ZMP
ENSDARG00000077920
Ensembl ID:
Human Orthologues:
CSMD1, CSMD2, CSMD3
Human Descriptions:
CUB and Sushi multiple domains 1 [Source:HGNC Symbol;Acc:14026]
CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:19290]
CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:19291]
CUB and Sushi multiple domains 2 [Source:HGNC Symbol;Acc:19290]
CUB and Sushi multiple domains 3 [Source:HGNC Symbol;Acc:19291]
Mouse Orthologues:
Csmd1, Csmd2, Csmd3
Mouse Descriptions:
CUB and Sushi multiple domains 1 Gene [Source:MGI Symbol;Acc:MGI:2137383]
CUB and Sushi multiple domains 2 Gene [Source:MGI Symbol;Acc:MGI:2386401]
CUB and Sushi multiple domains 3 Gene [Source:MGI Symbol;Acc:MGI:2386403]
CUB and Sushi multiple domains 2 Gene [Source:MGI Symbol;Acc:MGI:2386401]
CUB and Sushi multiple domains 3 Gene [Source:MGI Symbol;Acc:MGI:2386403]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32262 | Nonsense | Available for shipment | Available now |
sa9544 | Nonsense | Available for shipment | Available now |
sa23599 | Nonsense | Available for shipment | Available now |
sa12387 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32262
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108507 | Nonsense | 471 | 1873 | 10 | 35 |
Genomic Location (Zv9):
Chromosome 19 (position 46099719)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 44993326 |
GRCz11 | 19 | 44588899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTCACCCAATTTCCCCATTCAGTACGAGAGCAACTCGCAGTGTGTGT[G/A]GATCATCACGGCCAGCAACCTCAACAAGGTGAGAGCAAAACATATGACTT
Long Flanking Sequence:
CAGCTATTCAAGCCATCTGGTGAAATTGTATTAATTTCGCAATTATAAAGTTATTAAATTTTTTTCAAGTATTTCCCAAATTATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCTATTATATTTTTTCTTAGGGTCTATATTATAAGCTCCCTTAATCTATATATATATATTTTTCAATTGTCCACAGAACAAACTTTTATGTTTAGACGTGTTGAAAAAATCTCTCCTGTCAAACAGAAATTGGGGGAAATATGCAGGGGGGCTTATAATTCAGGAGGGCTAAAAGTTCTGCCTTCAACTGTACATTATATCGCAGAAAAACAAAATATCATAATGTCAGATTTCCCCAATATCATGCAGCTCTGCAGTAGTTTATTTCCTCCTTTCTTCTCTCTGCACAGTGAAAACTTGCGGATCAAACCTTCAAGGTCCGTCTGGGACTTTCAGCTCACCCAATTTCCCCATTCAGTACGAGAGCAACTCGCAGTGTGTGT[G/A]GATCATCACGGCCAGCAACCTCAACAAGGTGAGAGCAAAACATATGACTTTCATAAGGCTGTGAGGGTTTTTTTTTTTCTAAGAGATTTACTTTTATTTGGTTGTTGCTTGCAGGTAGAAAGAGTATTAAGAAAGTAAATTACTGTGTGTGTGTCATATTCTCATTTTACTAGGTTTAAGGCACGTACAGTGCTCAGCATAATTAAGTACACCCCTTTTTGAAAGAATATTTGCATCCATTTCTCAGTAAATACATTTTGGTGCGCTAAAAAAAATTCGATTTATTAAACATATATTTATTAACATCATATTTTAGTCACCGGACAGCTTTAAAAATAGAAAGATAACACATTTTATATATTGTTTGCTTTTTAATCTTTATTTCATATTTTTTTCCTTAACATAAACATTTGGGCTACTAGTTTTTGGACTGTTTTGTTAGATTAGCTCCAGATTTGGCTTCAGTACTGACTAAACTAATATACACTACCAGTCAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9544
