ZMP
btg3
Ensembl ID:
ZFIN ID:
Description:
protein BTG3 [Source:RefSeq peptide;Acc:NP_001007352]
Human Orthologue:
BTG3
Human Description:
BTG family, member 3 [Source:HGNC Symbol;Acc:1132]
Mouse Orthologues:
Btg3, Gm7334
Mouse Descriptions:
B-cell translocation gene 3 Gene [Source:MGI Symbol;Acc:MGI:109532]
predicted gene 7334 Pseudogene [Source:MGI Symbol;Acc:MGI:3647393]
predicted gene 7334 Pseudogene [Source:MGI Symbol;Acc:MGI:3647393]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41682 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa41681 | Essential Splice Site, Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41682
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100207 | Essential Splice Site | None | 159 | None | 5 |
| ENSDART00000131220 | Essential Splice Site | None | 160 | None | 5 |
The following transcripts of ENSDARG00000069065 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29062586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28494180 |
| GRCz11 | 10 | 28380805 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGCGAGGCAGAAGGAGTTTTCCACATGTGGATGAAAAGAAAACACGG[T/A]CAGTTTTTCTATTCCTATTTGCAGTGATAATGCGAGCTCACGTAGAATTA
Long Flanking Sequence:
TATTTAATGTTTTATTTGACGATTTATTAATTATTGTTTATAAAAGTATTAGATTATTTTTATTGATGTTACTTTTATAATAACAATTACAAAATTATAAAATGCAATAATATAATGATTTTAATGCACAGCAGCTTTTAACATTTTCCTAAACGACCACATTATTGACATAAGCCGAATAAGTAATTGTCCACTTATTTTGATTGCTGTACTGAATTAGTAATGGTCCACCTTTTTAATCGCTAAAGCAGCTATAATACTTCCACCTTGCGTTTATTTGTGCGTCTGCACATCAACACACTCCAAACATTGCGCAGCTTTTATTATCTTGAATCTTTCGCTTCACGAATCAAATGAATCGACTCCTGAGTCATTTCCTCCGAGCATGCGCACAAGACACAGTCACGTCACACACATAGTCGCGCGGGGGAGCTGGATTGGAAGTGGCTTGTGCGCGAGGCAGAAGGAGTTTTCCACATGTGGATGAAAAGAAAACACGG[T/A]CAGTTTTTCTATTCCTATTTGCAGTGATAATGCGAGCTCACGTAGAATTAATATATATTTTTAACGTCCAAATGTAAAATTAAAAACGATTTAAAAATGGGTGTTTTTAAAGAAACGGTCGGAAAAAAACAAGTGTTGATAGAATCGAGGCCACGTTAACTTCGGCTAACGTTAGGCTAAAGTGAGCTGGTTTAATAAACGTGGCATATAACATTTTTAAAAACGTTTTAATATGTCTGAAAGCAAAATGTGTGGGGTTGTGGTTTCAATATTTAACATCTCAACAATGCCACTGTTTTTGTTTCGTGGCGTTCAGTTTGGCGACTAAATGAAATTTCTCATAAAGATTAATCAGTTTTCTTACGCGACTAATGTCCATATGGACAATAACTATCAGTACGTTGCGTAAAAAAATAATAAATAAACGAAGATGTGAGAAATATGTTTGGTGTTTTGCTGTGACGTCTACAACTCTCTGTCTAGTCCGTGTTTCCGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41681
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:
C > T
Consequence:
Essential Splice Site, Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000100207 | Splice Site | None | 159 | None | 5 |
| ENSDART00000131220 | Essential Splice Site | 154 | 160 | 4 | 5 |
The following transcripts of ENSDARG00000069065 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 29053607)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28485201 |
| GRCz11 | 10 | 28371826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGGTCACGTCGGATTACCACTCTGGATCCTCCTCAGATGAAGACATCAG[C/T]TGTAGGGAGATCCAGTATACGACACCTCTTCACAACCAGCCTCCTTACCA
Long Flanking Sequence:
TAATGCATTTTAGCAATATTTTAGAAACTGCATTTAAATAATACCAGTATTGAATTCAACTAATTGCATTGAAGTTTTTTTTAACATGACTGCTTAAAACTGTCAACATTTTGAAAATGACACATTCAAAACATCATCATTGACATTTTAATTTAAATATTAAGTGTAAATAAAATGTTAAGTACAAGAAGGACTTTCATGGCACTGTATATGCTGGGGTGTTCATTACAAAGGTGCATGGTTTAAAACTATTAGTGACTTTAAAAGTCCTGGAATTTGGTGTCCATGAAAGAGTAAGAACTCTGTGATGTGTTGGTTTGTTTTTGACCCATCTTTTCTTCTGGCTACAGGTATGGCGAGAAGAATCATGGTTTCACTGTGGCCACTTTCTCAAGCGAGGACGATGATGATAAAGAGGATGTGACAAAGAAAGTGACGAGCGCCGTGGAGCGGGTCACGTCGGATTACCACTCTGGATCCTCCTCAGATGAAGACATCAG[C/T]TGTAGGGAGATCCAGTATACGACACCTCTTCACAACCAGCCTCCTTACCAGGTACACATGTCTTAAAATGTGTTTGTATGGTCTTATTACCACAGATGCATGATTTTTCATTATTATTATTATTATTTAGTTTGAAAAAAAGTCTCTTTTTTATAAAAATGATGATGTTTACTTGTATACAATGCATGTATAAAAGAATTATAAGCACAATACGTAAAGTTGTATTAGTAATTAGTTGTAGTAACATTATACATCTGACTGATTGTGCCACAGTTAAATTTCAACTTTACCCATTTGAGATTTTATTATTAGTTACATATAATGCACAAATAGATGTCACTGTTGTCTCTAACAATGTTTTCTGTTATCTTTGTTCTTATTAAAAGGTTGTTTATGCCAGTGCCCCAGGATGGCATCCGGTACCAAGAAAGAAATTTGGCCCGGGGAAAGGGCACTACCCTCAGCGGCCGCACTACATGATCCGCCCCCCCTGTAGACCC
Associated Phenotype:
Not determined