ZMP
si:dkey-8e10.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate deleted in malignant brain tumors 1 (DMBT1) [Source:UniProtKB/Tr
Human Orthologue:
CD6
Human Description:
CD6 molecule [Source:HGNC Symbol;Acc:1691]
Mouse Orthologue:
Cd6
Mouse Description:
CD6 antigen Gene [Source:MGI Symbol;Acc:MGI:103566]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31630 | Nonsense | Available for shipment | Available now |
| sa41130 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa14189 | Essential Splice Site, Splice Site | Available for shipment | Available now |
| sa34314 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31630
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 |
|---|---|---|---|---|---|
| ENSDART00000101300 | Nonsense | 164 | 560 | 3 | 8 |
| ENSDART00000132894 | Nonsense | 154 | 917 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 10549346)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9965928 |
| GRCz11 | 8 | 10004513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAAGCTGACATGGTATGCAAGGAGCTTGGTTGTGGGGATCATTATTA[T/G]ATTCCCAAAGCTGGAATATTTAAAACAGAACAGATCAAAAAAAATGTGCA
Long Flanking Sequence:
TATGACAAACTCGTATAAAAAAAAAAAAAACGAGAGATACTGAAATAGGACGTCTCAAGTTCTTTTCTCAAGTATGTTTTTTGTGGAGTAAATAAAACTGTGCCATTTATTCAAACAATAAACATGGGGACTTAATAATTAAATATATGTTTTTAGTCATTTAAAGATGTTGACGGTGATATATAATCTTACATTTGATTTCTTCATATTCATCCACAATTGGAAAAAATTGTTACAGAGTAAATTATATTTGACTATACACTTGCTATTGTAATCACATGTTGCATTGTCCTAATAGTCATTCCTTCTACGTTTTATTTATATCTAAATTTAGCCAGTAAATCAAAAGGTTTAGCATTTATACTTAAGTATTTATAGTGACAACTGACAATTATAGTAATGCAAAGATTGTCTTACGCATTTACTTTTTTATATTCTTGGCCAGATAAACCAAAAGCTGACATGGTATGCAAGGAGCTTGGTTGTGGGGATCATTATTA[T/G]ATTCCCAAAGCTGGAATATTTAAAACAGAACAGATCAAAAAAAATGTGCAGCTTAATTGTGTTGGGAATGAGAAGTACTCTTGGCAGTGTATGGAGCCGGCAGCAGACTGCAAGGATCGAGCCAATGTCATCTGCAGCAGTAAGTGAAGTCTATACTATTATGTTTACTTGTACATTATTCTGATTGGTCAGTCGCCCACTTTTCCTGCATTGCTGGTTCTGAATTTTTTCCTATTCCTCTTTGTTAAATGACTTTAAACCCAGAGTTATAAACCAAGACTAACCAGAAATGCATAGTCTGAGAAGGTGATGCTTTTGTACAAAGAAGTTACAAACTGTTTTTTTTAATTATTATTTTTATCACTATTTAATACTGATTATTTTCTCATCAATATTTACGTTTTTTTTATTTAGTTCACTTTTTTTGTGTTTATTCCAATCATCTCAAATATCTCCATTATGCCGTAAATATTTAGTTGGAATGTAGCGTTACGTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41130
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101300 | Essential Splice Site | 207 | 560 | None | 8 |
| ENSDART00000132894 | Essential Splice Site | 201 | 917 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 10549487)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9966069 |
| GRCz11 | 8 | 10004654 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGAGCCGGCAGCAGACTGCAAGGATCGAGCCAATGTCATCTGCAGCAG[T/A]AAGTGAAGTCTATACTATTATGTTTACTTGTACATTATTCTGATTGGTCA
Long Flanking Sequence:
AATATATGTTTTTAGTCATTTAAAGATGTTGACGGTGATATATAATCTTACATTTGATTTCTTCATATTCATCCACAATTGGAAAAAATTGTTACAGAGTAAATTATATTTGACTATACACTTGCTATTGTAATCACATGTTGCATTGTCCTAATAGTCATTCCTTCTACGTTTTATTTATATCTAAATTTAGCCAGTAAATCAAAAGGTTTAGCATTTATACTTAAGTATTTATAGTGACAACTGACAATTATAGTAATGCAAAGATTGTCTTACGCATTTACTTTTTTATATTCTTGGCCAGATAAACCAAAAGCTGACATGGTATGCAAGGAGCTTGGTTGTGGGGATCATTATTATATTCCCAAAGCTGGAATATTTAAAACAGAACAGATCAAAAAAAATGTGCAGCTTAATTGTGTTGGGAATGAGAAGTACTCTTGGCAGTGTATGGAGCCGGCAGCAGACTGCAAGGATCGAGCCAATGTCATCTGCAGCAG[T/A]AAGTGAAGTCTATACTATTATGTTTACTTGTACATTATTCTGATTGGTCAGTCGCCCACTTTTCCTGCATTGCTGGTTCTGAATTTTTTCCTATTCCTCTTTGTTAAATGACTTTAAACCCAGAGTTATAAACCAAGACTAACCAGAAATGCATAGTCTGAGAAGGTGATGCTTTTGTACAAAGAAGTTACAAACTGTTTTTTTTAATTATTATTTTTATCACTATTTAATACTGATTATTTTCTCATCAATATTTACGTTTTTTTTATTTAGTTCACTTTTTTTGTGTTTATTCCAATCATCTCAAATATCTCCATTATGCCGTAAATATTTAGTTGGAATGTAGCGTTACGTTTAAACTAAGTTCAGTAGTTACACACAAAGTAAAGAGCCGGGGGTTGGGGCTGGGGTGCGTGCAAACTGAAGAGCGGGAAGCGGGTATGGAGATGGTAGCGCGTTGGGTTTGGTGTATGGGGACTCGCATGGGGACTGTAATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14189
