ZMP
igf1rb
Ensembl ID:
ZFIN ID:
Description:
insulin-like growth factor 1b receptor [Source:RefSeq peptide;Acc:NP_694501]
Human Orthologue:
IGF1R
Human Description:
insulin-like growth factor 1 receptor [Source:HGNC Symbol;Acc:5465]
Mouse Orthologue:
Igf1r
Mouse Description:
insulin-like growth factor I receptor Gene [Source:MGI Symbol;Acc:MGI:96433]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20878 | Nonsense | Available for shipment | Available now |
sa38598 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31553 | Nonsense | Available for shipment | Available now |
sa11056 | Nonsense | Available for shipment | Available now |
sa2385 | Nonsense | F2 line generated | Not yet available |
sa5760 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa20878
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 |
---|---|---|---|---|---|
ENSDART00000046542 | Nonsense | 477 | 1380 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16325861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15308740 |
GRCz11 | 7 | 15557027 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAATGTTTCATTTTGTACTTTCTGTTTTTCTTAGGTGGGACTAAAATCT[T/A]AAAGTTTACTTCGAATAACACGAGGAGTAATCAAATCAAGCTGATGTGGG
Long Flanking Sequence:
TAATAAAAGTGCAGATATGAATATCAATCAATGACTAATGAAGTTTTGGATGAAAACAACACTACTTTAGGGGATTCAATCCAGCAATTAAATGCATTTACACTCTCCAAACTGTCTGTCTGCTGGTGAAGCATATTTAACAGTTGAATCTGTTTGTTGCTCTTATTCTGTGTTCTTCAGCACGTATGCCTTCGCTGCTTTGGATAACCAGCATCTGCAGCTTCTGTGGGACTGGTCACAGCACAACCTGACCATAAGTGAAGGAAAACTGTACTTCCGGTTGAACCCCAAACTCTGCATGTCCGAGATCCGCAAAATGTGGGCCAAGACAGGAATTAAGGACAACTTTGTGGAAAGAGATTTCCGCAACAACGGGGACCGTGCAAGCTGTACATGTTATTTATTATCACTTGATTGATTTATTCAGGAATGTAAACTTTAGTGTGCATTTAAATGTTTCATTTTGTACTTTCTGTTTTTCTTAGGTGGGACTAAAATCT[T/A]AAAGTTTACTTCGAATAACACGAGGAGTAATCAAATCAAGCTGATGTGGGAAAGTTATCGACCGTCTGATTCCAGAGATCTTGTCAATTTTATTGTGTACTACAAAGAAGCGTAAGTTTGGGTTTTGTTTAGAAGCTTTTTCTCAAGCAAGGTTATTATAGTTTTGCATTTTTAGATGCTTTTTAACAAAAAAGGCTCTAACTTTTAGTTTAGTTTTAGTTAGTTTCATCAATGGCTAGTTTAAATTTTTGTTAGCAAATGAATTTGTAAAAGCGCCTACCCCACTGCCCCCACCCCCCAAAAAATGTAAAATTTATTTATATAGCACATTGTGATTTTTATAAATCCCAAAGTGCTTTACAAAGAAGATGCAAGCAAGCAGTATGGACATAAAACAAAACAGCAATAGGCATAAAAGATGTAAAATCGGTCATACGAAAAAACTGTTTATTTTCAATGCCTAAAAAAAGAAATTCATTGATCCTTTAGTTAATTCCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38598
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046542 | Essential Splice Site | 723 | 1380 | 10 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16331857)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15314736 |
