ZMP
sema7a
Ensembl ID:
ZFIN ID:
Description:
semaphorin-7A [Source:RefSeq peptide;Acc:NP_001108357]
Human Orthologue:
SEMA7A
Human Description:
semaphorin 7A, GPI membrane anchor (John Milton Hagen blood group) [Source:HGNC Symbol;Acc:10741]
Mouse Orthologue:
Sema7a
Mouse Description:
sema domain, immunoglobulin domain (Ig), and GPI membrane anchor, (semaphorin) 7A Gene [Source:MGI S
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38090 | Nonsense | Available for shipment | Available now |
sa24691 | Nonsense | Available for shipment | Available now |
sa44317 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38090
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127274 | Nonsense | 126 | 640 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 27712218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26402312 |
GRCz11 | 25 | 26845514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACTTTTCAAAACTGCAAATTTGTATGTGGGACAAATGGAGAAGAGCCA[C/T]AGTGCTGGGAACTGGTAAGAGAACTTATTAGTAGTGCAATATTTTTGGTC
Long Flanking Sequence:
TGGGTACTGAGTCAAAGTAATCATTGTTTGCTTTGTTTTATTTTGTAAAACTATTCTATTTAAATGGAATAACATTTTTTATGAAAGAGATAAACCCGGTGTTGCTTGAATTTGTTACAGCTAAGGCATTTATTCTCAGATTCATGTTAACCATTGTAAATTCACTGTAAAACATGTTTTTTGTTGTTGTTGTTGTTTTGTGGGGTTTAGATTTCGCATTATAATAGAAAACAATAACTTGTTTAGATTGTCAGTATTTATTATATGTATTTATTTTCAGAATTTTACTCTAAATGCAAACTTGCCAAGATGTGGTGAGGTGAGTTTTATAATTCACTTGAAGAAGATAAAAAAGAACATATTTACTTTGACTTGTATATTGACTTGTCCTTCTTACTAATATTTCTCTATCTATATAGAGCTCTTGTGAAAATGTAGTCACAGTAATTGAGACTTTTCAAAACTGCAAATTTGTATGTGGGACAAATGGAGAAGAGCCA[C/T]AGTGCTGGGAACTGGTAAGAGAACTTATTAGTAGTGCAATATTTTTGGTCTCTGCTACATATTTAGAACAGTGCTGCATTTAAGTGTTTATTTCAGCTAAATTCAATCTAGTCATTTTACAAATACATTTAATACAAGTACAGTTATTATACTGCTATGGTAGGCTTATATTTAACTTTAATGTACATGTTAAAGACTGTTGATTGTTTTATATTCATACTCATAAGTATGTGAACATGAGCTTACATCTTGGTGGAAATAATTTCTACTGAAAGCATTAGACATTCTCAGGATTTATAATGTTCAGTTTATTATGAGTTAAATGATTGTAGGTAATAATTCATGTCCTGCATATGAATACATGTTAAAATGGCCTACATGTTAAAATATTCTCTTTCCCAGTATCCAAGAGAAAGCAATCATTCTGTTGTTAAGTCTGTAGAAGGCACAGGGATCTCGCCACATTCTAGTGAACAAAACTCCTTGTCTCTTGTAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24691
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127274 | Nonsense | 212 | 640 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 27713517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26403611 |
GRCz11 | 25 | 26846813 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTCCCACACAGAACCTACTTTTATCTCCAGTTTCCTGGCCAAGCGC[A/T]AAAATGACTCCTTGAATGAGAAGATATATGTCCTATTCCGAGAAAAAAAC
Long Flanking Sequence:
TTCAATGTTGCTTACCTTTTTTTAGCTTGTGAAATCTATTGAGCGATTTCTATATGATTTTACTTATTGTATGCATTTCCTAATTGAGAATATTTCTAAATGTCTTCCAAGGAAGGTTAAATAAGATTTAAGATACAATGTAAAATGGTAGCACAGTAAATTTAGTGCTTACATGCTTAGTGTGCTATTGTGTACACTTAGTGCTTTTTTACTTTAGTGTGCTCTTTAGTGGATGGGTATTTGCTGACAATGTGGGCTGAGCAAGCAAAAGGGCTATGTCTGCTGACCAGTCAGAATTTTACCTCTCCCAAGCTATCACTCTAGCCACTTTTTTCACACATCTGTCTATTGCTTGGCTATCACTTGCACCAAACGTCACATATAGCATATATAACTTGCAACTGAAGTTGAGGTCCATTAAAATTCATAAAATAATACATGATTTATGTCAACTCTCCCACACAGAACCTACTTTTATCTCCAGTTTCCTGGCCAAGCGC[A/T]AAAATGACTCCTTGAATGAGAAGATATATGTCCTATTCCGAGAAAAAAACTCAGACACTAGTCCAGAGGCGGATCCTTGGATATCTAGAGTTGCCAGAGTGTGTAAGGTATGTATGTTAAGCAGTTTGATTATTTAATACAAAAAAACATAAAGATGGATGTGTGATAAATAGTTTCTCTTAGTGGTACATTGTGTACGCTAATCTTACACAATGATTAAAAATCAGAGAAACTTAAACACATTTTGACTTTATAATTTAAAGGTGCCAAATGCATTCATTCAGTGTTTTAAATTGTTCTCTGATATTCACATATGCGTCTTAGGTATGTGTATGTATGCCGTTAATAGCACACCACATCTAATTAGATTTAATGCATCACTGTGTCTTTGTGTTTAGCTTGGCAAAAGATGAAGAATTTTTTCCTCATGTATCAAAATTCCTCATAAAAGCAGCAGGCCGTGTAAAGCTGATCACTATGAAAACAATTTTTTTTACCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44317
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 |
---|---|---|---|---|---|
ENSDART00000127274 | Nonsense | 569 | 640 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 25 (position 27733218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 26423312 |
GRCz11 | 25 | 26866514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATGCCAGTTATAGATGGGAACACGGGGGCAAAAGCAACCCATGTCAA[C/T]AGACCCAATCGGAATACCTCCTCCTAATCCCAGCTATGACGGCTGAGAAT
Long Flanking Sequence:
GAAATGCCAACCCAGCTGAGGCTCAAACCAGCGACCTTCTTGCTGTGAAGCGACAGCACTACGTACTGCGCCACCGCGTTGCCCACTAGCACAGTTATATACACATAAAAATACAAAGACTCCATTTTTATTTCATTGCTACAATAAGACATTTATTTCAGTGAGACTATAATGTTTTTCTGTTTGGATTTTGTTTCAGAGGAGGAATACAAAACATTTCTGATGGCAATGTCACTAAAGTATGTGACCACAAATCAGGTATATAACTAATCCAATAATTGTTTTAAGACACAAGACAAAATAAGTCTTCCAATCTCATGTATCTCTAACAAATGTTTTTAGTGGGAAGAGTTAGACGAGACGCTCAACAGTCATCTACTGCTCCCTCAAGGATTCAACACACTGTGGCCACTGATGTCCCCTTCTACTTATCTTGTCCGGTCGATTCACATCATGCCAGTTATAGATGGGAACACGGGGGCAAAAGCAACCCATGTCAA[C/T]AGACCCAATCGGAATACCTCCTCCTAATCCCAGCTATGACGGCTGAGAATTATGGCAATTACAGTTGTGTTTCCCAGGAACGTGATTACATCAAAGTTGTGAGAGAATATGAACTCCTTGCTAAGTCTGTTTTTAATGATGCTTTCAAGCTGAAAATACAAGACCGGCAGCTAATGGTAGCATTTGTCACGAGTGCCTTCTATCTGTGCTCACTTTAAGGTCAAGCTTGTTATGTAAGTGCTTCTGTCTTTAGGCATTTCTGACGACATTTAAGCTGATTAAAACATCAGTCACGTTGTCAAGAGGCTAGTGGTTCGTGGGCAAAGATAATTGTCTTACAAAGTCAGCACTGAAGTGCACATCCTAGAAGATAACTTCCCATTATATGTTAACCATCTATTTAGTATGTGCTGAATTGGTACAGTGGAGTACCAAAGTCTAAAACTCTTTGGAATCTGAAAATACAGTATTTAGCATTGACAGCGTTTTTTACATGCTGC
Associated Phenotype:
Not determined