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, Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000101300 | Essential Splice Site | 207 | 560 | 5 | 8 |
| ENSDART00000132894 | Splice Site | None | 917 | None | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 10551120)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9967702 |
| GRCz11 | 8 | 10006287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTAATAAAAYGTATAAAGCATGTAGAAATAAAAATGAAATTTTCTGCA[T/C]TTACAGACAAWGTCCGGCTTGGCAACTTTACGTCAAAGTGTTTTGGAGAW
Long Flanking Sequence:
GGTTTGTCTGTAAAACTGATTGTGATTTTTTTTTTTTTATGCTGCAATACTTGTTTTACACAGAACACAGGAGGTTCCGTCTTAGGGGTGGCAATAATGTATGCTCTGGATCAGTGGAGGAGTACAATTTCCCCAAAAAATCATGGGATCCTCTTAAGCAGAAAGATGTTAACCCTGACTACATCTGTACTCAATTGAACTGTGGCTCCACTGGAAACTTCACAAATGATAACGGAACAAACATCCTGACATGCTCAGGTAATGCTGGGTTTCTTACTTTAAATAAAATCACATCGTTACATCATTCTCATTACTAAGAGTGATGTTTAGATGAGTGTGGATGGTTTAAAAGGTGTAGCAAATAATAATAGGGTGATTTTATTATTATTAATATAAAAGTGACTTCTTAATCCATAAATACTTGTAGGTTACTTATCCATTAAGATACCTTTTTAATAAAATGTATAAAGCATGTAGAAATAAAAATGAAATTTTCTGCA[T/C]TTACAGACAATGTCCGGCTTGGCAACTTTACGTCAAAGTGTTTTGGAGATGTTTACGTTGTTGTGAATGGAGCTGAATATGGAGTTTGCTACCCTGATTGGAGTCAGGATCTGCTCCGTCAGCTGGGGAAGGTGGTCTGTCGAGAGCTCGGCTGTGGTGAGGTGATGGATGTGAAACGGGGATCTTGGAATACTGGTTTGCTGAGTAATGTTGAGTGTCAAGGTGATGAGGAGTCACTTTGGCATTGCCTGGCAAAGCATGAGCATCGATCACATCGATGCGACACAACTAAAGTTACATGTTCAGGTAACTGAGACGGTCTTTAAAATACTCAGAACATGCAAGAAATAAAGACCCTAATCACCCATATCTAGGCCCACACAGAATCTGCGCGTGTAGAAATCTGCTGATTTTTTAGCCCATCACTGAGTCTATTTATTTACTCATATAAATGTGTGTACATTTATATTTATTCAGTTTTTAAATGAATTTCAGTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34314
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 |
|---|---|---|---|---|---|
| ENSDART00000101300 | Nonsense | 296 | 560 | 5 | 8 |
| ENSDART00000132894 | Nonsense | 353 | 917 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 8 (position 10551387)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 9967969 |
| GRCz11 | 8 | 10006554 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAAGGTGATGAGGAGTCACTTTGGCATTGCCTGGCAAAGCATGAGCAT[C/T]GATCACATCGATGCGACACAACTAAAGTTACATGTTCAGGTAACTGAGAC
Long Flanking Sequence:
GGTTTCTTACTTTAAATAAAATCACATCGTTACATCATTCTCATTACTAAGAGTGATGTTTAGATGAGTGTGGATGGTTTAAAAGGTGTAGCAAATAATAATAGGGTGATTTTATTATTATTAATATAAAAGTGACTTCTTAATCCATAAATACTTGTAGGTTACTTATCCATTAAGATACCTTTTTAATAAAATGTATAAAGCATGTAGAAATAAAAATGAAATTTTCTGCATTTACAGACAATGTCCGGCTTGGCAACTTTACGTCAAAGTGTTTTGGAGATGTTTACGTTGTTGTGAATGGAGCTGAATATGGAGTTTGCTACCCTGATTGGAGTCAGGATCTGCTCCGTCAGCTGGGGAAGGTGGTCTGTCGAGAGCTCGGCTGTGGTGAGGTGATGGATGTGAAACGGGGATCTTGGAATACTGGTTTGCTGAGTAATGTTGAGTGTCAAGGTGATGAGGAGTCACTTTGGCATTGCCTGGCAAAGCATGAGCAT[C/T]GATCACATCGATGCGACACAACTAAAGTTACATGTTCAGGTAACTGAGACGGTCTTTAAAATACTCAGAACATGCAAGAAATAAAGACCCTAATCACCCATATCTAGGCCCACACAGAATCTGCGCGTGTAGAAATCTGCTGATTTTTTAGCCCATCACTGAGTCTATTTATTTACTCATATAAATGTGTGTACATTTATATTTATTCAGTTTTTAAATGAATTTCAGTAATATTATTGACTAATATGAAAATATTTATATGATTTATTTACAATACAGTTTGTAAAATAATATTTTATATGATAGACTTGCTTAGTTTACCAAATAAGGGTATTTAGATGGATTTGCATTGTAAACATTAAGCTTAAAAAGCTATTATTTTTTATGTCTAATATTTAGTTTTAAGTTACGATACTTCCAAAACAATTCCACATAAAAATGCAGATTTATTTTTTCAAAATTCTCCGCAGAAATGGCAAACGTCCGCAGATTCTATCTGG
Associated Phenotype:
Not determined