GRCz11 | 7 | 15563023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCGCAAAGCCTTCGAGAACTTCCTCCACAATGCCATTTTCACTCCCAG[G/A]TAAACCCTAGTTTGATCAGGAATGTGATTATTACTATTACTATATCTAAA
Long Flanking Sequence:
TTTCCGACAGCAATTAAGACTTTTTAGCATGAAACATCTGAAGCTTTCAGTGTCAGTGCATCTAGGGAAATTAGATCAAACACTGTTTGAAAACTCTTTTAGTTCTCGACTTCAAAATACACCAGGCTTTGCAATAATGAAATGATGTGCAACATGTTTAACATTGTCTGTATGTTATTAGTGCCGCTCTGTATTACTCATACTTGATTTTCTGTGGCACTGGTAAATAATTCCAGATTGTCGCAAGATCACAACAGGAAGAAAATATAACAATGTTTGTGTAAATCTCTGACAGAACTGAAGATCCCTGTAAGGGTTTCAGCCACGGGTTTGACAGACACTGAAGACACGAAGCCGACCAATCATGAAACAGGAGGACGAGACAAAACCCCCTGCTGTCCCTGCCCTAAAACAGAGGAGGATCTGAAGCGAATCGAGGATGACATCTACTACCGCAAAGCCTTCGAGAACTTCCTCCACAATGCCATTTTCACTCCCAG[G/A]TAAACCCTAGTTTGATCAGGAATGTGATTATTACTATTACTATATCTAAAAACCCAACTGATAGTGTTTTCAAAAGCACACCTTGTCATCACAGCAACAGAATTTCACCATGTTTAAGATTTTTATATATTTTTGGCTTTTGTTTCACCTGGTTTTTGGAGTCGTTTGTCGACAGAATTGAACTCTGTCTTCATGGTCAACTCCGCTCCATGTCCCAAGTTGGCCGACGTACATGGCGAGCCACTGGGGAATCTGGTAACACCGAAAAATTCGTAAATACTGAAGTAAGCTGGTAGAGCTACAATAAGCAGAGGCTGGCGGTGGCGTCACACTTCCCTGTAGCGTTCGTTTTAAAAATGAAATGCAGCCAGACGTACCTCTGGCTACATAATTTGTGCTCTCCAGAAATGTAGACAGGGTACCTTTCCACTATGAGCCTGTGTTGAAAATATATTACTCATATTTACTGAGAAATGGATAAAAATATTCAGTTTCAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31553
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046542 | Nonsense | 728 | 1380 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16341434)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15324313 |
GRCz11 | 7 | 15572600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATTTCCCTAATAGATCTTAATCTCTCTGGTTTCAGACCTCCAGACAGG[C/T]GACGGAGGGATTTGTTTGGTGTGGCCAACGTAACCTCTATTCACACTCTG
Long Flanking Sequence:
ACAATAAATGTGCAGCAATTTAAAAAAAAAAATCTTTTTTCACATTGTCATTATAGAGCATTGTGTGTAGAATTTTGTGGAAATAAGTTCTGATTTCTGATTTCAACTGTACATTTCAGTAGTTTCTCCTTGCGTCATTTGATTGTTATTACACATGACTCATTTTTCTGATTTTTCGTTTTGTTTTTGTTTTTATGTTTGTAATGTATTATTTTTATTTACCAAAATCTGGTTCAATTCCATGTCAACAGCTCCTTTTGAAATATTGTTCTCAGGGAAAAAATATGCCATGCTTAATACTTATTTTTTGTCACTGTAATTTTATGCTCAAAAATAAATTTCTGTTAACTAAAATCAGTTGTACTCCTATTCTGATTCATTCATTCAACTTTTTAATAAATGAGAATTCTTGTTGCCAGATTGAGCTTTTGTCATGCCTGAAGTTGTGCAATATTTCCCTAATAGATCTTAATCTCTCTGGTTTCAGACCTCCAGACAGG[C/T]GACGGAGGGATTTGTTTGGTGTGGCCAACGTAACCTCTATTCACACTCTGCTAGCGGGACACTGGAACCTGACCGAGGGAAACTTCTCAGATGACGAGCCGCCTAGACGAGAATTTTCCTTTCTGGAGAGGAAGGTGAAAGAGCGACACATTGAAATCACTGGCCTGCAGCCTTTTACCGTTTACCGCATTGACCTACACGCGTGCAATGAAGAGGTTCGACACTGCAGTGCCGCTGCATTCGTCTTCTCTCGCACCAAAGCAGCAGGTAAGAGCGGGACATCAAAACTTAAATAAGACTATAAAGAGGATAATTTTTAATTACAACAAATGAAAACATTTGGCATTCTATTAAAAATAAATGGTCATGAAATTTGAAAACAATAGAATTAATACTAACATTTCACTCAAATCAACAGCTAAAATTTTCCACGGGAAATTTTGAAGTTGTTTCATTGCACTGGGATTTACTTTACAATTAACACTATTTAAATAGTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11056
