Busch Lab

ZMP

CDR2 (2 of 2)

Ensembl ID:
ENSDARG00000037359
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.
Availability:
Order Allele From ZIRC
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.
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