ZMP
sema5b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate sema domain, seven thrombospondin repeats (Type 1 and type 1-lik
Human Orthologue:
SEMA5B
Human Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh
Mouse Orthologue:
Sema5b
Mouse Description:
sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and sh
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14533 | Nonsense | Available for shipment | Available now |
sa21542 | Nonsense | Available for shipment | Available now |
sa13826 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14533
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 |
---|---|---|---|---|---|
ENSDART00000087663 | Nonsense | 174 | 1101 | 6 | 21 |
ENSDART00000138345 | Nonsense | 111 | 1038 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 9 (position 38622804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 37760700 |
GRCz11 | 9 | 37570495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGATTCATACCGCATCCTYCTCTCAGGCAGGGAACATGAGCAGAGTGT[T/A]GGAGAGGGTGAACGGAGTGGCCCGCTGTCCCTATGACCCCCGTCATAACT
Long Flanking Sequence:
CCATTGGCATTTCTTTAAAGTTCCTTTAAAGGATTTCTGAAGGCAAATTTCCATTTCTGTTTAACCGAATGATTGGCCAGAATTCTAACCCAGTACACTAAATCCACAACCCCCCTTAATTTTCTTTAAATGTCTTTCCTGTCTTTTAATGTGATGGAGCTGCCAAAAGCTGGCCTTTTAACAAAATTATTCAATTAAACATTTAACATGGTGAATTTATGTCACAGCATGCATTTCTATATTTTGAAGATACCGCTGCTATTGTCATACTATAAAATGCCTCTTCCCCTGCAGCTGGAGTGTCAAAACTACATCCGGGTGCTGCTTGTCAACAAGACAGAGGTGGTCACCTGCGGGACAAATGCCTTCCAGCCTCTTTGCATCACCAGAGAGGTGAGCATCTATCAGTTAAATGAGCTGTCTAAACCGGAGCTTTTCTCAAAGTGTGCGTTTGATTCATACCGCATCCTCCTCTCAGGCAGGGAACATGAGCAGAGTGT[T/A]GGAGAGGGTGAACGGAGTGGCCCGCTGTCCCTATGACCCCCGTCATAACTCCACAGCGGTGGTGACTGAAAGTGGAGAGCTGTACGCTGCCACGGTCATCGATTTCTCTGGACGGGACCCTGTCATCTACCGCAGCCTTGGAGGAATGCCGCCTTTGCGGACCGCCCAGTACAACTCCAAATGGCTTAATGGTACATTAACCTCATCATCTCTTGTCTGATGGTTTCATATCCGTCAGAGATCGTCTGAAAAGCTTCAACGTTTCTCTTACAGCTCTTTCTTCTTTCTGTCCTAATATGAAGCAATGACAGAACGTTGGTCTTAAAGTGAAAAGTGATTATGAGACTTCGAGTTTGTGTATGCTAATAGCATTACCCAAAGGAAACAGCAATGAGGTTAAGCTGAAAACAAAATGTGCTTTTTGCTTAATTCTCCCAATGACTTGCTGTAAGTCTGAATTTGAAGTATTCTTGCATTTTTTTGTAAATATTAGAAAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21542
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 |
---|---|---|---|---|---|
ENSDART00000087663 | Nonsense | 202 | 1101 | 6 | 21 |
ENSDART00000138345 | Nonsense | 139 | 1038 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 9 (position 38622719)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 37760615 |
GRCz11 | 9 | 37570410 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCCCCGTCATAACTCCACAGCGGTGGTGACTGAAAGTGGAGAGCTGTA[C/A]GCTGCCACGGTCATCGATTTCTCTGGACGGGACCCTGTCATCTACCGCAG
