ZMP
sema3h
Ensembl ID:
ZFIN ID:
Description:
semaphorin 3h [Source:RefSeq peptide;Acc:NP_571125]
Human Orthologues:
SEMA3A, SEMA3C, SEMA3D, SEMA3E, SEMA3F, SEMA3G
Human Descriptions:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F [Source:HGNC
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G [Source:HGNC
Mouse Orthologues:
Sema3a, Sema3b, Sema3c, Sema3d, Sema3e, Sema3f, Sema3g
Mouse Descriptions:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3B Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3C Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3F Gene [Source:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3G Gene [Source:
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41220 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2459 | Nonsense | F2 line generated | Not yet available |
sa45324 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21304 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41220
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 |
---|---|---|---|---|---|
ENSDART00000062515 | Nonsense | 207 | 749 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 8 (position 26782966)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25910884 |
GRCz11 | 8 | 25930023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACTGCGTTTATTCGAAGTCTGGGGGAGCGACATGTGATTCGCACCGAA[C/T]AATACGACTCTACGTGGCTGCAAGGTGACACATGTGTAAATGTACACATT
Long Flanking Sequence:
AAAATAAATGAATTAAATTCAATTTAAAATTAATAAGTTACCTTGAGAATATGCAAACATACTGTAAATAAAGCTAAACATTGTAATATTGAAATAATAAAATAAATAAATAACTAAAGAATTAAACAAGCTTAAACTATTACAAAAACATGTAGAAATAAAATCATTTGAACAACTGAACAACCTTTTTTTTAGGCTGAGGAGCAAACACTGCAGGATGAAGACACTGAATCAGGGAGAGGAAAATGTCCTTTCGACCCTCACCAGAGAACAGCAACCGCCATCATAGGTGAGACGGCATGTTTACAGTTTGTCTGCAGTTTATATGTTTGTGTAAGAACATGCCAGTGTAACTCTGATCTAAATCTCTCTGTGTATGTGTGTCTGTTTTTTTTTCTTTTTCAGACGGAGAATTGTACGCAGGCATCTCATCTGACTTTCTAAGCCATGATACTGCGTTTATTCGAAGTCTGGGGGAGCGACATGTGATTCGCACCGAA[C/T]AATACGACTCTACGTGGCTGCAAGGTGACACATGTGTAAATGTACACATTCACCTCAGCTAACACTCTTAGCACTAATGAAAATACACACTGTATGTTGTTGACAGTGCGCTCTATCAGTTAAACACAAGGGAATGCAATCGCAAAAACAGATTCATGTGTTAGCTAACAGTATTTTTGTCTCTGCAGGCGCTGAATTTGTGCATGTTACAGCGATGTCAGAGAGTGATAACGAGGAGGATGATAAAGTCTACGTGTTCTTCACTGAGCGCGCTCAGGAAGCAGAAGGGGCTGCTGGGAAGGTCCTGTATTCCAGAGTGGCCCGCGTCTGTAAGGTATCTAGCAGTGTGCTCCTACGTGCCCGACTGCACTTGTGTGTCCCTCTGCCTGTTTGGCCACCTCTGCGAATCTGATAGGAAGTCCTGGGTGACATAACTATAAAATGTATTGCATGTATGAGTATATAATTATAATATTGTATGTAAATTATATATAAACATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2459
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000062515 | Nonsense | 262 | 749 | 7 | 17 |
Genomic Location (Zv9):
Chromosome 8 (position 26783297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25911215 |
GRCz11 | 8 | 25930354 |
KASP Assay ID:
554-3332.1 (used for ordering genotyping assays)
KASP Sequence:
GCAGAAGGGGCTGCTGGGAAGGTCCTGTATTCCAGAGTGGCCCGCGTCTG[T/A]AAGGTATCTAGCAGTGTKCTCCTACGTGCCCGACTGCACTTGTGTGTCCC
Long Flanking Sequence:
GTGTAAGAACATGCCAGTGTAACTCTGATCTAAATCTCTCTGTGTATGTGTGTCTGTTTTTTTTTCTTTTTCAGACGGAGAATTGTACGCAGGCATCTCATCTGACTTTCTAAGCCATGATACTGCGTTTATTCGAAGTCTGGGGGAGCGACATGTGATTCGCACCGAACAATACGACTCTACGTGGCTGCAAGGTGACACATGTGTAAATGTACACATTCACCTCAGCTAACACTCTTAGCACTAATGAAAATACACACTGTATGTTGTTGACAGTGCGCTCTATCAGTTAAACACAAGGGAATGCAATCGCAAAAACAGATTCATGTGTTAGCTAACAGTATTTTTGTCTCTGCAGGCGCTGAATTTGTGCATGTTACAGCGATGTCAGAGAGTGATAACGAGGAGGATGATAAAGTCTACGTGTTCTTCACTGAGCGCGCTCAGGAAGCAGAAGGGGCTGCTGGGAAGGTCCTGTATTCCAGAGTGGCCCGCGTCTG[T/A]AAGGTATCTAGCAGTGTGCTCCTACGTGCCCGACTGCACTTGTGTGTCCCTCTGCCTGTTTGGCCACCTCTGCGAATCTGATAGGAAGTCCTGGGTGACATAACTATAAAATGTATTGCATGTATGAGTATATAATTATAATATTGTATGTAAATTATATATAAACATAATTATATATGATAAAACCAAAAAATGTAGTAATAATTCTAAGAGTTTAAGCACACATTTTTTTTTTAAAATGAGAAATCATACTGTAATTTTGACTGTGAAGAATTATTAATAGTAGCATTACAAAAGTACCATAGTAGTATTGTGCTAAAGTGCTAATGCCATTGAACCGCTACACTGAAGAATGCTTTTCTTACTTTTGTCTTATTTCTTGTCCTAATATCTTAAACATTCTTAAATAAAGAAACATTTTCTAGACAAGTACACTCAAAAAATTATTCAAAGATACTTCCTTGGAATTACTTGTTTTTAAGAAAAGAGATTGTAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45324
