ZMP
olfm1b
Ensembl ID:
ZFIN ID:
Description:
olfactomedin 1b [Source:RefSeq peptide;Acc:NP_001003486]
Mouse Orthologue:
Olfm1
Mouse Description:
olfactomedin 1 Gene [Source:MGI Symbol;Acc:MGI:1860437]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa157 | Nonsense | F2 line generated | Not yet available |
sa16075 | Essential Splice Site | Available for shipment | Available now |
sa37229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa157
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037265 | Nonsense | 33 | 125 | 2 | 4 |
ENSDART00000135914 | None | None | 75 | None | 3 |
ENSDART00000139493 | Nonsense | 61 | 153 | 2 | 4 |
ENSDART00000140478 | Nonsense | 61 | 485 | 2 | 6 |
ENSDART00000146371 | Nonsense | 33 | 457 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 6738740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6859832 |
GRCz11 | 21 | 6782083 |
KASP Assay ID:
554-0018.1 (used for ordering genotyping assays)
KASP Sequence:
TTCTGTTTGTCCTCTGCCAGGTTTTACCCGCTAACCCAGAGGAGTCCTGG[C/T]AAGTGTACAGCTCGGCTCAGGACAGCGAGGGCAGATGTGTGTGTACAGTC
Long Flanking Sequence:
GCATTAACAAAAGGATTTTCATGGGTCCAGATTAAAAATGGAATATAACAGCAACAAACTGCAAAGCAGACCGAATGAAAATCTGTTTGCAGTGTTGTAATATTCCATAAGTACAGCATTGGTTTGGAGACTGTGGAGATTTAGGACTCTCCAGCGGATGTTCATCAATCCTCCATCTGTTCTTCACTCTCAGACAGACTGATTGGATCTGTAAGTCAAGAATGCCACACAGCTGAACGGGACCAGACCCTCTCTGTCTAACAGCTGCCGATCAAACGCAACAATACATCTGTTTGCTTAAATGAAGCTGAGAGTCATCTATCTGCTAGTAGAAGTCATCCTGCTGCGCTTTGATTGGCGGACAGGGATGTGGGTGTGGCCTGAAGCAGATGGGGTTTTGTGTAATCTTGTGTCATGTGTTTATAGTGAAGCTCTGAATGCTGTAATGTTTTCTGTTTGTCCTCTGCCAGGTTTTACCCGCTAACCCAGAGGAGTCCTGG[C/T]AAGTGTACAGCTCGGCTCAGGACAGCGAGGGCAGATGTGTGTGTACAGTCGTGGCACCTCAGCAGACCATGTGCTCGAGAGATGCCCGCACCAAACAACTGCGCCAACTACTGGAGAAGGTGAACTGCTGACCTGCAGCGCTCTAGTGGTTTGCCCTTGGGCATCATTTGATCTCTAATGCACTGTACGGTTGCCGCAGACGACCAGAGTTTTCCTCCAGAGATTAAAGTGACCCAGAGGCAACTCGCATTATCGTTCACATACAAACAGGGAGAGTTAATTAGTTCCTCTGGAGCAGGACGGGTGCTGAAGAAAACAGCTTTCCCTCTGATAGACAATGATGCAATTCCGCGAACACATCAGATCATTAGCAGATCTGGAAAAGCTGAAGCACTGACTAGTTTTCTGAAAGTCACTAGAATTGTATGTACAGAAATAGTAACACAAATATGTATATATATATATATATATATATATATATATATATATATATATATATA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa16075
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037265 | Essential Splice Site | 73 | 125 | 3 | 4 |
ENSDART00000135914 | Essential Splice Site | 23 | 75 | 2 | 3 |
ENSDART00000139493 | Essential Splice Site | 101 | 153 | 3 | 4 |
ENSDART00000140478 | Essential Splice Site | 101 | 485 | 3 | 6 |
ENSDART00000146371 | Essential Splice Site | 73 | 457 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 6741562)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6862654 |
GRCz11 | 21 | 6784905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATGYACTAAACTCATTGTATTCCCTGGYACCTTCTATATGTGCYTTTA[G/A]GTGCAAAACATGAYGCAATCAATCCAAGTWTTGGACCAGCGGACCCAGAG
