ZMP
erlin2
Ensembl ID:
ZFIN ID:
Description:
Erlin-2 [Source:UniProtKB/Swiss-Prot;Acc:A3QK16]
Human Orthologue:
ERLIN2
Human Description:
ER lipid raft associated 2 [Source:HGNC Symbol;Acc:1356]
Mouse Orthologue:
Erlin2
Mouse Description:
ER lipid raft associated 2 Gene [Source:MGI Symbol;Acc:MGI:2387215]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1659 | Nonsense | Available for shipment | Available now |
sa40490 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1659
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 |
---|---|---|---|---|---|
ENSDART00000098015 | Nonsense | 93 | 331 | 4 | 11 |
ENSDART00000131286 | Nonsense | 93 | 331 | 5 | 12 |
ENSDART00000141239 | Nonsense | 113 | 235 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 37091087)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 34873036 |
GRCz11 | 5 | 35473189 |
KASP Assay ID:
554-1606.1 (used for ordering genotyping assays)
KASP Sequence:
TACAGTGGAGGTGTAATGATCTACTTTGATCGCATTGAGGTGGTGAACTA[C/A]CTTGTTCCCTCAGCAGGTAAAATGATCTATTTGTCATTTATAATGTCGAA
Long Flanking Sequence:
GTAAACATATTGCATGATATGTTCATTTAATCTATTACACTCACTGAAACTGCAAATATTAAAGTTAACCATTGGTTCAGTAGTGTACAGTGTGAAACCAAAGTGCATAAACACTCAGGATTACTTTTTAACCCCAGTTAATTATTAGTGGTCTAAAACATGGAGAAGATAATCAAGGATTCTCTATAGGCAACTTGAGCTTTACTAACATTTCTCTATTTGTGAGGACATATAGTATAGTGTAATGAAATGTAATTTCTCGCTGGACAACAGTGCTACATTCTTGACATTTACTACAAAAGCTTTTAGAAGTAAACATGGTTGACTATTTCAAATGTAAAAAGCCTTTTTATTGTGAAGAAGAAAGTCTGCATAAGATGTCCATTTCCACTTGTGCCTTGTGGAATAAATTTCACACTCATTCATAAATGTTTTTTTTTTTTTTTGCTTTACAGTGGAGGTGTAATGATCTACTTTGATCGCATTGAGGTGGTGAACTA[C/A]CTTGTTCCCTCAGCAGGTAAAATGATCTATTTGTCATTTATAATGTCGAACCTACGAAAGAGGCTGTCATTAGGGGTGGACAACTGGAAACATTTTCCTGGACTCTTTAACATGGGACGGCCCTCTAAGAGCCTATTTGGCACAGCCTACTTGACTCATAAATATTTTATCCTACTTTCTGTGAATTTAAGCACCGACTATAACTGTCATTTATTTTATGCGCCCAATTCATCTCTCTCTTAACCCCATTGTCTGCTCTGCTACAGTTTATGGCATCGTGAGAAACTTCACAGCAGACTATGACAAAGCCCTGATTTTCAATAAGGTTCACCATGAGCTGAATCAGTTCTGTAGTGTTCACACGCTTCAGGATGTCTACATTGGTCTGTTTGGTAAGTATTTTGTTTTAGTGTACTAATAAGCTAAGCAGAGGTGGATCTCATGTTTCTTGGTTTGATACCTAAAAGTTTAATTTGCTGCTTTTAAACCTATAGCTTAAT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa40490
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098015 | Essential Splice Site | 185 | 331 | 8 | 11 |
ENSDART00000131286 | Essential Splice Site | 185 | 331 | 9 | 12 |
ENSDART00000141239 | Essential Splice Site | 205 | 235 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 37096220)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 34878169 |
GRCz11 | 5 | 35478322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTACTTTCCTTTGTTTAATATTTTGTGTGTTTGTTCATGTGTTCCTCA[G/A]GGAGAGTGAGAGAACAAAGTTACTGATTGCAGCTCAGACTCAGAAGGTGG
Long Flanking Sequence:
AAACAGGAACCTACTGTAAATGCACAAACAGGTGATACAGATATTGTGAAAACGAAGGCAGGAAACAGAACAAAGGACAAAAAAAGAATGGTGTTTTTTTGTTTTTTGTTTTTTTACTTAATCATACTTGATTCTTGCTGTTTTGTAATTTTTTTTCAAAGTTAAACATCTAATCAGAATTATTTACCAATATTTTTTACTTTAAACTTTACCCTCTAACACTAAATCAGCTAGATTAGTATCAGTAACACTTTTATTAGTAATTTTTGGAAACTGCATGGCTTACATACCTGCTAGATTCATGCCAGTAATTTGGTGTGCTCTATATAATGCAGTGATTGAATTAGGAGGACGTTTTTCTCTCACACTTGAACCACATCTAACAGAAACATATATATCTGATAATTGTGCAACTTCATCTGATGTGATCCTGCTCAACCAAACATAATTTCTTACTTTCCTTTGTTTAATATTTTGTGTGTTTGTTCATGTGTTCCTCA[G/A]GGAGAGTGAGAGAACAAAGTTACTGATTGCAGCTCAGACTCAGAAGGTGGTGGAGAAAGAGGCAGAGACAGAGAGGAAAAAGGCTGTCATTGGTAAGCAAAGATGTTTTTCTGAGTATTAAACCCGAGTCTGTCTTGTATCATGGTGAATTGGTTTCCGATTACATAAAAGTGAAATAATGTCACTCTGTTTTATCATGTTTGCAGAGGCAGAGAAGGTGGCTCAGGTGGCTGAAATCAAATTTGGACAAAAGGTTATGGAAAAAGAAACGGAGAAAAAGATCTCACAAATTGAAGGTAGGTGAATGTGTATTCACGAGTGTTCAGAGGTCCAAGAAATCATGGAGAATAAAACTAGATCAGACTAACCATATGGACATGTGGGCCTTCATCTTATTAAAATATCAGTCTTTATTTATGCTTCAGCATATTATTAAATAAACAAGTGACAATAAATACATTTATAATATTATTAAAAATATGGGTAACACTTTAGTTTAG
Associated Phenotype:
Not determined