Busch Lab

ZMP

LOC100000009

Ensembl ID:
ENSDARG00000075648
Human Orthologue:
SEMA5B
Human Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh
Mouse Orthologue:
Sema5b
Mouse Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa12594 Nonsense Available for shipment Available now
sa26663 Nonsense Mutation detected in F1 DNA Not yet available
sa33795 Nonsense Mutation detected in F1 DNA Not yet available
sa40625 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa26664 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa12594
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087661 Nonsense 224 1098 5 20
Genomic Location (Zv9):
Chromosome 6 (position 3979191)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 3948692
GRCz11 6 4109512
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCCCATCATTTACCGCAGCCTGGGGAACATGCCGCCTYTGCGCACYGCA[C/T]AGTACAACTCTAAATGGCTCAACGGTACAGCAAACAACAACAATTTAGTT
Long Flanking Sequence:
CCATACATGAAACAAGACTTTGCACTGATGTGTGTGTGTGAAAGCGTCTTAAACTTAAAAGTGTGTAATTGGTGTGTGTAATCAAAATTCATGAAGATTAGGTGTGAGGTGCTGAGGATTATGGGACATGTAGTCAGGTTTAGTGGTAGATGTGATGTGTTGAGTGCCCTCTAGTTTCTAGTGACCATGACAATTTGTTGTCTTTCTCTCAGGACGAGTGCCAGAATTATGTGCGAGTCCTCCTGCTGAACGGCAGTCGTTTGTTCACCTGCGGTACGAACGCCTTCATGCCCGTCTGTGTGACGCGTCCCGTGACGGACATCAGCAGCGTTCTGGACTCCATCAGCGGTGTGGCTCGCTGTCCCTACGATCCTCGACACAACTCCACAGCCATGATCACAGAGAGCGGAGAGGTGTACGCCGCCACTGTGACCGATTTCTCTAGCCGGGACCCCATCATTTACCGCAGCCTGGGGAACATGCCGCCTCTGCGCACCGCA[C/T]AGTACAACTCTAAATGGCTCAACGGTACAGCAAACAACAACAATTTAGTTTATACAATTCACCAATAGCCCATGTCTTTGGAGTATGGGGAAAACCGGAGCACCCGGAGGAAACCCACGCCAACATGGGGAGAACATGCAACCTCCACATAAGAAATGCCAACTGACCCAGCCAGGATTCAAACCAGCATCCTTCTTGCTTTGAGGCGACAGTGCTAACCACTGAGCCACTGTGTCGTTTCTTTTTAACATGTGTCTATTAGTTGAAACAATATATTATTATATACCAGTATACATAACAGCATATATTATATAACAGTATATTACAAGTCTGTGAAACTGATTTCATCCTCCTTTTTCTCTGTGCAGATCCTCACTTCATCTCGGCGTATGAGGTGAGCCGTTTCACATACGTGTTTCTGCGAGAGAACGCAGTGGAGCAGGATTGTGGGAAGACGGTTTTCTCTCGCGTGGCTCGCGTGTGTCAGAACGATATCGGCG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26663
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087661 Nonsense 239 1098 6 20
Genomic Location (Zv9):
Chromosome 6 (position 3979582)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 3949083
GRCz11 6 4109903
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTTCATCCTCCTTTTTCTCTGTGCAGATCCTCACTTCATCTCGGCGTA[T/G]GAGGTGAGCCGTTTCACATACGTGTTTCTGCGAGAGAACGCAGTGGAGCA
Long Flanking Sequence:
CATGATCACAGAGAGCGGAGAGGTGTACGCCGCCACTGTGACCGATTTCTCTAGCCGGGACCCCATCATTTACCGCAGCCTGGGGAACATGCCGCCTCTGCGCACCGCACAGTACAACTCTAAATGGCTCAACGGTACAGCAAACAACAACAATTTAGTTTATACAATTCACCAATAGCCCATGTCTTTGGAGTATGGGGAAAACCGGAGCACCCGGAGGAAACCCACGCCAACATGGGGAGAACATGCAACCTCCACATAAGAAATGCCAACTGACCCAGCCAGGATTCAAACCAGCATCCTTCTTGCTTTGAGGCGACAGTGCTAACCACTGAGCCACTGTGTCGTTTCTTTTTAACATGTGTCTATTAGTTGAAACAATATATTATTATATACCAGTATACATAACAGCATATATTATATAACAGTATATTACAAGTCTGTGAAACTGATTTCATCCTCCTTTTTCTCTGTGCAGATCCTCACTTCATCTCGGCGTA[T/G]GAGGTGAGCCGTTTCACATACGTGTTTCTGCGAGAGAACGCAGTGGAGCAGGATTGTGGGAAGACGGTTTTCTCTCGCGTGGCTCGCGTGTGTCAGAACGATATCGGCGGTCGCTTCCTTCTGGAAGACACGTGGACCACATTCATGAAGGCCCGGCTAAACTGCTCACGATCTGGAGACGTTCCCTTCTACTACCATGAGCTGCAGAGCACTTTCTATTTGCCCGAACAAGACCTCATCTACGGGGTCTTCACCACCAATGTGTGAGTGCATCAATAAATCAACTGCAGTCGCTTCAGTCAACCACGTGCTTTATGTTAAAGGGCCACAAGATCCCCATTTCAGCAGGGTGTTTTCACACCTTGAGTTTGAAAAAAGTCAGGAAAGTGGGCATGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAGGGAAAGAGTGATCAAAATTTGCATAAAAATGGGAGTTTCGATTTGGGCACACTCTGATTTTCACAGAGGCAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33795
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
ENSDART00000087661 Nonsense 250 1098 6 20
Genomic Location (Zv9):
Chromosome 6 (position 3979613)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 3949114
GRCz11 6 4109934
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACTTCATCTCGGCGTATGAGGTGAGCCGTTTCACATACGTGTTTCTG[C/T]GAGAGAACGCAGTGGAGCAGGATTGTGGGAAGACGGTTTTCTCTCGCGTG
Long Flanking Sequence:
GCCACTGTGACCGATTTCTCTAGCCGGGACCCCATCATTTACCGCAGCCTGGGGAACATGCCGCCTCTGCGCACCGCACAGTACAACTCTAAATGGCTCAACGGTACAGCAAACAACAACAATTTAGTTTATACAATTCACCAATAGCCCATGTCTTTGGAGTATGGGGAAAACCGGAGCACCCGGAGGAAACCCACGCCAACATGGGGAGAACATGCAACCTCCACATAAGAAATGCCAACTGACCCAGCCAGGATTCAAACCAGCATCCTTCTTGCTTTGAGGCGACAGTGCTAACCACTGAGCCACTGTGTCGTTTCTTTTTAACATGTGTCTATTAGTTGAAACAATATATTATTATATACCAGTATACATAACAGCATATATTATATAACAGTATATTACAAGTCTGTGAAACTGATTTCATCCTCCTTTTTCTCTGTGCAGATCCTCACTTCATCTCGGCGTATGAGGTGAGCCGTTTCACATACGTGTTTCTG[C/T]GAGAGAACGCAGTGGAGCAGGATTGTGGGAAGACGGTTTTCTCTCGCGTGGCTCGCGTGTGTCAGAACGATATCGGCGGTCGCTTCCTTCTGGAAGACACGTGGACCACATTCATGAAGGCCCGGCTAAACTGCTCACGATCTGGAGACGTTCCCTTCTACTACCATGAGCTGCAGAGCACTTTCTATTTGCCCGAACAAGACCTCATCTACGGGGTCTTCACCACCAATGTGTGAGTGCATCAATAAATCAACTGCAGTCGCTTCAGTCAACCACGTGCTTTATGTTAAAGGGCCACAAGATCCCCATTTCAGCAGGGTGTTTTCACACCTTGAGTTTGAAAAAAGTCAGGAAAGTGGGCATGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAGGGAAAGAGTGATCAAAATTTGCATAAAAATGGGAGTTTCGATTTGGGCACACTCTGATTTTCACAGAGGCAAAACAAACACATATGCAGGGCAGAAAGACAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40625
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
ENSDART00000087661 Essential Splice Site 327 1098 6 20
Genomic Location (Zv9):
Chromosome 6 (position 3979846)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 3949347
GRCz11 6 4110167
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTATTTGCCCGAACAAGACCTCATCTACGGGGTCTTCACCACCAATGT[G/A]TGAGTGCATCAATAAATCAACTGCAGTCGCTTCAGTCAACCACGTGCTTT
