ZMP
igsf9ba
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8DZ81]
Human Orthologue:
IGSF9B
Human Description:
immunoglobulin superfamily, member 9B [Source:HGNC Symbol;Acc:32326]
Mouse Orthologue:
Igsf9b
Mouse Description:
immunoglobulin superfamily, member 9B Gene [Source:MGI Symbol;Acc:MGI:2685354]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35860 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22617 | Essential Splice Site | Available for shipment | Available now |
sa35859 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35858 | Nonsense | Available for shipment | Available now |
sa18249 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35860
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 |
---|---|---|---|---|---|
ENSDART00000092705 | Nonsense | 203 | 1360 | 5 | 21 |
ENSDART00000138895 | Nonsense | 182 | 1309 | 4 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 18071395)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 19235209 |
GRCz11 | 15 | 19170941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGTGAGTGACGGCAGTCTGACGGTACAGGCCATCACCCGGGAGGAC[C/T]GAGGGGCCTACAGCTGCCGTGCCCACAGTGACCAGGGGGAGGCACTACAT
Long Flanking Sequence:
TTGGTGTGATGAGTCTGAACAGCAGGGTGGATTGTGTCACCCGTCCAGAAGGATGTCAACACACCTCAGAATATTGTGTGGGAGGAACAATAAGGCCAGTCTCCCTTTGGCTACAGCTTTCGATGTGTGGGGGATAAGGGTGCTTTTACGCTGGGCTCGTTTTTTTGGAATCTGGTACAATTTCTGCCAACATCAAACTCTAGTGCAAGATTATATCCATAAATGTAAAAGAAGACAAACTAAAATCTAAAAAATTGTGGTTGTCAGATCAGATTCTTACCGTTAAAAATACATGCAGACATCTTGTAAAAATAAGTCATTTTTAAAATGTGATATAATTTTTTTTTTTTTAATTTAATTTTTAGAAATTTAATTGTTGTATATAATTAAAAAATGTAATTGTAATATTTGGCAAACACAATAACTTGTGTTTTGTGCTTGTTTTGCTTTTGCAGGTGAGTGACGGCAGTCTGACGGTACAGGCCATCACCCGGGAGGAC[C/T]GAGGGGCCTACAGCTGCCGTGCCCACAGTGACCAGGGGGAGGCACTACATACCACCCGCCTGCTGGTGCAAGGTACTGATGGCTGCTCTTAAAGCACTGCGTGATAAAGCTGATACACTTTAATGAATCTTTTGTTTTGTATCAGTGGTTAGGTGTGGTTGCTAAGGTCATGTTAGACATTGTTACATCATAATCACTGGTGGAAAGAGTACTGAAAAACCATACTCCAGTAAAAGTACCATTTTCTAAAAGAATGTAGTGCAAGTAGAGTAAATGTATCTGTTCTAAACACTATTCAAAGTGTGTGTAAAAAGTCGTTCCTCTAAAAGTACTCAAGGGTAGTAAGTAGTGAGTATTACCTTGTGATATTACACCATATAAATTACCCTGAAAAATAAACATTTAGATTGTATCAGTGGTATCTTCTTTTAAGGGTGTTTCTAATTGCAAGTTCAATTATTTGGCTTTTTTTTTTAAATCAGAAATGTGAGATTAATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22617
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 |
---|---|---|---|---|---|
ENSDART00000092705 | Essential Splice Site | 417 | 1360 | 9 | 21 |
ENSDART00000138895 | Essential Splice Site | 396 | 1309 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 18047467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 19211281 |
GRCz11 | 15 | 19147013 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCTAGGTACCATGGGACAGTCCCCTCCGGCCACTCTGGTGCTAAAGG[T/C]GAGTCAGTGCATCTTAACGAGATCATATCAGAAAGAAAGTTTGCGTTCTT
Long Flanking Sequence:
AACATGCAACAAAACATACCCAGATCGGCATATTTTACATTTCACACAAATGTAGTCTGAGACATGTATGAATCTGGGATGTTTATTCCCTAAGTTCTTCATTCTTGTTCGAATCATACCCTCTCCACAGACCCTGCCCGTGTTGTGAACATGCCACCTGTCATCTATGTCCCAAGAAAGTTGCCAGGAATCATTCGCTGCCCAGTGGATGCCAACCCCCCTGTTACGTCAGTCAGATGGGAGAAAGATGGGTACCCCCTCAGAATTGAGAAGGTCTGAAATGATGGTATTTTTGAAGTCTGAAAGGTCAAGACTCTTAACTTTTTGACAACCCTCCACATCAATGCTTTTCTCCCAGTATCCTGGATGGAGCCAAATGACAGATGGAAGCATTCGGGTGGCAGAGGTCACTGAAGACTCCCTTGGCACCTACACCTGTGTGCCTTACAATGTCCTAGGTACCATGGGACAGTCCCCTCCGGCCACTCTGGTGCTAAAGG[T/C]GAGTCAGTGCATCTTAACGAGATCATATCAGAAAGAAAGTTTGCGTTCTTAAATGTCTTCATGTGACCACAGGACCCCCCTTACTTCAATGTGAGGCCCGGGGGGGAGTACCGTCAAGAGGCGGGAAGAGAGCTGGTTATCCCCTGTGCTGCTTCTGGAGACCCTGAGATTCCAACCATACAGTGGAGAAAGGTACAACAACCCAACACAAGTATGATATTTTTCAGCTATCCAAAGATTTACTGTTACTGTGCTTTGTCAAGGTTGGGAAGCCCAGCAGAAGTAAACACAACCTCTTACCAAGTGGTAGCTTACAGTTTGTCTCTTTGAGCAAAGAGGATCATGGGGAGTGGGAATGTGTTGCCACCAATGTCGTAACAAGCATCACTGCCAGCACACGCCTTTTTGTAATAGGTAAACGACTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35859
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 |
---|---|---|---|---|---|
ENSDART00000092705 | Nonsense | 590 | 1360 | 13 | 21 |
ENSDART00000138895 | Nonsense | 569 | 1309 | 12 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 18043374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 19207188 |
GRCz11 | 15 | 19142920 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTTCAGGGGTTGGAGCCAAAGACTGCCTATCAATTCAGTGTGCTGGCC[C/T]AGAACAAACTGGGCACCGGCCCCTTCAGTGAGGTAGTCACTGTGACTACA
Long Flanking Sequence:
ATATTTACATTTTTTTTTTTCGATTATTTTGTGTTTAATTACGGATTTTGCAGGTTTGCAAAAATTTGCGACTTTTTGTTTATTTTTCGTTGGATTCAGAGATCGCGGAATCGTGAAAAACTAGAGGGTTTGACTATATTTCAAGAAATATGTGATTTAATAATCAATAGTTTTTAAAGAAGTTCAGCGTAATTATTGTAACAACTATGATTCTATTCCTTAATTTCACCCTAAAACTCTGATGTTTCAAAATGTTCATAACAAGATAAGTGGTTTTATCTTCATCTTCTGAAGAGACATGAACACTTTATCTGATGAACAGTTTTCAACTAAGATATAAAATCCATTGTTAATGCAACTTTTTGTTACAATCCAACAGAAAAGTGAAGAATGACGTAGGAACCCATGATTGGCTTTCCATACCTGTGCCCGGCTCTCAGATGTGGTTAGTGGTTCAGGGGTTGGAGCCAAAGACTGCCTATCAATTCAGTGTGCTGGCC[C/T]AGAACAAACTGGGCACCGGCCCCTTCAGTGAGGTAGTCACTGTGACTACAGGAGGCAAGTGATACTTTCATACAAACTATGCTGTGTATTGGACCTCTGAATGACCACTTCCCATCATTCCTTTGTCTTTCCTAGGGTACCCTATTAGTACCCCTGAACCACTGGTGCTTCTAACTCCACCACGGTGCCTCACAGCCAACCGGACACAGCAGGGTGTATTGTTAACATGGCTTCCTCCAGCCAATCACACTTCACCAATTGACCGATACGTCATCGAATTTCGTCTTGGAGAAAAGTGGGAGGTTCTGGATGACTTGATTCCTGCCACTGAGACTGAGATTATAGCAAGAGATCTTATTCAGGTATAACTGACTGTGTACTTATTATTATTACAAACATTCATGGAAAATGTACTCATTTAAATGTAGAGTAGACTGGAAATAATAACTCCCTTTGATAAATATTAGCTGAAGTAATATGAGAGAATTGCAGCTGGGTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35858
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092705 | Nonsense | 843 | 1360 | 18 | 21 |
ENSDART00000138895 | Nonsense | 822 | 1309 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 18040268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 19204082 |
