ZMP
fto
Ensembl ID:
ZFIN ID:
Description:
Fto protein [Source:UniProtKB/TrEMBL;Acc:Q568I7]
Human Orthologue:
FTO
Human Description:
fat mass and obesity associated [Source:HGNC Symbol;Acc:24678]
Mouse Orthologue:
Fto
Mouse Description:
fat mass and obesity associated Gene [Source:MGI Symbol;Acc:MGI:1347093]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12749 | Nonsense | Available for shipment | Available now |
e37 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa34123 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa12749
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064913 | Nonsense | 119 | 568 | 3 | 9 |
ENSDART00000130028 | Nonsense | 131 | 579 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 37641209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 36042810 |
GRCz11 | 7 | 36314287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACACGTACCGTTATCTGGACACTCGTCTGTTCACCATCCCCTGGCACTG[T/A]GAAGGAGAAGAGGGCCAGAAAGATGAGAAAGGCAAACCTTGCTGTGACTC
Long Flanking Sequence:
ATTATATTATATTATATTATATTATATTATATTATACTAATGTTATATTATAGTAATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTTTGTAGTTTTCTGTTTTAGTAAATAGATTATACAGTTTGAACAGTACAAAAACCAGTAGGTCTGTGGAGCTTCATTAATTTAGACCCTCAAAGTAAGTGTATGCTTATACGTAATTACATTGTGCTGTATGTTTGTGTCTGTAATTTGACAGTGGGACTCCAGTTATGCGGGCCTGGCTTTGCGGCAGTCTGGTACCCTTCCAGAAGGTCTCCATGAGAAGGTTCAATCTGCTCTGTTAACTCTACAGCGGCATGGATGTCTCCTCCGAGATCTTGTCCGAGTTCGAGACCGGGACGTCTTCACGGCCGTTTCACGCGCTCTCGTGGGTCAGCCGGGCTACACGTACCGTTATCTGGACACTCGTCTGTTCACCATCCCCTGGCACTG[T/A]GAAGGAGAAGAGGGCCAGAAAGATGAGAAAGGCAAACCTTGCTGTGACTCCGACCTGAGGGACGCTTGTAAAGCATTATGGGAGCTCAATCAGTTCTTTTGCTCGGATGTAAAGCAGCAGACAAATGCAAGAGGTGTCAAGCGTACCCGCAGTGACACTGAAAACAGCGAAGATGCGCCAGGGGAGGGAATGTGCGAAGAAGAGAGTGTTAAGGACAGGTTAGTTGAGGAGAAAACCATAGAGGAGGAGGAGGAAGACAGTGGACAGGGCTGCTCTCATTCCTCACCTCCTTCATCCACTCCGCCAGCTGCTCAGGCCAGCCTGGTTCAGTTTAACGTCACGCTAATCAACTACATGAACCCTGCAGCCATGACCCAGCTGAAGGAAGAGCCATATTACGGCATGGGCAAAATGGCAGTCGGTTGGCATCATGATGAGAACCTGGTTCCTCTCTCACCAGTTGCCGTTTACAGCTATAGCTGCCCAGCAGAGCCAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
e37
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000064913 | Nonsense | 372 | 568 | 5 | 9 |
ENSDART00000130028 | Nonsense | 384 | 579 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 37629518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 36031119 |
GRCz11 | 7 | 36302596 |
KASP Assay ID:
554-0074.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGTTGCGTTGTATGCACAGATGATCTGAACCGGACACATCAGCACTG[T/A]GTACTGGCTGGTGACACAGCTAGATTCAGCTCAACTCACAGAGTCGCACA
Long Flanking Sequence:
TAAATTAATAATATTAAAACAAATTTGTGATCATTTACATACGAATATGTCTTCCTAAAACCATAAGAACTGTGTTTATCTTCAGAAAAGAAATGTCTTTAGATGAATATAATTTAGGTTTGTTTTATGTGATCTGTGAACAATGCTTACAACGATTAAATGTAGTTACTGATGCACAAATTGGCTTGAGGTTTCATTCTTGTATGTCTCTACCATAATGTACCATTCCACAAGAATTAAAGGGATAGTTCTGCCAAAAATCACAATTCTGTCACTATTTACTCAGCCTTTACATGTTTCAAACCTTTGAGTCAAACCTTTTTTTTCATTTGCCTAAACTGTCTTAATGTGTCATCCAATGATAAATGCACAACATGAGGGTGAAAAAAGTGATGGCAGAATGTTGTTGTTCTTAATGTTTTTGTTTCTAATCATTGTGTGTGTGTATGTGGCTGTTGCGTTGTATGCACAGATGATCTGAACCGGACACATCAGCACTG[T/A]GTACTGGCTGGTGACACAGCTAGATTCAGCTCAACTCACAGAGTCGCACAGGTGAGTGTCATCGCTTCAGTTCTACCTCCAACTTCTATAAAGTTCTTAACCAAAACCTCTCTATTTTTGCCTTACACTTAAACACCCCACACTAATATCAGTCATGTTTCTTCAGTGTTGTACGGGTACACTGGACTACATACAGAAACGTTGCTCTGAGGCCTTGGAGAATTTACACAGCGACCCCGAGAAGAACGCCAAGAGCCTGATTTCCCTCCTGCCCTCCATCCTCCAACGCATTGAGGATATCCACAACGAGGTGTGTATGAGAACACGAGTGTTTGCAGCAATGGAAAACCAAATCCCAAGCGCACGTCTCGGGCCGTAACAGATGAGGTTGCTCAGAGGTTTTTTAAAGGTTGTACTTTGCCATTAATTTTTCAAAGCTCAAACAATAGCCGTTCCAGTGGGCCAGACCATCAGTGTGGCCTTGCGTAGGTCTCCGTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34123
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 |
---|---|---|---|---|---|
ENSDART00000064913 | Nonsense | 447 | 568 | 7 | 9 |
ENSDART00000130028 | Nonsense | 459 | 579 | 7 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 37617163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 36018764 |
GRCz11 | 7 | 36290241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACCTGTGCTGCTCTTTTAGGTGGAGTTTGAGTGGCTGAGGCAGTACTG[G/A]TTCCAGGGCCGGCGTTACGCTCGATTCTGCAGCTGGTGGACTAAACCCAT
Long Flanking Sequence:
CCGCAAACTTATCCAGCATAGGTTTTTCAGAGCGGATGCCCTTCCAGCCGCAACCCAGTACTGGGAAACATCCATACACACTCATACACTACGCTCAATTTAGTTTATTCAATTTACCTAAAACACATGTCTTTGGACTTGGTGGGGGGGTGGGGGGTGGGGGGGGTGGAAACCGGAGCACCCGGTTCACACACAGAAATACCAACTGACTTGATCCAGAAACCTTCTTGCTGTCAGGTGGCTGTGCTAACCACTGAGCCACCACTGAGTTTCACACTTCATGAATTAAATGTATTGTTTGAGTTTTGGCCAGAACAACAGTACCAGTCTGTCCAACTAGCAATAGACAGAGACGACAATTGGGAAAAAATTTGAAACGTTCATATTTTTTTGCAGTTCATTGTGATGTCTCCAGCGGTGTGGAGATGACAGGCTGCAGCTTTAACATGTTGACCTGTGCTGCTCTTTTAGGTGGAGTTTGAGTGGCTGAGGCAGTACTG[G/A]TTCCAGGGCCGGCGTTACGCTCGATTCTGCAGCTGGTGGACTAAACCCATGGAGCAGATGGAGAAAGATTGGAAGGAAATGGAGAGAATGGTAAGAGAGTTGGAGTGAGGCCTCCAGATTTTTCGCTCAGTTCAGCGTCTGACACACAGCTTGCCAGTCGCAGTGTTTGTTTATGAAATGTTTTGGCTAATTTGATTCTGCTTTCTGCTACCAGTTGTAACCTCAGCGCTGTTTAACACATTTTACATTTATTTAAATCCGCAGTTCATGTGGTGAATGTGAAACAAGTGTGCAGGTTCTGTGTGTGGCCATCCAGACGACAAGAATGAGGGAGGCAGACAAATATGTACATGAGAGATTAGAACATTTGAATATGTAGTTTCTTTTATGATCATTTTATGTATATATAATTGAAAAAATGAAAATCCTTATCTGGAATATTATTATTATTATTGCTGTTATTATTATTATTATTATTATTATTATTATTATTATTATTA
Associated Phenotype:
Not determined