ZMP
ing3
Ensembl ID:
ZFIN ID:
Description:
inhibitor of growth protein 3 [Source:RefSeq peptide;Acc:NP_957231]
Human Orthologue:
ING3
Human Description:
inhibitor of growth family, member 3 [Source:HGNC Symbol;Acc:14587]
Mouse Orthologue:
Ing3
Mouse Description:
inhibitor of growth family, member 3 Gene [Source:MGI Symbol;Acc:MGI:1919027]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1532 | Nonsense | F2 line generated | Not yet available |
sa16070 | Essential Splice Site | Available for shipment | Available now |
sa6930 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa18549 | Nonsense | Available for shipment | Available now |
sa40231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15341 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1532
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037140 | Nonsense | 70 | 416 | 4 | 12 |
ENSDART00000122636 | Nonsense | 70 | 416 | 4 | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9670940)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10607567 |
GRCz11 | 4 | 10606416 |
KASP Assay ID:
554-1456.1 (used for ordering genotyping assays)
KASP Sequence:
GAAGATAATATGCTTTCCTAATRATCTCTTTCTGTTTACCAGGACTACTA[T/G]AAAGCTTTAGAAGATGCGGATGAAAAGGTCCAATTAGCCAATCAAATTTA
Long Flanking Sequence:
TGCTTATTATTTGTTAATGTTAGTAAGTAATTGCATTAGCTAATGTTTTCCAATGCAATCTTATTGTGAAGTGTTACCCATATTGTTTACTCCCGGAATCAGCTGCAAAATATATTGAACAATAAAAATTATATTGCAATTTAATTTAATAAAACATCTAAACTACATTCTAAGTGAAGCACAACATTTGCTTAACTGATATAATAAAGTTTGTATGTATAAGATGAGATCTTTACGCTGAAACTGACAGTGCATATTTTTTGTTACTAGCAAGATATGATATATTATTTTTTTGTTTTTATTTCATTTGTTATTCAATATTTTCCTTATTTTCATTATTATTTTTTAAATTGCATAATGATGAAATAATGATGAAATCATGATGAAACAACTGCTGGTTAAGTCATAACAATGATTGATAAAAAATTAATAATGGATAGTTTTGCATTAGAAGATAATATGCTTTCCTAATGATCTCTTTCTGTTTACCAGGACTACTA[T/G]AAAGCTTTAGAAGATGCGGATGAAAAGGTCCAATTAGCCAATCAAATTTATGACCTGGTGAGTAATTTACTGTAACTAGCAACACTAGCCTTTGTGTCAGTACTGTATGGTCCCAGTAGGTGGCAGCACATCACTAATAGTAAAAAGCCAATGGATTTCTGGGAAGCTTTTTTGTTTGCTATTTAAATGCATACTAATGCTTTTTCGTGAGATTTAATAGACGTTTTTAAATACATTTTTCCTAATGAGAAGTGACATTTGAACTTGTGTGTGGGTTTGTGTAATCCGTTGTGTGTTGATCTTGTGCCTCTTATGTAGGTTGATAGACATTTACGGAAGTTGGATCAGGAGTTGGCAAAGTTTAAAATGGAGTTGGAAGCAGATAACGCTGGCATCACAGAGATCCTGGAAAGACGTGAGTGACGCCTCTCAATCACCTTTTTTACAGATAACTGGCTAATTTCAAAAGATAAAAAAGGTAGGAGTTGGCAAGTTTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16070
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037140 | Essential Splice Site | 239 | 416 | 8 | 12 |
ENSDART00000122636 | Essential Splice Site | 239 | 416 | 8 | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9673485)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10610112 |
GRCz11 | 4 | 10608961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGTGCTATTTCCATGGCAGCAGCTCAGGCAGTGCAAGCCACAGCACAGG[T/A]AAACCGCCTAGTTTTACAYTACACYTAATTTCCTGTTCAAACTATTTTKG
