Busch Lab

ZMP

ENSDARG00000069754

Ensembl ID:
ENSDARG00000069754

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa39641 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39641
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000099354 Nonsense 32 320 1 4
ENSDART00000101749 Nonsense 28 317 1 4
ENSDART00000101750 Nonsense 23 246 1 2
Genomic Location (Zv9):
Chromosome 1 (position 34634590)
Other Location(s):
Assembly Chromosome Position
GRCz10 1 34653268
GRCz11 1 35385295
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTGATTGTCATCTGTGGACTGACTAAAGCTTCAATCAGACAGCATTA[T/A]TATGTGAATAGCTATAGGTCCTGGACTGAAGCTCAAAAATACTGCAGGAC
Long Flanking Sequence:
TATATTGCAAATGATCTTTTTTGTGAATTTTAACAAAGTAGCAAAATATTTTTTTAGGGATTAAAATGGAAGTAAATATATTTATTTTTAACTGGAAAGATATACTGGTGATGGAAAATATGTGGATAGATAGATTCAATTAGAATATTTAATGCACTGAACATGAGAAAGATCAAATGCCTTAAACTGAAGAATTATTAAGAGAATTGTTTTCATCACATTCTGTTATCAAAGTAGATTAAGAAATTTCCATATGAAAACACGAACAACATTTACATAAGTTTATATGTGAGTATAAATGTTCCGATTAATCTGGGTGTGGACATTGAGACCTCCTTACATTTATTTGCATATATTTCAAACTTTTTATACATAAAATGGACATTTCATCATCTCATACAACACAAGACTATTCAACATCTCACTGGAAAGATGAAACTCTCCATCCTTCTCCTGATTGTCATCTGTGGACTGACTAAAGCTTCAATCAGACAGCATTA[T/A]TATGTGAATAGCTATAGGTCCTGGACTGAAGCTCAAAAATACTGCAGGACACATTACACAGACTTGTCAACTGTCTCAAGTCAAGAAGAACAAAACAAGCTGATACATCTAGCAAATCAAACATACATTTGGATCGGCTTGTATAGGAACACATCCAACAGTAAGCAGTTTCTGTGGTCTGATGGCACCCCATTTTCTTTTTCCAACTGGGATGTTGGTCAGCCCAGTAAAGTTTACACCTATGGAGGTCAATGTGTTATCACCAATCTCAAATGGCTGAATGTAAACTGTAATTTATTAATTTCTTTCTTTTGCTACAACACCTCATTTACTGTTATTAAAGAGAAGAGGACATGGGAAGAGGCCCTGCTGTTCTGCAGATCTCACTATAGTGATCTGGCCAGTTTGACCACTGACAGAGAATTACAACTGGCCAAGCAAGTGACTGTGGAGTCTCAGACTGAAAGTGTGTGGACAGGTCTGCGCTTTCTGCTTGGTGA
Associated Phenotype:
Not determined