Busch Lab

ZMP

il17a/f2

Ensembl ID:
ENSDARG00000043934
ZFIN ID:
ZDB-GENE-061031-2
Description:
interleukin 17a/f2 [Source:RefSeq peptide;Acc:NP_001018634]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa42882 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa42882
Status:
Mutation detected in F1 DNA
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
ENSDART00000064513 Nonsense 26 140 2 3
Genomic Location (Zv9):
Chromosome 17 (position 12593841)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 12576363
GRCz11 17 12730429
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCAGGTTTTGCTAGGCTGTGCACTGGCAAGGCTCACAATTGCACAG[C/T]AAGAGCAGAACCGGTTGTGTGATACTGCTTTGACCATTTCTAATGACTTC
Long Flanking Sequence:
TTGCCAGCATAGAGTGATCTTTAATCCGTAGGTCAAATTACTGGCAATGAGTGGCAACATGTAAAAACAGCAAACACCTATCAACTGATCTGATGAGAAATCCAGGTCAGAGGTAGGCCTCATTATCTATGCTATCGCGATCAAGCTTGGCATAAATAGATGGGGTACATGAGAATCATTTTCACAGTTGAAGAGACAATAAGAAGACGACTTTAAGATGTTTCTGAACTTCTTTAGCGCTAAATACTTGGTGAGATGACCGTTCATTTGTAGATATTTTGTTGTAGCATAATACTGTTAGCTAGCATTATGCTAACACCATTGCTTCACTAAAGAGTTTGTTTTCAGGCATACATGTAATGCTTTGTAGCAAAATAGAGGCCTCAACTTGTTTTCTTCTTCTAAAAGTTGTCTTTAATGGTGAATTTAATGTTAACAGATAACAATCTTTCTCTCAGGTTTTGCTAGGCTGTGCACTGGCAAGGCTCACAATTGCACAG[C/T]AAGAGCAGAACCGGTTGTGTGATACTGCTTTGACCATTTCTAATGACTTCAATGGCTCTCAATCTGAGGACGGAAAGGGAAACGGCAGCATTCACAACCGCTCGCTGTCTGCGTGGAACTGGATGTGAGTTGAAGAGCTCTAAAATGAGTTTAATTCATGGCATAAACAAAGTTTGATGAGGTAATATACAGCTGAAGTCAAAATTATTAGGCCTGTTTTGGAGCAAAAATGTTGGTCACACTTTATTTTGATGGTCCGTTTGTTGAACTTAAGTTACTTTGCATCTACATGCCAACTAATTCTCAATATATTATAAGTAGACTGTTAGGTTGGAGTTAGGGTTAGTGTAAGTAGACATACGCTTGCAAAGTTTCTTATAGTCAGTTAAATGTCTGTTGAAGGAGCATATCAACAGATATTAATCAGACAGCCTACTAATACTCAAATGAACCATCAAAATAAAAGCTGTGTCTCATTTCAGAGGCTGCATCCTTCAAAG
Associated Phenotype:
Not determined