ZMP
ints1
Ensembl ID:
ZFIN ID:
Human Orthologue:
INTS1
Human Description:
integrator complex subunit 1 [Source:HGNC Symbol;Acc:24555]
Mouse Orthologue:
Ints1
Mouse Description:
integrator complex subunit 1 Gene [Source:MGI Symbol;Acc:MGI:1915760]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20113 | Nonsense | Available for shipment | Available now |
sa18206 | Nonsense | Available for shipment | Available now |
sa40146 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14215 | Nonsense | Available for shipment | Available now |
sa20112 | Essential Splice Site | Available for shipment | Available now |
sa40145 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20113
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083062 | Nonsense | 528 | 2194 | 10 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43604041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42305439 |
GRCz11 | 3 | 43011454 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCAGTCCTTCTGTTTAGGCCTCATGCAGGAGAGGAAAGAGGCCACTTA[T/A]GTGGACATGGAGTTTAAAGTGAGCACTGGATTGCTGCATTTGTGTGTTTT
Long Flanking Sequence:
CTTAGGAAAGTTTAACTAGCTTTGTTTCCATCCATGTATTTTTATATTCATGTCGTGATGTTGCATTAACATGCAGGATGGAAGATGTTAGGTGGGCCTCTGATATTAACTTTGTCCCACTTGCCAATAAAATTTATTATATTTTTTTTCTCTTGAACACACTTAATAGATGTGCTTTGTTTACAAAATATTAATGCAAAGATAAAATGTCAACTTTTACTAAATAAAAAGTTATCATATGTTAGTTTTGCTCATACTTATTAAAAAAAACTCTTGACCCTGAGTATCAGACTTTAAATGTTGCAGTTTTTTACAATTTTTTGTTTTCTCGTTTGTCTCTAGTTTCTTGCCATGGTCTTCCAGGACCTGCTGACCAATAAGGATGACTACTTGCGGGCCTCGAGGGCCTTGCTCAGGGAAATCATTAAACAGACCAAACATGAGATCAACTTCCAGTCCTTCTGTTTAGGCCTCATGCAGGAGAGGAAAGAGGCCACTTA[T/A]GTGGACATGGAGTTTAAAGTGAGCACTGGATTGCTGCATTTGTGTGTTTTAAGAATATCAGTTTTGCATGTATATAATTTGTTTTTGGTTTCCATTTTAGGAGCGTTTTGTCATCCAAGTGACGGATCTCTTGACCGTGTCCATGATGCTGGGGATTACAGCTCAGGTCAAAGAGGCCGGGATTGCCTGGGACAAAGGGGAAAAGAAGAGTAATACTGTTTTATACTGTTAGTGACACAAATATCCAACATTCAAATGTGTAGTATTGATCTTAATGATTATGTGTATGTATTTCAGATCTAGAGGTACTGAGGTCCTTTCAGAACCAGATCGCTGCTATTCAGAGAGATGCTGTGTGGTGGCTGCACTCTGTTGTTCCCACCATCAGTAAAGTGGGACCCAAAGACTACGTGCACTGGTATGGTTCAGAGGATTGCAGGATTTGTGCTGTTAAATAATGTTAGTAAAATGGTTATTGGTACTTAAAATAAAGCAGAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18206
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083062 | Nonsense | 624 | 2194 | 13 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43601337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42308143 |
GRCz11 | 3 | 43014158 |
KASP Assay ID:
2259-3977.1 (used for ordering genotyping assays)
KASP Sequence:
NNTTTTCAACAGCCTCCACAAGGTGCTTTTCACCGAGCAGCCTGARACGTA[T/A]TATAAATGGGAMAACTGGCCTCCTGAGAGTGACAGAAAGTGAGTTACCTC
Long Flanking Sequence:
AAATGTCTTAAATTTCAAAAACAAAAAGCCTTCAATTCACATAAATATTGGGCTGTAGGTCTTAAATAATTTTTAACAGGTCTTAATTTTTCTATGTCCATGTAAAGCTACGCAATGGGGCTAAGTTCATCTCAATTAAAGTTTTAACAGAAGATTATTTATTTACTATATTTACCAATGTGGTTTAATTATCTTCATTACAATAACATTTGTTTTAAACATTTTTTTAATGTTTTAACTGAACCAGTAGAAAAAATCTTTTGCGTTTACTCTTGTGTAAGTCTAAAATTTATTTCATAATGTTTTTAAAAGGTCTTAAAAAGTCTTAAATTTGACTTGATGATACCAGTAGAAACCCTGTGTTCAACTGCAACAAGGACACCTCAAAATAGTGTAACTTTTTCAATGTTATCAATGACACCCGTGCAGTATACTGATTGTTTTGTTGTGTTTTTCAACAGCCTCCACAAGGTGCTTTTCACCGAGCAGCCTGAAACGTA[T/A]TATAAATGGGACAACTGGCCTCCTGAGAGTGACAGAAAGTGAGTTACCTCTATTTTAGCATCTTGCAGATGTTTTCAGCATCTGTCTAATAAATGCTAATCTATCTCTCTTCTGTGTTAGTTTCTTTCTTCGGCTGTGCTCTGAGGTTCCTCTGCTGGAGGACACATTGATGCGCATCTTGGTGATTGGTCTGTCCCGTGATCTGCCCCTGGGCCCAGCTGATGCCATGGAGCTGGCTGATCACCTGGTGAAGAGAGCTGCAGGAGTTCAGTCTGATGGTAAGACAGCACTTCTGGTTACAGAGATGGTTTTCCTTATTTTAGAGTGGCCATGTGATGCTTTTTTGAAAAGGTCATTATTTAGTTTGTTGCATGTACCAATGTTATTTAGTAAAGGAAAACTATTTTAATTAATAAAATCAAATCAAAATTTCACAATAAAAGAAAAACTAAAACAAGATAAATTGAAATAAAATGATAATTAGCATAAAAGTTTTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40146
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083062 | Nonsense | 625 | 2194 | 13 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43601334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42308146 |
GRCz11 | 3 | 43014161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAACAGCCTCCACAAGGTGCTTTTCACCGAGCAGCCTGAAACGTATTA[T/A]AAATGGGACAACTGGCCTCCTGAGAGTGACAGAAAGTGAGTTACCTCTAT
Long Flanking Sequence:
TGTCTTAAATTTCAAAAACAAAAAGCCTTCAATTCACATAAATATTGGGCTGTAGGTCTTAAATAATTTTTAACAGGTCTTAATTTTTCTATGTCCATGTAAAGCTACGCAATGGGGCTAAGTTCATCTCAATTAAAGTTTTAACAGAAGATTATTTATTTACTATATTTACCAATGTGGTTTAATTATCTTCATTACAATAACATTTGTTTTAAACATTTTTTTAATGTTTTAACTGAACCAGTAGAAAAAATCTTTTGCGTTTACTCTTGTGTAAGTCTAAAATTTATTTCATAATGTTTTTAAAAGGTCTTAAAAAGTCTTAAATTTGACTTGATGATACCAGTAGAAACCCTGTGTTCAACTGCAACAAGGACACCTCAAAATAGTGTAACTTTTTCAATGTTATCAATGACACCCGTGCAGTATACTGATTGTTTTGTTGTGTTTTTCAACAGCCTCCACAAGGTGCTTTTCACCGAGCAGCCTGAAACGTATTA[T/A]AAATGGGACAACTGGCCTCCTGAGAGTGACAGAAAGTGAGTTACCTCTATTTTAGCATCTTGCAGATGTTTTCAGCATCTGTCTAATAAATGCTAATCTATCTCTCTTCTGTGTTAGTTTCTTTCTTCGGCTGTGCTCTGAGGTTCCTCTGCTGGAGGACACATTGATGCGCATCTTGGTGATTGGTCTGTCCCGTGATCTGCCCCTGGGCCCAGCTGATGCCATGGAGCTGGCTGATCACCTGGTGAAGAGAGCTGCAGGAGTTCAGTCTGATGGTAAGACAGCACTTCTGGTTACAGAGATGGTTTTCCTTATTTTAGAGTGGCCATGTGATGCTTTTTTGAAAAGGTCATTATTTAGTTTGTTGCATGTACCAATGTTATTTAGTAAAGGAAAACTATTTTAATTAATAAAATCAAATCAAAATTTCACAATAAAAGAAAAACTAAAACAAGATAAATTGAAATAAAATGATAATTAGCATAAAAGTTTTCAGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14215
