cxxc1l

Ensembl ID:
ENSDARG00000016187
ZFIN ID:
ZDB-GENE-040426-1142
Description:
CXXC finger 1, like [Source:RefSeq peptide;Acc:NP_956893]
Human Orthologue:
CXXC1
Human Description:
CXXC finger protein 1 [Source:HGNC Symbol;Acc:24343]
Mouse Orthologue:
Cxxc1
Mouse Description:
CXXC finger 1 (PHD domain) Gene [Source:MGI Symbol;Acc:MGI:1921572]

Alleles

There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa11489 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa11489
Current Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000083322 Essential Splice Site 115 570 4 15
Genomic Location:
Chromosome 8 (position 8271057)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCAGCCTGACACACMAGATTTYAAGTCAGACGGACGGCGTGGGTCACGAG[T/A]GAGGAATTCTGATYYATAAMAACTGYTCTTWGAATAATTGTATATCTAAC
Associated Phenotype:
Not determined

GWAS

This gene's human homologue has been identified in the following GWAS studies:

(GWAS data comes from http://www.genome.gov/gwastudies/.)

Register

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* quick link - http://q.sanger.ac.uk/oqnk3q2k