ZMP
ENSDARG00000075992
Ensembl ID:
Human Orthologue:
GIN1
Human Description:
gypsy retrotransposon integrase 1 [Source:HGNC Symbol;Acc:25959]
Mouse Orthologue:
Gin1
Mouse Description:
gypsy retrotransposon integrase 1 Gene [Source:MGI Symbol;Acc:MGI:2182036]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31352 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33289 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8491 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2125 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa31352
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109820 | Nonsense | 16 | 299 | 1 | 6 |
ENSDART00000126813 | None | None | 280 | None | 8 |
Genomic Location (Zv9):
Chromosome 3 (position 43436273)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42473207 |
GRCz11 | 3 | 43179222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGTCAAATCTTGCTGCACTACCAACGGGTCATGGAGGGTGACAAATA[T/G]AACTCATTGAAACAGTTTCTTCTTTTTGGAGAATATCCAAAAAATGCAAA
Long Flanking Sequence:
TTTTAAAGGTGACCATAAACAGCGTTGTTTTCGCATTTACTGTTTCTGATTAAGCAAGCGAAGGTGATATCCTGCAAACATTTGAAGAGAAATTATGGCTCTTCATTCATTAAACGTGTATTCCCGTTACTAATAATAATAATTTTACATAGCCTATCTTTGTGGTATTAGTAGTGTGTATAAACTGAAGAAAAAAAATCTGTATAAAATATGTGAATAATAATACAAATAAAAAGACATATTTAAACACAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATTTATTTATTTTTACAAGATTTCCTAATAGGTACGATACGTAGATATCCTGCACACGTAGATCACGTGGGTTGTTCAGCATCCATTATTGAAATTGCGCGCAATTATTTGATTTAGTCAAATCTTGCTGCACTACCAACGGGTCATGGAGGGTGACAAATA[T/G]AACTCATTGAAACAGTTTCTTCTTTTTGGAGAATATCCAAAAAATGCAAACAAACAGCAGCGTTTTGTATTGAAACGACGAGCTGGGAAGTTCTGTATGATAGGTAAGTCAAATAAAAGCGCACACATCAAAGATAACTTAGGCCCCATTAGTTAACTCTTCTTTTAGCACTGTAAAAACAAATATAACATTTTAATTAAAAAAAATGCAAAAAGACAACAAAACATTGTAAATCGCAATTAAAATTTTGGTTTTATTTCAGACCAATTTAACAATATAAAATATTGCAGAGTTTAATAAGATTTTTTTAAATAGTGTTGGCATGTCTTTCCACCAAAAATTATGTTAAGAAGACTGGTTTCCATCCATCCTTATGATGCGTTTCCACTGGGACCTTGGTAGCGGAATGTTTTCAATTAATTCATATGGAAGTTAAGCAGAAAACCCAGTCTTCACCATCACGTTCTTAGAAGCAGCAACAGTGAAAGCAGAAAGTTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33289
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 |
---|---|---|---|---|---|
ENSDART00000109820 | Nonsense | 40 | 299 | 1 | 6 |
ENSDART00000126813 | None | None | 280 | None | 8 |
Genomic Location (Zv9):
Chromosome 3 (position 43436202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42473278 |
GRCz11 | 3 | 43179293 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTTGGAGAATATCCAAAAAATGCAAACAAACAGCAGCGTTTTGTAT[T/A]GAAACGACGAGCTGGGAAGTTCTGTATGATAGGTAAGTCAAATAAAAGCG
Long Flanking Sequence:
CTGCAAACATTTGAAGAGAAATTATGGCTCTTCATTCATTAAACGTGTATTCCCGTTACTAATAATAATAATTTTACATAGCCTATCTTTGTGGTATTAGTAGTGTGTATAAACTGAAGAAAAAAAATCTGTATAAAATATGTGAATAATAATACAAATAAAAAGACATATTTAAACACAGACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATATATATATATATATATATATATATATTTATTTATTTTTACAAGATTTCCTAATAGGTACGATACGTAGATATCCTGCACACGTAGATCACGTGGGTTGTTCAGCATCCATTATTGAAATTGCGCGCAATTATTTGATTTAGTCAAATCTTGCTGCACTACCAACGGGTCATGGAGGGTGACAAATATAACTCATTGAAACAGTTTCTTCTTTTTGGAGAATATCCAAAAAATGCAAACAAACAGCAGCGTTTTGTAT[T/A]GAAACGACGAGCTGGGAAGTTCTGTATGATAGGTAAGTCAAATAAAAGCGCACACATCAAAGATAACTTAGGCCCCATTAGTTAACTCTTCTTTTAGCACTGTAAAAACAAATATAACATTTTAATTAAAAAAAATGCAAAAAGACAACAAAACATTGTAAATCGCAATTAAAATTTTGGTTTTATTTCAGACCAATTTAACAATATAAAATATTGCAGAGTTTAATAAGATTTTTTTAAATAGTGTTGGCATGTCTTTCCACCAAAAATTATGTTAAGAAGACTGGTTTCCATCCATCCTTATGATGCGTTTCCACTGGGACCTTGGTAGCGGAATGTTTTCAATTAATTCATATGGAAGTTAAGCAGAAAACCCAGTCTTCACCATCACGTTCTTAGAAGCAGCAACAGTGAAAGCAGAAAGTTTCCTGATGAAACTTGTGTAAGGGTGTTTTTTCCGCCAAGCGAAACGCAACACCAGCTGAAGCACTGTGCAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8491
