ZMP
tsc22d2
Ensembl ID:
ZFIN ID:
Description:
TSC22 domain family 2 [Source:RefSeq peptide;Acc:NP_956403]
Human Orthologue:
TSC22D2
Human Description:
TSC22 domain family, member 2 [Source:HGNC Symbol;Acc:29095]
Mouse Orthologue:
Tsc22d2
Mouse Description:
TSC22 domain family, member 2 Gene [Source:MGI Symbol;Acc:MGI:1919283]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14179 | Nonsense | Available for shipment | Available now |
| sa8884 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14179
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061315 | Nonsense | 378 | 556 | 1 | 3 |
| ENSDART00000146430 | Nonsense | 378 | 556 | 1 | 3 |
The following transcripts of ENSDARG00000041839 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 38092210)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 35230928 |
| GRCz11 | 22 | 35206677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCCYCARAGTGTGCCAAAGCAGAATGCAGCRCCCCAGCAGAACCAGCCT[C/T]AGGGAGTGCCCAGCGGGTCAGTTGTGGGACYGGGTGCACAGATGAGCCTC
Long Flanking Sequence:
CTCCAGTCGAGCTCCAGCAGCACCCCTTCGGTATTGCACCGCAGAACCCATTTGGCGATGCCAAATCTCCCAGCATGCCTTCCACAACCCAGCCGCAGCCGTTTTACGCAGGTAAACCGCTGCAGAAGCCCGTTCAGGTGCTTCAGACTTTAGTCACAGATTACAGAGCGCAGCATCAGCCTCCGGGCTCCCCGGTGGTCTCAGTGGCCACTCTTCCCTTGGTTACCCCCCTAACCCAGGGCCCATCGCCCATCATGACCCCTGCAGCCGGGGGTGTGCATTTACTCGGGATGGGCCTTCCCATTAGCCAGCCGGAGCATGCCGTTCAGCCGGGCATGGGCATGGTGGCGCAGGCCTTAGCGCCGCTCATCCAGCCAGCAGTAACCGTGTCTGTCAGCTCTCACGCCGGCGTGCAAAATGTGCCTGTTGTAATGTCCAGTGCCTCTAATACCCCTCAGAGTGTGCCAAAGCAGAATGCAGCACCCCAGCAGAACCAGCCT[C/T]AGGGAGTGCCCAGCGGGTCAGTTGTGGGACTGGGTGCACAGATGAGCCTCTCGGGTTTTGGCCCCATAGACGAGGGCCTGAGAAAGCCGGAGATGCTGCAGCAGAGCTCGGGACTCTCCATCAGACCCCTGAACCCCGAGGGCCTGCAGCTCCACACACCTGCGGTCAACAGCTTGTTCGGGATCGCCCTTCCCATCGACGGGGACGAGGACAGGTACTGCTTTTCTCTCGCTGTCATTGCTCATACGGGCGTTTGGTTCTTTTGCCAGTAAATAACACATTTTATTGCAGGTGTTTAAATATTTGCACATGAAGGACTCTTGTTGCTTTGAAAAGTTGGGTTTTTCCTAGGAAGTGTCTGAGGCAGAGTTTGTGCTCTGGTTTCTTGTTGAGTATTTTGCTTGTTTATTGACTTTTTTTTTTTAATGAATGTGGTTGGTTTAACACACAAACATGTCCTGGAGACCCATGGTATGGATGTTTTTCAGTGACTGTGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8884
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061315 | Essential Splice Site | 449 | 556 | 1 | 3 |
| ENSDART00000146430 | Essential Splice Site | 449 | 556 | 1 | 3 |
The following transcripts of ENSDARG00000041839 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 38092426)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 35231144 |
| GRCz11 | 22 | 35206893 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACAGCTTGTTCRGGATCGCCCTTCCCATCGACGGGGACGAGGACAGG[T/C]ACTGCTTTTCTCTCGCTGTCATTGCTCATWYGGGCGTTTGGTTCTTTTGC
Long Flanking Sequence:
CCTTGGTTACCCCCCTAACCCAGGGCCCATCGCCCATCATGACCCCTGCAGCCGGGGGTGTGCATTTACTCGGGATGGGCCTTCCCATTAGCCAGCCGGAGCATGCCGTTCAGCCGGGCATGGGCATGGTGGCGCAGGCCTTAGCGCCGCTCATCCAGCCAGCAGTAACCGTGTCTGTCAGCTCTCACGCCGGCGTGCAAAATGTGCCTGTTGTAATGTCCAGTGCCTCTAATACCCCTCAGAGTGTGCCAAAGCAGAATGCAGCACCCCAGCAGAACCAGCCTCAGGGAGTGCCCAGCGGGTCAGTTGTGGGACTGGGTGCACAGATGAGCCTCTCGGGTTTTGGCCCCATAGACGAGGGCCTGAGAAAGCCGGAGATGCTGCAGCAGAGCTCGGGACTCTCCATCAGACCCCTGAACCCCGAGGGCCTGCAGCTCCACACACCTGCGGTCAACAGCTTGTTCGGGATCGCCCTTCCCATCGACGGGGACGAGGACAGG[T/C]ACTGCTTTTCTCTCGCTGTCATTGCTCATACGGGCGTTTGGTTCTTTTGCCAGTAAATAACACATTTTATTGCAGGTGTTTAAATATTTGCACATGAAGGACTCTTGTTGCTTTGAAAAGTTGGGTTTTTCCTAGGAAGTGTCTGAGGCAGAGTTTGTGCTCTGGTTTCTTGTTGAGTATTTTGCTTGTTTATTGACTTTTTTTTTTTAATGAATGTGGTTGGTTTAACACACAAACATGTCCTGGAGACCCATGGTATGGATGTTTTTCAGTGACTGTGATGACAAGTATCCACAATTATTCATATAAATTCTATTAAATATTTATTAATTTAGTGAAGTATGTGGTTCTGAGATGGAAAAAGATATTAAAAACATTTTTAATTTATTTTTAAAAAATATTTTTTGTTTATTTATACAGATTTTAGAGGCCATGGATCCCAAACATGATAAAAAGACCTCCATATAGCTTCATATAGACGTTTTTCTTAGAACGCAAAA
Associated Phenotype:
Not determined