ZMP
fgf21
Ensembl ID:
ZFIN ID:
Description:
fibroblast growth factor 21 [Source:RefSeq peptide;Acc:NP_001038789]
Human Orthologue:
FGF21
Human Description:
fibroblast growth factor 21 [Source:HGNC Symbol;Acc:3678]
Mouse Orthologue:
Fgf21
Mouse Description:
fibroblast growth factor 21 Gene [Source:MGI Symbol;Acc:MGI:1861377]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10019 | Essential Splice Site | Available for shipment | Available now |
| sa38391 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10019
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 |
|---|---|---|---|---|---|
| ENSDART00000103511 | Essential Splice Site | 99 | 194 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 27134477)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN149943.1 | 10408 |
| GRCz11 | KN149943.1 | 10408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACATCTCTCTACCTCTGCGTCGATGATCAAGACAAGCTGAAAGGACAGG[T/A]ATGAATAGAAGTACTCCATTGCAATGATGYAMTATTCAGTTAAAAACCAA
Long Flanking Sequence:
GCATAGTTTGTGCATAAAGAGTATAGTTTGCTGTTAGAGAACCACTGTAACTCATGTAAATATCCTTCAAGTAAAAATGTCCTATCAGAAAAGATAACGAGTTCATAAAATCTGAGATACTGTGATTTACAATAACACATTTGTTGTTATTTTGGTTTGATGTAATGCTAACACTCTGTAAGTGCTGTTCTTTTTACAATATTAAAACCATGTTTACAGCTTAGTTCATTAAAAATAATATCAAGCTATTTTAACATTTATAATGAGAAAAATACAATTTCTTATGTGATGATTATGTCTCACGGTGGCGCTGGTTAGTTAGTATCTGAGGTTCAAAGGTGGTGTGTGTGCGACTGATCTGGGAACTGACGGAGGTGTGGTGTGGTTTACTGCAGGTGTGCTGGAGCTGCGTTCAGTCAAAGCGGGTGAAACCGTCATCCAGAGTGCAGCTACATCTCTCTACCTCTGCGTCGATGATCAAGACAAGCTGAAAGGACAGG[T/A]ATGAATAGAAGTACTCCATTGCAATGATGTACTATTCAGTTAAAAACCAAAAAGTATATAATTACACACATATATATAATATATTATATAATATATAATATGTATATAATAACACAATTAAAATTTTTAACAAATATATCATAAGATCACAGTCTAAAAAAAGTACACCCACATTAATATATGAGGGAAAATATTACATAAAAATTTACGAAAGAGGAATAATTATGAGAAAATTTTGTAGATTGCAAAAAAAAAAAAATGCAATACTTCAATACCTTTAAATATATTATGTTTCTATTTCTAATGATGTTTGTGACCAACTCTTATTTTAATTGAAATAACTTATATAACCTCTGGGTCTTAAAGAATCCCCCATCCACCCCTACTCCTCCCCTCTTTCCTAGACTAATCCAGGACAGGGCGACACGGTGACTCAGTAGTTAGCACTGTTGACTCACAGCAATAGGATCACTGGTTTGGGTCCTGGCTGGGTCAGTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38391
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 |
|---|---|---|---|---|---|
| ENSDART00000103511 | Nonsense | 162 | 194 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 3 (position 27132251)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | KN149943.1 | 8182 |
| GRCz11 | KN149943.1 | 8182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCCTGTTAGCAGAGCAGAGGACAGCCGGACACAGGAGGTGAAACAGTA[T/A]ATTCAGGATATAAACCTGGACTCTGACGACCCACTAGGAATGGGACATCG
Long Flanking Sequence:
ATAAATGCAACCACAGTGAGCAGAAAAGACAAAAATGTTAAAACCCAAAAACTTTGATCAATATTTTGTAGACAAACAATATGTAAGATCACTAAGGTTACATCATATAATTAATAGTTTTCTAATTATTAATGATATATACCTTTTTCACAGTAAGCTACATAAATTAATGTATTGTAAATGTCATCATTTTTCATTTTAAATATTGACAGTGGGCATTGAATTAACTGTTATGCTCACTTAATTTTTTGACAATTTTCACTAGAGACATGAGCACTTTTGATTGTCTGTATTCTCTGTTTTCTCTTTCAGCATCATTACTCTGCACTAGACTGCACCTTTCAGGAATTGCTACTGGATGGATATTCGTTTTTCCTTTCTCCACACACTAATCTTCCCGTATCGCTCCTCTCGAAACGTCAGAAACACGGCAATCCTCTTTCTCGCTTCCTCCCTGTTAGCAGAGCAGAGGACAGCCGGACACAGGAGGTGAAACAGTA[T/A]ATTCAGGATATAAACCTGGACTCTGACGACCCACTAGGAATGGGACATCGGTCACACTTACAGACCGTCTTCAGTCCCAGTCTGCATACTAAAAAATGAAGACATGCTTTACATTAGCACTGGACTGCAAGGTTAAAAATGATATGTTACTGTGCTTTTTTGTTTTTGTCAGGAACTGTATTTATTTAAATATATTTATTTATTTGCTGTGGTCTAATTTATTTAAATGAAGTAATTTATATATTGTTAATGCGATTGGTAACTTAAACATTTAAATGACAGACGTCTGCTGGAGCAGATTACACTTTCAGTTCTTTTTGTAGTTCACTGAGTCTGTATGATTTTTGCTTGATTAAAAATTGTAATAAATAATATTCCAACATGGCTCAGAGTTACACAATTCATAGAGCACACACATACACACCAGATAATACACCACAGAATGTTCTATAAGGCTTTTGAATTCACAAACTGCTCAGAACAGCAGTAACACTAAACTG
Associated Phenotype:
Not determined