ZMP
si:ch211-46o5.1
Ensembl ID:
ZFIN IDs:
Description:
Novel protein similar to vertebrate CUB and Sushi multiple domain containing protein family [Source:
Human Orthologue:
CSMD2
Human Description:
CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:19290]
Mouse Orthologue:
Csmd2
Mouse Description:
CUB and Sushi multiple domains 2 Gene [Source:MGI Symbol;Acc:MGI:2386401]
Alleles
There are 18 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10968 | Essential Splice Site | Available for shipment | Available now |
sa9832 | Nonsense | Available for shipment | Available now |
sa11417 | Essential Splice Site | Available for shipment | Available now |
sa36882 | Essential Splice Site | Available for shipment | Available now |
sa15257 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10968
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001805 | Essential Splice Site | 961 | 3604 | 18 | 70 |
ENSDART00000132471 | Essential Splice Site | 828 | 3456 | 16 | 68 |
Genomic Location (Zv9):
Chromosome 19 (position 37911453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 36775973 |
GRCz11 | 19 | 36363093 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAATGTGAACCAAACTTCCAGTGGAGTCGCCCCCTGCCCAGCTGCGATGG[T/C]ACAGTCCACYCTTTACCACCCAAAAAACAGGCACTAGCAGGGAAAAGGAC
Long Flanking Sequence:
ATAAATATCAATAATTATGCAAAATTTCATAAGTTTAATTATTGAGTTAATGCCTGATCAGTGATAAGTAAAAATTATTAAATACATAAATAAATAAATAAATGACAACAAAACAAAAACTAAATAGTATATGTATTGCTTCCATATATTAGTTAAATGTTGGCATTTTACTTTGTATATTATTATTAGCATTATACAAGTTAATAATTCAATACAATTACAGTTAAAATACATTGTCTGCTAGGAAATCCTCTCATCTAAATCATCAGCTTTAATCCCACATTACCCTTTGTGTTTTTCTGTCTTGTAGCTCTGCAGCTTCAGTCGGACCACTGTGTTGATCCAGGAATCCCAGTCAATGGTCAGCGACACGGCAATGATTTCTACGTGGGAGCGCTGGTGACATTTAGCTGTGAAGCCGGATACACTCTCAGTGACCACGAGCCCCTCGAATGTGAACCAAACTTCCAGTGGAGTCGCCCCCTGCCCAGCTGCGATGG[T/C]ACAGTCCACCCTTTACCACCCAAAAAACAGGCACTAGCAGGGAAAAGGACACATTAGAGACAGGTCATTTATTCAGTCGCTCCAAGACTCGAAAGGCCTTTACGGTTTGAAGCTCCACTTCTCCGTTTCCACCGGGCTTTGAATATTTAAGGCCATTATTGATTTTTCCCCTTGGGTAATGATAGGAATAATTCCGCCTCCATATGTTGATGTCCTTTAGAAGGGCACTTGGTGTAAAGTTGTTGGGCAGGATTGTGCTCAGCGGTTTGACGAATTGCCTTTATCTTTTTTTTTTTTCTTCTAGCGCTCTGTGGAGGGTTTATTCAGGGGAACAGCGGCACTATTCTGTCCCCTGGGTTTCCAGATTTCTACCCACATAACCTCAACTGCACCTGGATGATTGAGACTTCACATGGGAAAGGTGAGAGCGCCGGCTTCTGCTTTTGACAGTCTTCTTGAAGGGTTACGTTTATATGGAATTAAATATTCTTTTAGAAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9832
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 |
---|---|---|---|---|---|
ENSDART00000001805 | Nonsense | 1010 | 3604 | 20 | 70 |
ENSDART00000132471 | Nonsense | 877 | 3456 | 18 | 68 |
Genomic Location (Zv9):
Chromosome 19 (position 37904318)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 36768838 |
GRCz11 | 19 | 36355958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTCCTCTCGATCTCCACAGGAGTYCAGTTTACCTTCCACACCTTTCACT[T/A]GGAGAGTCCTCACGACCACCTTTTAGTTACAGAAAATGGTAGTTTTTCTC
