ZMP
si:ch211-260b17.8
Ensembl ID:
ZFIN ID:
Human Orthologue:
LRCH1
Human Description:
leucine-rich repeats and calponin homology (CH) domain containing 1 [Source:HGNC Symbol;Acc:20309]
Mouse Orthologue:
Lrch1
Mouse Description:
leucine-rich repeats and calponin homology (CH) domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17804 | Essential Splice Site | Available for shipment | Available now |
sa41424 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15164 | Nonsense | Available for shipment | Available now |
sa41425 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34651 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18420 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17804
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108629 | Essential Splice Site | 292 | 693 | 6 | 20 |
ENSDART00000135074 | Essential Splice Site | 292 | 655 | 6 | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26165915)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25321701 |
GRCz11 | 9 | 25132570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTTCCTGWCACTGACCGCCTCAGCTTGACACGACCCAGCAATGGGAGG[T/G]CAGTACAAACCGCAAAATAAAATAATTTTTTTCAGAAACTKAACAAAGTT
Long Flanking Sequence:
TTTCTAAACGCTGTCTACTTTTTGCATTTCATGAGCTGATGTTTGCAGATGTTTCCTGTTTCCCTCCTGTTTCAAACTTTTGACAGCCTCCTCTGTTTTGAAATGGATTCAGTTTAATGTGGTTTGGTAAGTTTGTGTTTGTGTGTTTTAGATTTGGCAGATCTACCTCTGGTCAAGTTTGATTTCTGCTGTAATAAAGTTTCTACTATTCCTGTCTGCTATCGAAAAATGACCCAGCTCCAATCCCTACAGCTGGAGAACAATCCACTTCAGAGTCCTCCTGCACAGGTACAGCAATACACACTCACTCACGCTCAAATATGTTACATGCCCATAATTGTTTCTGGCATTATTTTTGCTGCTTTCAGATCTGTATGAAGGGCAAGATTCATATATTCAAATACCTCGCCATGGAGGCGTGCCGGAGTGACAAGATGGCTGATGCTCTGTACCTTCCTGTCACTGACCGCCTCAGCTTGACACGACCCAGCAATGGGAGG[T/G]CAGTACAAACCGCAAAATAAAATAATTTTTTTCAGAAACTGAACAAAGTTGAGAAATGTTATGCTTAAAACAACAATACACATTTGTCAATGCAGAATTAAAATTACTTTTCTGATTTAAACTTGCTCACAGTTTACTTGGCCTTAAGTGGTTCCAAAAGAAGATATATTGATTCACATCCATTGTAGAAAAGAAAAAAGCAGCACTGGTAGTAAATAGCTACTGGTTGCAAAATTCTTTTTTAGAATATTTTTTCATTTTCAGTTTCATTTTTGGCTGAACTATACCTTTAAGTTGGGTTTTTAAAGGCCTGTGACCCATTGTATTTTTATTATGAATTTAATTATTTATTTAATTTCAACAATTTTTACAGAAAAATAAATTAAATGTTTCTTTGGAAGTAAATGTATCTTAACTATCTTAATACATTTGCACTGGAAAACAAGGCAAAATGGTTGAAAAAAAGCACCAGTTTTCCAAAAGTTGGAAAGTAATTTCCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41424
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 |
---|---|---|---|---|---|
ENSDART00000108629 | Nonsense | 371 | 693 | 9 | 20 |
ENSDART00000135074 | Nonsense | 371 | 655 | 9 | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26172494)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25328280 |
