Busch Lab

ZMP

LOC797571

Ensembl ID:
ENSDARG00000074322
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
sa24621 Essential Splice Site Available for shipment Available now
sa30216 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24621
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109937 Essential Splice Site 133 462 3 5
Genomic Location (Zv9):
Chromosome 25 (position 12758875)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 13095584
GRCz11 25 13192089
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAACAACCAACAACTATAAGCAGCTCGGTGTAGAGACTGCAGCAGAGG[T/C]GAATTCATGCACAGCATAGCATTTTTTAGAGCACAATATCATGTTTCATA
Long Flanking Sequence:
AATTAACTGTTTTTTCATCTACACAGTCAGTGAGAGGGAAAGACTGTGTGTGTGATCTACAATATTCAGATCCTGATTTCCCTGAGAATAAACTCGACAACGTTGAGCTCACTGCTTCACAATGCACTGGAAACATCACTTCAGAAAAGGTACAAAAAAATTTATAGTATTGTTCTCTTTATAAATCTAAATCAGGCTTGTATGATAAAATTGGACTTTTCTTAGTTTTATTTTACAATCTGTAATTGAAAGAAATTGTTTTCTTTTCAAATATGTTTAGATGACGGAGATTGACAGGCTTGTGTTGGGTCTACAACACCGCATCTGGCAGCTTGTGGACAACGTTTCCATGCTGGAAAAAGAAGACAACGGAAATCTGTACGCAGCTGTATCTCTGCGCATTATTGAATTAGAGTTAGCCGAGATTCAAGACCTTCTGGACAAACTTAACAAAACAACCAACAACTATAAGCAGCTCGGTGTAGAGACTGCAGCAGAGG[T/C]GAATTCATGCACAGCATAGCATTTTTTAGAGCACAATATCATGTTTCATATCATTCGATATTGATAATTATTGGATGTTTTTTAACAACACATATAGGATTGTTAGGATTTTTATATTTTAACCACTTTATTTTAATTTACCAACATTACTAAGGCAAATAGTTTTAATAGTCAAAAACAAAAGTAATTAAACTATTTGATATTAAAATAAAGACAAGTGTTTAAGAGACTCAAACTTATACAACTTATAAAATATTACAACTTGCGTGCAATGGTGAAGGTAGATCTACATCTGTAAGGTGTGAATAATAATGATACAGTAAACCTCAAACTCTGTAAACAAAACAAATTATAATAATGAAATCTGAGCTTTCAATTGAAGGAACTAATTATCATTATTCAAATACATGCTGAACATTACAAATAGTTAAGTTGAATGACTACATTACCCCTATACTAAAAACTCTTTCAGATGGGGAGCTAGTGGCTGGGATGCACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30216
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000109937 Nonsense 419 462 5 5
Genomic Location (Zv9):
Chromosome 25 (position 12756574)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 13097885
GRCz11 25 13194390
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGAGGAGATCTTTTACGCTTATGACACCAAAACCAACAAAGAGCGCTA[T/G]GATTTAAGAATTAAAATTAAGAAGATGCAGGCTAATATTAAGTTTATGAA
Long Flanking Sequence:
TTTATATTAGGTATAGTACCAACAGATACATATATATCAAGCTCAAATCCTACAACAAATACGATTCAGGGTCCAAACATGATCATGTACGGCAATGCTCTCTACTATAACTGCTACAACATATACTCTGTCTGTCAGTTCAACCTGACCACTAAAACTGTCAGTACTGTGGCTTTACCCAATGATGCAGGTTTTAATAACAAGTTTCCATTCGGACATCTCGGCACAACATACAGCTACACAGACATGGATTTTGTCACAGATGAATCAGGCGTCTATGTTATATACGCAACCACTAGCAACTTTGGAAATGTGGTGATCAGTAAAGTTGAGACTAGTAACCCGCCTGTTTTGGGCCAAACTTGGTCCACTTCTCTTCACAAAAAGACCGTCACAAACACTTTCATGGTGTGCGGTGTGCTTTATGCGACTCGATACCTGGATCAAGTAACAGAGGAGATCTTTTACGCTTATGACACCAAAACCAACAAAGAGCGCTA[T/G]GATTTAAGAATTAAAATTAAGAAGATGCAGGCTAATATTAAGTTTATGAATTATGACCCCAGGGATCATTTGCTGTATGTCTTCAATGATGCCTACATTGTGACTTATGAAACCAAGTTTGAGAGAGTTTAAGATTAACAATATCCTGCCTTTTATTCTCTTTTAAATGTAATGATTTGACGTATTTGGTATCTATGGTTGATATGTAATGCAAATGGAAAAACTTTTTGATATGTATCACACAACTTGGTCCTTTAAATAAAGAGAAAGTGAAAATACTGATACATCTGCGTGCTTACATTATGCTGCTTTTAAATATTCATGAATGCGATGTAGTAACTCAATGCATGCTTATGCTGCCCTCTGCTGGGTGTGTAATTTCACTTGTTTTACTTGTGAAGGCGATTAAGGGTTATGTCCAAACATTTATAAAAGACATTGTATTGAAAAGGACTTACCATGTGTCATGAACCATGAGACCACTCATCAGAGTTGTAGTA
Associated Phenotype:
Not determined