ZMP

si:ch211-278p9.2

Ensembl ID:

ENSDARG00000095274

ZFIN ID:

ZDB-GENE-081028-37

Human Orthologue:

NLRC5

Human Description:

NLR family, CARD domain containing 5 [Source:HGNC Symbol;Acc:29933]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22998	Nonsense	Available for shipment	Available now
sa28799	Nonsense	Mutation detected in F1 DNA	Not yet available

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.

Availability:

Order Allele From ZIRC

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

Mutation Details

Allele Name:

sa28799

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
ENSDART00000144941	Nonsense	359	466	1	1

Genomic Location (Zv9):

Chromosome 17 (position 7323326)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	7326100
GRCz11	17	7483278

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGCTGAACTGGCTTTCAATCAGCTGATGAAGGGCAATGTGATGTTCTA[T/A]GAAGAGGACCTGATTGAGAGCGGCATAGACGTCACTGATGCTGCAGTGTA

Long Flanking Sequence:

TCTTCATCAGTGGCTGTGTTGATGTCAAACCTCATCAGAGGAGATCTGCTTCCCTCTGCTCTCATCTGGATCACCTCCAGACCAGCAGCAGCCAATCAGATCCCTTCAAAATACATCAGCCGTCTGACAGAAATTCAGGGATTTAATGATTCTCAGAAGGAGGAATATTTCAGGAAGAGAATCAGCGATGTGGGTCAAGCCAGAAGAATCATCTCCCACATCAGAAGATCCAGAAGCCTCTACATCATGTGTCACATACCCGTCTTCTGCTGGATCTCAGCCACTGTGCTTCAGAAGCTCCTGAATGAAGATGACAGAGCAGAAATCCCTCAAACTCTGACTGAAATGTACATCCACTTCCTGCTGACTCAGATCAACATGAGGAACCAGAAGTATGAAGAGAGAGATCCAGAGAAACTCCTTAAGTCCAGCAGAGAGGTCATCGTGAAACTTGCTGAACTGGCTTTCAATCAGCTGATGAAGGGCAATGTGATGTTCTA[T/A]GAAGAGGACCTGATTGAGAGCGGCATAGACGTCACTGATGCTGCAGTGTATTCTGGGATTTGCACTGAGATCTTTATGGAGGAATCTGTGATTCATCAGAGGAAAGTCTACAGCTTCCTTCATCTGACCTTTCAGGAGTTTCTCGCTGCTTTCTTTGTGCTTTACTCTTACATAGTCAAAAATGTGGAGTCTTTAAAATTATTTCTGTATGAAGAAGATCAGCGTGAAATTAGTTTTTATGATCTATTAAATGCAGCAGTTGATGAATCCTTACAGAGTGCAAATGGACATCTGAACCTTTTCCTGAGGTTCCTGCTTGGTATCTCACTGAACTCCAATCAGAGACTCTTACAGGATCTACTGCCAAACAGAGAGAACAGTTCAGAGATCATTAAGAGAATCACACAATATATTAAAGTCCAAATCAAAGGTGATGAACATCTCTCAGCTGACAGATGCATCAATCTGTTCCTCTGTCTGCTGGAAATGAAGGATCAGAC

Associated Phenotype:

Not determined