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062515 | Splice Site, Nonsense | 374 | 749 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 8 (position 26795379)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25923297 |
GRCz11 | 8 | 25942436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGGTTTATAGAGCACACTGCTGAAGTGTGTGTGTCAATGTTCAGTG[T/A]CCCAGCAGCACATACGGAGGCTTCAGATCCACAAGGGAATATCCAGATGA
Long Flanking Sequence:
ATTAACATTAACTAATGAACCTTATTGTAAAGTGTGACCAAATATACTAAAGTATAAAATGTAGCAAAATGTACTGTCTTGCCATTCTTTTAGATATTTAAATAAGTACAGAATAAGTATGTTATATTATTTTGAAAAAGTACAGTATATCTGTGATGCTGAAGGATAGTGGATCAATAATTCACTTTTATTTTTACAAAAAAGTATTTAAAATATTACGGAAACATTACTTAAATTGCAAATCAAGTCAAGTTCAACTTTATTGTCATTTTACTACATGTGACTACATACAGTGGTGCCACATACTGTAAATAAAAAGGACAAATATGAACACAACTGGATGTAAGAGCTTTTCTAAATTTTATACATCTATTATAAATAACTAAATTCATATCCTTTGACACTTCTACTTTATTCCAGTGTTTACAATATTTGAATTGAACTAAAATACTGAAGGTTTATAGAGCACACTGCTGAAGTGTGTGTGTCAATGTTCAGTG[T/A]CCCAGCAGCACATACGGAGGCTTCAGATCCACAAGGGAATATCCAGATGACGTGATCTTCTTCAGCCGCACACATCCGCTGATGCAGGAGGTGGTTCGTCCTCTCGGTGGTCAGCCTTTGCTGATCAGAGTGGGCGTCCCTTATAAACTCACCCGTCTGCTTGTGGACAGAGTCGAGGCCGTAGATGGACAGCATGACGTGATGTTCATTGGCACAGGTATGTGTTTGTGCGGTAACAGGGCGGAACAAGCCTAAAACAGCGTAGCTGCCCTAGACTAGCAATATTGGGGATTACCAAAATTATTTTGACAAAAATGTTTCTGTAATAGTTCATTTACCAAGGGTAAGCATAACTATAAGTGCCACAATAATATTTCTAATGCTTTCATCTGTGTTTCCTGTGTAAATATTTAAAAAAAATAATTAATATAATAACTTAATTTTTTATTCACTTAACCAGTTATACATTTCACTACATATAGTACAAATAAATTGTAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21304
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 |
---|---|---|---|---|---|
ENSDART00000062515 | Nonsense | 388 | 749 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 8 (position 26795421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 25923339 |
GRCz11 | 8 | 25942478 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCAGTGTCCCAGCAGCACATACGGAGGCTTCAGATCCACAAGGGAATA[T/A]CCAGATGACGTGATCTTCTTCAGCCGCACACATCCGCTGATGCAGGAGGT
Long Flanking Sequence:
TATACTAAAGTATAAAATGTAGCAAAATGTACTGTCTTGCCATTCTTTTAGATATTTAAATAAGTACAGAATAAGTATGTTATATTATTTTGAAAAAGTACAGTATATCTGTGATGCTGAAGGATAGTGGATCAATAATTCACTTTTATTTTTACAAAAAAGTATTTAAAATATTACGGAAACATTACTTAAATTGCAAATCAAGTCAAGTTCAACTTTATTGTCATTTTACTACATGTGACTACATACAGTGGTGCCACATACTGTAAATAAAAAGGACAAATATGAACACAACTGGATGTAAGAGCTTTTCTAAATTTTATACATCTATTATAAATAACTAAATTCATATCCTTTGACACTTCTACTTTATTCCAGTGTTTACAATATTTGAATTGAACTAAAATACTGAAGGTTTATAGAGCACACTGCTGAAGTGTGTGTGTCAATGTTCAGTGTCCCAGCAGCACATACGGAGGCTTCAGATCCACAAGGGAATA[T/A]CCAGATGACGTGATCTTCTTCAGCCGCACACATCCGCTGATGCAGGAGGTGGTTCGTCCTCTCGGTGGTCAGCCTTTGCTGATCAGAGTGGGCGTCCCTTATAAACTCACCCGTCTGCTTGTGGACAGAGTCGAGGCCGTAGATGGACAGCATGACGTGATGTTCATTGGCACAGGTATGTGTTTGTGCGGTAACAGGGCGGAACAAGCCTAAAACAGCGTAGCTGCCCTAGACTAGCAATATTGGGGATTACCAAAATTATTTTGACAAAAATGTTTCTGTAATAGTTCATTTACCAAGGGTAAGCATAACTATAAGTGCCACAATAATATTTCTAATGCTTTCATCTGTGTTTCCTGTGTAAATATTTAAAAAAAATAATTAATATAATAACTTAATTTTTTATTCACTTAACCAGTTATACATTTCACTACATATAGTACAAATAAATTGTAATGTTTGTTTTTTTTTTTACTTGAGAGATGTTAAATGTGCCGGCT
Associated Phenotype:
Not determined