ZMP
si:ch211-1c4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate odz, odd Oz/ten-m (Drosophila) family [Source:UniProtKB/TrEMBL;A
Human Orthologue:
ODZ1
Human Description:
odz, odd Oz/ten-m homolog 1(Drosophila) [Source:HGNC Symbol;Acc:8117]
Mouse Orthologue:
Odz1
Mouse Description:
odd Oz/ten-m homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1345185]
Alleles
There are 17 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14203 | Nonsense | Available for shipment | Available now |
sa31428 | Essential Splice Site, Splice Site | Available for shipment | Available now |
sa11851 | Nonsense | Available for shipment | Available now |
sa16414 | Nonsense | Available for shipment | Available now |
sa16472 | Nonsense | Available for shipment | Available now |
sa20387 | Nonsense | Available for shipment | Available now |
sa20386 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14203
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 |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 551 | 2571 | 9 | 29 |
ENSDART00000144198 | Nonsense | 388 | 2389 | 7 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23176780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20889652 |
GRCz11 | 5 | 21393452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGRCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAA[C/T]AGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAG
Long Flanking Sequence:
ATAGAGGAAAAGAAGCTGGGGCTTCAAGCACAGATTGTGAACACACACCACTAAATTCCTCCATCCAATGCATAACCCCAGCAGGAAGAGAGCAGTCTCGTCATGGTACAGTGCCGCAACCAGCTGTGTATCAGCATGAACCACCAACAACACACAGAAAATCACCGCCACTCAGTTCAAAAATGCCCATATACTGCATGTTTGCTGCAAAATGGAGGAAAACAATGCATAAACTGCTTTTGACGTGCAGCAGCGCTACTTAGTAAACACACACTGATTCATGCATCCAGTCAGTATGAAATCTAAGACTTTGTTTGAAGGGAAACTTTTTGAGTGCACTTCTAAAGAGATGGTTTGATGATAGATGGCAATGAAAGGTAACAAAACTCTGTCATTTTTTTTTTTCAGAGGTTTGCCCTGTTCCTTGCAGTCCACATAGTGTGTGTGTTGCTGGGCGTTGTCAGTGCGAGGAAGGGTGGGAGGGAACCACTTGTGACAAA[C/T]AGCCCTGCCATCCAATCTGTGAAGAGCATGGAGAATGCAGGGACGGGCAGTGTGTCTGTCAGCCTGGTTGGGAGGGAGAGCACTGCACTATTGGTAAGTTCTTATAAGTTAATGCACACTGACAATAAGACATTTGCATTAAATCAGCATACAACAATGATTTCTGACACGAGACTGCACTAATGACTCCTGAATATTCCAATAGTATTTGGATGAAGCCTTTATTATGCACTCAATACATACACAGTGCACTCAATGAAGCTAGTGACATCACTGTGATCATTGCATGCAGCTCAGATTGCAAGTGCACCAGGTCTTTGCCAGCATGTCCTGGAAAATTCGGAAAAGTCCCATTGACTTCCATTTGACTTTCCACCAGGCTGTCATACAGACTTACAGTTGAGCTCATTTAACTCAGACTACCAATCTGCCAATCACTGATGATCTTTCAGCCACACGCTAGCAACCACTTACAGCACCCTAGCAACTGTCCCATAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31428
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 > C
Consequence:
Essential Splice Site, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040184 | Essential Splice Site | 641 | 2571 | 12 | 29 |
ENSDART00000144198 | Splice Site | None | 2389 | None | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23167554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20880426 |
