ZMP

LOC568355

Ensembl ID:

ENSDARG00000079107

Human Orthologue:

CLEC11A

Human Description:

C-type lectin domain family 11, member A [Source:HGNC Symbol;Acc:10576]

Mouse Orthologue:

Clec11a

Mouse Description:

C-type lectin domain family 11, member a Gene [Source:MGI Symbol;Acc:MGI:1298219]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa12477	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa12477

Status:

Available for shipment
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Availability:

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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000108496	Nonsense	216	273	4	4

Genomic Location (Zv9):

Chromosome 20 (position 4150107)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	4091786
GRCz11	20	3940112

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AACTGGCCTGTGTGGCTTGGGATAAACGATGAGCGCTCTGAAGGCCTCTA[C/A]CTGTTCGAGGACACGACACGCGTCACTTACTTCCAATGGAGGAAGCACTT

Long Flanking Sequence:

ACTTCCTAATCCAGATAGCTAAACTATGTTATGGCAGACATGCTGCCAATGCTGGTACTGATGTTTTAAAAGGGACTTACTTGGGAAGTATTTACCAGACTTGACGTAAAATCAGATCTGATCGGGTATTAGTAATGTACCAGGATGGGAAAGGTTTTTAGTCCAGGAATAAATACTACTTGAGGACATCAAACTACTCCACTTGACACTCATAAACCTTTGTGTGTTCTACTTGACACTAAATGTGAAAATGATTTAACAATTTATGTCTTTCCAGGCTGCCAGAAAGGCCGTAAAATAGGTTACAAATGCGTTCTGGCATACCGCGTGTACGAGACCTACGCAGATGCGTCCAAGAAATGTCAGGAGCGTGGAGGACGCATGGCCATGCCACGAGACCGCAAAGAGCAGGAAGCTCTGGCTGAATATGTGAAATCTGTATTCCATGGAAACTGGCCTGTGTGGCTTGGGATAAACGATGAGCGCTCTGAAGGCCTCTA[C/A]CTGTTCGAGGACACGACACGCGTCACTTACTTCCAATGGAGGAAGCACTTCCTATCAAGCCAGCCAGATGGCGGGAAACGAGAGAACTGTGTAGCCATGTCCTCAGATGATGGAGACTGGTGGGACACTTACTGTGAAAGACGCATGTATTATCTGTGTGAGTTTGATGTCTGATAAAGTCCCACGTGGCACATCTGACTTAAAATTTTGATTTACTTTCAGCTATAAAGACCAGCTATTTACTGCCTCCCCACTGAAGCCAAATGCAATTCTATAAGTTTAAACATCTTCATTCTCAGCTAGTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAACTTATCCAGCATGTTTTTACTCAGCGGATGCCCTTATAGCCGCAACCCATCTCTGGGAAACATCCACACACACACTCATACACTAGACAATTTAGCCTACCCAATTCACCTGTACCACATGTCTTTGGACTGTGGGGGA

Associated Phenotype:

Not determined