ZMP
CARD11
Ensembl ID:
Description:
caspase recruitment domain family, member 11 [Source:HGNC Symbol;Acc:16393]
Human Orthologue:
CARD11
Human Description:
caspase recruitment domain family, member 11 [Source:HGNC Symbol;Acc:16393]
Mouse Orthologue:
Card11
Mouse Description:
caspase recruitment domain family, member 11 Gene [Source:MGI Symbol;Acc:MGI:1916978]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20104 | Splice Site, Nonsense | Available for shipment | Available now |
sa6912 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45153 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11885 | Nonsense | Available for shipment | Available now |
sa9530 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa45152
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074647 | Nonsense | 149 | 1122 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41591120)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41454480 |
GRCz11 | 3 | 41596338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCAGCAGTCCAAGGCAAAAGACATGCAGCGGATGGACGTCATGACT[A/T]AATGCCGCACACTAGAAGACGAGCATAAAAAGCTGCGTCTAACCAACCAG
Long Flanking Sequence:
CATTTCCATGCTTTATTACACGTGGCATGCAAATGGTCTGGTAAACAACGGCGGACTTACAGCAGATCTCGCTTCTTGACATGTGGCTGTTTGTCACAATAAGAGACAAGCTTTGTTTGAGCATGGTTCATTGCTCCATCATTTGTGGTGTCGTGTTTCTGCTGTGTATTTAAATATGGCAGTCCTTGTGTTGTCTTTCTCCTGGCTTGCTGCTCACACAAGGGATGATTCTCTGTAAACCAGCATTCTGCAATGAATCTAGCTCCACCCTTTTGGCACTGTTCTGTTGTGTTAGGTATCGGTCACAAATGCATACTGTACTGTACCAAACCATACCACTTTCAAACGAGCCATTATTTGTGTAGTTGCATTTAATTGCCTGTTTTTGTCCTGCAGTGGAAGAGGGCCAGGAAGGCCTCATCCAGTTTTTAATGAATGAAGTCATGAAGCTTCAGCAGCAGTCCAAGGCAAAAGACATGCAGCGGATGGACGTCATGACT[A/T]AATGCCGCACACTAGAAGACGAGCATAAAAAGCTGCGTCTAACCAACCAGGAGCTGCTGACTTTCCAAGAGCGCTACAACAAGATGAAAGAAGAGCGCAATAACTATAACGATGAACTTATGAAGGTGAAGGATGACAACTATCAGCTTGCCATGCGCTACGCTCAGCTCAGCGAAGAGAAGAACATGGCCGTGATGAGGAGTCGAGACCTTCAGCTGGAGGTCAGAGAGATTCTGATTTGACTTGATTTTTTTTGCCTTCAAAATCTATACAAAAGATTTGACCACCGTCTCTCAATTTCCTCCAGATCGACCAGCTGAAGCACAAGCTGAACAAGGTGGAGGAGGAATGCAAAATGGAGAGGAGGCAGTCTCTGAAACTGAGGAACGACATTGAGAACCGACCCCGAAAAGAGCAGGTATTCGAGCTGGAGAGAGAGAATGAGGTCTTGAAGATCAAAGTTCAGGAGCTGCAGTCCATTATACAGGTGAAGACCCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20104
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 > A
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074647 | Splice Site, Nonsense | 332 | 1122 | 6 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41595747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41459107 |
