ZMP
zgc:65811
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393524 [Source:RefSeq peptide;Acc:NP_956846]
Human Orthologues:
CD81, CD9, TSPAN2
Human Descriptions:
CD81 molecule [Source:HGNC Symbol;Acc:1701]
CD9 molecule [Source:HGNC Symbol;Acc:1709]
tetraspanin 2 [Source:HGNC Symbol;Acc:20659]
CD9 molecule [Source:HGNC Symbol;Acc:1709]
tetraspanin 2 [Source:HGNC Symbol;Acc:20659]
Mouse Orthologues:
Cd81, Cd9, Tspan2
Mouse Descriptions:
CD81 antigen Gene [Source:MGI Symbol;Acc:MGI:1096398]
CD9 antigen Gene [Source:MGI Symbol;Acc:MGI:88348]
tetraspanin 2 Gene [Source:MGI Symbol;Acc:MGI:1917997]
CD9 antigen Gene [Source:MGI Symbol;Acc:MGI:88348]
tetraspanin 2 Gene [Source:MGI Symbol;Acc:MGI:1917997]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33074 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33074
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066142 | Essential Splice Site | 21 | 176 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 3 (position 2123790)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149855.1 | 18795 |
GRCz11 | KN149855.1 | 18795 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTGATTGGTTGATTATTGATTGATTGATTGATTGATTGATTGTCTCC[A/C]GCTGCTGGGCTTCAGTCTGGTGTCTCTGGGATTGTGGCTCCGCTTCGGCG
Long Flanking Sequence:
TTCACCTGGGTTTAATTCAGGTCAGGAGATGTGTTTATAATAATATATTTAACACACAAGCTTTATCAGTCTCCCTTTAACTGGCAAACACTAATGCAGAAGTGCGCCATCAGTCTGTTATCAACAGCTCATGTGGAAGGTCATCTTCAGTTCATTGAACACGTCGTCAGTGTTGATTTATATTGTGCCAGAGTGTGAACTATTCAGTAAAGCAGCTTCATATTTACCTGTAGTTCAGTTATACGTGTAGCTCACATATAAACACTGAGTGTGAATACACTGCTGAACAGCAGAACTGAAGACTGAAGCGTGGAGGATCTGACACTCACCACCACCGCCGCTGATGATGATGATGATGATGATGATGATGATGGTGATGATGATGGTGATGATGATGGTGATGATGATGATGGTGATGATGATGGTGATGGTCTTCTTCCTCTGTGGTGATGATTGATTGGTTGATTATTGATTGATTGATTGATTGATTGATTGTCTCC[A/C]GCTGCTGGGCTTCAGTCTGGTGTCTCTGGGATTGTGGCTCCGCTTCGGCGCTGAAACCAGAGGATTCTTCGACATCGACCTGAACACCAGCCAGTTCAACATCGGTGTGTGTGTGTGTGTGTGTGTGTGTGAATTTAAGTATATACTGTATGAGTGAGTGTATCTGAGTGTGTGATCTGATCTGACTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGGTGTGATGGTGCTGATGGTGTCGGGTGCGCTGATGCTGCTGGTGTCCGTCATCGGGAACTGTGGAGTCTGCTGCAGCAGCAAAGGCTCTCTCAGTGTGGTGAGCAGGACACACACTCGCATGCATACACACACGCTCATACACACACACTTGCATGTGAGCGAGAGTGAGCGAGCATATGTGTGTTTGTGGTCTTCAGTTCGACGGGCTGCTGTCTGTCCTCATCCTCATAGAGATCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined