ZMP
olfm2
Ensembl ID:
ZFIN ID:
Description:
olfactomedin 2 [Source:RefSeq peptide;Acc:NP_997882]
Human Orthologue:
OLFM2
Human Description:
olfactomedin 2 [Source:HGNC Symbol;Acc:17189]
Mouse Orthologue:
Olfm2
Mouse Description:
olfactomedin 2 Gene [Source:MGI Symbol;Acc:MGI:3045350]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5231 | Essential Splice Site | F2 line generated | Not yet available |
sa10851 | Nonsense | Available for shipment | Available now |
sa11276 | Nonsense | Available for shipment | Available now |
sa11140 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa5231
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109894 | Essential Splice Site | 49 | 483 | 2 | 6 |
The following transcripts of ENSDARG00000077847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 55058952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53952868 |
GRCz11 | 3 | 54207531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCATCCATCTCCNNTTTTTTTTCCTCATCTCTTSCTCTCTTTCTCCACGC[A/T]GGCCCTGTATCCAAGCCCGGAGGAGGGCTGGCAGATCTACAGCTCGGCAC
Long Flanking Sequence:
TCTGTAAGGTGTAGGGTCGAAATCAATACATTAGAAGTCCCCATTAAACATAGTACCTAATATTTACGTGTGTCTTTTTTAAAATGAACAATGTTATTTTGGCAATCAACATTATTCCACAAAGTTGAGCATTAAGCTTATTAATATTCCATCAACCGAAATGTTAATATGCAGAAAGGTTTCTGTGAGCTTTCCTTTAAAATGTCATGTCAGTGTAAAAAACAATAAAAATCAATGGCAAGCCCCCTTCTAAGATGAATCGTGTGTGTGTGCTTGTGTGTGAGCTTTTGAGCCATTGTTTTAAGACATCCATCTCCTGACTCCACCCGCTATGAAAAAGCAACATTATCGATCCAAGGTGCTCTATTTCCTCCAAGTGTCTAAGCTGATCAAAACCTCCTCCTCTCACAGATGCCACATTCTATTTTGCTCATGCATTTTGTCCTGTCTCTCCATCCATCTCCTTTTTTTTCCTCATCTCTTCCTCTCTTTCTCCACGC[A/T]GGCCCTGTATCCAAGCCCGGAGGAGGGCTGGCAGATCTACAGCTCGGCACAGGATGCAGATGGGAAATGTATCTGCACCGTTGTTGCTCCAGCACAGAACATGTGTAATCGAGACCCACGCAGCAGACAGCTCCGGCAACTTATGGAGAAGGTGACATTTGTCTGTTACTATCAGAATAAGCCAAATGACGCATGTTTTTCATGAGCAAATCCAAGCCAGAGTGATGTTTTGTACATATTACGCAGTCATTAAACACGAATCTCAAACATTACATAACACTGTTGGCCATTAGCAAAAGTTTGTTAAAGTACAACAAGCAAACAGCTGCCTAAAAGAGGACGCGTCCTAAATACTGCTGTGAAATTGGATTCATTCTGCTGAGCCGTTAGGATGTCTTTTTGTTTTTTTTCCCCATCTCTAATCATACTCATTAGACTAAGACCAGGCAAAGAACAAGTAGGGAAAAAAGTATAAGTGCCTCCTAAATCAGGAAATGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10851
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
The following transcripts of ENSDARG00000077847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 55088610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53982526 |
GRCz11 | 3 | 54237189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAAC
Long Flanking Sequence:
TCCAGCATCTCCTGCCCCACCCTTGGGCTGGTACGGGTCACGTGGTCTACAACGGCTCACTATACTACAACAAATACCAGAGCAACATCCTCATCAAGTACCACTTCCGGTCTCGAAGTGTCCTGGTGCAGCGGAGCCTTAGCGGTGCCGGCTACAACAACACCTTCCCCTACTCCTGGGGCGGATCATCCGACATCGACCTCATGGCTGATGAGAATGGTCTGTGGGCTGTCTACACCACCATTCCCAATGCCGGAAACATCGTCATTAGCCGTCTAGAGCCGCAAAGCCTGGAAGTGCTTCAAACGTGGGACACAGGCTTTCCCAAACGGAGCGCAGGCGAGTCCTTCATGATCTGCGGCACTCTTTATGTAACCAACTCCCACTTGGCCGGTGCTAAAATCTACTTCGCATATTACACCAACACCTCGACCTATGAGTACACTGACATCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAACGTCACGTTGTTCCAGGTCATCAAAACCGCTGAGGACTAAGTCATTCAGACTTTACAAACACATTTGCTCATACACAAATGCACACACACTATTATAACACACACATACACACACTTATGTGGAGGGGGGACTAAAGTTGAAACTTTTTTACTGCATTCCAAACTTCATAGAGTGCTATTAATTATCTAATGTTCTGAGGAGAGGAAGATTGGTACTGATAAATGGACGGAGCTTTTATTTTCTTTCCTGTGATGATTCAGCATGAGTACTTTCTTTTTATTTGTGGAAAAAGATGAATAAATAAACATCAAACTTTACCATTTTTCAAGTTTCAACTTTTTCTTTCCTTTGTTTTTTTCTTTTCTCCTAGATGCTGATGGTTACTAATGGCTGCATACTGTAGTAGCTAAAAAAAAAAGAAGCTTTTGTAAATGCCTGATCGCTCATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11276
