ZMP
si:ch211-106g4.2
Ensembl ID:
ZFIN ID:
Description:
semaphorin-3B [Source:RefSeq peptide;Acc:NP_001121818]
Mouse Orthologue:
Sema3b
Mouse Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B Gene [Source:
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2422 | Nonsense | F2 line generated | Not yet available |
sa41225 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12992 | Nonsense | Available for shipment | Available now |
sa41224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21310 | Nonsense | Available for shipment | Available now |
sa6101 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2422
Status:
F2 line generated
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 35 | 781 | 1 | 18 |
ENSDART00000027301 | Nonsense | 35 | 775 | 1 | 17 |
ENSDART00000062608 | None | None | 272 | None | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27461919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26589837 |
GRCz11 | 8 | 26608976 |
KASP Assay ID:
554-2700.1 (used for ordering genotyping assays)
KASP Sequence:
GCTTCATTGAGCGGAAGCTCACAATCCTCACCCCGGATGAAACTGTCTYA[T/G]AAAGGTAGTGCACTATATCWAATSCCTGTTATTTTATTCYCAGGTTCAGT
Long Flanking Sequence:
CTTATCTTAGACAGGACAGTAGCTTTAGACCATCTGCTACTGAAATAAAAAGTGTATGAGTGTGTGTGACTGCATATCTGAAATAACATGGCTATTATCGGACTGGGTTATTGTAGGAGTGGGTGACAAAGGGGTCAGGAAAGATGGAACAGTGTCAATGAAAAGAAGATGAAAGGTCTATAAAAGTTTTTTTTTTTGTTTTTTGTTTTGGTGTTCAGCTTTCAGAGTAAAGAGGAAACTCCACATCTACAGCATCACTGTAACAACAAGCAGGACAACTGAGAGCCGTCACGGCAACAGCTGCCAGGACAACCAGCATCCCACTCCACCATCTGTGTGGCAGCTGTCTGCGCTTTTTAACTTAAAAAAAGTTTTGGTCCTCCTCCTCCTCTGAAGATGATGATGATGATGTGCTGCACACTGGTCCTGTTTGGACTCATCGGCATCAGCGCTTCATTGAGCGGAAGCTCACAATCCTCACCCCGGATGAAACTGTCTTA[T/G]AAAGGTAGTGCACTATATCTAATGCCTGTTATTTTATTCTCAGGTTCAGTTTTATTTTTTCCTGAATTATTATTAATTTATTGCATATTACATTTTTTGTATTCAATATTTGTCCTTTTTTTCTAGACATTAATTTATTGGTAAAATACATTTTAGTAGTTAAGTAGTCCACTTTTGTCCACAATTGTCTACTATTTATGAAGATTTAATCAAAATGTACATTTTAGAAAGCCTGTTTTACATTTTCTTCACATTTAACTACAATTTAATTTTGATGTTGATCTGAAAATGCTTACCATGCTTTAACATGATAGGACTTCACAGTGGCTTAGTGGTTGCCAAGTTACCTCTCAGCAAAAAGGTCACTTGTTGCATGGAGTTTGTATGTTCTCCCTGTGTTTGTGTGGGTTTTCTCCGGGTGCTCCGGTTTCCCCAACAGACCAAAGACAAGCAGTATACTGTAGGTCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41225
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 116 | 781 | 4 | 18 |
ENSDART00000027301 | Nonsense | 116 | 775 | 4 | 17 |
ENSDART00000062608 | None | None | 272 | None | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27448664)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26576582 |