GRCz11 | 15 | 19139814 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAACCAAGAGAGCAATAACCAGTAAGAAGTACAGCGTGTCCAAGCAC[G/T]AGGCTGAGGTCACCACGCCCATCGAGCTGATCAGCCGTGGACCTGATGGC
Long Flanking Sequence:
TGTATTGACATGTGTTTCTATGTCCTTTTAATATCTATAATGTCTTATGCTGACATGTTGTTTGGTTGTACTAGTGTAGATGGCCTTCGAATGGCAGTCAGTGCTAAATGTAATCACTATTATGATGTGGATAAAGACAAATTACACCTAATTTTTTTGACAAAAAGCAGATAGAATACACAAGAAAAGGTTATATCATTACTTTATTTTGTATTACACGCGTCTTTTAGTGGTTCTAGTGGTTAGATTGTGCTGATTTTAAGATTTGTATTCCCCAGGGCTTACTTCTAAGTCCCGTGTCTTTTTTGATTGATAGGCTTTCCTCTGGGAAGATCAGTCCTGAGAGCATCGCTTCATCCCGGCCCCCATCTCTGGCCAGTGTGGGTGGTCATGGTCTTTACGTTAAGAAGTTGCCAAGCCCCAGGAAAGAGAAAGAGCTTTCCCTCTATAAGAAAACCAAGAGAGCAATAACCAGTAAGAAGTACAGCGTGTCCAAGCAC[G/T]AGGCTGAGGTCACCACGCCCATCGAGCTGATCAGCCGTGGACCTGATGGCCGATTCGTCATGGACCCCAATGACATCGACTCATCCCTCAAGCCCAGACGCATTGAGGGTTTTCCTTTTGTGGAGGAATCAGACTTGTATCCTGAGTTCCGCCAATCAGATGAGGAGAATGATGACCCAGGGCCCCTACCCCCAGTCATGGCCACCCTCAGGCCCCAGATTTCCCCTGTGTCCTCCAGCCAGGAGTCCTACATGCAGCCCCCAGCCTACAGTCCCCGGTTCCAGAGGCCAATGGAAGGTATGAGCATCTCGGAGGGTAGTCGGCTTCAGGCCACAGGGCAGAGCCGGGTCTCCCATTTTCACAGGGTCTTCCCTCCAGGCCCCTTCTATGGCTATATAGGTAGTGGTGCTGAAGTGGAGCTTCACCCTCCGTTTTACATGCCTGATGTTAGCCCACGTAGCTCTGCCATGTCCTCCTCACCTTCATACCCCCCTGAGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18249
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 |
---|---|---|---|---|---|
ENSDART00000092705 | Essential Splice Site | 1330 | 1360 | None | 21 |
ENSDART00000138895 | None | 1309 | 1309 | None | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 18038804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 19202618 |
GRCz11 | 15 | 19138350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGARAAGGACAGATGAGGAGATGCTCCCCTCAGAACCCTCTCCAGGG[T/C]AGGTGAACCGTACCATTGGAGGCTCCAAAATGACAAAGGAGACTGTTATT
Long Flanking Sequence:
GGAGCCCAAGCACACTGCACAGTGAGAGCTCGGACGGCTGGAGGTCTGAGGCCCAGCCTTGGATGAGCCCCAGGGCAGCTCGAAAGATGGATCTCGGCCTGCAGCAAGTGGTCCTGCAGCCGTCACGACTCTCCCCTCTGACCCAGACACCTCCTAGCTCACATGCCGGCTCTCCAGACATTCTCGTCCGCCCTCCTCCCCGCCCCAGCATCCTGCGGTCTTCCCGCTCTCAAGAGATGCCCGAGAGTGCCCGTCACCCTGCCAGTGTCTCCTTCTCCCGAAGGTCTCTCTCCTCTTCCCCTGCCACTTCACCTACCCAAGGCCAGAGCGGCCAACGGCCAAGCCTCAGCTACCGTGCCCACATGGCCTTTGCCACAGCCGCGGCCAGCTACCCCTCCCAGTCCCCTTCACCCCCTGCGGAGAGCAGTGATGCTTTCGGCCAGATGCCATCTCAGAGAAGGACAGATGAGGAGATGCTCCCCTCAGAACCCTCTCCAGGG[T/C]AGGTGAACCGTACCATTGGAGGCTCCAAAATGACAAAGGAGACTGTTATTCATCATCTGTGCCACAAAAGCAATGCTTTCATGCTTTTGTGATTTTTGATAAAAATACTTTACATACATCTTACTATAAACTATTTACATATGCACAAATGCCCATGTCCTCCAGTATAACTCCTTATTGGGTTCACAGGATAAATTTCCATACCTTTTTTTATTTTCTTTAAATTCTATTCTCATTTAAACTTAAAGCAGTGTAATTTTAATATTGGAAATAATCATAGTGTATAACATTTTTCATAATTAAGGATTTTCTAGTGCATCCATGATGATCCCATGGCTCTTCCTTCTTTGTCCTCTTTTGTGGGCTGATCACATCACTCACCCTCTCCAGCTCATTTCCTTCCATTTCTCTCACTTCCTCTAACTCAGGGCTTTGACCATCATGGTGGCCTTCTTAGGCGGCCTTCGTTGCCAGGGATGAGTGTGCACTCATCTCTTGCA
Associated Phenotype:
Not determined