Ensembl ID:
hypothetical protein LOC794050 [Source:RefSeq peptide;Acc:NP_001076365]
Human Orthologues:
CCL11, CCL13, CCL15, CCL16, CCL2, CCL23, CCL24, CCL26, CCL7, CCL8
Human Descriptions:
chemokine (C-C motif) ligand 11 [Source:HGNC Symbol;Acc:10610]
chemokine (C-C motif) ligand 13 [Source:HGNC Symbol;Acc:10611]
chemokine (C-C motif) ligand 15 [Source:HGNC Symbol;Acc:10613]
chemokine (C-C motif) ligand 16 [Source:HGNC Symbol;Acc:10614]
chemokine (C-C motif) ligand 2 [Source:HGNC Symbol;Acc:10618]
chemokine (C-C motif) ligand 23 [Source:HGNC Symbol;Acc:10622]
chemokine (C-C motif) ligand 24 [Source:HGNC Symbol;Acc:10623]
chemokine (C-C motif) ligand 26 [Source:HGNC Symbol;Acc:10625]
chemokine (C-C motif) ligand 7 [Source:HGNC Symbol;Acc:10634]
chemokine (C-C motif) ligand 8 [Source:HGNC Symbol;Acc:10635]
Mouse Orthologues:
Ccl11, Ccl12, Ccl2, Ccl24, Ccl26, Ccl6, Ccl7, Ccl8, Ccl9
Mouse Descriptions:
chemokine (C-C motif) ligand 11 Gene [Source:MGI Symbol;Acc:MGI:103576]
chemokine (C-C motif) ligand 12 Gene [Source:MGI Symbol;Acc:MGI:108224]
chemokine (C-C motif) ligand 2 Gene [Source:MGI Symbol;Acc:MGI:98259]
chemokine (C-C motif) ligand 24 Gene [Source:MGI Symbol;Acc:MGI:1928953]
chemokine (C-C motif) ligand 26 Gene [Source:MGI Symbol;Acc:MGI:3589281]
chemokine (C-C motif) ligand 6 Gene [Source:MGI Symbol;Acc:MGI:98263]
chemokine (C-C motif) ligand 7 Gene [Source:MGI Symbol;Acc:MGI:99512]
chemokine (C-C motif) ligand 8 Gene [Source:MGI Symbol;Acc:MGI:101878]
chemokine (C-C motif) ligand 9 Gene [Source:MGI Symbol;Acc:MGI:104533]


There is 1 allele of this gene:

Allele name Consequence Status Availability Estimate
sa43506 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
We currently estimate that this allele will be available during 2017.
G > T
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000061434 Essential Splice Site 94 136 4 4
ENSDART00000142164 Essential Splice Site 61 103 3 3
Genomic Location (Zv9):
Chromosome 20 (position 39357634)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 39430046
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
Flanking Sequence:
Associated Phenotype:
Not determined


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

(GWAS data comes from


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: