si:dkey-21h14.7

Ensembl ID:
ENSDARG00000001781
ZFIN ID:
ZDB-GENE-041210-93
Description:
tetraspanin-11 [Source:RefSeq peptide;Acc:NP_001038502]
Human Orthologue:
TSPAN11
Human Description:
tetraspanin 11 [Source:HGNC Symbol;Acc:30795]
Mouse Orthologue:
Tspan11
Mouse Description:
tetraspanin 11 Gene [Source:MGI Symbol;Acc:MGI:1915748]

Alleles

There are 3 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa40240 Essential Splice Site Mutation detected in F1 DNA During 2017
sa33406 Essential Splice Site Mutation detected in F1 DNA During 2017
sa33407 Essential Splice Site Mutation detected in F1 DNA During 2017

Mutation Details

Allele Name:
sa40240
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023638 Essential Splice Site 29 254 None 7
ENSDART00000138661 Essential Splice Site 29 254 None 8
Genomic Location (Zv9):
Chromosome 4 (position 10240178)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 11176805
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CACGGTGTGTCTCAAATACCTGCTCTTTGTTTTCAACTTTCTCTTCTGGG[T/C]GAGTCTGAACTCCACTTTGCTGGTATAGCTCTTATCAAAAAGGAAGGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33406
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > C
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023638 Essential Splice Site 118 254 3 7
ENSDART00000138661 Essential Splice Site 118 254 4 8
Genomic Location (Zv9):
Chromosome 4 (position 10249673)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 11186300
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
CCTCATCGAGCTGGTGGCTGGAGTTCTGGCCTATGTGTATTATCAGGCGG[T/C]AAGTGAACTCTTTCCACAACACTGACACACAAAACAAAGCTCTTAAGAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33407
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2017.
Mutation:
T > A
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000023638 Essential Splice Site 235 254 6 7
ENSDART00000138661 Essential Splice Site 235 254 7 8
Genomic Location (Zv9):
Chromosome 4 (position 10252366)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 11188993
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
TCACTTGCTTATCATTGGTGCTGTGGGAATAGGTGTGGCCTGTCTACAGG[T/A]AAGTCCCTCCCCCTTATGTAGATTATGAAATTAAAGGAATAGTTCACAGA
Associated Phenotype:
Not determined

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