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108507 | Nonsense | 1442 | 1873 | 27 | 35 |
Genomic Location (Zv9):
Chromosome 19 (position 45951766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 44849988 |
GRCz11 | 19 | 44445561 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCCTGGAGTCCCGATGAATGGCAGTCGTAATGGAGACGGTCGTGAGCCT[G/T]GAGACACAGTGACCTTCCAGTGTGATCCTGGATATGAACTTCAGGGAGAC
Long Flanking Sequence:
TACCGAGTGACGAAATGTGAAGGTTTTTTTTCCGTTCGCCATGCGGTATTAAATTCCATTAAAACAGAAGTCAGTTAAAAAAAAAAAGTTAAAAATTTAACACACAAAATTGCATGAAACTCTGTAGAGCCTGGTGATGCGAAAAAAGTGCTTCCTTGGTCTTATCCATGTTTCTTTGCACGTTAAACACACGTCGACCACAACAGAAAAAAAAAAAAAACCTGCAACTGCGTTAATTACGTTCATTTTTTTTACGCGTTGATTATTTCAAATCGTTTCAAAAACGCACTAATTTTGACAGCACTAAAAAAACATTTTTGGACACTTGCAATTGTAATCTAACCAATCTAATTCATGCATTTTTGACCCTATTGACATGCAGCGTCTTGCTTTAATTAACTGTTAATTGTTTGGATGCGGTTGCAGGTTCGGTGGCCACAGCCTGCAGGGATCCTGGAGTCCCGATGAATGGCAGTCGTAATGGAGACGGTCGTGAGCCT[G/T]GAGACACAGTGACCTTCCAGTGTGATCCTGGATATGAACTTCAGGGAGACGTGAAGATCACCTGCATCCAGGTGGAAAACCGCTACTACTGGCAACCCAGCCCTCCAGTCTGTATAGGTAGGAGATTCCAGTGGGATTTCATGAAATGCAATGGTTTTATTAAAACGGCTTGATGATATGGCTTTACTCTTGCTACACTTGTACTGCATTCAAGTCTGTGTGGGTTTTTTTCTGATCAGTTTGAACCCTAAGAATTTTATTAAACTGGTAAAACGTTTTTTTTTCATATCTGTATGTATTTGTTTCAGAAAATCATATTATACTTGTATATAGTAATGTCTTACTGATGAAGTGAATGTGAAAATAACACAATGCATATTTTGAAGGTCTTGTAAAGTTTTGTTTCGAGCTTAGCCTCATATTAGAAGCATTGTTTGACTCATATTCATAATCCATATTCATGATCTGAACACATCTAAGAGGCCGAGTTAATTGGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23599
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108507 | Nonsense | 1453 | 1873 | 27 | 35 |
Genomic Location (Zv9):
Chromosome 19 (position 45951731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 44849953 |
GRCz11 | 19 | 44445526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGGTCGTGAGCCTGGAGACACAGTGACCTTCCAGTGTGATCCTGGATA[T/G]GAACTTCAGGGAGACGTGAAGATCACCTGCATCCAGGTGGAAAACCGCTA
Long Flanking Sequence:
TCGCCATGCGGTATTAAATTCCATTAAAACAGAAGTCAGTTAAAAAAAAAAAGTTAAAAATTTAACACACAAAATTGCATGAAACTCTGTAGAGCCTGGTGATGCGAAAAAAGTGCTTCCTTGGTCTTATCCATGTTTCTTTGCACGTTAAACACACGTCGACCACAACAGAAAAAAAAAAAAAACCTGCAACTGCGTTAATTACGTTCATTTTTTTTACGCGTTGATTATTTCAAATCGTTTCAAAAACGCACTAATTTTGACAGCACTAAAAAAACATTTTTGGACACTTGCAATTGTAATCTAACCAATCTAATTCATGCATTTTTGACCCTATTGACATGCAGCGTCTTGCTTTAATTAACTGTTAATTGTTTGGATGCGGTTGCAGGTTCGGTGGCCACAGCCTGCAGGGATCCTGGAGTCCCGATGAATGGCAGTCGTAATGGAGACGGTCGTGAGCCTGGAGACACAGTGACCTTCCAGTGTGATCCTGGATA[T/G]GAACTTCAGGGAGACGTGAAGATCACCTGCATCCAGGTGGAAAACCGCTACTACTGGCAACCCAGCCCTCCAGTCTGTATAGGTAGGAGATTCCAGTGGGATTTCATGAAATGCAATGGTTTTATTAAAACGGCTTGATGATATGGCTTTACTCTTGCTACACTTGTACTGCATTCAAGTCTGTGTGGGTTTTTTTCTGATCAGTTTGAACCCTAAGAATTTTATTAAACTGGTAAAACGTTTTTTTTTCATATCTGTATGTATTTGTTTCAGAAAATCATATTATACTTGTATATAGTAATGTCTTACTGATGAAGTGAATGTGAAAATAACACAATGCATATTTTGAAGGTCTTGTAAAGTTTTGTTTCGAGCTTAGCCTCATATTAGAAGCATTGTTTGACTCATATTCATAATCCATATTCATGATCTGAACACATCTAAGAGGCCGAGTTAATTGGTACATATTGCTTTAGATGTCGACAACAGAACTTGTGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12387
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108507 | Nonsense | 1762 | 1873 | 33 | 35 |
ENSDART00000108507 | Nonsense | 1762 | 1873 | 33 | 35 |
Genomic Location (Zv9):
Chromosome 19 (position 45887616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 44785838 |
GRCz11 | 19 | 44381411 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTTCAGTAYAGTTGGACCAGAGACGGCCAAAGGCTTTCATTTTGTGTA[T/G]CAAGGTCAGTTTYTAGCTCTGTCAGAAATCTGTATGCTTATTCTATTTAC
Long Flanking Sequence:
GTTATTGCAAAAAAGAGCTGTAGGACTAAGCAGCATACAGAGCATCACAAAACCAATCCTGCTATCAAATACATGGTCAATGCAAGAGCATAAAAATACCACAGAAGATGTAAACAAATCGTTGTAGTGTAAGCAAATTCAGTGTGTTTATCTCATAATGTGGTCATCACGTCTGCTATAGTAGGATCCTTCAGTGGCTTTTTAGCTGAAAGATGTTTATTGGCATTTGATGGTTCAAGGCAAACCCGAAACCTTCTATTCAGCCGCTTCCTCTGTGCAAATATACATATATCAGAAGTCATTTGAAGCCAAAAGATTCAAGAATGATGCTTACTCTTGATGTTTCATGTGCTCTATAATGCAGTTCTAAGGCGTGTGTATTTATTCTGTGTGTGTGTGTGTTTTGCAGGGGAGTCTCTGCCCTTGAGTACTGGAAATCAAATAACTATCAAGTTCAGTACAGTTGGACCAGAGACGGCCAAAGGCTTTCATTTTGTGTA[T/G]CAAGGTCAGTTTTTAGCTCTGTCAGAAATCTGTATGCTTATTCTATTTACATACACAATGTCGGGACTGTGGTGGGACTTCATGAACCTGTAAAGCTTGGTATTTTAAAAATTAGGGATATTTTTTTTTTTTTATTAAAGCTGCATGAATCTTATAGCAACACACTCATTTTACAGCTTCCGCAGGGTTAACCCATTTTTTAATCCATTCAGCCAATCTCCGGATCTGGCAGGGGCACTTTTAGCTTAGCTTAGCATAGATCATTGAATCGGATTAGACCATTAGCATCTTGTTCCAAAAATGACCAAGGAGATGAGATAATTTTCCTATTTACCAAAGATTCTACTCAATTCTTTTTATTTTTTATTTATTTTTATTTTTTTTTATTCACAGTATGTAGGAAGGAAAATTAAAAGTTGATATGGCTATAGGAACTATACTTTCATTCTGGCATAATAATCAAGGAACTTTGCTGCTGTAGCACGTCTGCAGTAGGTGCA
Associated Phenotype:
Not determined