ZMP
NP_001007396.1
Ensembl ID:
Description:
differentially expressed in FDCP 8 homolog [Source:RefSeq peptide;Acc:NP_001007396]
Human Orthologue:
DEF8
Human Description:
differentially expressed in FDCP 8 homolog (mouse) [Source:HGNC Symbol;Acc:25969]
Mouse Orthologue:
Def8
Mouse Description:
differentially expressed in FDCP 8 Gene [Source:MGI Symbol;Acc:MGI:1346331]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36678 | Nonsense | Available for shipment | Available now |
sa10611 | Essential Splice Site | Available for shipment | Available now |
sa43130 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36678
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098504 | Nonsense | 47 | 218 | 1 | 6 |
ENSDART00000139665 | Nonsense | 47 | 193 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 31274007)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31424138 |
GRCz11 | 18 | 31402470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACAAAAAGATGCAGTGGTCAAGCTTATCCACCTTCGACTTAAACTA[C/T]AAGAACTACAGGTTTGTATGATCAGTCAAAATTGCAGAACATAATTTTTC
Long Flanking Sequence:
TGTTAGCTACCTGAAATTCTTAAGGGTGCATGTCCATCGAATAATACTGAATGCCTAGCACCGCATTGATGCTGTCATTCTAAAAAATGTTGTAGTGTCATTGAAAACAACTGAAAAGCTTTTTTAGGTGTTTTTCTTGTGGATTTTTAAATTAAAATCTAGAATTATGACATGTATGTATATCAAAAATAATAAACTAATAACTTAAGACAACAAGAAAATAAGTCACACTAGTTCTGAAATGTATGAGGTCAATCAAGTTAATGGTTGTGAATTAAACATTTTGGATGATCACTGTAACCAATGTAAGTTTTTTAATCATTTAGACTTAAGCACTGAATTGTGTGTGGATGTATGCACAGGGTTTGTTTGTGGCGTCTGATGTAGAGCAGCTGAAACTTGCCATAGAGGAGTGCAAGAGACTGATCCTGGAACTACCAGAGCATTCAGAGAAACAAAAAGATGCAGTGGTCAAGCTTATCCACCTTCGACTTAAACTA[C/T]AAGAACTACAGGTTTGTATGATCAGTCAAAATTGCAGAACATAATTTTTCATAAAAGTTCATTGTTCATAAAAGCCATAAATGAACATGCTGAATTTAAATTAAACTGCAAAATCTATTTGACTTAAGTCAAAATTTGTTTTTCAATAGGTACAGTTTTGAAAAAATGTGTAAGTTAAAAAACGTGTGTATATAATTTGAATGTGTATGGGTTTTATAAGCATTAAAGCCCACCTATTTTACCCCTTTTACAAGATGCAAAATAAGCCTTTGGTGTCTCTAGAATGTGTCTCTAAAGTTTTAGTTCAAAATACAAATCAGATAATTTATTATAGCCTGCAACGTATGCCTATTTTGGGGTCTAAGTACAGTGTAGCTATTATGTAGTCTGTGGCTTTAAATACAAATGAGCTGCTTCGCCCCGCTTAGCGCTCCCAAGTGCATGTTTGCTTCACCTGTGTTACATCAGGTATACAGCAGTCAGTGATGGGAACAGACATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10611
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098504 | Essential Splice Site | 153 | 218 | 3 | 6 |
ENSDART00000139665 | Essential Splice Site | 153 | 193 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 31265659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31432486 |
GRCz11 | 18 | 31410818 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACAAACAAGACTACAGATGTTCTGAATGCCGGACACCCATTTCATTGCG[T/A]GAGTCTTTTTGTATATGTAYAAAAGGTTCTTTTGCTTGGTTAATGAGTCA