Long Flanking Sequence:
AATGCCAACTGACCCAGCCAGGATTCAAACCAGCATCCTTCTTGCTTTGAGGCGACAGTGCTAACCACTGAGCCACTGTGTCGTTTCTTTTTAACATGTGTCTATTAGTTGAAACAATATATTATTATATACCAGTATACATAACAGCATATATTATATAACAGTATATTACAAGTCTGTGAAACTGATTTCATCCTCCTTTTTCTCTGTGCAGATCCTCACTTCATCTCGGCGTATGAGGTGAGCCGTTTCACATACGTGTTTCTGCGAGAGAACGCAGTGGAGCAGGATTGTGGGAAGACGGTTTTCTCTCGCGTGGCTCGCGTGTGTCAGAACGATATCGGCGGTCGCTTCCTTCTGGAAGACACGTGGACCACATTCATGAAGGCCCGGCTAAACTGCTCACGATCTGGAGACGTTCCCTTCTACTACCATGAGCTGCAGAGCACTTTCTATTTGCCCGAACAAGACCTCATCTACGGGGTCTTCACCACCAATGT[G/A]TGAGTGCATCAATAAATCAACTGCAGTCGCTTCAGTCAACCACGTGCTTTATGTTAAAGGGCCACAAGATCCCCATTTCAGCAGGGTGTTTTCACACCTTGAGTTTGAAAAAAGTCAGGAAAGTGGGCATGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAGGGAAAGAGTGATCAAAATTTGCATAAAAATGGGAGTTTCGATTTGGGCACACTCTGATTTTCACAGAGGCAAAACAAACACATATGCAGGGCAGAAAGACAGTGGCTGTGTTTACATGGATATCAGTAATCAAATTATTTGACAAATGATTAAATGGTTTGATGCCGCACGGCGAATGAGAGAAAAGAAACCTCCGCATTTCTCTGTAACTTAGGCCGTACTCACACTATGTACAGTTGCCTCAAACGGGGCCAAAGCACGCTTTTTCCCCCACCCGTCTCCCCCGACGGCCCGCACTCACACTACAATTAGGCCTGGGCACGCTTACGTCATCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa26664
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
ENSDART00000087661 Essential Splice Site 975 1098 18 20
Genomic Location (Zv9):
Chromosome 6 (position 4012411)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 3981912
GRCz11 6 4142732
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAACTCTAGTGCTGTCAAAAGGACAGAAGAGGAGCACAAACTGTGGAG[G/A]TGAGTCGAAAATTTACACCACCAGACAAAGATTGGAAACTTTAGCATTTT
Long Flanking Sequence:
CTCTAAGGATTTCTTTCAGTAAATGACTAGACAACACTGGCTTAGTTGTGATTAACTAAAAATAACTGACACAGCACAGAAGTTTCATTTATTTTTGGAATCCCAAAATAATAGTTGCTTTGTATGTTTTTAATAAGCTACAAGAACACAGAAATTCTCTTTAACTAACACACATCCTCTTAAAATATATAAATAATAGTTATTACATGTGCTCTGTTTTTCCTTCTCTGCTGTTTCAGGTGGGTGGGGGGCGTGGTCAGAGTGGGCAGAGTGTAATGGGGAGGGGCTTCAGCTCCGGGCTCGTACATGTGAAATAAGCCCCGCCTCCTGTCTTGGAAACTCCACAGATCAGAGACAGTGTCGGCCCAATGAGAGCGCAGGTCAGTTCAGTTCAGCTCAGCTTAGTTCCCTCTTTACATTCATTTCTGATTCACAAACACTCATCCTGTTTTTAACTCTAGTGCTGTCAAAAGGACAGAAGAGGAGCACAAACTGTGGAG[G/A]TGAGTCGAAAATTTACACCACCAGACAAAGATTGGAAACTTTAGCATTTTGAATGTTTTAAAAGAAGCCAATTTTGCTCACCAAGGCTGCATTTATTTGATGAAAAATAGTTAAAGGCTGTTACATTGGAACAGCTGGAAACAGGCCGAGTTCTTGCCAACCACAGAGGAGTGGGCTGACAGAAATCCCAGGTGGGCAATTTTTTGGGGGTGGGGTTAGGAGATAGATGCACTGTAAAATTCAAATTTAAAAAAACTGAACGGAATAGCAAAAGTATTGTAATAATGTTCTTGTTTGGGCTTGTTTCACCTTCGGGTGGGGAACTTTAATGCTGTGTGGAAAATTCCACTATGGAGATTTCGCTCAGAAAGCCAATCGTCTAAAAGAGTACATAATCGGGCCAATGAAATGCCAATGAGTTGGCAGCGTCAGCTTGCGCAGCTGATGATTGTTGCAATCAATTTGGCAATATAAGCATAGCGAGAGCAAGGTGAGGCATC
Associated Phenotype:
Not determined