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
The following transcripts of ENSDARG00000077847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 55088610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53982526 |
GRCz11 | 3 | 54237189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAAC
Long Flanking Sequence:
TCCAGCATCTCCTGCCCCACCCTTGGGCTGGTACGGGTCACGTGGTCTACAACGGCTCACTATACTACAACAAATACCAGAGCAACATCCTCATCAAGTACCACTTCCGGTCTCGAAGTGTCCTGGTGCAGCGGAGCCTTAGCGGTGCCGGCTACAACAACACCTTCCCCTACTCCTGGGGCGGATCATCCGACATCGACCTCATGGCTGATGAGAATGGTCTGTGGGCTGTCTACACCACCATTCCCAATGCCGGAAACATCGTCATTAGCCGTCTAGAGCCGCAAAGCCTGGAAGTGCTTCAAACGTGGGACACAGGCTTTCCCAAACGGAGCGCAGGCGAGTCCTTCATGATCTGCGGCACTCTTTATGTAACCAACTCCCACTTGGCCGGTGCTAAAATCTACTTCGCATATTACACCAACACCTCGACCTATGAGTACACTGACATCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAACGTCACGTTGTTCCAGGTCATCAAAACCGCTGAGGACTAAGTCATTCAGACTTTACAAACACATTTGCTCATACACAAATGCACACACACTATTATAACACACACATACACACACTTATGTGGAGGGGGGACTAAAGTTGAAACTTTTTTACTGCATTCCAAACTTCATAGAGTGCTATTAATTATCTAATGTTCTGAGGAGAGGAAGATTGGTACTGATAAATGGACGGAGCTTTTATTTTCTTTCCTGTGATGATTCAGCATGAGTACTTTCTTTTTATTTGTGGAAAAAGATGAATAAATAAACATCAAACTTTACCATTTTTCAAGTTTCAACTTTTTCTTTCCTTTGTTTTTTTCTTTTCTCCTAGATGCTGATGGTTACTAATGGCTGCATACTGTAGTAGCTAAAAAAAAAAGAAGCTTTTGTAAATGCCTGATCGCTCATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11140
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
ENSDART00000109894 | Nonsense | 455 | 483 | 6 | 6 |
The following transcripts of ENSDARG00000077847 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 55088610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 53982526 |
GRCz11 | 3 | 54237189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAAC
Long Flanking Sequence:
TCCAGCATCTCCTGCCCCACCCTTGGGCTGGTACGGGTCACGTGGTCTACAACGGCTCACTATACTACAACAAATACCAGAGCAACATCCTCATCAAGTACCACTTCCGGTCTCGAAGTGTCCTGGTGCAGCGGAGCCTTAGCGGTGCCGGCTACAACAACACCTTCCCCTACTCCTGGGGCGGATCATCCGACATCGACCTCATGGCTGATGAGAATGGTCTGTGGGCTGTCTACACCACCATTCCCAATGCCGGAAACATCGTCATTAGCCGTCTAGAGCCGCAAAGCCTGGAAGTGCTTCAAACGTGGGACACAGGCTTTCCCAAACGGAGCGCAGGCGAGTCCTTCATGATCTGCGGCACTCTTTATGTAACCAACTCCCACTTGGCCGGTGCTAAAATCTACTTCGCATATTACACCAACACCTCGACCTATGAGTACACTGACATCCCCTTCCATAACCAATACTCCCACATCTCCATGATGGACTACAATCCC[C/T]GAGAAAGAGTTCTCTACACCTGGAACAATGGACATCAAGTCCTCTACAACGTCACGTTGTTCCAGGTCATCAAAACCGCTGAGGACTAAGTCATTCAGACTTTACAAACACATTTGCTCATACACAAATGCACACACACTATTATAACACACACATACACACACTTATGTGGAGGGGGGACTAAAGTTGAAACTTTTTTACTGCATTCCAAACTTCATAGAGTGCTATTAATTATCTAATGTTCTGAGGAGAGGAAGATTGGTACTGATAAATGGACGGAGCTTTTATTTTCTTTCCTGTGATGATTCAGCATGAGTACTTTCTTTTTATTTGTGGAAAAAGATGAATAAATAAACATCAAACTTTACCATTTTTCAAGTTTCAACTTTTTCTTTCCTTTGTTTTTTTCTTTTCTCCTAGATGCTGATGGTTACTAATGGCTGCATACTGTAGTAGCTAAAAAAAAAAGAAGCTTTTGTAAATGCCTGATCGCTCATTAT
Associated Phenotype:
Not determined