Long Flanking Sequence:
CTTGTTTACTAAAATAACCTTGTGCATAACATTGGTAAGGTTTTATTTTACAAACAAAGTACTTTTGCATTCACAACAAAACACACATCATCTGCACAACATGCTGGAGAAGGCAACAATAATTCAAAGTGTTGCAACTTCTTTGTATATAGTTTTGAGTGACAATCTTCTCAAAGACTGATCTCAATTTGGTGACATTCTCGAACAAAGTATAAGGCTTGGATGCATCTTATAAAACTTTCATAGACAATATATTTTTGTGTTTGGGTCTTTGATACAAAATCGCATCATACAACTATTTTAATATCATGTTGAAACAGGAACATGTCTGGCTGACCACTTCTAAACTAATCACTGAAAATGAATAAAAACACAAGCTTGAACCATTGTTTATGTGACTGAAGCTCTTTATGATCTCTTAAGCTGCTCATATATAACCAGTGTTCTTCTCTTCCTCTCGATCTCCACAGGAGTCCAGTTTACCTTCCACACCTTTCACT[T/A]GGAGAGTCCTCACGACCACCTTTTAGTTACAGAAAATGGTAGTTTTTCTCAACCCCTGTGGAGATTGACCGGCTCGACACTTCCTCCTCCTCTTAGCGCTGGACTCTTCGGCAACTACACCGCTCAGATCCGCTTCCTCTCTGACTTCTCTGTTTCCTACGAGGGCTTTAATATCACTTTTTCAGGTACAGGGCTTTCTGATTTTTATAACAACTAGATCAGATTTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTATTTATTTTTTATTTTATTTTTTATTTATTTATTTATTATCATATTTATTTATTATCATATTTTTATTTATTTATTATCATATTTTTATTTTTTTATTCTCATAGTAATTTATTTATTTTCATATTTATTTATTTATGTATTTATTTATTTATTATCATATTTATTTATGTATTTACTTATACTAATGTTTGTTTATTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11417
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001805 | Essential Splice Site | 2177 | 3604 | 42 | 70 |
ENSDART00000132471 | Essential Splice Site | 2029 | 3456 | 40 | 68 |
Genomic Location (Zv9):
Chromosome 19 (position 37771389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 36635909 |
GRCz11 | 19 | 36223029 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAACAYGGCACGACGCGCAACTGGGATCATYCGTTTCCTCGCTGTGAAGG[T/C]ACGACCCTCTTTATTTCSTCCCCCACTTCAGTAAACATCTGCTGTGCTTA
Long Flanking Sequence:
GCAGTTGGCTGCCTGTGTGAACATTGATCAACATATTGCATTTCCGTGAAGTTCAGACTTCCATCATTGAAATCTGAGAGGAAATGACAGCATCTTTCATTGCCGGAGCTTTGATTGCCTTTGCTTTGAATCAAATCCCAAAGCTTTGTTGGGGCACAGCAATCAGTTGATTCCATGGGTACGGTTTACGTTTAATATTCAGAGTCTAGGTTTGGATTGGATCTTGGAGCTCAGAGCAATCTCTTTTTTAAATGAAACATACATTTTCATCCTCTATGTATCATGCATCAAGTATGTCTGTCTCTTTCAGCATATGAACTCCAGGAGTGTCCTGATCCTGAACCCTTCCATAATGGTGTGGTGGTTGGTGCTGGTTATAACGTGGGTCAGTCCATCTCCTTCGAGTGCTATCCAGGGTATCATCTGACAGGACACTCCATTCTTACCTGTCAACACGGCACGACGCGCAACTGGGATCATCCGTTTCCTCGCTGTGAAGG[T/C]ACGACCCTCTTTATTTCCTCCCCCACTTCAGTAAACATCTGCTGTGCTTATTTGCATTGTGAGAGAATAGATTTATTCGGCATGCTAATTGACATTTTTAGCTTTTTAAAATTTAAAATTTTAATTTTTGATTATAATTGTCATCCTAATTAGCTTTTTACAGGTAAAATATAAAGTAATATTTTCTATTTTTCTATATATTTTATTCTTAAAAAGAGTAAAATTATGAATTAGGATGACAAATATGGTCATGCTTTACGATAAGGTTTCATTTGTGTATTTACTAACAACAACTAATTATAAACAATACACATACAGCATTTATTAATCAAAGTTCAACATTTACTAATGCATTATTAACATCTGTAATAACGTAACGCAATTATAATTTTATTTAATTATATGTTTTATTAAATCCAATGAGGACTTAGAGAAACTTGTTCATGCTTTTATCACCAGCAGGGTGGATTACTGTAACGGTCTGTTGACATGAAGTAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36882
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001805 | Essential Splice Site | 2768 | 3604 | 53 | 70 |
ENSDART00000132471 | Essential Splice Site | 2620 | 3456 | 51 | 68 |
Genomic Location (Zv9):
