ZMP
ENSDARG00000015247
Ensembl ID:
Mouse Orthologue:
F8
Mouse Description:
coagulation factor VIII Gene [Source:MGI Symbol;Acc:MGI:88383]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15845 | Essential Splice Site | Available for shipment | Available now |
sa22404 | Missense | Available for shipment | Available now |
sa42320 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5870 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19072 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15845
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 |
---|---|---|---|---|---|
ENSDART00000014159 | Essential Splice Site | 338 | 2147 | 8 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1012866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 996210 |
GRCz11 | 14 | 1014474 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATMAACTCAGGCTGATGGAAACCYAATGCATGYCTCTGTGTTGTTCTCC[A/G]GCKGGTATGAATGCGTTCTTCACTGTTGAAAACTGTCCTGAACCYGCACC
Long Flanking Sequence:
CGCCATTGTGCTGCCCTGACATCCAGATATGATGGTTAAAATGCACATTCCTTTTTATTTCTCATGAGTAATTCTGTGTTTGTGGTTCGCTCAGGTCTGAGTGTGTGTGAGAAGAGTCCGCAGGTCTCCTGGCACCTCATAGGTCTGGGCTCCAGTCCTGAGATCCACAGCATCCAGTTTGAAGGACACACGCTGAAGGTGTTCGACCACAAGCGGGTGACGGTGGAGATGACACCCATGACCTTCACCACAGCCCTCATGAAGCCCTCGGCCACGGGGAGGTTTCTGATCTCCTGCAGGATCCACTCGCATCAGACAGGTCAGACTCGCTAAACTTACTCGCACTATACTGTCCTAATGAAAGCATTCAAAATCAAGGCATGATCATATTTTATAATATATATATTTTATTTAGTTTATTGTTGCTATCATGTGATACTTCAAGATGAGCATCAACTCAGGCTGATGGAAACCCAATGCATGTCTCTGTGTTGTTCTCC[A/G]GCTGGTATGAATGCGTTCTTCACTGTTGAAAACTGTCCTGAACCCGCACCGCTTCCCCTCCCGGACAAGAGAAACGTCAAGCACACTAATGACGATGAGGAGGAGGATGATGAAGACAACATGTTCTCTGTGGTGTTCAAACAAGGAGGTCCAATATCTGTGCTTCGCTCCAGCGCGAAGGGCCGACCCAAAGTGTGGCTCCATTACATCTCTGCAGAGGAGACGGACTGGGATTATACCGCTCAGAGCGGAGATCGGTACGCCTCACAACTCTGACATTACTTTCCTCTTTGCCATGATGACAGCAATATTGGACTAGATATTAGTAGTCAGCTTAAAGTGACATTTAAAGGCTTAACTAGGGTAAAGTAGTAAGGCAAGTTATTGTATAACAGTGGTTTGTTCTGGAGACAATGTAATATTGCTTAAGGGGGCTGATAATATTGACCTTAACATGGCTTTAAAACAATTAAAACTGCTTTTATTCTAGCCGAAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22404
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:
G > A
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014159 | Missense | 508 | 2147 | 10 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1015699)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 999043 |
GRCz11 | 14 | 1017307 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATCCAAACGGCCTGACCAGCGTTCAGCCTCTGAAGACAACAAACAAAG[G/A]TATGAACCACGGTGGCTCAGTGGTGAGCACTGAAGAAGCAAGAAGGTCGC
