ZMP
fgfr3
Ensembl ID:
ZFIN IDs:
Description:
Fibroblast growth factor receptor 3 [Source:UniProtKB/TrEMBL;Acc:B8JIA2]
Human Orthologue:
FGFR3
Human Description:
fibroblast growth factor receptor 3 [Source:HGNC Symbol;Acc:3690]
Mouse Orthologue:
Fgfr3
Mouse Description:
fibroblast growth factor receptor 3 Gene [Source:MGI Symbol;Acc:MGI:95524]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13480 | Nonsense | Available for shipment | Available now |
sa15832 | Nonsense | Available for shipment | Available now |
sa1675 | Essential Splice Site | Available for shipment | Available now |
sa10458 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13480
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 |
---|---|---|---|---|---|
ENSDART00000013534 | Nonsense | 120 | 804 | 3 | 23 |
ENSDART00000125883 | Nonsense | 120 | 802 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 13119347)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13127432 |
GRCz11 | 13 | 13258565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTGTGCTGCAGACTAAAAGCATCTCTCTCTTTCTTCATTTCTCAGATT[C/A]GCTGTCCTCTGGTGATGATGAGGACTATGATGAAGATGAGGACGAGGCAG
Long Flanking Sequence:
CACGCTCCGCTGGTATTTTAGGAGTGTGTGCGGTACACTTTTACCTGTGTAAATGTTCACAGAGGAGGAGCCGAAGACAGAATAATCTTCTTTTCAGGGTCACAGAGCCTTTTTTTTCTCCCTCTGAATGAGTTCATTTAGAAGCAGGATACGGGAGTGTGTGTTTATATGTGTGTATTTCAAGACATGTGTGTAAAAATACAGCTGTTGTCAGAAATCTCACTGAATCTCTGTTAACATCTGCCATCCATTAAGTGCTGTGTCTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCATGTGTGTGCGCATGTGTGTGCGCATGTGTGTGCGTGTGTGTAGTAATTGGTTTTGATTTGTTATCAGTTTATTTTCCTCATTCTGCAGTTCATATGAATGGTTTCATTGTTCATACAGAAAGGCCACTGTGCTGCAGACTAAAAGCATCTCTCTCTTTCTTCATTTCTCAGATT[C/A]GCTGTCCTCTGGTGATGATGAGGACTATGATGAAGATGAGGACGAGGCAGGTAATGGAAATGGTGTGTTTCGCTCTCTTATTTCTCATTTCATTACTGAGTTTTTGATCGAGTTTTGGTGAACTCTCTGTTGTATAATAAATGCATGAGATTGCTGTCTTTCATGGCTGGGGATCGGTTGCATCTCATTTCATCAGCTGCTTTTCCCCCCACTTGATGCTAAAACGCAAATTCTCTTGTGAGAGATGAAGGGGGAAGAAGAGAAATGATTTAAAATCTAACAGTGTTAAGTGGAATGTGACGAAAAAACACAGAATATGTTCAATTATGCGTGTAACAAGAGGAAGATTTTATTTCACAGTGTCTTAGAGTTGGTAAGTCCTCGATTCGGTGAGCCGAATTATGTTTTATGTTTTGTTTAAAGAGATTTTGAATCACTAGAATCACTGGTTGTGTCTATAAATCAGAACAGTTGTGACAAGAGCAGCAAATCATAACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15832
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 |
---|---|---|---|---|---|
ENSDART00000013534 | Nonsense | 560 | 804 | 18 | 23 |
ENSDART00000125883 | Nonsense | 558 | 802 | 17 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 13097699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13096067 |
GRCz11 | 13 | 13228542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTACGTGCTGGTAGAATACGCCTCTAAAGGGAATCTTAGGGAATACTTA[C/T]GAGCCAGAAGGCCACCTGGGATGGACTACTCATTCGACACCTGTAAGATC
Long Flanking Sequence:
ACACTAGCTGTCTTTGTGTTGTCTTCTGTAAGTGCCACAAAAATAATAATAATAATAATAATAATAATAATAATAATAATATAAACTGACAAAAGACAGAAATAATGACTGCAGAACATCAAGCTTTGCCCTCTCAGTAATAAATAACATTTTAACCATTGTTTAAAAAAAGAAACTGTTATTTTAACTCACATTTTAAATTCCTAGATGACGGCACAGATAAAGACCTGTCAGACCTTGTGTCTGAAATGGAGATGATGAAGATGATTGGGAAACATAAGAACATCATTAACTTGCTGGGAGCATGTACTCAAGACGGTCAGCACACAAACACACACACACACACACACACACACACACACACACACACACACAATACAAATTCAGCTTTGAAATTAGCCTTTGATTTTTCTAACTGAATGTGTTCTGACTGTGTTCACTCAGGTCCTCTGTACGTGCTGGTAGAATACGCCTCTAAAGGGAATCTTAGGGAATACTTA[C/T]GAGCCAGAAGGCCACCTGGGATGGACTACTCATTCGACACCTGTAAGATCCCAAACGAAACGCTAACATTTAAAGACCTGGTGTCCTGCGCCTATCAGGTCGCCAGGGGTATGGAGTACCTGGCCTCAAAGAAGGTAATGTGTCTGCTTATCTTAGTTTGTAAACTAGTTTGAACCGAAGTCATTTAAGATACGCGCCATGTTTATAAAGTTTATAATACTGACAGGTATTATTTTCCAAGTGTGTATTTATCAGACTTAAAAGATGGCCCTCTCTTTGTTTGTGTTGCCAGTGTATCCATAGGGACCTCGCAGCCCGGAATGTTCTGGTTACCGAGGACAACGTGATGAAGATTGCAGACTTCGGCCTTGCCAGAGATGTGCACAACATTGACTACTACAAGAAGACCACCAACGTAAGTCGACACTGATTATCAATCTCGAAGGAGAGAGCTCTTGGGTGGCATTGTGTTTTGGAGCACAGCAGATATGGTTATGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1675
