ZMP
si:ch211-260g14.8
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC558139 [Source:RefSeq peptide;Acc:NP_001124070]
Human Orthologues:
SELE, SELL, SELP
Human Descriptions:
selectin E [Source:HGNC Symbol;Acc:10718]
selectin L [Source:HGNC Symbol;Acc:10720]
selectin P (granule membrane protein 140kDa, antigen CD62) [Source:HGNC Symbol;Acc:10721]
selectin L [Source:HGNC Symbol;Acc:10720]
selectin P (granule membrane protein 140kDa, antigen CD62) [Source:HGNC Symbol;Acc:10721]
Mouse Orthologues:
Sele, Sell, Selp
Mouse Descriptions:
selectin, endothelial cell Gene [Source:MGI Symbol;Acc:MGI:98278]
selectin, lymphocyte Gene [Source:MGI Symbol;Acc:MGI:98279]
selectin, platelet Gene [Source:MGI Symbol;Acc:MGI:98280]
selectin, lymphocyte Gene [Source:MGI Symbol;Acc:MGI:98279]
selectin, platelet Gene [Source:MGI Symbol;Acc:MGI:98280]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15565 | Nonsense | Available for shipment | Available now |
sa11522 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15565
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000009440 | Nonsense | 78 | 856 | 3 | 15 |
ENSDART00000111022 | Nonsense | 41 | 835 | 3 | 18 |
ENSDART00000136834 | Nonsense | 100 | 648 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 34000791)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34073304 |
GRCz11 | 20 | 33976183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGATTGYTCACCTCAACGGAATTCTTCCAAGACGCAATGGCTRTTACTG[G/A]ATTGGTATTCGTWAAATTAATAACCAGTGGACCTGGGTGGGAACTAACAA
Long Flanking Sequence:
ATGGTTGTCAGTGGTTACAGGCATCCAACTTTCTTCAATATGTCATATTTTGTGTTCAACAGAGGAAAGAAAATCAAACAGGTTTGAGTAAATAATAACAGATTTTTTTTCAGATCAGTTTTTGGTGAAATATCCATTTAAGTATCAATTATTAAGATCATCTAAGTGATATAATTATTTTATTTTGCAGGACATTTGCAACAAGTTGCAGTTCTTTGCTTCGTTTGTTCTTATCTCTTCAGGTAGGAAAGTAAACCATATAACTGCATACTGTAAATAGTTCAAATAGTTCATTAATAGTTCCAATGTTTCATTTCTGCAGCGCTAAACTTATGGAGATGCAGTGAAGGTTGGTCATACCACTACTCAGACTCCACCATGACATGGCAAAATGCCAGAAACTGGTGCAGGCAGCACTACACCGACTTGGTGGCCATCCAGAACAAAAATGAGATTGCTCACCTCAACGGAATTCTTCCAAGACGCAATGGCTATTACTG[G/A]ATTGGTATTCGTAAAATTAATAACCAGTGGACCTGGGTGGGAACTAACAAAACACTTACTGCTGAAGCTGAAAACTGGGCAGAAAAGGAGCCCAACAACAAAGGAAATAATCAAGACTGTGTGGAAATATATATTCAAAGAGAGAAAGATGAAGGTAAATGGAATGATGAATCCTGCTCAAAATCAAAGACAGCGTTGTGCTACACGGGTAGGTAGCTTTTACGGATTTATAAGATCTTGTATGGCCTTCCAACCAATGCATTTAGATGAAAATGAAAAGTCATTCTGCTGTATTTGTTGTATAAATACAACCATCATCAAATAAGTATGCTGTTGTCTTTACCTTAGCTTCCTGCGCGAGTGACTCCTGTGTCAGTGGTCATGGAGAGTGTGTAGAAACCATAAACAGTCATACATGCTCATGCTTTGAAGGCTTCTATGGAAAAGTATGTGAAAATGGTGAGTAACATTTTCTGGTGATGTTTCCCATATCAGTTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11522
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 |
---|---|---|---|---|---|
ENSDART00000009440 | Nonsense | 83 | 856 | 3 | 15 |
ENSDART00000111022 | Nonsense | 46 | 835 | 3 | 18 |
ENSDART00000136834 | Nonsense | 105 | 648 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 20 (position 34000778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 34073291 |
GRCz11 | 20 | 33976170 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACGGAATTCTTCCAAGACGCAATGGCTATTACTGGATTGGTATTCGT[A/T]AAATTAATAACCAGTGGACCTGGGTGGGAACTAACAAAACACTTACTGCT
Long Flanking Sequence:
GTTACAGGCATCCAACTTTCTTCAATATGTCATATTTTGTGTTCAACAGAGGAAAGAAAATCAAACAGGTTTGAGTAAATAATAACAGATTTTTTTTCAGATCAGTTTTTGGTGAAATATCCATTTAAGTATCAATTATTAAGATCATCTAAGTGATATAATTATTTTATTTTGCAGGACATTTGCAACAAGTTGCAGTTCTTTGCTTCGTTTGTTCTTATCTCTTCAGGTAGGAAAGTAAACCATATAACTGCATACTGTAAATAGTTCAAATAGTTCATTAATAGTTCCAATGTTTCATTTCTGCAGCGCTAAACTTATGGAGATGCAGTGAAGGTTGGTCATACCACTACTCAGACTCCACCATGACATGGCAAAATGCCAGAAACTGGTGCAGGCAGCACTACACCGACTTGGTGGCCATCCAGAACAAAAATGAGATTGCTCACCTCAACGGAATTCTTCCAAGACGCAATGGCTATTACTGGATTGGTATTCGT[A/T]AAATTAATAACCAGTGGACCTGGGTGGGAACTAACAAAACACTTACTGCTGAAGCTGAAAACTGGGCAGAAAAGGAGCCCAACAACAAAGGAAATAATCAAGACTGTGTGGAAATATATATTCAAAGAGAGAAAGATGAAGGTAAATGGAATGATGAATCCTGCTCAAAATCAAAGACAGCGTTGTGCTACACGGGTAGGTAGCTTTTACGGATTTATAAGATCTTGTATGGCCTTCCAACCAATGCATTTAGATGAAAATGAAAAGTCATTCTGCTGTATTTGTTGTATAAATACAACCATCATCAAATAAGTATGCTGTTGTCTTTACCTTAGCTTCCTGCGCGAGTGACTCCTGTGTCAGTGGTCATGGAGAGTGTGTAGAAACCATAAACAGTCATACATGCTCATGCTTTGAAGGCTTCTATGGAAAAGTATGTGAAAATGGTGAGTAACATTTTCTGGTGATGTTTCCCATATCAGTTCTGACAATGAAAGGTG
Associated Phenotype:
Not determined