ZMP
ints7
Ensembl ID:
ZFIN ID:
Description:
Integrator complex subunit 7 [Source:UniProtKB/Swiss-Prot;Acc:Q8JGR7]
Human Orthologue:
INTS7
Human Description:
integrator complex subunit 7 [Source:HGNC Symbol;Acc:24484]
Mouse Orthologue:
Ints7
Mouse Description:
integrator complex subunit 7 Gene [Source:MGI Symbol;Acc:MGI:1924315]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa4883 | Nonsense | F2 line generated | Not yet available |
| sa6619 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa32279 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa4883
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000020703 | Nonsense | 598 | 964 | 13 | 20 |
The following transcripts of ENSDARG00000019300 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 12990809)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 13180055 |
| GRCz11 | 20 | 13076035 |
KASP Assay ID:
554-3571.1 (used for ordering genotyping assays)
KASP Sequence:
GAGACTACAGTGCAGCCATGAGCGCCATCTCTGAAGCACTGAAATCCTAC[C/T]AGAAGGGAATCGCATCTCTCACGGTCAGGATTCACTTTTATTTATTTTTT
Long Flanking Sequence:
CAAGCAGGCGCGCATTGAGGAAAAATAGACTGATTGCATCAAAAAGTAGCTCATATTATTGCGCGATGATAAGTAATAATATGAAAACGAAAGTAACGTGCGTGGTTTAAAAAATGTAAGAAGTAGAAAGTACAGATATTTGTGTAAGAAGTAAAAGTAAAAAGTTGTCAGAAAAATAAGTAGTAAAGTACTGATACCAGAAAAAAATACTTAAGTACAGTAATGAAGTATTTGTACTTTGCTACTTCCCATATTTGTAAGTAAATGATGACGGAATTTTTATTTTGAGGTGAACTATCCCTTTAATATGTCCACAGGGCTGCCATGATTTTTCCAGGGAGTTGTACCAGAGTCTTCGCACCCGTGTGGCCTCCGAACACTTTTACTTCTGGCTTAACAGTCTGATGGAGTTTTCCCAAGCGGAGCAGTGCCTTAGTGGCCTGGAAGATGGAGACTACAGTGCAGCCATGAGCGCCATCTCTGAAGCACTGAAATCCTAC[C/T]AGAAGGGAATCGCATCTCTCACGGTCAGGATTCACTTTTATTTATTTTTTGTCTAGTGATGCACCGATCTTGATTTTCAAACTGATTTCAATGGCTTGACTCCAAAAGAGATTAAAATTTTTTTCCTCTTTAATTTTATATTTTATTATGAAATGTAAAGGAGAGTGATGAATTAGTAACACTAGCCACATTTCCACTGTCAGGCCAGGGCAAGCTAGGGCTTTTATCGGGCCGGCCCGTGCCAATCGCCCAGAAGGTTGAGCAGTGAGGCCGGAGTCATGTCGCGTTTTCACTGTCGAGCTAATAGCTTGTAGCACGTCTCGTGAATCCCGCCCCCAGAATGTCCCCCGAATCAAATGTCACACAACCCGCCCACTTCAGCGAGAATCATGCAGATAAAGCACATCATCGCATCATCGCCGAAACAAAGGACATGTGACTGTACAGCATCACATTATGTTTATACGCACAGTCCTATGTGTTTCCATTCATTATTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6619
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 |
|---|---|---|---|---|---|
| ENSDART00000020703 | Nonsense | 666 | 964 | 14 | 20 |
The following transcripts of ENSDARG00000019300 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 12983163)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 13172409 |
| GRCz11 | 20 | 13068389 |
KASP Assay ID:
554-4958.1 (used for ordering genotyping assays)
KASP Sequence:
TCGCAACCACGATYGCTCTGTCCTCGGGCAGTGACTTGCAGCGCTGCGGA[C/T]GAATCTCCACACAGGTGCCCAAACACACGCTCCTATTTCTGCTCTYTTTC
