ZMP
insra
Ensembl ID:
ZFIN ID:
Description:
insulin receptor a [Source:RefSeq peptide;Acc:NP_001136144]
Human Orthologue:
INSR
Human Description:
insulin receptor [Source:HGNC Symbol;Acc:6091]
Mouse Orthologue:
Insr
Mouse Description:
insulin receptor Gene [Source:MGI Symbol;Acc:MGI:96575]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6016 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa1682 | Essential Splice Site | Available for shipment | Available now |
sa32968 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6016
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 |
---|---|---|---|---|---|
ENSDART00000008302 | Nonsense | 687 | 1353 | 10 | 21 |
The following transcripts of ENSDARG00000011948 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37284943)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37581653 |
GRCz11 | 2 | 37564110 |
KASP Assay ID:
554-3752.1 (used for ordering genotyping assays)
KASP Sequence:
GAGCCCCCACACAAGTGGACAACGAAGAGGAGCAGAAGTGGAACCAAACT[G/T]AGGAGCAGGGCCCTGATAGCCGCTGCTGCGCTTGTCCTAAAACAGAGAAA
Long Flanking Sequence:
CCTAAACCTAGCTCTGTTGTAGGAGTTGAGAATGAAATTGTTTACTACATAAACATAATTACATGATAAAAAGAACAACGTAAAATTAAGTTAACTCTTTGTTTTGAACTCGCTCATGTTCTTTTCTTGTACTTTTTTTTTCTTTCATTCTTTTTATTTTAGAGCCATCAGTGCCTCTGGACCCCATATCCTCGTCAAACTCCTCATCCCAGATCATTCTAAAATGGAAGCCACCAAACGATCCTAATGGAAACATCACTCATTACCTGGTCTTTTGCCAGCAACAGCCAGAGGCCAGCGAGCTCTACAAATTTGATTACTGCCAGAAAGGTTCGAAAACATACAGGAACATAATAACAATGCACACTTCCATTGATAGGTCTGGAGTTTGTAAGGTAATCTGTTGAGATCCTGTATGTTTCTGTTGATCAGGTATGAAGCTGCCCACCAGAGCCCCCACACAAGTGGACAACGAAGAGGAGCAGAAGTGGAACCAAACT[G/T]AGGAGCAGGGCCCTGATAGCCGCTGCTGCGCTTGTCCTAAAACAGAGAAACAACTGAAGAAAGAGGCGGAAGAGACGGAGTATCGAAAAACCTTTGAGAACTACCTCCATAATGAAGTGTTTGAGCTCAGGTAAATCTTCTTTCAGCTGTTGTGGAAAAAACTGTAACAGTATAATCAGTGATGAAAATTATTTAACCAATTAGATGATCCACCCAAACTATAAACTTCTCTGTGAATAACAGTACATTTAGCTATTTTTGGTTCCGATCTATGTAGTATGATATTAATCTTGTCATATATAAATAATATACCTTATGCATTACAGCTCTTTTACATGAATAGACAATCTGTATGTATGTATAACCTAGATCATGTAGACATGTTTATTCATAACATACTTTTTTGAAGACATTATATAAAGTTTTTTCTAAATTAAATGTGAATTGCATAAACATTAATGCATATACAGTAATAGAATGCATTGTTATTATATGAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1682
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 |
---|---|---|---|---|---|
ENSDART00000008302 | Essential Splice Site | 824 | 1353 | 11 | 21 |
The following transcripts of ENSDARG00000011948 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37279993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37576703 |
GRCz11 | 2 | 37559160 |
KASP Assay ID:
554-1628.1 (used for ordering genotyping assays)
KASP Sequence:
GACTCGATGCAGTATGGCAGCCTACGTCAGTGCCCGCACCATGCCTGAAG[G/A]TAGAGGATTTTTATTTATGATGCAGTGTTATTGTTTAGAATGTAGCTATT
