ZMP
tnni2b.1
Ensembl ID:
ZFIN ID:
Description:
troponin I, skeletal, fast 2b.1 isoform 1 [Source:RefSeq peptide;Acc:NP_001129964]
Human Orthologue:
TNNI2
Human Description:
troponin I type 2 (skeletal, fast) [Source:HGNC Symbol;Acc:11946]
Mouse Orthologue:
Tnni2
Mouse Description:
troponin I, skeletal, fast 2 Gene [Source:MGI Symbol;Acc:MGI:105070]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21031 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21031
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000025852 | Essential Splice Site | 3 | 176 | None | 6 |
| ENSDART00000144750 | Essential Splice Site | 3 | 176 | None | 7 |
| ENSDART00000147037 | Essential Splice Site | 3 | 133 | None | 6 |
The following transcripts of ENSDARG00000035958 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 40795778)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39132035 |
| GRCz11 | 7 | 39403052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCACCTTCAGAGGGGTCGCCACAAAGAGACAGCCAAGATGTCTGAG[T/A]AAGTATTGATTTACAAACATTGTGATGTTGAGATGTGATTACTAATCCCT
Long Flanking Sequence:
CTATTTTATTTTTTTCATATAAATTATTAATATGAACACAACAACTTATTTTAGATAGCAGAAGATCCAAACTCAGACTCCATCCCATCCATAATACAAGAAAAGGTCTAATATAGTTCTTCAGAGCACCAGGAAATATTTTTACAGCTGTGAAGGCTATCAGCTGTTGAGTGTTGAGGCTTAGGAGATTCTTCAAGAGGTCTGTCAGCTGTCCCGTCCTCTGTATTCCTACAAAAGAACGCTAAAAAAAGAGCTCAAGACAACTGCTTCTCAAATTCAACCCTTTAAACACCGGACACTTCTGTTGCTATTGCCACTTCCAGACATCCACGTACAGCAGCCATCTCTCTTGCACATTATCAGAAGCCAGATTTAGACCTCCAGATGACTGAATGTAAATTGTTTCCATTAGATTGAAGGCAGCAAAACTTACACCTACCCCGCACAGGCGTCTTCACCTTCAGAGGGGTCGCCACAAAGAGACAGCCAAGATGTCTGAG[T/A]AAGTATTGATTTACAAACATTGTGATGTTGAGATGTGATTACTAATCCCTGCAAATACATTTAGCATTAAGTAAAATTGTGTGTTTATGATAATACATGCAAGAATATGTGCTTAAATGAATCAAATATTAATATTTGCCACTTTGGAATGAGAAGGTTGTGAAATTTTTGTCAGTATTGGGTAATACTCATATTCTGTGACAATTTATTTACATTATGTAATACTTTTTTATTTAAAATAAAAAGCTCCTAAGAACTTTAACTTGGTGCTATTTTTGTAAGCCAATTTGCATTCTAAATGGACACAAGTGGACCAATCGGGATCATTTCAGAGGTCTGGATTAGTTATATAAAGAGCCATATCTAAATTTTTTTTTTTAAACCTTTATTAATCCGGGGTGGCCACAGCGGAATGAACCACCAACTTATCCAACAAGTTTTTACGCAGCGGATGCCCTTCCAGCCACAACCCATCTCTGGGAAACATCCACACACACACA
Associated Phenotype:
Not determined