Busch Lab

ZMP

arf5

Ensembl ID:
ENSDARG00000070472
ZFIN ID:
ZDB-GENE-030910-5
Description:
ADP-ribosylation factor 5 [Source:RefSeq peptide;Acc:NP_954969]
Human Orthologue:
ARF5
Human Description:
ADP-ribosylation factor 5 [Source:HGNC Symbol;Acc:658]
Mouse Orthologue:
Arf5
Mouse Description:
ADP-ribosylation factor 5 Gene [Source:MGI Symbol;Acc:MGI:99434]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa23226 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa23226
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103467 Essential Splice Site 110 180 4 6
Genomic Location (Zv9):
Chromosome 18 (position 7012572)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7590262
GRCz11 18 7549197
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGACAGAGAGAGAGTAGCAGAATCTGCAGAGGAGCTTTCTAAAATGG[T/A]AAGAGTTGCTCCATCTTTGTTTAAATACGATATATATATATATATATATA
Long Flanking Sequence:
GCTTTTACAGAAATGATCAATAATAATGTGTTAATGTTATTTCATTTTGTTTCTGAGTGCTAGCCCAACGTGATTCAGATAATCAATTTAGCTGGTTAATGTATATAAATGTTTATAACTCCTAACTAAAGTGTTGTTAAACTGTCTGTTTTCTTCTGATGGGCAGGTTTTAATGTAGAGACTGTTGAATACAAGAACATCTGCTTCACTGTGTGGGACGTTGGCGGTCAGGACAAGATTCGTCCTCTGTGGAGACACTATTTTCAGAACACACAGGTAAGATCTAGTTTAGGACTCACACGTGCTTCTTAGTCATTTCTGAGTACGTTTATCCTAAGCTTATCTTATCCTAAGTTTATTGAAACCCAGCTGCTTTATTGACTGCTTTTTAACTTTAAGTCTAAATGGTTTGTTTGTCTGTTCTCAGGGTTTGATCTTTGTGGTGGACAGCAATGACAGAGAGAGAGTAGCAGAATCTGCAGAGGAGCTTTCTAAAATGG[T/A]AAGAGTTGCTCCATCTTTGTTTAAATACGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAGATTGATAGATTGATAGATAGATAGATAGATAGATAGATAGATAGATATCTTGGCGTGTGAACTTAAGAGCGTGAGGTGGGATCATTAGTTCTCGCTGTTGCACTTTAGATCATTTTGGAAAGGCATTTTCTATCCAAGACTAAAAAGGATTGAGCCCTATGTGTGCACGTGCCTGCCTGTATGAATATGGTAATGACTCCACTTTGGCTTTTACCGGAGAAAAACTGTGTTCGTTGCAAGTTTGTCTTCGAAATTAATAACAGAAGAAAAAAATAGAGTGGGAGAGTTTAGCTGACGCGGTCAAAGCAGTGGGGTCTGAACATCGCACTGTGAGTGAATTAAAAAAGAAATGGTTCGATGTAAAGGTGCAGGTTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa635
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000103467 Nonsense 128 180 5 6
Genomic Location (Zv9):
Chromosome 18 (position 7014520)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 7592210
GRCz11 18 7551145
KASP Assay ID:
554-0544.1 (used for ordering genotyping assays)
KASP Sequence:
TGCARGAAGATGAACTGAGGGACGCCGTGCTYCTGGTTTTTGCAAACAAA[C/T]AGGATCTGCCTAACGCCATGGCTGTCAGTGAACTCACAGACAAACTCGGC
Long Flanking Sequence:
ATTTATGTTTTATTTTGTTTGTTGATTTTTAAATTGTATATTTATTGTTGAAAGATTCCTGCCATGAAGATAGCCTTGGTTGCTGACATGGTATTACATAAATAAATACATTACATTACGTGAGCGTGAAACCTGGCATACTCAACGTTTTTGTGTGTACGCAACATTGATACATGAGGCCCCTGGAGAATTTAGCTGTTACCCTAATCTAACACACCTGAACCAGCTAATCAAGTACTTTCTAGATATACTAGAAACTTCTTAGTAGGCATGTTGGAGCTAAACTCTGCAGGACACCGGCCCTCTAGGACCGAGTTTGGACACCCCTGATATAGATTATTAAACAATTTTTAGCATTTATTTATTGTTTTTTTGTGTGTTTGTTGAAGACATTAAATGTTCAACTAGATTAAGCCTTCATCACACTCTCTTTCACTTTCTTTATACAGTTGCAGGAAGATGAACTGAGGGACGCCGTGCTCCTGGTTTTTGCAAACAAA[C/T]AGGATCTGCCTAACGCCATGGCTGTCAGTGAACTCACAGACAAACTCGGCCTGCAGAGCCTACGCAGCAGAACGGTACACACACACACACACAAACACACACACACACACACATGTTTGTTTTTGTAAAAAGTGAGTACATTACATAGGTTTCCCATTCATTTTATACTGTCCAAACTGTATATTGTATTGCCCCCACCCTAACCCCAACCACCACAGGAGACAGTGTACAGTAGAGGTCTGCATTCCCGCGGCTGTCCCACGAGACAGATCCGACCAGATTTCTGAGGCGGGGGAATAGATTTCCGAGGCGGGGGAATAGATTTCCGAATTAAGCGCGGGAGTGGTCGGTAACTGCTTTAATTTTGCACGGGAGCAGGCCGTCTAGCAATATTTGCTGTGTTTAGGTTGTTTGTTGATGTGTGCGTGTATTTGTGGGCGCGCGAATGAGAGGTGAGAGGAACCCCCTCCCACCCCCGCTCTTTAGCGGGATCGGGCGTG
Associated Phenotype:
Not determined