ZMP
igsf9bb
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa44968 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37311 | Nonsense | Available for shipment | Available now |
sa37310 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32349 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa44968
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101136 | Essential Splice Site | 415 | 1339 | 9 | 19 |
ENSDART00000142907 | Essential Splice Site | 415 | 1325 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 24020038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 24705712 |
GRCz11 | 21 | 24742317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGCCTCGGTACCATGGGACCGTCCCCTCCCGCCCCCCTGGTGCTAAAGG[T/C]AAGGATAAAACCTTGTAGCTGCACCATTATTTCATTTGTTTGCGTCAATA
Long Flanking Sequence:
TTCAATAAAACCCATCATAACCAATGATTATCTCTCCAATGAATGCAGCAAAACTTAACATGGTTGTGTCAAATTTATACACTATTAGGATCAAATAAAGTTAATACAAAAATGTATTATCCTATATAACATATTTGTTTTGATGCATGTATAAATCCATGGATGTAATGGTTCAGTTATGTAGAAATAGTCATGAATCTGTGGATGTAGTGATGTAGGCATTGATCTTCTACAGGTTATGTGTTTCCTTAAGTTCATGACGTTGGTGTTGCAAAATCACCCTCTGCCTTTTAAGGTTCACTAAACTGTTAGTTCTTATTGTGTGCACTAAGGGTAATGGGACATCTCTCTATTGCAGTACCCTGGTTGGAGCCAAATGGAAGATGGGAGCATTCGAGTGTCTGAGGTGACAGAGGACTCTCTCGGCACCTACACCTGCGTGCCTTACAATAGCCTCGGTACCATGGGACCGTCCCCTCCCGCCCCCCTGGTGCTAAAGG[T/C]AAGGATAAAACCTTGTAGCTGCACCATTATTTCATTTGTTTGCGTCAATATAATGTGTTTGGTGATGGATAGGATCCACCCAAATTTTTGGTGGTTCCTGGAGGGGAGTACAGGCAGGAGGCTGGTCGAGAGCTGGTCATCCCCTGCGAGGCAGAAGGAGACCCATTCCCCAACATTACATGGAGAAAGGTAAGCCATGTCTTTCAAGGATCTTTACGAAGTCTTTGTCAAGCCAAATAAACTGCTTGCCAGAATTGTTTTTTCTTCTATTGGAGAAGGTAGGGAAGCCCAGCAGAAGCAAGCACAACGTCCTACCGAGAGGCAGCTTACAGTTCAAATCTCTCAGCAAGGAGGACCACGGGGAGTGGGAGTGTGTCGCCTCCAATGTCGCCACGAGCATCACTGCCAGCACGCACCTCCTAGTAATCGGTAGGAGGCGTGAAAACAAATGGTGTAAAACCCAATGACGCACAAACACAACTTGCAATATTTTTTTCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37311
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 |
---|---|---|---|---|---|
ENSDART00000101136 | Nonsense | 434 | 1339 | 10 | 19 |
ENSDART00000142907 | Nonsense | 434 | 1325 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 24019911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 24705585 |
GRCz11 | 21 | 24742190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCCAAATTTTTGGTGGTTCCTGGAGGGGAGTACAGGCAGGAGGCTGGT[C/T]GAGAGCTGGTCATCCCCTGCGAGGCAGAAGGAGACCCATTCCCCAACATT
Long Flanking Sequence:
AACATATTTGTTTTGATGCATGTATAAATCCATGGATGTAATGGTTCAGTTATGTAGAAATAGTCATGAATCTGTGGATGTAGTGATGTAGGCATTGATCTTCTACAGGTTATGTGTTTCCTTAAGTTCATGACGTTGGTGTTGCAAAATCACCCTCTGCCTTTTAAGGTTCACTAAACTGTTAGTTCTTATTGTGTGCACTAAGGGTAATGGGACATCTCTCTATTGCAGTACCCTGGTTGGAGCCAAATGGAAGATGGGAGCATTCGAGTGTCTGAGGTGACAGAGGACTCTCTCGGCACCTACACCTGCGTGCCTTACAATAGCCTCGGTACCATGGGACCGTCCCCTCCCGCCCCCCTGGTGCTAAAGGTAAGGATAAAACCTTGTAGCTGCACCATTATTTCATTTGTTTGCGTCAATATAATGTGTTTGGTGATGGATAGGATCCACCCAAATTTTTGGTGGTTCCTGGAGGGGAGTACAGGCAGGAGGCTGGT[C/T]GAGAGCTGGTCATCCCCTGCGAGGCAGAAGGAGACCCATTCCCCAACATTACATGGAGAAAGGTAAGCCATGTCTTTCAAGGATCTTTACGAAGTCTTTGTCAAGCCAAATAAACTGCTTGCCAGAATTGTTTTTTCTTCTATTGGAGAAGGTAGGGAAGCCCAGCAGAAGCAAGCACAACGTCCTACCGAGAGGCAGCTTACAGTTCAAATCTCTCAGCAAGGAGGACCACGGGGAGTGGGAGTGTGTCGCCTCCAATGTCGCCACGAGCATCACTGCCAGCACGCACCTCCTAGTAATCGGTAGGAGGCGTGAAAACAAATGGTGTAAAACCCAATGACGCACAAACACAACTTGCAATATTTTTTTCAATACATTTTTATCATTGTACTTCAGACTCGTTAAGGGTGCTTTTTTCGTTAAATGCTTACTTGTATTGTTGTTTATACTTTGCAACGTCATGAAACACCTGACTCACCATTTTTTAAAATTGTTCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37310
