ZMP
LOC798168
Ensembl ID:
Human Orthologue:
SEMA4A
Human Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Mouse Orthologue:
Sema4a
Mouse Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13803 | Nonsense | Available for shipment | Available now |
sa15476 | Essential Splice Site | Available for shipment | Available now |
sa39124 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42800 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36237 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13803
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 |
---|---|---|---|---|---|
ENSDART00000114601 | Nonsense | 200 | 739 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 45892938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43151128 |
GRCz11 | 16 | 43054886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RGACAAAAACGTAATTTCTCGCTGTCATAGYAGAGGAACACACAACAACT[T/A]GGAGCTTGAGACTGTACCGAAATTGCTACAGGGTTTGTTTGTTTTTCTGT
Long Flanking Sequence:
CAGCACCAGCTGTGGTCAATCATAAGCACGTAATCTTCTCGAAATTAGTTAATAAACTTCACTAAGTTTGGTTGGCTGGTGACATCACAAACCCTAAAATGTACATAAATCCCACCCCTGGCCATTATATTTCTTTAAACATGCACAAAATAATTAGCCAATCAGGGCACACTGATCCATCTGACCAATCAGAGGCCATTGTTTATTTTTTAGGGAGGGGCTTCATACAGTATAATCAGAAAGTTAAAAGACTGTTTTTAGGTGGATGACACAAAACTAAAATAAAACAATGCAAACAATATTGAGATTTTATTTCAAACATAGAACAAACACATTTAAGCGAACCCCATAAACGCAAACAAGCCTTGAATTAAAGCTGATTTTTAAAATGATGACCTCTTTGTTTACAGATGGAGAGCTGTATACAGCAACCAATGTCGGCTTCTTCGGGGACAAAAACGTAATTTCTCGCTGTCATAGTAGAGGAACACACAACAACT[T/A]GGAGCTTGAGACTGTACCGAAATTGCTACAGGGTTTGTTTGTTTTTCTGTAAAAATATTAATGCTGCCATGATGCTAATAACACATACAAGGCAAATGTTCTTGATGTCCTTACTTTAATATAGGCTGACACAGGAGTTGTTGGTTTGATTTGAGTTTACTTTACAAAACTCCTTCATGGGTGATTACAGTAACCTTGAGCAAACATAGGCTACTATTTTTATAGATTGAATAAGTTCCTTTTTGTTTTTTGTCTTAGAGCCTGTATTCATAAGCTCAACACATGTCGCCAGTGAAGGGAAGATCCTGCTGTTTTTTACTGAGAATGGGGACTTGAGCGGAGACTATTTTGGAAACTCTTTTACTGTGTCTCGTGTGGCACAGGTCTGCACGGTAAGACTTACAGTAATAATTAACCCTTAATCAAGTAACCCTTATGGTCACATAAACATATGACTTATGACATACGAGTCTTTACTATTATTCAATTTATTATTACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15476
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114601 | Essential Splice Site | 316 | 739 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 45891795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43149985 |
GRCz11 | 16 | 43053743 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGATTCWCCAGACAASACRCTGTTCTACGGGGTCTTCACTTCACAACGG[T/C]GACAAACATTTYTAGCAAATGCTCCATCATACTGTTCTGAAAGGTCTTGG
Long Flanking Sequence:
TATAAAATGATGTGATATTTTAGCCTTGAGAAAAAGGTTTTATTAGTTTTTATATTTTTTATGAATAATGCCACCTTTCTGTCTGTGATGGTACTGCACTTCAACTGTAACGATAATTAATTGACTCTTTATTAATTTTTTTTTCTAATGTTAGGCAGAAAAGGGACCTAATATAAGAACTATAATAACTTATATTTAACCTGTCCTCTCATTTGAGTCATAAAACACCGAAGCAGCACAAGAAGGAAGCGTTTGAGCTTGTCTGTTTTATAGGCTCCTCAAAACTAAATTTTTAATGACGTAATTCTTTATATCAGGATGACAATGGAGGAACCCTCACCTTACAAAGACGATGGACATCTTTTGCTAAGGCTCAGCTGGTCTGCCAACAAGGAGAAGATCTTCAGTTCAACAAACTTCAGGATATTGTCAAACTTTCCCCATCCGACAGTGATTCTCCAGACAAGACGCTGTTCTACGGGGTCTTCACTTCACAACGG[T/C]GACAAACATTTCTAGCAAATGCTCCATCATACTGTTCTGAAAGGTCTTGGGTTTTCTGTTTAAACATTTTCTTCCCATGTTTCTCTTATTCAGGTCGGTTTCATCTGGTCTGTCAGCGGTGTGTGCTTTCAGTCTGACGGATATTAAAGCTGCGTTTTCAGGGAATTACAAGACATTCGACTTGAGAGGAAATCACTGGTCACCTCAGCCAAATACAGACGGCAAACTCGGCAAGGTAACAGACTGAGAGAGATGTAATCTGTAACTTCACGAATCTTCCTAAATTTAGTTGAGGAAAAAAAATAATTATAAATAATTATAAATAGTTATAAACATAATTCAAGTTTAAAAAAATATTACTTTATTGTTTATTTTATTTGTATTTATTTGTACCATATTAGATATATTTTACTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTTGAAGTCAGAATTATTAACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39124
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 |
---|---|---|---|---|---|
ENSDART00000114601 | Nonsense | 533 | 739 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 45888834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43147024 |
GRCz11 | 16 | 43050782 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAAACACAGGCGGCAGGACGTGGAAAGAGGAAATGTCACAGAACAGTG[T/A]ATAGAGTTCAGAAATACTGCTGCAGGTAAACCGCTTCTGTGAGAACCAAA
Long Flanking Sequence:
CAGCGAAATGAACCACCAACTATGTTTTAAGCAGCAGATGCCCTTACTTTAATTTAATTGAATTATTTAATTTAATTTAATTTAATTTAATTTATTAATTAGTCTGTCTGTCTGTTTATTTAATTAATTAATTAATTAATTTACATTTTTCATCTAAAAACTAATGATTTTAAATTTATTTAAAACTATATAATATAATAATATAATGAAATACAAATCAAAGTAAATTTGGAAATCACTACTTTATTTTTTTTACCATACTGTCCCAACTTTTTCTAATTTGGGGTTGTATATTTGTGTTTTAATTGAATTAATGAAAACGTTTTTAAAAATGTATGTGTATAAACTAGTTTTAGTGTTAGCAATAACAACACAAGAAAAAAGCCCTAGTTTTTAAGTCCTTTTATCTGAAATAACAGATACCACTGTACTATTCTTATGTTTTTGTGTCTCAAACACAGGCGGCAGGACGTGGAAAGAGGAAATGTCACAGAACAGTG[T/A]ATAGAGTTCAGAAATACTGCTGCAGGTAAACCGCTTCTGTGAGAACCAAATGATTTGTAGACCTTAGATGTTTATTTTTAGCTCAACCCCAATTTGTTTTATCACACTTTTTATGTGAAGGTGCAAGAAGTATCTTAATTCCTGTAAAAATAAATCATAAAATTTGTGGGTAATAGCTGAAAAGAGGTTTTCAAGCATCTTATCTTTAGTAAAGTTATTAGTTAGACAGTTAACCTGCATTTGATATTCTTTTTATTGATACATAAAGTTAATTTTGATGCACAAAGTAAACATAAAATTTGATATACAAACTAAAACAGGATGTTTAGATTTCTTTTTGTTTTGTAATTAAATACAATAAAAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATACTTACCGGTCACTTTTTTAGGTACACCTGTCCAACTGCTAGTTAAGAAAAATTTCTAATCAGCCAATCACATGGCAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42800
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 |
---|---|---|---|---|---|
ENSDART00000114601 | Nonsense | 578 | 739 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 45886216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43144406 |
GRCz11 | 16 | 43048164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAACTGGCGAAGATGACCTGGAGATTCTCAAACAACAGCCTCGTTCCC[C/T]AGTTCCCGTACCTGCAGTGGACGGATGGCAGTCTGGTCTTCCCCGTCTCT
