Busch Lab

ZMP

LOC100003245

Ensembl ID:
ENSDARG00000086222
Human Orthologue:
C7orf52
Human Description:
chromosome 7 open reading frame 52 [Source:HGNC Symbol;Acc:22030]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa45275 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa45275
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129834 Nonsense 126 335 2 3
Genomic Location (Zv9):
Chromosome 7 (position 27266451)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 25869390
GRCz11 7 26140583
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTTTGTTCTCAACTGGTCAAGTCCAAGTACCCTGACGTTAAAGTCAGC[A/T]GACTGACCAGAGACGACCAACTGGGGCCAAAAGACTTCCAGAAGTACCGG
Long Flanking Sequence:
TGCTGTTTTTTTGACGCAGCTGAGGTGGAGATTGAGGCACACTCTGACAGGCACGGGGGAACGGTGGGCAGGGAGATCTAGAATTAAAGGCACAGGCAACAAAACCAGCTACATTGTGTTCAGAGCAGAAAATCATATATTTAAAAGCTATAATAAATAATCTGATGGGTGTTTTAAGCTAAAACTTTGCAGACACACTCTGGAGAAACAAATGACTCATCTTAAATCTTGAAAAAGGGGTAAAATAGGTGCCCTTTAAACAAAATGTGCAGTATTCCAGGTTTAAAAAGAAAATTTTTACTTTGTTATAGATATAACTTTTATACACCTACATTCTCCAGATTGCGCTGGAGTCAGTGTGCGTCATCGATGATGGCGAGACCATGCTGGTGGAAGGGCTTCGTGTCGCCCCACAGGAGCGGGGGAAAGGTGTAGCTGGGGTACTTCTGAGGTTTTGTTCTCAACTGGTCAAGTCCAAGTACCCTGACGTTAAAGTCAGC[A/T]GACTGACCAGAGACGACCAACTGGGGCCAAAAGACTTCCAGAAGTACCGGCTCATTACCAAACAGGTAAGACATGCTAACATGAAATATATAAATGTGTTTAGGCTGTCTTGAGTAAAATCAGCTAAAGCCACATTATCTTCGTTCTGTCGCATGATTCAAATAAAAAGGGAATCCTCCTGGTACGCTTCCGTGCTGAAGACCTAAAATTACGCCTTGGTGATCTCGGGCCCAATATCAGTGTAGCAGGAGAGGCTTTGTCCACCGCAAACATCCCGGTCTGCTTGGAGCCAGCAGAAGTGCATCAGCTCTTCTTAAGCGATGTGCTAATGCAGGACGTCCTACCCAATGCCACCATCGTTCAAGACTGGCAGCCTTTCAAGCCTCTACCCAGCAACATGGCCATCCTGATGAAGAAGGACATCGATTGGATGGTCGACGATGCCAAGCGCCCAACCATGACCAGCTTGTGCACCTTCCCATTTCACGTGCCAATCGGTG
Associated Phenotype:
Not determined