ZMP
dscam
Ensembl ID:
ZFIN ID:
Description:
Down syndrome cell adhesion molecule [Source:RefSeq peptide;Acc:NP_001025395]
Human Orthologue:
DSCAM
Human Description:
Down syndrome cell adhesion molecule [Source:HGNC Symbol;Acc:3039]
Mouse Orthologue:
Dscam
Mouse Description:
Down syndrome cell adhesion molecule Gene [Source:MGI Symbol;Acc:MGI:1196281]
Alleles
There are 12 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31795 | Nonsense | Available for shipment | Available now |
| sa21791 | Nonsense | Available for shipment | Available now |
| sa21792 | Essential Splice Site | Available for shipment | Available now |
| sa21793 | Essential Splice Site | Available for shipment | Available now |
| sa11753 | Essential Splice Site | Available for shipment | Available now |
| sa11007 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31795
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 |
|---|---|---|---|---|---|
| ENSDART00000098963 | Nonsense | 125 | 2023 | 3 | 33 |
| ENSDART00000125045 | Nonsense | 126 | 2024 | 3 | 33 |
| ENSDART00000136928 | Nonsense | 112 | 2010 | 2 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40158789)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 38874640 |
| GRCz11 | 10 | 38818047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAGTGTCGATGACGTAAACTCTTTCTCTGTAGTCTTACGGGAGCCCTA[T/A]ACGGTCCGTGTGGCGGACCAGACCGCGATGAGAGGCAGCGTAGCGGTCTT
Long Flanking Sequence:
CCAACAAACTGTTATTTCTGAATGCACTGAAGCTGGAATTTGGATGATTAGAAGCAAATCTATTTGTTGAACATGTACTACATGCCTAAAGCAATCACTCAATGTCTTTATCTCATTTTGGCGGAAGTGGCGTTTAGCGACTTTTGCATCAGAACTCTTGATATATAACTATAACTGTATAACTTCAGGTGTAACTATGTTTGTCAATCATAATTTAAAGTGTTAACATTATTAGTTACTAGTTAATTAAAGTGATTAGTTACTAATATAGTTATGCTTACTAATAACCTTAACTTTTCTGAATTTGATTGTATTGCAATAACGTGCACCTTTTGTAGAGCTGCTTTGAAACTGTAACTATTGTAAAAAGCGCTCTACAAATAAACTTGAGTTGAATTGAATTGAACTAAAATTGGATATTAAAAACATTTCAATGTTTCCATGATTTTGCAAAGTGTCGATGACGTAAACTCTTTCTCTGTAGTCTTACGGGAGCCCTA[T/A]ACGGTCCGTGTGGCGGACCAGACCGCGATGAGAGGCAGCGTAGCGGTCTTCAAGTGCATTATTCCTTCCTCAGTGGAAAACTACATCACTGTTGTGTCATGGGAGAGAGACACCGTACCACTCGTCTCAGGTAGGACACTGGCTGCTCATCTGCTGTTTTCGGCTTGAACATGCAAGGCTTTTATGCTGCACTCTAAAGAAAAATTCCATGTCATTTTTAAATTGACTGTACAAAAACATCTGTTAATTTACCATTGCCATGAATATTGTAGTTTAAAGTGCTTTGAATGTGCTTTTTTATTCAGTGTTTGATGTAATCACAAACACATGAGAATTGACATGAGGTCACATAGTTTATCTTTTGTTATTAACTAATGTGACTAAACTTTTTCTCTTTTAGGTAAGTCAGGATTATTAAATGTGTTTCTGTTATGCTTAATAGCAGAATAATGAAAGATATTTTTTTGAGAATTTGCTATAACTTTTGTTGAAAGTCAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21791
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 |
|---|---|---|---|---|---|
| ENSDART00000098963 | Nonsense | 207 | 2023 | 4 | 33 |
| ENSDART00000125045 | Nonsense | 208 | 2024 | 4 | 33 |
| ENSDART00000136928 | Nonsense | 194 | 2010 | 3 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40222397)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 38938248 |
