ZMP
fgfr4
Ensembl ID:
ZFIN ID:
Description:
Fibroblast growth factor receptor 4 [Source:UniProtKB/Swiss-Prot;Acc:Q90413]
Human Orthologue:
FGFR4
Human Description:
fibroblast growth factor receptor 4 [Source:HGNC Symbol;Acc:3691]
Mouse Orthologue:
Fgfr4
Mouse Description:
fibroblast growth factor receptor 4 Gene [Source:MGI Symbol;Acc:MGI:95525]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3514 | Nonsense | Available for shipment | Available now |
sa24005 | Nonsense | Available for shipment | Available now |
sa6682 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24004 | Essential Splice Site | Available for shipment | Available now |
sa37357 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
hu3514
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 |
---|---|---|---|---|---|
ENSDART00000100286 | Nonsense | 43 | 922 | 3 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 36516834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37506183 |
GRCz11 | 21 | 37191370 |
KASP Assay ID:
554-0053.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACTCCAGCAGATATCAGAGTTTCACGACACATACTTACTCCTGGATA[T/A]CCTGAGAATGCTACTGTGTTGGTCGGAGGACATGTGAAGCTGGTGTGTAA
Long Flanking Sequence:
GGCGCATGTGTTTTGTGTGTTTTGTTTAGCGTGTCTTTATTTTCCAGTTGACCATTCGCACCCTTTTCAGGGTCAGATACGGGCCAGGCTCTAGTTTTATTCATCGAAGTTCATTAGTGTATTGGTGGGAGAATGTTATGCTTCAGTGCTGGAGGTGACATTGCTTGGATAGGGGGCGTTCTTCACTCAAATGCTCGAAATCACATTCACCTCTAGGCCACAAGGAACACTGCTGTGAAGTCAAAGTTAGGTCATTCTCAGCCGAGAATTGTGTTTCTGTTCTCTCCTTTGTTTGTGGCTTTGTTTGCCTGATTTGCTCTAAAACAGTGGTGATCTTTGTGAGAAAGGCTCTAGTTAGTAATTAGCGTGGAGTTATGTTAATTAGACATGTTTATTAAATGTGGTTTATTCTACAGACTAATTACACCAGAAATGTTTGAAACCTCATTTTTTACTCCAGCAGATATCAGAGTTTCACGACACATACTTACTCCTGGATA[T/A]CCTGAGAATGCTACTGTGTTGGTCGGAGGACATGTGAAGCTGGTGTGTAAGCTCCACCAGCCAGCCTCAACACGTCTCCAGTGGTTCAAGAAGGACAGTAATCGCCTGGGGCCTGATGGATCACCAGTACTTACAGCTCTTACGGTGAGAAAGTGATTTAAAGATCCTCTATTATGCATATTTTCTGTCTTCAGGAACGAGGGAGTAATGTTACATTTGTTTCCCCTGCAGCCTCTTCTTGAGAACCTCTCCAAAGTCAACATATTTCCTTTGGTTAATATCTCTTTGGAAGATGCTGGAGAGTATGTATGCAAGGCGGAAAACTCAGCTGGTCAGGCTACTCGCTCTGCCTGGGTGGAAGTCTTAACGGGTAAGCCACACCATTTGATACCATCTAACTTACTCATCTTCAGGGCGGTTCTGTGGTTATTCTCTGAAAGGTCAGCTAGGTTAACCATTGGCGTAATATTACTATGAAAACCGGTTTATGAGTATTTAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24005
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100286 | Nonsense | 173 | 922 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 36516140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37505489 |
GRCz11 | 21 | 37190676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGTACTTAAACTCCGTTGTGACACAAACCGTCCTGGAGCTGTCCAGT[G/A]GTTCAAGAGTGGTGTTCGGGTGCAACACAATGCCCGTATCCAGATAAGAG
Long Flanking Sequence:
GGAACGAGGGAGTAATGTTACATTTGTTTCCCCTGCAGCCTCTTCTTGAGAACCTCTCCAAAGTCAACATATTTCCTTTGGTTAATATCTCTTTGGAAGATGCTGGAGAGTATGTATGCAAGGCGGAAAACTCAGCTGGTCAGGCTACTCGCTCTGCCTGGGTGGAAGTCTTAACGGGTAAGCCACACCATTTGATACCATCTAACTTACTCATCTTCAGGGCGGTTCTGTGGTTATTCTCTGAAAGGTCAGCTAGGTTAACCATTGGCGTAATATTACTATGAAAACCGGTTTATGAGTATTTAGGAGGTCAAAGAGACCACTAGAGTTGAAAGGTCACAGCTAAAATGTAATGTAGAGCCATTAGTAAATATTGCATTAATGTTTTGTTCCAGAAGTTTCAGAGGAGCCAACTGAGGAACCATCAGAGCACCTGCTGTTGGAGCTCGGGGATGTACTTAAACTCCGTTGTGACACAAACCGTCCTGGAGCTGTCCAGT[G/A]GTTCAAGAGTGGTGTTCGGGTGCAACACAATGCCCGTATCCAGATAAGAGCGGCAGTCATGGAAATTGCAGATGTTACCTATGAAGATTCAGGAGTATATGTGTGTATGCTACGTGGCACCAAAGAGGCTCTACGCAACTTCACTATCACAGTGGCAGGTAGGTTCTGCCGTATGTTGACTGATAAAAACAATAGTAGTGTTTTGAGTGCTCATATAATACATTTTCATGTGTCCCTGCAGATGCTGTAGGGTCGGGAGATGATGATGATGAAGATAATGGTCTTGATGACATTGGTCCTGAGACCGAAAATGACCAGGTCTACATATCCAGAGGTTAGTATACGTTGTAATTACAAATTCATTCCCATTAATTTGCGGTTTTAAAGTGATAGCTATAAATGTAACATTGGTTTCTACTTAGCACCATACTGGACTCACACTCAAAGGATGGAAAAGAAGCTGTATGCAGTCCCGGCTGGAAATACTGTCAAGTTCCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6682
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100286 | Nonsense | 405 | 922 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 36514493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37503842 |
GRCz11 | 21 | 37189029 |
KASP Assay ID:
554-5175.1 (used for ordering genotyping assays)
KASP Sequence:
CAGCCTCACATCCAGTGGCTCAAGCRTATAGAAATGAATGGCAGCCGTTA[T/A]GGGCCTGATGGCATTCCTTATGTGAAGATTGTGAAGGTATATAGGAAATC
Long Flanking Sequence:
GAAACGCTGTTGGTTGAGGCATCCAGACCAATTTTCTACCTGACCTGTGACAGACCTGTTTGTTAAGAACCCGGCGTGGGGTCAACTGCTGTGTCCTAGCAGAAGAGGGAAAGAGCAGGGAATAAAGAGCTCATCGACTTCAAAGCAGCCCAATGCATGGGCCTAGTTTTAAAAATCCCTTTATGGAACTAATTAGTGTGCGTTGATCAGCTTTGGAAAGTGCTGCATGTCTGTCCCTGTGCCTTAGTATCTTAATTTAAATTCTCTCGATTGTAAACTTGCATTTGTATAATTATTTTGCTAAATGTTAAGAAAAAGAACTAAATGTTCCAATTTCACCTTTCAGAACGCTCTCCACACAGGCCAATTCTTCAAGCTGGTCTCCCCAAAAACACTACAGCTATAGTGGGTGGAGATGCCCAGTTCCTGTGTAAAGTGTACAGTGATGCTCAGCCTCACATCCAGTGGCTCAAGCATATAGAAATGAATGGCAGCCGTTA[T/A]GGGCCTGATGGCATTCCTTATGTGAAGATTGTGAAGGTATATAGGAAATCATTCCTTACTTTTTTTTCTTGGAGACAAATCACATCATTATTTTGGTATAAAAATATTGATTTGTCTTGATTGTTTATTTAAACAGACAGGAAGCTTGAACATGTCTGAAGTTGAAGTCTTGTATCTTACCAATATCTCAATGGAGGATGCTGGAGAATACACCTGCTTGGCTGGAAACTCTATTGGTTTCTCTCATCAATCTGCCTGGCTCACAGTCTTATCAGGTAGGTTTGTAAAGACACAGGCATTAAATAAATAATATAAATCACTTACGCGTACAGATAGTAAAAACATGCCTGTCTGTACCACAGAGGAGGATGTAGCCAAGGAGGTGGACCTAATGGAGGCCAAATACACTGACATCATCATCTATGCTTCTGGCTTTTTGGCACTGGTGATGGCCATTGTGATTGTGGTCCTCTGCCGCATGCAGGTTCACCCCAGTCGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24004
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100286 | Essential Splice Site | 577 | 922 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 36513599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37502948 |
