ZMP
B6E445_DANRE
Ensembl ID:
Description:
Semaphorin 4b [Source:UniProtKB/TrEMBL;Acc:B6E445]
Human Orthologue:
SEMA4B
Human Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Mouse Orthologue:
Sema4b
Mouse Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11494 | Nonsense | Available for shipment | Available now |
sa13494 | Nonsense | Available for shipment | Available now |
sa44667 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11494
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 |
---|---|---|---|---|---|
ENSDART00000109243 | Nonsense | 444 | 849 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 31595922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29988264 |
GRCz11 | 7 | 30259414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTYCTGTCAGAAGTCAGCCTGTGCTYTTCACACACACTGTGCACTACACA[C/T]AAATCGCTGTGCACCACGTGAAGGGTCTCCACAGAGCTTATGACGTRATG
Long Flanking Sequence:
TTTAACTTACCAAGTGTACCAATATTACTGGAAAGGTCTGCATACTAAACTTCTGATGTGTTTATTTTACTTTTCTACTCTGCATACTGTTTGTTTCTAATCTGCTGCTGTGTTTTGCAGGAGTAAAGGTCTTGCTGGCAGTTCCGCAGTGTGTGTGTTCAGCATGGATCAGGTGGATCGAGCCTTTACTGGCCGTTACAAAGAGGTGAATCGAGAGACACAACAATGGTACACATACACTCAATCTGTACCTGAACCACGACCAGGAATGGTAAGACAACACACTCCCACATTTACACTCTACCTGTTCTGTACAAGTGGAGAGTCTCTTAGTGTTTTTTTTTCTTTTGTAGTGTATTACTAATGCCTCAAGGCAGCTGGGAATAGACTCCTCTTTGGATATGCCAGATAAGGTACTAAACTTTGTGAAGGACCACTTCCTGATGGACCGTCCTGTCAGAAGTCAGCCTGTGCTCTTCACACACACTGTGCACTACACA[C/T]AAATCGCTGTGCACCACGTGAAGGGTCTCCACAGAGCTTATGACGTGATGTTCATTGGCACAGGTATGTGAGGCCTTTATGAACATCAGATTTTCTGTGGTTATATTTCATTCCTAATAAGATGGTGATGTTGGGTTTTTGCAGCTGATGGGCGTCTGCAGAAGGCTGTAAATGTAGCTGGTATGATGCACATCATTGAGGAGATCCAGCTGTTCTCAGAACAACAACCAGTACAGCAAATAGAGCTGGATTCAGCTAAGGTGTGTTTGTGTTCTATATTATGTGGTTTACAAGGACACTAAATTGTATAGTGACATAGGTCTGACTGAAGTGTAATACTGATAAGGTGATTTTTCTTTACACTTAAAATCATACTTAACAGGGTGATATTCGCAGTTTAACAGGTTTTGATATTCAAATTTTTAAGGTTTACGGATAGAGGTAGGTTAAGTCCATATAATAAGCTATTTTTACAGTATAAAATACATTACACCTATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13494
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109243 | Nonsense | 655 | 849 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 31599952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29992294 |
GRCz11 | 7 | 30263444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTTGGTAGTCAGCGGCCGAGCAGGCAGYGACGAGGTCTTCTCATGTTG[G/A]KCARAAGAACGTGGCTTTTGGCAACTCTTGGCCAATTACTGCGTGAAGGC
Long Flanking Sequence:
TGTGGAAAAATTCCTTGCCCTGTTAAACAATTTAGAAAATATTTTAAAAAGAGAGAAAATAATAATAATTTTGACTTCAACTCTCTATATACAATCACAACAACAGTCTGTTTTTACAATCATTAGATGTCATGACAATACTGCTTTTTAGTTGGTGAAAGCCACAGAATTTGATATTTGACTTAAAGTTGGAACCCTACTTAACCATTACATAAAAGTCATCCAAGCATCTATAATCCAAAAAATTAAGTTGTAATATTTACCTCTTCTGCTCTCTTTCTAGTATCACCGCGTTCTTTCACAAATTCCGAAACATCAGATTGTGAGCTCATCATCATCCCAGCAAACACTCTTCAACTTCTACCCTGCAACCTTCGCTCCAACCACGCCCACAGAAAATGGCTATACAAACCAAACGTAAGTCACTTTCTGTTTCCCAGCGCAGATGGTGGCTTGGTAGTCAGCGGCCGAGCAGGCAGCGACGAGGTCTTCTCATGTTG[G/A]TCAGAAGAACGTGGCTTTTGGCAACTCTTGGCCAATTACTGCGTGAAGGCAGAGCCGTTATCTGAAACCACAACCAAAATCGGCCGCAAGGAAGCACCATTTTTAATCCAAAGCATAGCATCGGACATTCTGTCTGAGGAATCCGAAGCACACTCTGCTCAACATCGCATAAAGACGTACGGCACAGAACTGGCGGTGGTGTGTGTTTTATTAGCAGTATGTGTGCTTTCGTTTGGGCTTTCAGTAGTGTATCGACACAGAGGTCGGATGAAGGAGGTACTCAGAGGAGGAGAGCAAGCTGGAGGAGCCCAGAAGAGCACAGTCCACCCTGGGGAGAGCTTGCCTCTCAATGCTGGTGCACCTCCAACCTCGCCATCTGAACACAAAAGCTACCAGACGCTAGAGGAAAACTGTAGTTACATAATCGCTCCGGCAGAAACAAACGCACCGCAGAAATCGGAGGAAACACAGATACTCAAGCCAACACCACAGAATGGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44667
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 |
---|---|---|---|---|---|
ENSDART00000109243 | Nonsense | 839 | 849 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 31600502)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 29992844 |
GRCz11 | 7 | 30263994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAAGAGAGTCATGTGGAGGTCAGTGACATTAGCCCTCGTCCTCGGGTA[C/T]GACTAGGCTCTGAGATTAGAGACTCTGTGGTGTAAAATACTGCATATACA
Long Flanking Sequence:
CAGAGCCGTTATCTGAAACCACAACCAAAATCGGCCGCAAGGAAGCACCATTTTTAATCCAAAGCATAGCATCGGACATTCTGTCTGAGGAATCCGAAGCACACTCTGCTCAACATCGCATAAAGACGTACGGCACAGAACTGGCGGTGGTGTGTGTTTTATTAGCAGTATGTGTGCTTTCGTTTGGGCTTTCAGTAGTGTATCGACACAGAGGTCGGATGAAGGAGGTACTCAGAGGAGGAGAGCAAGCTGGAGGAGCCCAGAAGAGCACAGTCCACCCTGGGGAGAGCTTGCCTCTCAATGCTGGTGCACCTCCAACCTCGCCATCTGAACACAAAAGCTACCAGACGCTAGAGGAAAACTGTAGTTACATAATCGCTCCGGCAGAAACAAACGCACCGCAGAAATCGGAGGAAACACAGATACTCAAGCCAACACCACAGAATGGCTATAAAGAGAGTCATGTGGAGGTCAGTGACATTAGCCCTCGTCCTCGGGTA[C/T]GACTAGGCTCTGAGATTAGAGACTCTGTGGTGTAAAATACTGCATATACAGACTGAAACTCTTAATGTTCACTCGGTACAGTCAATGGGCAGCTTTTGTAAAGACTAATCATACTGAGCCTGAGGAAAAAGAGATGGGACATGCTCGGTTTGTGTATTGCCACATTTTAGTTGTTGGAGACAACGCCCTGAAATCTACTCTCACATCTTACAACTTTTAAATGTTATGACACAGTTTATTGTGTTGATATAAAAAAAAAAAGACAGTTAAAATATTTGTGATGTGGACGAGACTAGAGCGGATCGATGTACAGGAAAGGTGGGCAATGGGCTTTGTGTTGTATGACTGCTACTGGTGCTATAATCACTGCCAAGACAAAGAGTGATGAAGCTTCACTCAAGGTGGAAAAAACAGCTTTAAATGACTATTTGTGTTCCTAATGTTTAATGAGGGTACTTTCATCTTAAAAGTTGACTGTGACTGTGAATATCAGGCAGTTC
Associated Phenotype:
Not determined