ZMP
mfsd8
Ensembl ID:
ZFIN ID:
Description:
Major facilitator superfamily domain-containing protein 8 [Source:UniProtKB/Swiss-Prot;Acc:Q0VA82]
Human Orthologue:
MFSD8
Human Description:
major facilitator superfamily domain containing 8 [Source:HGNC Symbol;Acc:28486]
Mouse Orthologue:
Mfsd8
Mouse Description:
major facilitator superfamily domain containing 8 Gene [Source:MGI Symbol;Acc:MGI:1919425]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa42028 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa27950 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2646 | Essential Splice Site | F2 line generated | Not yet available |
| sa45459 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42028
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 |
|---|---|---|---|---|---|
| ENSDART00000050074 | Nonsense | 77 | 504 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 23983934)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 22513476 |
| GRCz11 | 12 | 22634695 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAAGTGCAGATGCCAGTTTTTTGGGATGGGTGGTTGCTGCATACAGTT[T/A]GGGTCAGATGGTGGCCTCACCCTTCTTTGGATTGTGGTCCAATCACAGGC
Long Flanking Sequence:
TTTGAAAGCGCACGCATGCACGCACGCACGCACGCACGCACCCACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATTGAATGGGACTCAATACTTGGAAGAACCCACCTGGGCTGTCCCAATTGGGACCCATCTGGTATTATTACTTATGATAATACTTTACATTTAAGTACAGCAGTTTTGTTTTAACTTTTTAAGAACAGTGCCATTTCTAATTAACTTTTAAAATCACATTTTAATTTAAACGTTGATGTTTAAAAAGTTGAAAAAGTTACAAAATGTTAAAAACTGATTAATTAGTTATATTTACAAATGTTTAATTGAACTGCCAAGTCCCTGTTGGTCTGTATATTGTAAGTTCATTAATCATGCTATGTCTTTTTAGATCGATGAAAGTGCAGATGCCAGTTTTTTGGGATGGGTGGTTGCTGCATACAGTT[T/A]GGGTCAGATGGTGGCCTCACCCTTCTTTGGATTGTGGTCCAATCACAGGCCTCGACGGGAGCCTCTAGTCTGCTCTATATTCATTAATGTCTCAGCCAACATTTACTACTCCTATGTCTACTTACCTCCCTCACACAACCAGATTCACATGCTCTTGGCTCGCACATTTGTGGGTATCGGAGCAGGTAAAAAGACTTTTTTTTGAAAGAATTTAATACATGCATGTAGAATATATTAAATTGATCAAAGGTAACAGTAAATATATTTGTGATGTATTTCACATAAATGCTGTCTTTTAAAACGTTCTTTTCACATCACAATGCTGAAAAATGTTTATCAGGACTTCATATAAACAGTGAATGGTACAATAATTATGCAAATTGATGATATAAAATGGTCAAATGTTTTTCGAGCACCAAATCAGCAAGATTCAACAACATTCAGCCTTGTCACCACTAAAATAAATGTAATTTTTTGATAAATGCAGTTTTTTTTAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27950
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000050074 | Nonsense | 137 | 504 | 4 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 23984113)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 22513655 |
| GRCz11 | 12 | 22634874 |
KASP Assay ID:
2260-5356.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCACACAACCAGATTCACATGCTCTTGGCTCGCACATTTGTGGGTATC[G/T]GAGCAGGTAAAAAGACTTTTTTTTGAAAGAATTTAATACATGCATGTAGA
Long Flanking Sequence:
CAATTGGGACCCATCTGGTATTATTACTTATGATAATACTTTACATTTAAGTACAGCAGTTTTGTTTTAACTTTTTAAGAACAGTGCCATTTCTAATTAACTTTTAAAATCACATTTTAATTTAAACGTTGATGTTTAAAAAGTTGAAAAAGTTACAAAATGTTAAAAACTGATTAATTAGTTATATTTACAAATGTTTAATTGAACTGCCAAGTCCCTGTTGGTCTGTATATTGTAAGTTCATTAATCATGCTATGTCTTTTTAGATCGATGAAAGTGCAGATGCCAGTTTTTTGGGATGGGTGGTTGCTGCATACAGTTTGGGTCAGATGGTGGCCTCACCCTTCTTTGGATTGTGGTCCAATCACAGGCCTCGACGGGAGCCTCTAGTCTGCTCTATATTCATTAATGTCTCAGCCAACATTTACTACTCCTATGTCTACTTACCTCCCTCACACAACCAGATTCACATGCTCTTGGCTCGCACATTTGTGGGTATC[G/T]GAGCAGGTAAAAAGACTTTTTTTTGAAAGAATTTAATACATGCATGTAGAATATATTAAATTGATCAAAGGTAACAGTAAATATATTTGTGATGTATTTCACATAAATGCTGTCTTTTAAAACGTTCTTTTCACATCACAATGCTGAAAAATGTTTATCAGGACTTCATATAAACAGTGAATGGTACAATAATTATGCAAATTGATGATATAAAATGGTCAAATGTTTTTCGAGCACCAAATCAGCAAGATTCAACAACATTCAGCCTTGTCACCACTAAAATAAATGTAATTTTTTGATAAATGCAGTTTTTTTTAAATCGTACAGATTCCTTGCAATATGAATTTTTATACAATTATAGATTTTTATAAGATTATGATTGAATAGCAAAATAATATTCAATAAAATGTTTATTTGTACAACTATGCCTCACTTGCAGATGCAGAACAAACACTCATCAAACAAAGTCAAAGCATTTGATTTCTTTGCTGTGTCTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2646
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000050074 | Essential Splice Site | 176 | 504 | 5 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 23984737)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 22514280 |
| GRCz11 | 12 | 22635499 |
KASP Assay ID:
554-3004.1 (used for ordering genotyping assays)
KASP Sequence:
AATGGCAAACATGAGTGCCTGTCAAGCTCTCGGCTTTATACTTGGCCCAG[G/A]TCTGTGTAAAGTATTTAAAGCATGTTACTTGCAGTATATTGCAAAAATAT
Long Flanking Sequence:
GTTCTTTTCACATCACAATGCTGAAAAATGTTTATCAGGACTTCATATAAACAGTGAATGGTACAATAATTATGCAAATTGATGATATAAAATGGTCAAATGTTTTTCGAGCACCAAATCAGCAAGATTCAACAACATTCAGCCTTGTCACCACTAAAATAAATGTAATTTTTTGATAAATGCAGTTTTTTTTAAATCGTACAGATTCCTTGCAATATGAATTTTTATACAATTATAGATTTTTATAAGATTATGATTGAATAGCAAAATAATATTCAATAAAATGTTTATTTGTACAACTATGCCTCACTTGCAGATGCAGAACAAACACTCATCAAACAAAGTCAAAGCATTTGATTTCTTTGCTGTGTCTTTCTGTCCTCCAGGTAATGTAGCAGTGGTGAGGTCCTATGTGGCTGGTGCCACTTCCCTGAAGGAAAGAACCAGTGCAATGGCAAACATGAGTGCCTGTCAAGCTCTCGGCTTTATACTTGGCCCAG[G/A]TCTGTGTAAAGTATTTAAAGCATGTTACTTGCAGTATATTGCAAAAATATCATTTGTTACTCTAATGAAGGCAAGTTATTGCAACGAGTAATTGCTTGTGTACTATTTCTAATATTGGATCAATGTGAATAAAGGCTTTTAAAAGTTCATCTGAAATCAGAATTTTAAATGTTTATTATTCAACTTAAGGGCTTCCATAGCAACTGTATCTCAATGTTCTCAACCAAACCCCTTTTGCCGCTAGTTTGCTATGAGGGAATCATAGATATATGTAAATATTGTTTTGGGATTATTTACAGTTTTAACCCAAAAAAATGACCATTCTGTCAGATGAAGAAGAGCCGGAGTCAGAGATTCAAATAAATAAATTAAGTTTACTGAAGATAGTTTGCAGTTTCATCCGCAGAAGCCAGCTTCAACACTCGCAATGAGTTCCTAGGCCGCTCTGCTTACAACCACAAATCAATAACAATTATACTCTCACATAACGTCATTACCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45459
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 > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000050074 | Essential Splice Site | 437 | 504 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 12 (position 23992765)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 22522633 |
| GRCz11 | 12 | 22643852 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAACCAACATGACGATTAACCAACTTCCCCAATTGTTTGCAAACACA[G/T]GGAGTTTACATGGGATGGCTGACTGCATCAGGAAGTGGCGCGCGGACCCT
Long Flanking Sequence:
AATCATGTGACTGAAGATTGGGTAGTGAATAATTAACATTAAAAATTGAATTCAAACTGAATTGCAATTTTAAATTGTAATAATGTCACACTACTACTCTAAAACACAGAACATAATAAACCCCAAACCTCTGGGGGGGTAGTGTGTATTGCATAAAAAATGTATTACATTTGTATTTATCATCTCCTCATCAACAGACATTAAGAATAACACTATACCACCAATACAACTGGCACCCACCCCAGCCTCAAACAGTTCCCTGGAGCCCATTGGATGCCCGTCCGAACAGACCTGGTGCTTGTTCACCCCTGTAATTCATCTCGCACAGTACATCACCTCTGACATCCTGATCGGAGTGGGCTATCCCACATGCAACGTCATGTCCTACACTTTATACTCAAAGATACTGGGGCCCAAACCACAGGTAAAACACTTTCTACTAATCCTTAAACCAAACCAACATGACGATTAACCAACTTCCCCAATTGTTTGCAAACACA[G/T]GGAGTTTACATGGGATGGCTGACTGCATCAGGAAGTGGCGCGCGGACCCTCGGGCCTGTCTTTGTTTCACACTTCTACACCATCCTGGGACCTCGCTGGGCCTTCAGTGCCATATGTGGCATAGTGCTAGCTGCGATTGTAATGCTCAGCGCCATGTACAAGCGTCTCGTCGCCTTCTCCATACGCCATGGACGGATTGCGGAATGACGGCATTACTGACAGGTGCCCCCTACCAACTTCTTAAAGAGACAGTTCATATGTAATACTCCTCAAGTGGTAACAAATCTTTTGTGTTTTCTGTTGGAAACAAAAAGAAGATTATTTGAAGAATGTTGTAATCTGGTAGCCATGGAATTTCATAGTAGGAACAAGAAGACTTTGGAAGTCCATAGGAAGCAGTTTCAGACATTCTTGACAATATCTTCTGTCCTGTTCAACAGAAGTTCAGCATATTATGACATAATTGTCATTTTTTTTGGTCAACTATCCCTTTATAGACA
Associated Phenotype:
Not determined