ZMP
si:dkey-42o15.2
Ensembl ID:
ZFIN ID:
Human Orthologue:
LRIG2
Human Description:
leucine-rich repeats and immunoglobulin-like domains 2 [Source:HGNC Symbol;Acc:20889]
Mouse Orthologue:
Lrig2
Mouse Description:
leucine-rich repeats and immunoglobulin-like domains 2 Gene [Source:MGI Symbol;Acc:MGI:2443718]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18052 | Nonsense | Available for shipment | Available now |
sa38577 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18052
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 |
---|---|---|---|---|---|
ENSDART00000112700 | Nonsense | 110 | 1044 | 3 | 18 |
ENSDART00000141986 | Nonsense | 84 | 1018 | 3 | 18 |
The following transcripts of ENSDARG00000078561 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 47778955)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 47839607 |
GRCz11 | 6 | 47838366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGGTGGCRGAGCAGCTGTTGCCRTATTCATCACTGGAAAGTCTAGACT[T/A]GAGCTCWAATTCTATATCMGAGCTTAAARCTGGATCATTCCCTCCCATGC
Long Flanking Sequence:
TTTGAGATTTAATTTTTATGCGAGGAAGCTTGCTCGGGTTTTAAATATTTTAATGATTGTTTCCATACTTATTTTTTTTGCATGCGAGTACCCCCAGATAACATTTAGTTTTTTTATTTACACATTTTCATTCATGTTATTTTGTTGTTTCTTTCTAGAAATTACTTTGGTAGACTTTAATAATTTGCTTTATTTGATTCTAGGTCTATAAATCAGAATGAACTTACAGCAGTGCCTTTTCTTGGAGACGCCTCATCCAACATCACTGTGCTGTCACTGTAAGTTTTCTCCTTCAGGCTCTTTATAACTGACAATACTGTTTACACTACACGGATTGCGTGATTTGTTTACTATTTTACATTTCATTAGGAGTGATAGGTTGTGAATATTGTTATGGGACGTCTGTAACCATCTGTTGTTTATTTTCAGTGTTCATAACCGAATCTCTGAAGTGGTGGCGGAGCAGCTGTTGCCATATTCATCACTGGAAAGTCTAGACT[T/A]GAGCTCTAATTCTATATCAGAGCTTAAAGCTGGATCATTCCCTCCCATGCAGCTAAAATACCTGTGAGTTTGTTTGTTTTTTTGCCTGTGTTTTTGAACTTGTGTATGTCGAGCACTTTAGTATAATGGCCCGATTCTGCTGAGTGGGACAGTATGGTACGGGTTGGTACGGGTCACCTTTATCAGGCTTGCATTTCCACTGCAAAAAGGTACCAATGGTAAGCGTGAGTATGACAGAAATTTCATTTGATGTCATTCTCGCTCAAGGAAATGTCAAAGTAAAGCTGTACGGGTCGTTCACATATCATATGAGAAGCACTTTACACACATAAATACTTGTGTATAAATGTTCATTACTAAACTTTCTATAAACAGAATTTGATTAACTGCAGATCAATGATGCAACATATATGTGAAGCAGTGCGAAATAGCCTACTGTAACATCTGCAGATATATAAAATAAATAGATGCAACATATATGAACACATTCAGACCTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38577
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112700 | Nonsense | 468 | 1044 | 12 | 18 |
ENSDART00000141986 | Nonsense | 442 | 1018 | 12 | 18 |
The following transcripts of ENSDARG00000078561 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 6 (position 47766097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 47826749 |
GRCz11 | 6 | 47825508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTTTCCTAAACCCCAGATCACAGCTCACCCAAAGACTGCTGTTGCGT[T/A]ACGTGGGACAAACGTCACTCTGAACTGCTCCGCCTTCAGCAGCAGTGACT
Long Flanking Sequence:
GTGCAACAGTAAACCTATGAAGCTTCAAAACATACATGTGCCAAAAATCCGCAGAAACAAATGCATCAGGACAGGGTAGGAGTTTACAATGGGACAATACTGTGCTTGCATGTTGTACTACTGACTCTATTGCCATTACAATGTATTATTCGTAGCGAACACACACTATTACTTGATGTGGGAGAAAAGATATAGGTGAACCAAGTCATTTAGCTTGTTTTGCTCTGTGACTTTAGCCATCTATGGAGGTTCAGAGAGCTCTTGAGTTTTAACTAAAGTATCTTAATTTGTGTTTTGAAGATAAATGAACATCTCAGAGGGTTAATTAATAACATAATTACATTTTTGGGTGAACAAACTCATTAAGGCCTTACTATTGGCTTCATTTTTTTGCTATTTAAAATAGCTTTTTGTAGCATTGATATGTTGTTGTTCCGTCTCTTTTGCAGGTGATTTTCCTAAACCCCAGATCACAGCTCACCCAAAGACTGCTGTTGCGT[T/A]ACGTGGGACAAACGTCACTCTGAACTGCTCCGCCTTCAGCAGCAGTGACTCTCCCATGAGCACGGCCTGGCGCAAAGATGGAGAGGTGCTGTATGAAGCTCAGGTGCAGAACTACGCTCGCTACCAGGACCAGCGCCTCCTCTACACCACCATACTCCATCTGCTCAACGTCAATTTCACAGACGAGGGCCAGTACCAGTGTGTGCTCTCCAACCATTTCGGCTCAAACTACTCCACTCTGGCCAAGCTCACTGTTAATGGTTAGTACATCACTACATTTATTTTATTTTTTTATAATGAGTCTAGATGAGATGTTTTGTTATAAGACAGGTTTACATTTACATTTTTATTCAGATAGGAATGTGTGTATTTATAATTTATGATCAAATCATAGTTGACGTACAAGTTGAGTATGCCACTCAATTTGCAGAAAAACAAGCAGTGCTTTAAGAGATCGCATTAATTGTGTGATAAAACCTATCCACTTGTTCAGTGTGACA
Associated Phenotype:
Not determined