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