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046542 | Nonsense | 995 | 1380 | 16 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16351351)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15334230 |
GRCz11 | 7 | 15582517 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAATGGGAAGTGGAGCGGGAGAAGATCACGATGTGCCGAGAGCTTGGA[C/T]AGGGGTCRTTTGGTATGGTGTATGAGGGCATCGCCAAAGGTGTCGTTAAA
Long Flanking Sequence:
AAACAAAAAATATATATACATGTATATATTCTTTTTTTTTTTTTTTGGTGGGGTGAGAGGCATTTGAAGTAGGTTCCTGCCCCAATAGAGCTTTATGTCTAGCAGCGCCCCTGTTACTACCTGCATATTGTTTGTAAATTAAATATTTATTAGCAATAAGTATTATTTATTTTTAATAAGCAGCTAATTTGTGGTTTATTGTGCTAAAAGTCCTAGTTAATGGTTTGTTAATAGCATGAACATTAAAAAAGTGTGACTAAACTTAACATAAATACTATACATGAAATTGCGCAAAATTGTATTTTGTACAATGAATTATGCTGAAGAGAGATTTTGAGGTAAAATGATATGTAGGGTTTGTTGAAAGTGACTAGTGTAGATATAGTGGGATAAGTATTGCTGATTAGTGACTATCTACGTGATAATGTATGTTTGCAGTGTATGTGCCGGATGAATGGGAAGTGGAGCGGGAGAAGATCACGATGTGCCGAGAGCTTGGA[C/T]AGGGGTCGTTTGGTATGGTGTATGAGGGCATCGCCAAAGGTGTCGTTAAAGATGAGCCGGAAACCAGGGTGGCCATTAAAACGGTCAACGAATCGGCCAGTTTACATGAGCGCATTGAGTTCCTTAATGAAGCCTCCGTGATGAAAGAGTTCAACTGTCACCATGTGGTGAGTTAAAGAAATCTCATCTCACTAGCTTAGTTAGACTCTTTTTCCCTTGTAAAAGTTTGACATGCATTACTCAACATTCGACGTGGATCTAAACCTTTCCTCAGAGTTGTCCTGAAACATTTAAACGTCTATTCTTCAATTTTTAAACACTTTCTACTCTTTACTTCAAGTTGAAGTTTTGATCCACTACAAATGTTGACTACTATATGCAATCTCTGATATTTAACATTTATAAATGAACCAATGAGCTTTCTAAATATTGCCAAATTTGGATTGCAGTAGCCTTACAACAAGAATAAACCATTAACATTGTAATGTTGACTTTTAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2385
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 |
---|---|---|---|---|---|
ENSDART00000046542 | Nonsense | 1357 | 1380 | 21 | 21 |
ENSDART00000046542 | Nonsense | 1357 | 1380 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16371607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15354486 |
GRCz11 | 7 | 15602773 |
KASP Assay ID:
554-3392.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCGGCCAACGGGCCCTCCATGGTCCTGAGGGGGCCKTTTGAGGAGGGT[C/T]AGCCTTACGCTCATATGAACGGGGGCCGGAAGAACGAGCGTGCCTTGCCT
Long Flanking Sequence:
TATACTTATATATTACAATTAAATCATGATAAATAATTAGCCTGATCATCTCAAATTCTTGTGTGTTTTTCTCTGAATGCCGTGTTGATCATCTCCTCTGTGTCTGATCCTCCAGGTTCGAGCTGATGCGCATGTGCTGGCAGTATAACCCCAAAATGCGGCCGTCCTTCCTGGAGATCATCAGCAGCATCAAGGAGGACCTGGAGGCAGGCTTCAAGGAGACCAGCTTTTTCTACAGCGAGGAGAACAAGCCCCCAGACACGGAGGAGCTGGACATGGAGAACGTGGGAACCATGGAGAACGTCCCTCTAGAACCGTCTTCCAGCCTGCAGCCCCTTGCGCCCTCAATATCCCCCCCTCAGCAGTGCACAGCTGCGGCCCAGAGCTGCTCGTCCCCGTCCTCGCCTCCTTCATCACCCAGCTCCACGGACAAACACCCGCTTCCGACATCAGCGGCCAACGGGCCCTCCATGGTCCTGAGGGGGCCTTTTGAGGAGGGT[C/T]AGCCTTACGCTCATATGAACGGGGGCCGGAAGAACGAGCGTGCCTTGCCTCTGCCCCAGTCTTCGGCTTGCTGATCGCCGGATGCGTCGGATGTGTGTCAAGCCACTGTGTGGTGTCCTGAGAAGAAATATTCAAGATATTCGTTTAGAGACGAAAAAAGAGAGAGTCCAGGCAATCAATTTTTTCAATCATACCTCAACGGACAAAGTTTGGAGTTCTTTGTTTTTTGTGCGTTCCGATTGAATTGTTGAATTGATGATTGAACTCATTTGTTATTTCCGCCAGACTGGATCACTGACTGAAAAAAAATATATATATATGAAAAGAAAAAAAAACATCACTTTCGCACTCAATAGGCTGTTTTTGTTACTTTTCTAAACTTCCAGAGCTGGTCTATGAGAGCCAGTAGTGGTACGGTGGCATTATTACAACATGCTCTGCATATCTCCAACTTGCGAGTTAATTGTCTTTGTTTCCAAAGACGTGCGTCTAAAAGAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5760
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 |
---|---|---|---|---|---|
ENSDART00000046542 | Nonsense | 1357 | 1380 | 21 | 21 |
ENSDART00000046542 | Nonsense | 1357 | 1380 | 21 | 21 |
Genomic Location (Zv9):
Chromosome 7 (position 16371607)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 15354486 |
GRCz11 | 7 | 15602773 |
KASP Assay ID:
554-3392.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCGGCCAACGGGCCCTCCATGGTCCTGAGGGGGCCKTTTGAGGAGGGT[C/T]AGCCTTACGCTCATATGAACGGGGGCCGGAAGAACGAGCGTGCCTTGCCT
Long Flanking Sequence:
TATACTTATATATTACAATTAAATCATGATAAATAATTAGCCTGATCATCTCAAATTCTTGTGTGTTTTTCTCTGAATGCCGTGTTGATCATCTCCTCTGTGTCTGATCCTCCAGGTTCGAGCTGATGCGCATGTGCTGGCAGTATAACCCCAAAATGCGGCCGTCCTTCCTGGAGATCATCAGCAGCATCAAGGAGGACCTGGAGGCAGGCTTCAAGGAGACCAGCTTTTTCTACAGCGAGGAGAACAAGCCCCCAGACACGGAGGAGCTGGACATGGAGAACGTGGGAACCATGGAGAACGTCCCTCTAGAACCGTCTTCCAGCCTGCAGCCCCTTGCGCCCTCAATATCCCCCCCTCAGCAGTGCACAGCTGCGGCCCAGAGCTGCTCGTCCCCGTCCTCGCCTCCTTCATCACCCAGCTCCACGGACAAACACCCGCTTCCGACATCAGCGGCCAACGGGCCCTCCATGGTCCTGAGGGGGCCTTTTGAGGAGGGT[C/T]AGCCTTACGCTCATATGAACGGGGGCCGGAAGAACGAGCGTGCCTTGCCTCTGCCCCAGTCTTCGGCTTGCTGATCGCCGGATGCGTCGGATGTGTGTCAAGCCACTGTGTGGTGTCCTGAGAAGAAATATTCAAGATATTCGTTTAGAGACGAAAAAAGAGAGAGTCCAGGCAATCAATTTTTTCAATCATACCTCAACGGACAAAGTTTGGAGTTCTTTGTTTTTTGTGCGTTCCGATTGAATTGTTGAATTGATGATTGAACTCATTTGTTATTTCCGCCAGACTGGATCACTGACTGAAAAAAAATATATATATATGAAAAGAAAAAAAAACATCACTTTCGCACTCAATAGGCTGTTTTTGTTACTTTTCTAAACTTCCAGAGCTGGTCTATGAGAGCCAGTAGTGGTACGGTGGCATTATTACAACATGCTCTGCATATCTCCAACTTGCGAGTTAATTGTCTTTGTTTCCAAAGACGTGCGTCTAAAAGAAAT
Associated Phenotype:
Not determined