Busch Lab

ZMP

ENSDARG00000086121

Ensembl ID:
ENSDARG00000086121
Human Orthologue:
MUC7
Human Description:
mucin 7, secreted [Source:HGNC Symbol;Acc:7518]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa6864 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6864
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123078 Essential Splice Site 69 343 3 3
Genomic Location (Zv9):
Chromosome 2 (position 47683750)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 47476048
GRCz11 2 47328552
KASP Assay ID:
554-4541.1 (used for ordering genotyping assays)
KASP Sequence:
GTATTCACCTGACCTAACTTACCATAAATTAATACCTGCTTATATTTTTC[A/T]GATTCCTCACAAKCAACCTTAGSACCTTCTTCAGAAACATCTTTTCCAAC
Long Flanking Sequence:
GTGCTCAAAAAACTAAAAACTTTGGGTGGGGATTTGGGTGGAGATATAGGTAAATAGAGTCATATTTACAGTTTTTGTGGACAACAAATGTTTTTGGAGCTTCATATGATTACAGTCGAACCACTGAAATCTTGCTTTGACAATCTTCAGTTCCTTTTCTGGACCATCTCTGGACCACAGTTGTCTAGGGAGGAGAAAAATCTTGGATTTTATCTAAAATATCATTTTAATATAATTTGTTATGTTTTTGTGAAGATGAACAAAACTCTCATGGGATTGGAATGACATGAGTGAGTATTTAACAATCAAATATTCATTTTTGCTAAAATCGTCTTAAAATAAAAGTAAAAACATTTATCAGAAATGTCTTAATTTCATTAGTTTTAGCACATCTGAAGCAGATGAAGAAAAAATTACAAACTACAGCCTTTTGTGTATTCTTTTATTATTGTATTCACCTGACCTAACTTACCATAAATTAATACCTGCTTATATTTTTC[A/T]GATTCCTCACAATCAACCTTAGGACCTTCTTCAGAAACATCTTTTCCAACTTCACTACCATCTTCATCAATAACACCACCAACTTCACCACTTCCATCATCAACCTCACCACAGCCATCAGCATCCTCAATATTATTTGCAACCTCATCATCACCAACTTCCCCACCTTCATCAACCTCACCATCATCTCCAGCATCCTCAACATCAATCCTAACCTCATCATCATCACAATCACCATTTTTACCAACGTCATCACCTTTCTTACCACCAACTTCACCACCATCTTTAGCATTCTCAACATCATTTCCAACCTCATCCTCACCACCACCTTCATCAACATCTACCTCACCATCAACTTCAGCATCATCGCCATTTTTACCAACATTATCACCAACTTCTCCACCTTTACCACCACCAACCTCACCACCTTCATTATATGTACGAACACCACCACCAACCTCAACACCATCTTCAACGTCCTCAACATTATTTTCAACCTC
Associated Phenotype:
Not determined