ZMP
trim3b
Ensembl ID:
ZFIN ID:
Description:
tripartite motif-containing 3b [Source:RefSeq peptide;Acc:NP_001073637]
Human Orthologue:
TRIM3
Human Description:
tripartite motif-containing 3 [Source:HGNC Symbol;Acc:10064]
Mouse Orthologue:
Trim3
Mouse Description:
tripartite motif-containing 3 Gene [Source:MGI Symbol;Acc:MGI:1860040]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6173 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15924 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6173
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008134 | Essential Splice Site | 45 | 748 | 2 | 12 |
ENSDART00000109183 | Essential Splice Site | 49 | 772 | 1 | 12 |
ENSDART00000136472 | Essential Splice Site | 49 | 752 | 2 | 12 |
The following transcripts of ENSDARG00000005397 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 26790145)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26194002 |
GRCz11 | 10 | 26155715 |
KASP Assay ID:
554-4398.1 (used for ordering genotyping assays)
KASP Sequence:
CACTACCACAATCCCAAAGTCCTGCCCTGCCTGCACACCTTCTGCGAAAG[G/T]TCTGTATCTGTTGCCACTTTGATTGATAATTAAARAGGGAAKGAGGAATT
Long Flanking Sequence:
ATGAAAACACTGATGCATAGTTTGATCTCTGTAGAACTTGGAGCAATCCTCCGGTCCAGCTTTGTCTTATTAATAGTTTTTTTTGTGTATAGATGTCTGTGACATTAGTTTTCACTGTGCTGATGGTTTATTTGCATCCTATTTGTTGTTCTGTTAGCGTAAGTAAATTTTTTTTTTGCAGTAATCTCACAGTTTGAATTTTGTCTGGTTCAATTCACCACTGTCATTTTACTCTTCCAACCCAAATCTTACTTGCCGCTGGTGTGTTTTTTTTATCAAATAAATGTTTTTGTTAACTCATCATTTTGTTCTTTTTAGGTTAAGGTTTGTCCTGGCCCTCGGCCACGTCTTTGGATGTCTGTCACAATGGCAAAGTTTGAGACCGGCCGCACAAGCCCAGTGGTCCGTCAGATAGACAAGCAGTTCCTGGTGTGCAGTATCTGTCTGGACCACTACCACAATCCCAAAGTCCTGCCCTGCCTGCACACCTTCTGCGAAAG[G/T]TCTGTATCTGTTGCCACTTTGATTGATAATTAAAGAGGGAATGAGGAATTATAGGAAGAAGATTCAGTAATGAGTCTCAATTGAACTCGTATACTTAGTGGCATTAAGCCTATTAAAATGAGTAATAAGGATCTTGTAATAGCGCCCTCAGTAATTGAAGCATGAATCGGCAGTTATCCTTTTTATAAGATGGCATATGAACTTTGAATACTTGCTTCTGACAGAATTTGGCACGGATGGGGACTCTGCACCTAGAACAGTTTTGACATGAGATGTGCGCAGTTTGACAATGAGACTCTCTCTGTTTGTTTTGGGCTTTGTATGTCAGTGGATGCTTTCCACTGTGATTGTCCGTGTTGTGACTGAAATTTCAGCAGCATTTGCCCTTCTTTTACTTTTGCTGTGTCTAACAGGAGGATCTAATTTATGAAATGAGACCTACTACTATAAGGATGTTTGGATTTGGTCTAAAAACAAAAAAGAAATTAAAACATTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15924
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008134 | Nonsense | 263 | 748 | 6 | 12 |
ENSDART00000109183 | Nonsense | 267 | 772 | 5 | 12 |
ENSDART00000136472 | Nonsense | 267 | 752 | 6 | 12 |
The following transcripts of ENSDARG00000005397 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 26778734)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26182591 |
GRCz11 | 10 | 26144304 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGGGAAARGAGCACATCCAGAGCAGCTGCAGTTTCACCGAACAGGCAT[T/A]GAGCCACGGCAGCGCTACTGAAGTCCTGCTGGTYCAGAAGCAGATGAGYG
Long Flanking Sequence:
AATATCTGTGGGTATAAGTTATAAGTGCAATTATAGAAGACTATAATATTTACAGATGGATGTACTATGAGCATAACATACAAGTCATATTAACAAGAATCATTGGTTTACAAATAGATGAACATACTGTACAGGTTGCCATTAATGATCAGGGATATGCAATTCAGTATGAACATAATATACATGTTGTTATTTGCTATAAACAGGAATTACAAATAGACATGTAGATATGTATATCATACATTTACGAATGTATAAGTGCTGTGGATATGTGCACTTACAAACTCTTTGAACTATACATGAAGATGATTTTGTTGAAAATTAGTCTTAAAAAAACGGTCTGAAAATGTGATTAATTTTTCAAGATAACTAATATGAAAGAAAAAGAAAAGGAAATTATCTTCTACCCTGTCTTCCGCAGGTTCTTCAGGCGCAGTTATCGTCACTCCTGCAGGGAAAGGAGCACATCCAGAGCAGCTGCAGTTTCACCGAACAGGCAT[T/A]GAGCCACGGCAGCGCTACTGAAGTCCTGCTGGTCCAGAAGCAGATGAGCGAGCGGGTGAGTGCTCTCGCCTGCCATGACTTCCCAGAACGCCCACATGAAAATGCCCACCTGGACTGCCAGATTGAGACTGAGGGCCTGCGACGCTCCATACAGAACCTGGGCGTCCTGCTGACAACGGGGGCTGTGGGACATACGAGCGTGGCCACCGGAGAGGGACTCAGACACGCTCTGGTCGGCCAGCATGTGACTGTGACCGTCACCACTAAAGATAAAGACAGCGAGCTCGTCAGGACGGGTAATGCGGCTCTCCGAGCAGAGATCATGGGGCAGGATGGAGCGCAAGTGACTGAGGCGGAGGTGGTGGATAATAAGAACGGGACGTACGAGGTTGGTTATACACTGAAGGGTGAAGGCGAGTACTTGTTCTCTCTGATACTGTATGGACAGCCGGTGAGGGGCAGCCCGTTCAAATTAAGGGCCATAAAGCCATCGGATGTGC
Associated Phenotype:
Not determined