ZMP
zgc:158262
Ensembl ID:
ZFIN ID:
Description:
Leukocyte receptor cluster member 8 homolog [Source:UniProtKB/Swiss-Prot;Acc:A4QNR8]
Human Orthologue:
LENG8
Human Description:
leukocyte receptor cluster (LRC) member 8 [Source:HGNC Symbol;Acc:15500]
Mouse Orthologue:
Leng8
Mouse Description:
leukocyte receptor cluster (LRC) member 8 Gene [Source:MGI Symbol;Acc:MGI:2142195]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42672 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1304 | Nonsense | Available for shipment | Available now |
sa10160 | Nonsense | Available for shipment | Available now |
sa19133 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42672
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113345 | Essential Splice Site | 14 | 839 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14015906)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12374997 |
GRCz11 | 16 | 12265899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCAAAATGGCGGCGAATGCGGCTCAACAAGCCCCGACACAAAACTGG[T/A]AAGGCGTTTTTATATCTCATTAATGACATCTTCACGTTTCTAACGAATTT
Long Flanking Sequence:
TTTCTGCATTTCCTTTTTAGCACAGAAAATATACTTAATACATTTATGACTGTACACATATTCTGGCCTGTTTGCCATTAAGCGTGTGTGTGGTTTGCTCTGCTCGTATGCAGAACATTCAGTCCTCCAAAAATGAAAAATAAATAAATCAAGTCCTCCAATGAGAGAACGCTGAAGAACATTTCCGGCGACTGCGTCCTCACCGGCAGCCATTTTGTTTGAGGTGTTGACATTCATCCGTTGAGTTCGGAGAACTAGTTGATATGGGCGTCAGTTTAACTCTGATATCGACAGGAACGTATTTAATTTAAGACAGTCGGTATACACTATTGTTAAACATTTTTGTAGCAGATTATATAGTAAATATTTTCTATTAAGCGTTAGTACGATTTCTTTTCTCATATTTGCGTAGATTTTTTCTACGAGCTAACAGTAACTAACTGGTTAGCTCTGGCAAAATGGCGGCGAATGCGGCTCAACAAGCCCCGACACAAAACTGG[T/A]AAGGCGTTTTTATATCTCATTAATGACATCTTCACGTTTCTAACGAATTTTGTCTGTTAAACGTGTCTCACCTAAAGGTTTCACTGCATATTTTGAGGTACAAATAGGTGTAACAATCGATTGAGATTTTGGCGTTCGCTAGCTTATCCGCTTCTCTTTGCAGATTTAACGAATTATTTCGTAGTATCGGCCTGCCATTTTTAATAAGTTGGATATAGGTTGATGTTTTTATTTTTATTTTATTTTTTTCTGTTAAAGGTAGTCCATACTAGAACTGGAATCGAGTGGAATTAACGTCTGTCTTGTTGTAAAGGCCTCATTGGTGACCAGCATATTTATCATTGCTAAGTTACACTGTTTCTTATCGTTATGGCTTTTAATCAAAAAAACTTTTAGCGAAACAAGCCAGACACAGTATGCTTAACAAATCTGAACAAGTTTTAGGAAATGCAATGACTCTTAAAATTCACTTGCCAAAATAACGTTACGAATATTACACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1304
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 |
---|---|---|---|---|---|
ENSDART00000113345 | Nonsense | 85 | 839 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14014948)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12374039 |
GRCz11 | 16 | 12264941 |
KASP Assay ID:
554-1219.1 (used for ordering genotyping assays)
KASP Sequence:
CAGACTCCTCTGCAATGCAGCAGCAGCAGTATTATCAGCAGTGGTATCAA[C/T]AGAACCAACAGCAGTATGCTGGTTACCCTTATCCTTATAACTACTACTAC
Long Flanking Sequence:
TCTTAAAATTCACTTGCCAAAATAACGTTACGAATATTACACCGTCTGCAGTCAGTTTTTGTTTGTATATGAACCTTGTTTTGTGTGGGTCACGGTGTGCTTGTGTAGATGTATGTAAATGTTTTTAAAAGGTCTGATATGCCGTGAACTAAAATCCATATTACGTTTACCTTACCATGTTTTCATCTGCAGGCCGTATGGTAATAATTCAAGTGGTGAAGGCCCAGTCCACGAGAACCCAGAATGGGAAAAGGCCCGACAGGCTCTAGCATCCATCAGTAAAAGTCAAAACTCTACCAAACCTTCAACTAATCAAACCACACAACAGGTTAGTGTTTCATGAGAATAGAGGTGGACATTTTTATCAGTTTTAAACCCATGCTTTATTGCGTGGTAAAATGGTTGATTTTTGATTTTTCTGTTAGGCTGGACAGTATCAGGCAGCAGTTACAGACTCCTCTGCAATGCAGCAGCAGCAGTATTATCAGCAGTGGTATCAA[C/T]AGAACCAACAGCAGTATGCTGGTTACCCTTATCCTTATAACTACTACTACCCCATGCCTCCGGTAAATAAATGCACTCCTACATTTTTGAACATGTATCTGTAAACAGTCCTTATCCATTTCCCTTTAAATCTTAACCGAAAGGTTAGCTGCAGAGAGTAAGCAGTTTTTTTTTTTTTTTTTTTTTTAAGCGTTTGTGTTTGATTGGAGCTTTTATACCACACACTGAAGCAGCATTGCTGTAATTATTTTGGTCCTTGGTCTATTTTTAACACACTGATTACGTTCAGTTAAAGTGATAATGCATTAGTTATGACCAAAAACAAATAGAAAAAATTGACAGCCGAAAAAGTAGAAGTTTTACCCAAAAAAATGCATGGACAATTTCCACTGGTTTTTATATTGTCAATCAAATGAACTGAAACGATTTAAAAATGCAACAAGTATTTGTTTGGGTCTGAACTACAAAACTACATTTAAAACAAAATTTAGTGTCAGTTT
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:
sa10160
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 |
---|---|---|---|---|---|
ENSDART00000113345 | Nonsense | 641 | 839 | 11 | 15 |
ENSDART00000113345 | Nonsense | 641 | 839 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14011202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12370293 |
GRCz11 | 16 | 12261195 |
KASP Assay ID:
2260-9323.1 (used for ordering genotyping assays)
KASP Sequence:
CAGTAAAGGCTCATTGGAAAAGCAATCAGGACTAYGTCTACGCATGTGAA[C/T]AAATGAAATCCATAAGACAGGATCTAACTGTRAGTGATGACTTTTAGTAC
Long Flanking Sequence:
