ZMP
si:ch211-69g13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to Down syndrome cell adhesion molecule (Dscam) [Source:UniProtKB/TrEMBL;Acc:A
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 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2791 | Nonsense | F2 line generated | Not yet available |
sa28403 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39033 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22586 | Nonsense | Available for shipment | Available now |
sa14192 | Nonsense | Available for shipment | Available now |
sa13818 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2791
Status:
F2 line generated
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 356 | 2020 | 6 | 33 |
ENSDART00000148350 | Nonsense | 187 | 1905 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6132508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6250301 |
GRCz11 | 15 | 6238254 |
KASP Assay ID:
554-2683.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCAGACGAGTTTGACATCACCTGGTACAGGAATGCGGAGAAGATCTAT[C/T]AGGGTATAAATGTACGAATCACGGGCATTAACAACGAGAACCTGGTGATG
Long Flanking Sequence:
TGGGCCAGCTGGAATTTTGATCGGAATTTGTCTTTTCTCCTTGTATTCGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACGGTCCAAAGACGTGGTATAAGGGAATTGGATGAACTAAATTAGCTGTAGTGTTTGAGTGTGTGTATAAATGTGAGAGTGTATGGGTGTTTCCTGATACTTGGTTGTGGCTGGAAGGGCATTCGCTGCGTAAAACATATACTGGAATAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGATAAATAAGGGACTAAGCTGAAAGAACATGAATGAATGAATGACATGTAAACGTGTTTTAAAGCATTGGTTTAATATATGTGCATTTTTGTTTTTATCTTTCCCAGAGCCTCTGAAAGCAGTGGTGAGCCCACGGAAGGTGAGGGGCAGCGTGGGTAGCCAAGTGTCTCTGTTCTGTAGTGTGACTGGCTCAGACGAGTTTGACATCACCTGGTACAGGAATGCGGAGAAGATCTAT[C/T]AGGGTATAAATGTACGAATCACGGGCATTAACAACGAGAACCTGGTGATGGAGGGAATGGCCAAGAGCGATGGAGGAGCGTATCAGTGCTTTGCTCGAAATGGAAAGATGTCCACCCAAGACTTAGTTCAGGTCGTCTTGGAAGGTGAGTCCATCTTGGTGGTTCTGTTCTGGGACGTAATGTCATGTGCTTCAAGCATTGCTGGAACAAAAATCTTCATTTAATATTCATTCTAATCTCATGTCATATACTTCATTTATTTTTCCTAAATAGTATGAATAGTATGAATAATATGTGAATAATTATAATAATAATAAATAATAATAAAAAAGATTTTAGCTAGATGATTTCAATTGAACTGACATAAATCCCTGTCATTTAAACAACTGCTTACGTTATCAATAAATTAAGTGTTCAAATTTTTATTTTAAATGTTTTTTATGCAGTCACCAAACCACATTAACTCAGTATTACTGATAGATAGATAGATAGATAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28403
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 1025 | 2020 | 17 | 33 |
ENSDART00000148350 | Nonsense | 856 | 1905 | 14 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6073422)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6191215 |
