Busch Lab

ZMP

chad

Ensembl ID:
ENSDARG00000045071
ZFIN ID:
ZDB-GENE-040426-1130
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
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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:
sa11952
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
Order Allele From EZRC
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