Long Flanking Sequence:
AATTTTGACTTCAACTGTATATCGTTTTGAATAATCGTGATTACAATTATGACCAAAATAATCGTGATTATGATTTTCCCCATAATCGAGCAGCCCTACCATTTAGCTTTTTATACTGAACCTGGGCTTAAATTACTTAATAATTTAATTGCTTAAGCATATTCAGATCTTACAGTGATGGTTTGACCATCCATCTAGTATGGGTTTTTTGTCTTTGTTACAAGATGCTTAGTAGTATACATGGTATATTAAATGTTTTACTAAATTCATTCAGATCTTAGTTGTGTAATTTATGAGCTGTATTTTGTTTTAAATGGTCATATTTCATTTCCAGGTTGCTATTACCGCTGCCATAGCAAGTGCATGAGTCTTATCAACAAACCATGTGTGAGATCAAAGGTCAGCCATCAGTCTGAGTATGAACTCAACATCTGTCCTGAGATTGGTCTGGACAAACAAGACTACAGATGTTCTGAATGCCGGACACCCATTTCATTGCG[T/A]GAGTCTTTTTGTATATGTATAAAAGGTTCTTTTGCTTGGTTAATGAGTCAGCATGGATATTTAGAATTTTCATTTTGCATAGAAGGTTGTTTGATATTGTGTTGTGTTGTGTAGGTGGTATTCCTAATGAGGCACGTCAGTGTGATTATACCGGTCAGTATTACTGCAGCAGTTGCCACTGGAATGACACTGCCATCGTTCCAGCAAGAGTCATACACAACTGGGAGTTTGAACCCCGTAAGGTACAAAAAAAAAACTCTGAGAAAAATGGATAATCTTGCTATATATTTGGCTAAGTTAGGTTTATAAAAGCAGAAAAAGCAGTTTAATCCATTAAAGCACCATTTTCTGCTTCTCCAAGATTTGTTCAAAACCAACTTTTGCAAACTAGTCCTACGTTTTTTTGCCTGATCGGAACCAAACAAATTCAGAAATATACTCTGGGCACTACATATCAATAAATATTGAAAAAAAGTTTAAATTTTGAAAGATTTTTGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43130
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 |
---|---|---|---|---|---|
ENSDART00000098504 | Nonsense | 210 | 218 | 6 | 6 |
ENSDART00000139665 | None | None | 193 | None | 4 |
Genomic Location (Zv9):
Chromosome 18 (position 31265294)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 31432851 |
GRCz11 | 18 | 31411183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAAAGCAGTTTAATCCATTAAAGCACCATTTTCTGCTTCTCCAAGATT[T/A]GTTCAAAACCAACTTTTGCAAACTAGTCCTACGTTTTTTTGCCTGATCGG
Long Flanking Sequence:
GAGTCTTATCAACAAACCATGTGTGAGATCAAAGGTCAGCCATCAGTCTGAGTATGAACTCAACATCTGTCCTGAGATTGGTCTGGACAAACAAGACTACAGATGTTCTGAATGCCGGACACCCATTTCATTGCGTGAGTCTTTTTGTATATGTATAAAAGGTTCTTTTGCTTGGTTAATGAGTCAGCATGGATATTTAGAATTTTCATTTTGCATAGAAGGTTGTTTGATATTGTGTTGTGTTGTGTAGGTGGTATTCCTAATGAGGCACGTCAGTGTGATTATACCGGTCAGTATTACTGCAGCAGTTGCCACTGGAATGACACTGCCATCGTTCCAGCAAGAGTCATACACAACTGGGAGTTTGAACCCCGTAAGGTACAAAAAAAAAACTCTGAGAAAAATGGATAATCTTGCTATATATTTGGCTAAGTTAGGTTTATAAAAGCAGAAAAAGCAGTTTAATCCATTAAAGCACCATTTTCTGCTTCTCCAAGATT[T/A]GTTCAAAACCAACTTTTGCAAACTAGTCCTACGTTTTTTTGCCTGATCGGAACCAAACAAATTCAGAAATATACTCTGGGCACTACATATCAATAAATATTGAAAAAAAGTTTAAATTTTGAAAGATTTTTGAAAAGTTGATTTTTTTTACAGAACAGTACACAAAAAAGTTCCATAATAATAGAAGCTAAATGTAGCTATAACTTTTGAATGGAATGAGGTAGGCCTGATCATACTGAACACTTTGACACTAAAACCACAGCTGTCATTCAAACTGTTAATTAAAGATTTATTAAAATATGAAAAACCTACTTTTGCAAGCTAATCCCTGCTTTTTGATAATTCACCACAAAATAAGTGTTGAAGTAATCTCTGGATTTCCTAGATAAGTAATTATTGAAAAAAGTGACATATTCTAAACAAATACAACATTTAAAAGGGTTTGAGATTTACAACTGTTAAAAACATTTGTCAAGATTCATTTTGTTTGAAATAATCAT
Associated Phenotype:
Not determined