GRCz11 | 5 | 21384226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCATCAAGGCTACATGTCTCATGTAAAGTGTGTGTGTGTGTGTGTTTT[T/C]CAGATGGTCTCATGGACTGTGTCGACCCAGACTGTTGTAGTCAGCAGGTG
Long Flanking Sequence:
ACTAAACTAAAAATAAACTGCAAAAAAAAATCGTAGCTCCTGAGACATGTTTCGCTCTCTCTTCAAAAATGTATACTGGGATACATGTCCATAATGAGCCTGGGTTGATTATAATGGGCAAAAAATGCATAAAACATGTATGTAAGGTGATTTGCGATTAACAAAAATATACTTTGTAAAAGGCATGTCCATGCAAAACAATATATATTTCAGAGATTTATTTGAGTAATTAGCGATTGAAACCAGCTTCAAATTAAACAGTGAAAGTCTGTAATAGGCATGTCCTTTTTTAAAGGCATCTAAGTAAACATATGTGTGAGTGTGTGTGAGAGGTTTCTGGGTTATTCTCTCTGAGACTCTCTCCTGTGGGAGGGTAAAAGCACAGATCCCCTTTAATGGAGCTGACAAATGAGATCATGTGCACACAGACACACGCTGAGCAAGGGCAACCTGCATCAAGGCTACATGTCTCATGTAAAGTGTGTGTGTGTGTGTGTTTT[T/C]CAGATGGTCTCATGGACTGTGTCGACCCAGACTGTTGTAGTCAGCAGGTGTGTGCGAGCGCCCCACTGTGCCAAGGCTCTCCTGACCCTCGTGACATCATTCAGCAGAGCCACACCTCTTATGAAACTCGCCCTTCGCGTCAGTTTTTCGAGCGTGTGCGATTCCTCATCGGACGGGACAGCACACACATACTACCAGGAGACCTGCCATTTGACAGCAGGTGAAAAACAAACGCTTGTAAATATTTGCACTCTCAAATGCACACAAAGTCTTTTTTTTTACAGGTGAAGCAGCATTTTTATATTTATTTTGGTCGTAAGATTAGCTTTTTTTTACCATACACATCATATTCCAGTGAAATCACTCTTCTGCTTTTGTATTTTTATGACTGCTGTGCAATACAGCAGAGATTCTGTGTAGAAGCAAAAGCAGATGCTGCTGTTTTATTAGGTCAGACACTGACAGACATCTTCGCTCAGACTTTGGTCACGATCTGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11851
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 746 | 2571 | 13 | 29 |
ENSDART00000144198 | Nonsense | 572 | 2389 | 10 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23162797)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20875669 |
GRCz11 | 5 | 21379469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTCGTTGGCGTGAACGTCACGYTTCAGCATAACCCTGAGTATGGGTA[C/A]ACACTCAGCCGGCAAGACGGCAGGTAACACACACTCTAAWGCACTTTGCA
Long Flanking Sequence:
GAAAAAACCTTAACAGATCCAAAAATGCATTATGAATATTGTGATGTTTTGTAAATACATCCACACACCACTGAAAGTGTTTGGTTAGCACATGCGAAGTGAACTCGCCTCTGGCTTTCCTATGCTGATCCAATACCAGCTTGTGCTTTGAGCAGTGTGACTCACCCCAAAAATAATCTCCCAAAATGATTTTTGCCATCATCGTCTAGTTTGAGGAAGTATGCGATCGATTGAAGCATGTATTGTATTTTTCTCTGATTACTGGAAAGAGAGTGCTGCTCTCCCAGCTTCGATCTCTCCTGACAGATCCTGGTTTCTCTTGCAGTGGCTGCACTCATTCTTTCCCTCTCTTTCCCTCCCTCTCTCTCTACCTCCCGTCTCTCTCTCTCTCTCTCTCTGTGCAGTCGAGTGTGTGTAATTCGAGGTCAGGTTTTGGCCTCTGATGGAACTCCTCTCGTTGGCGTGAACGTCACGTTTCAGCATAACCCTGAGTATGGGTA[C/A]ACACTCAGCCGGCAAGACGGCAGGTAACACACACTCTAATGCACTTTGCAAAGAAAGACATATAACAGAACACACACTGTTATAATCTCTCGTGAACATTCCTCTTTATTTATGCAGTGCATTCAGTATCTTCTGCTTGTTGTGTAGGTCCTGCATACTGTATCTACTCCATTCTATGCATACAGTGGGAGGCAAAAGTCAGCTAGTTGAATACAAAAAAAAAAAAAATAAATGGATTGGATATTTTACAAGAATTTCTTATTCTTTTGCTAACACCTACACTTCTGTTGCATGAAATTCAAGTTTGCAGTTATTCTTTGTTTGAGATTGTTGCCATTCCTCATTTTAAACAATGATTTTATAATATTGCAGAATGTCTTTCTTATTCATACTTCCATATATTATAAAATATAATTAACTGCAAAATGCAACGCTTTCAAATATCAGTACAGTAACTAAACAAGCGTATGGACAAGTTGTATAAAAACATTTTGGTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16414
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 1333 | 2571 | 22 | 29 |
ENSDART00000144198 | Nonsense | 1151 | 2389 | 18 | 25 |
ENSDART00000040184 | Nonsense | 1333 | 2571 | 22 | 29 |
