Busch Lab

ZMP

olfm1a

Ensembl ID:
ENSDARG00000018270
ZFIN ID:
ZDB-GENE-040718-194
Description:
olfactomedin 1a [Source:RefSeq peptide;Acc:NP_001002491]
Mouse Orthologue:
Olfm1
Mouse Description:
olfactomedin 1 Gene [Source:MGI Symbol;Acc:MGI:1860437]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa15214 Essential Splice Site Available for shipment Available now
sa221 Nonsense Confirmed mutation in F2 line Not yet available
sa40590 Nonsense Mutation detected in F1 DNA Not yet available
sa20573 Nonsense Available for shipment Available now
sa40591 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15214
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002908 None None 485 None 6
ENSDART00000051812 Essential Splice Site 22 125 None 4
ENSDART00000073950 Essential Splice Site 22 125 None 4
ENSDART00000134241 Essential Splice Site 22 457 None 6
ENSDART00000135610 None None 153 None 4
Genomic Location (Zv9):
Chromosome 5 (position 68309673)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 64051173
GRCz11 5 64732337
KASP Assay ID:
2259-6786.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCCTGAGTCTCACCCTCCTGGTGCTGATGGGTACYGAACTCACCCAAG[T/A]AGGTTTTCAAACGCCATTTTCAGCGGGATAATTAAGCAGATAWGATCRTA
Long Flanking Sequence:
GGACCCCCGCAGCTTCTCCGCTCCCTCGGTGCGCTTTTCTTTCGAATTTCCCCCGTCATCCCGTGTCACATCCGGTTCAGCACCGCCGCTTGGCCCCGCTTGTCAAATTTCCTGCCCACACCTACTCCCTCTCGTATTAACCAGCCAAGTTTGTCCTAGTGATGAAGTAATATTTACGGCGCTTTCCCCGTTCATCCCTGTTCATTCGCGATCGGGTCCAGAGAGGAGGCGAGGAAGCTGAGATGAGCTAAGAAAAAACAATGCAAAGCCAAAACCATCCCAATCTCATCTTCACCTCATTCTGCCGCTGAATTAAAACGCGTTGGGTTAAGATCCGTTCAAGAGGAAGCATCGAGCCGGACAGCTGCACGGGAGAAACAGCCTTGCATGTGATTTTTTGTATTCCCGGATCAGGTGGCATCGGCGGCGGAAGATGCAGCCTGCAAACAAGCTCCTGAGTCTCACCCTCCTGGTGCTGATGGGTACCGAACTCACCCAAG[T/A]AGGTTTTCAAACGCCATTTTCAGCGGGATAATTAAGCAGATATGATCATAATAAGCTTATTTCGTGATTATGAATCTGTCGGGATATTAACTAATATGATTTTAGGAGAAAAAAATTATCACAACGGGGTATTCTTCTAGCTTGAGGTTTATAATGGCACATGGCTAGAAGGGGTATTTTATAGTAACTTTTATTGTGAATTGGTGGTTGAAGATAAATGCATTTTAGCAGTGCGAGAGAGATGGGTTTTTATCATTTCTGTGATATTATTCTTGACGATAAAGCACTGTGGGGTTTGCTTGTGCAGTGTATTCTCATTATCCACACGCTGTGATTGTCTCTAACACTCTACAATCTCACTTTGAAGACGAGAATAGCAAGTGAATTGCTTTCTCCACACTCCACGACGATGCTCTCTCTATTCAGAAATGACTTTTCCCTTAAGCCCCTGACATTATTGTGGGGAAATCTCTGCTGGTGAGTCCATCAAATTGTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa221
Status:
Confirmed mutation in F2 line
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
ENSDART00000002908 Nonsense 67 485 2 6
ENSDART00000051812 Nonsense 39 125 2 4
ENSDART00000073950 Nonsense 39 125 2 4
ENSDART00000134241 Nonsense 39 457 2 6
ENSDART00000135610 Nonsense 67 153 2 4
Genomic Location (Zv9):
Chromosome 5 (position 68324390)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 64065890
GRCz11 5 64747054
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGCTGCCTGCGAACCCTGAGGAGTCGTGGCAGGTGTACAGCTCAGCG[C/T]AGGACAGCGAGGGCAGGTGTGTGTGCACGGTTGTGGCTCCTCAGCAGACC
Long Flanking Sequence:
ATTTTTGTATTTATGAATCATGTTTTCAATTTACAAATATTTTGTAAACATATTATTTTTGACAGCGATCTGGCTCCATAGCTAATTTGGTTACCTTTACGGTCTGTCCATATGTCACATCAGGAATAAGCTATGCTTTATAGCCACAGATTGAGAGCTGCGGTTCCAATCATAAAAGTTGGTGACGGTGTTTGTGAATGTTCATCTGAACGGCAGAATTTGCCAACTTAGTTGGCTAACAAAAGTTTTGGCAAACTCACCCCTGTTTTAAAGTTCTTGCACAGAGAAAAGCATCAACTGGCCAAAAACACTCACTCTGCCCTTGTGTACTGTTCAGGCAATTAACCTTCTCAAAGACTGCAGTGGCAGAAAGGATAAATTTGCTACAAAGCTGCTTCCTATAAAACACACGGCGATCAGTCACTGACCTTCTTTCTCTTTGTTTATCCCAGGTGCTGCCTGCGAACCCTGAGGAGTCGTGGCAGGTGTACAGCTCAGCG[C/T]AGGACAGCGAGGGCAGGTGTGTGTGCACGGTTGTGGCTCCTCAGCAGACCATGTGCTCACGGGACGCCAGGACCAAGCAACTGAGACAGCTTCTGGAAAAAGTAACCTTTGAAAATAATCCACACAAAGCCCCACTGACAGATTAAACCGCACGACGAATGGCTTTAATAAATCTTTTCAGTAGTGATGCACCGATCTCGGTTTTTCAAAGCAAAAATTGTCTGATTCCAATTGTCGTTGTACAACGAACTGAAGTGAGGAAATTTAAAATAAAATCCAGCCAAAACAAAGGTCATATTGAGTTCATTTCGGCAGATCAAAACAACTCATCTCAAAGCAAGCTTTCTGAGGGGAGTTCGCTTTGGCTCTTAAACACCTGTGGTGATTATGCAATCAGTAAGTGTGTTACAAAACTCCAGCTTCTTTGATTGATTCATATCTCATATCAGTGGAAGTCAGATAGGAAAACAGGAGAACAACATCCAAAACAATAACTTCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40590
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
ENSDART00000002908 Nonsense 96 485 2 6
ENSDART00000051812 Nonsense 68 125 2 4
ENSDART00000073950 Nonsense 68 125 2 4
ENSDART00000134241 Nonsense 68 457 2 6
ENSDART00000135610 Nonsense 96 153 2 4
Genomic Location (Zv9):
Chromosome 5 (position 68324477)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 64065977
GRCz11 5 64747141
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCTCAGCAGACCATGTGCTCACGGGACGCCAGGACCAAGCAACTGAGA[C/T]AGCTTCTGGAAAAAGTAACCTTTGAAAATAATCCACACAAAGCCCCACTG
Long Flanking Sequence:
TGGTTACCTTTACGGTCTGTCCATATGTCACATCAGGAATAAGCTATGCTTTATAGCCACAGATTGAGAGCTGCGGTTCCAATCATAAAAGTTGGTGACGGTGTTTGTGAATGTTCATCTGAACGGCAGAATTTGCCAACTTAGTTGGCTAACAAAAGTTTTGGCAAACTCACCCCTGTTTTAAAGTTCTTGCACAGAGAAAAGCATCAACTGGCCAAAAACACTCACTCTGCCCTTGTGTACTGTTCAGGCAATTAACCTTCTCAAAGACTGCAGTGGCAGAAAGGATAAATTTGCTACAAAGCTGCTTCCTATAAAACACACGGCGATCAGTCACTGACCTTCTTTCTCTTTGTTTATCCCAGGTGCTGCCTGCGAACCCTGAGGAGTCGTGGCAGGTGTACAGCTCAGCGCAGGACAGCGAGGGCAGGTGTGTGTGCACGGTTGTGGCTCCTCAGCAGACCATGTGCTCACGGGACGCCAGGACCAAGCAACTGAGA[C/T]AGCTTCTGGAAAAAGTAACCTTTGAAAATAATCCACACAAAGCCCCACTGACAGATTAAACCGCACGACGAATGGCTTTAATAAATCTTTTCAGTAGTGATGCACCGATCTCGGTTTTTCAAAGCAAAAATTGTCTGATTCCAATTGTCGTTGTACAACGAACTGAAGTGAGGAAATTTAAAATAAAATCCAGCCAAAACAAAGGTCATATTGAGTTCATTTCGGCAGATCAAAACAACTCATCTCAAAGCAAGCTTTCTGAGGGGAGTTCGCTTTGGCTCTTAAACACCTGTGGTGATTATGCAATCAGTAAGTGTGTTACAAAACTCCAGCTTCTTTGATTGATTCATATCTCATATCAGTGGAAGTCAGATAGGAAAACAGGAGAACAACATCCAAAACAATAACTTCATGATGAAGCAGCATGAATATACTGGAGGGCTAATCGCTCATGGAGAGGAGGTTTGAAACACAGACTTTTCGAACTTCTTGCCCTCAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20573
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002908 Nonsense 276 485 6 6
ENSDART00000051812 None None 125 None 4
ENSDART00000073950 None None 125 None 4
ENSDART00000134241 Nonsense 248 457 6 6
ENSDART00000135610 None None 153 None 4
Genomic Location (Zv9):
