ZMP

LOC556262

Ensembl ID:

ENSDARG00000077349

Human Orthologue:

SORCS3

Human Description:

sortilin-related VPS10 domain containing receptor 3 [Source:HGNC Symbol;Acc:16699]

Mouse Orthologue:

Sorcs3

Mouse Description:

sortilin-related VPS10 domain containing receptor 3 Gene [Source:MGI Symbol;Acc:MGI:1913923]

Alleles

There are 6 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32145	Nonsense	Available for shipment	Available now
sa23046	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa32145

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114236	Nonsense	119	1018	4	27

Genomic Location (Zv9):

Chromosome 17 (position 20211126)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	20361137
GRCz11	17	20380973

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTGTTTCTCTTTTGGCTGTAGCTCTACAGCTCTGTGGACTTCGGGAAG[A/T]AGTGGATTCTTGTTCACGAGCGAGTAACTCCAGGGAGATTTTACTGGTAC

Long Flanking Sequence:

ATCAGAACGATGCTGAGCTATCTGTACGTCTGTCCGACCAATAAGAGAAAGGTGAGTGTCTTCAAAACGCATGAAAGATATGGACGTATAAAACTGTCAGAGAGCAAATATCCAGCTAATAAAACTCATGCTCCCACTCTTTCTTGTCCTCAGATCCTGATTTTATCCGATCCAGAGGTGGAGAGTAGTTTACTTATCAGTTCTGACGAAGGAGCCTCGTTTCAAAAGTTCAATATTAACTTCTACATCATGAGTCTTCTGTTTCACCCTACGCAGGAGAATTGGATACTGGCCTATAGCCACGATCAGAGGGTATACACACACACACAGACATGCTCGCACAGCCTCAAGAGGGCCTGCTGAACAATTAAAAGCAGATAATGTGGATAATTAAGTGCGAGCGAGATAATTACCTTTGTTGGCTGTAGTTAGGGATCTTAAAGTGAATGTGTCTGTTTCTCTTTTGGCTGTAGCTCTACAGCTCTGTGGACTTCGGGAAG[A/T]AGTGGATTCTTGTTCACGAGCGAGTAACTCCAGGGAGATTTTACTGGTACGACACACACATACATACACAATCTTTTTTTTTTTTACTGATCATCAATCTCATATAACACGCCTACAGTGCAATTTCACACTGAAAATTAATCTGACTGCAAGAATACACCTGCACACACACACTCACGCACAATCACATACTGAAAATTAATCCAATATTAAACCCACTCTCTACATCCACTGACACTGATAAACTTACACACACACACAAACACACACACACACTGTCTATGTCTCTTTCCCTTCTTTCTTTCTATCTATCTATCTCGCTGTCATGTCACTTCTCTCTCCCCTGTGCTTCATATTCCCGTACGTGTGGAATTTTGATCAGGTTTTATATTTTAATCCCATCAGTGTGAGTTTGTGTGTTTGTGTGTGGGGTGCATCAGAATAACTGGTTGCCTGTCACATGCTCGATGAGCTGTGGAGACAACACGTCTTCACCTCTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23046

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114236	Essential Splice Site	461	1018	13	27

Genomic Location (Zv9):

Chromosome 17 (position 20176298)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	20326309
GRCz11	17	20346145

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGTCGACGGGGTTTTGATGACTCCAGAGACTGAGAATCGCATCATTAC[G/T]TAAGAATCATGTTCTCTGCCACACTGATCTCAATGGTCCAGAAGGGGTCA

Long Flanking Sequence:

CGGAAAGGAAGTAGAGTAAAGAGATGCGACACAAAAGCACAACGAAATGCAAAATAGATTGAATGTATAATGAGACTTCATCTGCATTTTACATGACTAATAATGATTAGAGGCTAATGTAAACACAACTGGGGTATGGTGAATAATTTTGTCCTGCTATTTTTCAACGAGCATATCTTAGATTTGATTTTAATGTAATTATGCAGATGCAGCCCACATTAAATGTTAATGCGGTGACTCCGCAACGACTTGTTTTTGTGCATCTGCAAAATATTCTCAGATGACTGAACAAATGCATCTTCTATTTTTATGTCTTTGTCAAATGTGCACAGTACAGTATATAAATCAGACGAGTGCTTTGCCAATGATATGATTTGTGTATGTGTGTGTAGGATTAGTCTGGATGAAGGCCGCCATTGGGACAAACTCAGCTTTTCGTCGACACCCTTATTTGTCGACGGGGTTTTGATGACTCCAGAGACTGAGAATCGCATCATTAC[G/T]TAAGAATCATGTTCTCTGCCACACTGATCTCAATGGTCCAGAAGGGGTCAGTAATGAACCTTCACCTACTGGGATCATTATTATCAGATTAAGTGTTTGCATTTGCATGTCTGGATGATGATCATTAGCACTGCTGTTTTACTAACACTTCCTTCTTATTAGTTCTTTATGGATTTTATGGCGCTAGAAGTCACTTTGTCAACTGTAAAGAATAAAAGTAAACAGATCCTGTTGTTTTCAAGCATCTCTGTCTGTCCTCGTAGATTCTTCGGGCACTTTAGTTACCACTCCGACTGGCAGCTGATAAAGATTGACTACAGCTCCCTGTTTGGGCGGAAATGCACAGACGGAGACTTTCAGACATGGCACCTCCATAACAAGGTTGTCACCTCACATTTTTCAGTAGCGCCTTACTGTTCGCTCTCAACAGCAATGCACTAATTCACTCACTCAACATTCAACATGAGTTTCTTTTGGCACTGAGTTCGCTAGTAATTAGG

Associated Phenotype:

Not determined