ZMP
si:ch211-284e13.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate insulin receptor substrate 1 (IRS1) [Source:UniProtKB/TrEMBL;Acc
Mouse Orthologue:
Irs3
Mouse Description:
insulin receptor substrate 3 Gene [Source:MGI Symbol;Acc:MGI:1194882]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18812 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33659 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa26532 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2220 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa18812
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 |
---|---|---|---|---|---|
ENSDART00000084890 | Nonsense | 112 | 513 | 2 | 7 |
ENSDART00000131831 | Nonsense | 123 | 1179 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 39692222)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37491612 |
GRCz11 | 5 | 38091765 |
KASP Assay ID:
2259-6232.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTATAATCTTACTGTCTTTTATTTTATATCTGTAGGTAAGACTCCTGAT[G/T]AGTGCGGCAGTGGAGGAGACTGTGGACTACCTTCCCCGGGCCCTGCCTTT
Long Flanking Sequence:
AAACCTTGTTGTCCTTGAATCTTTTTTTACATATCCTTGTAAAGCAAGGGACTTTTTGGCAAACGACAGAATCCACAATGGTACTAGCTTGAGAAAGGGTAGCACATCAATATATGAAGTCTTTTTTTGTTGTTGTTTAGAAGAAATTTGTAATGTCTAGGAATATTACATGTAACGAATAAAAGATTTATACAATAAATATAAAAAAATATGTAAATTAAAAATTTATCAATATAAAATAAACATTTTGTTTATATTAGTGGCTTAAGAAATCAAAGCTTTATTCAGTGTATAGTGTTCTTTATGGAAATATATTTTCTGACAATTCTGATTTGAAACAATTTAATGTTTTAATTATGTCTAAATAGATAAAGATAGACACATTTAACATCATATCTGCACAACAGTTCAATACAATACCATTAAATATTTGTGTGTTTATTTCACAGTTCTATAATCTTACTGTCTTTTATTTTATATCTGTAGGTAAGACTCCTGAT[G/T]AGTGCGGCAGTGGAGGAGACTGTGGACTACCTTCCCCGGGCCCTGCCTTTAAGGAGGTCTGGCAGGTTAAAGTCTGGCCAAAAGGTTTGGGCCAGGCCAGGAATCTAATTGGAATATACAGACTTTGCTTGACGGACAAAACAGTCAATTTTGTAAAACTCAACTCTGATGTTGCAGCTGTGGTCCTCCAGCTGATGAATGTGCGACGCTGTGGCCATTCAGAGAACTTTTTTTTTATTGAAGTGGGTCGTTCTGCCATGACAGGCCCTGGTGAATTCTGGATGCAAGTAGAGGATTCAGTGGTGGCACAGAATATGCATGAGACTCTTCTTGAGGCCATGAAGGCCCTGAGCGAAGAGTTTCGGCAAAGAAGCAAATCTCAGACTGTTGGGGTGAGCTGTGGAGGAGGAACTGCCTCTAACCCAATCAGTGTACCGTCTAGACGACACCATCCTAATCTACCACCTTCACAGGTTGGCTTTTCCAGACGTGCTAGAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33659
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 |
---|---|---|---|---|---|
ENSDART00000084890 | None | None | 513 | None | 7 |
ENSDART00000131831 | Nonsense | 465 | 1179 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 39691196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37490586 |
GRCz11 | 5 | 38090739 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAGTTACATCCTAATGGGTCACAGAGAAGGCTCTCACAAACGTGTTCAT[G/T]GACGCAGAGTCCTTCGCCGTTCATCTAGCCGCGAGTGTGAAGTTGAGCGC
Long Flanking Sequence:
ACACTTCCCCAACTCCACGGCATGGTTTCTCTAGGTCAAGGACAGCCAGCATTGGGGCTCGAACAGAGGATGGAGGGGGCAGAGCAACAGCACTCAGCACGAGTCCTAGTCTCAATGGGTCATCCTGCTCAACCACCCCAACCCTGAGACCTAAACCAACACGAGCACCCACTCCAGCAAAGATCACTCTTAGCCTAGCACGATATACACCAAACCCTGCACCTTCCCCAGCACCCAGTCTCTCATCCAGCTCTGGTCATGGGTCCGAGTGTGGGTTGGGTGGAGCCACCTTTGGAGCAGTCCCCATCTGCACCTATGCTCGAATTCCTCAGAGAGTGTCTATGTCAGGATCACCCAGTGATTATGGTTCCTCAGATGAGTATGGATCCAGCCCTGGAGAGCACTCTCTGCTAGCTGCTGGACTCCCTGCTGCCCTTGTTGAAGGTGGAGCTAGTTACATCCTAATGGGTCACAGAGAAGGCTCTCACAAACGTGTTCAT[G/T]GACGCAGAGTCCTTCGCCGTTCATCTAGCCGCGAGTGTGAAGTTGAGCGCAGGCTGCTCAGTAAGCGTGCTTCCTTACCCCCCACTTCTACCCAGGGTTTGGTCCCCCGCCGAAGGGAGGAGGAAGAAGAGGATGAAGAAGAGTATGCAGTCATGTCACGCAGTGCAAGTAGGGAATCTTTCACATCACGCAGAGGCTCAGGAGGTTCAGCAACAACATCATTGGTGCAGGAAAACTCTGCAGATAAAGGTGTGAGTACAAAAGGGGGTCCTGAAGACTCCTCAATTGACAGTGGTTACATGTCCATGTTACCAGGCGTTACAGCTCCTCCTGCTTCATTATCACTAGCAGTTTCTGGTTCAGATGCAGTGCCAAAGGGTGGAGATGAATACATGGCCATGACCCCCAATAATAGTGTCTCTCCCCCTCAGCACATTCGTCTACCAATCAGTGAAGGTTACATGATGATGTCTCCTAACAGTAGCTGTTCACCGGACTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26532
