ZMP
zgc:194678
Ensembl ID:
ZFIN IDs:
Description:
V-set and transmembrane domain-containing protein 2B [Source:RefSeq peptide;Acc:NP_001122250]
Human Orthologue:
VSTM2B
Human Description:
V-set and transmembrane domain containing 2B [Source:HGNC Symbol;Acc:33595]
Mouse Orthologue:
Vstm2b
Mouse Description:
V-set and transmembrane domain containing 2B Gene [Source:MGI Symbol;Acc:MGI:1914525]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21052 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21052
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110590 | Essential Splice Site | 231 | 260 | 4 | 5 |
ENSDART00000124876 | Essential Splice Site | 231 | 260 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 7 (position 46060879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 44733707 |
GRCz11 | 7 | 45072932 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGCCTCGGCCAGGCAATTCATCTATCCTGAGACAACAGCACGGATCCG[G/C]TGAGTGACAGTGCAACAGCGACACCGAGCGGTCGAGAGAGGAACATTTCA
Long Flanking Sequence:
TAAAAATACAATATAAGGCCTAAGTGTAGGATGTAAAATACAGATATATGCCAACAAAACCTGTTGAGATGTCTTGTTTTTGTCTGTCCGTGAGCAGACGGTGAGGGTCCAGGGCAATGCCATTTCCCACAAGCTGAGCTTATCGGCTGTGAAGAAGGAGGATGAAGGAGTGTATGAGTGTCGGGTTTTGGACTTGTACTCAGATGAGACTCAGGAATTTAAGGTGCAGGCCACACTGCGCGTGACTCCACGCGAGGGAATGCTGGCCGAGGAGGCCGTGTCTCACATCCAGAACCGATGGCCTTTGAGGAACAGCAACACAGCGACAGGTGGACGGGCCACTTCTGAGCCGGGCCAGGGTCAGGGAAAACCCCACGTGCCTCCGCCGGCTGGAATGGGACCTGCTCCCGCCTCAACGACTACGACCAGCTCTGCAGTCAAGTCGTCCGCTTCGCCTCGGCCAGGCAATTCATCTATCCTGAGACAACAGCACGGATCCG[G/C]TGAGTGACAGTGCAACAGCGACACCGAGCGGTCGAGAGAGGAACATTTCATTTAGTCCAGGGTTTCGTTTTGAGGATGTTGTAGTGGAATTACATTTTGAAGTCATATCGTATACGGGTTTAATTTGCAGTGTAGCCTACATTAAAATACATATGGCTAACTTTTGTTTAAGGACCTGACACATACAGCAATAGCCTATACAGTGTATGCTTTTTATTCATTTGTATTATATTGGTAATATTTTGCTTTAGCTTCTCATCTTTTTACATGTTTTCTGCTATGTGTCTGAAAAGGTTAGACACACACATACACGTTTGGTGGTGGAGAGGGAGGGGGTATTCCCATTGTTTCCACACTTTGGAACAATATGTCTCTTGCAATGTTATGATACCAACATCTTTAATATGTTGACATGCATGTGGACCCCGATAAGGAAAGCAGCTTATAAATCACTTCAAACAATGTTAGGTTGTTAAATCGTCACCTTAGAATTAAAAGGT
Associated Phenotype:
Not determined