ZMP
timm50
Ensembl ID:
ZFIN ID:
Description:
Mitochondrial import inner membrane translocase subunit TIM50 [Source:UniProtKB/Swiss-Prot;Acc:Q6NWD
Human Orthologue:
TIMM50
Human Description:
translocase of inner mitochondrial membrane 50 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:23656
Mouse Orthologue:
Timm50
Mouse Description:
translocase of inner mitochondrial membrane 50 homolog (yeast) Gene [Source:MGI Symbol;Acc:MGI:19137
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42531 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22624 | Nonsense | Available for shipment | Available now |
sa12674 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42531
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048423 | Essential Splice Site | 234 | 387 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 19454439)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 20557065 |
GRCz11 | 15 | 20492797 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGCGCCACTTTATGAGATAGTCATCTTCACATCAGAGACAGGCATGG[T/A]GAGTCTCAGGGGTGATCGGGACTGTCTGTTTTCCGCAATAATGCCATTTC
Long Flanking Sequence:
CACTTTTTTTGGATGCAAACCCAGTTTGAATTTTCTTATGACAGACGAATATTTCAGAGGCAGTGTCAATATGATTGATATAACATGAGGTCAAATAAAGTATTTTACGTGTGAAAATTACAGACAAAAATTTCGGATTCAGTGTACAATAAGCTTCTCTACTCTAGACAGAGTCTTCAGTGTCATGTTTGAAATGGAGATTTTCTGTAATAATATATTTGTATTTAATATTTTTTATGACTTTTTGATTGGTTTCAGACGTCCTTGCCAAATAAAAGATTACTTTGTTTAAAAAAACTTAGTATATAAACCATCTAGATAAAAAATTGTGCAAATAACAATTTTGCCCAAATAAATGTTGTTCTTTTTCCTGGATCTTTTCTGTTTCTTCTAGTTGGCCACAGGTTGGCGTTTTAAGAAGAGGCCTGGCATCGACTACTTGTTTCAGCAATTGGCGCCACTTTATGAGATAGTCATCTTCACATCAGAGACAGGCATGG[T/A]GAGTCTCAGGGGTGATCGGGACTGTCTGTTTTCCGCAATAATGCCATTTCAATTGGCTTATTTGTTTTCGCATACATTGTTTCAAATGCAGTTGAAAGGAAACGTTTCTTGAACCCTGCTTAGCATATCGGGATACAATAGATGCTATTTTGGGAACAGCAGCACACCTTGATATTTGTTGATTCTACAAACGCTCCGTCTTGTGCAGATGTATAACATTTCGTTAATAGGGCCATTAGACAGATCCTTATGCAAAGCTGCAGTCTGTTGGTGTTTGTGTGTGTCTGTTGTTGATCTGTTGGTGTGGCACACTTCTACAGTCATGCAAATTAGCCTTGTTTTGATTGAACAGCCTTTTGCTGTTGCTTTTTTGTTTCATTCTAATGTATGCAAAAGTCAGTTCAGCTGTTTGCCATTGTGGAAAAAAAGGCCCATGCGCCACCCTGATGCTTTACAAATGTTACAGACCATTTTGAGGATTTCTGATGGGAGAAAAACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22624
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 |
---|---|---|---|---|---|
ENSDART00000048423 | Nonsense | 333 | 387 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 19440487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 20543113 |
GRCz11 | 15 | 20478845 |
KASP Assay ID:
2260-8358.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGTGTTCAGCTATTGCCATCAGCGGGGTGGAGGATGTGCGTTCAGTAT[T/A]AGAGAACTACGCCCATGAGGAAGACCCTATTGAAGCTTTCAAAAGAAGAC