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109820 | Essential Splice Site | 51 | 299 | None | 6 |
ENSDART00000126813 | None | 3 | 280 | 1 | 8 |
Genomic Location (Zv9):
Chromosome 3 (position 43433267)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42476213 |
GRCz11 | 3 | 43182228 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATTGCTTAATACTGTTTTTATAAGATCTTAATACTTTAATTTRTTTTC[A/C]GAGGATGAATTGTTTTACATAAAAAACAATGCCCACAAAGAACAAAAATG
Long Flanking Sequence:
TGTCACTGCTCTAAATATATATGTTATATATATGTTATTTATACACAAAAGACTGGCTTGTTTTGTTTTCTAGTAAATTTGCTTACTACGTTCATTTTATTTATTTATTTATTTTTTCAAGCTTAGAGTGCTTACAGATTTTCTTTTATGTATATTTCAGATATGACTGTTTAACTTTGTTGGCTAGTTTTAGATTTTGGAATGAAAGCAAAACCCAATTATGGAATATCAAAGTACCAAAATTGTGTAAATCATAACTATATTGTGTATTTATTGTTTTCTTTATAGATTATGATATGGTGATTTAACATTTTAGTTATAATGGCTAAATGTATCCCCTAGTTGCCATTACTTTAAAGGTAAGCTTATTGGGATTGACAAAATTTTGCAGTTAGGCCTATTCCTTTTTCACTCCAAATGTGTGAAGAAGGCATATTAAATTGGAGCTTAATATTGCTTAATACTGTTTTTATAAGATCTTAATACTTTAATTTGTTTTC[A/C]GAGGATGAATTGTTTTACATAAAAAACAATGCCCACAAAGAACAAAAATGTAAAGTTGTCTGCAGTGCGGAGGAGGCAGATGCACTGTTTAAGCAATTTCACTGCAGTGACATGGGTGCACATGTTGGACAACTCAAGACGAGAGATGCCATTTCTCAGCGCTTTTATTGGCCTGGCATGTCTGCAGACATTGAAAAATGGGTATGCTTATTAACACTTAAACTAATATGTTTATATGACAACGTATAATATGCAAACAACTCATATATTTTCTGTTACCAGGTGTCGGAATGTTCAGTCTGCCAAAGAAATAAAAAAACCCTAAAGCTTGACACAGACTACACACCTATTAAGGTACAACGTCTAAATGTATATTTTAAAAAATTAAATGAATGAATGGATATATTAAAAGTAGGTAATTTCAAAGAAAATATGTTATTCTGAAATTTGTATTTTTGTACAGCCTATTTAAATTGATTAATGATTGTTATGTTTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2125
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109820 | Nonsense | 264 | 299 | 6 | 6 |
ENSDART00000126813 | None | None | 280 | None | 8 |
Genomic Location (Zv9):
Chromosome 3 (position 43431581)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 42477899 |
GRCz11 | 3 | 43183914 |
KASP Assay ID:
554-3355.1 (used for ordering genotyping assays)
KASP Sequence:
CTTTATTTTATCACATGTTTTTTAGGGTCCTATCTAAACTGGTAAAGGAC[A/T]AACCAAATACTTGGGACCAGTATTTGGATGCTGCCATGTTCGGACTTCGA
Long Flanking Sequence:
TAAGTGGGTTCAAGTCAAGTCAACTCAAAAATGTTCTGAAGTTTGTTGCCTTAAGATTTTAGGTTGAGTCACCTTTTTTTACAGTGTAGTTTCAGGGTAAATATACAGTGATTAAATTACTTATTGTCTGGAAAAAAGTAGTTACTGTTCAGTTTAGGTATACTTTAATAATTGTTGCTTCTCTTAAATCTTTTAAAGTCTTTAAATGACACCTTTTAAGCTAAACACTATCATCTTGCAAATAGCTAGTAAAATATTATGTACTGTTATCATAGCAAAGACAAAAAAGAATTACTCATCATTAGTTAATACAACTATTGTGTTTAAAACTATGTTAAGTGGAACTTATTTATAAACATTTGACAGAATTTTGCATTTCTTTAAAAAGAGTTACAATGTCACAGGACGGCTAATACCTTTGACTTCAACTGTATATTTGTACAGCCTTCTCTTTATTTTATCACATGTTTTTTAGGGTCCTATCTAAACTGGTAAAGGAC[A/T]AACCAAATACTTGGGACCAGTATTTGGATGCTGCCATGTTCGGACTTCGAACAAAGAAGCAGCTGACCACCCAATTCTCCCCATTTTACTTGATGTTTGGAAGAGAGGCACGCTATCCATGCGAAGTCCCTGAACATTTTGAGGTATTTTGTTGTAAATATTCTGGATTCGTTTTATGTCATTGCTATGTTAAGCTAAGTTATTTATTACCATTTTCCACAGCTTGATGGTTCATTTGAAAATGACTTCACCGAAGACATTGCCATTGACATCAAACGACATGAAAAAATCATGAACATTGTTGAAGACAATGTAAATAAATCTATCTCAAGGACAAGAAAAAGGCTGTCAAAGAAGGCACAATTTAGCCTTCAGGTGGGAGCAAAAGTGTGGAGAAGAAATGTCCGGAGTGAGCAGAGGAAAGGGGGGAAACTAGACCCTGAGTATTTTGGTCCCTTTGTGGTGACCAAAATACAAGGGAAGAGTGTTGATCTTGTGGA
Associated Phenotype:
Not determined