Long Flanking Sequence:
GGGTAGTCAATTTGATCAATAGACAAGGGTAAACATGGAAATGATATTCATCTTTTAAATAGTCTTGGTTGTTGTAACAAGATGCACTTTAACATGGTTGGCTGATTTTTATAGTAAAATTGAGTAAAATTATTTAATTAAAGCAATAAATAGCAATAGAATCCTTATAAGATTGGACTTAAATCTTGACCCTCTTGTGTGTTTCTGTGTATGCAGGCCATCAAGACAGCGCAGATCTCTGGTGGGCATTGCTAATAGGACGTCCTCTCGTCTTTTCACCACACCCTCCTCACTCCCCAATGGCTCTGCTACTCGTAGCCCAGAAGAGGAAGCAGAGGCCAACAAGATTTCACTGATTGTTCAGGCCAAGGAGTCAACAGTCATCTCCAATCTACGGCATTTCACCAGCTACCAGATAGAAATCCATGCATGCAACCATGGCAGTGACCCGACTCGATGCAGTATGGCAGCCTACGTCAGTGCCCGCACCATGCCTGAAG[G/A]TAGAGGATTTTTATTTATGATGCAGTGTTATTGTTTAGAATGTAGCTATTATTATTATTATTATTATTAGGTCTTTGTACAATTTAAAAAAAACATCTTGTATGTTTAAGAACTCAAAACTTCTTAGTCTAAAAACAGCTTCTAAGGTATTTTGCTAAAACAACAAGTTGATAAAATGTCCCTTTATCATATAATAGTCTGCCTAAACCCCGCCTTTTAGGAAGTAGATCAACACCTGCTTCTACTGCATCACTGCTTGTTTAGCTCCGCCCAGAGATCCATGCTGTTGTATGTAAACATGGACACGGAAACCAATGATTAAACGGCTATGAAGACGAAATCTGTAAAGTGTCAACTTGTGGAATAACAATGTGTTTATATTATGGCATCCTGCTAATCCCAGCATTAGGAAGCGTGGATGAGTTTTATTTATTTATTTATTTATTTTTAAACTTCCCGACCATGTAGGTAAGATCTTGGTCCGTTGTTCACCTCATTTT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa32968
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000008302 | Nonsense | 1153 | 1353 | 19 | 21 |
The following transcripts of ENSDARG00000011948 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 37269015)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 37565725 |
GRCz11 | 2 | 37548182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTAATTTCTGTTGATTTTATCTTGTGTACTCAGATTTTGGCATGACC[A/T]GAGATATTTATGAGACGGATTACTACAGAAAGGGTGGGAAGGGTCTTCTT
Long Flanking Sequence:
TTTTGCATTTTTAATTTTTATAGCTTTGAATAATTTAAAAAGAGCCACATATTGATAAATAATGTTATAACAGCTGTCTAAATATTAAGTTAAGATTGAATTGCCTCTTTTTACAGTTATGAAATAGTTTGATAACAAGCAGGAAATGTTCATGGGCCAATGACATGACCGCATTGAAATGGTCTATAGACATCTAAGGATAGCCCAAATCTAGACTAGTGGTCAAATAGACAGAATAGACAGACTTTATATGTGTAGTCATTCATTTCTTTTTATTTGATGACTAGTCTAATTTTGATCTATTCCTAGACGTCTATTAGATTTTCACTGACAGCCCAAATTTAGCCTTGTTTTAGCCAAGACAACCATGTTTAGACATCTATTAGTCTTGCTGGGAAAATACCTGTAATTGAATTATAATATATGTAATTATAATTAAATATGTGATTTAATTTAATTTCTGTTGATTTTATCTTGTGTACTCAGATTTTGGCATGACC[A/T]GAGATATTTATGAGACGGATTACTACAGAAAGGGTGGGAAGGGTCTTCTTCCAGTGAGATGGATGGCACCAGAGTCGCTGAAGGATGGTGTTTTCACAGCTCACTCAGACTGCTGGTGAGCTGACTGTCTATACGCACACAGCCTTACTAATACATCAGTAATTGTTGTTGCTCGTGTGTTTAGTCTTTCATGACCCATCTTGTGTTTGTTTAGGTCGTTTGGTGTGGTGTTATGGGAAGTCAGCACTCTGGCTGAACAGCCGTATCAAGGCCTGTCCAATGAACAGGTCCTTAAATTTGTGATGGAAGGAGGATATCTGGACAGACCAGACAACTGCGCAGACAGATTGTGAGTGTGTTGCTGACATGCTGTAACATGTCAGTGTTTGGTGCAAGGATACTGTATCTGACTTCAAAAAGGGTGGTTCTGTTTTGTTTCTGGCTAATGGGATTCATTTAGCAGATGTTTAATTAATTGTAGCCAGAGTGGATTCTATTTG
Associated Phenotype:
Not determined