ZMP
fancd2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC402960 [Source:RefSeq peptide;Acc:NP_991224]
Human Orthologue:
FANCD2
Human Description:
Fanconi anemia, complementation group D2 [Source:HGNC Symbol;Acc:3585]
Mouse Orthologue:
Fancd2
Mouse Description:
Fanconi anemia, complementation group D2 Gene [Source:MGI Symbol;Acc:MGI:2448480]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20790 | Essential Splice Site | Available for shipment | Available now |
sa20789 | Essential Splice Site | Available for shipment | Available now |
sa20788 | Nonsense | Available for shipment | Available now |
sa18469 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20790
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 |
---|---|---|---|---|---|
ENSDART00000064969 | None | None | 321 | None | 4 |
ENSDART00000075601 | Essential Splice Site | 552 | 1445 | 18 | 45 |
ENSDART00000125089 | Essential Splice Site | 552 | 1659 | 17 | 45 |
ENSDART00000128777 | Essential Splice Site | 552 | 1445 | 18 | 44 |
Genomic Location (Zv9):
Chromosome 6 (position 42256088)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42327142 |
GRCz11 | 6 | 42324678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTCAGTCGCCTGGCATTCGGACAGGAGCAGCATGGAGGACACATCCAG[G/A]TAAGAAACGCTTCTTTTGAAATACATAGTATACAATGTCTTTTAAATTTT
Long Flanking Sequence:
TTTAAGCGCTTATCTAGTTTATTGTATTTGATGCAGATGCACTAAACTACAATATCACTGCTACCATTTTAAAATGATGAATTCTTCACACATTATTCAAGCTATCCGGTGAAATGGATCTTATATTGCAATATATATCGCAGAAAGGCAAAATATTGCCAAGCAGTTTTTTCCAATATTTTCATAAATTTGATCATATTTTTTACTAGGTCGTAGGAGGAGCCATGGAAGTTAATTAGTAAACAAAGTGGAAACATATTTTATCTTTAACCTTCTTTTAACTTGAAATGTTGAACTGTTATAAATATTTTATTCAACTGTAGTTAATTATTACCATTGCTGGATTTATTAATGTAATATATTGGATCTGTGCATTGTCGGTGTTTTAACAGGGTATTCTGGATTACATGGACAACCTGACCTCACAGCAGATCAGACGTCTATTCCATCTGCTCAGTCGCCTGGCATTCGGACAGGAGCAGCATGGAGGACACATCCAG[G/A]TAAGAAACGCTTCTTTTGAAATACATAGTATACAATGTCTTTTAAATTTTTTTTAGTTAAGGTGGTCATCTCTCCTTCATCAGGATGACATGCACATCGTCATCCGCAAGCAGCTATCAAGCACTGTGCCCAAGTACAAGCGCATTGGTATAATTGGGGCAGTTATGATGGTGGGGAGTATGGGGGCCTGCAGGTACACTTTTTTTTACATTATACTTACTTTATTCTCAGTTACCCCAAGTAAATTTGTATGGTTTTTATCTTCTTCCTTTTATCCTCTTCTTCTTTATGAAGAAATAAACATGATGGCTCTCAGGGTGGCACGTTGCCTAAAGAGACAAACCGACAGGTAAGGGACATGATCTAATGGTTTGTGGATGTTCAGCTGACATTACTCTAATCTAGGCATGGGACAATAGCTCGTCATGATTTAGCCAAGTACGATGCGATCCAGGATTATCATCTATGTTGATCCTGGAACATCATTTTAGTTGGAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20789
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064969 | None | None | 321 | None | 4 |
