ZMP
sema4e
Ensembl ID:
ZFIN ID:
Description:
Semaphorin-4E [Source:UniProtKB/Swiss-Prot;Acc:Q9YHX4]
Human Orthologue:
SEMA4D
Human Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Mouse Orthologue:
Sema4d
Mouse Description:
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (se
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9636 | Essential Splice Site | Available for shipment | Available now |
sa9433 | Nonsense | Available for shipment | Available now |
sa19891 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9636
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056252 | Essential Splice Site | None | 766 | None | 16 |
ENSDART00000108861 | Essential Splice Site | 13 | 762 | None | 15 |
ENSDART00000109471 | Essential Splice Site | None | 766 | None | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 50142495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 49838027 |
GRCz11 | 2 | 49572257 |
KASP Assay ID:
2259-2692.1 (used for ordering genotyping assays)
KASP Sequence:
GAGGAACCACTGATGYGTCACAGGARAACTGAGAGACYAACTTGGAAAGG[T/A]AGGCGYATGGGAAGTTGCTGCTGGTCCGGTTTTGACTATTGCWGCATCGT
Long Flanking Sequence:
CACAAAGGTAGGAACACACTCGCATTCTACTTTTTTTTAAAGTGTGAACACAAAGTGTGTTTTTAGGTAGTAAGAAAACCAAAACGTGATTTTCTTTTGTTTACTACAATAGATAAGCTGGTTTTATCTAAGATCAGAGCTTCGAGAACATGACACTCTCCTACACTCCTCCTCTTTCACACACACACACTTGCTCACACTTGTAGTGGCTTGTCTGAGATTGAGGAGTTTCTAAAAGCATGTTTTTTTTCCTCTTTTCTCTCCAGCTGAAGAATGTCTTTTGCTTCACGCTGCAGGATTTAGGCAGTTTAGCGCTCTCTCACACAAAGCAGCAGACACCATGAGCTCCATTCACTGCAGAGCCACGACTCCCAACACACTTTCTGCTGTCTCTGACACTTAGAGCACTTTGATTTGTGCATTGGAGAGCTGGAATAGTGTGTGTGTGAAGAGGAACCACTGATGTGTCACAGGAAAACTGAGAGACTAACTTGGAAAGG[T/A]AGGCGCATGGGAAGTTGCTGCTGGTCCGGTTTTGACTATTGCTGCATCGTAAAACGTGTTTTCAGAGGAATTTAGAGCGATATTGTAATGCATTGGATTTGCATATATGGCCTCTGATTGTATTCTGCTGCACTTTTTTTGTGTGCATCTCAGTTTTTGGACATTTACACCACAAACTGATTTTTTCTTTGCAATTTTTAACCAAACTAATGCACAATGTTCTTTTTTTATTGTAGTTTAATTTATATACATTGTTTAGCATAAATGAGTACACCCCCTAGGATAATTTACAATAATATATTTGTGCATATACAATTAAAGTCAGCAATTATTAGCCCCCCTTTGTTTTGTTTTTTTTTCTTCTTTTTTAGTATTTCCCAAATGATATTTAACAGAGCAAGGAAATTTTCACAGTGGGTCTGATAAAATTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTCTAATTTTTTTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9433
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 |
---|---|---|---|---|---|
ENSDART00000056252 | Nonsense | 9 | 766 | 3 | 16 |
ENSDART00000108861 | None | None | 762 | None | 15 |
ENSDART00000109471 | Nonsense | 9 | 766 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 50150714)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 49846246 |
GRCz11 | 2 | 49580476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTATAACAAGAGCACTGAATGATGTCTCTGCTGGCTGTTCWGTG[T/A]GTTTTGTATGTCTGGAGTCCAGCAATGCTGACCGGTGGGCTKGGATCAAC