TACTTTCTCCTATGACTTCTTTCAGGAATATGGAAGACCTAGCCAGTGGCGTTGGTAAAAAACGTAAAGGTGGTAATGCAGGCCTTGACTTTCACGACCCAAATCGTGAAGCAAAGAAACAGAGCCGTGCAGCACGCTTCCACACTAAACTACGCACTGAGCCCCTGGTGTTAAACATCAATGTTTTTGACCTCCCCAACGGTACCCAAGAGGGATTAAGTTGGGATGACTGCCCCATAGTTGGCACCTGCCAGGACATCACAAAAAACTACCTCCGTCTCACCTGTGCCCCAGATCCTTCAACCGTCAGGCCTGTACCTGTGAGTGTTTCTCAGAATGTTGCTTGTCTTTTGAGCGAATGATTTGTGTTATTTGTGGTCTGTGGTTGTCAGTTTAATGCAAAAATTGCTTTAAAAATTGTGTTTTAGGTGTTGCGAAAATCCTTGATTGCAGTAAAGGCTCATTGGAAAAGCAATCAGGACTATGTCTACGCATGTGAA[C/T]AAATGAAATCCATAAGACAGGATCTAACTGTGAGTGATGACTTTTAGTACCATTTACCTGTCTTGCCTTTTTTAGTGTCTTATTTTGAAATGTCTTAATCAGGTGCAAGGTGTACGTACAGACTTTACAGTGGAGGTGTATGAGACGCATGCTCGCATTGCTCTGGAAAAGGTATGAAGGGAAATGTCTTTGTTGAATTAAGTCACAGTATTTTACTATTAATGTATTGGTATTAGACAACCAACCTCATTTTTCTGTTGTTTTTAGGGCGACCATGAGGAGTTCAACCAGTGTCAAACACAGCTGAAGGCGCTGTATAAAGACTGTCCATCAGACAACGTTGGAGAATTCACTGCCTACAGACTTATCTACTACATCTTTACTAAGAACTCTGGAGGTATAGCTATAAATTGCTTTTGCTTTACCAGCAGTTTAATATTTATTTTTATTATTTTGGGGTTCTTATGTATTCTCGTATGAAGCCTTTAATAATCTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19133
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 |
---|---|---|---|---|---|
ENSDART00000113345 | Nonsense | 641 | 839 | 11 | 15 |
ENSDART00000113345 | Nonsense | 641 | 839 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 14011202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 12370293 |
GRCz11 | 16 | 12261195 |
KASP Assay ID:
2260-9323.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTAAAGGCTCATTGGAAAAGCAATCAGGACTATGTCTACGCATGTGAA[C/T]AAATGAAATCCATAAGACAGGATCTAACTGTGAGTGATGACTTTTAGTAC
Long Flanking Sequence:
TACTTTCTCCTATGACTTCTTTCAGGAATATGGAAGACCTAGCCAGTGGCGTTGGTAAAAAACGTAAAGGTGGTAATGCAGGCCTTGACTTTCACGACCCAAATCGTGAAGCAAAGAAACAGAGCCGTGCAGCACGCTTCCACACTAAACTACGCACTGAGCCCCTGGTGTTAAACATCAATGTTTTTGACCTCCCCAACGGTACCCAAGAGGGATTAAGTTGGGATGACTGCCCCATAGTTGGCACCTGCCAGGACATCACAAAAAACTACCTCCGTCTCACCTGTGCCCCAGATCCTTCAACCGTCAGGCCTGTACCTGTGAGTGTTTCTCAGAATGTTGCTTGTCTTTTGAGCGAATGATTTGTGTTATTTGTGGTCTGTGGTTGTCAGTTTAATGCAAAAATTGCTTTAAAAATTGTGTTTTAGGTGTTGCGAAAATCCTTGATTGCAGTAAAGGCTCATTGGAAAAGCAATCAGGACTATGTCTACGCATGTGAA[C/T]AAATGAAATCCATAAGACAGGATCTAACTGTGAGTGATGACTTTTAGTACCATTTACCTGTCTTGCCTTTTTTAGTGTCTTATTTTGAAATGTCTTAATCAGGTGCAAGGTGTACGTACAGACTTTACAGTGGAGGTGTATGAGACGCATGCTCGCATTGCTCTGGAAAAGGTATGAAGGGAAATGTCTTTGTTGAATTAAGTCACAGTATTTTACTATTAATGTATTGGTATTAGACAACCAACCTCATTTTTCTGTTGTTTTTAGGGCGACCATGAGGAGTTCAACCAGTGTCAAACACAGCTGAAGGCGCTGTATAAAGACTGTCCATCAGACAACGTTGGAGAATTCACTGCCTACAGACTTATCTACTACATCTTTACTAAGAACTCTGGAGGTATAGCTATAAATTGCTTTTGCTTTACCAGCAGTTTAATATTTATTTTTATTATTTTGGGGTTCTTATGTATTCTCGTATGAAGCCTTTAATAATCTTGTTT
Associated Phenotype:
Not determined