ZMP
ifi30
Ensembl ID:
ZFIN ID:
Description:
interferon gamma inducible protein 30 [Source:RefSeq peptide;Acc:NP_001006057]
Human Orthologue:
IFI30
Human Description:
interferon, gamma-inducible protein 30 [Source:HGNC Symbol;Acc:5398]
Mouse Orthologue:
Ifi30
Mouse Description:
interferon gamma inducible protein 30 Gene [Source:MGI Symbol;Acc:MGI:2137648]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39829 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17401 | Nonsense | Available for shipment | Available now |
sa19758 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa39829
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078866 | Essential Splice Site | 45 | 255 | None | 7 |
The following transcripts of ENSDARG00000056378 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24532389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25107166 |
GRCz11 | 2 | 24762800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCCTTCACAATGGTGCAGCTCCGAGGACATAGCAGCTGAATGTGGGG[T/C]AAGAGTGACTCCTGTACCAAAACAAATGTAACTTTAGCAACCTTTTCTAC
Long Flanking Sequence:
AAAACACCGAGGGGTTTTCAGCAAGTTCAACGTGCTCTATTAAATTACAGAGAATTCATTCTTCTAAGCGAAAGAAAATAAAGTTCCTTATTGAAGTACATACAATTTTGGAGGGAATCTTAAGAATCTGCTCCTATGTAAAAACAAGAACTTCCCCAGAATGATAACCGTGTTGTGCCCATAGACTGTAAAACAGGTTGTGCCCAGCATTTACAGTGCTGTGTTTTGCCGGATTCTGATGACGTCACAACCTCAACCAATCGAAATATCGCACCTTTTTCGCTGGAGGAAGAAGAAAGTTTAAAATGTAGGACGTCCAGATTTTTATTCAGACTTCAAGACAAGCTGAACACTGGGAATCATCATGTTCGGCTTTAACCTGTGCGTTGTGCTCGTCGCCGTGTTTTCTCTGAGTAAATGCAGCGCTCGGTTTGTTTACTCCTGTAAATATCCGCCTTCACAATGGTGCAGCTCCGAGGACATAGCAGCTGAATGTGGGG[T/C]AAGAGTGACTCCTGTACCAAAACAAATGTAACTTTAGCAACCTTTTCTACTTAAATTGGATAAAATGAAACCAGAAGACGGTACGTTTTGTTTTTATTCATTTGTGACTATACATGTGGGGTAAGTGAAAACCAAAGCCAACTTAATTTACTACTTCCTCTTTTCATGAAAATAAACCGCTGGAGTCTCTATTATATCTGTAACTAGTCATTTGTGTCCGTACGTTTGCTTGCCACAAAAAAAAGTGAAGTTGAAGTCATTTGAAGTTTTTTTCAGGAATATTTGTGCTCTGACGTTTATTAACTCTTCTCTTTATTTGCTCGGCGCTTTCGGGGAAATCCCTACGTTTTGGGGACGTCGAGATGAGTGTGCACGAAACTTACTGTTCCCTTTATTCTCATTTAAGGTGCTGGAACAATGCATGAAGTATAACTCGACAAAGGCCGCTGACAAGGTGAAAGTGAGCCTCTACTATGAATCTCTGTGCCCAGGATGCAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17401
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078866 | Nonsense | 53 | 255 | 2 | 7 |
The following transcripts of ENSDARG00000056378 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24532819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25107596 |
GRCz11 | 2 | 24763230 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTACTGTTCCCTTTATTCTCATTTAAGGTGCTGGAACAATGCATGAAGTA[T/G]AACTCGACAAAGGCCGCTGACAAGGTGAAAGTGAGCCTCTACTATGAATC
