ZMP

LOC569427

Ensembl ID:

ENSDARG00000087625

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 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23196	Essential Splice Site	Available for shipment	Available now
sa36545	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23196

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127225	Essential Splice Site	19	466	2	5

Genomic Location (Zv9):

Chromosome 17 (position 53123353)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	52508920
GRCz11	17	52595220

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGAAGACATTATGAGTAGAAAGGTTGATGTTTTCCCTTGTGTCCTGCA[G/A]GCAGTGAGCCTCTGGGCTGAAGGCAGTGCCTCCAGTGGAGAGTGCATCTG

Long Flanking Sequence:

CCTTCTTCAATACACCTGCCTTGAAGTCTCTAGTATACCTAGCAGGGGTGTCCAAATTTTGCCCTGAAGGGCGGGTGTCCTGCATATAGTTGAGCTCCAACTTTCTTCAATACACCTGCCTGGAAGTTTCATGTATACCTAGAAAGAGCTTGATTAGCTGGTTCAGGTGTGTCTAAATGGGGTTAGAACTAACCTCTGCAGGACACCGGACCTCCAGGACCAAATTTGGGCACCACTGACCTAGAAAGAGCTTGATTAGCTGGTTCAGTTGTGTCAAATTGGGATTGAAACAATCCTCCAGGACCGAGTGTGAGCACCCTGGTTTAGATATTCAATTGATTCATGTGACTACTACAGTTAAGTGTGTTGGAGTGAACTCTATAGGGTTGCTACTCTCCAGTGTGACACCCCTGCCCTAATCCCTTCACCTTTAATCTCCAGAGAGACATCTTTGAAGACATTATGAGTAGAAAGGTTGATGTTTTCCCTTGTGTCCTGCA[G/A]GCAGTGAGCCTCTGGGCTGAAGGCAGTGCCTCCAGTGGAGAGTGCATCTGTGAAGCTTTCCTGCCCAACAGCACATTCCCAATCGGACAGCTCGTCCTGCTGGAGAGCACAGCCGTGGAGATCAAATACAAGCTGGAAATGGAGATTAGTAAGGTGTGGTACAATCTCAGAAACAATCACAGTCATTAGCTATGCTTGTGAATTAAACTTACGTGTAAAACTGGGATATTGCATAAAACATTCCACAATGGTGTTTGTTCTTCTCTGATAAATAAGTTGCGCCTCAGAAGACAAAGGTGAAACGCAATGAACGTGGTGAACGGAGGCGTGCACTTTCTGGTATGCATGCTGGGGTCAATTCACTGCGTTTCCATCTTAGTCTATCCGCAATTTTTTTAATCGAATAAACTGTTTATCCTTCTCAGTTGTGTGCAGACGTTTTCTATGTGCATTTTCAAAATGTTTGCAAAGCTTGGCATTTCCGTTGGACATAACAATTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36545

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127225	Nonsense	363	466	5	5

Genomic Location (Zv9):

Chromosome 17 (position 53118501)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	52504068
GRCz11	17	52590368

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACGGCGGACTCGAAGGGTAAACTAGTCCTAGGGAAGATCAATGAACAGT[C/A]ATTCGCAGTCGAGACGGTCTTTCAGACCAGTGTTTATAAACCCTCTGTCG

Long Flanking Sequence:

AATCAGACGAATCAGCAAGCCTATCGTGAGCCAGCTGAATGCAGACCTGAACGGAGCCTTCAAGTATGGTGGATGGGGAAAGGACTCCAAGCCCTTGTCCGGCTCAGAGAGCATGTACTGGTACTCGGGCAGCTCAGACACGCTGGTCAGCAAAATCTCCCAGTACTCGGCCTACTACACACTGATCACCAGGCAGAGCTTTAAAGCTCATCTGCTGTATGTGGATCGCCAGTACGACTGGCGCGGCGCTGGAAACAACTATGTAGTGAGGGAAAACAACCTGTATTATCAGTACAGAAGCCCTTTCGCGATGGCGAAGTTCAACATGACCAGTGCAAAAGTGGAGACCAAGGTGGTTCCCAAAGCCAGCGCCCAATTCTCCTACCATTACTCCGCCAACCAGAACCTGGACTTCGCCGCTGATGAGTCCGGCCTGTGGGTGACGTACGCCACGGCGGACTCGAAGGGTAAACTAGTCCTAGGGAAGATCAATGAACAGT[C/A]ATTCGCAGTCGAGACGGTCTTTCAGACCAGTGTTTATAAACCCTCTGTCGGCAACACTTTCATGGTGTGTGGGGTTTTATATGCCACAAGGTCTGTAGACACTAAAACCGAGGAGATCTTTTACACCTTTGACACCCGCACCGAAAAGGAAAGCTATGTTAGCATCCCCTTTGAGAAGTTCCATGACTTCTACTCTTACTTAGACTACAACCCCACCGATCAGAAACTGTACATGTTCAACAACGGTTACTACGTCAGCTATCATGTGTGGTTCAACCAGGAGGCCTCAGCAGATAAAAGCCTCGTCGACTGAGCGACTTGAGAATGTTGAATATGATGTTGTTCACCTGATGAACACAGAACAGCAGTGAACGTGACGTGTTTCTGTTTGTGTAATAAAGTTTGATGCGCAGAATGATGCATGTGTGCAGTTTTGTCTTTATATTGAATGTGATTTTATACAATTTCATTTCTTTTCATGAGGTCACTAGTACTTTGTT

Associated Phenotype:

Not determined