Busch Lab

ZMP

B6E518_DANRE

Ensembl ID:
ENSDARG00000070442
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
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.
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.
Availability:
Order Allele From ZIRC
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