Busch Lab

ZMP

LOC100330530

Ensembl ID:
ENSDARG00000039941
Human Orthologue:
OLFML2A
Human Description:
olfactomedin-like 2A [Source:HGNC Symbol;Acc:27270]
Mouse Orthologue:
Olfml2a
Mouse Description:
olfactomedin-like 2A Gene [Source:MGI Symbol;Acc:MGI:2444741]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa39523 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44431 Nonsense Mutation detected in F1 DNA Not yet available
sa19382 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa39523
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078436 Essential Splice Site 42 670 1 8
Genomic Location (Zv9):
Chromosome Zv9_NA921 (position 67042)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 8103826
GRCz11 21 8196365
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGGCGTGCTTGCTCATGATGTCCAGTCATGTTTCATCTCAGAGCAAG[G/T]TAAGAAAAAGTTCAAGATGAAAAACTAGCCTTGCATTCGTGCGCATTTAC
Long Flanking Sequence:
ACTGTTTCAAGAAAAGAGTCAAACCAATGGAGAAAAACTGTATTAAAGCTTGAACAATAACAGAACAGCATTTTTACTTTTAAATCTAAACAAAAGACTGAGATTACAATTAATTTGGATTCACAATATTTCCATCTAAACTAATAATAATAACAACAATTCAAAATTAGGCTATATAATTAATATTAAGGCACAAACTCATTAATTCAACGAGTTGTTAAAATCACATTCATCTTTTGTTGCCGCTGTTGTCCAGCAGGTGGAGGCATTGCTATAAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGGTCATGATGATGATGATGATGGTGAGTCTGTAGTCTTTACAGTCGCATGAACGCGCATCTCACACACTCGCACAGAGGAGCTTCACAGTCACACACCGCCGAGATGTGGAGGATTGTGGAGCTCGTGGCGTGCTTGCTCATGATGTCCAGTCATGTTTCATCTCAGAGCAAG[G/T]TAAGAAAAAGTTCAAGATGAAAAACTAGCCTTGCATTCGTGCGCATTTACTATATAAGCTTGCAACAATGTTTATTCGCTTACTGTAATATCACTCGTTAATTCTAAATCAGTTATTTGTTTCATGCATACTTTACTATAAACCTGCATGTAATAATTCATAAGAACAGTATCTATTTTAGTGAGTTTAATATTAATTAATTTAGATTTTTTCTTAAATAAAAGTTGTAATTAGTCTCTGAATGAGTTAGCCTAAACATTGTCTGCTGGAAGTTTAGTCTATGCAATGGCTTGTTTTCAGGGTTGTACTGTAGATAACAGCGGATATATGTGATCATGTGCACCTCCGTTCAGTGCATGCTCTGTTTATACTCCGTTGAAATGATTATAAGCACGGGTGGTTTCTTTGAAAGAGCGGGGATTAAACTCTTCAGTGGGGCACACACACTGCGCACAACGCACCGCTGGCACGAGTTCAAAGCTCTCGGGTTTATGACTGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44431
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078436 Nonsense 228 670 4 8
Genomic Location (Zv9):
Chromosome Zv9_NA921 (position 39337)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 8076121
GRCz11 21 8168660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCTGCTGCAGAAAGACTCCTCCCCCTCGAGCCCTAAAAGCAAAGCA[C/T]AGGTAAAAATACTCAGACAAATAATTCACCAAATGAATGCAAAACTGCAT
Long Flanking Sequence:
GAAACAGGACAAAACTCCACCAAAAATCAAATAGAGCTATTCAAACCATCTTCTGAAATTGCACATCGCAATATTTATTGCAGAAAAACAAAACATTGCAATATCAGTTTTTCCAATATCATGCAGCCCTACTGTGCATGACTCTGTATGTAACAAATAAATTAGCATTTGATTTAAATTGGAATAATATTTCACTGGTTTTTGATCAAATAAAAGATTCTTCATTGCAAATCCTTAACTTTTCAATATCATTTTGTGAGGACATATCAGCTTTATGTAAAGTTAAGTGATTTAAAGTTGTTTACCACTTCCAGGTGATAAAGAGTAACCTCTCCAGAGAGAATGACTTCGTGCGGGACAGTGTGGCGACTCTGACCAATCAGTTGCGGCAATATGAGAATCACTCTGACATCATGATGAGCATAAAGAAAGAGCTGTCCAATCTGGGCCTTCAGCTGCTGCAGAAAGACTCCTCCCCCTCGAGCCCTAAAAGCAAAGCA[C/T]AGGTAAAAATACTCAGACAAATAATTCACCAAATGAATGCAAAACTGCATATGGTTCAGTATATAGTGTTTACTGCATACCATTTATTAAAAGGAAAGTTCACCAAAACATGAAAATGTCCTCATCATCTGCTTAAACTTCAGTGGTTCTACACCTTTATGACTAACTCTCTTCTCTTCAGGTGAAGTTTTTTTTCCCTCTCCGCTGTCGCCACTGCCTCGCATGGTTCAGGATTGGTAGAGCTACGCATCGATGAATTGGCTCTTCAGTGTTTGAACTCTCAGTAATGATTAAATCACACTGAACTGAGCTAAACTGAACTGAACTTAAACATTAAAAACTGAACTACACTGTTCCAGTTACTGAACCACACTGTTCCAGTTACTATGACCATTTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATACAAATAAAGCTGAATTGAATTGAATTGAATTTTGAACCCAAAGGAAGATATTCTAAAGAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa19382
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000078436 Nonsense 667 670 8 8
Genomic Location (Zv9):
Chromosome Zv9_NA921 (position 15609)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 8052393
GRCz11 21 8144932
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTTGGGACAATGGACACCAGCTCACCTACAACATCGACTTTGCAGAG[C/T]AGGAGAAGAAATAAAATCGTGCAAATGAAACGCGCTTATAACTGCCTCAT
Long Flanking Sequence:
ATATCATTAAATACGACCTCAAACAGCGATATGTGGCCGCCTGGGCTCAGCTGCATGACGTGGTCTATGAAGACACGACACCATGGAAGTGGAAAGGCCACTCCGACATCGACTTCGCAGTGGATGAAAACGGGCTCTGGGTCATTTATCCATCAATCGACGAGGATTACGGACAGGCTGAAGTCATCGTTGTTAGTAGGCTTGACCCCAGTGACCTGTCGTTGAAAAAAGAGACCACGTGGAGGACGCGACTGAGGCGAAACTCATTCGGGAACTGCTTCATAATATGCGGAGTGCTTTACGCGGTGGACATTTACAATCAGAGGGAAGGAGAGGTTTCGTATGCGTATGACACGCTAACGGGGGCTGAAGCGGCTCCGCGTTTGCCTTTCATCAATGAATACGGCTTCACCACACAAGTCGATTACAACCCCAAAGAGAAGCTTCTGTATGCTTGGGACAATGGACACCAGCTCACCTACAACATCGACTTTGCAGAG[C/T]AGGAGAAGAAATAAAATCGTGCAAATGAAACGCGCTTATAACTGCCTCATTGGTTACACTAACCGAATGCATTCATGAAACAGGTCGTCATGCTCTCGTGAACTTTAATAGACACTTGTCAGAGGTTATATAAAGGGGATTATTACATAAGCTCTGCTCTATGATTGACTGCCAGTACTAGAATCCCAACAAATGCAAACTAAAGGCTTTGATTTGTTTCAAATGCATTAAACTCTATGAAGCAAAGTATAAATCAAGTGTTTTCCCGCTACATTTTTGGCTGCATCCGAAATAGACTACTACTCGAGTATATACTACATTTAAATTGACCAAATCTAAAGAATCTAAAGGCTTTGGGACTTGAGACTGCCCGTTCTGTAATTCGAACAAATGGAATCTAAAGGCGTTGATTCACATCAGTGTCCTAAATGCATTAAACTCCATGAAGCAAAGCATAAATCAAGTGTTTTCCTGGTACACGTTCGCTGCATCCGAAATCG
Associated Phenotype:
Not determined