ZMP
lhx8a
Ensembl ID:
ZFIN ID:
Description:
LIM/homeobox protein Lhx8 [Source:RefSeq peptide;Acc:NP_001003980]
Human Orthologue:
LHX8
Human Description:
LIM homeobox 8 [Source:HGNC Symbol;Acc:28838]
Mouse Orthologue:
Lhx8
Mouse Description:
LIM homeobox protein 8 Gene [Source:MGI Symbol;Acc:MGI:1096343]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18505 | Nonsense | Available for shipment | Available now |
| sa18198 | Nonsense | Available for shipment | Available now |
| sa180 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa18505
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 |
|---|---|---|---|---|---|
| ENSDART00000019078 | Nonsense | 3 | 332 | 1 | 8 |
| ENSDART00000144982 | None | None | 237 | None | 6 |
| ENSDART00000019078 | Nonsense | 3 | 332 | 1 | 8 |
| ENSDART00000144982 | None | None | 237 | None | 6 |
The following transcripts of ENSDARG00000002330 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 10997240)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 11422336 |
| GRCz11 | 2 | 11205935 |
KASP Assay ID:
2259-1657.1 (used for ordering genotyping assays)
KASP Sequence:
GTACAGGAGATCTGAGAGTGGATATWGCCTGTCATACTGGACAATGTACT[G/A]GAAAAATGAACAAACCACATCRAAAGAGAGCCCAAGCAAGAACACTGTAA
Long Flanking Sequence:
ATAGCAAAAACAAGATTCTAATTTTTAAAATATTGTTCTAGTTTCTATAAATTATCTACCATCTTAAATTATTATTATTATTATTAATGATACCTATAGGCCTAATATTCATCATCATTCATAACTATGTAGCATTAGGCCTATTTAAGATGTGTAGACTATTGTAACCAATCCTAAAAGTCGGTTTCAAAACGTCAGCAAAACTTGCATTCTTGATTTAACAAATATGACGGTGCTTACAGTTTGTTTATGGATCTTTTTTTCACGCAACTGAGCTGACTCCTCAACTGATAGGCGTGTGTAAATGTGACAGGGAGGTGCGGCCAGAGGAATGAGAACATGAGGAAAAGTTCCACCCTCACGGAGGAAAACAAAAGTTTGAGTTAAAACATGGTCGCGACGTGCGTTCAGCAGCAGCGGCAGCAGCACCTATATGGATTAATTCTCTCTGTACAGGAGATCTGAGAGTGGATATAGCCTGTCATACTGGACAATGTACT[G/A]GAAAAATGAACAAACCACATCGAAAGAGAGCCCAAGCAAGAACACTGTAAGTAACACGTTTAAAATGTTTTATTTGTTTTCTTTATTATTATTATTAATAAAAATAATTGTTTATTGTTTTATTATAATAAATAACCTAGGCTACTGAGGTGATCTCCTGGGGCTGCATGTTTTGTAGGATTTTCAAAGATAAAAATAATCTGAATATATTCATCTTCCATAATAAACAATGCAGGCACACTGTGTTTTATTTTTCATCACGTTAAACTATTATTTATCCTTGTTTGTCAGCAGCCGTCAACTCTGAATTACGGACCATCTTCAGCTGTGCCTCGGGCAACGCCTGTGCGCAATTATTATAAATTACGCGATGTGGAATTGTTTCTTCTTTTTTTCCACAGAGACAGTCGCTTTTTAGGAGTTTGGATTTAGTTAACATGCTTAAAAAATGTCTGAGTTTGGAAAGCAGAAAAAAACAATTACCAACAGGCTACTACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18198
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 |
|---|---|---|---|---|---|
| ENSDART00000019078 | Nonsense | 3 | 332 | 1 | 8 |
| ENSDART00000144982 | None | None | 237 | None | 6 |
| ENSDART00000019078 | Nonsense | 3 | 332 | 1 | 8 |
| ENSDART00000144982 | None | None | 237 | None | 6 |
The following transcripts of ENSDARG00000002330 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 10997240)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 11422336 |
| GRCz11 | 2 | 11205935 |
KASP Assay ID:
2259-1657.1 (used for ordering genotyping assays)
KASP Sequence:
GTACAGGAGATCTGAGAGTGGATATWGCCTGTCATACTGGACAATGTACT[G/A]GAAAAATGAACAAACCACATCRAAAGAGAGCCCAAGCAAGAACACTGTAA
Long Flanking Sequence:
ATAGCAAAAACAAGATTCTAATTTTTAAAATATTGTTCTAGTTTCTATAAATTATCTACCATCTTAAATTATTATTATTATTATTAATGATACCTATAGGCCTAATATTCATCATCATTCATAACTATGTAGCATTAGGCCTATTTAAGATGTGTAGACTATTGTAACCAATCCTAAAAGTCGGTTTCAAAACGTCAGCAAAACTTGCATTCTTGATTTAACAAATATGACGGTGCTTACAGTTTGTTTATGGATCTTTTTTTCACGCAACTGAGCTGACTCCTCAACTGATAGGCGTGTGTAAATGTGACAGGGAGGTGCGGCCAGAGGAATGAGAACATGAGGAAAAGTTCCACCCTCACGGAGGAAAACAAAAGTTTGAGTTAAAACATGGTCGCGACGTGCGTTCAGCAGCAGCGGCAGCAGCACCTATATGGATTAATTCTCTCTGTACAGGAGATCTGAGAGTGGATATAGCCTGTCATACTGGACAATGTACT[G/A]GAAAAATGAACAAACCACATCGAAAGAGAGCCCAAGCAAGAACACTGTAAGTAACACGTTTAAAATGTTTTATTTGTTTTCTTTATTATTATTATTAATAAAAATAATTGTTTATTGTTTTATTATAATAAATAACCTAGGCTACTGAGGTGATCTCCTGGGGCTGCATGTTTTGTAGGATTTTCAAAGATAAAAATAATCTGAATATATTCATCTTCCATAATAAACAATGCAGGCACACTGTGTTTTATTTTTCATCACGTTAAACTATTATTTATCCTTGTTTGTCAGCAGCCGTCAACTCTGAATTACGGACCATCTTCAGCTGTGCCTCGGGCAACGCCTGTGCGCAATTATTATAAATTACGCGATGTGGAATTGTTTCTTCTTTTTTTCCACAGAGACAGTCGCTTTTTAGGAGTTTGGATTTAGTTAACATGCTTAAAAAATGTCTGAGTTTGGAAAGCAGAAAAAAACAATTACCAACAGGCTACTACTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa180
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019078 | Nonsense | 199 | 332 | 5 | 8 |
| ENSDART00000144982 | Nonsense | 195 | 237 | 5 | 6 |
The following transcripts of ENSDARG00000002330 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 10999842)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 11424938 |
| GRCz11 | 2 | 11208537 |
KASP Assay ID:
554-0058.1 (used for ordering genotyping assays)
KASP Sequence:
GAGTGAATGTGGAGGGAGCTGTTCCCTCAGAGCAGGAAGTAAATCAGCCT[A/T]AACCGGCCAAGAGGGCACGCACAAGTTTTACAGCTGACCAGWTACAGGTT
Long Flanking Sequence:
TAAAAAATGGAAGTTCTTATCAAAGATTTGTTTCATACAGGAAATACGGAACACGTTGCGCTCACTGTGGCAGAAACATCCATTCAAACGACTGGGTTCGCAGAGCAAAAGGAAACACCTACCACCTGGCATGTTTTGCTTGCTTCTCCTGCAAGAGGCAGCTGTCTACAGGAGAAGAGTTTGCCCTGGTGGATGAGAGGGTTTTGTGTCGTGTCCACTATGACTGCATGTTGGACAACCTGAAGCGTGCCATGGAGAATGGTTAGAAGCTGCCTGGATTTTTATTTCAAGTGTTGAAATTTTCAGAGGATATCTAGTACCTGACGTTTTACAAAGAACACTGAATGTTTATCACATTTGCATTCATTCAGTTCCTGTGAAACAACGGATTGGGTTAAAATAATTTTTTTCTCATTCACTTTTTCATTTTGTGGTTTGCTCCAGGAAAAGGAGTGAATGTGGAGGGAGCTGTTCCCTCAGAGCAGGAAGTAAATCAGCCT[A/T]AACCGGCCAAGAGGGCACGCACAAGTTTTACAGCTGACCAGTTACAGGTTAATACAGCATATTTTTCTTTAAAAGTATTTAAAAGACTGGCTGCTTGACATTTTTAAAATTTGTATTTTTTTAAATGAAGGTGATGCAAGCCCAGTTTGCTCAGGACAACAATCCAGATGCTCAGACTTTACAAAAGTTGGCAGAAAGGACTGGTCTTAGCCGAAGGGTAATTCAGGTAAAACAGTTCTTCCAAAATTTATTTAATTTTCTGCATGAGATTTTAAATTTCTTTTTTTATTTGAATTGTTGTCCCAAGAATGATTTTATTTATTTACGTAAAAGTTTTACAAATATCTGAAGAACTTCATAAAAGTTTACTAAACTGGGAAAAATAGGCAAGTGTTATTCATTTTCTTTTAATTGTCTTAGCTTCATTTTATTGGGTAACGGACTTCATTTTGAATTAAATAATTCAATCTAGCAGTTTGTGCATTGTGATCTGAATGGTC
Associated Phenotype:
Not determined