ZMP
si:ch211-218o21.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate IQ motif and Sec7 domain 1 (IQSEC1) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
IQSEC2
Human Description:
IQ motif and Sec7 domain 2 [Source:HGNC Symbol;Acc:29059]
Mouse Orthologue:
Iqsec2
Mouse Description:
IQ motif and Sec7 domain 2 Gene [Source:MGI Symbol;Acc:MGI:3528396]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34453 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa14795 | Essential Splice Site | Available for shipment | Available now |
| sa7145 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15370 | Essential Splice Site | Available for shipment | Available now |
| sa38703 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa15249 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34453
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111680 | Nonsense | 56 | 1276 | 1 | 12 |
| ENSDART00000140410 | Nonsense | 153 | 1373 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38060943)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36916358 |
| GRCz11 | 8 | 36948792 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCTGAGAGCCGCATGACACGCCGCATCATCCTCTCCAACATGCGACTG[C/T]AGTATTCATTTGATGACCGGCATCCTCAACCACCCAACCCGACTCACTAC
Long Flanking Sequence:
TTCAGAGAGTTCCAGCAAATCTCCTTACGTGCACAGTTCTGACCGCTACGGGGACAACAGCTGTGGCCCGCCAGGCCCTCGGGTGCCTTTTGTGCCCCCTCCGAGCCCAGCTAGCCTTGCCTGGGCACAACGTACACGCAACCAACCAGCTAGTCTGGCCCTTCGCAAGCAAGAGGAAGAAGAGAACAAGAGGTGCAAAGCCCTATCGGACAGCTATGAACTCTCTACGGACCTGCAAGATAAGAAGGTAAGGCATACAAAAAAAATTAATCAAGATTCGCAGCAAATCACATTCCCTTAAATTAAATATAACCACTGTCATTGTGCAGGTGGAGATGCTGGAGAAGAAATATGGCGGCTACTTCGTGAGCAGACGAGCAGCACGTACTATCCAGACAGCATTCCGTCAATATCGTATGAACAAGAACTTTGAGCGCTTGCGCAGCTCAGCATCTGAGAGCCGCATGACACGCCGCATCATCCTCTCCAACATGCGACTG[C/T]AGTATTCATTTGATGACCGGCATCCTCAACCACCCAACCCGACTCACTACAGTCACAGTCCAGGAATGGGTCCTCCGCATTCTCCAACCAGCACCACAGAGCCAAGCTCTCCACGGCCAGAGTACACCCAACTGGAGGACACTTTCTCCAAACAAGTTAGTACTCAGTTGACTCTATCATAGCATGTGCTGGATGCCTTCCTTTAATACTCTAGGTAAATAAAGAAGCCAGAATCCTCTCTTCACTTTATTTCTTAGTTAAAGCTTTGTTTAGGGCCATCTATTGTTATGTCGTTCAAAAAATAATTGGATTCATACCTTACCACAATGTATCTTGATGGGTTCTGCGAATGAAGCCAATGTTGACTTCAGGAAAAGAATGAATAAAAATACACTTTTAATAATAAATTTATTCCAGTAAAAAAGAAGAATTAAACAAATACAAGAACAAAACTAAATTCTTTACTTTATCTCTCACTGAAAATAAAGGACCTAAGACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14795
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 |
|---|---|---|---|---|---|
| ENSDART00000111680 | Essential Splice Site | 107 | 1276 | 1 | 12 |
