xkr6

Ensembl ID:
ENSDARG00000043410
ZFIN ID:
ZDB-GENE-040724-153
Description:
XK, Kell blood group complex subunit-related family, member 6 [Source:RefSeq peptide;Acc:NP_0010122
Human Orthologue:
XKR6
Human Description:
XK, Kell blood group complex subunit-related family, member 6 [Source:HGNC Symbol;Acc:27806]
Mouse Orthologue:
Xkr6
Mouse Description:
X Kell blood group precursor related family member 6 homolog Gene [Source:MGI Symbol;Acc:MGI:2447765

Alleles

There are 2 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa4138 Nonsense Mutation detected in F1 DNA During 2014
sa19231 Nonsense Mutation detected in F1 DNA During 2014

Mutation Details

Allele Name:
sa4138
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063725 Nonsense 137 578 1 3
ENSDART00000131367 None None 385 None 2
ENSDART00000063725 Nonsense 137 578 1 3
ENSDART00000131367 None None 385 None 2
Genomic Location:
Chromosome 20 (position 18987075)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
TGCTGGTGCCGTCGGTCCTGGTCCAGATCCTGAGCTTCAGGTGGTTCGTG[C/T]AGGATTACACGGGGGGCGGCTTGGGCTCCGTGGAGGGTCTCAGCAGCACC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19231
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2014.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000063725 Nonsense 137 578 1 3
ENSDART00000131367 None None 385 None 2
ENSDART00000063725 Nonsense 137 578 1 3
ENSDART00000131367 None None 385 None 2
Genomic Location:
Chromosome 20 (position 18987075)
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TGCTGGTGCCGTCGGTCCTGGTCCAGATCCTGAGCTTCAGGTGGTTCGTG[C/T]AGGATTACACGGGGGGCGGCTTGGGCTCCGTGGAGGGTCTCAGCAGCACC
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

If you would like to be informed when the status of this gene changes (for example, a new allele is generated or an allele is made available for distribution) then please enter your details below:

* quick link - http://q.sanger.ac.uk/10ryglw0