ZMP
sema5a
Ensembl ID:
ZFIN ID:
Description:
Semaphorin 5a [Source:UniProtKB/TrEMBL;Acc:B6E511]
Human Orthologue:
SEMA5A
Human Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh
Mouse Orthologue:
Sema5a
Mouse Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37852 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32482 | Essential Splice Site | Available for shipment | Available now |
sa37853 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24468 | Nonsense | Available for shipment | Available now |
sa37854 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9240 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37852
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081759 | Essential Splice Site | 152 | 1078 | 5 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17112112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16418588 |
GRCz11 | 24 | 16563007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTACCTGCGGAACAAATGCATTCACTCCTATTTGCACCAATCGCACGG[T/C]AAGTAAACGCATCAATGCACGTAATATAATGCAGAGGTTTCCTGGCCTGA
Long Flanking Sequence:
AAATAAACTATATGAAAAAATGTGTTTGTTTAAAATTGTTCATGTTTTTTTTTACTTTAAGACTAATGTACACTAACAAAAACAGTATTTTATGCTTCAAGTGTAGTCATCAATGAAATCTGAAAGCTAAATCTAAAAGCTAATTTATTTATTTATTTATTTTTGTTCAAAACAATTGCAATTGGTTCAATTTACCGGCTAAAACATTTAAATTAACATTTTAGAACAAACAAACCTGTTTTAAAAGTTTATTTTCTCTTTTAAAACAAAAGTGTTTAAATTTAATTCTGACTATTCAATTTTTGTAAATCACCTGGTCAACATTTGTGATACTGATAAAGAAGGCTTTTTTCTACAGCTAACATGCTTTAACATATTTTCCATTATGTCTTTTTCACAGGAGGAGTGCCAGAATTACATCCGTGTCCTCCTCGTCAATGGTGACAGGCTGTTTACCTGCGGAACAAATGCATTCACTCCTATTTGCACCAATCGCACGG[T/C]AAGTAAACGCATCAATGCACGTAATATAATGCAGAGGTTTCCTGGCCTGATGTTACTCCACAGCTTTGTCTCAAACTCTCTCTCTCTCTCTCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCCCACATTGACCTCTTTTGACATTTTCATCACTGCGTGGGTTGTGTAGCATAGCATGTGGTGTTTCAAACTAAAGCCTGTGGTTTATTTCAATAAGAGTTTTGTTCGTGCTTCATCTCAGAAGAAGCTTTCTTGAGATTGGGACAAAAACAACAACAACAACATCCAAGGCCTGATACTCTAATAAACCATGTACTTGTAGGATCTCTAAGTCCTGTGTCCTTTGTGGAAAGTTCACACTTGATATGCAGGTATCGTAGAGACAGCTCGTGCTTTATCTTTGACAAATTTTTCCAACACATAGTTGCAATAACTGCCACTCAATTCAGCTGATTGAAAGATAAGCATCTCGCCAAGCACATTTACTGACATCCTCCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32482
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081759 | Essential Splice Site | 224 | 1078 | 6 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17116559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16423035 |
