ZMP
si:ch211-15l13.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5PNQ8]
Human Orthologue:
IQSEC3
Human Description:
IQ motif and Sec7 domain 3 [Source:HGNC Symbol;Acc:29193]
Mouse Orthologue:
Iqsec3
Mouse Description:
IQ motif and Sec7 domain 3 Gene [Source:MGI Symbol;Acc:MGI:2677208]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31400 | Essential Splice Site | Available for shipment | Available now |
| sa30852 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa6950 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31400
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 |
|---|---|---|---|---|---|
| ENSDART00000113971 | Essential Splice Site | 1029 | 1143 | 10 | 14 |
| ENSDART00000138846 | None | None | 602 | None | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 26007388)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 26714008 |
| GRCz11 | 4 | 26703206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAGACCATGGGACTGCTGGGCATGCAGTTCCACCTGTTTGAGAACGAAT[G/A]TAAGTTCCAACAGTTTTTTTATAGAATTATTTTTGAGTTTTTCTATCCTC
Long Flanking Sequence:
ACTATACACACACACACACACACACACATTACTGTTTAATTTGACAGTGCATAAAATTTACTGGATATTTTTTTCTAGATACTATTCAGCGTAAAGTGCAATTAAAAGGCTTAACTAGGATAATTAGGTTTACTAGGCTAGTTTGGTAAAATTTTGCAAATCACAGTGGTTTGTTCTGTAGACAATCAGAAAAAAAAATGCTAAAAAATTAACAACTGATTTTATTCCAACTGAAAGCAAACAAATAAGACTTTCTCCAGAAGAAATGAAATCTATAAGAATTATATAAGAGGGCTAATAATTAGATTTTCCTTTGGACTGATTTTTAACTGGATTACAATTCTCAGTGTAAATGCACCCAATAAACTCAATTATCATATCTGTGTTTTTTTCTTTACAGATTTTGAAATTGTGTCCAAAAAAAAAGAGTTCAGCTGCATACACCTTCTGCAAGACCATGGGACTGCTGGGCATGCAGTTCCACCTGTTTGAGAACGAAT[G/A]TAAGTTCCAACAGTTTTTTTATAGAATTATTTTTGAGTTTTTCTATCCTCCAAAATGGATAGAATATTTGTAATGTATAGAACAGTGGAGAATACTGTCAGAGAATTGTAGGAAGCAGAAAAAGGGGAATGATCAGCAAAGGACCTAGAGCCACAAATTGAACACAGGTCACTATGAGCACCTATGATCTGGGACTACTGTGTAGGTGGTGCATGATGGGATATGTCATTGTAATCTGTCAGTGTTTGCCACTGAAAAAGCCAGATCGCTGGTGACCATAACATTCCCAGATATTTACTATAAAAGCTTATTAGAAAAAACTTGCCTCATCCTACATTTACTTGTGCCCTATACAGTCTTAATAAACACTGGGTGCCTTTTAATCTGAAGGGACGATTTTTCTGAAGTTTAATTTAAATCAGGAGTAGGCCTTAATCTAGACTGCTGAATCATGGCTTTAAAAATTACTTTCTTAACCACAGATTATATACAGATTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30852
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113971 | Essential Splice Site | 1083 | 1143 | 11 | 14 |
| ENSDART00000138846 | None | None | 602 | None | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 26039822)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 26746442 |
| GRCz11 | 4 | 26735640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAAGAATCAATTGCTGAAGTGTCAGAGATGGAACAGATAAGAATTGAAT[G/A]TGAGTGGACTTTCAATTTCAGTTCAGTTCAATTCACATTTATTTGCATAG
Long Flanking Sequence:
GCGGAGAGGCAGATGGTCTCCCTGGTGAAACGTTATATCCCGAAACATTAGGCAAACAATGCAGAGGGATTGGAGTTTGGAATCACAAAAATCATGGGAGGACCCATATATCATTCAGGGGAGTAATTAAGTGTTTTACTTACAACCTCAGATGTGACAGTCTTTCTTTCTTATCCATCGACACATGCAAACTACAGTAGTTAAATTCACTGTGTAAGACATTTTTTATCCTGCTTTTATTTACTAAATGCCAATTTAAGTAGTTTAGATTGTCAATAAATAATAATCTACATTTCTATTTACTCTGTCTGATGTTGTCTGTTTTTCCTATGTTTCAGACTTTCCTCACGCCATGACGATTGTGTCTCCGTGTTCAGGCTCAGAAAAGAAGCAGGTGTTGAATTTCTGTGCTCAAAATGCAGAGGAGCTGCTCAAGTTCGTAGAGGACCTGAAAGAATCAATTGCTGAAGTGTCAGAGATGGAACAGATAAGAATTGAAT[G/A]TGAGTGGACTTTCAATTTCAGTTCAGTTCAATTCACATTTATTTGCATAGTGCTTTTCATGATACATATAGCTTAAAAACAGCTTTAGGAAAGAAAGCATGATTCTACTTTATGATTAGCATTTTATTAGAAGTAACATCAAAATAAAGTTCATATTGCAGACATTTACAAATGAATCAAATCATATTGTCATAAGCCCATATTTGTAAGTGTTGCTAGCCTGTTTTTAGCTAGACTTTGCTGTATTGTCTGCTGTTTATGTGTGAATCTTATGAAAACCTGATTTGAAAAAATTCAAACTAGATTTTTTTTTCACAAAATCTCTGTTAGAAAAGCAAATAAATTTTGACATTGTTTTAATTTAGACCCCCACCCCACCCCCTCCCCCTTTTTTAAGTTATTTTATTTTTTTATTATTTCCCAAATCATGTTTAACAGCGCAAGGAAACACAAAGTATCCCTGATAATATTTTTTTTCTTCTGGAGAAAGTCTTATTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6950
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113971 | Nonsense | 1139 | 1143 | 14 | 14 |
| ENSDART00000138846 | None | None | 602 | None | 6 |
Genomic Location (Zv9):
Chromosome 4 (position 26066067)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 4 | 26772687 |
| GRCz11 | 4 | 26761885 |
KASP Assay ID:
554-4762.1 (used for ordering genotyping assays)
KASP Sequence:
AAACTAGGTGTCAATTCACAACAGGCTTCAGACGTTCCAGCTCAATGCTG[C/A]ACCGCTGAGCCCTGAGAATGCTGCCCATCTCAACCACCAGAGGGAGCCCA
Long Flanking Sequence:
CATTTTAATTTAGGCTAAACTATCCTCTTAAGTCTTAAATTAAAAGTTAAATAGATAGTAATGGCATGCATTCGCATGTGTGGTGTCTGTACTACATTGTCCAGTTATCCTCTTCTCGTTGTTTAACACATCCCACCCTTCGTGTCCCTCTCTTTCCTCTTAATGCTCTAGTGGTTTCCAAGGGAGACACAAGGGCCCTCAGTGTCCTCTTAATAACCACCACAAACCTTCGTGTCACAAACACACGTTGCCCAAAACCCTGCACATTCGCATCCCCAATTTCAGCTACCCAGTTTGTTTGTGCCCAAGAACACAAAAGCAACCCCCCTTGTGCCACATCCAAACACAACACTTTGCGCATGTCTTTTGTGATGTGTGTTCACCAGAGGGCTGATGACGGTAGAAGGAGAAGAGTCTTATAACATATCATGCTATCTCTGACTGTTTTCTAAACTAGGTGTCAATTCACAACAGGCTTCAGACGTTCCAGCTCAATGCTG[C/A]ACCGCTGAGCCCTGAGAATGCTGCCCATCTCAACCACCAGAGGGAGCCCATCCAACAGCCACCATTGCAACGTGCCAGTCCCACAACCTCGTACTCTTACCACCCTGTGGCCCTGACTGAGCTACGACCTGACACCCTCATCCAGTGCCAGCAAATTGTCAAGGTCATCGTCCTAGACAAAGGTGGTCACGGGCACGTGGAGGCATTCCTTAGCCAGAGTCCCACACATCACCAGCTCATCCAGTCTGTTGTTACTACACCAGTGCATTCACCTGATGATGGAGACAGCCATGGGGGGAATGATGGCTCACAACCTCCGTTGCCTCCACCACCGCCACCATATAACCATCCCCACCAGTATATACCCCCAGATCCTCGAATTTCACTGCAGAGGACCCCAAGTGGCTCTCATAGCCTAATGTAGAGTCTAAACCCACAACAATTAGACACTCTTATATGCATATATTTATGGTTACAGACTTTATTGACTGCAGAAATGT
Associated Phenotype:
Not determined