Chromosome 5 (position 68352461)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 64093961
GRCz11 5 64775125
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACCAGGTGTGGTACATGGACGGCTACCACAACAATCGCTTCGTCCGC[G/T]AATACAAGTCCATGGCCGACTTCATGTATTCCGACAACTTCACCTCACAC
Long Flanking Sequence:
GTATGCCTTTTCAAATCATGTCCCATCTACTGAATTTTCCACAGGTGAACTCAAGTTAAGGTGCTGAAACATCTCAAATGGATCAGTGGAAACAGATTGTACCTGAGCTCAATTTAGAGCTTCATGCCAAAGGTAGTGAATACTTATATACATGTGATTCTTCAGGTCTTTTAGTTTTAATAAATTTGCAACAGTTTCAAAAACTATTTTTTACATTGTCATTATGGGGTATTGTGTGTAGAATTTTGAGAAATAAATGAATTTAATCCATTTTTGGAATAAGGCTGTAACATAAAAAATATGGAAAAAGTGAAGCGCTGTCAATACTTTCCGGATGCACTGTATATTTTAATAGGCACCTATGATGAAAATCATCTCTTGTAACAATCATTCCCTTTCCATTTGTGTTGTAAAATGTTTGATCCAACCCTCACGCTCGTTCATTTCTTCTCCACCAGGTGTGGTACATGGACGGCTACCACAACAATCGCTTCGTCCGC[G/T]AATACAAGTCCATGGCCGACTTCATGTATTCCGACAACTTCACCTCACACCGGCTTCCTCACCCCTGGTCGGGCACGGGACAGGTGGTCTACAACGGCTCCATCTACTTCAACAAGTTCCAAAGCAACACTATCATCAAATTCGACTTCAAGACCGCCACCATCAGCAAATCTGGCCAGCTGGATTACGCTGGATTCAACAACCGATACCACTATTCCTGGGGCGGCCACTCCGACATCGACCTCATGGTGGACGAAGGTGGGCTTTGGGCCATTTACGCCACCAATCAAAACGCAGGGAACATTGTGATCAGCAAACTCAACCCGGCCACCCTGCAAATCGTCAAAAGCTACACCACCAACCACCCAAAGAGGAGCGCGGGTGAGGCTTTTATGATCTGCGGGACGCTTTATGTCACCAACGGCTACTCAGGAGGGACAAAAGTCTACTACGCATTCCACACCAACTCCTCCACTTACGAATACATCGACATCCCGTTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40591
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
ENSDART00000002908 Nonsense 393 485 6 6
ENSDART00000051812 None None 125 None 4
ENSDART00000073950 None None 125 None 4
ENSDART00000134241 Nonsense 365 457 6 6
ENSDART00000135610 None None 153 None 4
Genomic Location (Zv9):
Chromosome 5 (position 68352814)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 64094314
GRCz11 5 64775478
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTGATCAGCAAACTCAACCCGGCCACCCTGCAAATCGTCAAAAGCTA[C/A]ACCACCAACCACCCAAAGAGGAGCGCGGGTGAGGCTTTTATGATCTGCGG
Long Flanking Sequence:
AGGCACCTATGATGAAAATCATCTCTTGTAACAATCATTCCCTTTCCATTTGTGTTGTAAAATGTTTGATCCAACCCTCACGCTCGTTCATTTCTTCTCCACCAGGTGTGGTACATGGACGGCTACCACAACAATCGCTTCGTCCGCGAATACAAGTCCATGGCCGACTTCATGTATTCCGACAACTTCACCTCACACCGGCTTCCTCACCCCTGGTCGGGCACGGGACAGGTGGTCTACAACGGCTCCATCTACTTCAACAAGTTCCAAAGCAACACTATCATCAAATTCGACTTCAAGACCGCCACCATCAGCAAATCTGGCCAGCTGGATTACGCTGGATTCAACAACCGATACCACTATTCCTGGGGCGGCCACTCCGACATCGACCTCATGGTGGACGAAGGTGGGCTTTGGGCCATTTACGCCACCAATCAAAACGCAGGGAACATTGTGATCAGCAAACTCAACCCGGCCACCCTGCAAATCGTCAAAAGCTA[C/A]ACCACCAACCACCCAAAGAGGAGCGCGGGTGAGGCTTTTATGATCTGCGGGACGCTTTATGTCACCAACGGCTACTCAGGAGGGACAAAAGTCTACTACGCATTCCACACCAACTCCTCCACTTACGAATACATCGACATCCCGTTACAGAACAAGTACTCGCATATCTCCATGCTGGATTACAACCCACGGGACAGAGCTCTTTACGCGTGGAATAACGGACATCAGGTGCTGTATAACGTCACCTTGTTCCACGTCATTCGCTCGGAGGAACTCTAAAGTGACTTTCTCTATCCGTCCGAGGTAGCATCGATGGAGTTTATTACCGGAAAATAGAGTAATGCCTGATTGATTGTTCAATAAAAGAAGACGTACAAATGTATCAAAAGTAATAGTTCGAGGCAACGTTACGAATAGCTGCCAACAAGGTCTTTTTCTTGTCTTTTTTTAAGCTTTCCTTAGATGATTCTGTTTGAATTCCTCACTGCAAAAACGTTTCG
Associated Phenotype:
Not determined