ZMP
chad
Ensembl ID:
ZFIN ID:
Description:
chondroadherin [Source:RefSeq peptide;Acc:NP_957357]
Human Orthologue:
CHAD
Human Description:
chondroadherin [Source:HGNC Symbol;Acc:1909]
Mouse Orthologue:
Chad
Mouse Description:
chondroadherin Gene [Source:MGI Symbol;Acc:MGI:1096866]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17612 | Nonsense | Available for shipment | Available now |
sa19040 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11952 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17612
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 |
---|---|---|---|---|---|
ENSDART00000066264 | Nonsense | 90 | 363 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 28083940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26421549 |
GRCz11 | 12 | 26512909 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGGCTTCAGTGAGATGAAAGGGCTCATTTCTCTGCACCTGCAGCATTGC[C/T]AGATCCGAGAGCTCTCCGGCCAGGCTTTCWAAGGGCTCAACAAGCTCATC
Long Flanking Sequence:
CAGCTTCCTTCCCTCCTTTTCTCTGACACACATACCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATGTTGCTCACCTCCAGCCCTCTCGCTCTGCTCTCCCACACACTCCCTCTCTTTACTCTGAGGCTGTGTGGACCACTTCAGCTGTCTGTATATGTTCCTGCCGCCACAGTTTCTCGGAGTAAAGCAGAAACCAGACCAAACATCCAGACAGCAATAAGCTCAACATGTACACTTTTCATGTCTTACTGGTGCTAGTGTGTCTACAGTTTTGTGCTCACACTGCTTTTGCAGCTCCAACTCAGTGCCCAAGCCAGTGCCACTGCCATGGGGACCTGCAGCATGTTATTTGTGACAATGTTGGGCTAAAGAAGATCCCTCGCATATCTGAAGCCACGCGTCTCCTCAACCTGCAACGCAACAACTTGGGGAATCTACCAACTGGGGGCTTCAGTGAGATGAAAGGGCTCATTTCTCTGCACCTGCAGCATTGC[C/T]AGATCCGAGAGCTCTCCGGCCAGGCTTTCAAAGGGCTCAACAAGCTCATCTACCTCTACCTGTCTGATAATGAGATCAGCACCATTAAACCCGGTGCTTTTGAGGATCTAACAGAACTCACCTATCTCTACTTGGACGGCAACCAAATCACAAGCCTTCCGAAGGGCATCTTTTCCCCCATGATCAACCTGTTCATCCTGCAGCTCAACAACAACAAGCTTCGAGAGCTGCAGCCTGGTACTTTCAAAGGTGCTAAGGATCTCCGCTGGCTTTATATGAGCGGCAACGAGCTGAGCTCCATACAGCCTGGTTCTCTTGATGAAGTGGAGAACTTGGCCATTCTAACCCTGGACCAGAACAACCTGTCCACATACCCTCTCCCGGCTATGAGCAAGCTGCGTGTTGTGGAGGAACTCAACCTCTCCAAAAACCCTCTCAGCCTCATCCCTGACCATGCATTCCGAAGCTTCGGACGCTACATGGAGAAGCTCCATCTAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19040
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 |
---|---|---|---|---|---|
ENSDART00000066264 | Nonsense | 100 | 363 | 1 | 4 |
ENSDART00000066264 | Nonsense | 100 | 363 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 28083970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26421579 |
GRCz11 | 12 | 26512939 |
KASP Assay ID:
2260-5432.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTGCACCTGCAGCATTGCCAGATCCGAGAGCTCTCCGGCCAGGCTTTC[A/T]AAGGGCTCAACAAGCTCATCTACCTCTACCTGTCTGATAATGAGATCAGC
Long Flanking Sequence:
CATACCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATGTTGCTCACCTCCAGCCCTCTCGCTCTGCTCTCCCACACACTCCCTCTCTTTACTCTGAGGCTGTGTGGACCACTTCAGCTGTCTGTATATGTTCCTGCCGCCACAGTTTCTCGGAGTAAAGCAGAAACCAGACCAAACATCCAGACAGCAATAAGCTCAACATGTACACTTTTCATGTCTTACTGGTGCTAGTGTGTCTACAGTTTTGTGCTCACACTGCTTTTGCAGCTCCAACTCAGTGCCCAAGCCAGTGCCACTGCCATGGGGACCTGCAGCATGTTATTTGTGACAATGTTGGGCTAAAGAAGATCCCTCGCATATCTGAAGCCACGCGTCTCCTCAACCTGCAACGCAACAACTTGGGGAATCTACCAACTGGGGGCTTCAGTGAGATGAAAGGGCTCATTTCTCTGCACCTGCAGCATTGCCAGATCCGAGAGCTCTCCGGCCAGGCTTTC[A/T]AAGGGCTCAACAAGCTCATCTACCTCTACCTGTCTGATAATGAGATCAGCACCATTAAACCCGGTGCTTTTGAGGATCTAACAGAACTCACCTATCTCTACTTGGACGGCAACCAAATCACAAGCCTTCCGAAGGGCATCTTTTCCCCCATGATCAACCTGTTCATCCTGCAGCTCAACAACAACAAGCTTCGAGAGCTGCAGCCTGGTACTTTCAAAGGTGCTAAGGATCTCCGCTGGCTTTATATGAGCGGCAACGAGCTGAGCTCCATACAGCCTGGTTCTCTTGATGAAGTGGAGAACTTGGCCATTCTAACCCTGGACCAGAACAACCTGTCCACATACCCTCTCCCGGCTATGAGCAAGCTGCGTGTTGTGGAGGAACTCAACCTCTCCAAAAACCCTCTCAGCCTCATCCCTGACCATGCATTCCGAAGCTTCGGACGCTACATGGAGAAGCTCCATCTAAATGACATGAGCCTGGAGAAGGTAAGTCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11952
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066264 | Nonsense | 100 | 363 | 1 | 4 |
ENSDART00000066264 | Nonsense | 100 | 363 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 12 (position 28083970)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26421579 |
GRCz11 | 12 | 26512939 |
KASP Assay ID:
2260-5432.1 (used for ordering genotyping assays)
KASP Sequence:
CTCTGCACCTGCAGCATTGCCAGATCCGAGAGCTCTCCGGCCAGGCTTTC[A/T]AAGGGCTCAACAAGCTCATCTACCTCTACCTGTCTGATAATGAGATCAGC
Long Flanking Sequence:
CATACCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATGTTGCTCACCTCCAGCCCTCTCGCTCTGCTCTCCCACACACTCCCTCTCTTTACTCTGAGGCTGTGTGGACCACTTCAGCTGTCTGTATATGTTCCTGCCGCCACAGTTTCTCGGAGTAAAGCAGAAACCAGACCAAACATCCAGACAGCAATAAGCTCAACATGTACACTTTTCATGTCTTACTGGTGCTAGTGTGTCTACAGTTTTGTGCTCACACTGCTTTTGCAGCTCCAACTCAGTGCCCAAGCCAGTGCCACTGCCATGGGGACCTGCAGCATGTTATTTGTGACAATGTTGGGCTAAAGAAGATCCCTCGCATATCTGAAGCCACGCGTCTCCTCAACCTGCAACGCAACAACTTGGGGAATCTACCAACTGGGGGCTTCAGTGAGATGAAAGGGCTCATTTCTCTGCACCTGCAGCATTGCCAGATCCGAGAGCTCTCCGGCCAGGCTTTC[A/T]AAGGGCTCAACAAGCTCATCTACCTCTACCTGTCTGATAATGAGATCAGCACCATTAAACCCGGTGCTTTTGAGGATCTAACAGAACTCACCTATCTCTACTTGGACGGCAACCAAATCACAAGCCTTCCGAAGGGCATCTTTTCCCCCATGATCAACCTGTTCATCCTGCAGCTCAACAACAACAAGCTTCGAGAGCTGCAGCCTGGTACTTTCAAAGGTGCTAAGGATCTCCGCTGGCTTTATATGAGCGGCAACGAGCTGAGCTCCATACAGCCTGGTTCTCTTGATGAAGTGGAGAACTTGGCCATTCTAACCCTGGACCAGAACAACCTGTCCACATACCCTCTCCCGGCTATGAGCAAGCTGCGTGTTGTGGAGGAACTCAACCTCTCCAAAAACCCTCTCAGCCTCATCCCTGACCATGCATTCCGAAGCTTCGGACGCTACATGGAGAAGCTCCATCTAAATGACATGAGCCTGGAGAAGGTAAGTCAGTCA
Associated Phenotype:
Not determined