GRCz11 | 8 | 26595721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTGTGCATGTGTGTGTGTGTGTGTGTTGCAGACGGATTGCGTAAACTA[T/A]GTGAAAGTGCTACACCACTATAATCGAACTCACCTATACGCCTGTGGTAC
Long Flanking Sequence:
TGTCTACCCTGGAATCCGGATGTTCCCGCTCCCACATGTTGTCGTAGTGATTCCCAGCTCTCTGGGAAATGTGGCACGCTCCAGCGAGCACATTCACAAAGGAAAAGAGAAACAGAGAGACTATAGGTGTCCATGTGTGTAAGTGTCAATTGAAAATGTCTTTGTTTTCATGCGTCAAAGAGAAAGTGCGAAAGATTACAGAGAGATCCGGGATCACAGTGTGCATGGAAAGGTCAGCACTCATGTCGTCAAGGATACATAATATAATAACGTTTCGTTTCTGATTTGCCCTGTAAAAGATCCCTCAAGAGACAACTCATGTGCTTGTGTGTTTCTGTTTTTGTATGTCTGGTCACTGATAGTCAATCCAGATGGGGACCGTCTCTCTCTCTCTCTCTCTTTGACAGATAAACTGGGGAAAGCATGTAAAATATGTCCTGCATAAAATTGATTTGTGCATGTGTGTGTGTGTGTGTGTTGCAGACGGATTGCGTAAACTA[T/A]GTGAAAGTGCTACACCACTATAATCGAACTCACCTATACGCCTGTGGTACGGGGGCTTTCCACCCCACCTGTGCTTATGTGGAGGTGGGACAGAAAATGGAGGTAAGTTTGTGTGTTTGGGGGTACTGTATATGATTGAGCTTGTGTGAAATCCAGTCCTGTTTGGTTTTGCATGGCCAAACACAATGCTAAAGTTTGCTTTTGCTCCACAGGATCATGTATTTAGAATCGATCCCTCTCTTGTAGAAGATGGAAAAGGGAAGAGTCCATATGACCCACGTCACACATCAGCTTCTGTTCTGATTGGTAAGATGCCACCCTTTATCTTTCTATTGCTTATATAAACAATCCAGAAAATGTTTAAAATACATCTAATTGAGCAAACATAGACATCTTAACCAAAACTAAACTGAATTTGATCAGTGAAAATCTAATCTAAAATTGCTTGGTTGGAATGCTGATACGTCATGACCAATCAGTAACCTTCTCTCTGTCATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12992
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 123 | 781 | 4 | 18 |
ENSDART00000027301 | Nonsense | 123 | 775 | 4 | 17 |
ENSDART00000062608 | None | None | 272 | None | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27448643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26576561 |
GRCz11 | 8 | 26595700 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTTGCAGACGGATTGCGTRAACTAYGTRAAAGTGCTACACCACTA[T/G]AATCGAACTCACCTRTAYGCCTGTGGTACGGRGGCTTTCCACCCCACCYG
Long Flanking Sequence:
GTTCCCGCTCCCACATGTTGTCGTAGTGATTCCCAGCTCTCTGGGAAATGTGGCACGCTCCAGCGAGCACATTCACAAAGGAAAAGAGAAACAGAGAGACTATAGGTGTCCATGTGTGTAAGTGTCAATTGAAAATGTCTTTGTTTTCATGCGTCAAAGAGAAAGTGCGAAAGATTACAGAGAGATCCGGGATCACAGTGTGCATGGAAAGGTCAGCACTCATGTCGTCAAGGATACATAATATAATAACGTTTCGTTTCTGATTTGCCCTGTAAAAGATCCCTCAAGAGACAACTCATGTGCTTGTGTGTTTCTGTTTTTGTATGTCTGGTCACTGATAGTCAATCCAGATGGGGACCGTCTCTCTCTCTCTCTCTCTTTGACAGATAAACTGGGGAAAGCATGTAAAATATGTCCTGCATAAAATTGATTTGTGCATGTGTGTGTGTGTGTGTGTTGCAGACGGATTGCGTAAACTATGTGAAAGTGCTACACCACTA[T/G]AATCGAACTCACCTATACGCCTGTGGTACGGGGGCTTTCCACCCCACCTGTGCTTATGTGGAGGTGGGACAGAAAATGGAGGTAAGTTTGTGTGTTTGGGGGTACTGTATATGATTGAGCTTGTGTGAAATCCAGTCCTGTTTGGTTTTGCATGGCCAAACACAATGCTAAAGTTTGCTTTTGCTCCACAGGATCATGTATTTAGAATCGATCCCTCTCTTGTAGAAGATGGAAAAGGGAAGAGTCCATATGACCCACGTCACACATCAGCTTCTGTTCTGATTGGTAAGATGCCACCCTTTATCTTTCTATTGCTTATATAAACAATCCAGAAAATGTTTAAAATACATCTAATTGAGCAAACATAGACATCTTAACCAAAACTAAACTGAATTTGATCAGTGAAAATCTAATCTAAAATTGCTTGGTTGGAATGCTGATACGTCATGACCAATCAGTAACCTTCTCTCTGTCATCATTTAGGTGATGAGCTTTATGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41224
