ZMP
ints2
Ensembl ID:
ZFIN ID:
Description:
integrator complex subunit 2 [Source:RefSeq peptide;Acc:NP_001018378]
Human Orthologue:
INTS2
Human Description:
integrator complex subunit 2 [Source:HGNC Symbol;Acc:29241]
Mouse Orthologue:
Ints2
Mouse Description:
integrator complex subunit 2 Gene [Source:MGI Symbol;Acc:MGI:1917672]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31784 | Essential Splice Site | Available for shipment | Available now |
| sa8636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21754 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31784
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023545 | None | None | 167 | None | 3 |
| ENSDART00000078791 | Essential Splice Site | 219 | 1210 | 4 | 24 |
| ENSDART00000143487 | Essential Splice Site | 216 | 1206 | 5 | 25 |
Genomic Location (Zv9):
Chromosome 10 (position 28707093)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28138687 |
| GRCz11 | 10 | 28025312 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGTTTCTCTGCCTTCTGGTGGCAAATGTCCCGGACAGCTTCAATGAAG[G/A]TATGTTCATCACCTACTATGAGTCTAATCTGTACATTTGATTTTTAAGAC
Long Flanking Sequence:
AAACGTTTTTGTGTCAAGCTTTTGTTACTTGTTAGTAGCACGCCAAATATATATTTTTATTCTCACAATCGATCAGTATCATCCTTCAGTATGTCAGAAACAAAGACTTGAGCTGAAGACTAAAAAGCTAAAATGTAATTTCAGCTCAGCCTTGTGATGTGGTACTCTTAAATAGAAAACATTAGTTCTTGACTTTAAATAATTCTGGCAAGGCACAGCAAGTTTACTTATTTAGCACATTTCATACACAATGGTAATTCAAAGTTCTTTACAGGAATAAAAGAAACAAGTATAAGAAAACAAAAACAACAAAAAATGAAAATTATTAAACTATATAAATATATAAATTGCATAAAATTGAAAATGAATAAATTCTGTTCCATCAGAGCTGCCATCTTTGCTGCCCATCATTGAAGTGGCTGAAGCTCTTCTTCACGTGAGGAATGGAGAGTGGTTTCTCTGCCTTCTGGTGGCAAATGTCCCGGACAGCTTCAATGAAG[G/A]TATGTTCATCACCTACTATGAGTCTAATCTGTACATTTGATTTTTAAGACTACGTTATTCATAAAAGCTAGTTAAATGCATGAGTAAATTCAGAGTTATTTGCCCAAATAAATGAACCTCCCCGAAAACTCTCCTCCAGCTTCACAAACACAATGAACATCTCTGAATTGAGTATTAGTCATGTGTTTAACTTTAATCCGATAATTTGTGATTAAGGTGCACAATTATGTGAATCACAAAATACAGGAATGCTGTGAGGTTTTTGAAGTCCCTTTTTTAGTTTTGGGTGCAGCACATTGTAGTAAAATCTAGAATTGGTCACATGCCTGTAAAGATCATTCAATGAAACATTTAAGCTTGTAGACTCCACTGCTGCTCACCAAAATGTGCATTAAAGAAAACAACAAACTCTGGGGTTGTTTGTTTTTGTTGCTACAGTTAAATTTCTTAATGATAGAACAAAATATAGGAATAAAAATAACAGACATACATCAGTCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8636
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023545 | None | None | 167 | None | 3 |
| ENSDART00000078791 | Nonsense | 335 | 1210 | 7 | 24 |
| ENSDART00000143487 | Nonsense | 332 | 1206 | 8 | 25 |
Genomic Location (Zv9):
Chromosome 10 (position 28699985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28131579 |
| GRCz11 | 10 | 28018204 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTTCAGAGAAAAAGAGAGAGCAGTTCGGTGCTGTGGCAGATGCGGAGG[C/T]AGCTGCTGTTGGAGCTGGTGGCCATTTTACCCCGYTCSCGCAGTACRCAC
