ZMP
si:ch211-236p22.1
Ensembl ID:
ZFIN ID:
Description:
Novel sushi domain containing protein [Source:UniProtKB/TrEMBL;Acc:Q1LVL7]
Human Orthologue:
CSMD3
Human Description:
CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:19291]
Mouse Orthologue:
Csmd3
Mouse Description:
CUB and Sushi multiple domains 3 Gene [Source:MGI Symbol;Acc:MGI:2386403]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42822 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42821 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17497 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42822
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074570 | None | None | 353 | None | 9 |
ENSDART00000143582 | Essential Splice Site | 58 | 429 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 50774849)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47628924 |
GRCz11 | 16 | 47564010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTTGCCAAGCAGACGCCACATGGAGCGGCACTCAACCACGCTGCATAG[G/A]TATATTTACTTTTAAGAACGTTTTCCTCTTATCAATAAATACTTTATCAT
Long Flanking Sequence:
CCAAGACCTCATGCATCTGTTGCTAGAGCGCCTTTAGAAGTCAGAAGAGTGAGGTTTACCTGCACAGCACTTCCCTAGCTGGCCTCTGTTACACTCACCCCAATAAACCTAACTCTCATCCCGGACGAGCCCCCACATGTTACTCACCGGTCCTTTAATCCCAGCTCAGACTGTGTTGGGTGCAGGAGGACTGGTGGGTTACACACCTTTTAGGACTGGGGGGTTACACAACTTTTACTACAAATTGAAGCAATTTTATTTAGAAAACTCATTTCATTAATAGTCGACCTCAAAAGACTCGATCTTTTATTTCTTTGTCTCCTCAGCCAAGTTCTGTGGTGATCCAGGAATCCCGAGCCGGGCCAGACGAGAGGGTCAGAGCTTCATCTTTAAAGCTGAGGTGATGTTCAGCTGCAGCGCCCCCTATGTGCTGGTGGGCTCCTCGACACGCACTTGCCAAGCAGACGCCACATGGAGCGGCACTCAACCACGCTGCATAG[G/A]TATATTTACTTTTAAGAACGTTTTCCTCTTATCAATAAATACTTTATCATTTAATCTTTACTGTTTTTCTCAGTCGCTTTGGTACATTTCTCAGATAAGAATTGAAATTCTCTCCTGTTTAATCTTCAGGTCATTGTGCTACCTGTGTACATCAAAAAAGCAGTTTCTTTGAACAAGTTGCAAATGCTTTTGTACATCTATGCAAATGATTATGTATTCTCTGATGTTTCCTACTTTATCAGCTATTCATGTCATGTTGATCAAAATTCATTATTTTGGTCTCTGTTGAATAGTCTCATCCCACACAACGTTTAATTGTTCATGTTCATGGCAGTTTACATGCAAAAGGGCTGAACATACATTTAGATTTTTCTGTGTGCTATGCTGTGTTGTCTTTTCCTTTTTGTATCACAATGACATGATTGGTCAACAAACTACAACACAAACAGCAAAAATAATTACAAAATAGCCATAGTTTACATCAGAATATCCATCCACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42821
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074570 | Essential Splice Site | 16 | 353 | 1 | 9 |
ENSDART00000143582 | Essential Splice Site | 83 | 429 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 50771505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47625580 |
GRCz11 | 16 | 47560666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCTGGCACTCCAGAATTCGGCTCTTTGAACAGCAGTCTGGGCTTTAAG[G/A]TAAGAAGCAGTGGAGCTTGGACTGTCTTGGCCTCTTATATCAAAGCCATT
Long Flanking Sequence:
