ZMP
CRISPLD2
Ensembl ID:
Description:
cysteine-rich secretory protein LCCL domain containing 2 [Source:HGNC Symbol;Acc:25248]
Human Orthologue:
CRISPLD2
Human Description:
cysteine-rich secretory protein LCCL domain containing 2 [Source:HGNC Symbol;Acc:25248]
Mouse Orthologue:
Crispld2
Mouse Description:
cysteine-rich secretory protein LCCL domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1926142]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27098 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21136 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27098
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130227 | Splice Site, Nonsense | 345 | 512 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 70247863)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 68852506 |
GRCz11 | 7 | 69102022 |
KASP Assay ID:
2259-9789.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTTTTATTCGTTAATCAATAAATTTTCTTTCTCCTTTTGTGTTTGCAG[C/T]AATCGAGTATTTGCCGTGCTGCTATTCACTATGGAGTAATTGATAACAAT
Long Flanking Sequence:
AAATATAATTTAATATACCAGGATTAATATAATTTAATAAAACTATATGAATATGTGAAACTATACTAATAGTTTAGGCGCTTCATTCCGCTGTGGTAAGCCGAAGGAAAATGAATAAATAAATAATAATTTAATCTTTTTTTTTCCCTTTTGCTTGTCAGCCCAAAATATCAAGTGTGAGACAAAAATGAGGGACAAATGTAAAGGAGCAACCTGCAATAGGTCAGTCGAACACTATTCATCATTCATTTTAGGATATTAATACATTTCAAACGTTCAGAAATTAACTGGTAATTTTTTTCTTCTATAACAGGTACAACTGCCCAGCAAACTGCTTAAATAAGCAGGGGAAAGTATGGGGAACGCTGTACTATGATGTTGTAAGTCATACTCTCTACTCTTTTTTATGATGATGATGATGATGGTAGTTTTATTCATTAATTTTCATTTAATTTTTATTCGTTAATCAATAAATTTTCTTTCTCCTTTTGTGTTTGCAG[C/T]AATCGAGTATTTGCCGTGCTGCTATTCACTATGGAGTAATTGATAACAATGGAGGACTTGTGGACGTCACGAGAAAAGACAGCTTCCCGTTCTTCGTAAAGGCAACCAAAAACGGCGTAGAGTCTTTCAGGTAATCAGAAAATAACCGTAAATTAGCAGTTATCTGTATTTTGTGATTCATGTTTTTATTTATTTATGCTTATGAATTTTATAAGGGGATCTTGATCTTTCTTCCAACAACTTTTAACCTTGAAAAGTTGGAAAAAAAAAAAGTTTTTATTGTAATTATGTCACGTTCGGTGATGGGAAAAAGGAGCGAGGACCCAAGCGCGGAGTAAATTGGATTTTATTAAATAATAAAAATAAAATAAAATGCAAAATAAACTACCCCGAGGGGGAAAACACTAATAAAACAAATAAACAAACAAACAAACAAACTTGACTGGGCAGGCAAGACAAGGCAAGGCTGGACACAGCAGGACAGGTAAAGATTTACAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21136
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130227 | Essential Splice Site | 388 | 512 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 70247995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 68852638 |
GRCz11 | 7 | 69101890 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCCCGTTCTTCGTAAAGGCAACCAAAAACGGCGTAGAGTCTTTCAGG[T/G]AATCAGAAAATAACCGTAAATTAGCAGTTATCTGTATTTTGTGATTCATG
Long Flanking Sequence:
AATCTTTTTTTTTCCCTTTTGCTTGTCAGCCCAAAATATCAAGTGTGAGACAAAAATGAGGGACAAATGTAAAGGAGCAACCTGCAATAGGTCAGTCGAACACTATTCATCATTCATTTTAGGATATTAATACATTTCAAACGTTCAGAAATTAACTGGTAATTTTTTTCTTCTATAACAGGTACAACTGCCCAGCAAACTGCTTAAATAAGCAGGGGAAAGTATGGGGAACGCTGTACTATGATGTTGTAAGTCATACTCTCTACTCTTTTTTATGATGATGATGATGATGGTAGTTTTATTCATTAATTTTCATTTAATTTTTATTCGTTAATCAATAAATTTTCTTTCTCCTTTTGTGTTTGCAGCAATCGAGTATTTGCCGTGCTGCTATTCACTATGGAGTAATTGATAACAATGGAGGACTTGTGGACGTCACGAGAAAAGACAGCTTCCCGTTCTTCGTAAAGGCAACCAAAAACGGCGTAGAGTCTTTCAGG[T/G]AATCAGAAAATAACCGTAAATTAGCAGTTATCTGTATTTTGTGATTCATGTTTTTATTTATTTATGCTTATGAATTTTATAAGGGGATCTTGATCTTTCTTCCAACAACTTTTAACCTTGAAAAGTTGGAAAAAAAAAAAGTTTTTATTGTAATTATGTCACGTTCGGTGATGGGAAAAAGGAGCGAGGACCCAAGCGCGGAGTAAATTGGATTTTATTAAATAATAAAAATAAAATAAAATGCAAAATAAACTACCCCGAGGGGGAAAACACTAATAAAACAAATAAACAAACAAACAAACAAACTTGACTGGGCAGGCAAGACAAGGCAAGGCTGGACACAGCAGGACAGGTAAAGATTTACAACATGTGATGACGAACTCGCACAGGACAGCAGACATGAGGGGTTTATAAACTGTAGGAAATTAACACACAAACAGATGAACATAATTAACTAATAATGGGTTAACAAGGAGGGTGGGACTAGACAATAGACGGAA
Associated Phenotype:
Not determined