GRCz11 | 9 | 25139149 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGTAGGAGACAGAAGTTCTTCTGAATCTCTGAAGGATCACCTGAGTTA[T/A]CGAGATTCTGCCCTTAGTTCACCATTCGTAAACTATATTAAAGTAAGTGT
Long Flanking Sequence:
GAAAATGCTCATAAACAATACAGAGTTTTTGTCATTGAAATAGATAGATGTTTTGATGCATGAAATGGGCTAAGTTCAAAAACACACATGTATTAAAATGTACTAGCTCATATATAAAGATAGACTTTTCATTTGAATATTGACTGATGCTATGGTGAATATTCTGGTATTTTTAAACGGTTCGAATATGATATCAGTGTAGGTTTTTGTGTCAGGATTTATCGAATTAAATTGGTGTCAGGATTTATTAAAGACATGCTGTCAAAAAATAGGGCTGAAAAGGCATGTATGGGTTTTTTGCTTCTAAACTTGCATGCATTTGTTGGAGTTTACCTTTCAGACACAACATTTATAAGAGGAGGATATTTAATTGATCATGCAATGTGATTTACTATGGTTTGTGTTAGTCAATTTACAGATTGTGTGTAATTGTAGTCATATTTTTTGTATTCTGTAGGAGACAGAAGTTCTTCTGAATCTCTGAAGGATCACCTGAGTTA[T/A]CGAGATTCTGCCCTTAGTTCACCATTCGTAAACTATATTAAAGTAAGTGTGGTCATTGCTATTTTTCAATGTGTGTGAGTTATCAGATGTTTATTTATGAGGTTGTTTTACTCCTCCCAGGTGTGTTTAGATTGGGTTCATGCACATTTTTTTTTTTACATTGTTATCGTTTGGCTACAATTGGGTGGGTGGAAAGGAACTGAGCCTTAAAAAAACATTAAACATTGGCTAGTAAGTTGGTTTGAGCTGTTGTTGTTGTTTTGAAAACGTAACCTGATGGTGTGTACATTATTCTATGCTGAACCAGCAGATTTGAGTAATTTTTCTGGTAATTTTCTCAGGTTTGAAAAATACAGTACATAATGGCACCATAACTGGCACCACAGCCCCCATTGTCCACAACAATGTTATTAGATCCTCAATTTCATTTTTGGTACCTGATTTCTGATTATTATGAATGGAAAATGATTAGAGAGGATTTTTGAAAATGTGTTTTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15164
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 |
---|---|---|---|---|---|
ENSDART00000108629 | Nonsense | 403 | 693 | 10 | 20 |
ENSDART00000135074 | Nonsense | 403 | 655 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26174139)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25329925 |
GRCz11 | 9 | 25140794 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGAGGTGCTGACTTCGACGAGCCCCTCAGGAWAGAGGAAGACACTAATTG[G/A]GYTTCAGAACRAACGTATGTTTATCTTCTTATTTTTAWCATCAGATCCTT
Long Flanking Sequence:
TGCTTCTGTAATTTAGTATAAATCTTTTTCTGTCTTTATCAGCCCCATTTCTTTTTTTCTGTTCATTTCTTGTCAGATTAATCAGCTGCCTCTCTTGGCATAGCGCTTTATGTTCCAGTAACTGTTAGTTTATCTGATAACGTCTCATTGCATCATGAGTTTGGCACAGACAGTGTTTATTTGTGCATTAGCATTTCACTTGTGAAGTCATCCACGTCTAGAGGGACATTGTTTGTATGAGGGGTGTGTGTCTGTGTCATTCCCGTGTGTGTGTGTCGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCACCATCTCAAACAGGCATGGGTGAATAAGGTTGATTTTAAATTCTAGCAAATCAGGCCTTTTCTCTGCAGTCACATGACAGAGTTTGCAGCTGGAGTTAATTGTGTATGTGTGTGTGTGTGTGTGTGTTTGAAGGGTCGAGGTGCTGACTTCGACGAGCCCCTCAGGATAGAGGAAGACACTAATTG[G/A]GTTTCAGAACAAACGTATGTTTATCTTCTTATTTTTATCATCAGATCCTTTTCTTCCTGTTTTTATGATGATCTGTTTTTCCTGTTCCTGTCCCCGACTGGGTCTAACAGGGCAAAAGTCAATATGATCAATCAGCTAAAGGAAGCTGTGGAGATGCTACAGGATCCTAACAGGTAGGTCAGTAGGCGATGGCTGGGGTGTTTCTTTATTAATTCCACACATTTTATAAGTTAGCAATTTTGTGTCAATTTTGTGTCAATCTCAATGACAACACATTTCAAACTCATTGTCAATAAAAAAATGCATTTCTTTGAGTTTTTTTAATATCTTATAATTGTGATATATATATGCATTTGAAGTCAAAGTTATTAGCCTGTGATTTTTTTTTTTGTTTGTTTTTTTTCAAATATTTCACAAATTATGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41425
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 |
---|---|---|---|---|---|
ENSDART00000108629 | Nonsense | 407 | 693 | 10 | 20 |
ENSDART00000135074 | Nonsense | 407 | 655 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26174149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25329935 |
GRCz11 | 9 | 25140804 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTCGACGAGCCCCTCAGGATAGAGGAAGACACTAATTGGGTTTCAGAA[C/T]AAACGTATGTTTATCTTCTTATTTTTATCATCAGATCCTTTTCTTCCTGT
Long Flanking Sequence:
ATTTAGTATAAATCTTTTTCTGTCTTTATCAGCCCCATTTCTTTTTTTCTGTTCATTTCTTGTCAGATTAATCAGCTGCCTCTCTTGGCATAGCGCTTTATGTTCCAGTAACTGTTAGTTTATCTGATAACGTCTCATTGCATCATGAGTTTGGCACAGACAGTGTTTATTTGTGCATTAGCATTTCACTTGTGAAGTCATCCACGTCTAGAGGGACATTGTTTGTATGAGGGGTGTGTGTCTGTGTCATTCCCGTGTGTGTGTGTCGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCACCATCTCAAACAGGCATGGGTGAATAAGGTTGATTTTAAATTCTAGCAAATCAGGCCTTTTCTCTGCAGTCACATGACAGAGTTTGCAGCTGGAGTTAATTGTGTATGTGTGTGTGTGTGTGTGTGTTTGAAGGGTCGAGGTGCTGACTTCGACGAGCCCCTCAGGATAGAGGAAGACACTAATTGGGTTTCAGAA[C/T]AAACGTATGTTTATCTTCTTATTTTTATCATCAGATCCTTTTCTTCCTGTTTTTATGATGATCTGTTTTTCCTGTTCCTGTCCCCGACTGGGTCTAACAGGGCAAAAGTCAATATGATCAATCAGCTAAAGGAAGCTGTGGAGATGCTACAGGATCCTAACAGGTAGGTCAGTAGGCGATGGCTGGGGTGTTTCTTTATTAATTCCACACATTTTATAAGTTAGCAATTTTGTGTCAATTTTGTGTCAATCTCAATGACAACACATTTCAAACTCATTGTCAATAAAAAAATGCATTTCTTTGAGTTTTTTTAATATCTTATAATTGTGATATATATATGCATTTGAAGTCAAAGTTATTAGCCTGTGATTTTTTTTTTTGTTTGTTTTTTTTCAAATATTTCACAAATTATGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34651
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 |
---|---|---|---|---|---|
ENSDART00000108629 | Nonsense | 521 | 693 | 16 | 20 |
ENSDART00000135074 | None | None | 655 | None | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26182834)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25338620 |
GRCz11 | 9 | 25149489 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGCATCTACTGTAGCTTCACCCTCTGTGCCGTGCTCGACTCCGCCCTG[T/A]CCCCTCCCCCTCACACAGGCCCCGCCCACCGATAGAGACACGCCCCCTAG
Long Flanking Sequence:
TTTAGCTGCTTAGAGGCTTCATGTTGCTTCCCCCTCTAACATCTAAGCTAGCATTTGCCTCATTCTCTGTGATCTGTTATTTATGTCTAACATTACCAGCCTTATCATGCCCCGAGTCTGACAGTTAACATAAATAATAGTCATTTGTACCGAGTGCATTAATAGCATGCCAGCAAACGTATTGAAATGCCGCTTACATTGACTTGTTTTTAATATTTTCTCTTTTTTGCTGTATGTACGTGTCATTTTGCTTTGCATATCCTCCCATTTCCTTCTCTTGTTTACATGTTTCCCTGAACTGCTGCTTGCCTGCTTGTTTGCTTTCTATTGCACAAACTACTGTTGCTTGGTTGGCACCTTCCTGTTTTCCCACTGATACCTGAAACTCCTGTGGTTTTCCAATGAAAATCACTTGTTTGACTCCTTCTGGGGCTGCCCTTTATGTTGACGCCTGCATCTACTGTAGCTTCACCCTCTGTGCCGTGCTCGACTCCGCCCTG[T/A]CCCCTCCCCCTCACACAGGCCCCGCCCACCGATAGAGACACGCCCCCTAGCCCAGCTGAAGGAGACATGCCAAGCAGTGGTAGGTCTGCTTAATGTATTGTCCTGTTCATTCACAATGCAAATCTGTGTGTTTTCTTGTCAGATGTATTTCTGGTCATTTTTTTTATACAGTCTCTATACAAAACCATCACACGCTGTGAAAATGCATACCTTTATTCACATTACATCATGCTTTTTAAAAAACTACTTGTAGAAAGGCACACAGGTTAGGACAAGGCTACACAAACATTGGAGGCTGTAAAAGTTATTTAATTTCCGGCTGTATGACAAATAGAGTCATTATTTCAAAAGGGGTATGATGATTTTCGATAGGCACTGTAAATACTGCCTGGCAAAAAAAGCAAACAGTTAGAGTCTATCAATGGATCATTGATGAAATAGTAAATATATGTGTCTGGCTTCTTTTATTTGATAACTATTGGCAACTTTAACTGTAACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18420
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108629 | Essential Splice Site | 584 | 693 | 17 | 20 |
ENSDART00000135074 | Essential Splice Site | 546 | 655 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 9 (position 26187456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 25343242 |
GRCz11 | 9 | 25154111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGGAGCAGCTAAGAGAAGAGCTGGAGCTCACAGAGMAACTTCGAGAGG[T/C]RCACAGACATTCTCATATNAAAAAAGATGTGTGTTTTAAATATATTAGTTG
Long Flanking Sequence:
GTTATGCAACTACAGCAGCACGCTCTGATGTGTGGAATGATACATTGTGCTCTTGTCTTTCTCAATATTCCTCTCTCTCTCTCTATCATGTCCACTGCTCCCCCTTCAGGGGAAATATTGTAAAATGAACAGCATTTCAGTCTCTTTAGAATTAGGGAGTGTTATTATGAGGAAAGAACTTAATAAATGTTTCTTGTTGGTTAAGAAGCATTAAGCCAGCATCTATTAACTGTTTTAGTCTCTTCATGTTGAATTGCCACATGTAACTTAAAGCTTTTGAGTTTGAGCATTCCATGATTGAAAATTAATGGTGTGTTTTTATTTTTGTGAATGTGATAGGAGATATAAGGTGCTGTGTGCAGACTGGTGACGCTTCAGTTGTGTGACAGTGTTTTTCAGGACGCACAAGACTCTGGAATCTGTGGATCCTCAGTTCACCATGAGGAGAAAGATGGAGCAGCTAAGAGAAGAGCTGGAGCTCACAGAGCAACTTCGAGAGG[T/C]GCACAGACATTCTCATATAAAAAAGATGTGTGTTTTAAATATATTAGTTGAGATAAAGTTGACAGAATATATAGCAATACAGTGACCCCACAGGGGACATGAAACACACATTTATATATATTTACAAATGAGGTTGAATGTAGAATGTTAACTCAATGTTGTTTTTGACAGAGTATTGAGAGCAGACTGAAAGTGGTTCTTCCTGAGGATCTGGGATGCTCTCTCAGTGACGGGGTCGTGCTTTGTCACCTAGTCAATCACATTCGGCCGCGATCAGTTGGCAGTATTCATGTACCATCACCTGCAGTGGTGAGACATCCTTGAATTATCCATAAAGCATACACACTAACATCGTGGGTCACCTTTTGGGGTGACTGATTTTTCCAGTTTTTTTATTTTTATGAAAGGCTCTAAGTGTGCTATATGTATTTGATTAAAAATACAATAAAATAAAAACTGTATTAGTGTGAAAAACTATTTTAGATTTTAAATAAAACTTA
Associated Phenotype:
Not determined