Busch Lab

ZMP

si:ch211-175l6.3

Ensembl ID:
ENSDARG00000071225
ZFIN ID:
ZDB-GENE-060503-201
Description:
hypothetical protein LOC561381 [Source:RefSeq peptide;Acc:NP_001038423]
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
sa7266 Nonsense Mutation detected in F1 DNA Not yet available
sa39993 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa7266
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
ENSDART00000040967 Nonsense 37 290 1 5
ENSDART00000141995 Nonsense 37 451 1 6
Genomic Location (Zv9):
Chromosome 3 (position 8117680)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 8087922
GRCz11 3 7973762
KASP Assay ID:
554-4443.1 (used for ordering genotyping assays)
KASP Sequence:
AGAATCCTGTAGTTTTATCATGCAGTCACAGYGTGTGTAAAGAGTGTCTT[C/T]ARCAGTTCTGGGGAACCAAGAATACTCARGAGTGTCCTGTTTGCCGGAGA
Long Flanking Sequence:
ATTTTGGCAATTAAAGAGTCAAAATCCTTTAATTTTCGTTAGTTAATTTTTTTATAAAGTTTTTTTTAGATGTTTTTTGTTAAAATTTGAACTAGAATCCTGAAGTTGTTTGACCTGTTTTATCACACACACAAAAGGAGATCAGAGATCTGCCCTCTTACAGCTCTGACCAGGAAGAGACTTATTATTTCTGCTTTCTGTCACTCAGACTCTTTTCATTTCTATACGGGAATTAAACACAATTGGAAATCAGCTAAGAATGAAGAGAAACCCCATTCAAGAAGGATTTCTGTGATATTTGTCTCTAAACAGGTGGCAGATCTTTGTTTACTTTTTATAATCATTTAGAAAGTGAACGTAAAGCTGAGATTTCTGGAGCTCAAACAGTGGAAATGGCTTCACTAAATGTATTCAAAGAACTTTCTTGTCCCGTGTGCTGTGAAATCTTCAAGAATCCTGTAGTTTTATCATGCAGTCACAGTGTGTGTAAAGAGTGTCTT[C/T]AGCAGTTCTGGGGAACCAAGAATACTCAGGAGTGTCCTGTTTGCCGGAGAAGATCATCAAAAGAAGAACCTCCAGTTAGTCTTACATTAAAAAACCTGTGTGAGTTGTTCCTGAAGGAGAGAAATGAGAGATGTTCATCAGGATCTGAGGAGATCTGCAGTTTACACAGTGAGAAACTCAAACTCTTCTGTCTGGGGGACAAACAGCCTGCGTGTGTGATGTGTGTTACTGTACAACAACACGACAATCACAAATTCAGACCCATCAGTGAAGTGGCTTCATCATACAAGGTAAGACAAGACCTGATGTAATAACTGACCAGTTGCATCTTGTGCATTTTGGTCAAGTATATTTTTACACAGGAGTTGTTATTGAGTATCTCTTTGTTTTATAAAACAAATAGTCTTAATAAGCTGCACTTTGATTTATTACACTGTTGTTTTATGTTACAGTATATATCAGTGTTTCTCAACTGGTGGGTTGCGACCCAAAAGTGGGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39993
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
ENSDART00000040967 Nonsense 203 290 3 5
ENSDART00000141995 Nonsense 203 451 3 6
Genomic Location (Zv9):
Chromosome 3 (position 8124377)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 8081225
GRCz11 3 7967065
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGAGATGAAGAAGAAGCTACAATCACTGCACTAAGAGAGGAAGAGGAG[C/T]AGAAGAAGCAGATGATGAAGGAGAAGCTGGAGGAGATGAACACACACATC
Long Flanking Sequence:
CAGGAGGAATGGGCCAAAATTCCTTCAAACTATTGTGAGAAGCTTGTGGAAGGATACCCAAAACATTTGACCATTGAATGTTTGAAAGTTATACAGTTTAAAAGCAAAGCTAAAAAAAATACCAAGGAAATGTATGTACATGTAAACTTTTGACTGTCTAGAAATTAATATAAAATTCTTAAAACACAATTATCTCATTATTCTGGCATTTAGCAAATGTAAATTTGTAAATGTAGAATTTATATGTAGAAATAAATAAATGTAGACATTTATTTTAAAAAAAATGTTTGTAAACTTCTGGGTTTAACTGTACTTAAGTCTATTTTAAATATTTTTGATGTGATGTTTTTGTATGTTGACTATTAAATGTGTCTGTGATTTGTTTTCAGACTCAAGCCGATCACACAGAGCGTCAGATTAAACATGAGTTTGAGAGGCTTCATCAGTTTCTCCGAGATGAAGAAGAAGCTACAATCACTGCACTAAGAGAGGAAGAGGAG[C/T]AGAAGAAGCAGATGATGAAGGAGAAGCTGGAGGAGATGAACACACACATCTCAGCTCTTTCACACACGATCAAAGACACGGAGGAGATGCTGAAAGCCAATGACGTCTGCTTTCTAAAGGTCTGATTTCAGATCAGTGATTGATTGATTGATGATGGATTGAGCTCTTGATGATCAGTTGTGTGTTTGTTCTGCAGGAGTTTCCAGTCTCGATGGAAAGGTGAGTGATCTGCTGGTGTCTCTGCTCTCTCTGCTTCTGAATCCTGCAGTTCTGACTCCTGAATGTTCTTCCAGAGTCCAGATCTCACAGCCGGATCCACAGACGCCTTCTGGAGCTTTGATTCATGTGTCTCGCTACTTGGGGAACCTGACATACAGAGTCTGGAAGAAGATGCAGGACAACGTCCACTACAGTGAGTCTCTACATCTCTGCTCACACAAACAGTGTTTCACTGAAGTACTTATACTAGTTTAAAGTGAAATACTGTGTAAAGTTTTTTG
Associated Phenotype:
Not determined