ZMP
zgc:73356
Ensembl ID:
ZFIN ID:
Description:
Mitochondrial import inner membrane translocase subunit Tim16 [Source:UniProtKB/Swiss-Prot;Acc:Q6PBL
Human Orthologue:
PAM16
Human Description:
presequence translocase-associated motor 16 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:29679]
Mouse Orthologue:
Pam16
Mouse Description:
presequence translocase-asssociated motor 16 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40010 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44557 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40010
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 |
---|---|---|---|---|---|
ENSDART00000054356 | Essential Splice Site | 1 | 129 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 12810649)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 12199703 |
GRCz11 | 3 | 12352646 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCGTCCTAAACCGAGCTGTATCCCATCACCACAGCTGTCCAACCATGG[T/A]ATGTTCAGAAATTCATATAATAATCTCTAGCGCTTTATGGTTTCTATGTC
Long Flanking Sequence:
CACTATCTCGCCAACTGGAACATATTTAAATCATGTTTTCTGTGTTATATTTCACCTGCAACAACAATACTGAACTTACATAAAGACGTGTTTGAACATTAAGGTCTGAATGCATATTATCCAAGGACCTGGGGAGATTTCTCTGCATGAAAGACTAATAAATGGGAGATTAACCTGCTGCTGCTTCTCCAATAAGGTTAAAGAGGAAGTAGTATGTCCCAAAGCTTGCATACTCTTCTGTTACACACTCAAAAGTCTAAACTTTTAGGGCGTAGTAGGAGTATGCGAATTGGGACGCAGCAGTGAATTAGCCATCCGGGTTTCTTACGTAGTGACGTAAGCGCCGTGCGTCTAATCTCTGCCTCCTCCAGCCAGCAGGTGTCAGTGCGCGTGCGTGTGACTTCTCTCGTCCGGCTTCATCAACCTTCATGGAGTTTCACACGTGAAAATATTCGTCCTAAACCGAGCTGTATCCCATCACCACAGCTGTCCAACCATGG[T/A]ATGTTCAGAAATTCATATAATAATCTCTAGCGCTTTATGGTTTCTATGTCTGTAGCGGTGTGTTTAGTCTCTGGACATGATACGTTAGCAGTTGATTATTCCGTAACATGATCGCATGAAACGACCTTGTATTCACATTTTCACCAAATTAATACTGTCATTTTACATTCTGAACAGAATATAGTTGTATGAACGTTTGTTTAACGTATATATGTGTGATGAAGTGATATGAACCTATATCAAGACATGTTTAATTGACAAACATGTTAGCTTAAAATACACTTATCTTATTTATGTACGTAATGTAATGTGCATTTATATGGCGTTTTTATTATTATAGTAAGTGATTAAGGTGCTTATTAAACGTTATTTATTGCTAGACTTTTATTATGAAACAGTAGAATGTCAGTGTGACGTCATATTCTTGCCATTTAACGTTACTAATATTGAGGAAAACTTGGTTTATTTGTTTTAGATTTTTCTGGTTTGATGTTGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44557
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 |
---|---|---|---|---|---|
ENSDART00000054356 | Nonsense | 44 | 129 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 12813564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 12196788 |
GRCz11 | 3 | 12349731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAATCAGCCAGTCAGGCGGCTGCGGAGGCTCGAGGTCAAGCGGGCAGA[C/T]AGTCTGCGGCGGCGTCCAGTTTCACAGGAATGACCTTACAGGAAGCCCAG
Long Flanking Sequence:
ATTGAAATAAAAGATTGTTAATAACTATTATAACACTTATTGCTTTTTCACCTTGTTTAGTATATGTGTTTGTTTATATTAAGTCAGTATTTGCAAGGAGAAACAATTAAATAATATTTTATGTTGCATTATGTTCTTTTAGGTATCATTTTAAATCACTACGATTAACATATTAATCACTATAAATATATTATTAATAACATATTAATAATTTATGTCATTATATAATATTTACTATTTTATTAAACTCATTGCATGCATGAAGTAAACGACATTTTAACAATACACTTTAACATCAAACTTTAAACTGAATGCTAGTATCTTGCAAAATATTATGTACTGTCATCACAGAAAAGACCCTATACATTGTTTATGTATAATGCACACACATTGGCCAGACCTAATCCTAATAGATGAGTGATGTTATTAATCAGGTGTGTGTTTGTGTGTGTGAATCAGCCAGTCAGGCGGCTGCGGAGGCTCGAGGTCAAGCGGGCAGA[C/T]AGTCTGCGGCGGCGTCCAGTTTCACAGGAATGACCTTACAGGAAGCCCAGCAGATACTTAACATCTCCACACTAACGCCAGAGGAGATCCAGAAGGTCAAACAAATTCACCAGCACACAAACATCACAGTGTTCCCACTCCGAGTAAATATGATATTAACTTTGTGCTTTCATTCTCTTTTCAGAATTATGAGCACTTATTTAAAGTCAATGACAAAGCTGTCGGCGGTTCTTTCTATATTCAGTCGAAGGTAAGAGATGACGCTGACAAAATCAACTGTGACTACAAAACCAGTCTTGTATATTTTTGGTTGTAACTGAAAATACATTATATGCATCAAAATTATACATTTTCTGTACTTTTATGCCAAAAAGTCATTAGAAGGTTTAGTACAGATCATGTTCTGTGATGATATTTGGTTAATTTCGTACTGTTAATTTTCCTGTGTCTTAAGTGTAAAAGTAGCATACAGAGGAAAAGAAAAACCAACAAGAAAATAA
Associated Phenotype:
Not determined