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 353 | 781 | 10 | 18 |
ENSDART00000027301 | Nonsense | 353 | 775 | 10 | 17 |
ENSDART00000062608 | None | None | 272 | None | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27446260)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26574178 |
GRCz11 | 8 | 26593317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTGCAGTGTGTCTCTATACTATGAACGACATTCGCCGAGCATTTTTA[G/T]GACCTTTTGCCCATAAAGAGGGACCCAATTACCAGTGGATTCCATTCCAG
Long Flanking Sequence:
AAAATCTCTATTGGTTCACTAACCTTCATGTCATGACTTCTTTATTTTGTGGGTGAAATATTAAAATCTTAATGTTTGAAAAATGTCAATACATAATGTTTTTGTCAAACAGAAATGACATGATGAGTTATTTTTTTGGAAACTGTGGAAACTTTTGAGTTTAATAATGAATTATTAAAATATAATGAATTGTTTAATGAATTGTTTAAAATAATTTTAATTTACTTTTCTTTTTTCCTTTTTTTTCTTTTTTACATATTTTAAACATAAAATGATAATGTGACGTGAATTCAGATAAACTGGGCATTTATGTGAGGACCAAAGTAGTACAAAATATTTGCATTCAGCATTTCTATGATTTTTATTTTTATCTCTCAGTATTGTAACGTTTTAACGCCCAGTGTGTGTGTATGTGTGTGTGTTTTGTGTCTTACAGTAGTGTATTTCAAGGTTCTGCAGTGTGTCTCTATACTATGAACGACATTCGCCGAGCATTTTTA[G/T]GACCTTTTGCCCATAAAGAGGGACCCAATTACCAGTGGATTCCATTCCAGGGTAAAGTGCCTTACCCACGGCCAGGCATGGTATGATAAGATGCTCTAGATCTCACATCATACACACCTGTAAAAAGTTTTTAAAATCTTTAATACACACTACCTGACAAAAGTCTTGTTGTCGATCCCAGTGGTAAGAGTAACAAAGAATAACTTGACTTCTAGTGGATCATTTGGAAAAGTGACAGAAGATATATTTTAATAATGTCTAATAAATCTGTTAAACTGCATCAATCATCACAAATACAGCAGAAGACCTATTGGAACCAGCATGGACTCAAGATTCTCACAGAAATCAGTCAAGTTTTGTGAAGGAAAAATCATGGTTTGGGGTTACATTCAGTATGTGGGCGTGTGAGAGGGTGGATGGCAACATCAACAGCCTGAGGTATCAAGACATTTGTGCTGCTCATTAAATTACAAACCACAAGAGAGGGCAAATTCTTTAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21310
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 |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 483 | 781 | 12 | 18 |
ENSDART00000027301 | Nonsense | 482 | 775 | 12 | 17 |
ENSDART00000062608 | Nonsense | 96 | 272 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27444098)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26572016 |
GRCz11 | 8 | 26591155 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGAAGCTGGAGCAACACTGAGCTGCTGCTGGAGGAGCTGCACGTCTTT[A/T]AGGTGAACACAAAAATGTGTGGCTTTTATTTAGAGGGATAACATAAACTA
Long Flanking Sequence:
TGTTTGAACTTGCTGACCTGTGTCACATGTTGATATCATGAGCGGATTATGTTTCCGGAATCTACAGATACAGTATCTCTCTCTCTCTGTCTCTCCCTCTTCCTCAGTGTCCCAGTAAGACCTTCGGCAGTTTCGAGTCCACCAAAGGTTTTCCTGATAACGTAATCCAGTTTGCACGGCACCATCCGCTAATGTTTAATCCAGTGACTCCTCTGGGTGGCCGACCGCTGTTCCTGCGCACCGGTATCCCATACACCTTCACTCAGATTACTGTAGACAGAGTCAATGCAGCCGACGGACACTATGATGTCATGTTCATCGGCACAGGTACAGTATTGACTGAATATTGAAGAGTGTGTGTTTAGAGGAAGAATACGACTCAGGTTAAAGTCTCTCTGTTTTTTTTTCCTGCAGATGTGGGCTCTGTGCTGAAGGTGATCTCGGTGCCCAAGGGAAGCTGGAGCAACACTGAGCTGCTGCTGGAGGAGCTGCACGTCTTT[A/T]AGGTGAACACAAAAATGTGTGGCTTTTATTTAGAGGGATAACATAAACTAAAACTCAATATAGTCAAGTACTCATGTAGAGATAAATTGTATTTCAATGAGGTTTCACACTTTTACAGTGTTCTTGAAGTAATTACAGTAAATTATACATATATATTATGTAAATTCACTACCGTTCAAATGTTTGGGGTCAGTTTTTTCATGTTTTTTAAAAACATTTTTTTATTTTAGAATTAATTTAAGGCGGCATTTATAAGGCGTTTAAAAACAACAATTCATTAAACTGTTAAATATTTATTAAAAATATAAATGGCTGCTTTCTTATTGTATGTAGGTTAAAATGAAAGTATTACTCCAGTCATTATTGATTTTATTACTATTAACATTAATAATAATAATAATAATAATAATAATAATAAAAATAATATTAAAGTGATTTCTGAAGGATGATGTGACTCTGAGTACTGGGGTAATGAAGCTGAAATTTCTTCTTTAAAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6101
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 |
---|---|---|---|---|---|
ENSDART00000015985 | Nonsense | 519 | 781 | 14 | 18 |
ENSDART00000027301 | Nonsense | 518 | 775 | 14 | 17 |
ENSDART00000062608 | Nonsense | 132 | 272 | 4 | 8 |
Genomic Location (Zv9):
Chromosome 8 (position 27442352)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 26570270 |
GRCz11 | 8 | 26589409 |
KASP Assay ID:
554-3925.1 (used for ordering genotyping assays)
KASP Sequence:
GGCTCAGACACAGGTGTTGTCCAGGTGCCTCTGCACCGCTGCAGTWTGTA[C/A]GGTAAAGCYTGTGCCGAGTGCTGTTTGGCTCGAGATCCGTACTGCGCCTG
Long Flanking Sequence:
CATCCACCTCACCTATAATCTGCCCACTGTATTCCTTAAAAATAGACAGAAACTTTAGAAGTGTGTGCTACAAAGAATAGTCCTAAAAATGTGGTTAACACATCATCAATGGATTATAACCACTGCATAATTGTTACTTAGTATCATTAAAATAATTTACGATTAGAATCCTTTTCAATAAAAATAAGCAACATCTCAAAAATAATACATTAAGCACGACAGACAATCTTTTTCTGACGCATTAACTTAGCATTGGACTCTTCTTGTTGCAGGACTCTTCGTCTATTATCAGTATGCAGATTTCCTCCAAACGGGTAAGAATACATCTTTTTTGAGAGGAGGGGAAATGTCAGCTATTTTTAAACAAGATCACAGGAGCACATGAAAGCAGCACATCAGTAAATCAAGCGGTGCTGTTCTTCTGTCTCTCTCCAGCAACAGCTGTATGTTGGCTCAGACACAGGTGTTGTCCAGGTGCCTCTGCACCGCTGCAGTATGTA[C/A]GGTAAAGCTTGTGCCGAGTGCTGTTTGGCTCGAGATCCGTACTGCGCCTGGGACGGACACACCTGCACACGATACCTGCCAAACACCAAACGGTACAGATGCACTCATTGGAGTCTAAAATTCTGAGACATATTCAATATTAGTTTCATACTGTTAGACCACACTTGTGACTGACAGTCAAACCTGATGATGTGTTAAGTTTTTAAATATGCTTGTGTGTGTGTGTTTTTATGCGTGTAGGAGGTTCCGGCGTCAGGATGTGAGGAACGGAGATCCTAATGCCCTCTGCTCAGGAGGTAAAACTGCAGTACCGTCAACAGCCTCAAGGAGGAGACATTTCTCTGTTTTTAATATTTATTCACAATGGCAAATAAATGTGGTTCATAAAAGGACAGTTAACCCAAAAATACTGTCATTCAAACCTGTTTGAGTTTCTTTCTTTTGATGAACACAAAAGAAGATATTTTGAAGAATGTTGGAAACTGTTAGCCCCTGACTAC
Associated Phenotype:
Not determined