Busch Lab

ZMP

trim35

Ensembl ID:
ENSDARG00000035009
ZFIN ID:
ZDB-GENE-030131-6185
Description:
tripartite motif-containing 35 [Source:RefSeq peptide;Acc:NP_956172]
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 2 alleles of this gene:

Allele Name Consequence Status Availability
sa35616 Nonsense Mutation detected in F1 DNA Not yet available
sa42319 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa35616
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049918 Nonsense 245 560 4 7
Genomic Location (Zv9):
Chromosome 14 (position 758203)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 741034
GRCz11 14 759416
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTCCATGTGGTCGTGTGTGCAGAGCTA[T/G]AAAGATGACCCTGACAGGTGAGTTTCTGAGCTCTGAATCCTCTCATCATC
Long Flanking Sequence:
GGATGGATGGATGGATGGATGGGAACAATAGATGGAAAGGGATGGATAGATGGATGTATGGGTAGATAGATAGATAGATAAATAACTGGATGGATGGATGGATAGATGGACAGACAAGATGGATGGATAGATGGCTGGATAGATGATTGGATAGATGGATGGATGATGGATGGATAGATGGACAGACAGATGGATAAATGGCTGGATGGATGGATGGATGGAGGGGTAGATGAATAGATGTACGGGTATATAGACGGATGGATAAATGGGTGGATAGATGGGTGGATAGATGGGATGATAGATGGATGGAAGGGTGGATAGATGGATGGATAAATAGATGGAATGATAGATAGATGGATGGATGAGTAAATCAATATAGACTTATTGTGTATATTGAGATTAGTTTGTAATCATCATCTCTCTCTCTCTCTCTCTCTTTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCATGTGGTCGTGTGTGCAGAGCTA[T/G]AAAGATGACCCTGACAGGTGAGTTTCTGAGCTCTGAATCCTCTCATCATCTGCATCTCCTGCAGTTCTGACTCTCAGATGATCTTCAGTTTTCAGAGCTTCAGTTTGAGTTCAGACTCAGAGGATCCTCCAGAGCAGCTGCTGGACGTCTGCAGACACCTGGGAAACCTCAAGTTCAGCGTCTGGCAGAAGATGCGGACCGCCGCTCAATACAGTGAGTCCTGGATATTTTACGAGCCCTGTTTTTGTTTTCTTTCCCATGTTTTTTTTTTTTCAATGAATTTCTAACGATTACTTTTATTTGATTTTTATTTTATTATTTTTTATATGGGAGGTTAGAGGTTGCTGGAGTGTTTACTGGAGTAGTGTTACATTCAATCAATAACATATTCATGCAGCACGTTTAATAAAGAAATTCAAAATATGAACATTTTCAGGATCTCTCTACATCTCTAATGAGACACTTCTGAATGTAATGTTTGTTCCTCCGCAGCTCCAGTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42319
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000049918 Nonsense 321 560 6 7
Genomic Location (Zv9):
Chromosome 14 (position 757625)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 740456
GRCz11 14 758838
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTGCGTGTGTGTGCGGGTCTGCGCTCGCTCCGCTTCAGCCGCCGCTG[T/A]CCTCCAGCTCTGTGTATTGCAGGTGGGCGTGAGGGTTACTCCAGTGTTTT
Long Flanking Sequence:
ATGATCTTCAGTTTTCAGAGCTTCAGTTTGAGTTCAGACTCAGAGGATCCTCCAGAGCAGCTGCTGGACGTCTGCAGACACCTGGGAAACCTCAAGTTCAGCGTCTGGCAGAAGATGCGGACCGCCGCTCAATACAGTGAGTCCTGGATATTTTACGAGCCCTGTTTTTGTTTTCTTTCCCATGTTTTTTTTTTTTCAATGAATTTCTAACGATTACTTTTATTTGATTTTTATTTTATTATTTTTTATATGGGAGGTTAGAGGTTGCTGGAGTGTTTACTGGAGTAGTGTTACATTCAATCAATAACATATTCATGCAGCACGTTTAATAAAGAAATTCAAAATATGAACATTTTCAGGATCTCTCTACATCTCTAATGAGACACTTCTGAATGTAATGTTTGTTCCTCCGCAGCTCCAGTGGTGCTGGACCCGAACTCTGCTCACCCTTGCGTGCGTGTGTGTGCGGGTCTGCGCTCGCTCCGCTTCAGCCGCCGCTG[T/A]CCTCCAGCTCTGTGTATTGCAGGTGGGCGTGAGGGTTACTCCAGTGTTTTGGGCTCTGTGGCTCTGGGCTCCGGGTCGCACCGCTGGGACGTGCATGTGGGCGACAGCAGCGTCTGGGCTTTAGGAGTGATCTCTGAATCCGCCCTGCAGACCCAAGACCAGCTGCCCGAATCTGGACTGTGGATCCTGGGCTTCCAGAGTGGGGAGTACGGCCAGGGCTGCTGCGGAGAGAGTCTGTCCCGGCTGGGGGTCCGACAGAGGGTCAGCAGGGTCACGGTGCTGCTGGACTGGGACGCCGGAAAGCTGACCTTCCTGGACTCACTCACAGGTTACTATATAAGTTGTTGTAGTTTAACATTTTTAATTTGTTTTTATTTTAATTCTATTTTTTTTTATGTTATAAACTTCATATTATTTTAGTTGTTGATTATTTAATTAGTTTGCAATTGCAATTTAGGCTATTTTCAGGACGTTTTTCAGTGAATGCTGTTAGTTTCCTT
Associated Phenotype:
Not determined