ZMP
fancg
Ensembl ID:
ZFIN ID:
Description:
fanconi anemia complementation group G protein [Source:RefSeq peptide;Acc:NP_991202]
Human Orthologue:
FANCG
Human Description:
Fanconi anemia, complementation group G [Source:HGNC Symbol;Acc:3588]
Mouse Orthologue:
Fancg
Mouse Description:
Fanconi anemia, complementation group G Gene [Source:MGI Symbol;Acc:MGI:1926471]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20504 | Essential Splice Site | Available for shipment | Available now |
| sa15941 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20504
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039369 | Essential Splice Site | 93 | 617 | 3 | 14 |
The following transcripts of ENSDARG00000024967 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 43115699)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 40896964 |
| GRCz11 | 5 | 41497117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCTAACCCAAGCGAGATGGAGGAGAGTCTGACCCGCAGTTTATTCAGAG[G/A]TAAGTACAGCAGCGTCGTTTATTGCTCATTTACATGCCGTATTGTGTGTT
Long Flanking Sequence:
GAAATTAGGAAGTATAAGGGCTCTGTTTTTATAAGGCTTTGACATGTCTGTTATTCCCTGTTTGGCTGATCGATGGAGTGAGGAGAACAACAACATAATTCTGGCTTGGAAGGTAACGTTAAGTTAAACAAAGGTGTTTTAATCGTTTACTTGAAATTGTAGCATTAGTCCTCCCACAGAAATACTCATCTACAGAATTTCCATTTCAGCAAAATGAACGGAGCCTTCAGCCCAATCAGGACGTTCGTAAGCGATGCTATTCAGAAAGCCTCAAACTACTTCAGAAAACCCAAGGTAACGTTAACTTACTGTCGTACAGGATTTACAGTAGGGTGCTAGTCTGCAGTTCCTAACCATAAATTGTGTTTGCACAGGACTACCAGCAGCTACTGAACGTCTGAAGCTCGAACTGACAGTTTCATACAACACGTGTTTATTCGCACTGGACTTCTCTAACCCAAGCGAGATGGAGGAGAGTCTGACCCGCAGTTTATTCAGAG[G/A]TAAGTACAGCAGCGTCGTTTATTGCTCATTTACATGCCGTATTGTGTGTTTCTAGCTGTGCTGTTCTGTTTGTGTGTAGCTTTAGAGGCTGCTGACTGTCCGGTGTCCAGCACTGAGCCAGTGAAGCTGTGGGAGGATGCTCTGCGCACTTTTGGCTGCTCTGTGTATTTGCCATATGTCCACAAGCTCCTGCTGCTCCAGTGGATGCTGTGGCTCATGCAGGGCCAGCTAGAGAGAGTGCTTACTCTTCTGACACAGATTGACAGCAAGGTGTGTTTATACAAATCAGTTTAAGATTCATTAGATCCTCCTTGTAGGTTTCTGAAGAAAGAAACTTGCGAAATGTACCTTATTTCTTTTCTTTAAAAATTAAACGGACACATCATATTGTAATGTAAATTGCATTAAAAGAGGAACTCTTTTAAAACATCTAAAAGAATCTGAAAGAGTTAAAAAATAAACATGTTTCTGTCTTTTATGTGTTAGAGTAATTGACATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15941
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 |
|---|---|---|---|---|---|
| ENSDART00000039369 | Nonsense | 273 | 617 | 7 | 14 |
The following transcripts of ENSDARG00000024967 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 43119093)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 40900358 |
| GRCz11 | 5 | 41500511 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATTATAGGAAGGCAKTGGAGGTAGATTTTTCTTGTCTTGGYGCACTTTA[T/A]CAAAGTGCTCTGGTGTTCAGACAGCTTGGCAATCCAAAGGCWGAAATGGA
Long Flanking Sequence:
GGGAACACAAACAGGATTTTAAAATGTGGGGAGGACATGTCCCCCTGTCCCCAGCAAAAATGCCCCTGGATGTGTAGTCGGTCAGAATTTTAGCAGATTTTTATAGCGATAGTTCACTTAAAAATGAAAATGTATTTGCTCGCTTTCAAGTGGTTCCAAACATTTATGAGCTTTTTTTATGTTGAACCATTGATTTTATGGTAACCCTTGACTTCCATAGTCACAAAACCTCTGTGGAAGTCAAAGATTACAAGTTTCTAGCTTTCTTCAAAATATCTTCTTTTGTGTTCAACAAAAGAAAGTAAATCAACTGAGTTTGTGACAAGTGAGGGGTGAGTAAATAATGACACAATGTTCCGCTTTTGGTGAACTATCCCTTTAAGTCCTGTATGTTTCTCACTGGCCATGTTTCTTATGTTCTTGCAGGATCAGCCCCATTGTGCTCTCCACTATTATAGGAAGGCAGTGGAGGTAGATTTTTCTTGTCTTGGTGCACTTTA[T/A]CAAAGTGCTCTGGTGTTCAGACAGCTTGGCAATCCAAAGGCAGAAATGGAGGCCTTGCATCTTCTTTACTCTGTAAGTCGTTGTGCACATAACGGCCATATAAAGTTTCAAGAGTCGCAGCCACATTAAAATACATAATTGAATCCCCTGAATGATCATTATGTGAATGAAGAGAACACAAACCACTCCTGAAATTGCTTTGATGCAGTGCTAATTAAACTGTGTGCATGATATCCAGTGTTTTTGACTATGCAATAGTACATCAGCTAAAGATGTTCAATATTTTTTACCAAAGTGCTCAGTTTATGAAGCAAATCATGTTGTAAAGTTTAATGGGCTGCTATTAAATGCACAGTGTGTAAAATTTATTTTAAATAAAATACCCCCCAAAACCCTAAAAGAGTGTTATATATTTAGTTGACTTGTGTATGTGCATTATTTTAAATGTTTTGAAGAATATTCAAATTCAGAAAATTACCATCGATTTTTCTGTTTGGTTT
Associated Phenotype:
Not determined