ZMP
si:ch211-136o4.1
Ensembl ID:
ZFIN ID:
Description:
cDNA, clone cssl:d0672 [Source:UniProtKB/TrEMBL;Acc:B0CLZ6]
Human Orthologue:
IGSF9
Human Description:
immunoglobulin superfamily, member 9 [Source:HGNC Symbol;Acc:18132]
Mouse Orthologue:
Igsf9
Mouse Description:
immunoglobulin superfamily, member 9 Gene [Source:MGI Symbol;Acc:MGI:2135283]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10840 | Essential Splice Site | Available for shipment | Available now |
| sa17448 | Essential Splice Site | Available for shipment | Available now |
| sa21707 | Essential Splice Site | Available for shipment | Available now |
| sa17395 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10840
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 |
|---|---|---|---|---|---|
| ENSDART00000111952 | Essential Splice Site | 20 | 1619 | None | 21 |
| ENSDART00000137456 | Essential Splice Site | 20 | 767 | None | 17 |
Genomic Location (Zv9):
Chromosome 10 (position 19069813)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 19082159 |
| GRCz11 | 10 | 19039593 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAACCTTCCTCTGTTGGAAGTCATTGTTGCAGTTCTGTGCCTATTCAG[T/A]GAGTATTTTACAGTATCTACTTCACAACTGACAGATGCACAATCATGCAT
Long Flanking Sequence:
CTGTAACAAGAGACAATTCAATCGTAACTTAAAGTTAAAACAGCTATCATAACATTATTTATCAATATGTGGCTCTTTTTGAAAGCTATAGAAATAAAAAATGTAAAACAGGAAATACGTTGGGACCATTGTTTTTGCTTACATCCTTCAAAATAGTCTATAAATCTCATGTTACAACCTTCTTTTCTGCGGTGTTTTGGTTCATACATGCAGATATGCATACAATGTTCACATAAGATCCCATAATCCTACTGTGTGCTCTGAGATTAAAGGAACAGGCAACCGAAACAGGCGTGGAAGTGTTTGGACATACTGTATATAGCAGTTGTCTGGATGCGTGTTTAACATAATGCTTTCTTTGTGGTTAAGGTTTGTTTGCTTGTTGTTTGATCTTGTGTGTTTGATGTTCTGCAGGTATGTGAATCTGTATGAACGCCCATCATGCGACTGAAGAACCTTCCTCTGTTGGAAGTCATTGTTGCAGTTCTGTGCCTATTCAG[T/A]GAGTATTTTACAGTATCTACTTCACAACTGACAGATGCACAATCATGCATTCTTCTCTTTTTGTACTCTGAAGCTGTTGAATGCTGGATTCTGATTGGTTTATGAATGTTTTAGTGTGTGCCATTATTTTTCTGCAGCAGAAGTTAAACCCAATTCTGAACATATATATTTGCAAATTTGGGGCATTTGTAAAATACAATGAAATTAAGAATCTGTGAATTTTCAATTGGCTTTTCCATAGGTGTCAAACTCCATTCCTATAGGGCCACAGCTCTGCACAGTTTTGCTCCAACCCTAATCAAAGACAGCCGATGCAACTAATCAAGGTGATCAAGACTACTAGAAACTATTTGGCAGGTGTAAGTTGTTGGTGGTTGGAGCTAAACTATGCAGAGCTGTGGTTTAAGACAATTGGTCTTTTCCCTGGTTTCCAAGACAAGGTTTGAGGCTAGTCCTAGACTAGTTTCAAGATACACACCAGTAATGTGTTTTTCTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17448
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111952 | Essential Splice Site | 84 | 1619 | 2 | 21 |
| ENSDART00000137456 | Essential Splice Site | 84 | 767 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 10 (position 19072556)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 19084902 |
| GRCz11 | 10 | 19042336 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCTTCATGCAGCTCGGAGTTCATCCTCGAGTACATCCTGACTATGATGG[T/C]AAGAACGTCTAACTTATGATGTATTTRAYACTATGTTATTATTATTAWTG
Long Flanking Sequence:
TATTATCCTCAATTACCAAATAATTACATATCTTTAATGTACATATTACATTGATGTTACATCATTATAAACACAGCTTTGAAAATCAAAGTTTAATTTCATTTACAGTATATGGTTTATTTGGTGAGTGAAAACACTGTAAAATGTTAATTGTTAATTTTTTCTTAGTTCAATTAAATAAAGATTGAAGGAAATTAACAAATCACATATTCTGCATTTTACAAAAACGTTCCAGCTTTTCATAACTGACCCAGGCAAGTTTTGACAGCATAATTGTTTGATTTGATGTTATTTCTAATTGTTTTAGATGACACAAGTGCAGCTGAAGAACATGTTCGTGCCAAAAAAGACAGTAGTGCAGTGTTGCCCTGCAGTTTACCAGCCCCGCAAAAGGACAGCTCAGCTTCTCAATATGTCATAGAGTGGGTTCGCCAGGGCTTTGATACCCCCATCTTCATGCAGCTCGGAGTTCATCCTCGAGTACATCCTGACTATGATGG[T/C]AAGAACGTCTAACTTATGATGTATTTAATACTATGTTATTATTATTAATGAGTTCAAATAATACGGTAGGGTTAGGATAGGGGTTTGTTTTAGGATAGGTTTTCTGTAATTATGCATAATTCATGTTTTTTTTTTACTATAATAAGTGTGTGTTGTGACAAGGACTAAGTAACAAGTAGTGTAAATATCCTAATAGCAAGCTAATTTAAGACCAGATGTTAATTTGCCATTATTGGTAACCATTTGATTTAAGGCTCTGTTTGTAACTCTTGTTCAGGGGGTTTCAAATTGTTTAAATGTATAATAAAATAAATCACACTTAAAATTTAATTTAAAATGTTTTATTATTTGCAATGTATGTTCAAATTATTTATTAAACTCGAGATGACATACATAATGAAAGTTTTATTTTTAATTAACTAATGTTAGCAAAGATTAATAAATACTGTAACAAATATATAGCTTATTTTTGCTAATGTATTCAATAATATTAACTAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21707
