Busch Lab

ZMP

fadd

Ensembl ID:
ENSDARG00000068099
ZFIN ID:
ZDB-GENE-070606-3
Human Orthologue:
FADD
Human Description:
Fas (TNFRSF6)-associated via death domain [Source:HGNC Symbol;Acc:3573]
Mouse Orthologue:
Fadd
Mouse Description:
Fas (TNFRSF6)-associated via death domain Gene [Source:MGI Symbol;Acc:MGI:109324]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa16977 Nonsense Available for shipment Available now
sa21084 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa16977
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098288 Nonsense 8 196 1 3
Genomic Location (Zv9):
Chromosome 7 (position 55004994)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 54049516
GRCz11 7 54319168
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGYGCCGTGTTAGCATTCAAACATGGACAAGAGAGGATTCCGAGCAATGT[T/A]GCTAGAAATTTCCGACAAGCTTACAGATGATAACGTGGCCAAATTAAAGT
Long Flanking Sequence:
GGTTTGTAAGGATTTTAATAGCTAGTGCAGTTGTATCCTTATGGAAAATCAAATGTAATGGCGTCTATTGTTTTGGACCTTTATTAGTGCTTTTTAAGACTAGCTCAAAATGCAAATTGTTTATATTATGCTACTAATGTTCAAAGGTCGAACTGTTGAAGCCAATAAAGTGATTCAGAAGAACAGTTCTGAATCACGAATCGGACACTGCTTAGCAAACGAATCATTAAGCTACAACATCAAAAAAAGAAGCCATTTCTAAAACAAGTCATCTTTAAAGCGAAATACATTTTGTCGTTTTGGTGTCCAGCAGCAGATCATTCAGAGCAGAGCAGAGCAGAGCAGCAGGGTGTCTTCAGAAGCAGGAGAGAGAGAGGGAGGGGATTTTACGAGTCCTCGCTAAACTTCAGACCGAGAGTTGAAAGCGAAAGCGGAGATGAGTCGAGCGGCAGTGCCGTGTTAGCATTCAAACATGGACAAGAGAGGATTCCGAGCAATGT[T/A]GCTAGAAATTTCCGACAAGCTTACAGATGATAACGTGGCCAAATTAAAGTTTTTGTGCACTGACGTCGGCATCGGGAAGAAAAAACTTGAGAAAATCGACACCGGGATTGAACTCTTCGAGTGCTTGATCGAAAGAACTGCAATTGGGCCTGAAAACACTGAGCTTTTACGAACACTTCTTGACAAAGTCGGTCAGACAGTTCTTATTGAAAAAATAGACGATTATGACAGGCAAACGTCAAGAAGCCCGGCTGGTGGTCTGGACGCGAAAGAGCGAGGTTGGTAACGTTACACTTGTACTGTAATTCTTGAAATTCTCATGTCTGTCAGTCAGGTGTAACGTCAGTGTGGTTTCCACTTAACGAAGTTCGATATTTTACGTGTAACCTTATAAACTACTGTAATTTTGGATGAAACAATGGTTTAAAGTCAGAGTAAGGTCTAATTTAAACGACATTTCTGTGTATTCTGTTGTTTTGTGTTACTTTTTTCACTGAGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21084
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098288 Essential Splice Site 188 196 3 3
Genomic Location (Zv9):
Chromosome 7 (position 55010772)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 54043738
GRCz11 7 54313390
KASP Assay ID:
2259-9529.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGGAGAGAGCTTTTTGTAATTACTGTGAATTTCCTTTATCTTAAGA[G/A]CAAAATAACTCTAAATCGTTTACAGATCTTCCTGAAGGAGTCGAGCACAG
Long Flanking Sequence:
TCTCCTACAGGCAACTGAATCTAAAGTTCTAAAACGATCACAAAAACAAGCGCACTTGTAGAATAAGGTCAATAGTCTGGGGAAGAACCAACCAACATTCAATTCAAACGCTTTCTGTGTCTCTTTTTAGAGAGAATCAACACAGCAACCGAAGTAGTGGTTGAGCAGCTGGGTAAAAAGTGGCCCTCCGTTGGAAGAAAGCTGGGGCTTCAGCAGACACAGCTGGAGGGAATCCAGGAGAAGCACAGCCGTGATCTGGAGGAGCAGGTCAGAGAGCTCATCAGACAGTGGATGAGGATCAAGAAGGAGAACGCCCGAGTGGAAGATCTCATTCAAGCGCTGCGAGACTGCAAACAGAACCTCACCGCTGATCTCGTGGAGAGAAAACTCAGGGAACTTTAAAAACAAAAACAACTTCACACCATTTTGTGTTTTTTGGAAGCTGTTGGAAAAAAGGAGAGAGCTTTTTGTAATTACTGTGAATTTCCTTTATCTTAAGA[G/A]CAAAATAACTCTAAATCGTTTACAGATCTTCCTGAAGGAGTCGAGCACAGCTTTTGTTCAGGATAATGAATTAGATAATATATTTGTACAGCGTTATTATATTGCAGGGCACGATATTATTGAATAATGAGTGTCTTAAAGGGATAGTTCATCCAAAAATGAAAATTTACTCACCATTTACTCTCTCTCAATGGGTTACAAACCTTGCTAAACACATTCTAAAGAAAGCTGAAAACTGGTAACCATTAACTTCCATTGTAGGAAAAACAATTACAATGAAAGCCAGTGGTTTTGAAATATCTCCTTTAGTGTTTAACAAAAGAGAGAAACTTGAAGGTTGAGTAAATGATGACTTTTGTTTTTTGGGTGAACTATCCCTTTAAAACAACACATCTGATTTACCCTTTGAAAAGCATTAGAATGGTGCAGTTTTTACAGAACACTCATCAAATGACACTGTTCTTGTATTGACTGATTCTGGCAGAGGATGTCTGACACTT
Associated Phenotype:
Not determined