ENSDART00000144198 | Nonsense | 1151 | 2389 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23115135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20828007 |
GRCz11 | 5 | 21331807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCT
Long Flanking Sequence:
AAAAACTACATATACAGTATATAGTCAGTATATGTAGGCTATATACACAGAAAATTATACTACTGACATCTTTCAAAGGTACATAGTGTATATTTCTATTGCATATTGTTACATATTACAGGTCTTATACAGTACTTGCATTTTGTTACTGCATTTGATCCAAAATGGTCTGCGGTGTGCCATTAGGCAACTATGCTGTGTGACTCTGTCATGCTGGGAGATTCAATTTGTGAATATTTTCCTGCCAGACTTGTTGGTATGACACATTTAAGAGTCCTGGCTGCTGCTGTATGCAGGTTTAATTAGAGAAAAATCTTTATTATTTAACTGCCATAGACAAGTGTTGCAGTTTTACTGCAGCGGGTCTCTGAGGGTTAATCGTTAAGCCCAACACTGAATGCCTAATGAACTAGACTTCCCTTTTTCCACTTCTTCTCCCTCTCATTCTCTCCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCTGACCTGGGGAATGTGCGCATTCGCCGGCTCACCGCTAACCATCCGCAGCTCAATCCCGAGGGGCTGTACGAGCTCGCCTCCGTGGCCGATCAAGAGCTCTATCTGTTCAGTCCAAACGGCACTCACCTGTTCACCCGCAGCCTGGTGACAGGGGACTACCTGCTTAACTTCACATACACCCCAGAGGGCCACCTGAGCAGCATAGCAAACAGGGAAGGCACCATAGCGCAGTTGCGGCGGGATGCTAATGGCGTGCCCCTGTGGCTCGTAGCCCCGGGCGGCCAGGTGTACTGGCTGACCATCAGTAACGCCGGGATGCTGAAGCGCATTTCGGCTCTGGCGCACGACCTGGCGCAGCTCAGTTATTACGGCAACACGGGGCTGCTCGCCACCATCAGCAACGAGAACGGCTGGACAAGCGTCTACGAGTAAGTGCTGTCCTTCGTCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16472
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 1333 | 2571 | 22 | 29 |
ENSDART00000144198 | Nonsense | 1151 | 2389 | 18 | 25 |
ENSDART00000040184 | Nonsense | 1333 | 2571 | 22 | 29 |
ENSDART00000144198 | Nonsense | 1151 | 2389 | 18 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23115135)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20828007 |
GRCz11 | 5 | 21331807 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCT
Long Flanking Sequence:
AAAAACTACATATACAGTATATAGTCAGTATATGTAGGCTATATACACAGAAAATTATACTACTGACATCTTTCAAAGGTACATAGTGTATATTTCTATTGCATATTGTTACATATTACAGGTCTTATACAGTACTTGCATTTTGTTACTGCATTTGATCCAAAATGGTCTGCGGTGTGCCATTAGGCAACTATGCTGTGTGACTCTGTCATGCTGGGAGATTCAATTTGTGAATATTTTCCTGCCAGACTTGTTGGTATGACACATTTAAGAGTCCTGGCTGCTGCTGTATGCAGGTTTAATTAGAGAAAAATCTTTATTATTTAACTGCCATAGACAAGTGTTGCAGTTTTACTGCAGCGGGTCTCTGAGGGTTAATCGTTAAGCCCAACACTGAATGCCTAATGAACTAGACTTCCCTTTTTCCACTTCTTCTCCCTCTCATTCTCTCCATGAATGTGTCCCCAGGTGACGGAGGTTACGCTCGCGATGCCAAGCTG[A/T]AGTCTCCCTCATCTCTAGCGGTTTCTCCTAATGGCTCCCTCTGCATCGCTGACCTGGGGAATGTGCGCATTCGCCGGCTCACCGCTAACCATCCGCAGCTCAATCCCGAGGGGCTGTACGAGCTCGCCTCCGTGGCCGATCAAGAGCTCTATCTGTTCAGTCCAAACGGCACTCACCTGTTCACCCGCAGCCTGGTGACAGGGGACTACCTGCTTAACTTCACATACACCCCAGAGGGCCACCTGAGCAGCATAGCAAACAGGGAAGGCACCATAGCGCAGTTGCGGCGGGATGCTAATGGCGTGCCCCTGTGGCTCGTAGCCCCGGGCGGCCAGGTGTACTGGCTGACCATCAGTAACGCCGGGATGCTGAAGCGCATTTCGGCTCTGGCGCACGACCTGGCGCAGCTCAGTTATTACGGCAACACGGGGCTGCTCGCCACCATCAGCAACGAGAACGGCTGGACAAGCGTCTACGAGTAAGTGCTGTCCTTCGTCTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20387
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 1930 | 2571 | 27 | 29 |
