ZMP

LOC100330293

Ensembl ID:

ENSDARG00000086776

Human Orthologue:

GPR35

Human Description:

G protein-coupled receptor 35 [Source:HGNC Symbol;Acc:4492]

Mouse Orthologue:

Gpr35

Mouse Description:

G protein-coupled receptor 35 Gene [Source:MGI Symbol;Acc:MGI:1929509]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa14229	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa14229

Status:

Available for shipment
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Availability:

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Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126730	Nonsense	278	296	3	3

Genomic Location (Zv9):

Chromosome 22 (position 3224014)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	3216719
GRCz11	22	3235987

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGCTGCGACGCACAGATTTGGTCGCATAATTTCGTYCRTGCCGCCATCTG[T/A]GTTTCTAGCATGAATTGCGCACTCGATTGTGTCACTTATTACTTYGCAAC

Long Flanking Sequence:

ATTTTCACCATAACTGCGATAAGCATCGTGCGTTTCATCGCCATCAAGTATCCGCTGAAAGCTCGCGAAATTTTTTCGCGCAGAAAAGCATTGGTGGTTTGCGCACTAATATGGCTGGTCACGTGCTCGCTTAGCGTAGCTTTCCATCGTGTGGACGATCCCAAGCATAACAGTACAATTAAATGCTTCCAGAAGAATAAAAAAGAGGAATTACCATTGACGTTTATTCTCGTGCTGAATGTCGTCGGGTTTATTTCGCCGTTTCTAATCATGACGTTCTGCTCAATCAGAGTTATATTCACGCTTAGGAAGCAGCTGGACATCGGCTCGCGCGCGGAAAAAATGCAGTGCATTTTTATAATGGTGGCGAATTTGTGCGTTTTCGTTGTGTGTTTCTTTCCCGTTCATTTCGGCTTCCTGCTCAAGTACATCACTCAGGCGCACAAATACAGCTGCGACGCACAGATTTGGTCGCATAATTTCGTTCATGCCGCCATCTG[T/A]GTTTCTAGCATGAATTGCGCACTCGATTGTGTCACTTATTACTTTGCAACAAGAACATCGTGGACGATACGGTGCTGCCGTCAGAAAACACATGAGGGATATAAGTGCCATTATAGCAGCACGAGAAGCTCGCAGTGACAATGTTTACGCATACGTTTACACATGAATAAGACAATAATATGATTAAGTTGCTTCTTGAAAGTTTTCATTTGACAAGTTACTATATATATATATATATATATATATACACACACACACACACACACACACACACACACACACGCACATATATATATATATATATATATATATATATATATATATATATATATACACGTGATTGTCATTACAGCATTTGACGATAGTTTCCTTCAGAGTTCACACAACAACAGTTAGTTTTCGTTATGTCAAATGTAATTTTGGGCATTTCGTTTTTAAGTTCAACTGCAGTTAATTTCTCCTCATTTGAATCATGTCCATCTATGAAAACACTCTCTTGC

Associated Phenotype:

Not determined