ZMP
si:ch211-267e7.7
Ensembl ID:
ZFIN ID:
Description:
LOC567907 protein [Source:UniProtKB/TrEMBL;Acc:A7MBT4]
Human Orthologue:
OLFML2B
Human Description:
olfactomedin-like 2B [Source:HGNC Symbol;Acc:24558]
Mouse Orthologue:
Olfml2b
Mouse Description:
olfactomedin-like 2B Gene [Source:MGI Symbol;Acc:MGI:2443310]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45097 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19726 | Essential Splice Site, Missense | Available for shipment | Available now |
sa11701 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45097
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010370 | Nonsense | 3 | 466 | 1 | 7 |
ENSDART00000128505 | None | None | 679 | None | 10 |
ENSDART00000131501 | None | None | 258 | None | 2 |
ENSDART00000135558 | None | None | 150 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 20374611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20947221 |
GRCz11 | 2 | 20605193 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTGAGATTGTTCTTGCAGCTCTTCTTGAGGAATCTTCATAATGGGAT[T/A]ACTGTTATATATTTTTTGCTGTGTTTTTTGTTTGACACGCGCCAATGTGG
Long Flanking Sequence:
TTTCTAAATAAATAAATAAATACAAAAATATGTTTCTTCAAAAACCTTAAATTTCTCCTCTGGTGACATATTTATTACCATTTACTTACGTCTCTACTCTTGGTTTGGTTGTGTGGCACATGTGCATTGAAAAGCGCGGGATTATGTGATTGATCAGATGACTGAACTCCTCCTTTTCTTCTCTGCCCACTGACTCCTGGTCAAACAGCAAACCTTCACATATCATCATCCATTCATCACCGGCTCTCCATCTCACTCAAGGTCTTCCCTCTATCTGAAAAAGCCAAGAGCACTGATTTCCACTAATCTAGGACTGTTTTGACGTCATCGAGGACAATTTTTGCATATTCATTGATTAATAGAGTTGATTGGCATGTGAAAGTATTTACATTAGGTTAAATTACATAATAATTTTTTTTCTGGGACGGTCGGACAGAGAAGAGTAACATCTAACTGAGATTGTTCTTGCAGCTCTTCTTGAGGAATCTTCATAATGGGAT[T/A]ACTGTTATATATTTTTTGCTGTGTTTTTTGTTTGACACGCGCCAATGTGGAGCAGCAGGCAACTGACAATACAGACAACCGCGCAACACTAGAAGATGAGATGGACAATCAAGAAAACATACTCACACAGGTAATTGCTCTTGATTATTGAAAGCTAATTATTGCATGAACATATGACTTATTATTATTAATGGAATTCGGCAAGATAACTATATTATAGACTAATATGATTTTATGTATCAAACATATTATTTAGAATTGATTATTATTGTTATCATTATTATTGTTGTTGTTGTGCTAGATTTTTATAGAAATGTATAATGTACTGTATATATAATTATTAATACAAAAATTCTGTTAATATCAACAATTAATAATAGTTAATATATCAACAAACTAATAATAATAAAAACAATAATAATAATAATAATAATAATAATAATAATAATGTTATTAATAATATAAATATAATAATGATGATGATGATGATGATTATTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19726
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010370 | Essential Splice Site | 225 | 466 | 4 | 7 |
ENSDART00000128505 | Missense | 195 | 679 | 4 | 10 |
ENSDART00000131501 | None | None | 258 | None | 2 |
ENSDART00000135558 | None | None | 150 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 20378007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20950617 |
GRCz11 | 2 | 20608589 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGCCTTCACTGCAGAAGAACGCAGCAGCGGCTTTTGCTCACACTGAG[G/A]TACAGATGCAGTATATTCTAGCACGATCTTTTAGAAGAGCCTAAATGGAA
