ZMP
ENSDARG00000089599
Ensembl ID:
Human Orthologue:
CUZD1
Human Description:
CUB and zona pellucida-like domains 1 [Source:HGNC Symbol;Acc:17937]
Mouse Orthologues:
Cuzd1, Dmbt1
Mouse Descriptions:
CUB and zona pellucida-like domains 1 Gene [Source:MGI Symbol;Acc:MGI:1202881]
deleted in malignant brain tumors 1 Gene [Source:MGI Symbol;Acc:MGI:106210]
deleted in malignant brain tumors 1 Gene [Source:MGI Symbol;Acc:MGI:106210]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43026 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23207 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43026
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 |
---|---|---|---|---|---|
ENSDART00000128412 | Nonsense | 116 | 586 | 2 | 10 |
Genomic Location (Zv9):
Chromosome 18 (position 4356868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 5106640 |
GRCz11 | 18 | 5721393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACACAAACAACCCCTACAGCAGCACCTATAATGACTACAACTACCT[T/A]GGCAACATCCAAAGCATCAACTACTTTACCACTGAGCAAAATTCCTCTTC
Long Flanking Sequence:
GATTCCTACAACACCCGAACCCACAACAACCACCACAATAATTCCTACAGCAACCCCCACAACAACATCCGAACCCACAACAACCACAATACCCGAACCCACAACAATGACCAAAATAATTCCTACAACAACACCCGAACCCACAACAACAACAACAGTACCCGAACCCACAACAACGACCACAATAATTCCTACAACAACCCCCACAACAACACCCGAACCCACAACAACGACCACAATAATTCCTACAACAACATCCACAACAACACCCGAACCCACAACAACAACCACAATAATTCCTACAACAACCCCCACAACAACACCCGAGCCCACAACAACAACCACAACAACACCCAAACCCACAACAACAACTACAATAATTCCTACAACAACACCCACAACAACACCTGAACCCACACCAACCCCTACAATAACTCAAACAACTCTTACAACAACACAAACAACCCCTACAGCAGCACCTATAATGACTACAACTACCT[T/A]GGCAACATCCAAAGCATCAACTACTTTACCACTGAGCAAAATTCCTCTTCAGTTTTCTCTGCAAGGTATGTTTGGAAGGTTTGTACACTAAGCTTCAAAATTATATTGATATGTGTATTTAATCTAACACTATTCATACATTTCAGTTGACAATCCAGCACCATCTTGTGTTGAGGGTGAATATCTGCCACAGTTACTCTATCCAACACCTTCGGATGGAGAACTCTTGCAGGCTCGTGTAAATCATCAGTTTGAGTTCAGAGTGAAGGCTGTTGCATTATTTTCAAGGTATTTTGGGAAAAGGCGTACTTGGGCTTGTTTAAAATGAAACTGAAATAAACTGCAACTTAATTTGCAATTGCATGTTAGTACACTACCCTTGCCTGGTTCCTCTATGCATACTACAGTAACCATGTCTTCCAGAATGAAAATAGGGAAAAAGAAGTCTAATGTTATTTGTCTCTCGGTTTTATATCTTGTTGTTGCTTTCGTCATCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23207
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 |
---|---|---|---|---|---|
ENSDART00000128412 | Nonsense | 579 | 586 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 18 (position 4360999)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 5110771 |
GRCz11 | 18 | 5725524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTGCGGTGTGATCTTCTACACATCCAGGACACCCGGGATCAGAAAA[C/T]AACCCTTGTCATCACACGACTTTTAAACGTGTCAGCGTTTTTTTTCCAAA
Long Flanking Sequence:
TTATTTACAAGCACAAATGTATAACTGAAATGAAACAATTTTTCTGTTGAACTCTCATTGTCTCTTGGCTTTTTGTCTTCTTCCTCTCCCCCTGCTCATCTGTAGGTGTTCATCAGCTGCTCCATCATCGTATGCCAGGCTGGCGATCCCAACACTCGCTGCTCTCAGGGCTGCATCAACAGCACCGCCGCCCCACCTTCACACAACATTAACAAAAGAGACGCCCCTATTGAGACCAGCAGTTACTTCATCTCCCAGGGACCCATACGGCTGAGGAGGAGCCCATCACGTAAGACAGCATAACTTCATTCATATTTACTAACATGATTGTATCCTAAACTAGTTTGTTTACAACTGCAACCTTTACTCACATTTCAGAGGTGACTGTGAACTTGGGATTTAATGTAAACCTTGCTGTCGTCGCTGGGTGTCTGGTGGCCATTGCTGCTATGATTTGCGGTGTGATCTTCTACACATCCAGGACACCCGGGATCAGAAAA[C/T]AACCCTTGTCATCACACGACTTTTAAACGTGTCAGCGTTTTTTTTCCAAAGCATAATGCAATGATTATACTGCGAAAACACTGTTTCTAAGCTTGTTGGTGGAAAGAAATATTTGGTGATGTTTTCTTGCTTTTGCAATCATTGTTGTAATAATTGGAAGTTTTTAAACTAATTTCGAGAGGAGCACATGATATAATTGACTGCAGCTGGCCACCTATCTACACTCATTTGTTAGCCAATCAGATCTATCCTAACTCACTATAAGTAGCCTAGCTAGATATTACTCCCTTATCTTCGTTTTCCGAAGAAACCCCCCCATCCACCCCCTTTCTCCTCCTTTCCTCCTTTAAAAAGGGGAGCTCTCGAGAACCACCTGATCTCGGACTCCCCTCACATGCTCTATGGACCTGGCGGGAGCCCTGGGCTCAACTATCTCCGAGCTCAGGGTTCTCTCCCGGGACAGCATGCCAAACCTGCTAACAGTTGTCAAGCAATATCTA
Associated Phenotype:
Not determined