GRCz11 | 21 | 37188135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATTTCATGTAATGGTGAACTAACTAGTTATTTAAATTCTCTCATGCCA[G/A]TTTGACTTTAGGGAAACCGCTTGGAGAGGGTTGCTTTGGTCAAGTGGTTA
Long Flanking Sequence:
GGAGGCCAAATACACTGACATCATCATCTATGCTTCTGGCTTTTTGGCACTGGTGATGGCCATTGTGATTGTGGTCCTCTGCCGCATGCAGGTTCACCCCAGTCGGGAGCCTTTTGATACGCTCCCAGTACAGAAACTCTCCAAATTTCCTTTGCGCAGACAGGTAAGATGACACTCCTGAATAAACCTCATGATAATTGTCCAAGATCATGGTATTCAGAAGAGCTTTCTGGATTCTAATCATGTATGTTTTGGACTCTATCGCAGTATTCAGTGGAGTCCAATTCTTCTGGAAAATCAAGTGCGTCACTGATGAGGGTGGCTCGTCTTTCCTCCAGTTGTTCCCCAATGCTGGCTGGAGTTATGGAGTTTGAACTGCCTTATGATCCTGATTGGGAGTTTCCAAGAGAGAAGTAAGCAGTACCAGCAGCTGTAGCTGTAAAAGATGTTTCATTTCATGTAATGGTGAACTAACTAGTTATTTAAATTCTCTCATGCCA[G/A]TTTGACTTTAGGGAAACCGCTTGGAGAGGGTTGCTTTGGTCAAGTGGTTAGAGCAGAGGCGTATGGGATAAACAAAGAGAATCAAGATCATATGGCAACTGTAGCTGTTAAGATGCTAAAAGGTATGCGTGTACATGACATGTAGATGTTGTATTAATGTATTGAGCATTTCTGAATTGAAGACTAAAGAGGGATTTATCTGTCAGATGATGCAACCGATAAAGACCTTGCAGACCTGATCTCTGAGATGGAGCTCATGAAGGTTATGGACAAGCACAAGAACATCATAAATCTTCTTGGTGTTTGTACACAGGACGGTAAGCTAAACACTGTTACATCTCTTTGTTGCATGAACCTTATTTGGCCACTTGACATTGAAATGTATATTTCTGGTTCAGGTCCGCTGTACGTGCTGGTTGAATATGCATCAAAAGGTAGCCTACGGGAATATCTCCGAGCTCGTCGACCTCCTGGCATGGACTACACCTTTGATGTGACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37357
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000100286 | Nonsense | 784 | 922 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 21 (position 36511667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 37501016 |
GRCz11 | 21 | 37186203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATCCTACATAGTCTCCTGACATATTTGACCTCTGGTTTTCACAGATG[G/A]TCTTTCGGGGTTTTGATGTGGGAGATATTCACATTGGGAGGATCGCCGTA
Long Flanking Sequence:
AGATGTGTAATGTGTCCATGCTGACTGGCAGACAGCTTAATAGAAAATAATTGGAGAAAGGGGGGGGCAGGGAGTATTAGCAAAGGAGTGGGCAGCCATGTTTCTGTGGATCAAAAGAAAGTGGAGTGCTTTGGCTCGGCCTGTGTGGCAGCTAACTGTCCCGCTCACAGCCCTGTTGTTTCCAATTTCAGGGACGTCTGCCAGTGAAATGGATGGCACCAGAAGCCTTGTTTGACAGAGTCTACACACACCAGAGCGACGTGTAAGTCTGGCTAATCACTGCAGCTATGCCAAAGAATCAGCTGAGCAGAGATCCCTCTGGCTGGAATGCCGGTCAATTTAGATTAACCAGATTGCACTGTTGTAGTTTAATCCTGATTTAGATGGTGGATGTTTTAATGACTAAAGTATATGACTAACAGGAGCATCGAATTAGTACTGCTCAAGCTGATTATCCTACATAGTCTCCTGACATATTTGACCTCTGGTTTTCACAGATG[G/A]TCTTTCGGGGTTTTGATGTGGGAGATATTCACATTGGGAGGATCGCCGTACCCTGGGATACCAGTAGAGGAGCTTTTTAAGCTGCTGAAGGAAGGCCATCGGATGGATAAACCCTCCAACTGCACCCATGAACTGTAAGAATCAGTCTGATTACCCAAACATTGTGTTTACTTTACACTCTCAGAAATAAAGGCACAGGAACTGTCACTGAGGCAGTACCTTTTTAAAAGATACAAATTTGTACCCACATAATTTACAGCGGTACCTCAAAGGTGCATATTAGTACGCAAATGTACCTAAAAAGTACCTTTTGAAAAGGCACTGCCCCAGTGACAGCTTTTGTACCTTTATTTCTGATAGTGTATCACTTTAAGGTGATTTACTTATGTTCCCATTGCTTTTATAGCTACATGAAGATGAGAGAGTGCTGGCATGCAGTACCAACTCAAAGACCAACGTTCAAACAACTTGTGGAAGAGCTCGATAGGGTGCTGGTGTCA
Associated Phenotype:
Not determined