Busch Lab

ZMP

ENSDARG00000094098

Ensembl ID:
ENSDARG00000094098
Human Orthologue:
NLRC5
Human Description:
NLR family, CARD domain containing 5 [Source:HGNC Symbol;Acc:29933]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa36314 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36314
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000139373 Nonsense 130 272 4 4
Genomic Location (Zv9):
Chromosome 17 (position 7330755)
Other Location(s):
Assembly Chromosome Position
GRCz10 17 7333529
GRCz11 17 7490707
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCTGAGGGAAACAGAACGGTGACATGTGTGAAGAAGAAGCAGCCATA[T/A]CCTGTTCATCCAAAGAGATTTGATGAGTGTCTTCAGGTTCTGTCCAGAGA
Long Flanking Sequence:
ACATTCGAATGTTATTTAATATGAAACTATTCAGATGGCGCTCTGTGGTGGATCAAAAAATGAACAGTGTGCTGAGTTGTAGCTGGGCACTGCAGACAGCCGACTTGTGGTGCCAGTGCGCGTGTCCTATTATAGATCTAGGTTTAGAATTCTTAAATTTCATGGTGTTGTGTGGTGCGGTGCATCGCTGAGCGGCACATACCTCATTTAGTGTCATCTTCCTTATTATGTAAACTTTACAGGGTGTCACATATTTTGTTATAGTGTGGATCATGGAGGAGACATCAGGATCAAAACAGGACCACAGAAATGTAGGTCTCTATCTCACACACCCAAAACCCACTATAATTGTTGTGTTGTGATAAGCTGTACACCTCATCATCTCTTTTCTTGTGTTCAGATATCTGTGATCTCACACTGGATGTAAACACAGCACACAATAAACTCGCTCTGTCTGAGGGAAACAGAACGGTGACATGTGTGAAGAAGAAGCAGCCATA[T/A]CCTGTTCATCCAAAGAGATTTGATGAGTGTCTTCAGGTTCTGTCCAGAGAGAGTCTGACTGGACGCTGTTACTGGGAGGCTGAATGGAGTGGGAACATTTCTATATCAGTGGTATATAATGGTATAAGCAGGAAAGAATGGAGCGATGATAGTTTGTTTGGATTCAATGAAAAGTCCTGGAGTCTGATCTATTGTAATGGCAGTTTCACTGTTGGACATGGTGATATAAGCATAGAAATACATGTCCCTCACTGCTCTAACAGAGCAGGAGTGTATCTGGACCACTCAGCTGGCACTCTGTCCTTTTACAGCGTATCTGACACACGCAGACTCACACACTTACACACATTCAAAATCAAATTCACTGAAACACTCTATGCTGGAATTGGGTTTTTTTCTGTTGGTTCAGTGTCTCTATGTGGAATTAAACAGCTTCCTGTGAGAAAGAACTGAACTATCTATGGTGTCTGACACACATTCAGCACCATTTTCACCAAACC
Associated Phenotype:
Not determined