ZMP
lhx1a
Ensembl ID:
ZFIN ID:
Description:
LIM/homeobox protein Lhx1 [Source:UniProtKB/Swiss-Prot;Acc:Q90476]
Human Orthologue:
LHX1
Human Description:
LIM homeobox 1 [Source:HGNC Symbol;Acc:6593]
Mouse Orthologue:
Lhx1
Mouse Description:
LIM homeobox protein 1 Gene [Source:MGI Symbol;Acc:MGI:99783]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15189 | Nonsense | Available for shipment | Available now |
sa42561 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15800 | Nonsense | Available for shipment | Available now |
sa39051 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15189
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 |
---|---|---|---|---|---|
ENSDART00000005641 | Nonsense | 22 | 405 | 1 | 5 |
ENSDART00000134373 | Nonsense | 22 | 97 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 27059150)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 27777390 |
GRCz11 | 15 | 27710266 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGCTGCGAGAGGCCTATATTGGACAGGTTTCTCCTTAATGTTCTGGAC[A/T]GAGCATGGCACAKCAAGTGCGTACAGTGCTGCGAGTGCAAATGTAACCTA
Long Flanking Sequence:
ACTTTAATGCACATCCTCACCAATGCTTCACCTTGTTGACAACGACGACGTGCTTTTCACGCAATGATGTGCTTACCTTTGTAGCCAACGAACAGTTGGTGTTTTGAAAGATTTCTCTATGCTGGCTTCATTTATGCACCTCAAAATTTGGGACGGAAGAGGACGAGAAATGATGACTGACTACTGAAGCACTACCTCATGAGAAAATCTTCTATCGTCTTCATTTTGGACCCCTACAGGTCCACCCACAAACGCAGAACTGGTGAATATATTTAAAACTTCTTCATCTTTTCGTTTCAACCCTGTTCGCAAAGACTGACTTGGAACATCCTTCAGCGATACAACTTTTCCTCCTCTCTTTTAAAAGAGAGAAATCAGGAGCAGAGCCTCAGGTTGTGGACACCACGGCAGTAACTGTGGGAGCACATCCAAAGACGATGGTCCACTGTGCGGGCTGCGAGAGGCCTATATTGGACAGGTTTCTCCTTAATGTTCTGGAC[A/T]GAGCATGGCACATCAAGTGCGTACAGTGCTGCGAGTGCAAATGTAACCTAACAGAGAAATGCTTCTCTCGAGAAGGAAAACTATATTGCAAAAACGACTTCTTTAGGTAAGTTCCTTGCGTGAGTTAATTCGACCAAATATTTTACTTGTGGGGTTTTTGTGATAAATGGATAATTAATCGTTTATAAAGTAGCTATTATGTAGGCCCACTTCAGAAAATCTAGTACAGATGTCTACCATAATAATACAAATATTCTACGAACAAGATGAATATATTACCCGTTGTTGTGTATCTATGGTATATCTATGAAACATTTCTATATAAAATATATAATGTATCGTTAATATATGACAGAAATAAATCCAGAAGACACCCAAAATTATTTCATTTTAAAATTACACATTTACATTTTAAAGAGGTTCCACAATTGAGCTTAAAACAACATCACTTTAAAAGGTGAAATCACATTTTTTAAAGTCACTCAAAAATAACTAAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42561
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 |
---|---|---|---|---|---|
ENSDART00000005641 | Essential Splice Site | 57 | 405 | None | 5 |
ENSDART00000134373 | Essential Splice Site | 57 | 97 | None | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 27059042)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 27777282 |
GRCz11 | 15 | 27710158 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCTTCTCTCGAGAAGGAAAACTATATTGCAAAAACGACTTCTTTAGG[T/A]AAGTTCCTTGCGTGAGTTAATTCGACCAAATATTTTACTTGTGGGGTTTT
Long Flanking Sequence:
AGATTTCTCTATGCTGGCTTCATTTATGCACCTCAAAATTTGGGACGGAAGAGGACGAGAAATGATGACTGACTACTGAAGCACTACCTCATGAGAAAATCTTCTATCGTCTTCATTTTGGACCCCTACAGGTCCACCCACAAACGCAGAACTGGTGAATATATTTAAAACTTCTTCATCTTTTCGTTTCAACCCTGTTCGCAAAGACTGACTTGGAACATCCTTCAGCGATACAACTTTTCCTCCTCTCTTTTAAAAGAGAGAAATCAGGAGCAGAGCCTCAGGTTGTGGACACCACGGCAGTAACTGTGGGAGCACATCCAAAGACGATGGTCCACTGTGCGGGCTGCGAGAGGCCTATATTGGACAGGTTTCTCCTTAATGTTCTGGACAGAGCATGGCACATCAAGTGCGTACAGTGCTGCGAGTGCAAATGTAACCTAACAGAGAAATGCTTCTCTCGAGAAGGAAAACTATATTGCAAAAACGACTTCTTTAGG[T/A]AAGTTCCTTGCGTGAGTTAATTCGACCAAATATTTTACTTGTGGGGTTTTTGTGATAAATGGATAATTAATCGTTTATAAAGTAGCTATTATGTAGGCCCACTTCAGAAAATCTAGTACAGATGTCTACCATAATAATACAAATATTCTACGAACAAGATGAATATATTACCCGTTGTTGTGTATCTATGGTATATCTATGAAACATTTCTATATAAAATATATAATGTATCGTTAATATATGACAGAAATAAATCCAGAAGACACCCAAAATTATTTCATTTTAAAATTACACATTTACATTTTAAAGAGGTTCCACAATTGAGCTTAAAACAACATCACTTTAAAAGGTGAAATCACATTTTTTAAAGTCACTCAAAAATAACTAAATTGGAAGAAATTTCTCCAGCGATTCAACAGCTTTACACAGAGCTTTGCATGATTTTATTAGATTTAGGACTTACATTCACACTAACAAGAAGTGTGATCCTAAGTACTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15800
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 |
---|---|---|---|---|---|
ENSDART00000005641 | Nonsense | 114 | 405 | 2 | 5 |
ENSDART00000134373 | None | None | 97 | None | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 27057573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 27775813 |
GRCz11 | 15 | 27708689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTCCACAGGAGAGGAATTGTACATCATAGAYGAAAATAAATTTGWCTG[T/A]AAAGAYGATTATTTAAGCAACACGAAYGGAAAAGACTCAAATCTCCTATC
Long Flanking Sequence:
TTTAATGCACATTACTAACCTGCTCAATAAACGTATATGTTTTTTTAGGCCTACAGTGGAAAAAAAGTACATGCTAATGCATATATAAATATTATTTTGTTTGCGTATTCTAAAATGCTGTAACCAATAACAATTAACCAGGTAAATATTTTTCCCAAAAAATAACTTTGATGGTAATACTTAACATTTAGGAGCATTCGAATTTTATATGAACTCAAATAAGTGATGCTATTCAATAAGTCTCGCCTGAGCTTATGCAGATAATTTCGTATTTTTCTTTCGTTTTACTCCTGTATATTGACCTTTTTTTTGGTCTGTCCATTTTGCAGGCGCTTTGGAACAAAATGTGCGGGTTGTGCTCAGGGGATCTCGCCGAATGACTTGGTCCGGAGGGCACGGAGCAAAGTGTTTCATCTGAACTGCTTCACATGCATGATGTGTAACAAGCAGCTTTCCACAGGAGAGGAATTGTACATCATAGACGAAAATAAATTTGTCTG[T/A]AAAGACGATTATTTAAGCAACACGAACGGAAAAGACTCAAATCTCCTATCAGGTAAGTAAATGATGCTAGAATTGAAAATATGTATTGCATGCTGCAAGCGGGTTTATTTCCCCCCACATATTTTTTGCTTTTTGATTAAATGTTTATTAGCAATTCATATTTTGTTGTAAAACATTTTTTAAACAATAAAGACAAATATTGTTCAGAATAGGGCTGTAGATTGAAATGTTTTGTTTTCTTAAACAGTACACTAAAATAGATCTTCAGATGGGGCACGACAATCTAAACAAGCTTGTTTAGAATTTTCTCTACCAATTTCCATGTCAAATGAATTGCATTAAATTAGTAGCCTATCGCGATGTTGGTCAGTTTATTTACTAATAATAATTTCACTGTCGTAGACTAGTGCATCGTGACAGTTCTTTCAACTGTAAATACCATTATTTCTTTGTTCCTTGTTTGTAGATTAATTTCTTTTTTTATTCTTTCGAAATTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39051
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 |
---|---|---|---|---|---|
ENSDART00000005641 | Nonsense | 147 | 405 | 3 | 5 |
ENSDART00000134373 | None | None | 97 | None | 3 |
Genomic Location (Zv9):
Chromosome 15 (position 27056885)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 27775125 |
GRCz11 | 15 | 27708001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCAGTTACAGCTTGCAGTGATCCTAGTTTATCGCCAGATTCTCAAGAC[C/T]AGCTACAGGACGATGTCAAGGATGCGGAAATCGCAAATTTATCGGACAAA
Long Flanking Sequence:
TAAAGACAAATATTGTTCAGAATAGGGCTGTAGATTGAAATGTTTTGTTTTCTTAAACAGTACACTAAAATAGATCTTCAGATGGGGCACGACAATCTAAACAAGCTTGTTTAGAATTTTCTCTACCAATTTCCATGTCAAATGAATTGCATTAAATTAGTAGCCTATCGCGATGTTGGTCAGTTTATTTACTAATAATAATTTCACTGTCGTAGACTAGTGCATCGTGACAGTTCTTTCAACTGTAAATACCATTATTTCTTTGTTCCTTGTTTGTAGATTAATTTCTTTTTTTATTCTTTCGAAATTTGTTTTTGTGCTTTATTTATAGTGTTTATTTATTTATTTATTTTACATTCCAGTGTTTAGTGTTCAGCGCATCTCAGGTCACCATGTCTAATTCAGATTTTTTTTTTCGACTCCCTTTTTTTCCGACGGCCCCTTTTCCCTATTCAGTTACAGCTTGCAGTGATCCTAGTTTATCGCCAGATTCTCAAGAC[C/T]AGCTACAGGACGATGTCAAGGATGCGGAAATCGCAAATTTATCGGACAAAGAAACGGGTAACAATGAAAATGATGACCAGAACCTTGGAGGCAAACGGAGAGGACCGCGTACCACTATTAAAGCAAAGCAACTGGAGACACTGAAAGCGGCATTCGCGGCGACCCCCAAACCAACCAGACACATCAGGGAGCAACTGGCGCAAGAGACGGGACTCAACATGCGAGTTATTCAGGTAAAATTGCACATTATTGCATAAATTTGATGTGTGTGTTATTAATTACATTATTGCTTTGGTCCTAACAATTGCAAGGATCAAAACGCTAAAACATGAATGTCGATATTGATATTTGAAGAATAATATAGCTTATAGCATGCGATTCTTAAGCATCTTGTGGTATAAATTTCTCTCTTTGGATGAAATTGTGAAAAGCACACGCGCGCCTTCTTTGTGCTTCTCATTGCCAATCCTTGAGGCAAGACTATTTGAATTAAAATGAGG
Associated Phenotype:
Not determined