ZMP
B6E518_DANRE
Ensembl ID:
Description:
Semaphorin 7a [Source:UniProtKB/TrEMBL;Acc:B6E518]
Human Orthologue:
SEMA7A
Human Description:
semaphorin 7A, GPI membrane anchor (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:10741]
Mouse Orthologue:
Sema7a
Mouse Description:
sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A Gene [Source:MGI S
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11887 | Nonsense | Available for shipment | Available now |
| sa42747 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45580 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa2870 | Essential Splice Site | F2 line generated | Not yet available |
| sa22868 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11887
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115260 | Nonsense | 14 | 632 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 31697529)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 29502615 |
| GRCz11 | 16 | 29437238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTGAGCAACATGAATCTGCTCGTACTAGCAACTCTTTTCTCAGTGGTTT[T/A]GGCCGAAAAATCACCTCGGCTGAAATTCATCGTKAATGGTAAGACTTTAT
Long Flanking Sequence:
TAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATATAGATCTCTAACAAATATAAACTGATATTAAGTGTGATAATACATATAAAGTGACAAACAAGCAAATGTAATCGAGAAGCTCTGAAACTAGTAAATAAAGTGAGTGTTTTGCTCTGTTAGTAGTTGTCAGTGGGGTGAGCGCATGTCTGCTCGCTCCTTCTCTCTTTCAGGAGGTGTGACGTGAAGGCAATTACCGCTCAGCTTCTCGCGGAGCTCTGAGGGACAGACAGGCGAGGCGGCGTCCGCTTATCGCACGCGCACTTCTGCAAAAAACAACCCCAGTCCTTCAGCGAGAGCACTCTTTCATTAGCTTGTCGTCACTCTAATTAGAGCACCGCTGAGCAACATGAATCTGCTCGTACTAGCAACTCTTTTCTCAGTGGTTT[T/A]GGCCGAAAAATCACCTCGGCTGAAATTCATCGTGAATGGTAAGACTTTATTTGTCTTTAACGTTACAGTTTCAGTCTGCATAACGCATACGTATTTTTTTCTGTGGAAAGTTCTGGATTTTTCTAAAGCCATGTTTATCCTTACTCTAGCACAAATTGCATCTTATTTTTCCCTTGGGAGAAAAAAAAACTGCTGCGTATCTACTTCCGTTAGGATAAAATAAATCAAATGGCAATGTTGGTGACTGGAAGCAGGCCAATACAGGGCACTGATTGCATTACATAGCTGTTTTGAAAACAAAAACCGATTGAGGCTCATGTTCACGTCATGACTTCACATCATGACGTATATATGTGATATTAATCGTGGTTAAGAGTGCGTAAGTTTATTTATTGCACTACACTGATAAATAAGCTGTAGCATCGCGTTATTTGGGGAAAATGTAAACACAAATACATTTAATCATGCTGTCAATAAAGCGGTGTTTATAGCCTAAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42747
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115260 | Essential Splice Site | 73 | 632 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 31694024)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 29499110 |
| GRCz11 | 16 | 29433733 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTCATCTATAAGCTCAGTTTTCGTGATAAAGAAGTGCATGACATTCAG[G/A]TAGGGGGGCCGACACTGTAACCCAGAGCCAAAGTAGATCTATCACTGCTC
Long Flanking Sequence:
