ZMP
fgf13l
Ensembl ID:
ZFIN ID:
Description:
fibroblast growth factor 13, like [Source:RefSeq peptide;Acc:NP_991265]
Human Orthologue:
FGF13
Human Description:
fibroblast growth factor 13 [Source:HGNC Symbol;Acc:3670]
Mouse Orthologue:
Fgf13
Mouse Description:
fibroblast growth factor 13 Gene [Source:MGI Symbol;Acc:MGI:109178]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34919 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34919
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000020096 | Nonsense | 110 | 193 | 4 | 5 |
| ENSDART00000145532 | Nonsense | 99 | 182 | 3 | 4 |
The following transcripts of ENSDARG00000056633 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 27358869)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 26761663 |
| GRCz11 | 10 | 26723376 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCGGTGTTTGAGAACTATTACGTGACCTACTCGTCAATGATCTACAGA[C/T]AACAGCAGTCGGGCCGAGGCTGGTACCTGGGTCTCAACAAAGAGGGTCAA
Long Flanking Sequence:
TCAGATTTCAGAGGTGCCAGATCCGGACAGGCGAGTTTCGGCACAAATTAAGCCCTGCTGTTGGAAGTATATCAGCATACTAAAATAAAAGCTTCAGCAACTTTAAGTTCACAAAGACTATCAAACTATTTATCCTATTGGTTGTTTTTAATTTTTACTTTATTTAGACAGCATGCATTAGAATGTTGATACCAAACTATGACAACAGATATTTGCATTAAACAGAATCTTACCATCAATATTAGCCTGAACTATCTTCATTTTGTCTGCTCTCACTTTCTTCATCTCCCTCGCACACACACTTTTTTTTCTCAGTTATGCAGATACTCCTCCACAAACACATCAGAATATTGCTCTTCCCCTCATTCTCCCAGTCTCTAATGTTTCTGTTGTCTTCTCTGCCCATTTCACTCTCACAGGAGCACTTCACGCCGGAGTGCAAATTTAAAGAGTCGGTGTTTGAGAACTATTACGTGACCTACTCGTCAATGATCTACAGA[C/T]AACAGCAGTCGGGCCGAGGCTGGTACCTGGGTCTCAACAAAGAGGGTCAAATCATGAAGGGCAACCATGTAAAGAAGACCAAGCCGGCTGCTCACTTCATCCCCAAACCTCTTAAAGGTTTGTTCAAGTGTCTCCTGTTTTGATCGTCAGACTGATGGCTTTCTAAAAATAATATGTTTGAGACTGGGGGAGATATTGGTTGACAAGAAATTTAGTCGCTTGTTGGCTTTCCAGCACGTTTTTGCTGTTGTTTCATGTTATGAATAGAAATGTGGGTATCACTTTATTTTGATGGTCCCATCAAATGCATTTTATTAAATTTTTACTTACATTGCATCTACATGCCAACTAATTCTCAATAGATTCTAAGTAGACTGTTAGGTTGGGGTTAGGGTTAGTGTAGTTTGACATGTACTTGCATGTAAGTATTTTATAGTCAGTTAAATGTTGAAGGAGCAATATCAGGAGCAATATCAGCAGATATTAAGCAGACAGTCTAC
Associated Phenotype:
Not determined