GRCz11 | 24 | 16567454 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGCTTCCACCTCTGCGTACTGCTCAGTACAACTCCAAATGGCTCAATGG[T/G]AGGCTTAAAATATGAATGAAAGATTGAATTGAATTGAATTGAATTGAATT
Long Flanking Sequence:
CAGAAGACATGGCCAAAAGTTGGAAGAACATTTCTACTGTAACGAATGATTTGAACGGTGAAATAGTTTTCACTGCTACATCAGCTCCTCTGGCTGAAACTAACAACTAACTTAAATGAAAATGTTTGGATGTACAGTATTTTCTCTGCACAGATACTGTATTTATTATATATATATATTTTTTTTTTGTTTTGTTTTTTTCAATTTGTGTTTACCTAGATATTTGCTAGCCTTTGAAATTGAAGAAGTGCAGTATTTCTGAATTCAATCTCTTTCTCTGTACAGCTGACTAACCTGACTGAGGTCCATGATCAAATCAGTGGGATGGCACGGTGCCCCTATAACCCTCTGCATAATTCCACCGCCCTCATCACTTCCAGTGGAGAACTGTATGCTGCAACTGCAATGGACTTTTCAGGCAGAGACCCAGCCATCTACCGCAGCTTGGGAGGGCTTCCACCTCTGCGTACTGCTCAGTACAACTCCAAATGGCTCAATGG[T/G]AGGCTTAAAATATGAATGAAAGATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTGAATTAAAATGAATTGAATTGAATTGAATTGAATTTATTTGAATCGAATTGAAAACAATTGAGTAATCTTAGTTTAGGCATATATAATTTCATGAAAACGTAACAAGTTAGGGTAGTTCACCTAAAATTAAGATTGGGTCATTGTTCATTTACTCTCATTTAATTCCAAACCAGTGTAACTTTCTATTTGTAACACAAATGGAGATTTTACAGTATACAGACTGGCAGTCTCCATCACTTTTATTGACTGAGACTGTCATCTATCATCTGTGTTTTTGCTAATTTAAGGACGGAAAATCTGCCTTGCGCCATGGCGCATAGTCTAAAAGGGTTGAGTTTATTTTCTTAATGAGTTATAGGTGTGTTTTGAGAATAAACCAATTAGAGTCTCATCTCCCATTCCCTTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37853
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081759 | Essential Splice Site | 699 | 1078 | 14 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17180091)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16486567 |
GRCz11 | 24 | 16630986 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGGCGAAGAACGTGTGAGAATGGAAATGAATGCCCTGGATGCAGCACT[G/T]TATGTAACAATAATATTAATACTAAGTTTATTTTTAAATGAGTATCTCAA
Long Flanking Sequence:
AAGTGAATTAAAACACCACTATCAAGTTCTAAAGCTGATGTTTTATTTAAAGTATGGTCCTAACAAGTAACCTTATAAAACATGTTCTGTTAATGTAGTAGAACAAAATGTTCAAGTGTGATCAAATTATAATTACCATAGACCTTGTTTTGCTCAATAATTAATAGCCCCCATTATGAAACCTGTTTGGAAAATTTCATGGGCATCCAAAATATTTTAATTTGTGCATCAGAGGATTCATAATTCACAAAGACCTGTGTTTATATTGTAAAATCAGAATGACTAAATAACTGCGAGATGAGTTCGTGAATGAATGTTTGTATTCTGAGATATGTGTTTTCATCTTTCTTAGATACTGCAATGAACACCTGCCGTGTCCTCCGCATGTCTATTGGTCAGCTTGGTCTCCTTGGGAGCGCTGCACAGTTCCTTGCGGTGGAGGAATCCAGTCACGGCGAAGAACGTGTGAGAATGGAAATGAATGCCCTGGATGCAGCACT[G/T]TATGTAACAATAATATTAATACTAAGTTTATTTTTAAATGAGTATCTCAAGAAATTGAAAGCGTGTCTTTAGTGCTTATTTGTAGGTTGGATCAGTATAATATTACAAGAACTAATGTGGCATTATGACCAAGCCTATGGTTTATTTACAGTTCCCTCCACAAATATTGGCACTTCTGGTATATATGCGTAAATGGGGCTATGTCTTTAAAAATGTATTATTTTTTATAAAAAACATGCTTGTTTAGAATAAAAAGTTGCTAACCTGACGCAGTTTTATCAAAAATCTAATATATTTGCTATATATAAATGCTTATGTCTGTAATATAAGTATCATTAGCACCCATATGGACTCATATAAGCATATTTTGTAAAGCTCATTACCATGGATATTTTATAGTTGTTTTAGTTCAACTGGGTGACCAGGGGGGTATTCCAGAAAGTAGGTTATGTGAAATACCCGGGTATGTTTAAGAGTAAGTAGGTGGATAACCCCAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24468
