ZMP

ENSDARG00000087569

Ensembl ID:

ENSDARG00000087569

Human Orthologue:

OLFM4

Human Description:

olfactomedin 4 [Source:HGNC Symbol;Acc:17190]

Mouse Orthologues:

E030002O03Rik, Olfm4

Mouse Descriptions:

RIKEN cDNA E030002O03 gene Gene [Source:MGI Symbol;Acc:MGI:2443346]
olfactomedin 4 Gene [Source:MGI Symbol;Acc:MGI:2685142]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa44248	Nonsense	Mutation detected in F1 DNA	Not yet available
sa9650	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa44248

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124557	Nonsense	219	375	5	7

Genomic Location (Zv9):

Chromosome 25 (position 12751591)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	13102868
GRCz11	25	13199373

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCAAGTCGTATATTTCTGGTGCCTGGGGCCGCGATGCTCTACTAACGGAT[A/T]AGGAGCGTTATTGGGAACACTGTCTAGTGAGTGGACACAAGGATGGCCAC

Long Flanking Sequence:

TTGGTGACATGTCTGTGGGTGTCACCATTCAAAATGAAAGCACGGCTTTTCGCTTATGATGTCTTTATTGCTCATCATCATAAATTAAAATAAGGACGCATGACAGCTAAGCGGGACTCTGCAAAATAAACCCTGAAACTCTGACCAATGTGAGAACAGTTTACTACCATGTGACTTGTTTAGCTCTTTTGGTCCATTTAAAACTGCCGTGAGAAAGCGAACCGCACCAAGAAAAAGAGCAACATTGTAGCAATGTTAATCCCTGTTTTGGAACAAATGAATTGATTCACTTGTGTGGAAGCACCCCTAGAGAACCTACTTGCTACTCAAATGCTATTTTCAGAATTATAAAACTCCACAATTATTGAAAGTACATTTTTGCAGGTTCTTGTCATCAGCGCATCATGACCAGAATAAGTTCTCCAGTTGTCACCAAGCTCAATTCCATCAGCAAGTCGTATATTTCTGGTGCCTGGGGCCGCGATGCTCTACTAACGGAT[A/T]AGGAGCGTTATTGGGAACACTGTCTAGTGAGTGGACACAAGGATGGCCACACTATCAGAATGTACAACTCATATGAAGACTTCATGGCTAACAGGAACTACAAGGATGAACAGATTGCACCATCTTACAGCAGTAAAAATGCAGTTCGAGGTTCTGGCACTATACTCTACAACAATACCGTATATTATCAATGCTACGACAAAGCTGAAATCTGTAGCTTCGATATTACAAGTCAATCAACCAAGCGTATGAAATTGGATGGTGCCGGAATTGACAACAAATTCCCGTTCTGCTACTACAGCTGTCGTGATTGGACAGACATCGACCTGGAGGCTGACAGAGATGCAGTGTGGGTGATTTATGCCACTGAGGAGAATCATGGGAACATCATTTTGAGTCGCTTAGACCCGGTGGAGCTCAATATCACACACACATTTAAGACGCATCTCTTTAAGAGGTCAGTGAGCAGCACGTTTATGGTGTGTGGAGTCCTTTATGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9650

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
Order Allele From EZRC

Mutation:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000124557	Nonsense	275	375	5	7

Genomic Location (Zv9):

Chromosome 25 (position 12751761)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	13102698
GRCz11	25	13199203

KASP Assay ID:

2261-9453.1 (used for ordering genotyping assays)

KASP Sequence:

CCATCTTACAGCAGTRAAAATGCAGTTCGAGGTTCTGGCACTATACTCTA[C/A]AACAAYACCGTATATTATCAMTGCYACGACAAAGCTGAAATCTGTAGYTT

Long Flanking Sequence:

GTGACTTGTTTAGCTCTTTTGGTCCATTTAAAACTGCCGTGAGAAAGCGAACCGCACCAAGAAAAAGAGCAACATTGTAGCAATGTTAATCCCTGTTTTGGAACAAATGAATTGATTCACTTGTGTGGAAGCACCCCTAGAGAACCTACTTGCTACTCAAATGCTATTTTCAGAATTATAAAACTCCACAATTATTGAAAGTACATTTTTGCAGGTTCTTGTCATCAGCGCATCATGACCAGAATAAGTTCTCCAGTTGTCACCAAGCTCAATTCCATCAGCAAGTCGTATATTTCTGGTGCCTGGGGCCGCGATGCTCTACTAACGGATAAGGAGCGTTATTGGGAACACTGTCTAGTGAGTGGACACAAGGATGGCCACACTATCAGAATGTACAACTCATATGAAGACTTCATGGCTAACAGGAACTACAAGGATGAACAGATTGCACCATCTTACAGCAGTAAAAATGCAGTTCGAGGTTCTGGCACTATACTCTA[C/A]AACAATACCGTATATTATCAATGCTACGACAAAGCTGAAATCTGTAGCTTCGATATTACAAGTCAATCAACCAAGCGTATGAAATTGGATGGTGCCGGAATTGACAACAAATTCCCGTTCTGCTACTACAGCTGTCGTGATTGGACAGACATCGACCTGGAGGCTGACAGAGATGCAGTGTGGGTGATTTATGCCACTGAGGAGAATCATGGGAACATCATTTTGAGTCGCTTAGACCCGGTGGAGCTCAATATCACACACACATTTAAGACGCATCTCTTTAAGAGGTCAGTGAGCAGCACGTTTATGGTGTGTGGAGTCCTTTATGCAACACGTTATGTTAATACTTATCAAGAGGAAGTGTTTTATGCTTTCGATACAACCACTGGTCAAGAGATAAACTCTCTTTCTTTGCCTTTCGAGAAGGTTGCTGCTGGAATAGCCAATCTGAACTACAATCCTGTTGACAGGAGGCTTTACATGTATAATGATGGCTATCT

Associated Phenotype:

Not determined