ZMP
igf2r
Ensembl ID:
ZFIN ID:
Description:
cation-independent mannose-6-phosphate receptor [Source:RefSeq peptide;Acc:NP_001034716]
Human Orthologue:
IGF2R
Human Description:
insulin-like growth factor 2 receptor [Source:HGNC Symbol;Acc:5467]
Mouse Orthologue:
Igf2r
Mouse Description:
insulin-like growth factor 2 receptor Gene [Source:MGI Symbol;Acc:MGI:96435]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23790 | Essential Splice Site | Available for shipment | Available now |
sa23791 | Nonsense | Available for shipment | Available now |
sa23792 | Nonsense | Available for shipment | Available now |
sa14455 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23790
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 |
---|---|---|---|---|---|
ENSDART00000061101 | Essential Splice Site | 394 | 2459 | 9 | 47 |
Genomic Location (Zv9):
Chromosome 20 (position 42621892)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42693051 |
GRCz11 | 20 | 42590161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGCGATGTAAAGAAGATTGCTGGAAGATACCAGAACCAAACCCTGAGG[T/C]TCACTTCATGTGATTCTGATATGCATAAACCTTAAATGTGGCTCAAAACC
Long Flanking Sequence:
TGTTTTTAAATCTGCCACTATGCTGACACATAGGCTTTTGTAGCTCCGCCCTATTATGAAAAAGAGCAAAATCTCATTTGAATTTAAAGTGACATTCACCAAAATGGCACAATTAGGATCAAAGCCTAACGGGGCAGTTTTAAAGAGTTATAAAACATTATTTGTGAGGTACTTTGAGCTGAAACTGCACATACACACTCTAGAGACATCAGAGACCTAATTTACATAGGTCCCTTTTAACATAAACAAAAAGCGCAGTTGTGGTTCATCAAGTATCCTGCTTTACCTTTCTTCCTATTTCTTTTATTCTAGCCACAGATACACCATACATGGCTGAGGCCAAAAATGGCAAGGACACCTACTTTTTCTATCTGAACGTGTGTGGAGGGACCAATGCTGGACAGTGTTTTGACGACAAAGGATACATCTCTGCCTGCCAATTCAAAGAGAATGGCGATGTAAAGAAGATTGCTGGAAGATACCAGAACCAAACCCTGAGG[T/C]TCACTTCATGTGATTCTGATATGCATAAACCTTAAATGTGGCTCAAAACCAACTGGTTATGAACATTATCTTTTTTTCTTTTTTGTTTAAATCTTTAGATATTCAGATGGTGATCTCACATTAATCTACCCAGACGGCAGCAGATGCAGCACTGGATTCCAGCGCATGACTATTATTAACTTTGAGTGCAATGCAACTGCTGGTGAGTGATAGTATTGACAGTGACAGCTATTCCGAATCTGATAACTTTTAGCAATATTGTATATATAATCTTTTAAAAAGACACTACTTCCATTCCATGTGTTTGAGAGATAAAAATAATTAAACTGGATCAGATTATGGAAATAAAAATGGAGCTGTACACTGAAAAGTCTTTAAAATTTACTGTAGCAAAACAGAAACTTTGAATTATCTGTTAAAGGGCCATGAAACCCCCTCATTTCAGCAGGGTGTTTTCACACCTCAACTTTGGAAAAAGTCAGAAAAGTGGGCGTGTCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23791
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 |
---|---|---|---|---|---|
ENSDART00000061101 | Nonsense | 751 | 2459 | 16 | 47 |
Genomic Location (Zv9):
Chromosome 20 (position 42634201)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42705360 |
GRCz11 | 20 | 42602470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGAGGATGAGTACACGTATAACTTTAAGTGGTACACTTCCTACGCCTG[T/A]CCAGAGAGATTACATGAGTGTGTCGTGACAGACCCCGAAACTCTTCAACA
Long Flanking Sequence:
TTTTGTAGTCAAGAGTTACACTTGATGTTTAGTGTGTAAAATATGATTTCTACAGCCAATCAGACTTGACCGTAGGTGGACTTAATCTCTCTTTGCTTTACCTCTTCAGCGGCAAATCGTCTTGGAATCTCGGCCAGTTCAACTCCAAGCTTTCTTATTATGATGGCATGATTCAGCTGACCTACAGAAACGGCTCTCAGTACAACAACAAGCAGCACACGCAGCGATCCACACACATCTCCTTCCTCTGTGACCGAGAGGCTGGTCCAGGAAAACCAGAGTTTCAGGTATCGCACCTGCTCCTTTGTTATGTTTGTGCTGAATGTAGATATTTTTAGCCCTACATAAGGTGACTCTGCATAATAAATGGCCTGCATGTGTGAAATTTTTTTTTTTGTGTTTGAAACTTTGCATTGACTTTGCATTTAAAAGACTTTCTTTCTTCTGCAGGATGAGGATGAGTACACGTATAACTTTAAGTGGTACACTTCCTACGCCTG[T/A]CCAGAGAGATTACATGAGTGTGTCGTGACAGACCCCGAAACTCTTCAACAGTATGACCTGTCCAGGTTAGTCTGCATTCAGCAAATAACTGTTATTAGCGCATGACTGAAATGTTACAAAATTTTGACATGTTTTGATTTTGGTTGCACTTAACTTGGTTTAAAGGGAATACACACAGTCCAGCCCGAAATTATTCAAACCCCTGGGAAATTCTGACTTAAAGTTACTTTTAGTTTAAATTTTAGTACTTGGCTGATGATTTCCTTATATAGCCATTAACCAAAAAAACCCAAGCACATTATTGGTTGACCCAGTGTTGCTTTTTGGCATATTTAAACAAACACTATAAAAGACTAACCTATTAAAGACATGTACTGTATTTGTCTGAATTGATGGACCAATTTATGAACAATTTACTCAAAAAAACTACTTTATTTATTGTGCATGAATGTTTGATTTAATTTAATTTTTTTTAACCTTTTTTTCTTACAGTTCATAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23792