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 |
---|---|---|---|---|---|
ENSDART00000081759 | Nonsense | 739 | 1078 | 15 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17195799)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16502275 |
GRCz11 | 24 | 16646694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGTGAATATCTCAGACAATGGTGGCCACTACGAGCAGCGCTTCAGATA[C/A]ACCTGTAAAGCTCGAGTCCCAGAGCCCGGCCTGCTGGAAGTTGGACGACA
Long Flanking Sequence:
GAGTTTAGATAATGAAGTGGCCAGCTCAATCATCTGACCTCAACCCAATTGAAAACTTCTGAGATGCATTTTCTGAGTCTCAAGTGTACTTTGTACATATTACTGGGTATAAATATTACAAATTAACATATCATACTCAATAAATTGCTATATATATATATATATATATATATATATATATATATATTAATTATGCATTTATCCTACTAAAATGGGTGTGGTTTTGTTTATTTTAACTTTGATAAGTATTGATCCACTTCAAATTTTCACTACTGTATATTTAATCTGGATATAAGTAATCTGTATTTTAAACTGTGTAAATGTATAACATATAATATACTTCATATAATATATAATATATTTCATTGCTTTTTTATACAGGAATTCCAGTCCTGTAACACCCTCCCCTGTCCGGATCTGAAGAAGACCACGCCCTGGACCCCATGGACCCCAGTGAATATCTCAGACAATGGTGGCCACTACGAGCAGCGCTTCAGATA[C/A]ACCTGTAAAGCTCGAGTCCCAGAGCCCGGCCTGCTGGAAGTTGGACGACAGCGAATCGAAATGAGGTACTGCTCCAGCGACGGCTCCACGGGCTGCTCCACTGACGGTGAGATCTCATTCTGTCTCCGTTCTTCATTCGTCACCCCGCTCTTTCCTTTTCTCCGCTCTCATCTGGCTCTTTGATAAAGTGAGCCCGCAGTGACTTTGAGGCAAAGCCACTTGATCTATTTGTCCATCAGGAGAAAGACAACATGATGTGTTCTAGAGCTTCTTTCTCTCTTTCTTTCGCTCTTTCTCTCATCTATGTGGGCTCAATACATCAGCTTTTGGAGTGGCGTCTTATTCAACAGAAGTGCTCTTGGCTGCATTCGGCCTCAGACAGACACAAGGAACATGCTAATGAAGTCAGATCAGCTGCTGTGATTTATTTATTTATTTTTTAATTAAAGGAATAGTTCACCCTAAAATGAAAATTACAACATAATTTACTCACTCTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37854
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081759 | Nonsense | 855 | 1078 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17234127)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16540603 |
GRCz11 | 24 | 16685022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTTTCCTTATCTTTCAGTGGACGGGAGCTGGTCGTGCTGGTCACCTT[G/A]GTCGAAATGCTCAGTGACATGCGGCGGAGGCCATTACATGCGCACACGCT
Long Flanking Sequence:
GCATACATATTAAATTATACCCCTTAATTTGTATTTATATATTTATTTTAAGCTTTCCATTACGGATCACATTTAAATGTAATAAAGCTAAAAGTGCTTATTCTGAATGACTGCTCTTTACAGCTCAAAAGTATGGAGAAAATGATCCCAAAACATATCAACATGCTGATATCAACATGAACAATTGTTACACATTTACACGCACATTCCCGCTTAGGAAATCTCAAAAATATTTAGGAAATATATTCTCATTTAAATGTAATGAGTCTGAGTAAATAAGCAAAAGCATAGAAAAGAAATACACATTCTCCTCCATCTGTTGTCAAGTATTTATAGTTGCCTTCACCATCAATGTTATTCTGCAAAATATTTCCACTATTTACTAAAAGAAATGTCACCCACTTTCCCCAAAATTATTCATGACCGAAGCATGGTAGTTATTTAAGCGTTGTCTTTTCCTTATCTTTCAGTGGACGGGAGCTGGTCGTGCTGGTCACCTT[G/A]GTCGAAATGCTCAGTGACATGCGGCGGAGGCCATTACATGCGCACACGCTCCTGTAACAACCCTCCACCTGCCTATGGAGGTGACATCTGCCTGGGTTTGCATACTGAAGAGGCCCTCTGCAACATCCAGCCCTGTCCTGGTATGCACACACATTTGATTATTTTTAACTGGAATGATGGTACTGATTAAAAGAACACAACATCCAAACAATTACAAAGAGTCCATTATGTTTCACAGTACAAACAATGTGCAGATAAATAGCAACTAAATTTCTTTTACAGGACATTATTATTAATAAATACAAGTCACTTTTATTAATCAGTTGGATAATTGCATACTAAGGATAGAGATGATCGTTTTTTACAAACACTTAAACTACTTATTATAGCAGATACAGATTGGTCAATTGTTTAGAGTCTTTCTTACTCAGTCCAGCAATTTGTAATCCTCTTACACACACAGTCTAATAACGTGTCCTAGGCTAGGCTATAAATTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9240
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081759 | Essential Splice Site | 902 | 1078 | 17 | 21 |
Genomic Location (Zv9):
Chromosome 24 (position 17234269)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 16540745 |
GRCz11 | 24 | 16685164 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGGGTTTGYATACTGAAGAGGCCCTCTGCAACATCCAGCCCTGTCCTGG[T/A]ATGCACACACATTTGATTATTTTTAWCTGGAATGATGGTACTGATTAAAA
Long Flanking Sequence:
TGATCCCAAAACATATCAACATGCTGATATCAACATGAACAATTGTTACACATTTACACGCACATTCCCGCTTAGGAAATCTCAAAAATATTTAGGAAATATATTCTCATTTAAATGTAATGAGTCTGAGTAAATAAGCAAAAGCATAGAAAAGAAATACACATTCTCCTCCATCTGTTGTCAAGTATTTATAGTTGCCTTCACCATCAATGTTATTCTGCAAAATATTTCCACTATTTACTAAAAGAAATGTCACCCACTTTCCCCAAAATTATTCATGACCGAAGCATGGTAGTTATTTAAGCGTTGTCTTTTCCTTATCTTTCAGTGGACGGGAGCTGGTCGTGCTGGTCACCTTGGTCGAAATGCTCAGTGACATGCGGCGGAGGCCATTACATGCGCACACGCTCCTGTAACAACCCTCCACCTGCCTATGGAGGTGACATCTGCCTGGGTTTGCATACTGAAGAGGCCCTCTGCAACATCCAGCCCTGTCCTGG[T/A]ATGCACACACATTTGATTATTTTTAACTGGAATGATGGTACTGATTAAAAGAACACAACATCCAAACAATTACAAAGAGTCCATTATGTTTCACAGTACAAACAATGTGCAGATAAATAGCAACTAAATTTCTTTTACAGGACATTATTATTAATAAATACAAGTCACTTTTATTAATCAGTTGGATAATTGCATACTAAGGATAGAGATGATCGTTTTTTACAAACACTTAAACTACTTATTATAGCAGATACAGATTGGTCAATTGTTTAGAGTCTTTCTTACTCAGTCCAGCAATTTGTAATCCTCTTACACACACAGTCTAATAACGTGTCCTAGGCTAGGCTATAAATTATAACCATCATTTTGTTGTAGCCAAACATTTTCAAAGCATTTGATAATGGTTGATATTTTCGCATTTTGTCTGTGTTGCACAAGCCCATATATACATTAAAACAACAACATACTTCCAAAATCAGATTGTTTTTAGAGACATCATT
Associated Phenotype:
Not determined