TTATTTTTTGCTTTGTTTTGGTTTCTGTTCAACACAAAGTAAGATATTTTGAAAAAATATTGTAAACCTGTAACCATCAGCATACATTGGAAATACAAATATTAAAGTCAACATTCTAAAAAATATATTTCCTTGTGTTTAACAGGAGAAGGAAACTCATGGTTTAGAAAAATCCACAGCAAAATATATTGGAAACATTCGACGCATTTAAATACTGTAGGTTCATTAGGCTCCATTTGTTTTGCTGTCTTATTCAAATTTAATGACTATAGTTGTATTTTCATTGTTTTCTCTGTAACAATATATGAACATATATACCAGACTTGTGTACGCACTTCATTTCTGTCTGTTTGTCTTTAGAATCACCTCGATTTCGCTTCATAAAACCAGAGAACTTCACTACAGTTTACCACCAACAGGAGACTGATGTCCTGTATGTGGGGGGCCAAGGGGTCATCTATAAGCTCAGTTTTCGTGATAAAGAAGTGCATGACATTCAG[G/A]TAGGGGGGCCGACACTGTAACCCAGAGCCAAAGTAGATCTATCACTGCTCTAAATCCTGACCTAGATAGCTGGTACTCAGCAAGTAACAAAAAAACTGTGCTATTATTTATGGAGCAGAACAATGTCTTATAACGGAGGCTCTGTAATACGATTACTTTGCGGTTGGGTAAAGAAAGCATTTCTTGCCAAGGACAGATGGTTATGGTTTCTTACCATTTAACTACAGCAATTATACTATGTTCTGTTTTCTATAACAGAATATAGCTCTAACATGATGAGAACAAATCATCCCTACAGTACATTATTATGAATGCAAGGCTGTGTGATTAGTACTGTTGTTGATGTACTCACAGATCCCTGTGGTGATGGATGAGAATGCAAAAGAGTTGTGCCACTCTAAATCATCCCAATGGAAGGTAAGAGAGACAATCCTGCAGTATTCAGCCAGTTTAGACCTCGGGTAGCTTGTGATTTCAGGCAAAGAAAAGGATTATCTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45580
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 |
|---|---|---|---|---|---|
| ENSDART00000115260 | Nonsense | 273 | 632 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 31685266)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 29490352 |
| GRCz11 | 16 | 29424975 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACATTCCTGAAGGCACGTGTGATGTGTGGGAAATCTGGAACTCCTGTA[C/T]AGTACAACAACTTCAAGCAGGCTTTTGTTCTGACCTCTCATCTCCGCACT
Long Flanking Sequence:
GTAATGAAACCCAAATTATTGAGGATAAGTGAATGTTGCCATGTTGTGCCTTTCAAATACAGCTATACTAATAGCCCCACAACTGTTGAAATCAACTAATACTGCAAATGGTTTACTATACTTTCAAATGCAGCATAGTTTGAATCTATAACAATACCAAATGTCTTACCCTTCTTAGATCCGCAGTTTGCAGGAGCCGCTGTGATACCACACGAGGAGAAACTCAAAAATGAGATCTACTTCTTCTTCAGCGAAGTCAACAGCAGCTCCAGTCTAGATGAAGAGCCGTACAGGGCACGGATAGGACGAGTCTGCATGGTAACAAGCTTTTAGCAGTTCCTGCTTCATATACAGCACACTGCTGTAAGGACACAAGCTTTCGGATGACCTTTATATCTGTGTTTCAGGTCGACGAGGGAGGGCTTCAGAATGTGCTGCCTAACTCCTGGACTACATTCCTGAAGGCACGTGTGATGTGTGGGAAATCTGGAACTCCTGTA[C/T]AGTACAACAACTTCAAGCAGGCTTTTGTTCTGACCTCTCATCTCCGCACTGGCTTGATCTACGGCATTTTCTCCAATGCCTGGTAAGCAGATGTCTGAGAGTCTGAGAGTGAGTAGGATGGTAGCATTTGACATCAGACTGCTGAATAATGCCTCTGGCAGAACTACATTCAACACAGAAAAACATCCCTATAGATTAACGCTCAAAACACATACTTATATATATACATTTTTGTGCCAAAATTTTGGTCGCCCAACAGTTTTGGCGTTTTAGAAAAGTTTTAATGACCTTCTAGATATAAGACTGGTCTCTGCATTAAGATATAAACAGATATGTGCACAAAATTGAGAAAGTTCAGAGTAAGATGGCTCCTGCTAGTAAAAGATGGTAATTAGTATGCATCCATATACAAGACCCAGAGTCTATCTTATAATTTTTGTGGTTTTTTAGCTTTTTTCCTGTCCAGGCAATCCCATACTGCCTCTATAATACTATATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2870
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115260 | Essential Splice Site | 300 | 632 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 31681388)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 29486474 |
| GRCz11 | 16 | 29421097 |
KASP Assay ID:
554-3210.1 (used for ordering genotyping assays)
KASP Sequence:
AGTANNNATGCACAGGCTTCAAAAATCTGTGTCTCCTGTTTATGTTTTTCAAC[A/T]GGAACACGACCGTAGTATGTGCGTACTCTATTGAAGATATTGACAAAGCC
Long Flanking Sequence:
TATATATATTTTTTTTTGACATACGATTATTTAGCTTACCCCATTGGCAGATTGTTTAGCTTGCTTTAAGAAAAAACTCACTTAATGTTGGCATTTTATTTTTTTAAAACAAGACAATATGTTTGCTTGTCTAGAAAAGGCTTCTTGATTTAAGAATGTTTAGATATTTGGATTAGAAACAAAGACGAAAATCTAAGTAAGATAAGCAAATGTTGCAGTGTAGATATCTTATCACCACATCACAACTGATTCATTTGCAGCCCGTTTGGTCTGCTGTTTGTTTTTGATGTGCAATATGTATTTAATATTGGTTTCAGATCTTCAAAAGATATAAAGCATTTCACTAATTTTGTAGATAATGCTTCTGTGAAAAACGTATCATGAGTTAAAGACCAAAATGTAAAAAATAATTATCAGCTAATTAGTTTTTGCATATGAGCGAAGGTGTACAGTAATGCACAGGCTTCAAAAATCTGTGTCTCCTGTTTATGTTTTTCAAC[A/T]GGAACACGACCGTAGTATGTGCGTACTCTATTGAAGATATTGACAAAGCCTTTTCTTCATCCAAACTGAAGGGCTACAACTCACCGTTGGCAAATCCACGTCCTGGAACGGTAAACACACAAAGTCAAAGCAAAGTCAAAATTAGCTTAACAGAGGTTATACAGTATTTTTAATCACGTTCTTATGCATTATATCACATCTATTAGATACTAAAACAAAAACACAACCTGATTCATCATTTGTGTGGTCTTCCTCCATCCAGTGTGCTTTCAAGAATAACACTCAAGCTCATAACCAGAAGATCCTGAGTGTGATCAGGGATCACCCAGAAATTGAAGAAGTGATCGGCCCGGTCCATGACGTTCCTCTGGAGTTGTCTGTTCAAGACCACTTCACTCATATTGTGGCAGACACAGTCTTGGCTGTCAATGATGAACACTACAGCATCATTTATCTGGGCACAGGTACAGTAAACTGCAGAGAAATGTGCTAAAGAGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22868
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000115260 | Nonsense | 580 | 632 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 31674806)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 29479892 |
| GRCz11 | 16 | 29414515 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCATCTCAGGCTCCTCCTGCGTCCTGGCTCCGACCCCCGAGCTGCCCT[T/A]GAAGGAGGGTGTTTTCCGTTGTCTGGCGGAGGAGAGCGGCCTGCAGCAGG
Long Flanking Sequence:
TAATTAACCTAGTTAAGCCTTTAAATGTCGCTTTAAGCTGTATAGAAGTGTCATAAAAATATCTATTAAAATATTACTTTCAGTCATCATGGCAAAGATAAAATAAATCAGTTATTAGAAATAACTTATTAAAACTATTATGTTTAAATACGTGTTGAATAAACAAACAGGGGGGCTAAAAATTTGGGGAGGCTAATAATTCTGTCTTCCAACTGTATATTGCTAAATAAATAGGCACTGTCCTTAATGTACACTATAAGTACCACATAATCATTTCATCACACTAAAACATTTCCCACCATTCTCTAAAACAGCTCCTAAAGCCCGCAGCACTATCCCCAAAGAAGTTTTAGTAGATAAAGATGGGCCGGTCCTGCTGCCCTGCCCCGTTCGCTCCTATCACGCCTCTTACCGCTGGGAGAAAGACAACTGCATCAAGACGTACCCCTGCACCATCTCAGGCTCCTCCTGCGTCCTGGCTCCGACCCCCGAGCTGCCCT[T/A]GAAGGAGGGTGTTTTCCGTTGTCTGGCGGAGGAGAGCGGCCTGCAGCAGGAGGTGGTGTCCTATAAGCTGGTGTTCAACGGTGGGCCACTCTCCACCTCTCTGGCCTCCACACTGGGCTCCACTCTGCTGCTGGCTGTCACCGCACATTGGCTCCTGTAGATCCAGATTAAGGAAGAAACCAGTGTTATGCTAAGGTCAGCAGAGCATGAGTTCAGCTTAACTGCAGGAGCGGCTGGTCTCGGTATAAACTGAGCTTCTTGTGTCTTATTCGGAGCAATCACTATAGAGCTGCACGATTAATCGGTAAAAATCGCTAGCTTAATTCAGACACCCACATTATAATAGTTTAATTATTTTTTTTATATTTTATTTATTTATTTTATTTTTTTCAAAACAGTTCAGAACAAAACAAACAAAGAAAACATTTTAAAGGAACATGGAAGCAAAAAAAGGCATACCATACAAGTGTCAAAGTTCACCAAATACAATCTCATTTACA
Associated Phenotype:
Not determined