Long Flanking Sequence:
TAACCCAGTACACTAAATCCACAACCCCCCTTAATTTTCTTTAAATGTCTTTCCTGTCTTTTAATGTGATGGAGCTGCCAAAAGCTGGCCTTTTAACAAAATTATTCAATTAAACATTTAACATGGTGAATTTATGTCACAGCATGCATTTCTATATTTTGAAGATACCGCTGCTATTGTCATACTATAAAATGCCTCTTCCCCTGCAGCTGGAGTGTCAAAACTACATCCGGGTGCTGCTTGTCAACAAGACAGAGGTGGTCACCTGCGGGACAAATGCCTTCCAGCCTCTTTGCATCACCAGAGAGGTGAGCATCTATCAGTTAAATGAGCTGTCTAAACCGGAGCTTTTCTCAAAGTGTGCGTTTGATTCATACCGCATCCTCCTCTCAGGCAGGGAACATGAGCAGAGTGTTGGAGAGGGTGAACGGAGTGGCCCGCTGTCCCTATGACCCCCGTCATAACTCCACAGCGGTGGTGACTGAAAGTGGAGAGCTGTA[C/A]GCTGCCACGGTCATCGATTTCTCTGGACGGGACCCTGTCATCTACCGCAGCCTTGGAGGAATGCCGCCTTTGCGGACCGCCCAGTACAACTCCAAATGGCTTAATGGTACATTAACCTCATCATCTCTTGTCTGATGGTTTCATATCCGTCAGAGATCGTCTGAAAAGCTTCAACGTTTCTCTTACAGCTCTTTCTTCTTTCTGTCCTAATATGAAGCAATGACAGAACGTTGGTCTTAAAGTGAAAAGTGATTATGAGACTTCGAGTTTGTGTATGCTAATAGCATTACCCAAAGGAAACAGCAATGAGGTTAAGCTGAAAACAAAATGTGCTTTTTGCTTAATTCTCCCAATGACTTGCTGTAAGTCTGAATTTGAAGTATTCTTGCATTTTTTTGTAAATATTAGAAAAACATGACAATGTTCTCAGATTTGCCAAGAGACATAAAACTCAGAACAGAAGAAAAATAAAATAAAAGAGGTTTTAATTTGAGCTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13826
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 |
---|---|---|---|---|---|
ENSDART00000087663 | Nonsense | 703 | 1101 | 14 | 21 |
ENSDART00000138345 | Nonsense | 640 | 1038 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 9 (position 38569341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 37707237 |
GRCz11 | 9 | 37517032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGTGCAGTGCAGATTGTGGTGGAGGTGTGCACTCTCGCTCCAGGAACTG[T/A]GAGAATGGAAATAGCTGTCCAGGSTGTGCGCTGGTACGTATACCTGAAGC
Long Flanking Sequence:
CGTAGTTTGAACAAAAGACATTTTCTGAGTGCATTTTTAACTGCTTCAGAAAAGTACAACTCCTGAGAAAAACTGCTTAGTTACATTAATTTGTAACTCTGCACCACTGAATATAATGACTTCTCAAATTGTATAAAAATGCTACTTAAAATTATTATCTGATAATCTTCCCTTCTGCTGCAACTGCCAAATCAAATAAGATGCACATTTTAAATGTCAGTAACATTTAACATCAGTCTCATATCCAAATGCTTGTAAAACTTGTGGCCATTTTCAAGTGATTTTTTTAACCTCTTTAAGCTACCATTTCTTTTAAATTTTATCAACTCACAGCAGCCCGACTAAGACTCATGATATCAGTGAAACAAATTTTTTATGCTCTTCAGATTCTGCAATGAGAAGGTGTCATGCCCTCAGCCTATCTTCTGGTCATCATGGTCTCCCTGGTCCAAGTGCAGTGCAGATTGTGGTGGAGGTGTGCACTCTCGCTCCAGGAACTG[T/A]GAGAATGGAAATAGCTGTCCAGGGTGTGCGCTGGTACGTATACCTGAAGCACACTCTCTTACATATGCACACACGCACACACACACACACACACACACAAACACATGCGCACACACACGCGCACACACACACACACACACACACACAGTAGCCTTGAAGCCTCCTGCTCGAGCATGATAACCAAGCCGCTCTCCTCCTAGAAAGATACGCGTGATGTACTGTAGAAGCAGAGCTCATTTGTGATTCAGAGTAGACTGAGTGGACTCGACAAATCTAATACACTGTTTCATTGTGGAGATTTATGCAGTTCTGAGACTGTCACTTACATTAAGTTGATCATCCACCCTGCCTGCTGACATTCTTGAAGTTATTTACAGTGCATTCATCATCTTCAAACTGAAAACGAGATAAAACATATATACATAAATTTATTTGGGCATGCTTTTTGTTGCCAAGACAGAAAGGCATATGCTTATAGAGTGCAAAACTGCATGCACACT
Associated Phenotype:
Not determined