GRCz11 | 15 | 6179168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCACAAACACTTGCAAAATGGCTTGATCCGAAGCTACCAAGTGTGCTA[T/A]CGGGAGTTCGGGACAGGAGGCAGCCCACAATACAACACCATCAACGTCGA
Long Flanking Sequence:
ATGAAGTTATTGTATGGAAACCAGGATTTTGTGTGTCATTTTAGCAGACTGCATTCAAAACAAAGCTGTTTTTAGTTTAACAAAAAGGGTTTTGAGAAGTTCTGAGTTCCAAAAACAAATGTTTTCATAACACCGTGACACCTTTTATTTCAAAAGATCAATGCCATTTTTGATTACTCAGTTCATGAGCCCTTTAGGAAAATGCTGAATGAATGGAGTATACATAAATGTAAACAATGTGATGTTAAAGTTTAACAGTTTTGCTAGAGGGATCCAGTTTCTAAAAGTATTTATGATATGCCTGTAGGTTTTAGCACACCCATACAATTTCTAAACACTCAAAATACAGTGTTTTCCCATCAGTAGAAAAATACTTGCTTTTACAAATTGAAAAGTTATATTTTATGATCTCTTAATATCAAGTTCTGTTTTGCTGTATCTTTCCAGCCCCCCCACAAACACTTGCAAAATGGCTTGATCCGAAGCTACCAAGTGTGCTA[T/A]CGGGAGTTCGGGACAGGAGGCAGCCCACAATACAACACCATCAACGTCGACACCACGGGAGACATTGAAACCCTCACTCTTGATAACCTGAAGAAGTACACGCAGTATGAGGTGCGGGTGCAAGCAGCCAATCGAGCAGGAATGGGGCCAACCTCAGAGGAAATCACCATCACCACGCTAGAGGATGGTTAGTCGCCTAATTAAGTCCATTTCCCTGTGTTCTCAAGTTATTGAAATATAATATGTACCAAGGGCATAGATGTGCTCTTGACATTAGTGGGGAGTGGGGACATACAATTCTAGAGTGCATGCATTGCAAAAATAGTTTGGTAACACTTTATTTTGATGGTCCGTTTGAGTAATATTAGACTTTCTGCTAAATATATGTTGATATGCTCCTTCAACAGACATTTATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCGCTTTATTAATCTGGGGTCGCCACAGCGGAATGAACCGCCAAATTATCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39033
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 1254 | 2020 | 21 | 33 |
ENSDART00000148350 | Nonsense | 1085 | 1905 | 18 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6061116)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6178909 |
GRCz11 | 15 | 6166862 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTTGAAGCCGCACCTGATGTTTATTTCCGTCGCTTGACCAACTTGAAC[C/T]AGAATTGGCAGTACAGCATCTGGGTTGTGGCGGTGACTGCGGCAGGTCGT
Long Flanking Sequence:
CTTCAGTCTCCTGCCGAAGCTCAGACGCCGCGCTTTGAGAAACTGTCAATCACAGCTGTCAATCACGATGACACGCCCAGCATTAAATTACTGCTAAAAACAAACTGTTAACAAAAATGAAGATCTGCACCTATTTCAGCACAATAACCAGTGCCTTAATTGACCAGAACTATCTTTCGGGACATTTTATTGCAAGTGTAATATTTTTTTTTATTTGGGCTCAAGTCTCCTTCATTAACACGGAGGAGGCGGGCTTTATGACTTGTACTGCAGCCAGCCCCCAGGGGGCGATCTAACGGCCGAGACCTTCACTCAAACGTAGGCTTGCGGCACACTTGGTTGTAGCTAGACTCTACAGGAAATTGACTCTCGAGGAGTAGTTTATAGGGTGGAATTTGTTTTTGTGGCACTTACATTTTTTTTATCTCATGTCATTACAGGTGATTAGTGAGTTTGAAGCCGCACCTGATGTTTATTTCCGTCGCTTGACCAACTTGAAC[C/T]AGAATTGGCAGTACAGCATCTGGGTTGTGGCGGTGACTGCGGCAGGTCGTGGGAATACCAGTGAAATTATCACCGTAGAGCCCCAAGCTAAAGGTATGGAAGATATGGCAATCACTCCATAACACGGAATACCTAACACTAAAAGTATTTTCCTTAATAAAAAAAAAAAAAAGGTTTTCTGTTTATTATTAGAATATTGCAGAAAATGAGCCTTTAAAACCAAATGTGACCCATAAAAACACGATTTGTTAATTATGAATTTTAAAGTTTTATGAACTTCCACATATGATAACCTTTTTAATATGTGTAACTTTTCATTTTAAGTTTAAAATAGTTTGCAAACATTTTGTTTAGTTTACCTGTTCAGTGTGATGTCATTTAATGTCTCCAAAAGACTCTACAATCCCATTTATTTTGCCTTTTCCGAGCAAAGAAAAAGAAACAGATCAAAAAAAAAAAAATGTTTTCTTACTTAAAGTTTTTGTCTTGTTTCTAGTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22586
