Busch Lab

ZMP

tram2

Ensembl ID:
ENSDARG00000030092
ZFIN ID:
ZDB-GENE-040426-2024
Description:
translocating chain-associated membrane protein 2 isoform 2 [Source:RefSeq peptide;Acc:NP_998236]
Human Orthologue:
TRAM2
Human Description:
translocation associated membrane protein 2 [Source:HGNC Symbol;Acc:16855]
Mouse Orthologue:
Tram2
Mouse Description:
translocating chain-associating membrane protein 2 Gene [Source:MGI Symbol;Acc:MGI:1924817]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa23807 Nonsense Available for shipment Available now
sa43532 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23807
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043938 Nonsense 10 371 1 11
Genomic Location (Zv9):
Chromosome 20 (position 47841280)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 47639283
GRCz11 20 48116588
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAGTCGGGAACTTGTAAAATGGCTTTTCGCAGGAGAAACAAGAGTTA[T/A]CCCTTCTTCAGCCAAGAGTTTCTCATTCAGAATCACGCGGACATTGTCTT
Long Flanking Sequence:
TGATCAACAAGAACCAATCACAGTAGAGTGTGATTTTAGAAAAATGAACACAATGAATTATATAACCGATTTAATCGAGAACTGTAAGCGATTACATTTACTATTCAATATAGAAATACATTTTTATAATAATATGAAAAGAATACATGATATATTGTCCAATTAATTAATACAGTTTTAGGCTACGTTACCAGATTTATGGTAAAGACGAATGTTTAATGAATTTGACTAAAGATGTATTAGTATTATTATAACTAACTTATTTTACTAATTATGATTGTAATGTTACAAAAATTGCACTCATATTGGTCGGTCCACGCATTCATTCATAACACTAACAGCGCATGCGCTTTAGCTTTAATTCGTGGCTAAAGCGCGCATGCGCAGTGCGCTTGGAGAAGTTTGGAGTGATTCGTGGAAGTTTTAGATTTGGAGGAAAAAAAGCACAGCTGAAAGTCGGGAACTTGTAAAATGGCTTTTCGCAGGAGAAACAAGAGTTA[T/A]CCCTTCTTCAGCCAAGAGTTTCTCATTCAGAATCACGCGGACATTGTCTTCAGTTTGGTGATTTTCATTTTGATTGGGCTGATGTTTGAGGTGAGTTCAAGAGTTGTGGATCTTCTTCTTCTCCGAGTCTTTGCCAGCTGTTTTTCTGTCTGTCTGCCTATCTCAACGCGTTTAAATACAAACTAAACACTCAGTTTTAAAGCCAACAACGAGCACAAACACTATTACACAAAACCTACTTTTATTAGACTCAAATCACATCATATATTCATGTTTTTTTGTGTGTTTTTTTTTTTTTTTTTTTTTGTAAAAGTAAGTGTCAGACACGCTTATTTACATTAAAAACACGACACCACCATCTCTTTGGTCGAGCTTTTAAAATAAAACGTAGTGTTGTAAGGTACATTGAAAACACTGTCGCCATCACCTGGGCCCTGACGTCTGCAGTCTGATGAGGAGGAAGAAACTCCACGTAAACTCCAGAAAACATTGTTTATTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43532
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043938 Essential Splice Site 292 371 9 11
Genomic Location (Zv9):
Chromosome 20 (position 47856907)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 47655132
GRCz11 20 48132438
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGACTCTTGATTTGGAGACGGGAAACTTCAACACTCTGTCCATCAGG[T/C]GAGACTTAGAATTTTTTTTATTTTTCAAAGTAGCATTTAGCATTAAACAT
Long Flanking Sequence:
GAACATGCTAACTCCACACTGAAATGCCAACTGAAACAGCAAGAAGTCACTGGTTTGAGCCTCCTGCCCACTGTGCCACACCCACTGTGCCACTGTGCTGCCCTAGTCTTATACAATCTTTATCTTTTAGTCTTTAATAAGCAATCTATTCTTTGCGGATACACGTGTTGCGATATCGATGCTCAAACAATATATTGTTCCTCTCTAAATGAAAGAAATTACATTTTAAAATGTATTCTAATAGAAAGCAATTCATTATAGCTGCACTAATATTTCACAATATTGCAGACTTTCCTGTGTTTTGGATCAGAGAAGTGTCGACACATGAGGCTTACGCGTGTGCTTGTGTTTGTAGGTTTGAGATGTGGTCTGTGGGCTTTGTTCTGACTCGGATGATCACTCTGACGCTCATGTTTTTGGCCGTTGGCTTTGGTTTGGCTCGTTCTGAAAACCAGACTCTTGATTTGGAGACGGGAAACTTCAACACTCTGTCCATCAGG[T/C]GAGACTTAGAATTTTTTTTATTTTTCAAAGTAGCATTTAGCATTAAACATGTTGGTAAACAGTTTAAAAACAATCTTGCAGGATAATCTTGGTTAAAATGACCATATTTAAAGGCCACCTGTTATGCACAATCAGCTTTTGTAAAATATTTGGATGGAAATGTCTGTAGGCACTGCTGTATTAAGCCTGGTTTATACTTCTGCGTCAAGTGACCAGCGTAACTCATGGCGCAGGCAACGCGCGTGGCTGTGCATTTATACTTCTGCGCGCTGTCTCCGTTGGTCTGCATTAACACTTCCGAAACGCTAGTTGGCAGTAAGGTGTAAATGTTCCTCTGTGTCGAGTTTCTTCGCTGCTGTTTTGCTTTTCCTTAACACTTCCTGGTTGTAGAAGTGACTCAAACTCGCTCATTTTGAGGCAGGAACCGGCGGACGTGCAACAACTTTAACTATGAGGTAAACACAAAACAAAACTTTCCATCCGGAGCTCCTTCACGGGAC
Associated Phenotype:
Not determined