Busch Lab

ZMP

TRIM35 (12 of 41)

Ensembl ID:
ENSDARG00000092407
Description:
tripartite motif-containing 35 [Source:HGNC Symbol;Acc:16285]
Human Orthologue:
TRIM35
Human Description:
tripartite motif-containing 35 [Source:HGNC Symbol;Acc:16285]
Mouse Orthologue:
Trim35
Mouse Description:
tripartite motif-containing 35 Gene [Source:MGI Symbol;Acc:MGI:1914104]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa17348 Nonsense Available for shipment Available now
sa36154 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17348
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000135053 Nonsense 55 348 1 6
Genomic Location (Zv9):
Chromosome 16 (position 29075863)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 26951637
GRCz11 16 26825079
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTRGAGTGTCCTGTTTGCAGGAGACGATCGTCCAGAGATGATCCTCCTTG[T/A]AATCTTGTKTWGAAGAACTTGTGTGAGTCACTGACAGCAGACAGAGCTTC
Long Flanking Sequence:
AGACTGAATACTGATCATGCCAGTGACATGCAGATTCTCCGGGTCATGAAACGCTTCTGAAATGATCGATGCTTTGAATCGCTTTTGTCACGTGACCAAGTGTTTCGAAACACTTTAGTCACGTGACCTGGGTGTTTCGGATCATGCTTCGGTACAGTGTTTCGAAACACTTGTGCTTCGGGATCTCGACACTGTGTCGAAACGTCAGTTTCACGTCAGCCATCCCTAGATATCTCACTGGATGAGAATACAAAAGACCAATTGAAAGTGAAAGAAAGATCTAGAGATAATTTGGTTGAACGCTGAAGAATGGCTTCTGTGAAAACAGTGTCTGTGGAAGACCTTACCTGTCCTGTGTGCTGTGAAATCTACAAGAATCCTGCAGTGCTGTCATGTAGTCACAGTATATGTAAAGAGTGTGTTCAGCAGTTTTGGAGCCTGAGAAATACTCTGGAGTGTCCTGTTTGCAGGAGACGATCGTCCAGAGATGATCCTCCTTG[T/A]AATCTTGTGTTGAAGAACTTGTGTGAGTCACTGACAGCAGACAGAGCTTCAGGGTCTGAGCTGGACTGCAGTTTTCACAATGAGAAGCTCAAACTCTTCTGTTTGGATGATGAACAGCCTGTGTGTCTTGTGTGCAGAGATTCACAAAAACACACCAATCACAGGTTCAGACCTGTTGATGAAGTTGTTCCATCTTACAGGGTAAGTCACATATTGGCAGCTTCAATTAAATAACGCGTAAAAAGTTAAGAGGAATGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGCGTGTGTGCGTGCGTGCGTGCGCGTGTGTGTGTGTGTGTGTGTGTGTGTAATACCTCATCATGCTGATAGATGGCAGTACAATAAAACATAACCTGTCACCGAAAGCCTCAGTTTCCAATGTATGTCGTTTTCTTTGGTGTTCATGTTATTTAAAAAATAGATATGAGAAAATATTAGCTTGAACAGTGAGAAATGAAAGAATTTAATTCCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36154
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
ENSDART00000135053 Nonsense 244 348 5 6
Genomic Location (Zv9):
Chromosome 16 (position 29077118)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 26952892
GRCz11 16 26826334
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACTCACTGCAGTTCTGACTACTGAATGTTGTTCAGAGCTCAGAGTTCA[C/T]AGCAGCAGGATCCACAGAGGATTTCAGGAGCTTTGATTAATGTGGCAGAT
Long Flanking Sequence:
AAATGCTGAGGTAAATTTCTCTGTTTTCATTTTTATTTTTTATTCAGACTCAGAGTGAGAGCACAGAGCGGCAGATTAAAGAGGAGTTTAAGAAGCTTCATCAATTTCTGCACGATGAAGAAGAAGCTTTAGTCTCTGCACTGATGAAGGAGGAAGAGCAGAAGAGTGAGATGATGAAGAACAGGATTGAGGAGATGAACAGACAGATCTCAGCTCTAGCAGATACTATAAAAGACATAAAAGAAAAGATGAATGCCAGTGACACCTCATTTCTACTCGTGAGAAATGATTGTTTTTTTATTTAAAACATTTACCATGTGTTTCGATTCAAAGCACCATTGATATAATATTGAAACACTGATCATGTTCCGTTCTATTTCCCAGAGCTTTAAAGGCATCATGGGAAGGTAAGTGAGTCACTGTGTCTCTCGTGTTTGTGATTATGAGCTCAAACTCACTGCAGTTCTGACTACTGAATGTTGTTCAGAGCTCAGAGTTCA[C/T]AGCAGCAGGATCCACAGAGGATTTCAGGAGCTTTGATTAATGTGGCAGATTATCTGAGAAACCTCACCTTCAGAGTCTGGAAGAAGATGCAGCAACTTGTTTACAACAGTAAGTTCTCATTGATTTGAGATATCATGCACTGTAACAAATGAGCCCATTTTGGATAGATGCATTTCTTTGTCCCAAATCATGTCTTAGAAACTCAATGATGCTAAAAAGTTTCTATAAAGATTCTTTGGTAAAAACATTTCCTGAAATCGAAGATGACAGTCACACAAACCTATAGATTATTTAAAAACACAAAACATATTCATATCAGATGCTCCCAGCTCTGTTTTGTTTAGACTTCCATGTTGGAGATTTTGTCTTATAGGTTTAGTCCATCCTTAAAAGGACAGTTCTGTCATCATTTACTCAACCTTGACTTTCTCCAAACCAGTTTAAGAGTTTTTGATTTGTTAAACACTAAGGAAAATATTTTGAAGAATATTGAAAAACTG
Associated Phenotype:
Not determined