ZMP
CDR2 (2 of 2)
Ensembl ID:
Description:
cerebellar degeneration-related protein 2, 62kDa [Source:HGNC Symbol;Acc:1799]
Human Orthologue:
CDR2
Human Description:
cerebellar degeneration-related protein 2, 62kDa [Source:HGNC Symbol;Acc:1799]
Mouse Orthologue:
Cdr2
Mouse Description:
cerebellar degeneration-related 2 Gene [Source:MGI Symbol;Acc:MGI:1100885]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21992 | Essential Splice Site | Available for shipment | Available now |
sa35175 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21992
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054363 | Essential Splice Site | 114 | 563 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 1201018)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 968376 |
GRCz11 | 12 | 1003963 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGAAGCTGACGCAGGAGAACCGAGCAGCGCAGATAAAGATCCAAGGG[T/A]GAGGCTCCAGACAGCAGCTGCTCACGGTGTCCTAAAAGTAGGAAGATGTA
Long Flanking Sequence:
ATGGATGATAGATAGATAGATAGATAGATGGATAGATGGATGGATGGATGGATGGATGGATGGATGATAGATGGATGGATGGATGGATGGATGGATGGATGGATGGATGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATGGATAGATGGATGGATGGATGGATGGATGGATGATAGATAGATAGATAGATAGATAGACAGACGGACGGACGGACGGACAGACAGATAGATAGATAGATAGATACATAGATACTGTTGTCTTCAGCTGTGTGTGTCATGGTCTGATGTTGATCTGTTGGTGTTCCAGTATCTGTCCAAGCAGGTGGATCTGCTGCGGTCGGTCAGTGATCAACATGCTAAACTCTACGAGCAGCTGGACGCCAGTTCACAAGAGCTGGAGCTGAAAAACCAGAAGCTGACGCAGGAGAACCGAGCAGCGCAGATAAAGATCCAAGGG[T/A]GAGGCTCCAGACAGCAGCTGCTCACGGTGTCCTAAAAGTAGGAAGATGTAGAAACTTTTGCGTGCGCAAGAGTGTTCAAGCTTCGCTACGAACCACTTCCTCATTAATGAACCGCTCTGTTGCTTAATGACGTGCCCTGTCAGTCATCCTTCACATCATCCACATTCTATCATATTTAACGTCCGCTTGAAATCAAAATGTACAATTTTGCCAGCTCATCGTTATTATAAAGGTGAAAAAATATCCAGGAAAAATGTGTTTGTTTTAGTAGCTTTCAATTAAAACTTGAGCATTTGATTCTGCATCCTTCTGCTGACGTCAGCCTGAGGGTTTTCATAGCACTTGCATATTAATATCCTCAAACACGCCCCTCTTACTGTTAAGCTGCGCTCACGCTGGACTTTTCCAAGTAGGTATCGCTGCAGCCCGGAGACCTGCAAGTGGGAGGGATTACACCGCAAGTAGGTTGGGTGACCTCCAAGTGGGAGGGACTTAAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35175
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000054363 | Nonsense | 456 | 563 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 1206894)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 974252 |
GRCz11 | 12 | 1009839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCTATTCAAGATGATGAAGTGCGTGTAGTCAGCCCGAGTGGGCGGGGCT[T/A]GCATAATGGAATGCCTCTGCTGGATGATGGAGTGGGTGTGGTCAAACACA
Long Flanking Sequence:
AATACTAGATGATGAAGTGGGTGTGCTTGCGCAGATTGATGATGAAGTGGGTGTGGTCGGACAGAGGGGGTGGAGCCTGCCAATGCCGGATGATGAAGTGGGTGTGGTTAAGCAGAAGGGGCGGAGACTGCACAAAGACATGTCTATGTTGGATTATGAAGTGGGTGTGGTCCAACAGAAGGGGCGGAGTCTAAAGCATCAGGCCTTGTCTCTATTGGCTGATGAAGTAGGCGTGATGGGTCAGAACCTGCAACAGAGTTGGTGTTTATTGGATGAAGAAGTGGATGTGGTGGGTCAGAGTGGGCGGAACCTGCAGCATCAAGGCGGATCTCTGTTGAATGATGGAGTGGGCGTGGTCACCCAGAGTGGAGGTGGTCTTTATCAGGGTGTGTATCTGGATGAATGGGATGTGGTAGGCCATAGTGGGCGGAGCCTGCAGCATCAGGCAGCATCTATTCAAGATGATGAAGTGCGTGTAGTCAGCCCGAGTGGGCGGGGCT[T/A]GCATAATGGAATGCCTCTGCTGGATGATGGAGTGGGTGTGGTCAAACACAGGGGGCGTGGCCTGCAGCATCAGGGCGCGTCTCTGCTGAGTGAGGTGGATGCGCAGTACGTCGCCCTGCAGGAGAAGTACGATGCGCTGCTGCGCCGCTGCCAGAGCGACACGCCGACACACAACCAGAACACTGTTCCAACACACACACACTCCACACACAACCAGCAGCCCGAGTACAAAGCCCTGTTTCAGGAGATTTTCACCTTCATTCAGAAGAGCAAGGAGGACCTGAAGGAGAACAGGACCAAGCCCGATCAGGCTGACTGTAAATAAGCACAAAAAAAAGTGGGGCAGAAGATTTTCCACTCAGGTATTACTGGTATTGGCAGTAAATGTTAGTTTCATAGAAACAGCAGGCAAAGCACACAATGGAAAACACAATTTTAAAGGAAACAGACATGCTTTTTATTATTTATTTTAATTTTATTTAATAATTTGAGACTTTATT
Associated Phenotype:
Not determined