Busch Lab

ZMP

ZNF518A (2 of 2)

Ensembl ID:
ENSDARG00000090188
Description:
zinc finger protein 518A [Source:HGNC Symbol;Acc:29009]
Human Orthologue:
ZNF518A
Human Description:
zinc finger protein 518A [Source:HGNC Symbol;Acc:29009]
Mouse Orthologue:
Zfp518a
Mouse Description:
zinc finger protein 518A Gene [Source:MGI Symbol;Acc:MGI:1919922]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa12306 Nonsense Available for shipment Available now
sa22390 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa12306
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125420 Nonsense 411 819 2 3
Genomic Location (Zv9):
Chromosome 13 (position 51481054)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 50190716
GRCz11 13 50505635
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAACATAGCATTTCATCGTCAGTGATTGAGAGATGTAATAGCCAASAA[C/T]AAGATGTCTACGATAACCRGGACTTCAATAACCTCCAAYATAATCCAGTC
Long Flanking Sequence:
AATGGCCGTCCACTTTACTGGACACCAATGGCATCTTAGTGGATCCAGAGAAGACTTTGGAAGAAACGAAGCAGTTTCTTGAAAGAACGGTTGTTAGTGGTAAGAAGTGGAGCATGTCTCTAAAAGATGAGCAGGACTTTGCTCCCCCACATTTAAATGGGATAAACCATTGGCGTGTTGGGAAAGATAAGATATCCGGACTGATGGAGAAAAACAATATAACCGTTCCCCCAGATTGCACTACGAAAGTGGTCGGATTCAAGATGGTGGACGGCAAAAAGCATTTAGTCCTCAGAGTCATTCCTTCAGACAAGCAAGATGAGGCGTTCAGATCTAACACTGTGAAACCAACCAATCAATCTTCGGTTGAGCCAAACGACACTGTTAAAGCTTCAGGAAACTGTTCTCAGGGGACTCCGGAAAGGATTTTATCCCCGGGACGATGTGCAACTCAACATAGCATTTCATCGTCAGTGATTGAGAGATGTAATAGCCAACAA[C/T]AAGATGTCTACGATAACCGGGACTTCAATAACCTCCAACATAATCCAGTCAGAAAGACCAAAACAACCAATCTACGGTCCTGTGATGAAATAAACACTCATGCAGAACATCCAAAAGAGCAAGAAAAGCCTCTCAGTGGGTCAGAGCAAAACTCTAATGAGGATCTGAGCTCTGATGTGGGATCTGCGCAAGAGAAACGCGACCTGGCATTGGATCCAAATGCAGATCTGTGCTCCACTTTTGGGTTTGATTGCATTAGTCCATCTTTGAATAACCTGAGCGAGTCATTGTGTGGTTTTCAAAGTGCAGATGGAGGATTGTTATTCCACAGCGAAAGCACAAACAACTGCGACCCCAGAGAGGCTGCTGTGTTCCCGGTGGGTCAGTATGACTGCGAGAGGGAGAATCTGTGTGTTTCAGAGCTGAATCAGACGGTGGAGGAGCTGCCTTTGACTACAGTCAGACACTTACTGGATGAGTCTTCAAGTTCGGATGAACCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22390
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000125420 Nonsense 670 819 3 3
Genomic Location (Zv9):
Chromosome 13 (position 51487465)
Other Location(s):
Assembly Chromosome Position
GRCz10 13 50197127
GRCz11 13 50512046
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCTCGAGACACTCCGACAACCCTTCGACTGATTCCCTTCAATTCCACA[C/T]AATCCCTCAAAATCCCTGCTGAGAACCAACCCGTTATAGTCCTCAACCAT
Long Flanking Sequence:
GGCGATGAGGTCCTACAATATTCTGAGAAGGTTTTTAAAATGGTATTGAAATTACCTTTTGGATTCCTGTATATAACCTGTACTAGTATCCAGCTTGAACTGACATTTAAAGAAAATAAATTAAAATATTATAGGAAATCATGTGTGAAAATCCTTGCTCTGTTCAACATAATTTGGGAAATATTTATAAAATGCTAATAATTTTGACTCCAGCATACAATCATATACTCTTCTCCATGTTTTGATCAGGAACAATCGAGCGACATGAGCCAGAAAACACCAGCATCATCTTCTCTGAGGATTCAGACTCGTCCACAACTGTTCCTGAGTCAGCCGCCGGCTCCATTTCATCACTAAACAGAAAGCGCATGGGAGAAGAATCCTCAACAGACTCCCAACAACAACCCGTCAGTAAATCCCCAAAGCCATCCATTCTCCATTGGGAACCGGCGTCTCGAGACACTCCGACAACCCTTCGACTGATTCCCTTCAATTCCACA[C/T]AATCCCTCAAAATCCCTGCTGAGAACCAACCCGTTATAGTCCTCAACCATCCAGATTCTGATATCCCCGAAGTGACGAACATCATGAAAGTCGTGCACAAACACAAAGCTGCGATCCAGCGTGTGGTTTTGTCTCGTAAAACTCTCCGTGCGCTGTCGGAGTTTAATTGCAATGCATTCATTTCAACGAATCTCCTCACCAGTTATCACTATAGGAGGGAATGGCCAAATAGCAGCGTTAAGGAGAGATTCAGCTTGAAACTGAGACTCAAAAGAGTGCGTGGAAGAAAGTATACCGTGGTGCCGACGCTATCAGAAAGCGCTGTTCTGCAGCCGACGTTCACATGCTGGTTTTGCGGGCGTGTTTTCAGGAATCAAGAAGCTTGGGTTGGACACGGACAGAGACATCTGACTGAAGCCACCAGAGGCTGGAAGCAGATCTTCAACACATAGAAGACCTGAATCAGAGAGTTAGACGTTTATAAATGCAGTGAGAGCTAA
Associated Phenotype:
Not determined