ZMP
LOC555913
Ensembl ID:
Mouse Orthologue:
Dmbt1
Mouse Description:
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 |
---|---|---|---|
sa23057 | Essential Splice Site | Available for shipment | Available now |
sa23056 | Essential Splice Site | Available for shipment | Available now |
sa8765 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23057
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 |
---|---|---|---|---|---|
ENSDART00000028591 | Essential Splice Site | 28 | 487 | 1 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 21692214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21842363 |
GRCz11 | 17 | 21862199 |
KASP Assay ID:
2261-0941.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAACACAACCGTTTCACTGACCTTCAACGATGTTGAGTACGACACTAT[T/G]TGAACAATTTTAGAACTGAGGCTCTATAGTAAAAAATGTGTTGAATGTCC
Long Flanking Sequence:
TTTTCTCTCTCCTTCTGCTTGCTAGCTTGGAAAAATGCTGTGATTACATCAAAGTATATAATGGTCCTTCAATCTTCCACCCATTTCTGGGAGAAATAAAGGAGTTCAGAAACCAGTCTTTCAAATCCAGCAGCAATGATCTGACTGTGGTTTTCTTCAGTGATCACAGTGTATCAGGAAAAGGATTCCATGCAAACTGGCTCTTTGTTGGTATGTGATTAAAAGAGATTAATATAACATTTATGATATTACACATTTTAACTATTTATTCTGCTAAGCCAAACATTCTCTCAGAATTGAATTTGTGACTCACGTTTTGTTCTTTATCATTCTCTATTAGAAGAATCATGTGGTGGCAATATGACAGACTGGACGGGTGAATTGTTCAGCCCCCGATACCCTAATAACTACCTTGATAACTCATATTGCACATGGACCATTCACAGCACAGAAAACACAACCGTTTCACTGACCTTCAACGATGTTGAGTACGACACTAT[T/G]TGAACAATTTTAGAACTGAGGCTCTATAGTAAAAAATGTGTTGAATGTCCTCCTTTCAAAAAAAAAAAAAAAAAACAACAATATGGTTTGTCTCTCCTTTCCGTTTGCTAGTTTGGAAACATGCTGCGATTACATCAGAGTGTATGATGGTCCTTCTACTCTCCACCCTTTACTGGAGGAAATACGGGACTACAGGAATCAGTCCTTTAAATCCACAGGCAACACTCTGACCGTGCTTTTCTACAGTGACAGCAGTGTAACAAGAAGAGGATTTCATGCAAACTGGATATTTGTAGGTATGTGATTAAGATGAATATGACTTGATTTATGCTATTACACAGCAATTCTCTAATTGACTTTGGAAAACACTTTAGTGAAAGACATCCTCCACTTTCATAAAATAAAATATATGATGTCAAAACAAAGTCGTATACAATATTTACATAGATGGTCCATCAAAAAGAGCAAAACATGCAAACTGCAAATATTGCACCTGATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23056
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028591 | Essential Splice Site | 28 | 487 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 21692104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21842253 |
GRCz11 | 17 | 21862089 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAAAAAAAAAAACAACAATATGGTTTGTCTCTCCTTTCCGTTTGCT[A/G]GTTTGGAAACATGCTGCGATTACATCAGAGTGTATGATGGTCCTTCTACT
Long Flanking Sequence:
AACCAGTCTTTCAAATCCAGCAGCAATGATCTGACTGTGGTTTTCTTCAGTGATCACAGTGTATCAGGAAAAGGATTCCATGCAAACTGGCTCTTTGTTGGTATGTGATTAAAAGAGATTAATATAACATTTATGATATTACACATTTTAACTATTTATTCTGCTAAGCCAAACATTCTCTCAGAATTGAATTTGTGACTCACGTTTTGTTCTTTATCATTCTCTATTAGAAGAATCATGTGGTGGCAATATGACAGACTGGACGGGTGAATTGTTCAGCCCCCGATACCCTAATAACTACCTTGATAACTCATATTGCACATGGACCATTCACAGCACAGAAAACACAACCGTTTCACTGACCTTCAACGATGTTGAGTACGACACTATTTGAACAATTTTAGAACTGAGGCTCTATAGTAAAAAATGTGTTGAATGTCCTCCTTTCAAAAAAAAAAAAAAAAAACAACAATATGGTTTGTCTCTCCTTTCCGTTTGCT[A/G]GTTTGGAAACATGCTGCGATTACATCAGAGTGTATGATGGTCCTTCTACTCTCCACCCTTTACTGGAGGAAATACGGGACTACAGGAATCAGTCCTTTAAATCCACAGGCAACACTCTGACCGTGCTTTTCTACAGTGACAGCAGTGTAACAAGAAGAGGATTTCATGCAAACTGGATATTTGTAGGTATGTGATTAAGATGAATATGACTTGATTTATGCTATTACACAGCAATTCTCTAATTGACTTTGGAAAACACTTTAGTGAAAGACATCCTCCACTTTCATAAAATAAAATATATGATGTCAAAACAAAGTCGTATACAATATTTACATAGATGGTCCATCAAAAAGAGCAAAACATGCAAACTGCAAATATTGCACCTGATTGTGAAAATAAAGTACTTCCAATCCTATTTTTTTCCTTTTCAATACATATAGTAGTGATTGAACAGATCCTCCCTCAGACGACCCCTGCCACCACTATACAGTACTAGATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8765
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 |
---|---|---|---|---|---|
ENSDART00000028591 | Nonsense | 187 | 487 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 21690445)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 21840594 |
GRCz11 | 17 | 21860430 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GRAAKGTCTGCTTCAAYGACACCACACATCAGGCATTTCACTCTWCTTCA[C/T]GWTACTTGACTGTTGTCTTCASGAGTGACTTTTCTGGTGTTRGCCATGGG
Long Flanking Sequence:
AAACATATGTGCAGAGTATCTTTTATGGTCCTTTTACTCTCTTTTTCATTATGCTTGGACACTAACTAATTCCTGCATTTATTTTGGGGCATCGGGATATCCAGCTACTCACCCTCAGTGTGGAGGACAACTGTATGACTCCGGGATGTTTTACAGTCCAAACTACCCAAACTATTATCCTGACAATGCCTACTGTGTGTGGTATCTTTCTGCTCAGCAAGGACAGAGGATCTTCTTGACATTTGCTGATGTGCAGTAAGTGTGATTAATACAAAAAAAAAATCATCATCATTATTAACTTATACTACTTGAGAGTATTACTGTATGTGTAGTATCATGAAATTCCTCCATGTGGAACAAAAATTTCTGTTTCTTTCAGACTGGAGCGCTGCTGTGACTGTGACTACATTACCATTCACGACGGCTCTTCCACTGGTTATCCACAGCTGGGAAAGGTCTGCTTCAACGACACCACACATCAGGCATTTCACTCTTCTTCA[C/T]GATACTTGACTGTTGTCTTCAGGAGTGACTTTTCTGGTGTTAGCCATGGGTTCAAGGCTCTTTTCACCAGCTCTCTCACTGCAAATGAAGGTAAAAATCTAACATATATAACTTTAATGCTAAACAATTGTAATTGTTATGAGACAAACACTTTGTCTCTCTAATGCCTTAAATGTTGTAAATAAGGGCATAAAATTATTGGTATTGCAGGCAGTGTGGATTGTACCTCAGACAACATGGTGATTGTACTACAGAGTTCTTACCTGAACTCACTAGGGCTGAGTGGAAATGACCTTTATGTTGATGACCATCTCTGCAGACCTAATATTAGCAGAACTGAAGTTGTGTTCAGATTCCCCCTCGACACATGTGGAACTGCCAAAGAGGTTTGATGTTGACATCCAACATGGCTCCAATGCCAAATCTGAAATCAGTAGCTTTCTGTCAAATATTTTACATATGGATTTGCTTAATCAGATTAGTTAAAGATGAATCACCCA
Associated Phenotype:
Not determined