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 |
---|---|---|---|---|---|
ENSDART00000101136 | Nonsense | 1132 | 1339 | 18 | 19 |
ENSDART00000142907 | Nonsense | 1132 | 1325 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 23981493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 24667167 |
GRCz11 | 21 | 24703772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCAAGCCTCAGGGCCTTCCAGCCAAGCGTTTACCTATGCAAGAGGCA[C/T]AGAGTCTAGGGCAGCTAAGACACACAAGCCACGGTATGGGTGTACCGGTA
Long Flanking Sequence:
GCCAGTTCTACAGCTATTTGGGAAGTCCAGGAGAACCTGAGCCTCCTCCTCCCTTCTACATGCCAGACACCAGCCCTCTCAGCTCTGTAATGTCCTCTCCTCCATACCACCTAGAGGGGCCTTTTGGTCATCCCACCATACCAGAGGAAATTGGTGAGGGTGAGATTCAGCATTATGCAGTCTCTGGCTACACCCTTCCCTTGGCACACCCCTCCACCTCGCGCTCTCCAGACATCTGGCAGAGACCAGATTTCACCTTTGCTACAATAGAGGGTCCTCACTTTATTTTCCCACCACCACACCCTTTGCATCTTCATCCGGAACCTCCCCTTCCTCCCCCTCTTGTTCTTCCTCCTAGTGCCCTCCAGCCCTCCACACTTCAAGTTTCTCCTTACCCTGGTATCCTGCAGCTGGAGGCCCCAAAGAGCCGCCCAGGCAAGTCTCCCAGCAAGGTCAAGCCTCAGGGCCTTCCAGCCAAGCGTTTACCTATGCAAGAGGCA[C/T]AGAGTCTAGGGCAGCTAAGACACACAAGCCACGGTATGGGTGTACCGGTATTGCCTTACCCTGACCCGGTGTCTCACATGGTTGGCCCAAGCTCGTTCGGAAGCCTGGACACAAGATGGTACGAGCTTACACCCAGGCTTAGCCCCAGGCAGCCCCGTAGGATGGAACCCAGCATGGTTGTTCTCCAGCCATCCCGCCTCTCACCTCTAACTCAGAGCCCTATTAGCTCTCACGAAGGCTCACCAGAGATTGTAGTTCGTCCCAGACCCCGTCCTAGTATGATCCAACCCCCGATTCCTCCTGAGATGTCTGAGATCACCCTTCAACCTCCTTCTTCAGCTAGCTTCTCTAGGAGGTCCTCCCCTTCCTCTTCTCCTGCTCAAGGCCAAGGCAGCCGAAGGGCAAGTCCCAGCTACCGATCCCACATGGCATTTGCCACCTCAGCGGCAAGCTATCCGTCACAGTCCCCTTCACCTCCTGTAGAAAGCAGCAACATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32349
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 |
---|---|---|---|---|---|
ENSDART00000101136 | Nonsense | 1271 | 1339 | 18 | 19 |
ENSDART00000142907 | Nonsense | 1271 | 1325 | 18 | 18 |
Genomic Location (Zv9):
Chromosome 21 (position 23981076)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 24666750 |
GRCz11 | 21 | 24703355 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTTCTCCTGCTCAAGGCCAAGGCAGCCGAAGGGCAAGTCCCAGCTAC[C/T]GATCCCACATGGCATTTGCCACCTCAGCGGCAAGCTATCCGTCACAGTCC
Long Flanking Sequence:
CCCCAAAGAGCCGCCCAGGCAAGTCTCCCAGCAAGGTCAAGCCTCAGGGCCTTCCAGCCAAGCGTTTACCTATGCAAGAGGCACAGAGTCTAGGGCAGCTAAGACACACAAGCCACGGTATGGGTGTACCGGTATTGCCTTACCCTGACCCGGTGTCTCACATGGTTGGCCCAAGCTCGTTCGGAAGCCTGGACACAAGATGGTACGAGCTTACACCCAGGCTTAGCCCCAGGCAGCCCCGTAGGATGGAACCCAGCATGGTTGTTCTCCAGCCATCCCGCCTCTCACCTCTAACTCAGAGCCCTATTAGCTCTCACGAAGGCTCACCAGAGATTGTAGTTCGTCCCAGACCCCGTCCTAGTATGATCCAACCCCCGATTCCTCCTGAGATGTCTGAGATCACCCTTCAACCTCCTTCTTCAGCTAGCTTCTCTAGGAGGTCCTCCCCTTCCTCTTCTCCTGCTCAAGGCCAAGGCAGCCGAAGGGCAAGTCCCAGCTAC[C/T]GATCCCACATGGCATTTGCCACCTCAGCGGCAAGCTATCCGTCACAGTCCCCTTCACCTCCTGTAGAAAGCAGCAACATTTTTGGGCAGATGCCAACCCAGAGGAGGACTGAGGAGGAGATCCTTCCATCAGAACCCTCTCCACCCCAGTTATCAGCTTCAGGGTAGGTGCACAAGGCCTGAATTGTGTGGTCTAAGCCATGTACCATGTGGCCTAAGTGTAACATCTATGACCCTTTGGGGATATCAGTGCGGAAATGAGCACACATTTTATTCTTAGTCTTAAACTACATCTTGTTAATATGGGCTAAATTTAAGTGTTTGATGCTTGCCTTAAGCTGGTCTTAGTAATGAACTCATGCTTTCATAGAAACACTGCCCCAGATGCCTTGCATTATTCAAAACCATTCAAAACCATTTTCTACATAGACAAGTTGTGCTAAAGTTTTCTATGCCACTGATTCTGCTTTCATGTCAGACATCAAATTTCATTCATAAGGT
Associated Phenotype:
Not determined