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 |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 1376 | 2020 | 23 | 33 |
ENSDART00000148350 | Nonsense | 1207 | 1905 | 20 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6057987)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6175780 |
GRCz11 | 15 | 6163733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGTGTTGCCAGCAACAACTGGGGTTCCGATGAGATCATGCTAAATCTT[C/T]AGGTCCAAGGTGTGTTTGTAATCTTCAGAGACAGCCTTTTTTAATTTAGA
Long Flanking Sequence:
TCTGTTGAACACAAAAGAAGATAAAAACTAGTCGACTTCCATATGTTTTGCTAGCTTCCTACTAGTGATGTTGAAGGTTACTGGTTTCCAGCATTCTTAATATTATCTTCCTTTGTGTTTAACAGAAGATTTTTGTTTTTTGGAAACACATGAGCTGAATAAATAGTGAGTAAAAATGTTTTTGGAGGGTGAACTATCTTTTTAAATCTGTTCAGGTATGTCTGGCCAGACTTGCAAATGAAACTTATAGCACCTGAAATAATTAGTTTGATTGTGTTTTTTTATTCATTTCATTATTTTGCTTATGAAGCTGATATCTTGAAAAACTGATCATGCTTTCTTACAGTAATGGTACACCTGCTCCAGTTTCAATCGATGGTCGTCGCAGCGCTCACAACAATGGCAGCTTTGTTATTCGTACCGTCAAAGCAGAGGATTCTGGGTATTACAGATGTGTTGCCAGCAACAACTGGGGTTCCGATGAGATCATGCTAAATCTT[C/T]AGGTCCAAGGTGTGTTTGTAATCTTCAGAGACAGCCTTTTTTAATTTAGAATTTAAAATTGGTAAGGCGAGAGGAAATTTCTTGGTGCCATTTGATAATATTTTTAATTATTTTTATTTTTCATTTTATTTTAGCTGCTGCTTTTATTTCTATTATACGGTTGCACTTTACAATCAATATGGTTGTATATTCTAAAATGTAATTGTAAAAAAAGAAATACATTGTAAAAATATTTTTCTTACTTAAAGTTTTTGCCTTGTTTCTAGTCCAAATATTTAAAAATTCTTCAATCAAGAAGAATTTTCTAGATAAGCAAAACATATTGTCTTGTTTTCAGAAATGTTATGTCCATTTTTTTCCCTTGAAACAAGCAAAATAATCTGCCAATGGTAGAAAACAAGATTACTTAGCTTGTTTCAAGGAAAAACTCACTTCATTTTGACTTATTATTTCGGAAAACAAACTCTGGGCTCTATCATACACCCAGCGCAATAGGGCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14192
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 |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 1447 | 2020 | 25 | 33 |
ENSDART00000148350 | Nonsense | 1245 | 1905 | 21 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6055564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6173357 |
GRCz11 | 15 | 6161310 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCCCCAGTGAGCGCTCTTACCGTCTGGAGAATCTGAAGTGCGGTACTTG[G/A]TACAAGTTTACTCTGACTGCACAGAATGCARTAGGTCCCGGACGCATCAG
Long Flanking Sequence:
ACCACCGGACCAACCACGTCTTACCGTGACCAAAACCACGACCACCTCCATCACGCTCTTCTGGATCCCCGGAGACAATGGCGGAAGCTCCATCAGAGGTTAGACTGCCTTGATATTTTGCGCTCCACATTTTCACCTATTCTCCACTGGGTGACAAAAATGAAACACTATCAGCACAAACCTGTCAAATGTTTCAAACTGAGATTTATTCCACACGCCGTTATATTTTAATAAACTTAAAGGTCAACTTTGCATCGTACAGCAAGTGCTCTGTATCAATTTGCAGTGCCTGTAAAAATTCATAAACAAAGTTTGGCATTTGAGGTTTATTTATTAAAATGGACACATCACTGAGCATACAGTAAAGTGTTTTTTTGTGGTTCTCTCTGTTCAGGCTACATTTTACAGTACTCAGAGGATAACAGTGAAGAATGGGGCAGTTACTCCATCAGCCCCAGTGAGCGCTCTTACCGTCTGGAGAATCTGAAGTGCGGTACTTG[G/A]TACAAGTTTACTCTGACTGCACAGAATGCAGTAGGTCCCGGACGCATCAGTGAAATCATTGAGGCCAAAACCCATGGAAAAGGTACACATCTGTTAATAATGTCAAGCTCTTGTGGCTACACTGCTAAAAATGACTTTATTATTGGAGTTTCTGTTTTGTTTTTTCTGTTTTGGTTATGTTAAATCAAGAAGTATTTTCTAGAAAAGAATAAGCAGAATAATTTTGCAAAATAATTGTGCTTTCGCTGAGAAATAAGATTATATTGCATACCCCATTTATTTTGCATGTTTTAAGGATAAACTCACTTAATTTTGAAGTATTATTTCTAAAAATAAGAGTGTTTTTTGCTTTTTTAGAAAATGCTTCTAGATTTAGGAATTATTTAATATTTGGACTAGAAAAAAAACTCTTAAGTTAAATAAAACTATTTTTGCAGACAAGTATATGAACATTAATGAATTTACCTTTAGCAAGGTACGGTATGACATGGTTTGCTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13818
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 |
---|---|---|---|---|---|
ENSDART00000098038 | Nonsense | 1980 | 2020 | 33 | 33 |
ENSDART00000148350 | Nonsense | 1865 | 1905 | 30 | 30 |
Genomic Location (Zv9):
Chromosome 15 (position 6034077)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 6151870 |
GRCz11 | 15 | 6139823 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGAGAGGCGGTACAGCAGTGGCAGCCGGGAACTGCCTCTACACTGCCA[C/T]AGCGCGAGCCGGGCGACCTRGCYCAGGCCGCCAAACTCAGCAGCTCCCAG
Long Flanking Sequence:
GCTAAGCTAAAAACTGTAAAAACCAAGTCTCCTTTTGCATTGAACTTGCTGTTTATGTTTACACAGCTACATTACACATCAACTAAAGTTTAAAATATGATATCATAGTGGACCACCCCTTTAAGTAAGCAAGACATACGAAATGGACCAGAACTGAGAACCGCTGGTGTAGATGTAGCCTTAAAATGAAATAGTCTTTTGATCATTGGTTTTTAAATGCTCACACTTACATGCTCCCTGTTTATTTTGTAGCAGGTGAACTGGTCCATCTCCCCCCTTACCTACGCATGGACTTCCTTTTGAACCGGGGAGCGGCCTCTTCAGGTCGGGAGGCCACAGGACAGACTTGTATGGACCCACAGAAGAGCCGGATTACAAAGCGGCCGGCGTTGCTTGCCCCCACCCCCTCCGAGACCCCCTCTTCAGCCCTCTCTTCCTCCGGGCCCCCCAGCAGAGAGGCGGTACAGCAGTGGCAGCCGGGAACTGCCTCTACACTGCCA[C/T]AGCGCGAGCCGGGCGACCTGGCCCAGGCCGCCAAACTCAGCAGCTCCCAGGAATCGCTGCTAGACTCCAGAGGACACCTGAAACAAAGCAACAACCCCTACGCAAAGTCCTACACACTTGTATAACACAGGACTACAGCTACGGACCACGTTGCACTGTCACGCACACACAGAAACAAACAAACAAACAAACAAAAAACGTGAGGACCTGCTGCAAAGACGAGAGCTTTTCTGATTCAGAGATGAGTCCTGTACATACATTCTGAATTCCTAAAGAAGTGGATAGTTTTCTTTGCATCTGTCTTTCTATCTATCTCACTCTCCCTCTCTCTGTTTCTCTCTGTTGTTTTTTTTTTTTTACTCTTTCTTCCTTTCTTTCGCTCACCTCTCTTCCCTCTTCTCTAAGTTGGAATCTTTTTATTTTATTTGACGTACGTTATTTTAAATACCACCGTTATGAAGATTGCCAAAATTATTTATTTAAATTGACAGAGGAACTAC
Associated Phenotype:
Not determined