Long Flanking Sequence:
ATGCCATGAAGGATTAAGGCAGTTCTGAAGACAAAAGAGGGTCCATCCCAGTAAATAGTAATGTGTACCTAATAAAGTGGCCAGTGAGTGTATATATATTTTACATTAAGCAAAGTTTAAAAGTTTCCCCTTACAGATTTTAATTTCAGTTTATATAAACTTTTACATTGACCTTTAACCGTTTACATTTAAATTAAAATATAATAATATAATTCATTCACAATAAATATAAATAAAATAACTCTGATTGTCGTCTAGCTTGTAAAGTCCAAAACACACTTGTTGATTGCCTCATTATGATGAACTCTATGTCATTTTGAATGAAAGCATCTGCAAAGTGAATAAATATTAATATCTAACTGTAAAACTTCTGAACTGTCTGTCTTTCTCCAGTGTTGTTCAAGACTGCACACTTGAATGAAATTGTGGTCCTGCCCTGTCAGTCAAAATCCAAACTGGCGAAGATGACCTGGAGATTCTCAAACAACAGCCTCGTTCCC[C/T]AGTTCCCGTACCTGCAGTGGACGGATGGCAGTCTGGTCTTCCCCGTCTCTCTAGAGACCACAAACACCTACCGCTGCGTGTCTGAGGAGCTGGGCTTTCAGCAAACCATCGCCACCTTTTCTGTAAATCTCCCTGTGGTTCCTCGATCTCGCATGTCTCCATCACACCAGCAGCCTGAGCACATTGACTTCACCACAATTGAGCTTGATGAATCTGAACCTATAAATGAAGAAAAAATAAATGACAGGAGCGAGGAAAAACAAGCCAGCACTTATCACGATGCTGGAAAAGACACTCTGTGCATCTCACAGAAGAGCTACTACTCTGAAATGGTCGCTGTCTGCATCTTTTTTGTCATTTTTTGTTTCTGCATACTGGCTTTTTTTGTGGTCCTGTGGAGGAATGGCAAGAGGTGCAACAAAATTTTACCTCAGGAGCAGCCTCAGAAAGGCACAGAGTCGGACAAAATCTGCCAGACAGAACTGTAACAAAAGCAGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36237
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 |
---|---|---|---|---|---|
ENSDART00000114601 | Nonsense | 735 | 739 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 16 (position 45885743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 43143933 |
GRCz11 | 16 | 43047691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTACCTCAGGAGCAGCCTCAGAAAGGCACAGAGTCGGACAAAATCTG[C/A]CAGACAGAACTGTAACAAAAGCAGAGCTAAAAGAGCTGTATCAGGGTGCT
Long Flanking Sequence:
AGATTCTCAAACAACAGCCTCGTTCCCCAGTTCCCGTACCTGCAGTGGACGGATGGCAGTCTGGTCTTCCCCGTCTCTCTAGAGACCACAAACACCTACCGCTGCGTGTCTGAGGAGCTGGGCTTTCAGCAAACCATCGCCACCTTTTCTGTAAATCTCCCTGTGGTTCCTCGATCTCGCATGTCTCCATCACACCAGCAGCCTGAGCACATTGACTTCACCACAATTGAGCTTGATGAATCTGAACCTATAAATGAAGAAAAAATAAATGACAGGAGCGAGGAAAAACAAGCCAGCACTTATCACGATGCTGGAAAAGACACTCTGTGCATCTCACAGAAGAGCTACTACTCTGAAATGGTCGCTGTCTGCATCTTTTTTGTCATTTTTTGTTTCTGCATACTGGCTTTTTTTGTGGTCCTGTGGAGGAATGGCAAGAGGTGCAACAAAATTTTACCTCAGGAGCAGCCTCAGAAAGGCACAGAGTCGGACAAAATCTG[C/A]CAGACAGAACTGTAACAAAAGCAGAGCTAAAAGAGCTGTATCAGGGTGCTGGATGAGTCATTCTTGATCCACAGTTTGGAAAATAACAACGTTTACGCTTCGAAATGAATCAGAGGGGATCGGTGTAATGGGTTTAATATGGGTCATGGGATTTAAAATCATTTTTGATATGTGTGATATTTAATGTAATCATATTATTTTATCTAAAAACAGGGTTAGTCAGCTCTGACACATGAATGAAGACTTGTTTGTACCATTTAAAGTCTTAATAGAACTTTAACATACACTCTAAAAATGCTGGGTTGTCTTAATGCAACATTGGGTCAAATATGTACAAATCCAAAAATTGTATTTAAAAAACATTATTCAACCCAACTGATAGATTTGTCGATTAAGTGCTCAGCATAAATGAATACACCCCTCACAAATCTATTTTAAATATAAAATATATCTAAATATATCTATATCTATATCTATATAAATATATCTTATCTATCTAA
Associated Phenotype:
Not determined