ZMP
ENSDARG00000079765
Ensembl ID:
Mouse Orthologue:
Ccdc48
Mouse Description:
coiled-coil domain containing 48 Gene [Source:MGI Symbol;Acc:MGI:3611451]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41900 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41901 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41900
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111157 | Nonsense | 166 | 583 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 39072787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37639806 |
GRCz11 | 11 | 37907011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGGAGGAGGACAGCGAGAAGATCCGGACCCGCACAGAGCCTGGATCAT[C/T]AGCAGATCAACACTACTGTGGAGAACAAGAGAAGCGTAGGTAAGAAAGAG
Long Flanking Sequence:
CAGTCATGCAGGTTTCGCGGATTCGCGCGGCGCGTAAAAGCGAGTGGCTGAAAAGCGCGCTTTCGCACCACTTCAGCCCGGACCCCTGCGCGGAAAACGAGATCGTGGTTTTGGCTACCGGTGTGGACCAGTATCTCCAGGAGGTGTTTCATCACTTGGCCTTTAACAACGGAGAAGATCTCGTCTCGGATGAGGACTTTAGGAGTCTGTGTTTAGTTTTGGGCATCACCGGGAGCGCGGAGACTGATGGACTTCCTCGCGTGCTCAACTTTAAAGACTTCCACGCGCGACTTTGCGGGTTTTTCTCTTTAAAAGCCCCGGAGGGTGAGAAAGGAGCTCGACTGCTGGTCAGCGAGGAGACCGAACACATCGAGAGGGAGATCAGACTCCGCTGTCCGCGCGTCCGGAGGAGAAAGTGTGTCAGTTTCGATCTGTCCGCCGAGCAGCAGAACCGGAGGAGGACAGCGAGAAGATCCGGACCCGCACAGAGCCTGGATCAT[C/T]AGCAGATCAACACTACTGTGGAGAACAAGAGAAGCGTAGGTAAGAAAGAGCTTATCATATATACACACACTTGTTCTTATTCCATAGACAACTGAGGTAAAGTAGGTTTTATTCGCACATTTATTCAGTGAAAACCTATGACACGGTCCCAGTATTTTTTAACCATGCTACTTTGAATATTGGGTCAGATATTGCATGTAAATATGACTTCAAAACAGCACTATTTAACTGACTGTGAACAATGTTGTGCTTTGATAGTAATTCATTGGCTATTATGATTTCACACTTGTTCTTACTGTGTATCTTGATTGGGACTCCCCAAGACGTAATTGTGTTCCTGGTGTACAAACTCTACATTCAATCCTCCTACCTCAACCCTACCCTGAACCCAACCCTCACAGGAAACAATTTCCATTTTACACTTTTAAAAAATCTTTTTTATGCTGTATGATTTATTCAATTCAGTTCAGTTCAATTAATATTTATTTGTATAGCCCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41901
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111157 | Nonsense | 186 | 583 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 39074938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 37641957 |
GRCz11 | 11 | 37909162 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGATCTAATTTGGCTTCATTTACTGCAGTAGATATAAGCCCGCAGAGA[C/T]GACTGCAGGAGCAGCTGGAGCTGGAGAACGCCAGTCTGAGGGAGCTGGTG
Long Flanking Sequence:
AGAAAATCAAGCTGTAGAATGGCCCAGCCAATCACCTGATCTGAATCCAATAGAGTAAAAACAATAAAGATCAGATTTAAGACACACAGAGCCAACAAGATTTTTACAGTCTGTTGAAGTCTGTGAAAAACTCACACCCAAGCAATGCATGTGACTTCATCATCCATATGAGAGACGTCTTTAAGCTGCCATCACTTAAAAAGCCTTTTATATAAAGTGTTAAGTATGTTTTAGTAGTTCAGTACTTTCTCCTCGTGTCATTTCATTGTTATTACACAGAACTCATTTTTCAGATTAGTTTTTTTTGTGTGCATTGTTTGGGTTTTTACCAAAATCGTGTCCAATCCCATGTCAAAAGCTCCTTTAGATGTATTATTCCTAGAAAAAATCATTGAAAATAATTCAATAATTACCCCCCCCCCCCTGTAAATGATAAATGTCTTTGCTACTGGAGATCTAATTTGGCTTCATTTACTGCAGTAGATATAAGCCCGCAGAGA[C/T]GACTGCAGGAGCAGCTGGAGCTGGAGAACGCCAGTCTGAGGGAGCTGGTGGAGGACCTGCGTTCAGCCCTCCAGAGCAGCGACGCACGCTGTATATCACTAGAGGTGGCATTACGCCGAAAACACACTCTTGGCACAACCCTAGAGAAACAAGACTGCAAAACCAAAACCCAACACCCCAAACACATGGACTGGGACTCCAGAAGAGGCACTAAAGACCTGCTGCGAGAGCTGGAACTGATCCGTGCGTCCAGAGACGGGCAGCTGGAGGAGGCCATGCGCTTTAACCAGAGGCTGGAGGAAGAGCTGATGGCGGCTTACGGAGAGCTGACCCGCATGCAGGAGACGCTGGAAAACGTCAGGACGGAAAACAAACGGATTAAGAAGAGGACGGAGGAGGTCAGGGGAGCACTGGCTGCAGGACTGGAGCACGTTAAGACCTTACAAGACCAGGCCAAACAAGCGGATCTGCTCCGAGAGCGCGTCCAGAGTCTGGAGAAG
Associated Phenotype:
Not determined