ZMP

os9

Ensembl ID:

ENSDARG00000020301

ZFIN ID:

ZDB-GENE-060929-32

Description:

protein OS-9 [Source:RefSeq peptide;Acc:NP_001068576]

Human Orthologue:

OS9

Human Description:

osteosarcoma amplified 9, endoplasmic reticulum lectin [Source:HGNC Symbol;Acc:16994]

Mouse Orthologue:

Os9

Mouse Description:

amplified in osteosarcoma Gene [Source:MGI Symbol;Acc:MGI:1924301]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa40745	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38566	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa40745

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113440	Essential Splice Site	123	669	None	15
ENSDART00000133305	Essential Splice Site	157	703	None	15

The following transcripts of ENSDARG00000020301 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 6 (position 39146265)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39217865
GRCz11	6	39215401

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTATATATTTTGTAGTTACAAAATTAAAATCTTGTTGATCTTTTTTTTTC[A/C]GGCATCTAAGCAGCATAAGCTGAAGAGGTATCACAGTCAGTCATATGTCA

Long Flanking Sequence:

ACCACTTAGAAGGCAGGTTAAATCTTTTATCTAATGTGTCTTGGATAAATTGAGTTTTACATGGTCTAAAAAATATATATGCACTGCCTGTATAAACATGTTTTTTATTAGTAGATGGAAAGGAATTTAGAGAATTTAGGACAGAAGCCTTTCAGGAAAATGCACTGCCTATAAATATATACTATTAAATATTTCAAGATGTTTGAAATGTGTTCCCTATATGTGATCGCAGATTCGGAGATCAAGGGAGATGTACTGTTTTTGGGATATTATGATACAGAGTTTGACTGGACGAATGAAACTGCAAAGGTAAGGTCAGGTTTGTTAATCTTGATTTGCTTGTCCTAATAAAATGTCTGTAAATGTTGTCAATTCAAATTAGGAATTCTGATACTAGCAGTAAATATTTTTTATTAACCACTTTTATGTTAACAAGTCTGTAGTTATCTTCTATATATTTTGTAGTTACAAAATTAAAATCTTGTTGATCTTTTTTTTTC[A/C]GGCATCTAAGCAGCATAAGCTGAAGAGGTATCACAGTCAGTCATATGTCAATGGCTCAAAATGTGACTTAAACGGCAGTCCCAGAGAGACGGAAGTCAGAGTAAGATACTAAGTGCCATATTCCAGACTATAGAGAAAAATAATGAAGAAAGAGTATTATTGAAGTCAGTCTAATGGCTAACAATAAACAATAAGGACACTAGTTAACTGTTGTGACTAGTCTTCTTAATTCTGCTGCTGTATGCACACACACTGTAGAATACCTTCACTATACAGATGTTGAGCTCATTAGACCTCAAGTAATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATACATACATATATACATACATACATACATACATACATACATACACACACACAATTTAAGGTTAGATAGATCCTTAAATGGATCAATCCTAGGTAGATCAAATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38566

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113440	Nonsense	324	669	9	15
ENSDART00000133305	Nonsense	358	703	9	15

The following transcripts of ENSDARG00000020301 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 6 (position 39141861)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	6	39213461
GRCz11	6	39210997

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTACAACTCTCTTACAGACCCCTCAGGAGCCACAGGACAACCAATTACAT[G/T]AAAATGATTGTAAGACAATTATTTTAATTAAACATAAAGTAACTATGTTG

Long Flanking Sequence:

GTCACCAATGTATATGTTTATCATATTAGTTTTTGACCTACTAACTACAAAATGAATTAAAATGGCAATCTCTGACATTGTATTACAGTATTTATTTTCACATCTTTTTATAAAACATTCAGGTGTGTCGTCTTGTGCATGTATAGTTTGTAGCTTTTTTGTTTATTATTTCAGTCTTGCTTTTACATTCTTGTTCTCTTCTTTAAGCTGTCTCTTTAGCAGCTTCCATGCAGCCTTCAAACAAATATCTGTGTATGTGTGATATAACAGAGGGTGAAGTTGCTGAGAAGTCGACGAGTGAAGAGCCAGAGGACAAAGACTTCTGGGAAGGAGTTACCAAACCAGCACACACAAAGCCAAGCACACCTGACACAGAGGTACAAACTGTCTGGAAATGAACATAATGTGAACCAGACATCTTCATAGTGAGATTTGGTCATTTACTTCATTTTACAACTCTCTTACAGACCCCTCAGGAGCCACAGGACAACCAATTACAT[G/T]AAAATGATTGTAAGACAATTATTTTAATTAAACATAAAGTAACTATGTTGCATAAGAAGTTTTTTTTTCTTGAATCAAAAATGTAGCATCAGTTTTATTTAGTTTATTAATGAGTACCATACACAACCAGAATTACAGTATCTATGAAGCTAAAATTGGTCTTGATTTAAGGGTGATAAATTTATAGATGTTATGTAACAAGTAAAGCTGTGCTGTACAATCAAAACTTTATTTTTAACAATTTGTAAAATTTCTGCCATGAAACTATGCGCAAGCAGGCTGATTGGTTACCTAATCTGCCCCTGCGTCATGAGTTGAAATGCTCTGCGTCATTTTACGCTGTCAAGCTGCTGCATGTTTTTGGAGACCCTCTTCCACCCCAGCTCCACCTGTGTTTGGATCTGCTATGGCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAATTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAG

Associated Phenotype:

Not determined