Long Flanking Sequence:
GAGCTGTGTTACACACTGCATGGAAGGTCATTTTCAAAAACCCATAAAAGGGGCTCTTTAAAGTCCTGCAAAATGATATTTAAGCTAAAATGATCCAGTACAGTATATATGTTGTTTAATCTGCTTAATCAAATGCTCTGTTTACACATTGTGTACTTTTAATCGGCTAAATTAAAAGGGAAAAACTAGTTTGAAGCATTTGGAGAAAAAAAAAATGTCCAGTTTTGATTTCTATTGGGTAGATCTTTGTATGCTGTCTTGCTAATTTTTCTGTTATTTTTAGCTCTTTGTGACTGACTCTAAATGTGTTTGATCTTTAGGCTGCCAGTACGCCGCTCAGTCCGCTGACATTCCAATGTGAGTTTGTGAAGCTGCGTATAGACACTCTTCAGGCTCTGTCTCAGCTCATTTGCACCTGCAACAGTCTGAAGACCAGTCCTCCTCCTGCCATCGCAACCACGATCGCTCTGTCCTCGGGCAGTGACTTGCAGCGCTGCGGA[C/T]GAATCTCCACACAGGTGCCCAAACACACGCTCCTATTTCTGCTCTTTTTCCTATTTTTATTTATTTAATATTTTATTTATATATATATTTTTTACTTGTTTAGTTTGATCATTTATTTGTTTATTTACATGTATTTATTTATCCATCTGTTTAAAGTTTTATTTAATTTTTATTTATTTTATATTTTAATTATTTATTATAATTATTTTTTATATTTTTATTATAATAAAGTTTATCATATATTTATTTACATGTATCTATTTATGTGTTTAATGTTCTATTTATTTTATTATTTATTTATATTTATTTGTTTATCTATTCATTTATCTATTTTATTTAATATTTTAATTATTTTTTATTTGTCTATTTAATACTTTATTTATTTTTATTCAGTTATTTTATTTGATTGATTATTTTATTTATTTATTCATTTATCTATTTGTATATTTTAACTTTTTAATTTATTTAATTATATCATATATTTATCTAATTTATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32279
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020703 | Nonsense | 689 | 964 | 15 | 20 |
The following transcripts of ENSDARG00000019300 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 12982431)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 13171677 |
| GRCz11 | 20 | 13067657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTCCATGGATGAGTTTAGAAGTCTCGCAGCTCGCTATGCTGACCTGTA[C/A]CAGTCTTCGTTTGATGCGGACTATGCCACCCTTCGCAATGTTGAACTGTA
Long Flanking Sequence:
TTTATCATATATTTATTTACATGTATCTATTTATGTGTTTAATGTTCTATTTATTTTATTATTTATTTATATTTATTTGTTTATCTATTCATTTATCTATTTTATTTAATATTTTAATTATTTTTTATTTGTCTATTTAATACTTTATTTATTTTTATTCAGTTATTTTATTTGATTGATTATTTTATTTATTTATTCATTTATCTATTTGTATATTTTAACTTTTTAATTTATTTAATTATATCATATATTTATCTAATTTATTTAATATTATGTTTATTTTATTATTTATTTTTTTAAATATTTTATTTATTTTTATGTATGGTTATTTTATTTTTTTATAAATTTATTTACATATTTAGGTATCTATTTAATGTTTTTTTTTGTTGTTGTTGTTTGTTTGTTTTTTACTTATTTATTTGATTTTTGTGTACATTTGCTCAGATGAAGTTTTCCATGGATGAGTTTAGAAGTCTCGCAGCTCGCTATGCTGACCTGTA[C/A]CAGTCTTCGTTTGATGCGGACTATGCCACCCTTCGCAATGTTGAACTGTATCCTTTCTTTCTTGTAGAGCAGTGTCTCTACAAGATCTAGTTACAAAAAAATCATCTGTACTTTTCTTAATGACTTTTTTCCTAGACAACAGCAGAGTTGCTTACTCGTATCTTATGTTATCGAAGCTTTAATAATCGATCCACAAACAGCCAGGTAAAAATGCTATGCTACTATCCCACATCAAATTCAAATAAGAAAATAGGATCTTAGTTTCTGGCCTTAAATGAATTGTATAATAGATTTTAGTTGTAATGTCTCAAAAAGTGCACATTTTAAAGACAACATCCGGTTCAGTTTCCAGGAGTTTGGCACTCATGGATCAATTCTGGCAGAGAGCGAGTATGAGCTGAGAATGATGGCTGTGTTCAATCATGTCCTGGAGGAAGTGGAAAATCTAAGCAGGAAACACCCTCCTGTTTCTTACCTGGTACTGCGTTTCTAAGAGTATC
Associated Phenotype:
Not determined