Busch Lab

ZMP

zgc:73356

Ensembl ID:
ENSDARG00000037356
ZFIN ID:
ZDB-GENE-040426-1776
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.
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.
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