Long Flanking Sequence:
TCGAAGCATTCGTGAGCATGTCACTTGCGAAAGCAGTTTTGGTTAATGCTATTGCTAGGTGTATTTCAGGATGTGGTGAGTTTTTTTTTCTTTCTTTTTTTTTAAGCTGTTCTAGCTTTGTGTCATTCTGAGGCTTGAAAAAGCAGAATCGTGTGTCTCTGTCAAGGTCCCAGAGCAAAAGCTTTCATCCTCTGCATTAGCATCACTATAGAAGTGACAGAAATACTTCTGCCAGCACCCCTGCCTGTACTCTCTCTCTTTCTCTCTCATTCAGATGGCCTCACAGCGCTCTTTGCTGCTTCTTTGAAGGGCATTCTTTGCAGCTAAAGTCATATATCTCAGTATGGAGGATCTCCGAACTGAAGCAGGGCAGAAGACAAGGATGAGAAAGCTTTGACAGAAAGACCACAGAGGAATTTTGCAATCGCAGACCGAAATCACGGACTGATTTTTTTTTTATAACAAGAGCACTGAATGATGTCTCTGCTGGCTGTTCTGTG[T/A]GTTTTGTATGTCTGGAGTCCAGCAATGCTGACCGGTGGGCTGGGATCAACACTGGATAGCCTACCTCGGAAAACAGTGCCAATTGGAAGTAAGTTGACTTTTTGAAAATCACATTTGATTATTATTAGAAAAAAGTGCCAGTGCTGTTTGTCACTATCATTGGCTAATATTTATAAATGCACTTGGGTACTTAAAAAAATTACATTCATTAGATACATAAATAGTAGTAAATTAATATTTTATTTCCATTTTCTTATTCAAAGGTGCTGAAATTTTAAAGTGCTTTCAGCTGTATTTTTAGCAGCATATTAAGCTTAAAATCATGTTCTTATACAGTTAAAGTCAGAATGATTCACTCTTCTGTGAATTTCTTTTCAAATATTACCCAAATTATGTTTAACAGAGCAATGACTTTTTTACAGTATTTTCATAATATCTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTTGGTTAGAATAAAAGCAGTTTTAAGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19891
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 |
---|---|---|---|---|---|
ENSDART00000056252 | Nonsense | 161 | 766 | 7 | 16 |
ENSDART00000108861 | Nonsense | 157 | 762 | 6 | 15 |
ENSDART00000109471 | Nonsense | 161 | 766 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 50157424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 49852956 |
GRCz11 | 2 | 49587186 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGTAAGCTGACTTTAGAGATCCTCCAAGAAGATACGAAAGGGAAATG[T/A]CCGTTCGACCCTTTTCAGCGATATACATCTGCAATGGTCGGTACGTACTG
Long Flanking Sequence:
ACTGTAAGTTGCAGTATTATAATCACTTATTAGCATTAATACATTTTTACTACTACTTTGGTAATTAGTGATGTAACATATTATACAAATATGAAGATGTTTAAGACTTACAAAAGCACCGTCTGAGGAAGTGGCTTTTGTATGTTTATTTACAGCAGATAAAAGGAAGTGTGTGTTGTAGCTTGGTCAGACATTGTGGTCAGAAAAGATCTTTGAGTTATTCCCCGTGTTGTTTTTGTCTTCTTCTTTAGAATGACTGCAAAAACTATATTCGAATTCTTCATAAAAAGGACGACGGCAGAATGTATGTCTGTGGAACCAAAGCGTTCAACCCCACCTGTGGCTATTTGGTAAGTGTCATCCATTTAATTCAGTGTTTGTTAGTGACCACAAATGTAGAATGTGCATCGTTTATTTGGTTGTTGCATGTTATTCTCATAGTCCTATGCGGATGGTAAGCTGACTTTAGAGATCCTCCAAGAAGATACGAAAGGGAAATG[T/A]CCGTTCGACCCTTTTCAGCGATATACATCTGCAATGGTCGGTACGTACTGCTTAGTTGTTTATTGACTAGATAATTTGTATTCATATCTGCAACACTCACAGTTTCATTTATTGCAAGTATTTTTACACATATAGTAATCTCTGCCTCGGTTTTCTCTCTCAGATGGAGCGTATTACTCTGCTACTTCAATGAACTTTCGGGGTTCAGAGCCGGTGATGATGCGCAGCACAGAGGAAAGCATTCGAACTGAGTTTACAAGCACCTGGCTCAGTGGTGAGAAAGTGTTCATGTCTAAACTAACCACCAAACACAATGTGAAAAAATGCAAGAGCACACTCAGTACGATACCCTTGTACATAACCACAACATACTTGCAAACTGAATGCACAGCTTATCAGATTTTTAGAACAAAGGCTACTGATAAACTGTTAAAGGTCCCATGAAATTAAAGTTTTTTTAGTCAATATCAGTATGTTAGTTTAAGGATATCTATAGTATA
Associated Phenotype:
Not determined