Long Flanking Sequence:
TATGTTTATTTTGAGGGTATCAGGGAGCAAAAGAAATAGTTAACATGATGATTATCAATTCCAACTAATATGAAAAATCTTATGATGAAGATTTTTTTCCATCCATATAAAATGAACAAATTCATGTTCTGTAAGTTAGCAAGTAAATGAAAAGATGTGGATGACATCTGAACTACAGTTTTACAGTCAGTATTATGGCAGAAGCAAAGTACTAAACATGAATTCCTTGCTTTGTGCGCTTTCTCACAAAATGCCTGATAACTATGTTGGGTCAGTATGCAGATAGTGGGAGGCAGTTTGAAAACGTTCAACCACACAATCAAACGAGTTTTCATCTACCTCTGTAAGTGGCTAAATATGAATAATCTTAAGAGAGTTTAGTGTCTTTGTGTTTAGCATCGTCCACTTGTCCACATCTTAATAGCAGATGTAAACTCTGAACTATTTGTTCACTTCAGAGAAAAAGAGAGAGCAGTTCGGTGCTGTGGCAGATGCGGAGG[C/T]AGCTGCTGTTGGAGCTGGTGGCCATTTTACCCCGCTCCCGCAGTACACACGTCCCCAACGACAGCGACATGGACACAGAGAGCAGCTCGGGTTATTCTGGCCTTCGGGAGGAGCATGTGGTGAAAGCCAGTGCACTGCTACGACTCTATTGCGCTCTGATGGGGATTGCCGGTCTTAGGTATGCTATATTTTAGGACTTTTGCACAAGCAAGGCTGGAAAACTACTAACATTATGATTTTTCATTTTTCTACAATTATATATTGTGATTTATAGAACTTCACCAGATGACTTGCGAAAGCTTTATTAGTTTTGATTGATTGGAATGAGCTTGTAGGGGAGTAAATAATGCATAAAATGTAATGCACAAATGATATGCTTAAATCAATGCAATAGAGCAAAGATAAAACTGAAATGAACAGTGCTTTGAGGTTTTTCAGGATAATTAAATTATCTTCAGGTACAGAAATTGAATAATCAAATGTAAAGTAACACTGCAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21754
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000023545 | None | None | 167 | None | 3 |
| ENSDART00000078791 | Essential Splice Site | 436 | 1210 | 8 | 24 |
| ENSDART00000143487 | Essential Splice Site | 433 | 1206 | 9 | 25 |
Genomic Location (Zv9):
Chromosome 10 (position 28696052)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 28127646 |
| GRCz11 | 10 | 28014271 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCTCCCTGTCTTTCTGTAAACTGCTGGCGTTCCCCACTCTTGTCAGG[T/C]ACAGCTTTTTTGCTACCAATAATCCATCCTTTAAGATAAATGAGCATTTA
Long Flanking Sequence:
CATTTGTTGGTCTATGAATTAAAAAGGTGCTTGAATTAAAATTAATGTTTTTTTTTTAAGTCTTTGAATCTGGTGTCCATGAAAGGGTGGAAACTGGTCAAATCTGGTCAAATAAAATCCTGACTCATGTGACTATTGTGGATGTGCACATTGCTATATCGATGCTGAACTGATATATTGTGCAGCACCAGTGTAGTAACTTTTAACCACACATAATTTAAGCTGCTTAACTTAATTCCCCCTTAAAAGGAAATTCCTGGCTTTGTTCCACGGAGAGGTTGTAGATGTATGGAAATTAATTCCTCAAGTCTGATTTAAAATGAGTTCGTAAAAACCGTTTCCAAGTCTCATTTCAAGAGTTTTATCTCCACAGGCCCACAGATGAAGAGGCAGAGCAGCTGCTGCAGTTGATGACCAGTCGTCCACCAGCTACGCCTGCTGGAGTGCGCTTCGTCTCCCTGTCTTTCTGTAAACTGCTGGCGTTCCCCACTCTTGTCAGG[T/C]ACAGCTTTTTTGCTACCAATAATCCATCCTTTAAGATAAATGAGCATTTAATGATGGGTCATAATATACACTAATTTAACGTTTCTTTACACCTGTAATACTCCAGAAAAGAGTATAATTGAGTTATTGAGCTATTCTCTACAAAGTATTCATTTTGAACTTCTGAAACGCTACCATCAAAGCTGATATGCTATACAACCTAATCAAAGACCTTGGTCAGTTTTATTTTCGAAGAATAACTGCTAATTTGTGATGATATGCATGCTAATGATTGGGGACTTCAGAAAATTGACTGAATATATATAATATATATATATATATTACTGCCTGTATTTTTATTAAAGATTTGTCACAGTTAACTGGGGAAACTATTAGCAGTTTTCATATTTTTATTTTAAGTAAATGAATTAAAAATATATATTTAGTTATTAATTATTATTATTGTTTTTATTATTGTTGTTGTTATTAATCAGACAAATTAATGAAGTATTTCTATAATG
Associated Phenotype:
Not determined