ZMP
nod2
Ensembl ID:
ZFIN ID:
Description:
CARD15 [Source:UniProtKB/TrEMBL;Acc:Q1AMZ9]
Human Orthologue:
NOD2
Human Description:
nucleotide-binding oligomerization domain containing 2 [Source:HGNC Symbol;Acc:5331]
Mouse Orthologue:
Nod2
Mouse Description:
nucleotide-binding oligomerization domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2429397]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21011 | Nonsense | Available for shipment | Available now |
sa10156 | Nonsense | Available for shipment | Available now |
sa18880 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21011
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 |
---|---|---|---|---|---|
ENSDART00000052380 | Nonsense | 79 | 970 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 38955148)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37291788 |
GRCz11 | 7 | 37563046 |
KASP Assay ID:
2259-9172.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCATGCAGTTATTTTTTGGCTGCGATTGAGCAAGAATTAGCTGAGGAG[C/T]AAAAGGCTGGACTATGTTTTGGTAATGGATGCGTTATGGTGGGCAAGGAC
Long Flanking Sequence:
TTGGCATCACAATAAATGTTAGAATGAGGAACATACGCCCACATTTACACGATAGGCTACCTGTTTGTGCTGATGTTTAAGAAATGTAATAATATCACAACATACTGTAACATCTGAGTCTGACATCTAATTTATGCCACAATATGATTCTTCAGTGAGAGGTTGTAATGTTTTCTGTCTCATCTTTTTAGTTGAGTTCTGTTGTGACTGGGCTATGAGGCGAGATTCAGTTCACTATGAACGCTCAACAGTTGATCCTCAAACAGCGAGCAGAGCTTCTGGCAGTTCTATGTGGTGGAGGTAGCGATGAACCTCTGGAGAGTGTTTTGGACCTGCTACTTGCTCAGGAAGTTCTTGTCTGGGAGGATTACCTTAGGGTACGAGTGGCAGAGAAACCCTTGTGTGCTAACATCAGGCAACTTTTAGATTTGGTGTATGACAAAGGAGAAGATGCATGCAGTTATTTTTTGGCTGCGATTGAGCAAGAATTAGCTGAGGAG[C/T]AAAAGGCTGGACTATGTTTTGGTAATGGATGCGTTATGGTGGGCAAGGACAGACCAGCCACTGCAACTTCAACATTACTGGCTGACAGGCCAATGTTAGTGAGACGGCTCAGAGATAATATTGATGGAGCACTAAATATTTTACTGACGACTGGTTGTTTCTCCATCAAAGATTGTGATAGTGTGCAGCTACCTGTATACACACCCTCACAACAGGTAATACCACCTTAAACTATGAGTTTGTTTTAATACACAAATAATGAAATTTCATGTGCCACATGACTATCTCAATATAATTTGCAGTGTATCTTTTCCTATTGTACTGAAATCATTTTGGCCTATGTAGCATGTTCATCGGGCCAGATTTATGAATGGACAATCAGTTTGTATGATCAAGGGGGCCCTGTTACAATGTGGAGAAATAAATAAATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATGTAAAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10156
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 |
---|---|---|---|---|---|
ENSDART00000052380 | Nonsense | 911 | 970 | 8 | 10 |
ENSDART00000052380 | Nonsense | 911 | 970 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 38948801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37285441 |
GRCz11 | 7 | 37556699 |
KASP Assay ID:
554-6143.1 (used for ordering genotyping assays)
KASP Sequence:
ATAATGGTGTGGGCAGTGCCGGTGCATGTGCTCTGGCTAAATTTATCCGA[C/T]AGAACAAAAGTCTGGAAGAATTGTGGTGAGTGSCTTCAGCTTTTTTTAGT