ENSDART00000144198 | Nonsense | 1748 | 2389 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23085328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20798200 |
GRCz11 | 5 | 21302000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTA[C/A]GACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTT
Long Flanking Sequence:
AATGGGTGAGGTGATAATCCTGTGAGACAGAGAGACGAGTAAGACGGCTGAGCGGTCAGACAGGTAAACAGGTTATACTCTTCCACCAATAAACATACAGGCTGACATTTAATCTTCCTTTTGTCACTTGGCTTGCACTCCCCTCCTGCTTGGCTGATCTAAAAGCGCTTTGAATCACAATCAGCCGTCTGACAGTGGCGGAGTTCATCCTATCTCACACTGTGGCAAAACTGACTCGTGTTTTACCTCACCTCTGTCTGGCTTTCTGCTAACTTCTTTCCACTCTGTTTCTCGCATTCAGGTCCTCTGGTGAGCAGACAAATATACCGTTTCAGCGAAGAAGGATTGGTTAACGCTCGCTTTGACTACAGCTACAACAACTTCAGGGTCACCAGCATGCAAGCTATGATCAACGAAACACCTCTTCCTATTGACCTCTACCGATATGTGGACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTA[C/A]GACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTTCAATCCCAATGGGCAAGTGATCGAGGTTCAGTATGAGATTCTGAAATCCATCGCCTACTGGATGACGCTGCAGTACGACAGCATGGGACGCGTCACAAACTGCGATATTCGCATTGGTGTGGACAGCAACATCACACGGTACGCATATGAGTATGATGCCGATGGCCAATTGCAGACGGTTGCCATTAATGACCGCCCACAGTGGCGTTACAGCTACGACCTGAATGGAAACATCAATTTACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTTCGAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGATGGGTTCTTGCGTCTTCGAGGCAACTTACTCTTTGATTACGGTTCGAATGGACTGCTAATGGGTGCCTATGATCGGGACAGTGAGCAGAGAGTGTGGTACCGTTACGATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20386
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 |
---|---|---|---|---|---|
ENSDART00000040184 | Nonsense | 2044 | 2571 | 27 | 29 |
ENSDART00000144198 | Nonsense | 1862 | 2389 | 23 | 25 |
Genomic Location (Zv9):
Chromosome 5 (position 23084988)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 20797860 |
GRCz11 | 5 | 21301660 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTT[C/T]GAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGAT
Long Flanking Sequence:
AAGGATTGGTTAACGCTCGCTTTGACTACAGCTACAACAACTTCAGGGTCACCAGCATGCAAGCTATGATCAACGAAACACCTCTTCCTATTGACCTCTACCGATATGTGGACGTGTCTGGACGTATCGAGCAATTCGGGAAGTTCAGTGTCATCAACTACGACTTGAACCAGGTCATCACCACACATGCCATGAAGCACACTAAAATCTTCAATCCCAATGGGCAAGTGATCGAGGTTCAGTATGAGATTCTGAAATCCATCGCCTACTGGATGACGCTGCAGTACGACAGCATGGGACGCGTCACAAACTGCGATATTCGCATTGGTGTGGACAGCAACATCACACGGTACGCATATGAGTATGATGCCGATGGCCAATTGCAGACGGTTGCCATTAATGACCGCCCACAGTGGCGTTACAGCTACGACCTGAATGGAAACATCAATTTACTGAGTCACGGCAACAGTGCGCGATTGACACCATTGCGTTACGATCTT[C/T]GAGATCGTATCACGCGGCTTGGAGAAATCCAGTATCGCACTGATGAAGATGGGTTCTTGCGTCTTCGAGGCAACTTACTCTTTGATTACGGTTCGAATGGACTGCTAATGGGTGCCTATGATCGGGACAGTGAGCAGAGAGTGTGGTACCGTTACGATGGGCTTGGGAGGAGAGTGGCCAGTCGCTCTAGTGACGGAGCACAGCTGCAGTTCTTTTATGCCGATCTGATGGAACCAACGCGGGTGACGCACCTTTACAACCACAGCAGCGCAGAGATCACCTCCCTCTATTATGACCTACAGGGACATCTCATCGCAATGGAAATGAGCAGCGGCGAAGAATTCTACATAGCATGTGACAATGCTGGAACTCCACTTGCGGTTTTCAGTAGCCGTGGCCATGTAGTGAAGGAAGTTCGGTACACACCGTATGGAGATGTTTACCGGGACTCCAATCCTACCTTTTCTCTGATCTTCGGATTTCAGGGCGGCCTCTATGAC
Associated Phenotype:
Not determined