ZMP
sema3ab
Ensembl ID:
ZFIN ID:
Description:
Semaphorin-3ab [Source:UniProtKB/Swiss-Prot;Acc:Q9W686]
Human Orthologue:
SEMA3A
Human Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A [Source:HGNC
Mouse Orthologue:
Sema3a
Mouse Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A Gene [Source:
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23237 | Nonsense | Available for shipment | Available now |
sa13929 | Nonsense | Available for shipment | Available now |
sa6502 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23237
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061886 | Nonsense | 344 | 778 | 10 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 8880919)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9457895 |
GRCz11 | 18 | 9427085 |
KASP Assay ID:
2261-1874.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTCTCTGTTTGCAGTAATATTTTTAAGGGTTCTGCGGTCTGCATGTA[C/A]AGTATGGCAGATATCAGGAGAGTGTTTTTGGGCCCATATGCCCACCGTGA
Long Flanking Sequence:
AAGTAAACACTACATAACAGAAACAAAAGTAAATCATTTCTGGTTTGTATTTGACAGAATGATTTTGGAGGCCACAGGAGTTTGGTGAACAAATGGACCACCTTTCTGAAGGCCCGTTTAGTCTGCTCAGTTCCTGGCCTCAACGGCATCGATACACACTTTGATGAACTGCGTAAGTATGAAAAACAATGTTTTACTTGTTTAACATGTTTGGTTGACAACTTACAGCACCTCACTCTGATCATTTCCAGAGGACGTGTTTCTCATGAGCTCTAAGGATCCTAAAAACCCCATTATCTATGCTGTATTTACAACATCCAGGTAATAAAACATCCAATTTACACCACAGTATACTGTTATATAACTGCATATTCTGTTATCTTCTATTCAGAGCATGATAATTGTGTTTTAGGTCCCTAAAGATGAACCTGTGAAGCAGTTGGTAATTGTTGTTTCTCTGTTTGCAGTAATATTTTTAAGGGTTCTGCGGTCTGCATGTA[C/A]AGTATGGCAGATATCAGGAGAGTGTTTTTGGGCCCATATGCCCACCGTGATGGACCCAATTACCAATGGGTACCATTTCTGAGTCGAGTACCATATCCAAGACCTGGCACGGTAAGATGGCCATTCAGAGCTAATGTACATCATACCTTTTTTATGGCTCAAATCAAAGTGAAAGGTCTGCTTGTATCCTAACATGTTCTCCCGAATCTGAACAGTGTCCCAGCAAAACATTTGATGGTTTTGAATCAACAAAGGACTTTCCTGATGATGTCATCACGTTTGCCAGAAGCCATCCAGCCATGTACAACCCAGTGTTTCCTATCAACAACCGTCCAATCATAATCAAAACTGATGTGGATTACCAGTTCACTCAGATAGTAGTGGACAGGGTTGAAGCAGAGGATGGCCAGTATGATGTCATGTTTATCGGCACCGGTGAGTTGAATAATGTTTTTTGGTGACGCTGTGCTTTAAATAGTTTATTTTGGTGGTCCCCTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13929
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061886 | Nonsense | 503 | 778 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 8883985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9460961 |
GRCz11 | 18 | 9430151 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTYAGGGAAGTCACAGTGTCTTGGCTTTGTCTTTACAGCAACARCTCTA[T/G]CTTGGATCTGCCATCGGGGTTTCTCAGATGCCWCTTCATCGMTGTGACGT
Long Flanking Sequence:
GATAGCTTGAAAAATATTCATGTAGCTCAGCATTTTGTTGACACAGGTGTTATACCGTACACCAGCTAGATTTATCATGTAGCAAAAACTTAACACAGCTCTCAGACTAGGTTACACACACACAAATACACACACATATGCTTAGTTGGCCTCAGTCTACATTACGCAGAGCAGGAGCTGCTGTCACAGTCAGTCACACAACGCGACAACACGAGGTTTTGCCATTAGAGGCCACACACACACACACACACTCACAGCAGCTGCTTTTACATTAAGGAGTGCAGTGTGAGCTCCCCTTTAGGCGGTGTGAATAATCAAGCAGACACTGAGAGCTTATCTAAAGGCATATATAATTAAACAGCTGGGTATGAAACGGTGAAAACTTCCCTTATCCTCAGTCAAGCAGTCATTAACTCTGTCACATCACAACAAAAAACTTTGTGGTTCCTGTTTCAGGGAAGTCACAGTGTCTTGGCTTTGTCTTTACAGCAACAACTCTA[T/G]CTTGGATCTGCCATCGGGGTTTCTCAGATGCCACTTCATCGATGTGACGTCTATGGGAAGGCCTGCGCTGAATGCTGTCTGGCACGTGACCCTTACTGCGCATGGGATGGCTCTCAGTGTTCCCGATACTTTCCAACAGCTAAGAGGTACAATGAGGATACACAGAAACACTCCACAGTTGATCTGAGATGAAGATGACAGATGACATTTTTTCCACAGTGGGCTCTTGAGTTCGTCTTAGGTTTTTTTTTAATACATGCCTATTATAATTCAATGTGTGTGTTTTCTGTATGTGTGTGTGATAACATTTAATTCAAACAAACTTTTAGTAATGACATTGCTATTTAAGGCTCAAAACCAAAACACTATGATATTAATAGAATATCTGTTTTTTTATTTATTATTAATTATTAATACTATTTTACTATTATATTTAACACTAATATTCATTTAATATAAATACTAATGTTGTATGTATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6502
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 |
---|---|---|---|---|---|
ENSDART00000061886 | Nonsense | 729 | 778 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 8893604)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 9470580 |
GRCz11 | 18 | 9439770 |
KASP Assay ID:
554-4618.1 (used for ordering genotyping assays)
KASP Sequence:
TCGATCAGCTCTGCGAACAGGTGTGGAAGAGAGAACGCAAACAACGCAGA[C/T]AGAAAGCCAATCTACTGCACGCCAGCCAATCACACACCAGCCAGATCCTC
Long Flanking Sequence:
TCTTAAATGTTAGTTGTTTAGATCAGTGTCTAGTATGGATCATCAAGCTCTTGTTTATAATTATTTGACTACAAACATTTATCTAATCATACATTTGGGTTAATAGGGTCAACTGCAGCCAAAATACCTGAACAGCTGTTGTCCATAGTATGCTTACAGTGTTGTGTGTCTGTGTTTTGTTTTAGATAAAGTCAGACGAGCGAGTGTTGGGCACAGAACAGGGTCTTCTGATCCGAAGCCTCCATCAGAAGGACTCAGGTGTGTATTACTGCCATGCCGTCGAGCACGGCTTCATCCAGACCCTCCTCCGTCTCACGCTCAACGTCATTCCTGCCGAACACCTGGATGATCTGCTTCACCGAGACCCACCAGACACCAACGATCCCGCCAACGGCAAGATGTGGTACCGCGACTTTCTGTCCCTCATCAATCCGCCGAGCCCCAACAGCGTCGATCAGCTCTGCGAACAGGTGTGGAAGAGAGAACGCAAACAACGCAGA[C/T]AGAAAGCCAATCTACTGCACGCCAGCCAATCACACACCAGCCAGATCCTCCACTCCAGCCAATCACACGCCAAGTGGAAGCTGCTACAGGAAAACAAGAAAGGGCGCAATCGCAGGACCCACGAGATGCAGCGGGCGCCGAGAAGTGTGTGACATGGACACCAAATATATCTATATAAATAAAAAACTTCTGCTGTTCTACAGACATACCGCTGCAGACAGGAAATGGGGAATTTCACTTCCTGTCATGTATGTGTGCAAGAGAGATGAAACTTCATTCACACTATGTATCGAGACTCAAACGGTTTTGAGAGGACGCGAGGATGCCTGTAAATATGACATGAATACAAAACCATACTGTGAAACAGGTTTCAGTCCGTATTAAAACCTGTTTCGTTTATGAGGGAAAAACATGGATGCTGAAAACCACTGTTTAACCTCTGTTTAGCTGAAGCACAACCCCAGTGCATTCTGGATTATGATCTTGTCTGTAATATTATG
Associated Phenotype:
Not determined