Long Flanking Sequence:
CAGCTTAATGAAAATGTGCATTAGAGTCATTTTTAATTTTTTATTTCCAGCTAAATAATTGCAAACATATTGAGAATATTTTTTATAACCACACAATCCTAATCCTAATTACAGTGACAAGGGAAATGAACCACAATAACAATTTGTCATAATCATACAGGCACATATGTTTATTGTGTGTGGTAACTGCTTAAATGGTTCTCAAGAAACGAGCTTTATGATGCAATGAGATTACTGATCACTTATGTTGCGCTGTTTCTCACAAATGTTTTCTGGTCATATACTGAATGTGATTTTTTTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTTGCAGGCTGCAGAGCGAACAGCACATCCTCCTCTAACAGCATGTATAACGTCAACTCGTCCCAATCACTCACCTCCTCATACAACCTGAGCCCACTTCCGGCCGGGCCTGCAGCAGGAGCGGGTGCTATTTCCATGGCAGCAGCTCAGGCAGTGCAAGCCACAGCACAGG[T/A]AAACCGCCTAGTTTTACACTACACTTAATTTCCTGTTCAAACTATTTTTGGCCTCATAGGAGTCTCTTTCATACTTCCTCCAACGGTTATTTTCGTGTCAGTTATTATGTTATCGAAGCCGGTGTTAATTTCAGCACTCACTGCACTTTAGTATTATAACTCGAGGGAAATCACATCGACACATCCTGTCCTGTATTTTTAGATTATTTTCATTATTGGTGTTTCTTATTTAATTCTAGTGAGACTCCATTTTTCAATCACCTTTTGCTTTTGTTGTTATTGTGTGTATTTTTTTTTGTTATTACATTTTTGATACACTGGTAAATAATATAAAACAAATTACCGCAGTCTTTCATGTAGCGGGTTTCTTGGAAATGATTAACCCCTGTTTGTACAGGCTTTTAAGATGGTTTTTTGTTAATTTGACTGATCACAGATCATCAATGGAGATATGTTTTTCTTTATTGGTAGTGTTTGAATTACTCTCTTGTGTACTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6930
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037140 | Nonsense | 250 | 416 | 9 | 12 |
ENSDART00000122636 | Nonsense | 250 | 416 | 9 | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9675497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10612124 |
GRCz11 | 4 | 10610973 |
KASP Assay ID:
554-4542.1 (used for ordering genotyping assays)
KASP Sequence:
AAAYACTGTGTGTGTTTCAGATGAAAGAGGGCAGGAGAACATCCAGTCTC[A/T]AGGCCAGTTATGAAGCGGTCAAGAACAATGATTTCTTGGGWCGAGATTTT
Long Flanking Sequence:
ATAACGGATGAAAAATAGCCTTTTTCTAGTACTTCTGGTGCACTTTCTGCAATGCTAATTAATGTATACTGTCCCTGCCAAATATATAATTATATATACAAATATTATCTGGAGAGACTTAAAATGAAATATTTTTAAATGTGAATCCTTCCAGAATTGTGCAATGTTTTTAACAAAAGTAAATCTTAAAAAACTGTTTTAGTTTTTTTTATCTTATTATTTATGCATTTATCTTATGTATTATTTGTTGATGTTGATGACTTTTTATAGTTAAAATATTTGTATAATTATAGAAAAGTGGTATTTCTAAAACGTTGTAAACTTGATTATTTTTTGATCCATGGCATAGGCAGAGAAGCTGGTATGGCATTAAATAAATAAATGAAATACAATAAAAACTAAATGCATGAAAATCTAAGCTAATTTCAAATATATTTAATAGTTTATAAAAAATACTGTGTGTGTTTCAGATGAAAGAGGGCAGGAGAACATCCAGTCTC[A/T]AGGCCAGTTATGAAGCGGTCAAGAACAATGATTTCTTGGGTCGAGATTTTACCATGAGTCGAGACTCCAGCAGTTACTCGTCTTCTGCGTTGGCCAGTACGCTCACGCAACCCCTCACATCCACCAACAGCTCTGACTCCCGCACAGCACGCAAGACCAAGTAAGACACACACACACAGGTGCCACAATAAAGAGCCACGTGACCATGCTCGATTTTAAACACTTCATTGCGTTTTTTTTTTCCTCCAGAAGCAACACTAAGTCTTCCAACCACCAGTCCTCTTCATCCTCCTCTTCCTCTTCACTGTCATCCTGCTCGTCATCTTCAGCTTTGGCTCATGAACTGGTACAAACCACAGTCACAGAAACAGACACCAGCAGTCAAGTGGACTGGACTTACGACCCCAATGAACCCAGATACTGCATTTGTAACCAGGTACATTTATGTAGCATCATCTCTCATGCAGTGTATGCATTTAAAATGAACTATCTAATGAAAA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
See FAQs for more info.