ENSDART00000075601 | Essential Splice Site | 864 | 1445 | 27 | 45 |
ENSDART00000125089 | Essential Splice Site | 864 | 1659 | 26 | 45 |
ENSDART00000128777 | Essential Splice Site | 864 | 1445 | 27 | 44 |
Genomic Location (Zv9):
Chromosome 6 (position 42248560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42319614 |
GRCz11 | 6 | 42317150 |
KASP Assay ID:
2259-7987.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATGATACCATCTTCTTCAGTCGTTCAACAAAAGAAAGGAAAGAAAGG[T/C]AAGGTTGCTGGGGAAATGACCAAACTTGAATTCTGTTGGTGTTTAGGACA
Long Flanking Sequence:
CCGACAAATCTGCAGCAACTGTGTGTTGCTATCCTGTCAATTTGGACTGAAATCTCTGAGGAATATTTGCAGTACCTTGTTGAATCTATGACATGAAGGATAGAGGCAGTTCTGAAGGCAAAAGGGGGTCCAACCCTGTACTATAAGGTGTACCTAATAAAGTGGCCGGTGAGAGTATATTCATGTTTGAATTTAGCTTTTGCTTTTTGAGCATGTGTGTTCTTTATTGTAAATGTATTCACTTATATTTATTTATGTATATATAATTATCTATTTATTTCATGTAAAATATTATCTATCTTCGGCGACCCCGGATTAATAAAGGGATTTTAGCTGAAAATGGATGAATGAATTATCTATCTTCCATGTTAACATTCTTTTTTGTATATTGTTTTAGCTACACCAGGCTACATTCCTCCTCAGGCTAACTTTGATGGAGAGAGTGCTGATGTGATGATACCATCTTCTTCAGTCGTTCAACAAAAGAAAGGAAAGAAAGG[T/C]AAGGTTGCTGGGGAAATGACCAAACTTGAATTCTGTTGGTGTTTAGGACATGGGTAATGATGATGATATGAGCAAAAATGATATCTCAGTATTATTTTGGCTGAATTATGACAAAATATTTATATGTGTTTTACTCAACAAATGTTATTAAAGTTTATGATGTTTACTGGAAATTCACAGCTCATGCACCTCCGAAAGCAAAAAGATTTTGTTGACAGAGTTTTTAAAGATGGAGAAAATACCTGTGAAATGAAAACGGCACTTCTCAAACAGCACAAGTAGCCAATCTGTCAGCAGCACATTAAACTATCAGAGCATGAACTAAAGTGTATGGGTTATTTTAAAGTTTGTAATATAAAGCATGACTTCAGGACAAAGTGGACTCTGTTTGTCACTATTATTCCGATGCGCTCATATTAAACTGTTGCATTTAAATATAAGTCGCATTGCTAACCATGTTGTTAAATATATCACTATGTTGCACAAACTCGTCATACCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20788
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064969 | None | None | 321 | None | 4 |
ENSDART00000075601 | Nonsense | 893 | 1445 | 28 | 45 |
ENSDART00000125089 | Nonsense | 893 | 1659 | 27 | 45 |
ENSDART00000128777 | Nonsense | 893 | 1445 | 28 | 44 |
Genomic Location (Zv9):
Chromosome 6 (position 42247941)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42318995 |
GRCz11 | 6 | 42316531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACTCCTCTGGTGACAAGTCACAGCTAGAGGGAGCAGCAGATGCAGAA[G/T]AGTCCCAACCGGTAAAAACCCCATATATTGTCTCTACTTTTATTTACACT
Long Flanking Sequence:
TTTATATGTGTTTTACTCAACAAATGTTATTAAAGTTTATGATGTTTACTGGAAATTCACAGCTCATGCACCTCCGAAAGCAAAAAGATTTTGTTGACAGAGTTTTTAAAGATGGAGAAAATACCTGTGAAATGAAAACGGCACTTCTCAAACAGCACAAGTAGCCAATCTGTCAGCAGCACATTAAACTATCAGAGCATGAACTAAAGTGTATGGGTTATTTTAAAGTTTGTAATATAAAGCATGACTTCAGGACAAAGTGGACTCTGTTTGTCACTATTATTCCGATGCGCTCATATTAAACTGTTGCATTTAAATATAAGTCGCATTGCTAACCATGTTGTTAAATATATCACTATGTTGCACAAACTCGTCATACCGCCCAGCCCTATTGTATAGTATTTTGTTGCTTAGAGTCATCTGGAAGGAAGAGGAAGGCCTCAGCGAGTAAAAACTCCTCTGGTGACAAGTCACAGCTAGAGGGAGCAGCAGATGCAGAA[G/T]AGTCCCAACCGGTAAAAACCCCATATATTGTCTCTACTTTTATTTACACTCACTGAAACAAACATCTGGTAGACTGACTGTGAAACTGGGCTGTTTCAAATGGAAATTGAAAACATATTTCTTCTGAGTTATTTGGGGCATTGTGTCACCTGGCAAGACACTGCAGAAAAGTAGCAGAAAAATACTGTAAAAATGAATTGAAGTTATCACCATACTTAATTAAGAAATGCAAAAATAATTGTCATAAATGAGCAAACAAGACATTATGTCATTACATATGAACAAACTTGCACACATTGTTAACAATCATCTGAACATAGGATGAATTCTGGTTTACTTGTTTTCTTAGTTGACATATTAAAGCCTAAAATATTGCGAACAGACAGGGGCTTTGCGATTTGTGAGATTTTTATTTATTATTTTTTATTTTTTCTATAATTTTTACAACTTAATGAATAATAATAAACACATGTGACGTCTATGTATTTCTACCATGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18469
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 |
---|---|---|---|---|---|
ENSDART00000064969 | None | None | 321 | None | 4 |
ENSDART00000075601 | Nonsense | 1407 | 1445 | 43 | 45 |
ENSDART00000125089 | Nonsense | 1407 | 1659 | 42 | 45 |
ENSDART00000128777 | Nonsense | 1407 | 1445 | 43 | 44 |
Genomic Location (Zv9):
Chromosome 6 (position 42224274)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42295328 |
GRCz11 | 6 | 42292864 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGTTTGTTTTGTTTTTGCAGGGTGAAGAGATTCTCTCTCAGAGGTCA[C/T]AGGCAGCTGATGAAGAGGAGGAAGAGTCCTCTCAGCTACAGAGCGAAGCA
Long Flanking Sequence:
TTTTAAATAGAGTGATGGTGCAATTAAGCATTAACAGTGGTTTCAACCATTATAGGGGTGGCCAAATGTATATTAATATTACCTATTATTAGAATTATTAACATTATTATTTATAAGTGTATCTGCATCTGCCTCGTAAAACATGTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGGGAACCCAGATTAATAAAGGGACTAAGCTGAAAAGAAAATGAATGAATTAATTAATTATTTAAAATACAGATCAGAGTGAAATATTTCTCGGTATTTAACAACTGACCCCCCTATACATCTTGTTATGACCTTCTTCAGGAGGGATCGAGTGTTAATCAGGGTTGTTAATCCCCCCTAAACTCCCCTGTAATTCGCACCCTGGATATAAGGACACCATTTGGAGCACTGGGTGCAGTTTAGTATTTCTGGATTATACAGAGATGTAAAACATTTTTGTTTGTTTTGTTTTTGCAGGGTGAAGAGATTCTCTCTCAGAGGTCA[C/T]AGGCAGCTGATGAAGAGGAGGAAGAGTCCTCTCAGCTACAGAGCGAAGCAGAGGTAGGTTGGCCTCCATTTTTCGACATAAATGCTCTTGTAATCTAATCTGCTGGAATTCTGAACATAAACTGTTTATTCCTACTGCACAGGATGCACAATAAGATGTGAACTTTGCTGATGGGAAATTAAATATTTTTGTTACAATGCCAAAAAATCATTCATTTCTTTGCTTTACATGCAAGTGTTGTAATCTAGGTCAATTGATTAGTGTTATTCGATCTAACATTTTATCATTTGCTGTTTTTTATTTTTATTTTTAAAGAAGGCTCTCAAGCTCAAAGGCTTTTTATTTCAATAATGTTGAAATTTTGGTAATGTTGTGAAATATTATTACAATTCAAAAGAGTTCTTTTTCTACTTTATGTGTTTTGATGCTTGTGATAACAAAGCTAAACTTTCAGTATCCATTGACCGGAGAAAAACAATTGAACAACACTGGATAAAATT
Associated Phenotype:
Not determined