ZMP
insrb
Ensembl ID:
ZFIN ID:
Description:
insulin receptor b [Source:RefSeq peptide;Acc:NP_001116701]
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 |
---|---|---|---|
sa16909 | Nonsense | Available for shipment | Available now |
sa6697 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32383 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16909
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 |
---|---|---|---|---|---|
ENSDART00000105823 | Nonsense | 310 | 1348 | 3 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 11063496)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10923664 |
GRCz11 | 22 | 10953346 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCATACGTCATCCACAAYGGGGCCTGCATCCCAGAATGCCCRTCCGGATA[C/A]ACCACCGTCAACTCCACCTCGTACGTATCAATTTTCTCCTCAACAAAATA
Long Flanking Sequence:
GTAAACCTAGAATGGATTTAGAAACAGATATGCTAATGCTTGAACCTGCAAGTGGACAGAGCACATCATCCTACCCGAGTGTACAACACACAATGAAGAGTGCGGGAGACGTAACTCTAAGACGTATTTACATTGTTCGCCTGTATTATTCTGCCTATTTCATTGACAATCTAACAATATTTCCTTTTTTTTCCTTCAGTTTGTCCTTCTGAATGTGTCCACGGAGCCTGTACGTCCCATAAGGAGTGCTGTCACGAGCAGTGTCTGGGTGGCTGCTCTGTGCCGGGGAACTCCACCAAATGCGTGGCCTGCCGCAACTTCCTGTACGGCGAGGCGTGCGTGGACCGCTGTCCGCCAGGATACTACACCTTTAAGAGCTGGCGCTGCGTGTCCCTTCAGTTCTGCCAGGACCTGCACAACCAGTGTAAGGACAAGAGCGGAGACTGTCACGCATACGTCATCCACAACGGGGCCTGCATCCCAGAATGCCCGTCCGGATA[C/A]ACCACCGTCAACTCCACCTCGTACGTATCAATTTTCTCCTCAACAAAATAAAGAAATGCCATTTTTCATGTGTAACAGAGGCCAGCTAGTGAAGTGCTATACAGGTAACCCTCACTCCTCTGAGATCTAAAGGTGCTCTAGCATAAGATGCTAGAGGTCATGGTCTTTAGCCCTACTTGTCAGAGCAACCGACTCCCATGCAAAGAATTGCCGGTTCGATCTTAGCTCAGACCGGGTTGGGTACAGTAGGACCGGTGGGTTAAATTTAAGGGCTCGTCCGGGATGGGAGTGAGGTTTAGGGGGTTAGTGTAACAGAGGCCAGCTAGCGAGTTTCTATGCAGGTAAACCTCACTCTTCTGAGATCTAAAGGTGCTCTAGCCTCAAGTGCTAGAGGTCATGGTCTTTAGCCTTCTTGTTAGAGCAACCGACTACCATGCAAAGAATTGCCGGTTTGATCCTAACTCAGACCGGGATGGGTACAGTAGGACTGGTGGGTTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6697
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 |
---|---|---|---|---|---|
ENSDART00000105823 | Nonsense | 481 | 1348 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 11049510)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10909678 |
GRCz11 | 22 | 10939360 |
KASP Assay ID:
554-4884.1 (used for ordering genotyping assays)
KASP Sequence:
TTAATTKTTTAGCMRTAAAGTAGACCCGATCTKCATTCTGTCCTRCAGGT[G/T]AAAGTCACATACTCAAATTTACACAAATCCGCACCATGAGCGACAAGATC
Long Flanking Sequence:
AAATCTGCAGAAATCTGTGGAATTCTGCGGAAAATCTGCGGAGTTCTGCAGAATTTTGCGCGTGCAGATTCCGTGTGGGCCTACTTATGACGATATGAATGACCATATGGTATTAAGTCTGTATAGTACCAATATACATTGACCCTATTTAAAGGACTATTTGTTTTTTACATATTTCTCACTTTATTTAGAACTTCGGGGCAAATGTTTGATAATGTAAAATATAAAACAAATATTAAATAAAAAATGAACAAAAACCCAACACAAAACATTGGTAAATAAAATGATTGTTAGCATTTTTTTATAAATGATTAAATATAATATGAAACTACAGACCTTTTATTTTTGTTCATTGTCATATTGCACAGCTCTGCTGGAAACCTTTTAAATGTGCTGCTTTTAAAGATTTAAATTTGATGGTTTGTACTGGAAACCATTAGAGCATCTGCATTAATTTTTTAGCAATAAAGTAGACCCGATCTTCATTCTGTCCTGCAGGT[G/T]AAAGTCACATACTCAAATTTACACAAATCCGCACCATGAGCGACAAGATCCTCATCCGATGGGAGTCCTTCTGGCCCTCGGACTTCAGAGACCTGCTGGGATTCATGGTGCTCTACAAGGAAGCGTGAGTGTGGTCCTTTCAGTATCTATTGTGCTTCACTATTGAAGCTGTTTATATGATGTAAATGAAGGCCTGATTTAAAGATCCTTCACATATTTCATATTTTGAGTGTGCAAATAGGCGGAAATGCAGTCACTTTTCGAGGTTTACAACATAGAGAGTTGAAGTGAACTGCATGACATGTGACAAGAACCAACCAATCAGCTTCACAGTTATTTAACCATGATTGTTCGTATGTAGTTCTGCTCATTTTAAATCCTATAAAACAAAATTATATTAAAATAGTTTTGAAAATGTTGCTGCACGTCCTCCTTTTTTATATTATTATGAGAATTTTTTATTGTATGACTAATAATGTTTTAAAATATTATAATGTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32383
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 |
---|---|---|---|---|---|
ENSDART00000105823 | Nonsense | 858 | 1348 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 22 (position 11041591)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 10901759 |
GRCz11 | 22 | 10931441 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATCAGATGGAAAGAGCCCAAAACTCCTAACGGCATGATCATACTGTA[T/A]GAAGTCAAGTATCTACGGATGTCTGATAACTACGTAAGTGTTATAAATTA
Long Flanking Sequence:
TGGAGGACTATCAGCACTGCAAGTTTTAGATGTCTCCTTTGTCTGTCACACCCGTTACAGATCTTTAAGCCTCTGCTCAAATGATCTGAATCTGGTGTATTTGGGTAAGGAGACATGGAAGATGTGCAGAGCTGGTGGTCCTCCAGGAACGAGGTTGAGAAACACTGCTTTAGATCATTGTATCCCAACCCTGTTCCTGGAGGCATACCAACAGAAGATTTTTGGATGTCTCCCTTATCTAATCATTAACTTCAGGATTCAGCTGTTTGATTATGGGGAGGTTGAAAATGTTGTGTTGGTGTGCCTTCAGGAGCAGGGTTGAGAAACACTGCTTTAGATTATAGAAAGGTATTGGAATGTATTGAGTTTCCACTTGTTTTCATAGTGAAAGCTGATGTCATTGCCGAGCCAGTGACTCACGAATTTTTTCCTGACGAGCCGGATGTTGTTTACATCAGATGGAAAGAGCCCAAAACTCCTAACGGCATGATCATACTGTA[T/A]GAAGTCAAGTATCTACGGATGTCTGATAACTACGTAAGTGTTATAAATTATGGTGTGTATGTATATGCCATAGACATAAAAATGTCTACCTGCTGTAATGTTTTTAAATGTTTTTGGTCTCTCAGGAGGATCAAATCTGCGTGTCCAGAATTTCCTATGAGAAAAACCATGGCTATCGATTAAGAGTAGGGCATCCTGGGAATTACAGTGTGCGAGTTCGTGCCACCTCGCTGGCTGGCAATGGTTCTTGGACTGATCCTGCATACTTTTATGTTCAAGACAGTAAGCTTTACTTTATGTACTATACCTTTTTTCTGAATTTAGCAGCACTTCTGTCTCTAACAAACATGTTTTGCAGGGGAAATGAGCATGAAAATCGTTATCATCCTAGCCATCTGCATTTTCTTACTGGTGATTCTGGCCAGCGTAGGCTACTTTGTCTTGAAGAAGAAGTAAGTTTAAGACATTAAATCAAGCCCTTATTCATCGCATAAACAGTG
Associated Phenotype:
Not determined