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
swim bladder ZFA:0000076 |
aplastic PATO:0001483 |
abnormal PATO:0000460 |
Mutation Details
Allele Name:
sa18549
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 |
---|---|---|---|---|---|
ENSDART00000037140 | Nonsense | 253 | 416 | 9 | 12 |
ENSDART00000122636 | Nonsense | 253 | 416 | 9 | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9675508)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10612135 |
GRCz11 | 4 | 10610984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RTGTTTCAGATGAAAGAGGGCAGGAGAACATCCAGTCTCWAGGCCAGTTA[T/A]GAAGCGGTCAAGAACAATGAWTTCTTGGGWCGAGATTTTACYATGAGTCG
Long Flanking Sequence:
AAAATAGCCTTTTTCTAGTACTTCTGGTGCACTTTCTGCAATGCTAATTAATGTATACTGTCCCTGCCAAATATATAATTATATATACAAATATTATCTGGAGAGACTTAAAATGAAATATTTTTAAATGTGAATCCTTCCAGAATTGTGCAATGTTTTTAACAAAAGTAAATCTTAAAAAACTGTTTTAGTTTTTTTTATCTTATTATTTATGCATTTATCTTATGTATTATTTGTTGATGTTGATGACTTTTTATAGTTAAAATATTTGTATAATTATAGAAAAGTGGTATTTCTAAAACGTTGTAAACTTGATTATTTTTTGATCCATGGCATAGGCAGAGAAGCTGGTATGGCATTAAATAAATAAATGAAATACAATAAAAACTAAATGCATGAAAATCTAAGCTAATTTCAAATATATTTAATAGTTTATAAAAAATACTGTGTGTGTTTCAGATGAAAGAGGGCAGGAGAACATCCAGTCTCAAGGCCAGTTA[T/A]GAAGCGGTCAAGAACAATGATTTCTTGGGTCGAGATTTTACCATGAGTCGAGACTCCAGCAGTTACTCGTCTTCTGCGTTGGCCAGTACGCTCACGCAACCCCTCACATCCACCAACAGCTCTGACTCCCGCACAGCACGCAAGACCAAGTAAGACACACACACACAGGTGCCACAATAAAGAGCCACGTGACCATGCTCGATTTTAAACACTTCATTGCGTTTTTTTTTTCCTCCAGAAGCAACACTAAGTCTTCCAACCACCAGTCCTCTTCATCCTCCTCTTCCTCTTCACTGTCATCCTGCTCGTCATCTTCAGCTTTGGCTCATGAACTGGTACAAACCACAGTCACAGAAACAGACACCAGCAGTCAAGTGGACTGGACTTACGACCCCAATGAACCCAGATACTGCATTTGTAACCAGGTACATTTATGTAGCATCATCTCTCATGCAGTGTATGCATTTAAAATGAACTATCTAATGAAAACAACACATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40231
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 |
---|---|---|---|---|---|
ENSDART00000037140 | Nonsense | 262 | 416 | 9 | 12 |
ENSDART00000122636 | Nonsense | 262 | 416 | 9 | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9675534)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10612161 |
GRCz11 | 4 | 10611010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATCCAGTCTCAAGGCCAGTTATGAAGCGGTCAAGAACAATGATTTCT[T/A]GGGTCGAGATTTTACCATGAGTCGAGACTCCAGCAGTTACTCGTCTTCTG
Long Flanking Sequence:
GTGCACTTTCTGCAATGCTAATTAATGTATACTGTCCCTGCCAAATATATAATTATATATACAAATATTATCTGGAGAGACTTAAAATGAAATATTTTTAAATGTGAATCCTTCCAGAATTGTGCAATGTTTTTAACAAAAGTAAATCTTAAAAAACTGTTTTAGTTTTTTTTATCTTATTATTTATGCATTTATCTTATGTATTATTTGTTGATGTTGATGACTTTTTATAGTTAAAATATTTGTATAATTATAGAAAAGTGGTATTTCTAAAACGTTGTAAACTTGATTATTTTTTGATCCATGGCATAGGCAGAGAAGCTGGTATGGCATTAAATAAATAAATGAAATACAATAAAAACTAAATGCATGAAAATCTAAGCTAATTTCAAATATATTTAATAGTTTATAAAAAATACTGTGTGTGTTTCAGATGAAAGAGGGCAGGAGAACATCCAGTCTCAAGGCCAGTTATGAAGCGGTCAAGAACAATGATTTCT[T/A]GGGTCGAGATTTTACCATGAGTCGAGACTCCAGCAGTTACTCGTCTTCTGCGTTGGCCAGTACGCTCACGCAACCCCTCACATCCACCAACAGCTCTGACTCCCGCACAGCACGCAAGACCAAGTAAGACACACACACACAGGTGCCACAATAAAGAGCCACGTGACCATGCTCGATTTTAAACACTTCATTGCGTTTTTTTTTTCCTCCAGAAGCAACACTAAGTCTTCCAACCACCAGTCCTCTTCATCCTCCTCTTCCTCTTCACTGTCATCCTGCTCGTCATCTTCAGCTTTGGCTCATGAACTGGTACAAACCACAGTCACAGAAACAGACACCAGCAGTCAAGTGGACTGGACTTACGACCCCAATGAACCCAGATACTGCATTTGTAACCAGGTACATTTATGTAGCATCATCTCTCATGCAGTGTATGCATTTAAAATGAACTATCTAATGAAAACAACACATTAAACCAATATTGTGGCATTTAAAAGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15341
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037140 | Essential Splice Site | 378 | 416 | None | 12 |
ENSDART00000122636 | Essential Splice Site | 378 | 416 | None | 13 |
The following transcripts of ENSDARG00000034326 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 4 (position 9676611)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 10613238 |
GRCz11 | 4 | 10612087 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTTTGTGCAGGTGTCKTACGGAGAGATGGTCGGCTGTGATAACCAAGAWG[T/A]AAGTCAACCCTTCATCTTTAGGGACACACACAGACAACATTTCCTCTTCA
Long Flanking Sequence:
ATTTATGAGGAGAGTTGTAACCAATATTGAAACATTAAGTGATGGAGATTTTAATATAATCCTTATATAAACAATAGGAACAAATGCCAGGGAGGAAATGTATATGTTTATATGTTTTTAAACTATTTACACCTATATATTTTTTACAATTCTCACTGTAGAAAGTGTGTGACTGGGTTTGCAGGAGGAGTCTGGGTGTGTGTGTGCTGTTAGTTGGCATATGAGTGCAAAAGAATTGTCTCCCTAAGAATGCGTTTGTTTTATGGCCTCAAAGTGATATAGCTTTTGTCAAAGTATATCAAAAATAGAAATGTGTGTGTGTGTGTGTGCGTCTTTGAATAGTCATCAAAGACTAAACTTGCACAGTCTTTGTTTGCAGGTGCGCTTCTGTGACACTCGGCTGCAGGTGTGCACTGCTGCGTTTGTTGCTCTATGTCTCATTCTCTCTGTCTTTGTGCAGGTGTCTTACGGAGAGATGGTCGGCTGTGATAACCAAGATG[T/A]AAGTCAACCCTTCATCTTTAGGGACACACACAGACAACATTTCCTCTTCATAAAACACATACTGGATCACTCTGTCTGGGCTCTGACAGCTTTTGTGACCCCTGGGCAGCCATGATTTTTGTAGCGACGATGGCAAACAACATCAGCATTATTATTTTGAGTGAAAACGGATGTTGAACTATGTACAGTATATCGTTTGAGCATCGATATTACAGTGTGTGTCTCCAGCAATAGTCACGTTGCAGGATTAGATTATTTATTAACCATTATTTGCTGTTTGGCATGTTTTTATCCACTCTTGGGTGATTTTGAGTCTTAAATTTCGCCACAACTTTCTCTGTGTTTCAGCAAATGGAATGAATTTTGGTGATCAATCTTATTTTGGCAAATATTTTGGGGAAATGCTTTTAAAAATTCAACACTTTAGGCATATTTACTATTTTTTTTCCTCATTGACTTCCATTATAATGATATTTATTGATTGCAAATCCATGACACCA
Associated Phenotype:
Not determined