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 |
---|---|---|---|---|---|
ENSDART00000061101 | Nonsense | 1100 | 2459 | 23 | 47 |
Genomic Location (Zv9):
Chromosome 20 (position 42645127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42716286 |
GRCz11 | 20 | 42613396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATGAGAAGTCATATGTTCCTCTGGACACCTCGGATCAGGCCCGGTTT[C/T]AGAAGTTTTACGTAAATGTGTGTAAACCACTGCCTCGTGTTCAGGGCTGC
Long Flanking Sequence:
AATTTGTGGACTGCATCAAAGAGAGCTGTAATGAAATCACTTCTCACTTGATTTCATAGCACGGTATTTGATGGTCCTGTAAAAAACTGATCCAATGAATCTTTGTGTCGTCTTTTCTTTCTAACCAAGATAATAAATGGCCTGTGCACTGCAAAGTTCTAACAAAGAGGTGCTGTTTTCTGTTCTGCCTTTAGTACATGTATCTAATATGCAGTAAAATGTCTTTGCTTATGGCAAAATCAGTACTGGAATCGTTACTCTAACAAAATATAGTTGTAGCACCAGAAAAAGAAAGTCACAAAATGTCACCATTTGGTCACAGTCTGAAGCCCCGCTGAAGTGTGCCATTTATGTATCACTGTTATCATGATTTGGATATGAAAGTCAAACTAATTCCTCTTTCATTTCCAGATTCACAGGGCCGGGAGTATGACCTGGGTGACCTCAGTCTGGATGAGAAGTCATATGTTCCTCTGGACACCTCGGATCAGGCCCGGTTT[C/T]AGAAGTTTTACGTAAATGTGTGTAAACCACTGCCTCGTGTTCAGGGCTGCCCTGGTGAGTGTCTACAGTGCAGATTTGAGAGCCGATTTCCCACTATTTTGTCTAATGGTTAGAATAAATGTCAGTTCCAGTAGTATGACCATGTGAGGACAGAATTTCTTGGTATGGTTGGACAAGTGCACTGTTTATTTATATTTCATATAGTACCAAAAATAGAAATATCCGATCATTGTCTGTATTGCTCTTACCTTACCAAGGTAATAGCTGGCGCATTTGTATTACGTTCCAAAGAGTTTCATTATCAGCACAACAGTGGAACATTAAGCTTAAATTGATGAGAGTGGCTTTCAAAGTGCCTTGTTTCTAGCATGGATCTGAGTACCATGACATACCAGGAGATTAGTTTCATAGTGACTTCCGTGCAATGCAGTCAATGTCAGAATAAATGATCCACACATTTGAATCGGTGCCAAATGTGAAAAGGAAGTGTGCTATTTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14455
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 |
---|---|---|---|---|---|
ENSDART00000061101 | Nonsense | 1219 | 2459 | 26 | 47 |
Genomic Location (Zv9):
Chromosome 20 (position 42648823)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 42719982 |
GRCz11 | 20 | 42617092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCTGTCACAGGTGAAAACTKCAAAGTCACAGACCCCAAGAGCGGTTA[T/A]GAGTACAATCTCACACCGTTGGCTGGAMARGACTATGAAGTGAAGAGTTC
Long Flanking Sequence:
GTGAAACGCCTGTGTGAACGTGGATCGTTTTAATTCTCAAACGCCATTTAAAAACTAAAACGTATTAATGTAAACAAAGGCTAAAGCTTAAAATCATACTTGCCCCGTCTTATAGTAGTGTAAATTAATTACCGTGCAGAAAGATCAAAAGATCCGAAAGATCAAATAGCAAGATCATAAGTGACTTAAAATCATTTTCCAGCATTGTTGTATTTTAATTATGGAACGTTTCTCCAATATTAAAAAAAATATATATTGTTCTTTAACCTTTATTCCTTTCTTCTGTTAAAAGGGTGCACCGATGTTCGATCGCAAAGATGGCTGTGAGTTTGTTTTCATCTGGAGAACCTCAGAAGCTTGCCCAATCAAAAGAGTCCATGGTAAGATGAACAGTCAGTCCATTTGAAGGCAATGAAAAAATACTTGGATTTTGACTAATTTTAGCTGCTCTCTGCTGTCACAGGTGAAAACTGCAAAGTCACAGACCCCAAGAGCGGTTA[T/A]GAGTACAATCTCACACCGTTGGCTGGACAGGACTATGAAGTGAAGAGTTCGACCTATGAGTATCATTTCGCAGTCTGTGGCCCAATTACAACCTCTGTCTGCCTTCACGATGCCAGCCAATCTGTGTCCTCCTGTCAGGTCGAGAACCAAAAGCACAGGATTGCAGGTGAGCTTATTTGTTTCTGTTTGTTATCAAGGTGAGCTGTTTAATGTCTAATAGAGCTACGTCAATGTAGTGATTAGGGCTGCATAATATATATCAAAAAATTATCACAATAATTATTTGCACTTTTCTGAGATATGGATATTGCATTTACTATTAAGTCAAGTATTTATCTGCTGCATGCACATGTCAGTTGTATATTCAAGTCTGAACAATCAGATGGCTCCTTTACTATTATTATCTCTGCCTCATCAGTAATTCCTGTTAAGTGGAAATAAATACTTGTGCTGGGAGACAAGAGAGGAAAATGACAGCAGCCTATAAGAATCAGAATTTT
Associated Phenotype:
Not determined