Long Flanking Sequence:
AGGCTTGGAAATAATAACATCACATCAGTTGGAGCAGAGCAGCTGGCAGAAGGCCTAAGCTACAACCAATCTTTACAGTTTCTGGGGTGAGGTCTATGAAAGGAATGAAATATTGTATGGTATTTTTATTTAATACCTATATTAAATCACAATTTCTTTTTACTTCTAGATTATGGGGTAATAAAGTTGGGGACAGGGGAGCTGAGGTATTGGCGGATGCGCTGACGAATAGCAAAACACTAATATGGTTAAGGTAATATTGTATATATTGATCATAAATCTGTATTCTGTAATGCATATGTTTTAACATATTTTGCAACATGCAAAATGATGATAAGCAAAGAAAAAAGGTTGCCTAGATCATATAAAATTTGCAGAGCCGTGAGTCACTCAGTGCAGCATGTTTTATTTTTTGTGGTGGTGTTGCGTTGGTTTGTTTCAGTCTGGTGGATAATGGTGTGGGCAGTGCCGGTGCATGTGCTCTGGCTAAATTTATCCGA[C/T]AGAACAAAAGTCTGGAAGAATTGTGGTGAGTGGCTTCAGCTTTTTTTAGTTTTCATTTTCTGAGTCAGACTAGGATGATCTAACTCTATTACTCCTAACCAGGTTAAACAAAAACTCCATCTGCAAGGAGGGGGTTGATTGTCTGATAGAGGCACTGAAAATGAACACTAGTGTTAAGAAAGTCTGGTAAGGATATTTCCCAGCATTTTAACTTACCATACACTGGTTTTTACTTTGAAAAAGTAATTGATTGAAATGTGGAGTTAGACTTTCAATTAGAATTTCACATTAAAACATTTACAGTTTTAATTTGGACTTTTTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGTAAATATTATATTATCCATGTCTATGGTTTGTGTTTTGAATAATATTATATCCTTACTACAAAGACTCTTTGCTTTGTGCTCTTAAAGGCTGAGAGGAAATAATCTGAGCCCACAGGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18880
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052380 | Nonsense | 911 | 970 | 8 | 10 |
ENSDART00000052380 | Nonsense | 911 | 970 | 8 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 38948801)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 37285441 |
GRCz11 | 7 | 37556699 |
KASP Assay ID:
554-6143.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAATGGTGTGGGCAGTGCCGGTGCATGTGCTCTGGCTAAATTTATCCGA[C/T]AGAACAAAAGTCTGGAAGAATTGTGGTGAGTGGCTTCAGCTTTTTTTAGT
Long Flanking Sequence:
AGGCTTGGAAATAATAACATCACATCAGTTGGAGCAGAGCAGCTGGCAGAAGGCCTAAGCTACAACCAATCTTTACAGTTTCTGGGGTGAGGTCTATGAAAGGAATGAAATATTGTATGGTATTTTTATTTAATACCTATATTAAATCACAATTTCTTTTTACTTCTAGATTATGGGGTAATAAAGTTGGGGACAGGGGAGCTGAGGTATTGGCGGATGCGCTGACGAATAGCAAAACACTAATATGGTTAAGGTAATATTGTATATATTGATCATAAATCTGTATTCTGTAATGCATATGTTTTAACATATTTTGCAACATGCAAAATGATGATAAGCAAAGAAAAAAGGTTGCCTAGATCATATAAAATTTGCAGAGCCGTGAGTCACTCAGTGCAGCATGTTTTATTTTTTGTGGTGGTGTTGCGTTGGTTTGTTTCAGTCTGGTGGATAATGGTGTGGGCAGTGCCGGTGCATGTGCTCTGGCTAAATTTATCCGA[C/T]AGAACAAAAGTCTGGAAGAATTGTGGTGAGTGGCTTCAGCTTTTTTTAGTTTTCATTTTCTGAGTCAGACTAGGATGATCTAACTCTATTACTCCTAACCAGGTTAAACAAAAACTCCATCTGCAAGGAGGGGGTTGATTGTCTGATAGAGGCACTGAAAATGAACACTAGTGTTAAGAAAGTCTGGTAAGGATATTTCCCAGCATTTTAACTTACCATACACTGGTTTTTACTTTGAAAAAGTAATTGATTGAAATGTGGAGTTAGACTTTCAATTAGAATTTCACATTAAAACATTTACAGTTTTAATTTGGACTTTTTAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAGTAAATATTATATTATCCATGTCTATGGTTTGTGTTTTGAATAATATTATATCCTTACTACAAAGACTCTTTGCTTTGTGCTCTTAAAGGCTGAGAGGAAATAATCTGAGCCCACAGGAAG
Associated Phenotype:
Not determined