ZMP
fgfr2
Ensembl ID:
Description:
Fibroblast growth factor receptor 2 [Source:UniProtKB/Swiss-Prot;Acc:Q8JG38]
Human Orthologue:
FGFR2
Human Description:
fibroblast growth factor receptor 2 [Source:HGNC Symbol;Acc:3689]
Mouse Orthologue:
Fgfr2
Mouse Description:
fibroblast growth factor receptor 2 Gene [Source:MGI Symbol;Acc:MGI:95523]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10729 | Nonsense | Available for shipment | Available now |
| hu2987 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10729
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 |
|---|---|---|---|---|---|
| ENSDART00000007408 | Nonsense | 421 | 817 | 9 | 18 |
| ENSDART00000080914 | Nonsense | 419 | 815 | 9 | 18 |
| ENSDART00000080916 | Nonsense | 444 | 840 | 8 | 18 |
| ENSDART00000098269 | Nonsense | 355 | 751 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 46957498)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46209849 |
| GRCz11 | 13 | 46346314 |
KASP Assay ID:
2260-6940.1 (used for ordering genotyping assays)
KASP Sequence:
CTAAGAAGCCTGATTTCAGCAGTCAGCCAGCAGTGCACAAGCTCACCAAA[C/T]AGATCCCCCWGCGCCGCCAGGTAACAGAAAGTAGATAAAGAGTTCCAGAA
Long Flanking Sequence:
CAGTGCAAATTTAGATAGATTTAGTGTCTTTGAAAAACCCTCAGTGTGTGATGTGTGTGTGTGAGTGTGTGTGTGTGTGTCTCTTCCTCTCTCATTTCTTCCCATTCTTCCTACTGACCCAATATCCTTCCCAGATACCTTAATGTCCTTCATAAGCATCTTATAATATGCTTTACCAACATTAAAGTTTCTGGTTCGGTATTCTTCACCTGTATCATAATTTATTATTGGTCACACTTTATTTTAATATACAATTCACTCTGTTAACAAAGCATCAACTGAGACCTTTAGCACAGTCAAACACTTCTGAATATTGCTTCACAGCTGAGACGAATCCCATCGAGACGGATTATCCTCCAGATTATGTGGAGATCGCCATCTACTGTATAGGTGTGTTTCTGATCGCCTGTATGGTGGTGATCGTGGTGGTTTGCCGGATGAGGACGTCGGCTAAGAAGCCTGATTTCAGCAGTCAGCCAGCAGTGCACAAGCTCACCAAA[C/T]AGATCCCCCTGCGCCGCCAGGTAACAGAAAGTAGATAAAGAGTTCCAGAAACCTTATACACACTTACATTCACACTAATAATGACAATAAGCACGTTTACATGGACACCAATTCTCCGATTTTTATACGATTAGGACAATACTCTGATCAAAAGTCCACTATGTAAACAGCGATTTTTTTTTTTTATTACCTTATCCAACTAAACATAAATGGAGTTAAGACTTGGAGTATTCCTATTTTACTGGCATTATTGAAGTGCAGTACAGACATGTAAACACCACAATCAAACTATTGCCGCCGTGTAGGACTTTTAGGCGCATTTTTTGATAGGATATTCCATACACACACAGCTGTTTCACACAGCTGTTTGTTATGCCACAGCCATGTCACCCTGCAGCCCAAGACCGGTTACTCACTGAAGCTAAGCAGGGCTGAGCCTGGTCAGTACCTGAATGGGAGACCACTAGGGAACACTAGGTTGCTGTTGGAAGTGGTGTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2987
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 |
|---|---|---|---|---|---|
| ENSDART00000007408 | Nonsense | 547 | 817 | 12 | 18 |
| ENSDART00000080914 | Nonsense | 545 | 815 | 12 | 18 |
| ENSDART00000080916 | Nonsense | 570 | 840 | 11 | 18 |
| ENSDART00000098269 | Nonsense | 481 | 751 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 46933179)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 46185530 |
| GRCz11 | 13 | 46321995 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGAGATGATGAAGATGATTGGCCGGCACAAGAACATCATCAATCTGT[T/A]GGGAGCGTGCACACAGGATGGTGAGGGATTTATTTTCACTATAGAAAGCC
Long Flanking Sequence:
TAGTATGATCGAGTATTTTTGGAGTGTACAACAGCAGGCATGTCTAAACTCGGTCCTAGAGGGTCGGTGTCCTGCAAAGTTTAGTTCCAACCCCAGTCAGACACGCCTTGGCTAGCTAATCAAGCTCTTACTAGGTTTTCTAGAAACATCCTTGCAGTTGCCTAAGGCAAGTTAGAGCTAAAATCTGTAGGACACCAGCCCTCCAGGACCGAGTTTGGACACCCCTGATCTACAGTGTAAACCCAGAACAATGAGAAGAGTTGTATCCCATGATAAGACGAAGCTTGCAGCCAAGCATGCAGTTCCCTAGTACTACTTTACAATGTCATATGATCTCAGCTGAGCAGGAAATAGGAAGAATGGCTTTTTCTGAATGAGGTTTAATTGTTTTGTTTGTCTGATCTTTCTAGATGATGCGACCGAGAAGGATCTTTCTGACCTGGTGTCAGAGATGGAGATGATGAAGATGATTGGCCGGCACAAGAACATCATCAATCTGT[T/A]GGGAGCGTGCACACAGGATGGTGAGGGATTTATTTTCACTATAGAAAGCCTACATTATCAGTCCTCTAAATCATCAACATGATCAAAACTTTGCTGAAAAACCTGTTCCACACAACCAACTGCACGCCTTTGTCATCTGATTAATTGTTTATAGCTTATTAGCAAGTAATCATCTGCCTTCAGCTCAGGATTCACACATGCATTTTGCTATAAAATATCTACTGATTTTAATAAAGTAAATGAAGTAAATATTTAATATTTCAGAAATATTTCCAAGTAAACTAAATCAAATTATAAAAAATAAGTAAAAATCAGGCTTTTGAGTCATTGTTTTGCTTTCTATAATTGTTTTGCCCTCACAAAAAAAGCAATACTTGGAAGCTATATTTCAAAATAATGCATTTTACTGTCATCTTAAGACATTTTATTGGTTGATATAAAATTGCAATTAATATCTATACAGTTTATGTTGGTAGTCTGCTATACTTTTATATTTAAAA
Associated Phenotype:
Not determined