| ENSDART00000140410 | Essential Splice Site | 204 | 1373 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38061099)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36916514 |
| GRCz11 | 8 | 36948948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCCACGGCCAGAGTACACCCAACTGGAGGACACTTTCTCCAAACAA[G/A]TTAGTACTCAGTTGACTCTATCATAGCATGTGCTGGATKCCTTCCTTTAA
Long Flanking Sequence:
GGCCCTTCGCAAGCAAGAGGAAGAAGAGAACAAGAGGTGCAAAGCCCTATCGGACAGCTATGAACTCTCTACGGACCTGCAAGATAAGAAGGTAAGGCATACAAAAAAAATTAATCAAGATTCGCAGCAAATCACATTCCCTTAAATTAAATATAACCACTGTCATTGTGCAGGTGGAGATGCTGGAGAAGAAATATGGCGGCTACTTCGTGAGCAGACGAGCAGCACGTACTATCCAGACAGCATTCCGTCAATATCGTATGAACAAGAACTTTGAGCGCTTGCGCAGCTCAGCATCTGAGAGCCGCATGACACGCCGCATCATCCTCTCCAACATGCGACTGCAGTATTCATTTGATGACCGGCATCCTCAACCACCCAACCCGACTCACTACAGTCACAGTCCAGGAATGGGTCCTCCGCATTCTCCAACCAGCACCACAGAGCCAAGCTCTCCACGGCCAGAGTACACCCAACTGGAGGACACTTTCTCCAAACAA[G/A]TTAGTACTCAGTTGACTCTATCATAGCATGTGCTGGATGCCTTCCTTTAATACTCTAGGTAAATAAAGAAGCCAGAATCCTCTCTTCACTTTATTTCTTAGTTAAAGCTTTGTTTAGGGCCATCTATTGTTATGTCGTTCAAAAAATAATTGGATTCATACCTTACCACAATGTATCTTGATGGGTTCTGCGAATGAAGCCAATGTTGACTTCAGGAAAAGAATGAATAAAAATACACTTTTAATAATAAATTTATTCCAGTAAAAAAGAAGAATTAAACAAATACAAGAACAAAACTAAATTCTTTACTTTATCTCTCACTGAAAATAAAGGACCTAAGACTGACAGTATACAGAAGTCTGTTTAAGCGTGCTCCTGGTTTGTACTTTTATACTGTATTCAAGCCTTTGAATACAAAAGTGCCCCTAATGTTTTAAGCTATCAATGTTTGATATACTTGAGTATATCTTCAAAAATGTTAATACAAAGAAGAAAATCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7145
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111680 | Nonsense | 378 | 1276 | 2 | 12 |
| ENSDART00000140410 | Nonsense | 475 | 1373 | 3 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38064245)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36919660 |
| GRCz11 | 8 | 36952094 |
KASP Assay ID:
554-5280.1 (used for ordering genotyping assays)
KASP Sequence:
CACCRCTCTCATCTTCCTCRTCTGCACCACTGCCCCCTGGTGGCTTGGAG[C/T]AACAGTGCTGCTCAGATGGGGATAATGACTCTCTGAACTCCACCACAAAC
Long Flanking Sequence:
GGGGGGGTGTTGGAAGTGGAGTCGGTGGCAGGGAAGACAGTCGGGACACAGAGGGCGGAGGAAGTAGCAATAGTCGCCGAAGCACACCTTGCACAGAGTGCCGTGATTACCGTTTACGGGGAGGGCATCTACCACTACTTACAATTGAACCACCAAGTGACAGCTCAGTGGACATGAGTGACCGCTCAGACCGAGGCTCCCTTAGCAGACAACTAGTGTATGAGCAGGACTCAGCAGGAGGGTCGCCTCAAGGGACTTTAAAACATAACCCTAATGCTCGTTCACAGTCCTCCACAACTGCACAGGGTCAAACCCGTCCAGCTAGCCGATCGATACCGTCGCATATCCCTCACCACATGGCGCACCACCATCACCATCACCACCACCACCATCATCACCAGTACCCAGACACCCCTTCGTCATCGTCCTCCCCTCAACAGCCCCCTACCACACCGCTCTCATCTTCCTCGTCTGCACCACTGCCCCCTGGTGGCTTGGAG[C/T]AACAGTGCTGCTCAGATGGGGATAATGACTCTCTGAACTCCACCACAAACTCTAATGAGACCATTAATTGCAGCTCAGGATCCTCATCAAGGGACAGTCTGCGGGAGCCCCTACCTCCATTGGGGAAACAGACGTATCAGAGAGAAAGCCGGCATAACTGGGACTCTCCTGCCTTTAATAATGATGTGGTTCAGAGAAGGCAATATCGCATTGGGCTCAATCTCTTCAACAAGTAAGAGAAAATGAAAACCTATCTTCTACCACTTTACCTGAAAGGGGTGTTTATAAGACTCAGGAAATATTCATAATCACATGGCACATGTCATGAATATGAAGGAGATTTTATGCATGCTGTATTATTAACCCTAATCATTAGCCCCTTTCACACATACAGACCTTTCCGGAAAATTGCCGGTCATTTGTGAACAGGCCCTTTATGAAAATACTGGTAAATTCATTCCGGCAATTTTCCAGAAAGAGAAATCGTCACATTACTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15370
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111680 | Essential Splice Site | 550 | 1276 | 5 | 12 |
| ENSDART00000140410 | Essential Splice Site | 647 | 1373 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38068313)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36923728 |
| GRCz11 | 8 | 36956162 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATCTGCCCCTCAAATATTTGCTCTCAAATATTAYTTCTCTATTTCAC[A/C]GTCAGAGGTATTGCRTTTRTAATCCAGCACTGGTAAGACAGTTCCAGAAC
Long Flanking Sequence:
TTTGAGGAAATTTCAAGCTCAGATAAAAGTCCAAGGAGAGGCCCAAAAAGTGGAGAGACTTATTGAGGCTTTCAGGTAGCTAAATGTGCTCTCAGTAAATAATATACTTAGCACTTTAAAATAATCACATTGAACAATGATATCTGTTGGTTACAATGAATATAACAGCATTCATGGGATAGTTCACCCAAAAATGAGTTTATTTATGGGTTTCTTTATTCTGTTGAACACAAAAGACAAAATTTATTTAAAAAAAAAGCTATGAACCTGTAATCATTAAAATAAACAGTCAATGGTTACAGGTTTTCACCGTTCTTAAAAACATCTTTTTAGTATGTTCAATAGAAGAAAGAAAGTCCAACAAATGAAGGGACAGTAAATTCTGACTTCATTTTTAGTTCTAGGTGAACTATACCTTTAAAGAATCATGTTTTATCATGTTTACCATGTTTTATCTGCCCCTCAAATATTTGCTCTCAAATATTACTTCTCTATTTCAC[A/C]GTCAGAGGTATTGCGTTTGTAATCCAGCACTGGTAAGACAGTTCCAGAACCCAGACACCATCTTCATCCTAGCGTTTGCCATCATCCTGCTCAACACAGATATGTATAGCCCCAATATCAAAGCGGAGAGGAAGATGAAGCTGGACGACTTCATCAAAAACTTGCGAGGTGCTGTTCAAATCCCTCTCTCTTAAGCGTCACACATTCACACACTAGATCTTACTCGAGGGGTCAACCCGCAATCTGCTTTTAAATGTGTCATCTAGCTGTGAGGGATTTCACAAGCGTATGCTAAATCTCTTCTTGTGTGTCTGTCAATTTTTTCTTCCTTTCTCAGGGGTGGATAACGGTCAGGAGATCCCACGTGACTTACTAGTCGGAATCTACCAGCGCATTCAGAAGTGGGAACTGAGAACCAATGATGACCATGTTTCTCAGGTCCAGGCAGTAGAGAGAGTCATAGTGGGCAAGAAACCAGTGAGTACTACCGAGTGGTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38703
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111680 | Nonsense | 660 | 1276 | 7 | 12 |
| ENSDART00000140410 | Nonsense | 757 | 1373 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38071821)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36927236 |
| GRCz11 | 8 | 36959670 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGTAAATACCTTTTCTTTGATTAAAGGTTTTGTCTCTGCCTCACCGG[A/T]GACTGGTGTGCTGCTGTCAGCTCCATGAAGTCCCGGACCCTAATCGTCCT
Long Flanking Sequence:
ACCGGTTAGCATTTAGGCAGATCACTGCACCTTTAATGAAGACCGCAATAATAATAGACACCAATGAACGCATTTATGAAGGGATTAAGTGTTCTACAAACAAGTTTAAATGGGTACAAATACTTTACAATAAATCAAAACCTCTAGTGTTAAATTAATGTTAGTGATTAAATAACTCTTAATCAGAAAAATCACAGACACTGTACAAGGACTGTGCTTGTATGCTAATGTACACATAAAAAGTCAACTTTGGGCTGATCTTTCAGACTATTGTGTGGACTGTATGGATTTGGTTTGGGTTAGTTGAATAAATTAATAATAAATACATTTCAGAAGATATCGAGTAGACATTCTACAAACTCTCTGCAAGTTTGTGACTTAAATGTACTTGTCAACAGAATTCATAAGGAGGATCATCACATGATTTGATAACGATTAGTAATGTGAAAGTGAAGTAAATACCTTTTCTTTGATTAAAGGTTTTGTCTCTGCCTCACCGG[A/T]GACTGGTGTGCTGCTGTCAGCTCCATGAAGTCCCGGACCCTAATCGTCCTCAGAGGTCTGGAGTCCACCAGAGAGAGGTCTTCCTCTTCAACGATCTGCTTGTGGTAATATTAATAATCCATTATTCATATAACAAAAGATTTGGTCTTACACTTTAGCAAATAATCTGCATAATTGTGTCTAGTAAAGTCACTACATATTAAATAGCTTCTTTTTCTTTATTACATTACAAGGTTACAAAGATTTTCCAGAAGAAGAAAACTTCAGTAACTTACAGTTTCAGGCAGTCCTTCCCTTTGGTGGAGATGCAGGTTCACATGTTCCAGAACTCCTGTAAGATTTTAAACTGGTTACTTATTGTTTTTCTTACATATTCTACATATACATCTACATGTGTTTATACAATACCTCAATAGTTTGTGTCAGAAGTTTTCCTGACACAGAATAGATGTATTTGATTGTATTTATTTGCTCCAAAAAATAATTCAGTATTATTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15249
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111680 | Nonsense | 833 | 1276 | 10 | 12 |
| ENSDART00000140410 | Nonsense | 930 | 1373 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 38076359)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 36931774 |
| GRCz11 | 8 | 36964208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATGGGAAGGCCTAGTCTGGATGACARCTATTCACCRGGAGAAGGCCTT[A/T]AACGTACTGCTCTCAGCTCCTCACTGAGGGACCTGTCTGAATCAGGTGAG
Long Flanking Sequence:
ATGCACATGCTGGAATTTAATGGGTAAATGTGTTTGTGTCATAGTTTACCACATTTTTCTTGGGAAAAAAAAAGTTTATCCTACTATCCCAAACTCTCAAATTGATCTGCATATGGCATTTGCGTTAAGAAATTTTTTAATGCAGTAATCCAAAATGCTCATAAAAATAGGTGAATGAAAAGCTACTGAATTTTCAGTTTTGAGTGAACTATTCTTTTCAAACTAGATAAAAAAGCACATTCCAAACACCTTGCTTTAATTAGTTCAAGCAAATCATGCTTGGTAAAGATAAAAGGTGTTAGTTCATAAACCGTCCTCTCATGTTTCTTGCGATTTATCCTCCTGCAGCTGAGCTAGAGAAGCAGAAGGGAGTAATGCGGCCCAGCCTGCTCACCAACAGTATTATGGCAGGAGGAGTGGGCGGGGTCAAGAATGAAGTAGTGAATGGCACTATGGGAAGGCCTAGTCTGGATGACAACTATTCACCAGGAGAAGGCCTT[A/T]AACGTACTGCTCTCAGCTCCTCACTGAGGGACCTGTCTGAATCAGGTGAGACACTATGCTATGCCAAATGAGGGGCAAATATAAAATGTTAAATTAACAGTTTATACCAGTGGTCACTAAATTTGTTCCTGGAGAGCCTTTGTCCGAGTTTAGTTACAACCCTAATCAAACACACCTGAACAAGCTAATCAAGGTACCTGGTAAAGCCGTGGTCATGCTGCACTTTTCTCCAATAGACTTTCATTCATACTCGCACAAATACGGCAGACTGGAAACGCAAGCTCATGCGACAAGTTTCGCAGTTCGCTGCGTTGCAAAGTTCAAGCTTGGTGAATTCTGACCTAAAAAATTACATCATATGACTGTGTGAGACCAATCAAAGGTCAAAACATGACTTTTTTGTGCAGGAATAATAAATATGGACCGATCTCTTACTTTTTTAACATCTAATCATCTTGTTTAATCCCACCCTTTTTTGCAGCGTCAAACGATAGAATTTT
Associated Phenotype:
Not determined