Chromosome 19 (position 37716245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 36580765 |
GRCz11 | 19 | 36167885 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTGTGAGCAGGACCACCGCTGGTCCGGGAAGACTCCTGTCTGTATCCG[T/C]AAGTGTTGCTTAAGCAGCAACTCTCTTATCTGAGGTCTTTTGACAGTTTT
Long Flanking Sequence:
GAATATTTTTATGTAAAAACCATGACATCACATGAGTTGCACATGAATATCTTCCATAACCACACATTTTTACGTGTTCCACATATTTCAGATGTAATTTTAACATCACTGCACATGTGTAGCTTATGTCTATAAGGGACGAGGACCTGATCAAGATTTTAGTTATTTCAAAATTCATTAAAGCCTGCAAAAGCTAAATTAATTAAACCTAAAGTTATCAAGCAAATACATTTAAGAAATGGATGCAGTATTATTATTAATAATTCAGTCAATCACTCTTTTATGTGCTCTAAACAAGCATTTGCACCGTTTTTTTTTTCAACAGCTGGACACTGTGGCACACCAGAGCCTATAGTGAATGGTCAGATCATTGGAGAAAACTACAACTACAGAGGCAGTGTTGTTTACCAGTGTAATCCTGGATTCCGGCTCATCGGCGTGTCCGTTCGCATCTGTGAGCAGGACCACCGCTGGTCCGGGAAGACTCCTGTCTGTATCCG[T/C]AAGTGTTGCTTAAGCAGCAACTCTCTTATCTGAGGTCTTTTGACAGTTTTATGCCTCAGATGAATGAAATAATCATGTAAATGGCATTAACTTGTTTGCTGGTTTCTCCACAGCCATCACATGTGGACATCCAGGCACTCCTGCTAATGGTGTGACGCAAGGAACACAGTTTAACCTAAATGATATTGTGCGTTTCGCATGCAACCCTGGTTACGTTCTACAAGGTGCGCTCAAGTCTCAATGTCAATCCAACGGCCAATGGAGCAACGCTCTTCCCAGGTGTAAAAGTAAGTTATTTGGATTTATCTTCAGCGGCGCTCCTTTGGATGTCACTTGATAAGAGAGTGTGAATAGTATTTTATCAGGTTTAAATAGCTTGAGTGCTCTATTGAACTTTGCTTTATAACTTTATAACTGCTGGCGAATAAAAGTTTGTCTTCTAATAATAATGGAGGTAAGCATTTACATGAAAATACTTATAAAGACTTGGATGTGTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15257
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001805 | Essential Splice Site | 3008 | 3604 | 57 | 70 |
ENSDART00000132471 | Essential Splice Site | 2860 | 3456 | 55 | 68 |
Genomic Location (Zv9):
Chromosome 19 (position 37701249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 36565769 |
GRCz11 | 19 | 36152889 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGTCTGGCTAAYGGGAGCTGGGTGGRCATCCAGCCYGAATGCCACGR[T/A]AAGAAATATGAANCGCCATGCGCAGCTGAACGTACATGATTWATCGCTTC
Long Flanking Sequence:
CTTTGTATGTGTGTTTTGAATAAAATTTAATTAAAAAAATCACCAACAAAAAAAAAGAAAAAAAAAAAGAAAATTTCTGTGGTGAAGCAGGTTTACAAGTGTTGACTTTTTTATTAATTAATTAATTAATACAATTAATTTAATTTTGTTTATATTTATTTAAATTTATTTAATTTTCAAGGCCACACAAAAATACTTCTTTTATCTCTGTAAAAAACAGAAAGAAATTAGAATTTGTAAAATACAATGCATTCACATGAAACTAGTAATAAAGCAAAGCGTCCAAATAAATGCTGATAAATGTGTGCTGTTTCAGGGGATTCTGCTGGTCTGTGTGGAGATCCAGGCATTCCAGTACATGGGATCCGTCTGGGAGAAGAGTTCACCACAGGGAGTGTTGTCCGATTCAGCTGCGAGCCTGGATACCAGCTGAAGGGCTCCTCCGAGCGGACCTGTCTGGCTAACGGGAGCTGGGTGGGCATCCAGCCTGAATGCCACGG[T/A]AAGAAATATGAAACGCCATGCGCAGCTGAACGTACATGATTAATCGCTTCCACTTCCAGAAGATTCTGCTACAACCAGAACTGTAGCCTATGCAAATTTATCAGCCAGCAACTGATTTCAAAGCAGTTTGTGTCTAAACTTTGTGCAGTTGGCGCATTTCAGGTAGTCCATTGCAATATGAATCAATTCCAAGAGAATCAAGTTTCTATCAAGGGGAACACACAGTTGGAGTCAGATTTATTTTAACACCCTTTGATTTTTTTTGGTCTTTTTTTAAATATTAGGTTTAACAGGGCAAGGACATTTTCACAATATTTCTGATAATGTTTTTCCTTCTGGAGAAAGTCTTTTGTTTTATTTCAGCTAGAGTAAAAGCAGTTTTTATTTTTTTATGAGCCATTTTAAGGATAAAATGATTAGCCCTATGAAGCAATTTTTTTCCAATTGTCTACAGACCAAACCATCATTATACAATAACTTGCCTAATTACCCAAATCCGC
Associated Phenotype:
Not determined