Busch Lab

ZMP

zgc:92411

Ensembl ID:
ENSDARG00000022437
ZFIN ID:
ZDB-GENE-040808-52
Description:
CD81 antigen [Source:RefSeq peptide;Acc:NP_001003735]
Human Orthologue:
CD81
Human Description:
CD81 molecule [Source:HGNC Symbol;Acc:1701]
Mouse Orthologue:
Cd81
Mouse Description:
CD81 antigen Gene [Source:MGI Symbol;Acc:MGI:1096398]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa32210 Nonsense Available for shipment Available now
sa43122 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa32210
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000037813 Nonsense 59 238 2 8
Genomic Location (Zv9):
Chromosome 18 (position 27264931)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 27338186
GRCz11 18 27320564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTCCTCATGCTCCAGTTTGAAGGAAATCAAGCACCGGGAACTTTTTA[T/A]ATCAGTAAGTGACTTCTGCTCACATGCTAAATTTGGCCAAAGGCCCATTC
Long Flanking Sequence:
CAATCCTGAAGCCTCTTGAGATGCGTATTGTTTCCCGTCATTGTACTTTACGCACTGCCAACACCAAAATATATCTGCCTGACTTCCACAATTCTCTGAGTGAAGCTGCTGCTTCCTGCTCCGCCAATTGCAAAAAAATAAACAAACAAACGGTATCACAGAGGACTGGCTCTCAGTGCTGAACAGGACCCCCACCCCTTCTTTGTGCGTGAATAACACTAAACCTGTCAGATGTTTCTTCCCCAAACGCAGGAAGAAATGACCTCAGGAGTGACCTCCGGAAAAAGAATTGAAGCAAACATTTCTGGGCGATGACATCTGTTGAAGGTTCTAATCAGTCATTTAATGGAGAATTTTTGCTAAGATATTTCTGTTTTTCTTTGTTGCTAGCTGGCTGGTGGTGTGATTTTGGGTGTAGCTTTATGGCTTCGTCACGACAGTCAAACCAGCAACCTCCTCATGCTCCAGTTTGAAGGAAATCAAGCACCGGGAACTTTTTA[T/A]ATCAGTAAGTGACTTCTGCTCACATGCTAAATTTGGCCAAAGGCCCATTCACTACAATGACCATAACTGCTCTAATGATAAAGATATAGTTTTATGAAACACTCTGAATTGAATGGAATAGCAGTCTATGCCTAAATCAGTAATGGCACACAGAAACAATATTGCTTCTATAGGTTTTATGATACTGGTGTCAAACTGATATATTTAAAGTGGTACCAGTACCTAGAAATTGCAAAAAAAAAATGATAAATAAGAGCCCCAAAACAAAATTGGAAGACTTTTATTAATTAAAAAAAATCTTGCACAACATATTATATATATATATATATATATATATATAAGTATTATCCTTTTAATCTCTGCAGACCTGGTATTGGGTTCAAAATGACATCATCATTCACTTCCTTTAACTTGTAAAGGTTTGTGTTGGGTGTGTTGGTTTAGTTTCTTTCCTGCAGACATTTATCACTTTGACATTCATTTTACTAAACAGATTGGGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43122
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000037813 Essential Splice Site 219 238 8 8
Genomic Location (Zv9):
Chromosome 18 (position 27279889)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 27353144
GRCz11 18 27335522
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACTCATATCCTTTCAAATGATTATGCGCTTAATTTCTCTCTACTGTGC[A/T]GGTTTTTGAGATGATCTTCACCATGGTCCTGTGCTGTGCGATCCGCAATG
Long Flanking Sequence:
ACCAGTATTGGGCTGCAGAATGATATGGCTGTGTCTAATAATAGATGCAATGTTTCTACTGTACAGTCTATATTCTATACCCCTCTACCCCTCAATCCAACCTTCACATGAAACAATCTGCATTTTTACTTTTTCATAATACTTCATCCTGTGTGATTTATTAGCCGTTTTTCTCATAATGTTAAGTTTTACTGGTTTTGCTATACTTATGGGGACAGTTGGTCCCCACAGAAATACATGGTACGCACATAAACACACACAACCGTGGATTTGATTTAGAATGCAAAATAATTTGATTATATTTTTTGATGTTGTGCACTTCAGAGCTGCCACGTGAAGCTAAGAAACCTGTTCTCTGAGAAGCTTCATGTGATTGGACTGGCTGCTCTAGTTATTGCTGTCATTATGGTAAGAATAATACACACACATACAGACCTGTACTAAGAATATATACTCATATCCTTTCAAATGATTATGCGCTTAATTTCTCTCTACTGTGC[A/T]GGTTTTTGAGATGATCTTCACCATGGTCCTGTGCTGTGCGATCCGCAATGCTCCTGCGTATTGAGTTGGTGAATGATGACCAGGCTAATAAATGATGTTTGATGTATTTTTTTCTAGTGGTGGTCAAAAGGCCATTTCACTTCTGCATTGCCTCTCTCGTTTTAAGTTCAGGTGTCCAAACGCTGAACATTGATCCCTGTGTTTGTAGAGTGGACTGTCATTGTGAATGTGCCAGAATACACACCAAGGGCTTTTAAAAATTAACCAATAGCCAACATCAGAGAGGAGGGATAATGTGATTGATGAATAGCATTGCGTTTGTGTTGTATTGTTTTATGTTTATTTAATCATTTTATTAAATCTTTACTGGTTTACTTTAATTATCTGTTCTTCAACTTTTAGTAATAATTTTTGTGTGTTTGTTTATTTGTAAAGTAAATCAATGTAATGTTAATAGAGATGGATTTCAGCAGCCCCTAATGATGGTGTCATAAGAATCT
Associated Phenotype:
Not determined