[C/T]AACTGGAGGAGCAACTAAAAGATGTTACGGTAAAGCTGCATTCAATTCTGACCAAAAAAAGTTTGTTCTTGCATGTAATGTCTCTCTTCTACAATACCTGACATTCATTTGACCTTCATTTGTTTTTCAAGGACACCACAGCCCCTTTAGTTTCCACAGAGACCAAGGATTGTTTATGTGTTTGGTGTTTAAACGAATGCCTGTTATATGTGTAGTGTACTTTAAGTGCAACATACATTTTCAGATTAGCGATGCTCAGAACTTGTAAACAAAAAACTATAGATCTAAAAAAATGGTTCTCTCACATTACTATGAATAGGGGAAAAGTATAATGCTCAGTATGGCCACAGAAGTGAAGGAAGTCCTGCCTTCTGGCCGAAATAGCAAATTGTCTTTATAGCCGCACTGTTTTGTGGGGAAGGGTCTGTTCAGATTTGCTTGTTTGTTACAACAAGCCCTGTCATTTTGTGAATACTGGGTGCCTGCGTAGATTTTCACAG
Associated Phenotype:
Not determined