ZMP
si:dkey-49n23.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to semaphorin 3 family (Sema3) [Source:UniProtKB/TrEMBL;Acc:Q1MTG9]
Human Orthologue:
SEMA3D
Human Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D [Source:HGNC
Mouse Orthologue:
Sema3d
Mouse Description:
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3D Gene [Source:
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24202 | Nonsense | Available for shipment | Available now |
sa37551 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24202
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059965 | Nonsense | 582 | 1008 | 16 | 21 |
ENSDART00000133335 | Nonsense | 527 | 703 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 33507054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30868592 |
GRCz11 | 22 | 30817787 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATAGTAAGTTAAAAGTGTTCATTGCTGTCTGTAGGCTCAGAGAATGCT[G/T]AACTGAAGACGGTTTACGGCGTGGAGACAAACTCAACTTTCCTGGAATGT
Long Flanking Sequence:
CAGAGTTCATTTTTGGGTGATACTGTATCCCTTTTACTCATGTAGCATGCATAAAAGTGCACATGCTGTGAAATATAGTAGAAACCACATCTTGACCCTAACCTCTTTTAATCATTGCTGAAGACAATATTGAAAACCATCAGCAAACCTGTCAAATGGTGGTTGTGAGGGTGGGTAACATCCTCTTATGGTCCACAGGCGCGCCCGGAGACAGGATGTGAGGTATGGAGACCCTTGGAGCCAATGTCAGGACATGAGAGACGGTAATAAATCACTTTACAACTTTTCATCTTCATGTTGTATATGATATTTCCCAGTCCTCGAATAAAGAGGACGCTACTCCCTCTAGTGTACAAAATGGATATTGACATACAACACCAGTTAATATGGGATGCATGTTCTAGGTCTTTCTGTGAATAACTAATTTTAAAAGAAAGTATACGATAAATATTATAGTAAGTTAAAAGTGTTCATTGCTGTCTGTAGGCTCAGAGAATGCT[G/T]AACTGAAGACGGTTTACGGCGTGGAGACAAACTCAACTTTCCTGGAATGTGTCTCAAATTCACCACAAGCCACTATCAAGTGGATATTTCAGCCAAATCACAGTCAAAACAGCAAAGAGGTCTGTCGACATACTCTTTAACTGAATATTAAATCAGAGTCAATATGTGTACAGTATATTTATACTGAAAGGTTTAGTTTTCCCAAACAATGAAAATTAATCATTAATTACTTACCCTCATGCCATTCCAAATCCATCTTTGGAACACAAATGAAGATAGTTTTCATAATATTTTAGATATTTAGAGACTGTCTTTTGAGATTTATAGATTTAGAGACTGTCTCTTGAGTTTTATAGATTCAGAGACTGTCCTTTGAGATGTATAGATGTAGAGACTGTCTCTTGACAGTCTATTTATCCAAAACTCTAATTATTTAAATAATTCCTTAAAGTTCAGTTAAAAGTTTGAGAGTTTTGGGTGAACACAAGTGCCTTTATGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37551
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 |
---|---|---|---|---|---|
ENSDART00000059965 | Nonsense | 940 | 1008 | 19 | 21 |
ENSDART00000133335 | None | None | 703 | None | 16 |
Genomic Location (Zv9):
Chromosome 22 (position 33447740)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30808871 |
GRCz11 | 22 | 30758066 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAACGCCTACAGCTGCGTGATTAACAACACCATCAGCAACAAGACTAAA[C/T]AGTTTAACACTGATGAACACTGTCCGATATGTAAAGGTATGTGAGGGAGT
Long Flanking Sequence:
CAGTGACTATCTCTATTGAGTGCATTGTGTTTGACATTACAAGTCTGAGACATGCAGTCTTGGCTTGCAAATGCACTCAGATACTATAGATTTTTTCCCTTTCCAGGTCTTCTTATATCTCCACACATAAGCAGAACGAAAATTCAGTCAATAACTTAAACAAGTTTTATTAGACTTTTAAGAGTGAGACACTGCAGGACTCCATTTTGTTTCCCGATCTAAAAATGTTTTCTTCTTTATTTCCAGCTCAACTTTTCAATCCAGAAATCACCTGTGAGATTTCAAAAAAAAATTCTGAAGGTTCATCAGTTTCTCGCTGTAATCTCCTATGTTCAGTGGTACATGTGAGAGATGTAAGTCTCTCCTGGTACAAAGAAAACAGTTTAATCTCCAGCATCAGTGTGTCTGATCTCAGCAACAGTCTCTCTCTGGAGGTGGACTATGAGGATAAAAACGCCTACAGCTGCGTGATTAACAACACCATCAGCAACAAGACTAAA[C/T]AGTTTAACACTGATGAACACTGTCCGATATGTAAAGGTATGTGAGGGAGTTTATGCACTGAACTAATCTCTCAGCCATGAATTTAATAAAGTGGCTTTGAAATACAGTAACTGATAAGATGTACAGCATGTTTTTATATTGTAAGTTTTACGGTTTGCCTACAATAAAGTATTTATACCTATGGTACTTTATTGAATTTGTTAGTAGTTTTACTTTTTCTTTGTCTTTTCAGTTTCTTGCTTTAGATGGATATATCTTTTAATGCTGCCTTTTGTAGCATTTATTTGCATAATTTCCTCTGTTGTGATATGCTTCTGTAAAAACAAAGCCGGATTTCAAAAAGGCAAGTCTTATATGGCAAACACATACATTTTTTTCCTCAAAGTACTAATATATTTTAATGAACTGAAAATAAAACATCATGTGTCTTTCTGCTTTTCAGTAAACCTGGAAGCTGGGCATGCAGAAAAAAAATCTGCTCTGACCACCACGGATCAAGT
Associated Phenotype:
Not determined