Long Flanking Sequence:
AATGTTTTAACATTTTTATAATAAGATTTTATTAATTTCTTTTTATTATCTTATTTGTATAAAACTTCCAATTTATTTTCTTTCTTTAAATGTAGTTTTATGTAAATATCCACTTTTTGCTGTCATTTTTGTTGTTTATTTAGTGAGATTTATATTTGGGCAATTAACTAACTTTAGTAAAACTGCTAAATATTATTCAGCAATAACTGTGATTGTCTGTCCTGCAGGACGTGTCTTGTTTGAACAGAGACACCTCTAAAGTCATCGTGGTGGACTGTAAGCGGGAGGCTTTCGGTCTGCAGCCCTTCAACGGTTTGGCGCTGTGCAAGTGGGATGGAAACTCAGAGGATCGCACTCTGTATGACCTGGCTGCTTTCCTTAAAAGTGAGTTAGTGCACTATTAGAAATAATTACATCTTGTTTCGGAACTTTCATTTGTTGACTTGTTATTTGGTGTTCAGCTATTGCCATCAGCGGGGTGGAGGATGTGCGTTCAGTAT[T/A]AGAGAACTACGCCCATGAGGAAGACCCTATTGAAGCTTTCAAAAGAAGACAGGCACAGCTTGCACAGGTATGCACTTCAGTTTCATGATTGAGTCACAGGATTTACATTAAATGCAAGACGCTGCTGGTTTTTATTTTCCCTATGCTCCTGTACTTTGGGGATTTGGACTTTTTTCTTTTACAAATTCTTTTTACAATTTTAATGTAAAGGAAGCATCAAAATATGCTTAAACTCAAGTGTTTAATTTATAACACTTCATCAGTTTGTCTGAAGATTTCAATTACAATACATATTTGTTAGAGCTGTGAACCTACACTAGTCTCACAGTTTGGTTATGATTACCATGCCATCAATTCGGTTCAATTCGATATCTTGGTGCATTATGGTGAATAGATAATGCTTTCCATACACAGTTTTAGATTTTCTTTACAGGAGCAATTCTTGTATTAAAATGTATAAATATATTTATATACTATTTGTAATAAAATGTTGTCCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12674
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000048423 | Essential Splice Site | 355 | 387 | 10 | 11 |
Genomic Location (Zv9):
Chromosome 15 (position 19440419)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 20543045 |
GRCz11 | 15 | 20478777 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAAGAYCCTATTGAAGCTTTCAAAAGAAGACAGGCACAGCTTGCACAG[G/T]TATGCACTTCAGTTTCATGATTGAGTCRCAGGATTTACATTAAATGCAAG
Long Flanking Sequence:
CAATTTATTTTCTTTCTTTAAATGTAGTTTTATGTAAATATCCACTTTTTGCTGTCATTTTTGTTGTTTATTTAGTGAGATTTATATTTGGGCAATTAACTAACTTTAGTAAAACTGCTAAATATTATTCAGCAATAACTGTGATTGTCTGTCCTGCAGGACGTGTCTTGTTTGAACAGAGACACCTCTAAAGTCATCGTGGTGGACTGTAAGCGGGAGGCTTTCGGTCTGCAGCCCTTCAACGGTTTGGCGCTGTGCAAGTGGGATGGAAACTCAGAGGATCGCACTCTGTATGACCTGGCTGCTTTCCTTAAAAGTGAGTTAGTGCACTATTAGAAATAATTACATCTTGTTTCGGAACTTTCATTTGTTGACTTGTTATTTGGTGTTCAGCTATTGCCATCAGCGGGGTGGAGGATGTGCGTTCAGTATTAGAGAACTACGCCCATGAGGAAGACCCTATTGAAGCTTTCAAAAGAAGACAGGCACAGCTTGCACAG[G/T]TATGCACTTCAGTTTCATGATTGAGTCACAGGATTTACATTAAATGCAAGACGCTGCTGGTTTTTATTTTCCCTATGCTCCTGTACTTTGGGGATTTGGACTTTTTTCTTTTACAAATTCTTTTTACAATTTTAATGTAAAGGAAGCATCAAAATATGCTTAAACTCAAGTGTTTAATTTATAACACTTCATCAGTTTGTCTGAAGATTTCAATTACAATACATATTTGTTAGAGCTGTGAACCTACACTAGTCTCACAGTTTGGTTATGATTACCATGCCATCAATTCGGTTCAATTCGATATCTTGGTGCATTATGGTGAATAGATAATGCTTTCCATACACAGTTTTAGATTTTCTTTACAGGAGCAATTCTTGTATTAAAATGTATAAATATATTTATATACTATTTGTAATAAAATGTTGTCCTTTAACACAGTCAGATATATTAACTGTACCTATAAACAACAAAAGCATTTATAGCAAATAATATAAACAAAT
Associated Phenotype:
Not determined