GRCz11 | 3 | 41600965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTGTGATGGGTTTAAATGAGCATCATTTAATCTAATAATGCACAGTA[C/A]CTGGAAGAGAAGGAGGACCTTGAGTTGAAGTGCTCCACTTTAGTGAAGGA
Long Flanking Sequence:
AATGCATTATTAAAAATCTATGTTTTGCCTTTTATCGTTAGTTAAAACATTGTGAGTTAACAAACTAAAATGACTAACTAAATAACTAATTAAATCATATTGTAAAGTGTTACTGAGTTAAAAAAAAACACATTTATAACAATAATGGCACATTGAAATTATATAAATCTTATAACTTCCCATTTTTATTCATAGCATATGAATGATAACTCATTAGTAATCAGAATTCCACATTCAAAACAAAACAGCAGAATGAAAATGTATACAGTTGTTGAGCATTTTGCCTGTAAATGATGAAATTTCATGCAATCAGCAGAGTTTGAGTTGCATGAAAATGTTTAGTCTGGAGTAAATGTTTGAACTGGAATATAATAACAACAATCTCAATTCTGTTGTTCTGAAAATTTCCTCTCGAGGTCATGTGATGCAATGTTGAACAATGCCATTTATTTGCTGTGATGGGTTTAAATGAGCATCATTTAATCTAATAATGCACAGTA[C/A]CTGGAAGAGAAGGAGGACCTTGAGTTGAAGTGCTCCACTTTAGTGAAGGACTGCGAAATGTACAAGAACCGCATGAATACCATCATGGTGCAGCTGGAAGAGGTGGAACGTGAACGGGACCAGGTTGAGTACTAATGGGTTTCTAACGATGGCTTTAGATCAGCTCATTTCAGGCTGCTTAAAAGGGTTACTGATAGACATTTGTTTTCTCCATCCCACAGGCTTTCAAATCGAGAGATGATTCTCAACATCTCGTCTCTCAGTGTCTAATCGACAAAGACAAGTATCGCAAGCAAATACGAGAGCTGGAAGAAAAGAGCGATGAGCTTCAAATCGAAATCGTACGAAAAGAAGCCAAGATAGTCAACCTGGAGTGCAAATTGAGAAGGATGGCTAAGGAAAATGGGTTGGATCAGGTGAGAAATGATCTGTGTGATTTAAAAGTTGTTGCTTTTTGCTTAACTGAAAATAATTAACATGGCCTTTTTATGATGTTTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6912
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074647 | Essential Splice Site | 438 | 1122 | 7 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41596165)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41459525 |
GRCz11 | 3 | 41601383 |
KASP Assay ID:
554-5457.1 (used for ordering genotyping assays)
KASP Sequence:
CCTGGAGTGCAAATTGAGAAGGATGGCTAAGGAAAATGGGTTGGATCAGG[T/C]GAGAAATGAWCTGTGTGATTTAAAAGTTGTTGCTTTTTGCTTAAYTGAAA
Long Flanking Sequence:
CATGTGATGCAATGTTGAACAATGCCATTTATTTGCTGTGATGGGTTTAAATGAGCATCATTTAATCTAATAATGCACAGTACCTGGAAGAGAAGGAGGACCTTGAGTTGAAGTGCTCCACTTTAGTGAAGGACTGCGAAATGTACAAGAACCGCATGAATACCATCATGGTGCAGCTGGAAGAGGTGGAACGTGAACGGGACCAGGTTGAGTACTAATGGGTTTCTAACGATGGCTTTAGATCAGCTCATTTCAGGCTGCTTAAAAGGGTTACTGATAGACATTTGTTTTCTCCATCCCACAGGCTTTCAAATCGAGAGATGATTCTCAACATCTCGTCTCTCAGTGTCTAATCGACAAAGACAAGTATCGCAAGCAAATACGAGAGCTGGAAGAAAAGAGCGATGAGCTTCAAATCGAAATCGTACGAAAAGAAGCCAAGATAGTCAACCTGGAGTGCAAATTGAGAAGGATGGCTAAGGAAAATGGGTTGGATCAGG[T/C]GAGAAATGATCTGTGTGATTTAAAAGTTGTTGCTTTTTGCTTAACTGAAAATAATTAACATGGCCTTTTTATGATGTTTGATAACATATCAGCTATTGGACAATCTTCAAATAGGATAAACCTTCTTTTACATTAGAACATGTCCTTTTTATAAGACAGTGACAATCACACTATTATTTATTTGCAGACATCTCTTGTTATAGAAATGGCATTAAGTGTAACATTAGTTTACCACATACCAAAAAAAACCTCTTGTAAGACATATTTAGAAGAAGAATCCTTTGACACATTTAAAAAAGGCTTTAAGAAGATCACACCACAGCCTTTCTCCCTCTCTTTCAAACACACACATACTTTTAAATATGTATACATATATTTGGGTTGACATTCACTTTTTTGATCACCAGCCACTGTTGCTGGTAGTTTTCCAACATTACTAGCCACTCGCCATTTTCACTAGCCACAGTTTTGTTTTTGGGAAAATATATTTTCTAAATTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45153
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074647 | Essential Splice Site | 587 | 1122 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41607232)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41470592 |
GRCz11 | 3 | 41612450 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCCTTCAGACACTGCAGATACTGACAGTGGAGACAATGCCGATATGGG[T/A]ATGAACACACATAAATCATTTATTCCGCCCACTTGCTGTCTGAATCATAC
Long Flanking Sequence:
TCTGGTTATCTCTATGATCATGCATGGACGGATCATAAAGGTTTCTGTACAGTTGTACCTATCTCTTTAAAGTGTTTTATATTCAATATATATATTTATATTCATTGTCAATTATAAGAAAAAATATATAAGTTTTTATTCATTTATTTATTATTTATTATAAGAATTTTATATTGTAAACATGGGTGATAATTCTTAATTTTAATGGGTAGTTCAGTGTATCCAAATTACATGAAACGGGAACCTTGTCTAACAACATTTTGTTTAAACAAGTTCTGTTTGAACTAATGTTGCCATAACGACGACAATAATACAAACACCGAAAAGACTTCCTTGCATTTCCTCAACAATCCCATAGTTAGCATTGCTAGAAACTAAAGTGCAATGATAGTAATTTGTTGCTGGGAGTGAAGAGTAAAACTGACTGTGCTGTATCTTTCTTTCAGCTTTCTCCCTTCAGACACTGCAGATACTGACAGTGGAGACAATGCCGATATGGG[T/A]ATGAACACACATAAATCATTTATTCCGCCCACTTGCTGTCTGAATCATACACTTAAGTGACTCGTCTTTGTAAAAATGTCTCTTTTCTTTTCTGCAGATGACCATGAACCATCATCCATCAATTCATCTTCCTCTTCCCACCAGTCTGAGATAATGGATTCGTATGATCTGGAGCAAGTCAATAACATCTTCAGGAAATTCTCGTTGGAGAGGTTTTTTTTTTTGTTTTATTATTTTAGTTATAATCTTAGAGTACTTCTATAATGGGTCTTTGAGCACTTCACTTTTTGCTATTCTTAAGAGGGAAGAAATCTCAGTTTCTGTCATCTCAATTTATCCAGACTCCACAATATCACTCTTTTGATTTTTTCCTTCTTCTCTAGACCTTTTCGTCCTTCATTGACCTCAGGCCCTCCACGAAACTCATTGCGAACGGTTCAGAGCCTTTCTCTCTCTGGAGAAAACCTTTTGTCTGAAATCACTCTGATTGGTGGAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11885
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 |
---|---|---|---|---|---|
ENSDART00000074647 | Nonsense | 829 | 1122 | 17 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41610213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41473573 |
GRCz11 | 3 | 41615431 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCCCAGAGCCCAGYAGCTCCTCTTGGTGAAGATTCAGAAGCTGATGTGT[C/T]GAGGAGGCCGAGAAGATGTCGACACTCTGAGAGTGATCCGGGTCAGTTYC
Long Flanking Sequence:
TGCTTTGCTTTGACCCTCCGCTTTCTCGTTTCCAGGCTACAGGCGGCTGGTGAAGGATATTGAAGACGGCACAGTGGTATCTGGAGACTCCTTCTACATACGTCTCAATCTGAACATCTCCAGCCAGTCTGATAACTGCTCGCTGAATGTCAGATGTGACGAGGTCCTCCATGTTCTGGACACCATGCATCAAGACAAATGCGAATGGCTGTGTGCCCGTGTCGACCCTTTCACAGACAAGGACCTGGACAAAGGCACCATACCGAGTTACTCAAGGTGAGGAAGAAATGAGTGACCATTATTGTGTCGGTTTTCAAACCAAGTGTGAACACTGGTCTATTGCCTGCTGCAGATTGCCTGTCAGTGTGTTGGTGAGCGTGTGGGTGTGCATTTTTTTTTTGTCTGTTGACTGTGACGAGAAGCTGTTAAGTGAACTTAGCTGTCACCTCCTCCCCAGAGCCCAGCAGCTCCTCTTGGTGAAGATTCAGAAGCTGATGTGT[C/T]GAGGAGGCCGAGAAGATGTCGACACTCTGAGAGTGATCCGGGTCAGTTTCTTATGGATTGTTGGGGAAATGCATCTTGTTTTGGGTTTCACATTCATAGATGAGGGTAAACTGATTCTGCACAAACTGAAAGGCAATTACAGGGACAGTAACTTATAGAGTTATACTGTTTGGTAACTTATAGAACCTAGAAAGTCTGTCATAATTTATTTATTTTGATGACTTTACTTCGTTGGCAGAAACTCACTGTTTTATTCTTTTTATTCATTAATGGCAAAATGACTTTAATTTATTCTGTTTGTTTTATGCATCTGCTGTATGGAAAACTAAGAGTGACCCTTCAAAAATAAATTGAAGAAGCAGTTTATCAGTTTAGTAATTAATACATACACTTTATACAAATAAATCATCTTTAAATGGACAATTCATGTTTTAAAATGTGAATTAATTAAACAATACAAAGTATTAGGATCTCTTTCACATGGTCAGTCTCTTTAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9530
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074647 | Nonsense | 994 | 1122 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 3 (position 41619710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 41483070 |
GRCz11 | 3 | 41624928 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGACAAAAGATGAATTCCTCATGAAACAGAAGATAGAGCCCATCATTTA[T/A]TCCAAAGAAAAGCAGGCGGGCACGTATGAATGCATCACCCCAGAAAATAT
Long Flanking Sequence:
TAATTTGAACAAATTTAAAAAAAATATTTTCGAGTGTAACAAGAACATCATCAAATAAAGTTTACCAGTTTAAATTACTATACAGCTACTTATTTACAGCTTCATGGTCAAAGAAACAGCTTAAGTTTCAGAGTTTGCAAAGAGAAGTTTAAAACAAATTGCTTTAGATTTATATACAAAAGAAAAGCACATATCAGCAGATTCTTTCAATAAGTCTCAGAATGTGAGAATGAAATGCAAATACTAATTGTTTGTTAAGATCACAGCTTTTGTGTTTGACTAAACATCCCCAGCGGAGTTTTAATTGTAATGGATCTTCAACTAGTTATTACTTTAATAAAAAGATTCACAAATGCGATGTTGATTCACAGCCGCAATGCTTTAAATCCTCACAGTGTTTTCCCTAACATGCCTGTTTATAACTTCTAATTCATCTTCTTCGCAGACATTGTGACAAAAGATGAATTCCTCATGAAACAGAAGATAGAGCCCATCATTTA[T/A]TCCAAAGAAAAGCAGGCGGGCACGTATGAATGCATCACCCCAGAAAATATAGAAGCCGTTGCCTTCAAGGTACAGTAATAAATGCTCTTTTCAGAAGAATTTAATAATAGCTAAATTATGTTTTTGCTTTTCATGTGCTGTCATTTCTTCTGCTTACTCAAGAGGCTTGTCAGATATTTATGCGTTCGCTGTTTTGCCCAGCAATTTTATTTCAAAGTGCTTCCACTCAGTGAGAGCATTAACACTTTCCCAAAGACATCCGTGCGATTTTTCACACGGCATCTGTCCTAAACTCTTAGGCCCCGTTTACACTAGTGCGTATTAGTTTTAAAACGGCGTTTTAGAATGAAAACGATCCGCGTCCACACTCGCGTTTTACCCAGCGTTTCTGAACTGCTCTCCGTCCACACCAAAACGCTGAAAACGCACATCACGTGACCACACACACACACTTTGGCAATCGCTGGAGCCCATCTACCCAGATGAGAGCTCTGCTAGTC
Associated Phenotype:
Not determined