Long Flanking Sequence:
AGCTCCATATCACTCCACTGAAGGATTAGAGTTCACTCACAGCTACACCAGTCAGAAAGCACATCAGAACACGACAGAAGGCTTTGGAGGAGATGTGAAAGTAACTAGTGCAGTTTGAGGAGGGAAAACACCGGACTAATACAACATCTGAGCAGTGGATTTAGCTGTGGTGACCATAATATAATCGGAATAATCATTAGAAATTGCAAACTGAAGGTCACCACATTAGCTGTGCATTATTTTCTAATAATTCACTGCCCTGTAGTTAATTACTCGTTGAAATTAGAGCAAATCTTACTTTGATGAATTGTTAATTATGAAAAAATAAGATGTATGATAAATGTAGAGTGAGTTTGATGCTAACTTTAAAGTCTGATGTCATTAACTTGTCTCTTTTGTTTCTCTCTATCAGATTGTGTTTAAAAATATGGCCAGTCGTCCATTCAACATTTATCCAAACGGCCTGACCAGCGTTCAGCCTCTGAAGACAACAAACAAAG[G/A]TATGAACCACGGTGGCTCAGTGGTGAGCACTGAAGAAGCAAGAAGGTCGCTGGTTCGAGCCTCAGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTAGCGTGGGTTTCCTCCGGGTGCTCCCCCACAGTCCAAACACATGCGCCATAGGGGAATTGATGAACTAAATTGGCCGTAGTGTGTGTGAATGAGTGTGTATGGGTGTTTCCCAGTGCTGGGTTGCAGCTGGTAGAGCATCCGCTGTGTAAAACATATGCTAGAATAGTTGGTGGTTCATTCCACTATGGCGACCTCTGAAATAGAAACTAAGCTGAAGGAGATTGACTGAATGAATGAATGAACCAGTGGTTTTCCTGTTTCTGACAGAAGGGTAACTCATTCATACATTTTCTTGTCAGCTTAGTCCCTTTATTAACCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTGAGCAGCAGATGCCCTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42320
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014159 | Essential Splice Site | 509 | 2147 | 10 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1015705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 999049 |
GRCz11 | 14 | 1017313 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACGGCCTGACCAGCGTTCAGCCTCTGAAGACAACAAACAAAGGTATGA[A/C]CCACGGTGGCTCAGTGGTGAGCACTGAAGAAGCAAGAAGGTCGCTGGTTC
Long Flanking Sequence:
ATATCACTCCACTGAAGGATTAGAGTTCACTCACAGCTACACCAGTCAGAAAGCACATCAGAACACGACAGAAGGCTTTGGAGGAGATGTGAAAGTAACTAGTGCAGTTTGAGGAGGGAAAACACCGGACTAATACAACATCTGAGCAGTGGATTTAGCTGTGGTGACCATAATATAATCGGAATAATCATTAGAAATTGCAAACTGAAGGTCACCACATTAGCTGTGCATTATTTTCTAATAATTCACTGCCCTGTAGTTAATTACTCGTTGAAATTAGAGCAAATCTTACTTTGATGAATTGTTAATTATGAAAAAATAAGATGTATGATAAATGTAGAGTGAGTTTGATGCTAACTTTAAAGTCTGATGTCATTAACTTGTCTCTTTTGTTTCTCTCTATCAGATTGTGTTTAAAAATATGGCCAGTCGTCCATTCAACATTTATCCAAACGGCCTGACCAGCGTTCAGCCTCTGAAGACAACAAACAAAGGTATGA[A/C]CCACGGTGGCTCAGTGGTGAGCACTGAAGAAGCAAGAAGGTCGCTGGTTCGAGCCTCAGCTGGGTCAGTTGGTGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGTGTTAGCGTGGGTTTCCTCCGGGTGCTCCCCCACAGTCCAAACACATGCGCCATAGGGGAATTGATGAACTAAATTGGCCGTAGTGTGTGTGAATGAGTGTGTATGGGTGTTTCCCAGTGCTGGGTTGCAGCTGGTAGAGCATCCGCTGTGTAAAACATATGCTAGAATAGTTGGTGGTTCATTCCACTATGGCGACCTCTGAAATAGAAACTAAGCTGAAGGAGATTGACTGAATGAATGAATGAACCAGTGGTTTTCCTGTTTCTGACAGAAGGGTAACTCATTCATACATTTTCTTGTCAGCTTAGTCCCTTTATTAACCCGGGGTCGCCACAGCGGAATGAACCGCCAACTTATCCAGCAAGTTTTTGAGCAGCAGATGCCCTTCCAGCCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5870
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014159 | Nonsense | 929 | 2147 | 17 | 37 |
ENSDART00000014159 | Nonsense | 929 | 2147 | 17 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1019096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 1002440 |
KASP Assay ID:
554-3730.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGACRGCGCTCTAGGCTAGTTATGAACAGTACAAGGCACAGTAGATG[G/A]CGCTCTAGGCTAGTTTTTAACAGCAGACAGTGCTCTAGGYTAGTTATTAA
Long Flanking Sequence:
GATACTATTTAACAGCAGATGGTGCTTTAGGCTTGTTATGAACAGGACATGACACAGTAGATGGCGCTCTAGGCTAGTTTGTTACAGCAGAAAGTGCTCTAGGCTAGTTTGTAACCGCAGGCAGTGCTCTAGGCTAGTTATTAACAGTAGAAGGTACTCTAGCCTAGTTTTTAACAGTAGATGGCACAGTAGATGACGCTCTAGGGTAGTTTTCAATAGTAGATGGTGCTCCAGGCTAGTTTTTAACAGCAGTCGGTGCTTTAGGCTAGTTTTTACAGTAGATGGAGCAGTAGATGGTGCTCTAGGGTAGTTTTTAATAATAGATGGTGCTCTAGGCTAGTTTTTTACAGCAGACAGTGCTCTAGGCTAGTTTTTTACAGCAGACGGTGCTCTAGGCTAGTTATTAACAATAGACGGCACAATAGATGGTACTCAATGATACTTTTTAACAGCAGACAGCGCTCTAGGCTAGTTATGAACAGTACAAGGCACAGTAGATG[G/A]CGCTCTAGGCTAGTTTTTAACAGCAGACAGTGCTCTAGGCTAGTTATTAACAGTAGACGGCATAATAGATGACGCTCTATGATACTTTTTAACAGTAGATGGCACTCTAGACTATTTTTTTATAGTAGATGATGATCTAACAGCACCGTCTGCTGTTAAATCCTAGCCTAGAGCTGCAGTTAAAAAACTAACCATGAGTGCCAAGAAAACTAGCCTAGAGTGCCATCTACTGTTAAAAACTAGCATATAATTGTAATATAATATATATCCAGCTGGTTATTTTATGCAAAATAAAAGATAATGTAACTTGTAATTATTTGCAATCTATCAGGTCGTTTCATACACCATTTTTACATTTAGGATTGAAACTATACGCATGCATAGATGGTAGTAAATGCTGCTGATGTTGTTACAGGTGACGTCAGATAAAGAGAAGAAGCTGTTGTTTACGGTGTTTGATGAAAACAGAAGCTGGTACTTCGAGGAAAACATCAAGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7229
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014159 | Nonsense | 929 | 2147 | 17 | 37 |
ENSDART00000014159 | Nonsense | 929 | 2147 | 17 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1019096)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 1002440 |
KASP Assay ID:
554-3730.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGACRGCGCTCTAGGCTAGTTATGAACAGTACAAGGCACAGTAGATG[G/A]CGCTCTAKGCTAGTTTTTAACAGCAGACAGTGCTCTAGGYTAGTTATTAA
Long Flanking Sequence:
GATACTATTTAACAGCAGATGGTGCTTTAGGCTTGTTATGAACAGGACATGACACAGTAGATGGCGCTCTAGGCTAGTTTGTTACAGCAGAAAGTGCTCTAGGCTAGTTTGTAACCGCAGGCAGTGCTCTAGGCTAGTTATTAACAGTAGAAGGTACTCTAGCCTAGTTTTTAACAGTAGATGGCACAGTAGATGACGCTCTAGGGTAGTTTTCAATAGTAGATGGTGCTCCAGGCTAGTTTTTAACAGCAGTCGGTGCTTTAGGCTAGTTTTTACAGTAGATGGAGCAGTAGATGGTGCTCTAGGGTAGTTTTTAATAATAGATGGTGCTCTAGGCTAGTTTTTTACAGCAGACAGTGCTCTAGGCTAGTTTTTTACAGCAGACGGTGCTCTAGGCTAGTTATTAACAATAGACGGCACAATAGATGGTACTCAATGATACTTTTTAACAGCAGACAGCGCTCTAGGCTAGTTATGAACAGTACAAGGCACAGTAGATG[G/A]CGCTCTAGGCTAGTTTTTAACAGCAGACAGTGCTCTAGGCTAGTTATTAACAGTAGACGGCATAATAGATGACGCTCTATGATACTTTTTAACAGTAGATGGCACTCTAGACTATTTTTTTATAGTAGATGATGATCTAACAGCACCGTCTGCTGTTAAATCCTAGCCTAGAGCTGCAGTTAAAAAACTAACCATGAGTGCCAAGAAAACTAGCCTAGAGTGCCATCTACTGTTAAAAACTAGCATATAATTGTAATATAATATATATCCAGCTGGTTATTTTATGCAAAATAAAAGATAATGTAACTTGTAATTATTTGCAATCTATCAGGTCGTTTCATACACCATTTTTACATTTAGGATTGAAACTATACGCATGCATAGATGGTAGTAAATGCTGCTGATGTTGTTACAGGTGACGTCAGATAAAGAGAAGAAGCTGTTGTTTACGGTGTTTGATGAAAACAGAAGCTGGTACTTCGAGGAAAACATCAAGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19072
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 |
---|---|---|---|---|---|
ENSDART00000014159 | Nonsense | 1836 | 2147 | 31 | 37 |
Genomic Location (Zv9):
Chromosome 14 (position 1031672)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 1015016 |
GRCz11 | 14 | 1033280 |
KASP Assay ID:
2260-7111.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGTATAGTTGGAGGCCTAAACTGATTTTTGTTTTAACAGAATGCAAT[C/T]AGCCCATAGGAATGCAATCAAGATGGATCACCAACAAACAAATAACAGCG
Long Flanking Sequence:
AATAGATAAATAACAATACTGAAGCACTGTGATGACGAGCTGACGGAGACCTGATGCCTTTTCCAATCAGCAGAACAACATTTCAGATCTGCAACAATGGAAAGCTGAAAAACATGGAGAGCTGCAAGCCAACATTAATGACACAAAAACCCTCAAATGCACATCTATATCTGTGAACAACTACATCACAGCATGCAGACTGATGAGTTTATTCACTAATGTGTTTCTATCATAGTTTATGCACACTATCGGATGTTTATCTTGCTCAATTTATATGCTTACCTTTTTTATAGGCATTTTCAAAATTCCTGAGCATCTTCACATTTCCATTCAGAGTTATTTTATGTGATATTTTAAACTGTGCATAAAAATAGGTGGATGGAAACATAGCTAATAGGAGATTGTCATGGATGTTTCTTTGCATTGTGTTTGTGCAGTCATGTCTTCTATCACTGTATAGTTGGAGGCCTAAACTGATTTTTGTTTTAACAGAATGCAAT[C/T]AGCCCATAGGAATGCAATCAAGATGGATCACCAACAAACAAATAACAGCGTCTGATTACTACGGTAAGAAAAAACAACACAAAATGATATTACTAAAAGACACAGGACTTAAAGAGGCCACATGAAGCTTCATTATGCACAAGTATTCTATAGCAGGAATACATTTAATACACTTCAATAAATCAAGCAAGTTGCAGTACAAACCGCAAGTCACATTACATGATTTGACTGATTTCCACCTCAAATTGGGGTTTGTGAAGGATTTAATTCAGACGGCTGGAAACGGCACATGATACATTGCCATAACTGCTATTCGCATTCATTCATTTTCTTTTCGGCTTAGTCCGTTTTTTAATGAGAAGTCACCACAGTGGAATGAACCGCTATAAATGCTATTGTATTATTGCTAATTATTGTTTTCTTCATTATTGTTGGCAGCCTGAAACTGACATTTAATTTAGATGAATTGCACAGCCTTAGTAGAAACACTGTTTTAAGCA
Associated Phenotype:
Not determined