ZMP
ncana
Ensembl ID:
ZFIN ID:
Description:
Neurocan [Source:UniProtKB/TrEMBL;Acc:Q75T39]
Human Orthologues:
ACAN, BCAN, NCAN, VCAN
Human Descriptions:
aggrecan [Source:HGNC Symbol;Acc:319]
brevican [Source:HGNC Symbol;Acc:23059]
neurocan [Source:HGNC Symbol;Acc:2465]
versican [Source:HGNC Symbol;Acc:2464]
brevican [Source:HGNC Symbol;Acc:23059]
neurocan [Source:HGNC Symbol;Acc:2465]
versican [Source:HGNC Symbol;Acc:2464]
Mouse Orthologues:
Acan, Bcan, Ncan, Vcan
Mouse Descriptions:
aggrecan Gene [Source:MGI Symbol;Acc:MGI:99602]
brevican Gene [Source:MGI Symbol;Acc:MGI:1096385]
neurocan Gene [Source:MGI Symbol;Acc:MGI:104694]
versican Gene [Source:MGI Symbol;Acc:MGI:102889]
brevican Gene [Source:MGI Symbol;Acc:MGI:1096385]
neurocan Gene [Source:MGI Symbol;Acc:MGI:104694]
versican Gene [Source:MGI Symbol;Acc:MGI:102889]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33063 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15838 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33063
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000097691 | Nonsense | 323 | 1125 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 57630445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 59459254 |
GRCz11 | 2 | 59550675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTGTGGGCCCCCGGGGGTCTCAGTGTCCCAATGAAGAGCCAGGAGTC[A/T]GAAGAGTTTCTCCTGCAGAGCTCAGCAACGGGACGAAGAGATTCGATGCT
Long Flanking Sequence:
AATAAATAAATAGAGAAAAATAAAGCTAATAATTGAATAAAAGAAACAAATAAACATTAATACAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAAACTTATTACTGATCAGTATCAATCACAGCATAGGAGTCATTCAATGTGCTTTCACACACAATAATCCAGTTTGTGTGTTGATGTTTTATTCATGTGTGTGTTCCTCCTCCAGGTGAAGTGTTTTCCTCATCAGTGCCTGATAAACTCACTCATGCTGAAGCTGCGGCTCACTGTGAGTCTCTGGATGCTCGTCTGGCCTCTGTCGGGCAGCTCTTTCTGGCCTGGAGGTCTGGACTGGAGCACTGTGGCCCGGCTTGGGTCTCTGACGGGACACTAAGGGTCTCTGTGGGCCCCCGGGGGTCTCAGTGTCCCAATGAAGAGCCAGGAGTC[A/T]GAAGAGTTTCTCCTGCAGAGCTCAGCAACGGGACGAAGAGATTCGATGCTTTCTGCTATAGAGGTACAGCTGACGGCACTATCCAGAGGAATTATTTAGATTATATATGTACAGTTGAAATCAAAATTATTGTGATTTTATTTTTCAAATATTTCCCAAATGATGTTGAACAGATTCAGGAATTTTTCACAGTATTTCCTATCATATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGCTACAATAAAAGCAGTTTAACACTATTTTAAGGTCAATATTATTAGCCCCCTTAAGCAATATTTGTATTGGATTGTCTACAGAACAAACCACTGTTATACAAGGCATTGTTAGGTGGTTGCTAAACAGTTGCTAAATGGCAATGCTCATGTACATGTTTGATCAAATGCTAACACTTAGTAGGCATTTCTAGCATATGTTATTGCACTTAGATAATCATTCATAGCATGTAGCTAATCGTTATTAGCACTTGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15838
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 |
---|---|---|---|---|---|
ENSDART00000097691 | Essential Splice Site | 903 | 1125 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 57676686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 59413013 |
GRCz11 | 2 | 59596916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTGTGTGYCTGTGTTTGCCCAGCTACAGCGGAGACCGAWGTGAGAGAG[G/A]TGAGAAAACAACTCGTCCATTATMACATCACACTCCAAATTAATGAGTTT
Long Flanking Sequence:
AACTAAGTTGTCCGTAGTGTATGTGTGTGTGTGTGTGTGTGTGTGAAAGAGTGTGTATGGGTGTTTCCCAGTACTGGGTTACAGCTGGAAGGGCATCTGCTGTGTAAAACATATGCTGGAATAGTTGGCGGTTCATTCCACTGTGGCAACCACTGACCCCTTTCTCTTGTCATTCATGTTATATTTGCATTACATGTACTGGAAATGTAATATTTAATTTCAACTTAATTTCGATTACCAAATAGGTTAGTTTGGTTAACATTTGACTTTATAATAGCAGTACTAAACAAGTGTATGTGCAATTATTAAATGTTTTGTTTTTATACACAAAAATGTGTATAATTCTGTTCATATGAGTTAATATTTGAATGTTTTTGTTCTGTCAGATGTGGACGACTGTCAGTCGAACCCCTGTGAAAACGGCGGGACCTGCATTGATAAAGAGGACTCCTTTGTGTGTCTGTGTTTGCCCAGCTACAGCGGAGACCGATGTGAGAGAG[G/A]TGAGAAAACAACTCGTCCATTATCACATCACACTCCAAATTAATGAGTTTCACATTTGAGAGTTTCCCTGCTGACAAAATCCAACTTAGATCAGCTCATAAGAGCCAGGCGGGAAGTTTGTGGAAGAGCATGTACAGGAGATACAGCTGAGGGCTCATTCCCCCTCCTGTGAATTTCTTTTTCAAATATTTCCCAAATGTTGTTGAACAGATCTAGGAATTTTTCACAGTATTTCCTATAATATTTTGTCTTCTGGAGAAAGTCTTATTTGTGTTATTTCAGCTAGAATAAAAGTGGTTTTTAATTTTTTTTGAGGTAAAGTTTATTTATGAACTAATTTCAAGAGGATCACATGCTTATGATTGCTTGTGGCCGGTCCCATATTATTAGACTGGCTTGTGAAAGCAAGCCAGACTACTGAAATCCTATTTTTCTTCTGAGACTAAAAATCAAACACTATCTCCTCCTAGAGCTTCCGAGCAATGACCACCAAGCTCACA
Associated Phenotype:
Not determined