Long Flanking Sequence:
ATTATAACAGTTGTGGCATTTAATTATCAAATTTCAGTAAAAAAATAGAAATAGAAATTTTATTCTGTTTAAAGTGGATAAGACATAATATTTTCACATACAATTTTTTTTGTGAAAATTATCATGAATTATTATTATGTACATATATTTATTAAACAATAGATATAATTGTCTATTATTATTATATATACTTATCAGCCTAATTAGAAATTAGATTACAAAATAATGATAATAATATTATATTTGTTTTACAAAATGTGTCGGCAAACTAATTGTTTTGATAATCAACAATAAAACCAACATTCTGACAAAATTCATGCAAACAGAAAAATGAAATTAATATTTAGCAAACATGATCACACAATTATTATTATTATTATTATGATTAATTGATTATTTGTGGCACCTAATCAAAAGTGAGCACTTAGTAATAAAAAATATAACATTTCTTTATGTACTAAACTCATTGTATTCCCTGGTACCTTCTATATGTGCTTTTA[G/A]GTGCAAAACATGACGCAATCAATCCAAGTATTGGACCAGCGGACCCAGAGGGACCTGCAGTACGTGGTAAAGATGGAGGATCAACTCCGTGGCCTGGAGACCAAATTCAGACAGGTGGAAGAGAACCACAAACAAAACATCGCCAAGCAATACAAGGTAAACACCCACAATGCGCACCTCAGGCCATATGGATGCAACACACGCACAATAACACACCCCAGACTGCATGTATCTTATAAATCCTTGTGTGCTTTTAGCGAAATATGCAGACCTGTGCGATATAAAGCATTGTTTTTGACCTTAAAATCAGCTAAATATTTTCAGGATCTGCAGATTTCAGTTTCCACACTTGACACATGCATGAAATGTGATTTTGTTTGCACTCTGTAACACAAGTGAGTGTGCATGTGAGTACGTGAGTCTCTGTGTGTGACTGCCAATGTGTTAGCTAGTTAGCGAGTTAGCTCCCTGTGCTGAGTGTGTTGTTTCTTGCTTGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37229
Status:
Mutation detected in F1 DNA
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037265 | Nonsense | 109 | 125 | 3 | 4 |
ENSDART00000135914 | Nonsense | 59 | 75 | 2 | 3 |
ENSDART00000139493 | Nonsense | 137 | 153 | 3 | 4 |
ENSDART00000140478 | Nonsense | 137 | 485 | 3 | 6 |
ENSDART00000146371 | Nonsense | 109 | 457 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 6741671)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 6862763 |
GRCz11 | 21 | 6785014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTACGTGGTAAAGATGGAGGATCAACTCCGTGGCCTGGAGACCAAATTC[A/T]GACAGGTGGAAGAGAACCACAAACAAAACATCGCCAAGCAATACAAGGTA
Long Flanking Sequence:
TTGTGAAAATTATCATGAATTATTATTATGTACATATATTTATTAAACAATAGATATAATTGTCTATTATTATTATATATACTTATCAGCCTAATTAGAAATTAGATTACAAAATAATGATAATAATATTATATTTGTTTTACAAAATGTGTCGGCAAACTAATTGTTTTGATAATCAACAATAAAACCAACATTCTGACAAAATTCATGCAAACAGAAAAATGAAATTAATATTTAGCAAACATGATCACACAATTATTATTATTATTATTATGATTAATTGATTATTTGTGGCACCTAATCAAAAGTGAGCACTTAGTAATAAAAAATATAACATTTCTTTATGTACTAAACTCATTGTATTCCCTGGTACCTTCTATATGTGCTTTTAGGTGCAAAACATGACGCAATCAATCCAAGTATTGGACCAGCGGACCCAGAGGGACCTGCAGTACGTGGTAAAGATGGAGGATCAACTCCGTGGCCTGGAGACCAAATTC[A/T]GACAGGTGGAAGAGAACCACAAACAAAACATCGCCAAGCAATACAAGGTAAACACCCACAATGCGCACCTCAGGCCATATGGATGCAACACACGCACAATAACACACCCCAGACTGCATGTATCTTATAAATCCTTGTGTGCTTTTAGCGAAATATGCAGACCTGTGCGATATAAAGCATTGTTTTTGACCTTAAAATCAGCTAAATATTTTCAGGATCTGCAGATTTCAGTTTCCACACTTGACACATGCATGAAATGTGATTTTGTTTGCACTCTGTAACACAAGTGAGTGTGCATGTGAGTACGTGAGTCTCTGTGTGTGACTGCCAATGTGTTAGCTAGTTAGCGAGTTAGCTCCCTGTGCTGAGTGTGTTGTTTCTTGCTTGCAGGGCTAACTATAAAGACATGATAGGAGAGCCAGAGGCCAGAAGAAGCAGGTCTAACCCACGATTGGCTGAAGTGGGCGTCAGTCACGCTGTTTATGTCACGATTCTCATAT
Associated Phenotype:
Not determined