Long Flanking Sequence:
AGAGTAACCACTAAATTAACAAGATTTACTCTAAAAAGTTTTATTTGTATGCACAGGGAAGAAAAAAAAAAACTTTTTTCACTTCAGCACAATCACAGGAAAGCAAATCCAGTCATGGTACATCAGGGAAAAATAACAGGGGGTCTCATTATTTATTTTTGATTATACCATGGCCTAAAAACAACAATGTGCTTTTTATTCGCTTTTCAGTATTACTGTGGCAAAAGAAATCACTGTCTGCTTTCAAATGTCACAACTGGACAAAGGGGAATTGGGTTCAGGTGGTTGGGCGGAACTGCCACCCATGGTCCTCTATTGTGTTTACGTTCTCCTTGCAGTCGTTTTCCGGAAACCTGACAAAGGAGAAAGTGAGCGTGAAAGGTGAAAAGGGGCAGGGGAAGGGGGCCCGCTCCAACCAAAGACAGGAGAAGAAGAAACGTCTCAGTGTGCTGGAGCCTTCACTGCAGAAGAACGCAGCAGCGGCTTTTGCTCACACTGAG[G/A]TACAGATGCAGTATATTCTAGCACGATCTTTTAGAAGAGCCTAAATGGAAGTATTCACCCAAAAATGACAATTTGTTGTTAATTTACTAACCTTCAGCTGTTCAATATGTAGGTGACATTTCTTTAGTAGAACATTAAAGGAAGAGTTCACCCAAAAAGAATATGACCACATAATTTATTTCACCCTCAAAAGCTTTAATACACCCTCAGTGTATATGACTTTTTTCATCTTTACGCCGATAGAATGATACAAACAGTTAGAATAGTTTTAAATGTTATTCTGGCTTTTCTATGCTGTATATTGGGTGTTGGTTAGTAGCAATTTTCATTGTTACATCATTGTTAATGTATGTCTTCTGAAGAAGTTCAATGTGTTTTTGTAATGATGGAAGTTAAAATATTTCAAATTTTTATTGAATAGACTTGAATGACTTTTGGCGGACAATTTCCAACGGAAACAATTTTAGACGGCTAGTTTTCATATCTGACTAACTGATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11701
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010370 | None | None | 466 | None | 7 |
ENSDART00000128505 | Nonsense | 524 | 679 | 9 | 10 |
ENSDART00000131501 | None | 103 | 258 | 2 | 2 |
ENSDART00000135558 | None | None | 150 | None | 3 |
Genomic Location (Zv9):
Chromosome 2 (position 20383650)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 20956260 |
GRCz11 | 2 | 20614232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAGAGCTTTTTCTCGWGATATAATCAGGTTTGATCTTCGTCTCCGGTA[T/A]GYTGCAGCCTGGACCACCCTTCATGACGCAATATTAGAGGAGGAGGAGGC
Long Flanking Sequence:
TTACTCTGTGCACAAGCACAGCCCACTAGGCAACATCAGACTGACCCTGTCAGTTAAATGCAAATTCGCCAGGTCTTGAAACGCTTCTGAAATGATCGATGCTTTGAATCGCTTTAGTCACATGACCCGGTGTTTCGAAACACTTTATTAATGTAACCTGGGTGTTTCGAATCACCTTAATCACGTGACCTGGGTGTTTTTAGATCATTCTTCAGTGAAGTGTTTCGAAACACTTGGGCTTCGGGATGCTGACACTGTGTCGACACATCAGTTTTACATGAGCCATTAGTACTTAAAACTGGATCATCATTAAACTTAAACTTTCTATTATGTTAAAACATGACATTGATTTCTTTTCTTTTTCTCATAGGGCAGGTCAGCAACTCCTACAAACTCCCCTATAACTGGATTGGCACCGGCCATGTCGTCTACAGTGGCTCTTTCTTCTACAATAGAGCTTTTTCTCGTGATATAATCAGGTTTGATCTTCGTCTCCGGTA[T/A]GTTGCAGCCTGGACCACCCTTCATGACGCAATATTAGAGGAGGAGGAGGCCCCTTGGACTTGGGGAGGACATTCAGATATTGACTTCAGTGTGGATGAAAGTGGGTTATGGTTGGTGTACCCAGCTCTGGATGACGAGGGGTTTCACCAGGAGGTGATCATTCTGAGCAAACTCCGTGCCTCTGACTTACAGAAAGAGAAGAGCTGGAGGACAGGTCTAAGGAGAAACTACTATGGAAACTGCTTTGTCATCTGCGGTGTTCTATACGCCGTCGACAGTTTTGAGCGCACACATGCCAATATTTCTTATGCGTTCGACACACACACGCATACCCAAATGATTCCTCGACTCCCTTTTATAAACAACTATACCTACACCACACAGATTGACTATAACCCTAAGGAACGTATGCTTTATGCTTGGGACAATGGTCATCAAGTGACCTATGATGTAATATTTGCTTATTAAGTGAAGTTTATTTATAGACTTTCGAGAGGATC
Associated Phenotype:
Not determined