Long Flanking Sequence:
TTTGTTTACTCCTGTAAATATCCGCCTTCACAATGGTGCAGCTCCGAGGACATAGCAGCTGAATGTGGGGTAAGAGTGACTCCTGTACCAAAACAAATGTAACTTTAGCAACCTTTTCTACTTAAATTGGATAAAATGAAACCAGAAGACGGTACGTTTTGTTTTTATTCATTTGTGACTATACATGTGGGGTAAGTGAAAACCAAAGCCAACTTAATTTACTACTTCCTCTTTTCATGAAAATAAACCGCTGGAGTCTCTATTATATCTGTAACTAGTCATTTGTGTCCGTACGTTTGCTTGCCACAAAAAAAAGTGAAGTTGAAGTCATTTGAAGTTTTTTTCAGGAATATTTGTGCTCTGACGTTTATTAACTCTTCTCTTTATTTGCTCGGCGCTTTCGGGGAAATCCCTACGTTTTGGGGACGTCGAGATGAGTGTGCACGAAACTTACTGTTCCCTTTATTCTCATTTAAGGTGCTGGAACAATGCATGAAGTA[T/G]AACTCGACAAAGGCCGCTGACAAGGTGAAAGTGAGCCTCTACTATGAATCTCTGTGCCCAGGATGCAGAATGTTTCTTACATCTCAGCTCGTGCCAACCTTGATTATGTTGCAAGACATCATGGAGATTGATCTGGTTCCATATGGAAACGCACAGGTATATTTACACTACTGCACGCCGCTCTTTAGGCAGTTTACTTATAGTGTGAATAGTCTATCACAACTTGAGAAACGTGATTTTTTTCCCTTCACAATTCTAAATATTTAAATCACAATGTCCCTTTTCCTACACTTTGTAAATATATTTGTATATAAATATATTTTTATTGGTATTTAACAAAACTATACATGGTACTGTATAATACAGAATTAAAAAAATGGCAGACTTAATTTTTCCCCCCACTATCCCCTCAACATAAATTTATGAAATAAAAACAAACATCCTCTGAGAAAAAAAAACAACCTAAATTTGTTTTAACAAGTTAACAATAAAAGAGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19758
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078866 | Nonsense | 72 | 255 | 2 | 7 |
The following transcripts of ENSDARG00000056378 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 24532876)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25107653 |
GRCz11 | 2 | 24763287 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGGCCGCTGACAAGGTGAAAGTGAGCCTCTACTATGAATCTCTGTG[C/A]CCAGGATGCAGAATGTTTCTTACATCTCAGCTCGTGCCAACCTTGATTAT
Long Flanking Sequence:
GCTGAATGTGGGGTAAGAGTGACTCCTGTACCAAAACAAATGTAACTTTAGCAACCTTTTCTACTTAAATTGGATAAAATGAAACCAGAAGACGGTACGTTTTGTTTTTATTCATTTGTGACTATACATGTGGGGTAAGTGAAAACCAAAGCCAACTTAATTTACTACTTCCTCTTTTCATGAAAATAAACCGCTGGAGTCTCTATTATATCTGTAACTAGTCATTTGTGTCCGTACGTTTGCTTGCCACAAAAAAAAGTGAAGTTGAAGTCATTTGAAGTTTTTTTCAGGAATATTTGTGCTCTGACGTTTATTAACTCTTCTCTTTATTTGCTCGGCGCTTTCGGGGAAATCCCTACGTTTTGGGGACGTCGAGATGAGTGTGCACGAAACTTACTGTTCCCTTTATTCTCATTTAAGGTGCTGGAACAATGCATGAAGTATAACTCGACAAAGGCCGCTGACAAGGTGAAAGTGAGCCTCTACTATGAATCTCTGTG[C/A]CCAGGATGCAGAATGTTTCTTACATCTCAGCTCGTGCCAACCTTGATTATGTTGCAAGACATCATGGAGATTGATCTGGTTCCATATGGAAACGCACAGGTATATTTACACTACTGCACGCCGCTCTTTAGGCAGTTTACTTATAGTGTGAATAGTCTATCACAACTTGAGAAACGTGATTTTTTTCCCTTCACAATTCTAAATATTTAAATCACAATGTCCCTTTTCCTACACTTTGTAAATATATTTGTATATAAATATATTTTTATTGGTATTTAACAAAACTATACATGGTACTGTATAATACAGAATTAAAAAAATGGCAGACTTAATTTTTCCCCCCACTATCCCCTCAACATAAATTTATGAAATAAAAACAAACATCCTCTGAGAAAAAAAAACAACCTAAATTTGTTTTAACAAGTTAACAATAAAAGAGTTAAAAAAAAGTAAAGAAAAGAAATAGATGAAAAGATCGCTTTAAGTAGACAATAATTGCT
Associated Phenotype:
Not determined