ZMP

OMG (2 of 2)

Ensembl ID:

ENSDARG00000089444

Description:

oligodendrocyte myelin glycoprotein [Source:HGNC Symbol;Acc:8135]

Human Orthologue:

OMG

Human Description:

oligodendrocyte myelin glycoprotein [Source:HGNC Symbol;Acc:8135]

Mouse Orthologue:

Omg

Mouse Description:

oligodendrocyte myelin glycoprotein Gene [Source:MGI Symbol;Acc:MGI:106586]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15202	Nonsense	Available for shipment	Available now
sa42570	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15202

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
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Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000129474	Nonsense	111	395	2	2

Genomic Location (Zv9):

Chromosome 15 (position 30217278)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	31038985
GRCz11	15	30919726

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

KCACCACCTTCCTGTCGGTCTGCCAAGAGCTCTTTGGGATATACGTGCCT[C/A]AGGAAAYTACATCCGCCAACTGGAGAAGAMCRATACAGCCTACCACTGGA

Long Flanking Sequence:

CAGTAACAACAGATATTAAGCCGACAGTCAACTAATACTCAAAAGGACGATCAAAATAAAGTTTAACCTTTCATTTTTTAACTAGTAAGCCTGATGCGAATACAGTTTTTTTGGGGGAAAAAAAGACCTTAAAAATTTGTTTTGTGACAAGTATCCCTTTGTTTTGTTTTTTTACAGGAAAGCCCAAATTGCACCTGCCTCAATGCCGGCTAACCTGTTGCTCCTCCTCCTTTTTGGGGTGCGTGTTCTGGCCATTTGCCCACCAATGTGCACCTGTAGCAGAGGCCATAGAGTGGTAGACTGCTCTGCGCGAGGGTTGGCAATACTTCCCGAAAGCTTGCAGCACAACATTCATTTCCTCAACTTGTCTTATAACAGGATCCAAAATCTTGATGGGCTCCTCAAACATTTCGACCACTTAAGAACTCTGGACATCTCCTATAACCATCTGCACCACCTTCCTGTCGGTCTGCCAAGAGCTCTTTGGGATATACGTGCCT[C/A]AGGAAACTACATCCGCCAACTGGAGAAGAACGATACAGCCTACCACTGGAACCTTCAAAATCTGGATTTGTCATTCAACTTGCTGGAACGTGCAGTTTTGATTAACAACACACTGTCCAATCTACAATCTCTTAATCTTAGTCATAACAAATTCTGGACTGTCCCGACGAACATGCCCTACAATTTGGAAATGGTGGACCTTTCTCACAACTACTTGCTGCAGATCCTGCCAGGTTCTCTTGATCGCCTTCCTAGATTGAAGAGATTTTACCTGCATGCCAATCGCTTCACATCATTAAGCAAAGATATTTTTAATCAACTGGATGATCTGCAGCTCCTCACACTCGGAGACAACCCTTGGGCTTGTGAAGATGAGGAGAATATAAACCACCTGCTGACTTGGATGCAAAAAACCCCTGCAAAGGTTTTGGGCTGCCCCTGCTACACTAGACCTACATGTGGCGAGGTCCACCTGGCCACCAGGAGAACCTGGCACTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42570

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
ENSDART00000129474	Nonsense	234	395	2	2

Genomic Location (Zv9):

Chromosome 15 (position 30217646)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	31039353
GRCz11	15	30920094

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTGGATGATCTGCAGCTCCTCACACTCGGAGACAACCCTTGGGCTTGT[G/T]AAGATGAGGAGAATATAAACCACCTGCTGACTTGGATGCAAAAAACCCCT

Long Flanking Sequence:

CTTATAACAGGATCCAAAATCTTGATGGGCTCCTCAAACATTTCGACCACTTAAGAACTCTGGACATCTCCTATAACCATCTGCACCACCTTCCTGTCGGTCTGCCAAGAGCTCTTTGGGATATACGTGCCTCAGGAAACTACATCCGCCAACTGGAGAAGAACGATACAGCCTACCACTGGAACCTTCAAAATCTGGATTTGTCATTCAACTTGCTGGAACGTGCAGTTTTGATTAACAACACACTGTCCAATCTACAATCTCTTAATCTTAGTCATAACAAATTCTGGACTGTCCCGACGAACATGCCCTACAATTTGGAAATGGTGGACCTTTCTCACAACTACTTGCTGCAGATCCTGCCAGGTTCTCTTGATCGCCTTCCTAGATTGAAGAGATTTTACCTGCATGCCAATCGCTTCACATCATTAAGCAAAGATATTTTTAATCAACTGGATGATCTGCAGCTCCTCACACTCGGAGACAACCCTTGGGCTTGT[G/T]AAGATGAGGAGAATATAAACCACCTGCTGACTTGGATGCAAAAAACCCCTGCAAAGGTTTTGGGCTGCCCCTGCTACACTAGACCTACATGTGGCGAGGTCCACCTGGCCACCAGGAGAACCTGGCACTCAGCCGCATTCACAGAACAACCGTTAGGTGCTGATGCTCGCCATCCTGGCCACAGAGTCCCACTGCATGCAGTTACTTCTGGGTACTTGTCCAAGTCAGCCCAGTTGAATGTGGCTCTCAATGCAAATGCAATGAATACTTCTGAGGCAGGCGAGCAGGTACTGATCTTGGGTGGAGGATTTCGTACATCAACTCCACATAGCCTGTCCACACAGTCAAGCACAACAATTCGAACACGTAGCACCAAGAAGGCCCATCCAGGCAAAGCTCAGAGCACAAGCCATCAAATCCACAAACGCAGCTTTGAAACCACCATCTGGAGCCTTTTATGTACTGTTGTCATTCTCCGTGCTTTGTGATTCTGCATAATC

Associated Phenotype:

Not determined