ZMP
vangl2
Ensembl ID:
ZFIN ID:
Description:
Vang-like protein 2 [Source:UniProtKB/Swiss-Prot;Acc:Q8UVJ6]
Human Orthologue:
VANGL2
Human Description:
vang-like 2 (van gogh, Drosophila) [Source:HGNC Symbol;Acc:15511]
Mouse Orthologue:
Vangl2
Mouse Description:
vang-like 2 (van gogh, Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2135272]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa12076 | Nonsense | Available for shipment | Available now |
| sa18862 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12076
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 |
|---|---|---|---|---|---|
| ENSDART00000033316 | Nonsense | 219 | 526 | 4 | 8 |
| ENSDART00000033316 | Nonsense | 219 | 526 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 6182842)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 5217270 |
| GRCz11 | 7 | 5338986 |
KASP Assay ID:
2259-8397.1 (used for ordering genotyping assays)
KASP Sequence:
GTGCGGGTGCTGGAACCCAGAGAGCGYGACTACAGGGGMATTGTGGGATA[T/A]GCGGTGTCGCTGGTGGACGCGCTGCTYTTCATYCAGTATCTGGCGCTGGT
Long Flanking Sequence:
AGTCATGTGATGTTATATTCTCGTGTGTCTCTCTCTCAGGATGATAACTGGGGTGAAACCACGACGGTGGTGACGGGGACGTCGGAGCACAGCGTCTCCAATGAGGACCTGACACGGGCCTCTAAAGAGCTGGAGGACTCGTCCCCGCTGGAATGCCGTCGCTTCGCCGGGCCGATCGTGAGCGGGGTGCTGGGTCTGTTCGCTCTGCTGACGCCGCTGGCTTTCCTTCTGCTGCCGCAGCTGCTGTGGCGAGATTCCCTGGAGCCCTGCGGGACGCCCTGTGAGGGCCTGTATGTGTCTCTGGCCTTCAAGCTGCTGGTGCTGCTGATCTCGTCCTGGGCCCTGTTCTTGCGGCCGTCTCGCTCCACGCTGCCGCGCTTCTTCGTCTTCCGCTGCCTACTCATGGCGCTGGTCTTCCTCTTCGTGGCCTCCTACTGGCTGTTCTACGGCGTGCGGGTGCTGGAACCCAGAGAGCGCGACTACAGGGGAATTGTGGGATA[T/A]GCGGTGTCGCTGGTGGACGCGCTGCTTTTCATCCAGTATCTGGCGCTGGTGCTGCTGGAGGTTCGACACCTCAGGCCGGCCTTCTGTCTCAAAGTGGTGCGCACCACCGACGGGGCCAGCCGCTTCTACAATGTGGGACACCTCAGGTGAGATTACGCATTGGTTGAGTGCTTGATTCTGATTGGCTGATGAGTAGGCATAGGATTCTGATAGCAGGGCTGCTCAGTTATGGGAAAAATCATAATCATGTTTATTTTGGTTATAACTGTAAACACAATTACCTTAATAATTTTCAGTGGCCCATATGACCAAACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATATATACATATATATATATATATATATACACATATATACACACATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18862
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 |
|---|---|---|---|---|---|
| ENSDART00000033316 | Nonsense | 219 | 526 | 4 | 8 |
| ENSDART00000033316 | Nonsense | 219 | 526 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 7 (position 6182842)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 5217270 |
| GRCz11 | 7 | 5338986 |
KASP Assay ID:
2259-8397.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCGGGTGCTGGAACCCAGAGAGCGCGACTACAGGGGAATTGTGGGATA[T/A]GCGGTGTCGCTGGTGGACGCGCTGCTTTTCATCCAGTATCTGGCGCTGGT
Long Flanking Sequence:
AGTCATGTGATGTTATATTCTCGTGTGTCTCTCTCTCAGGATGATAACTGGGGTGAAACCACGACGGTGGTGACGGGGACGTCGGAGCACAGCGTCTCCAATGAGGACCTGACACGGGCCTCTAAAGAGCTGGAGGACTCGTCCCCGCTGGAATGCCGTCGCTTCGCCGGGCCGATCGTGAGCGGGGTGCTGGGTCTGTTCGCTCTGCTGACGCCGCTGGCTTTCCTTCTGCTGCCGCAGCTGCTGTGGCGAGATTCCCTGGAGCCCTGCGGGACGCCCTGTGAGGGCCTGTATGTGTCTCTGGCCTTCAAGCTGCTGGTGCTGCTGATCTCGTCCTGGGCCCTGTTCTTGCGGCCGTCTCGCTCCACGCTGCCGCGCTTCTTCGTCTTCCGCTGCCTACTCATGGCGCTGGTCTTCCTCTTCGTGGCCTCCTACTGGCTGTTCTACGGCGTGCGGGTGCTGGAACCCAGAGAGCGCGACTACAGGGGAATTGTGGGATA[T/A]GCGGTGTCGCTGGTGGACGCGCTGCTTTTCATCCAGTATCTGGCGCTGGTGCTGCTGGAGGTTCGACACCTCAGGCCGGCCTTCTGTCTCAAAGTGGTGCGCACCACCGACGGGGCCAGCCGCTTCTACAATGTGGGACACCTCAGGTGAGATTACGCATTGGTTGAGTGCTTGATTCTGATTGGCTGATGAGTAGGCATAGGATTCTGATAGCAGGGCTGCTCAGTTATGGGAAAAATCATAATCATGTTTATTTTGGTTATAACTGTAAACACAATTACCTTAATAATTTTCAGTGGCCCATATGACCAAACNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNATATATACATATATATATATATATATATACACATATATACACACATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined