ZMP
lhx2b
Ensembl ID:
ZFIN ID:
Description:
LIM/homeobox protein Lhx2 [Source:RefSeq peptide;Acc:NP_001035099]
Human Orthologue:
LHX2
Human Description:
LIM homeobox 2 [Source:HGNC Symbol;Acc:6594]
Mouse Orthologue:
Lhx2
Mouse Description:
LIM homeobox protein 2 Gene [Source:MGI Symbol;Acc:MGI:96785]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6091 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21179 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6091
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 |
---|---|---|---|---|---|
ENSDART00000033846 | Nonsense | 72 | 396 | 2 | 5 |
ENSDART00000136250 | Nonsense | 31 | 134 | 2 | 3 |
ENSDART00000148020 | Nonsense | 103 | 427 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 3254261)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 3028710 |
GRCz11 | 8 | 3087459 |
KASP Assay ID:
554-3748.1 (used for ordering genotyping assays)
KASP Sequence:
GCTGCGGAGGCAAGATTTCGGATCGCTACTACCTGCTCGCCGTGGACAAG[C/T]AATGGCACATGCGCTGTYTGAAGTGCTGCGAGTGTAAACTGAACCTGGAG
Long Flanking Sequence:
ACACGCAAATGGATGCATGCACAATATAATACATTCTATCTGTTGTATCCTCTTTATATGCATGATCCTCCGTTGTCACGGGAAATGTTAAAAAAAATTAAAGTAGCCTATATATCGGCTCTTATTCACTCTAAACTTGTGTATTTATCTTCTGAATTTGTTCTCACGCCCCTCCCATTCTATACACAAGTGAGCACTATTTTACTCTTAGCATGTTTTTTTATACCCAGCAAATGCGTAAAATAGTGTTTACACTCATCCCTAAAGCCATTACCATTATAATTTACAAATCTGCCTTTTAATATCATTGCTGCAACATAAGAGAGAATGGTGGAGAAAAAAAATCTGTGTTTGTGTAAGATTGGGATTTGAGTTCGTGCATTTAATGAGTCTGTGTGTTTCCGCAGAACATGCCTTCAATCAGCGGGGATCGGGTGGCTCTGTGCGCCGGCTGCGGAGGCAAGATTTCGGATCGCTACTACCTGCTCGCCGTGGACAAG[C/T]AATGGCACATGCGCTGTCTGAAGTGCTGCGAGTGTAAACTGAACCTGGAGTCTGAGCTCACCTGCTTCAGCAAAGACGGAAGCATCTACTGCAAAGAAGACTATTACAGGTGAGCCAACTCATTTGGCTACGTAAAAAGTTGATTTTAAGTTCATTTTTTCGCATTAGGAGTTTAGTTTTCGTTGTGGATAAATAATAAAAAGACAAAAGTTGTATTTTGTAAAGATATGCATTTGTTTGTAGATATATTAGATCTATTTTCTTACTTCAATTTAACGAAAAACAAAGACGCAACTAATTTCCATTGTGGGCATAACAATAATGTTGTTTTAATGTATTTTTTTTCTATTTAAAATACAAAATAATCAATGTCAATATTTCAGAAAGGATTGATTTTACTAGAATTTGTTGTTTGCTCATAATAATCTTTTATGTTTGTTTAAATTAATAAAGCATCGGGATGTTTTTTGTCTATTGCTTTTTTTTTTTTTTTTTTTTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21179
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 |
---|---|---|---|---|---|
ENSDART00000033846 | Nonsense | 84 | 396 | 2 | 5 |
ENSDART00000136250 | Nonsense | 43 | 134 | 2 | 3 |
ENSDART00000148020 | Nonsense | 115 | 427 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 8 (position 3254297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 3028746 |
GRCz11 | 8 | 3087495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGCCGTGGACAAGCAATGGCACATGCGCTGTCTGAAGTGCTGCGAGTGT[A/T]AACTGAACCTGGAGTCTGAGCTCACCTGCTTCAGCAAAGACGGAAGCATC
Long Flanking Sequence:
TATCTGTTGTATCCTCTTTATATGCATGATCCTCCGTTGTCACGGGAAATGTTAAAAAAAATTAAAGTAGCCTATATATCGGCTCTTATTCACTCTAAACTTGTGTATTTATCTTCTGAATTTGTTCTCACGCCCCTCCCATTCTATACACAAGTGAGCACTATTTTACTCTTAGCATGTTTTTTTATACCCAGCAAATGCGTAAAATAGTGTTTACACTCATCCCTAAAGCCATTACCATTATAATTTACAAATCTGCCTTTTAATATCATTGCTGCAACATAAGAGAGAATGGTGGAGAAAAAAAATCTGTGTTTGTGTAAGATTGGGATTTGAGTTCGTGCATTTAATGAGTCTGTGTGTTTCCGCAGAACATGCCTTCAATCAGCGGGGATCGGGTGGCTCTGTGCGCCGGCTGCGGAGGCAAGATTTCGGATCGCTACTACCTGCTCGCCGTGGACAAGCAATGGCACATGCGCTGTCTGAAGTGCTGCGAGTGT[A/T]AACTGAACCTGGAGTCTGAGCTCACCTGCTTCAGCAAAGACGGAAGCATCTACTGCAAAGAAGACTATTACAGGTGAGCCAACTCATTTGGCTACGTAAAAAGTTGATTTTAAGTTCATTTTTTCGCATTAGGAGTTTAGTTTTCGTTGTGGATAAATAATAAAAAGACAAAAGTTGTATTTTGTAAAGATATGCATTTGTTTGTAGATATATTAGATCTATTTTCTTACTTCAATTTAACGAAAAACAAAGACGCAACTAATTTCCATTGTGGGCATAACAATAATGTTGTTTTAATGTATTTTTTTTCTATTTAAAATACAAAATAATCAATGTCAATATTTCAGAAAGGATTGATTTTACTAGAATTTGTTGTTTGCTCATAATAATCTTTTATGTTTGTTTAAATTAATAAAGCATCGGGATGTTTTTTGTCTATTGCTTTTTTTTTTTTTTTTTTTTGAAATATGATGACGCAATAGGCCTCAAAATTATGTTAC
Associated Phenotype:
Not determined