ZMP
igf2bp2b
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC557028 [Source:RefSeq peptide;Acc:NP_001082843]
Human Orthologue:
IGF2BP2
Human Description:
insulin-like growth factor 2 mRNA binding protein 2 [Source:HGNC Symbol;Acc:28867]
Mouse Orthologue:
Igf2bp2
Mouse Description:
insulin-like growth factor 2 mRNA binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:1890358]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14577 | Nonsense | Available for shipment | Available now |
sa12673 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14577
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 |
---|---|---|---|---|---|
ENSDART00000088166 | Nonsense | 368 | 446 | 8 | 10 |
ENSDART00000088170 | Nonsense | 262 | 340 | 11 | 13 |
ENSDART00000136148 | Nonsense | 358 | 436 | 11 | 13 |
ENSDART00000137127 | Nonsense | 358 | 436 | 10 | 12 |
ENSDART00000141303 | Nonsense | 400 | 478 | 10 | 12 |
ENSDART00000141457 | None | None | 82 | None | 3 |
ENSDART00000144916 | None | None | 103 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 29432742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 29641357 |
GRCz11 | 1 | 30445288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGGTGAAGTTGGAGGCGCATATAAAGGTGCCAWCAASTGCTGCAGGA[C/T]GAGTCATTGGRAAGGGGGGCAAAACGGTAGGTGTGCTTGTTTGTGTTTCA
Long Flanking Sequence:
CAGACAGTCAGTTGTAATTTAATGATTTGATGCAATAATACAACCCATTGTTTAAAGGCTGCAATCACAGTGCTGCAGAACCCAGCTGAAATATAGAAGTAAACATAGAAAGTAGCAGTTGAGATTCTTTTTTATTGCTACCTAAATGCTTAAAGAAGACTAAATAGAAAAAAAATCTGTGTTTTGTGCTTCTTTAGATTGCTGCACCAGAGAGCCCTGATGAACCCGAGAGGATGGTCATTATCACTGGACCACCAGAAGCTCAGTTCAAGGTAAAAGATGCAATCTGATTGCTTAAACTCCCAGTCGTAAAAATAGATTCTATTAGGCATGTTTCACATCCACCTGTATATTTGTTCTTCATTTATCTTGTTTGTATATGTGTGTGGTTGTAGGCACAGGGAAGGATATATGGGAAGCTGAAAGAAGAGAATTTTTTCACAGCTAAAGAAGAGGTGAAGTTGGAGGCGCATATAAAGGTGCCATCAACTGCTGCAGGA[C/T]GAGTCATTGGAAAGGGGGGCAAAACGGTAGGTGTGCTTGTTTGTGTTTCAACTTTTCTCATCAAGGGACTGAACATGACTGATTGTATTCTTCTTTTGTTCTTTTTTTTTAAGGAAAATACAGTGCTCATCATATATGAGTACACCCCTCACTAATCTCTCATTTAAATTAATATTTTCTATAGGAAGCTATATTATATTTGTGCATATACATTCGTTTAGTCAGTACTGAAGCCAAATCTGGAGCTTATCTAACAAAATAACTTACAATAATGGTTAAAAAATTAGTAGCCCAATTTTATATGTTAGGGGAAAATAGTAAGTTTTTTTTTCAGTTTGGTGACTGAATTATTATTTGGTGACTGATTTATTTATTACTAAATAAATCTGTTCAACAAATCTGCAATGTGCAAATGCACCAATATACATTACCCATATTCACTGAGAAATGGATAAAATATTCTTTTTCAAAATGGAATGTACTCATTTATGCTGAGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12673
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 |
---|---|---|---|---|---|
ENSDART00000088166 | Nonsense | 368 | 446 | 8 | 10 |
ENSDART00000088170 | Nonsense | 262 | 340 | 11 | 13 |
ENSDART00000136148 | Nonsense | 358 | 436 | 11 | 13 |
ENSDART00000137127 | Nonsense | 358 | 436 | 10 | 12 |
ENSDART00000141303 | Nonsense | 400 | 478 | 10 | 12 |
ENSDART00000141457 | None | None | 82 | None | 3 |
ENSDART00000144916 | None | None | 103 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 29432742)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 29641357 |
GRCz11 | 1 | 30445288 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAGGTGAAGTTGGAGGCGCATATAAAGGTGCCAWCAASTGCTGCAGGA[C/T]GAGTCATTGGRAAGGGGGGCAAAACGGTAGGTGTGCTTGTTTGTGTTTCA
Long Flanking Sequence:
CAGACAGTCAGTTGTAATTTAATGATTTGATGCAATAATACAACCCATTGTTTAAAGGCTGCAATCACAGTGCTGCAGAACCCAGCTGAAATATAGAAGTAAACATAGAAAGTAGCAGTTGAGATTCTTTTTTATTGCTACCTAAATGCTTAAAGAAGACTAAATAGAAAAAAAATCTGTGTTTTGTGCTTCTTTAGATTGCTGCACCAGAGAGCCCTGATGAACCCGAGAGGATGGTCATTATCACTGGACCACCAGAAGCTCAGTTCAAGGTAAAAGATGCAATCTGATTGCTTAAACTCCCAGTCGTAAAAATAGATTCTATTAGGCATGTTTCACATCCACCTGTATATTTGTTCTTCATTTATCTTGTTTGTATATGTGTGTGGTTGTAGGCACAGGGAAGGATATATGGGAAGCTGAAAGAAGAGAATTTTTTCACAGCTAAAGAAGAGGTGAAGTTGGAGGCGCATATAAAGGTGCCATCAACTGCTGCAGGA[C/T]GAGTCATTGGAAAGGGGGGCAAAACGGTAGGTGTGCTTGTTTGTGTTTCAACTTTTCTCATCAAGGGACTGAACATGACTGATTGTATTCTTCTTTTGTTCTTTTTTTTTAAGGAAAATACAGTGCTCATCATATATGAGTACACCCCTCACTAATCTCTCATTTAAATTAATATTTTCTATAGGAAGCTATATTATATTTGTGCATATACATTCGTTTAGTCAGTACTGAAGCCAAATCTGGAGCTTATCTAACAAAATAACTTACAATAATGGTTAAAAAATTAGTAGCCCAATTTTATATGTTAGGGGAAAATAGTAAGTTTTTTTTTCAGTTTGGTGACTGAATTATTATTTGGTGACTGATTTATTTATTACTAAATAAATCTGTTCAACAAATCTGCAATGTGCAAATGCACCAATATACATTACCCATATTCACTGAGAAATGGATAAAATATTCTTTTTCAAAATGGAATGTACTCATTTATGCTGAGCACT
Associated Phenotype:
Not determined