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083062 | Nonsense | 1284 | 2194 | 28 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43588675)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42320805 |
GRCz11 | 3 | 43026820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGTGTGCMAAAAGATACTAGCATTATGTGTGTTATTGCCTGTTAGATTA[T/A]ATGGCTCATCTGGTGGAGGTCCAGCATGAGAGAGGAGCCACAGGAGGACA
Long Flanking Sequence:
TGTTTTCCTGGTCATTGCGCCTTTGCCATGTGCTGTGTATATGCAGACGATCGGATACGAGTCACTTTTAAAAGATGATGTAAGCAGGTCATCAAAAAAATCAAATACAGTCACAAAACCGGAATTGATCATCAAGATCTGCAGTGTAAATGCAGCCATATTGTCAGCCATCATAAGATATCATTAAAACAACAGGTACACTGTGATCTTAGATGATAAATAACTCACCCTTCTAGTGTCCATCTGATTTTCTCTGTCATTTTCAGCTCTGCAAGATCTGGAGCCCCAACAGCTACTGTTGTTTGTCCAGTCTTTCGGGATCCCCGTCTCCAGCATGAGCAAACTGCTGCAGTATCTGGACCAGGCCGTGTCTCATGATCCCCAAACACTGGAGCAAAACATCATGGACAAGAGTGAGGCTCTTTCAGTTGTCTTTTTTTCTCCATTATTGAGTGTGCCAAAAGATACTAGCATTATGTGTGTTATTGCCTGTTAGATTA[T/A]ATGGCTCATCTGGTGGAGGTCCAGCATGAGAGAGGAGCCACAGGAGGACACACGTTCCACACTTTGCTCAGCGCTTCACTTCCTCAACGTAGAGGTCAGGATTTATTGCTTTACGCCATGGGTTGAGTCAGCAATGATTAATGGTGCTGTTTTACTGCACGGCGTGATTAAATTCTCTACTAATGAATCCTCTGCTGGTCTTGTGTGTTACAGACAGCTCAGAGGTGAGCAGGGCTAAAGTGACTGTTGAAACACCCCATGGCTCTGTGAAGATGAGAGCAGTGAGTCAGGTGCCAGTAATCGGCCCAGAGGATGATCTTGCTGGGGTCCTACTACAGGTACGACATTTTATTCTTGGCCTTAGTCTTTTAGGTTTGAGCAGGGTGCAGCCATTGGACCCTTATTGGCTTGAGACTTTAAGTTTCATCCACTTGTATTGGTTTTTACCTCTGAGAAATAGCTTGTTATGCTACTTCATGTTGCAAACTGGTATTTTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20112
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 |
---|---|---|---|---|---|
ENSDART00000083062 | Essential Splice Site | 1540 | 2194 | 32 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43583394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42326086 |
GRCz11 | 3 | 43032101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAGAGCTGGAGAAAAGTGCAATGCTGAACCTGAACTCATCAGAAAAGG[T/C]ATTTTAGTGGGATTTTTTTCACCAGGAAATATAGTTTTGACTACTTACAG
Long Flanking Sequence:
TCTATTGTTGTTTGCTTTTGCTTACTCTCTACTTCTGTTTTTCTCAATCAGAGGTCGGTTTCTCAGGACGTTGGCTTCTCGTCACTGTTCTTTAACGCCGTAGTGCAAATGTTGACGTGGTTGGAGAACTCGGCGGTAGACACGGGTCCTCTCCACAGCCTCCTGAAGTCTCTGGCAGCGCAGTACTCTCACAAACATCGCATCACAGATGGTGAGCAGCTCCCGATCCTGATTCTTAGCCATACAGATCACTTTTACTAGCGTGTAATCCAAATGACGACAGAGAAATAGGGAAAACATGTGAAATAAATGCAGTCAGCAGAATATATGCTCTGCTAGTGTGTTTGATTCTGTCTTGTGTCATCAGTTCGTACAGGATTTCTGCATTTGGCTGAAGCGCTAGCTTACAGACGGGACTCTGAAGTGGCAGTGAGGGGCATTATTGCTTCTCTGAGAGCTGGAGAAAAGTGCAATGCTGAACCTGAACTCATCAGAAAAGG[T/C]ATTTTAGTGGGATTTTTTTCACCAGGAAATATAGTTTTGACTACTTACAGCAAGGGTGTCAAACTCAAATTTGGGCCATTTTCGTGACTGACAACTCAGAGGAGGCATATTTACCATTCAAGCACAAGAAAAAAGTGGTAACCTGATGTAATTGATGCGTCTTAGGAGAACAGACATGACGTTTAAAATTCAAGCGTCACCTGTTACCAGTGATAATGCAAATCAGCATGTTTGTGGAATCACACACATAAAGTTGTTTGTACCTGGCATGGAGATACAATTAGATTGTAGTTTAAACACTTGTGGTTGAATGCATTTAAGAAACCATTATAGACTACCTACACTCTACGTACTGGCCTAACATGTAATCCTTCTGGCTTCTGAGAAAGTGCACCTAAACAAGTTGTTCGTTCTAAATAAATTTAAAATAAATTAAAATTTTCTAAATTAAATAAACACAGGGAATTTAATTAAATTATATTTTAATTTATTTTATTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40145
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083062 | Essential Splice Site | 1797 | 2194 | 38 | 47 |
Genomic Location (Zv9):
Chromosome 3 (position 43567031)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42342449 |
GRCz11 | 3 | 43048464 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTTTATTGGCAGTTTAAGTAGTTATTTATTGTTTGTGTGCTGTTTAC[A/G]GTATAATGAGTAAGAAGTGTCAGACGCTGCTGCTTCAGATCTATCTGCAC
Long Flanking Sequence:
TTCATATATCTTACTGCTTGTTTTAAAGGACAAAATTGTATTGCAAATAATATATAAATATATTTATCTATTTTAACACAAGAATTCCTGTGCTGTAAAATAAAATATTATATTGTGTATAAAAAACATCGTCAATGCACCGTGATGCTCTGAGATATCGAATTGAACCGAATTGATGGCATGATAATCACAACCAAACTAAACAGTTAGACCAGTGTCTATATAGTTCATAAACTGTTTATTTATTTATTTATTGATGCTTTAAAACTAATTTGTTACACCACTAGACCCACTAATGTGACCTGGTGAATCCAAAAGTGGGTTTAAAAAAAATCTGCAATAAAATGTTAACCAGTCGCTGCGTTGTACATGTTCCTCATATTTTTAACCTAAACTCCTGATGCTGATTTAATATAAAAAGATTTAGAGAATCAGAACAGGCTCTTCTTAGCTTTTTATTGGCAGTTTAAGTAGTTATTTATTGTTTGTGTGCTGTTTAC[A/G]GTATAATGAGTAAGAAGTGTCAGACGCTGCTGCTTCAGATCTATCTGCACTTCCCGGAGGTCATCCAACACATCCGCCTACCAGAGGCCACACTGAGCGGCGAGGGGGCAGCAGACGGCAGCACATGCAAGGTACCGGCTGCAGAGACTGACACCTCCTGTTAATAGCACTGCACAGATTATTAATACTCTGCTTGTTTTCTTTCTCTCTCTATGTGTGTGTGTATCCGCATATTCAGTTGGACGTCCTCGTGCATCGGCTCATCACTCTGCTGGCTGACACTGGAGACTCCAAATCAGCTGAAAACCGTGTGTCTGATGCCAATCTGGCCTGCAGGAAACTGGCTGTCTCTCACCCGGTGCTCCTGCTCAGGTTTGCACAACACGCATCACAGCTTTCTGTTCCTTCCAACAAACTGTTGAATGTGTGGTTATGGGTTGTACTCATATGTGGGATTTATAATATATGAATAAACAGTAATGGCTTTCTATAGGTCATGT
Associated Phenotype:
Not determined