Busch Lab

ZMP

tmem132e

Ensembl ID:
ENSDARG00000090830
Human Orthologue:
TMEM132E
Human Description:
transmembrane protein 132E [Source:HGNC Symbol;Acc:26991]
Mouse Orthologue:
Tmem132e
Mouse Description:
transmembrane protein 132E Gene [Source:MGI Symbol;Acc:MGI:2685490]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa12525 Nonsense Available for shipment Available now
sa12566 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12525
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130565 Nonsense 318 631 5 5
ENSDART00000130565 Nonsense 318 631 5 5
Genomic Location (Zv9):
Chromosome 5 (position 62375070)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 60010260
GRCz11 5 60684027
KASP Assay ID:
2259-6657.1 (used for ordering genotyping assays)
KASP Sequence:
ACAACCTCAATGGCACTTCAGMGGATGATAAGGTGGTCACGGTGGCACAA[C/T]AACCCCAACAGCGGTGGCCAGTCRTCATCGCTGAGGGTGAGGGCACAGGA
Long Flanking Sequence:
ATGAATTTTTGTTATTGTATAAGTGAATAGTATGTCATTTGGGATGCAACTTGGGTCCTCAGATTCACTAAAAATTCTGTTGAATGTTGCAACCTCCAGGTGGTGGTTTGGACCACCCAATTCTAGTTTTGTAACTATCTGCCAAAGACACAAAGGTATTTTTAATCTCATCTGGAGATCACTTTCTACTTGTGTGTTGTGTGTGTGTGTGTGTGTACTGACACATAACTGTGATATGTTGCTTTTTGTTCTTTGCCTTTTTGACTGCCAGAGTGCATCACAGGCACCGAAGAAAGAGTTCAATTACAGATTTTCTTTTTTTATATGGTGTTTAAGTGTTGATACTCACAATGTCTTTTGTTTTGTGTTTATAGGAGGCCAGCTTTTCCATCTGGGTTTACTACAGTGACAATACAGCAGCTCCACTGAGTATGTATGATCCTAAAGACTACAACCTCAATGGCACTTCAGCGGATGATAAGGTGGTCACGGTGGCACAA[C/T]AACCCCAACAGCGGTGGCCAGTCATCATCGCTGAGGGTGAGGGCACAGGAGACATAGTTCATGTGGAGATGACCATCTCTGAAACCTGCCAGAAGACCAAACGTAAGAGCGTAATTGCTTCATCTTCTGTGTTTGTCAAAGTCCGATTTGGAACAGATGAAGACTCTGAGGAGGATATGGAGATGGAGACTGAAATAGACACTAGAATGCCTGCCAACACAAGAAGGCCCGCTATTGATTCCAATGTGGGTGGTGCAGGGTATGAACCATCTAATGAGCAACCCGCAAGTGTACCCATTGATTACACAAACTTCCCTACGATAAGCAATCCGGAAGAACCAACTGAAGAAGACGAAGAGGATGATGAGTTTGTGCACAGTCCACGTAGCATGACTGACCTAGAGATCGGCATGTATGCTCTTCTTGGGGTGTTTTGTCTTGCTATACTGGTCTTTCTTATAAATTGTATCGTGTTCGTATTGAAGTATCGCCATAAGCGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa12566
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000130565 Nonsense 318 631 5 5
ENSDART00000130565 Nonsense 318 631 5 5
Genomic Location (Zv9):
Chromosome 5 (position 62375070)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 60010260
GRCz11 5 60684027
KASP Assay ID:
2259-6657.1 (used for ordering genotyping assays)
KASP Sequence:
ACAACCTCAATGGCACTTCAGMGGATGATAAGGTGGTCACGGTGGCACAA[C/T]AACCCCAACAGCGGTGGCCAGTCRTCATCGCTGAGGGTGAGGGCACAGGA
Long Flanking Sequence:
ATGAATTTTTGTTATTGTATAAGTGAATAGTATGTCATTTGGGATGCAACTTGGGTCCTCAGATTCACTAAAAATTCTGTTGAATGTTGCAACCTCCAGGTGGTGGTTTGGACCACCCAATTCTAGTTTTGTAACTATCTGCCAAAGACACAAAGGTATTTTTAATCTCATCTGGAGATCACTTTCTACTTGTGTGTTGTGTGTGTGTGTGTGTGTACTGACACATAACTGTGATATGTTGCTTTTTGTTCTTTGCCTTTTTGACTGCCAGAGTGCATCACAGGCACCGAAGAAAGAGTTCAATTACAGATTTTCTTTTTTTATATGGTGTTTAAGTGTTGATACTCACAATGTCTTTTGTTTTGTGTTTATAGGAGGCCAGCTTTTCCATCTGGGTTTACTACAGTGACAATACAGCAGCTCCACTGAGTATGTATGATCCTAAAGACTACAACCTCAATGGCACTTCAGCGGATGATAAGGTGGTCACGGTGGCACAA[C/T]AACCCCAACAGCGGTGGCCAGTCATCATCGCTGAGGGTGAGGGCACAGGAGACATAGTTCATGTGGAGATGACCATCTCTGAAACCTGCCAGAAGACCAAACGTAAGAGCGTAATTGCTTCATCTTCTGTGTTTGTCAAAGTCCGATTTGGAACAGATGAAGACTCTGAGGAGGATATGGAGATGGAGACTGAAATAGACACTAGAATGCCTGCCAACACAAGAAGGCCCGCTATTGATTCCAATGTGGGTGGTGCAGGGTATGAACCATCTAATGAGCAACCCGCAAGTGTACCCATTGATTACACAAACTTCCCTACGATAAGCAATCCGGAAGAACCAACTGAAGAAGACGAAGAGGATGATGAGTTTGTGCACAGTCCACGTAGCATGACTGACCTAGAGATCGGCATGTATGCTCTTCTTGGGGTGTTTTGTCTTGCTATACTGGTCTTTCTTATAAATTGTATCGTGTTCGTATTGAAGTATCGCCATAAGCGC
Associated Phenotype:
Not determined