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013534 | Essential Splice Site | 645 | 804 | 19 | 23 |
ENSDART00000125883 | Essential Splice Site | 643 | 802 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 13097282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13095650 |
GRCz11 | 13 | 13228125 |
KASP Assay ID:
554-1621.1 (used for ordering genotyping assays)
KASP Sequence:
CCTTGCCAGAGATGTGCACAACATTGACTACTACAAGAAGACCACCAACG[T/A]AAGTCGACACWGATTATCAATCTCGAAGGAGAGAGCTCTTGGGTGGCATT
Long Flanking Sequence:
GAATGTGTTCTGACTGTGTTCACTCAGGTCCTCTGTACGTGCTGGTAGAATACGCCTCTAAAGGGAATCTTAGGGAATACTTACGAGCCAGAAGGCCACCTGGGATGGACTACTCATTCGACACCTGTAAGATCCCAAACGAAACGCTAACATTTAAAGACCTGGTGTCCTGCGCCTATCAGGTCGCCAGGGGTATGGAGTACCTGGCCTCAAAGAAGGTAATGTGTCTGCTTATCTTAGTTTGTAAACTAGTTTGAACCGAAGTCATTTAAGATACGCGCCATGTTTATAAAGTTTATAATACTGACAGGTATTATTTTCCAAGTGTGTATTTATCAGACTTAAAAGATGGCCCTCTCTTTGTTTGTGTTGCCAGTGTATCCATAGGGACCTCGCAGCCCGGAATGTTCTGGTTACCGAGGACAACGTGATGAAGATTGCAGACTTCGGCCTTGCCAGAGATGTGCACAACATTGACTACTACAAGAAGACCACCAACG[T/A]AAGTCGACACTGATTATCAATCTCGAAGGAGAGAGCTCTTGGGTGGCATTGTGTTTTGGAGCACAGCAGATATGGTTATGCATTGTATTTTAAATGTTAAGATGACTGTTGTTAAATCAGTGTTCAGGAAAATTTAAAGATGCGTTTGTGAGCAGCTGAATGAGGTTTGGAATTGGTAGAGTGTGTGAGTATTGGCATGGATTTAAACACATGACTGTTTACCTGGCACACCATGCATTGTAGGAAACAGTATTCAGAGTCGACTAACTAAAACTATTATTACTTTCATTTTGATCATCTAAGGCCAAGTTTTCTTGAATGGAGAATACTGAACTCTCGTCACACTCACATAACAAATTTCAAGATCAGTGACAAATCATACATTTGATTAAGTTTGTTAAATAAATAGTAGCAGCAGTTTAGGTTTTATGTTCGACTGAACTCAAAAGAAGATATTTTGAATAATCTGGAAACAGGTAGCCAGTGATATTCTAAATAGG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa10458
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000013534 | Essential Splice Site | 750 | 804 | 22 | 23 |
ENSDART00000125883 | Essential Splice Site | 748 | 802 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 13 (position 13088122)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13086490 |
GRCz11 | 13 | 13218965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAGCTGGTGGAGGACCACGACAGGGTTCTTTCCATGACCTCCACTGAC[G/T]TAAGAGCTCTGGTGCATCAAACCAAAMACCTTAAACCTTTCACACTCAAC
Long Flanking Sequence:
AACTTTCTAATAGCAAAAAATAAATAAATAAATAAACAACTTCAGAAATATCTTTCAAACTTTAAAAAGCTAAATTTTCAGTGTGTTAAAAAACTGCTCTCCTGCTTGCTAGACAAAATGAAGTATGCACCTTCACGCGCAGTCTAGTAACACATACACAATTATAGTCTATACTACAAAAAAGATTTGTAGTTTAATGACTTCATAAAACAACACAACAGACATTCGAATCTCAAATGTAAATATGGTGTAATATAAAGTTCAATTTGGTGCAGTAAGAAAGGTCAGGATGGCTACTATTGGCCATTCTAGTAGTTATAGACTTCCTGTAGTTCTAATGTTAATTAAAAAGCACAATGGTAATGCTTTGTTTTGTATGTTGTGATCTGTGCAGGTACATGATCATGCGAGAATGTTGGCATGCTGTTCCTTCACAAAGACCCACGTTCAGACAGCTGGTGGAGGACCACGACAGGGTTCTTTCCATGACCTCCACTGAC[G/T]TAAGAGCTCTGGTGCATCAAACCAAACACCTTAAACCTTTCACACTCAACTCCTACAGCCAATCCTGACAAATCCTGCGTTTAATATTTTAGGAGTACCTGGACCTCTCTGTACCGTTCGAGCAGTATTCACCGACCTGTCCGGACTCCAACAGCACCTGTTCCTCTGGCGATGACTCTGTGTTTGCCCACGACCCCTTACCTGAGGAGCCATGCCTCCCTAAACACCACCACAGCAACGGGGTCATACGAACATAAAGAAAAAAAAAACAGGGAGCTTTAGGGTTTGGCTGCACTGGACCAGCATGTGGCAGAGAAGCGCAGTGTGGGGATCTCATGAAAGCTTCAGACTTTCAGCTGTTCGCAGGTTTGAAGGACGGATTTAGCTTTTCTCCTTCAGCACCTGCTTTTCTTCCAAATCATTATTCAGCTTTTTGTCTTTGAAAAGAGAATTCCTATTTTTGTATTCGGCCAGTTTCGTTTTTCCACAGTGAGAAGGGT
Associated Phenotype:
Not determined