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111952 | Essential Splice Site | 184 | 1619 | 4 | 21 |
| ENSDART00000137456 | Essential Splice Site | 184 | 767 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 10 (position 19090615)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 19102961 |
| GRCz11 | 10 | 19060395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTGGTCCAAAGACGGAGCACCAATAAAACCTCAACACAAAGTAAAGG[T/G]CAGAATGAAGCACTTTAAAACCTTACGAAATACTGAACAGCTGCGATTGC
Long Flanking Sequence:
TGTTTGTGAAGCCCTTTGAGTTGCATGTATGTAGGAAAAGTGCTATACAAAATAAAATGTATTATTATTATTATTAAAATTATTATTATTATTAAAATTATTATTATTATTATTATTATTATTATTATTATTATTAATATTATTATATGTAATGTTATTTAAAAATAAGAGATAATCGACCTATGTCTCTTGCTGAAAAGTAGCTGATGGGATCTATTTGTATGTATATACTGTCCAACACTCAGTAGAACCTTTTATTTTGAAGATTTTCTCCTCAAATATATTACTCTTTATTGCTGGAAACTGTTCTGGGTTTGAGAGATAATAACAGTTTTCTGTGCTTGTAGCTCCTCCAGTGCTGACAGAAACCTCTCCTCCTGAGGTGGAAGTGTTTGTTGGTAGATCATTAACCCTGAAGTGTGCAGCGCAGGGAAATCCGCGGCCTACAATCACCTGGTCCAAAGACGGAGCACCAATAAAACCTCAACACAAAGTAAAGG[T/G]CAGAATGAAGCACTTTAAAACCTTACGAAATACTGAACAGCTGCGATTGCCCTTCTTGTCCTCTTGTATTTCCTGTTGGAAGTTGGGTGTGACACATTAAAAGAGCTTGTTCTGTTTTTAAAGAGCCAAATACATATTAGTGCAGTGTTTGATGGTACAAACATAAATGAAACCCCTGAAAACAACATTAGCATTTTTCATTAATTTTCCTACTAAAGAAACATGAATGAAAAATTAAGAAAGATCAATGTAAACATACAATAAAAAAAAACATAGTTTAAAAGAAAAATAAAAAATACATTAAAATAACATATTTAATTGAAAATGATAACATTTACAAAAGTATCTAACTACATTTACAAAAATACTCAGATTTTTTTTTGTTGTAATATGTTGTTTTGTCAACTTTTTCCACTTATGCTTTCACTTTTATACCCACTTTATCTTAAAAGCTATCAGATTTCATAACAACAACACATTTTGATTGAACTGACTTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17395
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111952 | Nonsense | 1566 | 1619 | 19 | 21 |
| ENSDART00000137456 | None | None | 767 | None | 17 |
Genomic Location (Zv9):
Chromosome 10 (position 19116163)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 19128509 |
| GRCz11 | 10 | 19085943 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGARCAGCATTACTAAAGATGATGACAGTWCAAATTTAGACCAAAAA[C/T]AAMAAGGTAAGAAAAATGWTAGCCTTGTATGTTGTAACACTAAGGGCTCT
Long Flanking Sequence:
GGACAGTGACAGAGATGAAGCAGCTCTATTAGATCCTGAACAAAATGGAAGGTATGACTGAATTCCCTTTGTCTTTCACTTAACATTCATTATTCATTTTACAGTTTTAGTTATTTATTTTGCATTGAATATCATGGTTTGTAGATGTAGTGCCAATGGCAATTCAGTATCTTGGCAATTAAATTGGTAATACCAAAAGTATTTGTTATGCTGCCATTTTAATACAATCTTTTTCACTTAAATTTTGCCATGGTGATTGCATGCTGTTTGGATTAAACATTGCAACTTTACTTGCATGTATCACATTATTTTTTTATTTTCTTACATTTTTTTTTAGAAGAGACTCTGTGGATGAGAGTTATGAATGGGAACCAGCTTATGTCCCAATGCGTCCTGTAGTGTCAATGAATAAGACAGGTCTACAAAAAGAATTTAAAGGAAGCCAAAGGAAGCAGAGCAGCATTACTAAAGATGATGACAGTTCAAATTTAGACCAAAAA[C/T]AACAAGGTAAGAAAAATGTTAGCCTTGTATGTTGTAACACTAAGGGCTCTATCATACACCCGGCGCAAAAAGGGCAAGGCGTGTTTGGCACAATTTTTTGCTATTTTTAGACCAGTGCAACCCTAATTTTCATGTTTTGTACCACATTGTTTAAATAGCAAATCCATTTGTGCCACTTTGTGAACTCATGGGCATGTTGGTCTATAATAGATGTGGTAAGGTGCATCACTGGTGCGCTGCTATTTTAAAGAACTGAAATAGACTGCACCATTAACCAACTGAAAGCAAGCTTAAACATTGCTTATTATACACAGGATGTACAGCAATACACAAATATCTTCACAAATGAAAAAAAAAAAAGGATTCAAATGTTACAAAAAGATTATTTTCTGCATAAATATAAAAACTGTGCCTCATCTTGAGGGGCTTTTCAGTTTATTCATGACAATTTGAATTTGTATAATGTTATTATTAGTAGTAGTGTTATTTAACATATGCAT
Associated Phenotype:
Not determined