ZMP

snx12

Ensembl ID:

ENSDARG00000019060

ZFIN ID:

ZDB-GENE-040426-787

Description:

sorting nexin 12 isoform 1 [Source:RefSeq peptide;Acc:NP_957417]

Human Orthologue:

SNX12

Human Description:

sorting nexin 12 [Source:HGNC Symbol;Acc:14976]

Mouse Orthologue:

Snx12

Mouse Description:

sorting nexin 12 Gene [Source:MGI Symbol;Acc:MGI:1919331]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23971	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa23971

Status:

Available for shipment
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Availability:

Order Allele From ZIRC
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Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000003335	Essential Splice Site	55	162	None	4
ENSDART00000126678	Essential Splice Site	55	153	None	4
ENSDART00000133478	Essential Splice Site	55	160	None	6
ENSDART00000140811	Essential Splice Site	55	283	None	5
ENSDART00000147375	Essential Splice Site	55	151	None	6

Genomic Location (Zv9):

Chromosome 21 (position 29215295)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	30434539
GRCz11	21	30471234

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATAGGAGTCGGTCGTAATCGCTTCACCACCTACGAAGTCCGGATGAGGG[T/A]AGGCCGAATAACCGTAATTGTGTGTTTGTTCCGGAGAGGCTGCGGCTCGG

Long Flanking Sequence:

GGAGCCCTGAAGAGCCCACCCTTTCAAGTTTATCTCAAACCTGATAGGTCAATCTCCTGTCAATCATCAAAAAACAGACCATCTATTGGATAGCTCAGTAAAAATAGGCGGGTCATAAAGTAGGTCTCCCAAACTGCTGCACATATCATCGCATCGGGGAGAAGCGCAGGATTTCCTGTGGCATTGCTGAAGTGGACGCATCCAAGTTTTACATTCGAAGAAGTACCTAGCCCACTTTCACCAACGTCGATTTAATGTCTTAACCAAAACCATCTCATTCGTACGTGCTCAAGACTACACCTCGACGTAGTTAGTCTGCAAGAAGTCTTCGAAGATGTCCGAAGCCACAGTGGCCGATACTCGCCGGTTAAACTCCAAACCGCAGGATCTGACGGACGCCTACGGCCCTCCCAGCAACTTTCTGGAAATCGACGTGTACGACCCGCAGACTATAGGAGTCGGTCGTAATCGCTTCACCACCTACGAAGTCCGGATGAGGG[T/A]AGGCCGAATAACCGTAATTGTGTGTTTGTTCCGGAGAGGCTGCGGCTCGGTTCGGCCTAACCATTAGTTAGCCTGCGAGCTAACATGCTAACTAACACCCCATTCGAACTTAAAGACTGTGAAGCTTCACAAAAGCGGGTTATATTTGATAGAACTGCAATTTTTTTGTCTAAATATTTTTTCTTAGTGCGCATGTCTGATTTAGGCAGCCTGTCGGATAGACATTGAGCTTATTTGGCTGTTGTTGTTATTCTGTCCTTCAGCAACATTTACTGTCGAACTGTTGTTTTGCATGTCATAAAATGTATAATTTGATGCGTTATTGTTACACTTGTATCAATTTATTAATGTAGTGTATTAGATGTATTCGAGAAAGCGTATTGTGTACAGTTTTATCATCGACCGATGCTAATGTAATGATTTATTCTGCGTTCTCCATTGAAATGCAGACAAATCTTCCCATTTTTAAACTGAAGGAGTCGGTTGTCAGACGAAGATAC

Associated Phenotype:

Not determined