ZMP
si:ch211-278p9.2
Ensembl ID:
ZFIN ID:
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 |
|---|---|---|---|
| sa22998 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22998
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000144941 | Nonsense | 225 | 466 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 17 (position 7323730)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 7326504 |
| GRCz11 | 17 | 7483682 |
KASP Assay ID:
2261-0597.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTCCCTCTGCTCTCATCTGGATCACCTCCAGACCAGCAGCAGCCAAT[C/T]AGATCCCTTCAAAATACATCAGCCGTCTGACAGAAATTCAGGGATTTAAT
Long Flanking Sequence:
GAACAGCCAAAATACAAGACACTCCAATCTACTGCAGTGACATCTTCAAACCCTTACAAGAACCAGAACATGAGCAGAAAGACCAGATCAAGACTGTTCTCACTAAAGGCATCGCTGGAATTGGAAAAACCGTCTCTGTGCAGAAGTTTATTCTAGACTGGAGTGAAGGAAAAGCCAATCAGGATGTAGATTTCATGTTTGTGCTTCCATTTCGAGAGCTGAACTTGATTAAAGATCATCAGTACAGTCTTCACAGACTTCTGCTGGACTTTCATCCTGAACTTCAAGATCTGGACTCAGAGATGTATGAGGAGTGTAAAGTCGTGTTCATCTTTGATGGTCTGGATGAAAGCAGAATCACACTGAAGTTTTCAGACATTGAGAGAGTTAGTGATGTGAATAAGTCTTCATCAGTGGCTGTGTTGATGTCAAACCTCATCAGAGGAGATCTGCTTCCCTCTGCTCTCATCTGGATCACCTCCAGACCAGCAGCAGCCAAT[C/T]AGATCCCTTCAAAATACATCAGCCGTCTGACAGAAATTCAGGGATTTAATGATTCTCAGAAGGAGGAATATTTCAGGAAGAGAATCAGCGATGTGGGTCAAGCCAGAAGAATCATCTCCCACATCAGAAGATCCAGAAGCCTCTACATCATGTGTCACATACCCGTCTTCTGCTGGATCTCAGCCACTGTGCTTCAGAAGCTCCTGAATGAAGATGACAGAGCAGAAATCCCTCAAACTCTGACTGAAATGTACATCCACTTCCTGCTGACTCAGATCAACATGAGGAACCAGAAGTATGAAGAGAGAGATCCAGAGAAACTCCTTAAGTCCAGCAGAGAGGTCATCGTGAAACTTGCTGAACTGGCTTTCAATCAGCTGATGAAGGGCAATGTGATGTTCTATGAAGAGGACCTGATTGAGAGCGGCATAGACGTCACTGATGCTGCAGTGTATTCTGGGATTTGCACTGAGATCTTTATGGAGGAATCTGTGATTCAT
Associated Phenotype:
Not determined