ZMP
tnni2b.2
Ensembl ID:
ZFIN ID:
Description:
troponin I, skeletal, fast 2b.2 [Source:RefSeq peptide;Acc:NP_001003423]
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 are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17285 | Essential Splice Site | Available for shipment | Available now |
| sa38632 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17285
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099001 | Essential Splice Site | 27 | 187 | 3 | 6 |
| ENSDART00000139240 | Essential Splice Site | 16 | 176 | 5 | 8 |
| ENSDART00000146702 | Essential Splice Site | 16 | 176 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 40784647)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39120904 |
| GRCz11 | 7 | 39391921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCTGGCCAGTGTTAAATATCCAAGTGGCATTTGTTCATTGTTTGTTGT[A/C]GAGTTTGATTCTGGGTATAGCCAAAGACCTGCTGTCGGCTGAGCAGAAGC
Long Flanking Sequence:
AACTGCTTTATGCTAGCCAAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATCAGACATAATGTGAAAAATTCCTTTCTCCTCCAGACTTCAACTGTATATATTATGTAAATACAAACTTTTATCTTGGATTGCGATTAATCTTTTGACAGCACTAATATTTTCACATTCAATATGCCCATGTGTGTTTGTCTGTCCTAGATATATGTGAAAGGGAATGCAAATCCATTCTCACATGTTATCTGAGATGCAGCTGTCTGTGAGTGTGCACAGAAAACTGCATGCTAATACCAAAACAACACCTCTGTTGCATCTTCTTCGTCGTGGTGTTTCATTCATATGAATCACTGACCAACTGTGATTCGTTAAACCACTATAAAAATAAAAATGGCAAGTGGGAGTAACTGTTACACGCCTCTACTAATATCCACATGCATTTTGCTGGCTGGCCAGTGTTAAATATCCAAGTGGCATTTGTTCATTGTTTGTTGT[A/C]GAGTTTGATTCTGGGTATAGCCAAAGACCTGCTGTCGGCTGAGCAGAAGCAAACAGAGGTGGACAGAGTTAATTACATGGAGGAGAAATGTCCACCTCTCTCTCTGCCAGGCTCAGTGCAGGAATTACAGGTACGCATGTACAGTATGAAGCCTTTCAACATTTCAGTATTTATAAGTATATAACTCAGTTGTTAAAATTCTCTTCACTCTGCTCAGGAACTGTGCAAAGAGCTTCATCAGAAGATTGATGTGGTGGATGAGGAAAGATACGACATGTCTCTCAAAGTGGCCAAGAGTGACAAAGAGGTTTTTGTTTTTCTCATTCCTCCGTCCTTATCCATCTCACTCCTCTACTTTGGCTTGAATTTACAGCACATCACACTCTGTATTCTTGTAGATTGAGGATCTGAAGATTAAGGTTCAGGATCTGATTGGTAAATTCAAGAAGCCCGCTCTGAAGAAAGTGCGTATGTCTGCTGATTCCATGCTGCAGGCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38632
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000099001 | Nonsense | 101 | 187 | 5 | 6 |
| ENSDART00000139240 | Nonsense | 90 | 176 | 7 | 8 |
| ENSDART00000146702 | Nonsense | 90 | 176 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 7 (position 40785049)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 39121306 |
| GRCz11 | 7 | 39392323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTTTGGCTTGAATTTACAGCACATCACACTCTGTATTCTTGTAGATT[G/T]AGGATCTGAAGATTAAGGTTCAGGATCTGATTGGTAAATTCAAGAAGCCC
Long Flanking Sequence:
GTGGGAGTAACTGTTACACGCCTCTACTAATATCCACATGCATTTTGCTGGCTGGCCAGTGTTAAATATCCAAGTGGCATTTGTTCATTGTTTGTTGTAGAGTTTGATTCTGGGTATAGCCAAAGACCTGCTGTCGGCTGAGCAGAAGCAAACAGAGGTGGACAGAGTTAATTACATGGAGGAGAAATGTCCACCTCTCTCTCTGCCAGGCTCAGTGCAGGAATTACAGGTACGCATGTACAGTATGAAGCCTTTCAACATTTCAGTATTTATAAGTATATAACTCAGTTGTTAAAATTCTCTTCACTCTGCTCAGGAACTGTGCAAAGAGCTTCATCAGAAGATTGATGTGGTGGATGAGGAAAGATACGACATGTCTCTCAAAGTGGCCAAGAGTGACAAAGAGGTTTTTGTTTTTCTCATTCCTCCGTCCTTATCCATCTCACTCCTCTACTTTGGCTTGAATTTACAGCACATCACACTCTGTATTCTTGTAGATT[G/T]AGGATCTGAAGATTAAGGTTCAGGATCTGATTGGTAAATTCAAGAAGCCCGCTCTGAAGAAAGTGCGTATGTCTGCTGATTCCATGCTGCAGGCTCTGCTGGGCTCCAAACACAAAGTGTCCCTGGATTTGAGAGCCAATCTTAAACAAGTCAAGAAAGAGGTCAAGGAGGAGGTGAGGGCACATTATAATTCCTCGAGTAAATCGGTCAAATACCAATTTGCCAATCAAATTCCAACATAATAATTCTTTGGTCATTTGTTTAGGATAAGGAGGCTGTGGGAGACTGGCGTAAGAACATTGAGGATAAGGCTGGCATGGGCGGCAGGAAGAAGATGTTCGAGTCTGAGGCTTAAACAGGCAGCCATTTTACTTCTGAAGTTGATTTCTGATGGACTTTCTATTGCACGTTTCACTGTCAAAAAGTGCTTTTGCATTCAAACTACACATCCAACAAACCGTAACTACTCTAATCATAATATTGAGACTGCCATGTACTAC
Associated Phenotype:
Not determined