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084890 | Splice Site | None | 513 | None | 7 |
ENSDART00000131831 | Nonsense | 556 | 1179 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 39690923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37490313 |
GRCz11 | 5 | 38090466 |
KASP Assay ID:
2259-6231.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGCAGGAAAACTCTGCAGATAAAGGTGTGAGTACAAAAGGGGGTCCT[G/T]AAGACTCCTCAATTGACAGTGGTTACATGTCCATGTTACCAGGCGTTACA
Long Flanking Sequence:
GGTTGGGTGGAGCCACCTTTGGAGCAGTCCCCATCTGCACCTATGCTCGAATTCCTCAGAGAGTGTCTATGTCAGGATCACCCAGTGATTATGGTTCCTCAGATGAGTATGGATCCAGCCCTGGAGAGCACTCTCTGCTAGCTGCTGGACTCCCTGCTGCCCTTGTTGAAGGTGGAGCTAGTTACATCCTAATGGGTCACAGAGAAGGCTCTCACAAACGTGTTCATGGACGCAGAGTCCTTCGCCGTTCATCTAGCCGCGAGTGTGAAGTTGAGCGCAGGCTGCTCAGTAAGCGTGCTTCCTTACCCCCCACTTCTACCCAGGGTTTGGTCCCCCGCCGAAGGGAGGAGGAAGAAGAGGATGAAGAAGAGTATGCAGTCATGTCACGCAGTGCAAGTAGGGAATCTTTCACATCACGCAGAGGCTCAGGAGGTTCAGCAACAACATCATTGGTGCAGGAAAACTCTGCAGATAAAGGTGTGAGTACAAAAGGGGGTCCT[G/T]AAGACTCCTCAATTGACAGTGGTTACATGTCCATGTTACCAGGCGTTACAGCTCCTCCTGCTTCATTATCACTAGCAGTTTCTGGTTCAGATGCAGTGCCAAAGGGTGGAGATGAATACATGGCCATGACCCCCAATAATAGTGTCTCTCCCCCTCAGCACATTCGTCTACCAATCAGTGAAGGTTACATGATGATGTCTCCTAACAGTAGCTGTTCACCGGACTTGCACGGCATTAGTGGATGCATATGGGGCAGCAGAGGCAGCATGGAGAGTCGAGCAGGCAGTGACTACATGAACATGTCACCTATAAGTGCCAGGTCAGCTTGCAGTACTCCTCCATCACACCCAGAGCAACAGCCACTGCAGCCAAAGATGGTCTATTCATATTTTTCATTACCACGTTCCTACAAACACGCCACTCTCTCTGCCCGTTTTGAGGATAATCTGGAGAGGGTTTGCATGGGAAGAGGTGAAGCTGCAGGAAAAACTGGACATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2220
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 |
---|---|---|---|---|---|
ENSDART00000084890 | Nonsense | 498 | 513 | 7 | 7 |
ENSDART00000131831 | Nonsense | 678 | 1179 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 5 (position 39690557)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 37489947 |
GRCz11 | 5 | 38090100 |
KASP Assay ID:
554-2778.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGGTCAGCTTGCAGTACTCCTCCATCACACCCAGAGCAACAGCCACTG[C/T]AGCCAAAGATGGTCTATTCATATTTTTCAYTACCACGTTCCTACAAACAC
Long Flanking Sequence:
AAGAGTATGCAGTCATGTCACGCAGTGCAAGTAGGGAATCTTTCACATCACGCAGAGGCTCAGGAGGTTCAGCAACAACATCATTGGTGCAGGAAAACTCTGCAGATAAAGGTGTGAGTACAAAAGGGGGTCCTGAAGACTCCTCAATTGACAGTGGTTACATGTCCATGTTACCAGGCGTTACAGCTCCTCCTGCTTCATTATCACTAGCAGTTTCTGGTTCAGATGCAGTGCCAAAGGGTGGAGATGAATACATGGCCATGACCCCCAATAATAGTGTCTCTCCCCCTCAGCACATTCGTCTACCAATCAGTGAAGGTTACATGATGATGTCTCCTAACAGTAGCTGTTCACCGGACTTGCACGGCATTAGTGGATGCATATGGGGCAGCAGAGGCAGCATGGAGAGTCGAGCAGGCAGTGACTACATGAACATGTCACCTATAAGTGCCAGGTCAGCTTGCAGTACTCCTCCATCACACCCAGAGCAACAGCCACTG[C/T]AGCCAAAGATGGTCTATTCATATTTTTCATTACCACGTTCCTACAAACACGCCACTCTCTCTGCCCGTTTTGAGGATAATCTGGAGAGGGTTTGCATGGGAAGAGGTGAAGCTGCAGGAAAAACTGGACATAGTGCTTATGATTGTGGAGGAGACACACCTGTGGGCTCCGGTGGCGGTGGACAACTTTCTCTGTCCTCATCTTCTTTTTCCTCCAGTTCAGCTAGCAGTGAAAGCCTTGAAGACAGATCGTTGTCTCTTTCTGTTGGTGGAGTGGGACGAGCAGCTAGGCTGAGCACAGGACACAGGGTACGGGGAGCTCACCCCAAAATTACATCCCAACACCATCACCAGCAGAGTTGTGGGCCAGGGGTTCCGAAACAGGGTCATTTACAGACAAGGAAAGACAAATCATCCAGCTATTTTGTGGATATGTCCAAAGCCAATACCCTGCCGAGAGTCAGGGAGACTTTGCTCCCAACGGCATCTCAGAGCCCTGGA
Associated Phenotype:
Not determined