| GRCz11 | 10 | 38881655 |
KASP Assay ID:
2260-3581.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGTTCAACTACCGCTGCATGACGAGACATCGCTACACGTCCGAGACA[C/T]GACAGAGCAACAGCGCACGGCTCTTTGTGCCAGGTAAAAGTGCTTGATGA
Long Flanking Sequence:
CAGAAAGCAGAGCAAATGGCGTTCTCAATCAAATCTGACACAGACGTCTCCTCTGAGAGAGCGCGCGGAGGCCCTGGCAGACATTATTCCTCATAAAGTTTTACGACCTGCATATTCTGTGTTATCAAACCATTAGCGTGAAATCAGTGCTCAGTGGTACATGAGCGGCGGGCCAATCAAACCCGCACGTGACCGGCAGGAATCACTGTGCTAAATCAGCCGGTTCCTGCTGAGGCTGATGGGAAAAAAAAAAAAAAAAAAACAAGATTCTGTTAACCGTGCCTCATTATGACACGCAAATGCTACAGATTAACTGTGTTTAATGTTCAGCGATTAATTACGGAGATGTTTACCTCAGTCTAATAATGTCGATTTTTGTGTTTTTAGGGGCTCGATTTCTCATCACGTCCACGGGGGCCCTGTACATCCTGGATGTGCAGAAGGAGGACGAACTGTTCAACTACCGCTGCATGACGAGACATCGCTACACGTCCGAGACA[C/T]GACAGAGCAACAGCGCACGGCTCTTTGTGCCAGGTAAAAGTGCTTGATGATATGATACTATTCAGTGGGATGAGACATGGAGGGACGGGGGGATGGATGGATGAATAAATGCACAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGAGTGGATTAATGGATGAATAAGCAGAATTGGCAAATAGATATGAATAGTCAATATTTGAATTGATAGATAAATGGAGGTTCTATTTGGATTGTTAAACAGTTTGGATGGATGGAATTATTAATGCGTGGATAGGCAGACAGTTGAATAAATGGATAGATATACAGATGGATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21792
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098963 | Essential Splice Site | 502 | 2023 | 8 | 33 |
| ENSDART00000125045 | Essential Splice Site | 503 | 2024 | 8 | 33 |
| ENSDART00000136928 | Essential Splice Site | 489 | 2010 | 7 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40231425)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 38947276 |
| GRCz11 | 10 | 38890683 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACTTCCATCGCAATGTCAATGTTCTTTTAAAGAGAAGTGTTTCTGTTTA[A/G]GGTTCCGCCGACATTCGACCAATGAAAAACCTCACTGCCATAGCTGGGTG
Long Flanking Sequence:
TTTAACAGCAGATGGCGCTCTAGACTAAGTTTAAACAGCAGGTGGTGCTCTAGACTAGTTTTTTTAACAGCAGATGGTGCTGTATGCTTATTAAACAGCTGTTCTCTGCTTGCATCCAGTTCCTTAAAATATGGAAAGGTTTAGGAAAGAAGCCAGGGATTCTCAACCGGTGGGTGAATATAGGGCCTCGATGAGCAGCAAGATAGTTTAAAGTTCAAAGCTTAAAGTTAATGTAAATATTATCCTATAACTGGTTGATTTCATTGTAAATAATGGAGATACAAAACACGTCTTATTGACTTTAATAGTATTTGTTTTACCTACTAAAGGAGAGTGTGATCTTGTTTTTGTGTTGTCTCCTTCTGTTTTCTTTCGATGTTAGAAAGGCCCTCATCCATGAACCTTAAATGTACATGTTTTTGTTTTCTTTGCTACATTTTCTGCAAATTCGACTTCCATCGCAATGTCAATGTTCTTTTAAAGAGAAGTGTTTCTGTTTA[A/G]GGTTCCGCCGACATTCGACCAATGAAAAACCTCACTGCCATAGCTGGGTGGGACATGTACATTCACTGCCATGTGATTGGCTACCCATATTACTCCATCAAATGGTTCAAAAACTCCAACCTCCTCCCTTTCAATGACCGTCAGCGAGCATTTGAGAACAACGGCACGCTGAAGCTGCTGAACGTGCAGAAGGAGTTGGATGAGGGCGAGTACAGCTGCCATGTGCAGGTGCAGCCGCAGCTCTTCAAGAACCAGAGCGTCCACGTCACGGTCAAAGGTACACTGAGTTTAATAATCACATTAATAACACCAATTCCTACTCCTTCCACTTGAAACAGAGTGTAAAAACAGAGTGCTTCAAATAAACCCCTAAATATTGGGACTGCACTACACAAACACATACAATGACATTCTTCATGTGTAGTGGCTAAAACAACACTGTATTAATTTGGTACACCAAAAACAAATGTACCAATTAACCATTAACATAATATAATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21793
