Busch Lab

ZMP

LOC796113

Ensembl ID:
ENSDARG00000087319
Human Orthologue:
CECR6
Human Description:
cat eye syndrome chromosome region, candidate 6 [Source:HGNC Symbol;Acc:1844]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa40248 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40248
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123953 Nonsense 173 395 1 1
Genomic Location (Zv9):
Chromosome 4 (position 11375640)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 12312267
GRCz11 4 12311116
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCATTTTTGGATGCAACCTCGGCGAGTTTACCTTCGCCTACCTTGCATG[G/A]CTGATCTACGTGATCGCGTCCACCCCAAAAGTGGTGCTCGTGTTGGAAAC
Long Flanking Sequence:
GAAATCATAAAAGACATCTCCCAGCCCGACTCACCTGTCTCATCAGCACCAGAAAACGGACAGCTGCTCTTCATCCGAAGCGTCGCGTCCAGGAGAGACACGCAGACCACCAGCGGCAGTGCCAACCTCGAGGAGGGCAGCTCCCAGCCCCTGGTCTCCTCCTCAGCCACAGCTCAGCCCCAATCCTACACCATGACATCTGGAGAATTCATGCAATCCACCCCGACGTTCGCGCAGAGGTCCAGGAAGAACCTGTTTTATAAGATCCTGTGCTTCCTCGTGCTCGTCCTCCAGGGCGGCATGCTGGATTTCTACCTCATCGTCTTCACGGATCTCTACTGGTGCTCGTGGATCGCCACGGATTTAGTGGTCATTTCTGGATGGGCGATCTTTTTCATGAAGAACGCAAGGTCTAAGCGGGAACGAGCGTGCGGTTTCCACCAGAAGAGCTCCATTTTTGGATGCAACCTCGGCGAGTTTACCTTCGCCTACCTTGCATG[G/A]CTGATCTACGTGATCGCGTCCACCCCAAAAGTGGTGCTCGTGTTGGAAACGTCCATTCTGGATCTTATCGCCCTGAAGGTGCCCTTTGGCGTCACCGGGTTTAAAATCACCATGTTGCTGTGCGCGCCTTTGCTTTACTGCCTCATCAACTCCATCATTGAGGATCCCAACGGTGCCACCCGTTTCCACTCCCAAGGCTGCTTCGTGAGCACCTGCCTGGACATCCTGGACAGCTTTATATTGGTGGAGGTGCTTCTGAAGAACGAGATACCCAATGTTTACCTTAGATACACGGTCATATCCGTGTATTTCATCGCACTGGGCGTACCGGTGGTTTGGCTTTATGAGTTGACGGCCTCGGAGATGAACTGTCGCTGGGTTTGGGCGAGGTTCTTCACCGGCGTGCTGCTCAACGCGCCGCTGTTGGTGGTCCGGTGTTTCCTCGTTTTCGTGTACAAAACCCCAGTTTCGGTGTTTATGTTCAAGAACATCTTCTTTTT
Associated Phenotype:
Not determined