GACAACGCGAGAGCCGTCCACTACGCCACTAATTGTACCTGGTATAGCCATTAAACTAATTTTCTAGTGAGATGCTAGTGGTCCAATCCAATTTAATGATTGATGCTAAGCTAAGCTAAAATTGTTCTCGTCAGACCCGAAGATCGTCTGAATGGGTTCAAAAATGATAAAACTCAACTAGTAAACTCCAATTTCCTATTTTCCCATCTAACTGCCTACTTGCAAAAAAAGGTGAAGTGTTCCTTTAACCTTGAATGTCACATCCATACACTCTTAATATCCACTCCAACTTTGATCTATGAACGTTACATGAACATTACGACCCTCTTCTCCAGGTCACAGCCATTACATCAACCGCTACATCTTCTTTTCATAATCCAATTATAAGGATCTGAAAATGACAGTTTCGTTCTTTCTTCACCGCAGAACCGACCCGAACGACTTGTGAAAACCCTGGCACTCCAGAATTCGGCTCTTTGAACAGCAGTCTGGGCTTTAAG[G/A]TAAGAAGCAGTGGAGCTTGGACTGTCTTGGCCTCTTATATCAAAGCCATTATGACGAGAGTTAGTTCAAAAGGCCCCATTTCTGTCAGTTGTAGCCTGCTTTTATCTTCAAGTGCGAAAACGGCCCCTTTCAAATGGCACAATGTGACTTTTGATGTGCCTATTAAGGGCTGAAAGTCATATTTTCCATCATCGCTGAGACAAAAGGATATTCGCTCGCCGGGTGACAGAATCATCCGAAGGCGTTAATGCCACATGAGAGAGTCGAGTGCGAGGTTTTGTCATCTTTCCGGACCGGCCCGTATTTTATGAGTGCAATTGATTTATTGTCAAGTTGATTCAGTCAAATGCTGTTTGAAGAGCAGTTTCAGGATGTGTGACTGACTGACTCTTAATGTCTGGAGAGAGTTTACTATTCAGACGCTCATGATATCCAGCCCAGTGCATTTGATGCCACTTTTAGGGTTAGTAGTGGTCAACTGTGTCAATGTTTTAATAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17497
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 |
---|---|---|---|---|---|
ENSDART00000074570 | Nonsense | 41 | 353 | 2 | 9 |
ENSDART00000143582 | Nonsense | 108 | 429 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 16 (position 50765159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 47619234 |
GRCz11 | 16 | 47554320 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTCAGACGGGCCACTTGTTACTGGGCTCCACCACACGCACRTGTCAG[C/T]AGGATTTGACCTGGAGTGGCTCTCAACCTGAATGCATCCGTGAGTCTCAC
Long Flanking Sequence:
CAAATCCGTTGCTAAGGCATACTTTATGTAGGTCGATTAAATTATGCGCCAAAAACAGGTTGACAACACTTGTTAATAAATACAAAATACATTCTATATTAAAAATATAAGCTGTATCTCGCAAAAACCGATGCATCTTGATTTGCTTCCAAAATTTCATTCATCCTCTGCTGCTCTACCGATGCACTCGCATTGTGCACGCGCATGACCGCGTATCGATACATATCGATTAATCTTCCCATCCCTACTGTAGACTGATGTAATTTTATGCCGTTCAGGCTTATAACCGTAATATGTGAGCAAAAATTATTCCCTATTCTGGGTCACCATGGGTTGAGAGGACGTGAATGCGGTGTGTGGGTGTATATATGTATGTGTCTGTGCTGTGTATGTGTGTGTTTTCTGACAGGCTTATCTCTGCTTCTCAGGTTGGTAGTACAGTGAAGTTTGTCTGTCAGACGGGCCACTTGTTACTGGGCTCCACCACACGCACGTGTCAG[C/T]AGGATTTGACCTGGAGTGGCTCTCAACCTGAATGCATCCGTGAGTCTCACTCACTCAACACACACACACAGACAGACTGGTTCTTATATCTCTGTGGGGACTCTGATAGACGTAATGATGTTTCTACTATATAAACATTATATTCTTTCCCTCTACCCCTAAACCAAACCCACAGAGGACACACTCTGCATTTTTACATTTTCAAAATAAATCATTCTGTGTGATTTAAAAGCATGTTTACCTCAATTTTGTTTACCTCAAGTCCCCTTAAGTCTGTGTGCAGTCAGGTTTGAGTCCCCATTGGGATATGAAAACAAGTACACACACATGCACACACTTCTACATGATTTTGGTGCATTTGTGTGTGTGTTGTACTTCATCTTTTCAGGATTTTTTTTTTTGAGGCAAGTCATCTATTTTGCAAGTTATGTTATAACATTTATTTCCCCCTGCAGGAGATTTGTTTTCCATATGCACGTCATTCCATATGAAAGTGAAAA
Associated Phenotype:
Not determined