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098963 | Essential Splice Site | 726 | 2023 | 10 | 33 |
| ENSDART00000125045 | Essential Splice Site | 727 | 2024 | 10 | 33 |
| ENSDART00000136928 | Essential Splice Site | 713 | 2010 | 9 | 32 |
| ENSDART00000098963 | Essential Splice Site | 726 | 2023 | 10 | 33 |
| ENSDART00000125045 | Essential Splice Site | 727 | 2024 | 10 | 33 |
| ENSDART00000136928 | Essential Splice Site | 713 | 2010 | 9 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40234810)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 38950661 |
| GRCz11 | 10 | 38894068 |
KASP Assay ID:
2260-3584.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCGGATGGAGAGCCCAGGCCCACTATTGAGTGGAAATACTCCAAAG[G/T]TACCGAGATTCACCCACATCTACCTATTTTTTTATTTGGTCTTGTTGAAT
Long Flanking Sequence:
GCTTAAGGGGGCTAATAATATTGACCTTAAAATGTTTTTTTAAAAAATGCTTTTATTCTAGCCGAAATAAAACAAATATAACTTTCTCTAGAAGAAAAAATATTATAGGAAATACTGTGAAATGTTTCTTGCTCTGTTAAACATCATCTGGAAAATATATTTAAAAAAATTCACTGAAGGGGCTAATAATTTTGTTCTGTAGATGCGACTATGATTGCTTATTATTTTTTCTGTTTGCAGCGCACACCTTCGCAATCTAATATAAATACTGAATTGAATATGAATTTTTGAGAATTTTGATGCATGAATGTATACATTTTCTTTTAGCATTGCTCTGTAGATACGGTCAAAGATGCAACTAGAATGAGGTTTTGTTGTAGTTCCACCAAGGTTTAAAGTCCAGCCTCAGGACCAGGATGGAATCTATGGGAAATCAGTGATCTTGAACTGCTCTGCGGATGGAGAGCCCAGGCCCACTATTGAGTGGAAATACTCCAAAG[G/A]TACCGAGATTCACCCACATCTACCTATTTTTTTATTTGGTCTTGTTGAATACATAAACATTGCTTAATCATCATATGTTTGCTTGCGATAGTAAATTATAAGTAATATGTTATTAAAGAATGACATTTGAATTGTGTTTATTTTTCTTTTAATAACAAAAAAAGCTGATTTAAGAATGAATTTGACTACTTTTTCAGTGGGGAATGAATGTAGGAATGGGCTGTACACTGAAATGTAGTTTTCATAGATTTTTTATTTATTTACTGTAAATCATTTTATCAAAATAATAATTTTATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATTATTATTATTATTATTATTATTGTTATTATTATTATTATTATTGTTGTTGTTATTGTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATATGCTGTGATTTCTTAAATGAATTTTTTAAAAACATTTTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11753
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098963 | Essential Splice Site | 1094 | 2023 | 18 | 33 |
| ENSDART00000125045 | Essential Splice Site | 1095 | 2024 | 18 | 33 |
| ENSDART00000136928 | Essential Splice Site | 1081 | 2010 | 17 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40268613)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 38984464 |
| GRCz11 | 10 | 38927871 |
KASP Assay ID:
2260-3585.1 (used for ordering genotyping assays)
KASP Sequence:
AATGCAATCATGGCTAATGTGTCAGATTTGTGTTGGTTTTGTGTTTCTCA[G/A]TTCCCAGCAGAGCTCCAGAGAAGGTGGTGGCYACCGCTGCATCCCCAGAG
Long Flanking Sequence:
GGTGGTGCAGGCCAGCAACAGCGCCGGTCCGGGGCCTGCCTCCAGTGAAGTGCGGGCCACGACTATGGAGGACGGTAAGCTACCGTCACACAATCAGCTTTTGGGTCGAGTGAGTCATTTTCGAGTCGTTTGTGGAGTTTGCATGTTCTCCTTGTGTTGGCATGGGTTTCCTCCGGGTGCTCCGGTTTTCCCCACAGTCCAAACACATGGACGACATGGTGCTATAGGTGAATTGGGTAAACAAAATTAGCCCTAGTGTGTGTGTGTGTGAGTGTAAGAGTGTGTATGGATGTTTCCCAGTACTGGGTTGCGGCTGGAGGGGCATATGCTGCGTAAAACATATGCTGAAATAGTTGGCGGTTCATTCTGCTGTGGTGACTCCTGATAAATAAGGGACTAAGCTGAAAGAAAATGAATGAATTCCAGTTTTGTATCTAATTAGCGTCTTTAAATGCAATCATGGCTAATGTGTCAGATTTGTGTTGGTTTTGTGTTTCTCA[G/A]TTCCCAGCAGAGCTCCAGAGAAGGTGGTGGCCACCGCTGCATCCCCAGAGAGCATCTCTCTGTCCTGGCAGACTCCGGCTCGAGAGGCTCTGAACGGCGTCCTACAGGGCTTCCGCATCATCTACTGGGCCAATCTACCAGACGGAGGTACAGTGCACACCCTTAAACAACAATACTTACATTTATAATACTTAGGCTGTATCGCTTCAAGGGCGACACAGCGGCACAGTGGTTAGCATTGTCGCCTCACAGCAAAAAGGTTGCTGGTTTGAGTGCAAGCTGGGTCAACTGGCATTTCTGCGTTGAGTTTGCATGTTCTCCTTGTGTTGGTGTGGGTTTCCTCCATGTGCCCCGGTTTCCCCCAGTCTGAGGACATGCACTTTAGGTGAACTGAATAAACTAAATTGGCCTCAGTGTATGAGTGCGTGTGAATGAGTGTATGGATGTTTACCCAGTATTGGGTTTCAGCTGGAAGGGCATCCACGGCGTAAAACATATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11007
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
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098963 | Essential Splice Site | 1577 | 2023 | 27 | 33 |
| ENSDART00000125045 | Essential Splice Site | 1578 | 2024 | 27 | 33 |
| ENSDART00000136928 | Essential Splice Site | 1564 | 2010 | 26 | 32 |
| ENSDART00000098963 | Essential Splice Site | 1577 | 2023 | 27 | 33 |
| ENSDART00000125045 | Essential Splice Site | 1578 | 2024 | 27 | 33 |
| ENSDART00000136928 | Essential Splice Site | 1564 | 2010 | 26 | 32 |
Genomic Location (Zv9):
Chromosome 10 (position 40291641)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 39007492 |
| GRCz11 | 10 | 38950899 |
KASP Assay ID:
2260-3586.1 (used for ordering genotyping assays)
KASP Sequence:
CATCTKTTTGTGCATGAAATGCTAAACATKGATTTATTWTGTTTGTCAAA[G/A]GCACCATTCCTCCATTGGTGAAGACTCTGGTGAAGGACCCCGTGAAGAAA
Long Flanking Sequence:
AAAGTCCGGTGTGGACCAAAGCTAAACGCACGTCTCTCAGCAAGAGCTACAACCTGCTGGACCTGCAGGAGGCCACGTGGTACGAACTGCAGATGAAGGTGTACAACAGCGCCGGGCTCGCCGAGAAACGAGTCAAGTTTGCTACGCTCAGCTATGATGGCAGTGAGTAAATCTCTCTTTTAATGCAGAAGGGTGTTGTTGTTGTGCCACTAAGGTTGCCAGGTTAGACTGACAGTTTCTATCTTCAAAACACATCCACTACAGAAAAAACATAACATAAGTTACATAAAAATTAATGCTGTTTAATTATAAATTGTGATTAATCGCATCCAACATAAAAGTTAATTTTTTGAACACCTTCCTGGCAGAATGAGATTCGTACACATATTTATTTATTTTTTTTTGGAGGATATTCTGTTCGTAGTGAGCTTTTAACCTGCCTTTTAAATCCATCTGTTTGTGCATGAAATGCTAAACATGGATTTATTTTGTTTGTCAAA[G/A]GCACCATTCCTCCATTGGTGAAGACTCTGGTGAAGGACCCCGTGAAGAAAACCAGCAATGAAGGGATGAAGATGATGGTGACGATCTCCTGCATCTTGGTGGGGATGGTGCTGCTCTTCGTCCTGCTGATGGTGCTGAGGAGGAGGAGGAGAGAGCAGAGGCTGAAGCGGCTCAGGGGTCAGAGACTCCAAAATACACACCACTGCACTTTCACCGTAGATTTAGAACACAGCATATGTCGCTGTTTGAGATTTGACTCACATCAGCTGTATTTTGCATGACTCTATGGTACTCCTATTTTCAGTTGATGTTAATGAAGCTTATTGTTTGTTCCGCAGATGCAAAAAGTTTGGCTGAAATGCTTATGAGGTAAACACTTTTGATTGTTTTGTTTTTATAAAGCAACCCAATATAGAAGTTCAGGCATCACTGACTTGCCTTCTTTTCATTTTAAATCCATATGACCTTTTTTGTCCTAAATATTGTTAATTAAGTTGGCA
Associated Phenotype:
Not determined