ZMP
zgc:63670
Ensembl ID:
ZFIN ID:
Description:
Leucine-rich repeat and fibronectin type III domain-containing protein 1 [Source:UniProtKB/Swiss-Pro
Human Orthologue:
LRFN1
Human Description:
leucine rich repeat and fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:29290]
Mouse Orthologue:
Lrfn1
Mouse Description:
leucine rich repeat and fibronectin type III domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:213
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa8956 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10889 | Nonsense | Available for shipment | Available now |
sa42629 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8956
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099023 | Nonsense | 231 | 584 | 2 | 5 |
ENSDART00000124704 | Nonsense | 231 | 742 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 45463224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 45896191 |
GRCz11 | 15 | 46111352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACGCTTTTCCAGCACGCGCAGGTTCTGTCCGAGCCCAAGACTTCCAGCT[C/A]GTCCAGGCTGWCGGTCAGCTTYGGRGGAAACCCTCTGYACTGTAACTGCG
Long Flanking Sequence:
GTTTGTTTGTTTATTCAGTTGTTTTTATCTTTATTACTTTTGTTAATATTCTTAACTTTACAAAGTAGTTTGTTTGTTTTTTACTTTAATTTTGTGCACTTTTTATTTAATTTATTTCCAGTCGATCATTATAGTGCTAATTTTCAAACGTTATCTTCTTTCCAATGAAGGCCTGATGAACCTCAGACACCTGATTTTAGGAAACAACCAGATCCACCACATTGAAGAGTCCTCCTTTGACGAGTTCGTCGCCACCATCGAGGATCTGGATTTATCCTACAACAACCTGCGGACTTTACCATGGGAAGCCATCGCTCGAATGACTAACATAAACACGCTGACCTTGGACCACAACCTGATCGACCACATCGGTGTGGGCACGTTCACGCTGCTCACCAAACTAGTGCGTCTGGACATGACCTCCAACAGGCTGCAGACTCTCCCTCCGGACACGCTTTTCCAGCACGCGCAGGTTCTGTCCGAGCCCAAGACTTCCAGCT[C/A]GTCCAGGCTGACGGTCAGCTTCGGGGGAAACCCTCTGCACTGTAACTGCGAGCTGCTATGGCTGAGACGGCTGACCCGAGAGGATGATCTGGAGACTTGTGCTTCTCCTGAACACCTGATGGACAAATACTTCTGGTCCATTCAGGAGGAGGAGTTCATCTGTGAGCCGCCGCTCATCACCAAACACCAGGTCAGAACACTGATATTCAGTTCTGAATAGTAGAGATGTAACAATTCACTGAATACTATAACATCTCAAATTTCCTCACCTCTAGATTCGATGATGTCATTATTAAAAGCATTCTGGATACGAGCCCGTTCTGAATATCAATGATGTAACGATTTCCTGAATACAACAGCAGGAGTGTAATGATTCTCTTAACTCTTGATTTGATGATGTCATCTTTAGAATCATTCTATATAGATAAGTGATTAGAGCCAGTTCTAAACAGCAGGAATGTAACAATTTGCTGTGTCCCATTTGGTCAACTTATGATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10889
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099023 | Nonsense | 339 | 584 | 3 | 5 |
ENSDART00000124704 | Nonsense | 339 | 742 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 45468104)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 45901071 |
GRCz11 | 15 | 46116232 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGCTTCCCGGACGGCAAACTGGTGCACAACAACTCCCGCACCMTTTTATA[C/A]GACAACGGCACGCTGGACATCCTGATCACCACACTGAAGGACAGCGGYGC
Long Flanking Sequence:
TTTTAAATTAACCAGTAAAGTCGTTCCGGAAATTTTCCGGATATTTACCGGTATCCCTGTGTGAAAGGGGCTTATGTGACCGTTAGAAAATTACATTCTATGTAGTATGCATGCGAGTAGTATAAGGACATTTAAACTTACTACATACTACTACTTGTTTCGGTTCTTTCTACTACTACCTGCATTGCTTTACTCTCATTCATGAATTCTCTTGTGTGGCATCATGGTATGGTTCTTGCTGGAACTAATAGGTCATCCAGGTACTTCTCAGGAAACTCTCTTGTAGCTCTTTCCCTCACACACACACTGTCAAAGTTTCCAGTTCTTCAGTTTGAGCATGCATTAAAGCTGATGTTCTCACCACAGGTCACCAAGCCGTATGTGATGGAGGGTCAGGGCGTGACTCTGAAGTGTAAAGCCATGGGTGACCCTGATCCCGCAATCCACTGGCGCTTCCCGGACGGCAAACTGGTGCACAACAACTCCCGCACCATTTTATA[C/A]GACAACGGCACGCTGGACATCCTGATCACCACACTGAAGGACAGCGGTGCCTTTAACTGCGTGGCGTCTAATGCTGCGGGCATCGCCACCGCTGCCGTACATGTACACATGATCCCGCTACCCCTGCTGGTCAACAACACAGGCCACATGCGGGAGGCTGACCCAGGACTCTCCGACATCAGCACCTCCTCCAGGTCCAGCAGCAACGACAGCAAAACACACAGCAAGAGGGTCCTGGTGGAGAATCTGACCGCTCACTCCGCCGTCATACACTGGCCCTCAGAGAGACACATTCCTGGCATCCGCATGTACCAGATCCAGTACAACAGCACTGTTGATGATACACTCGTCTACAGGTACAACACACACACACACACACACACACACACACAGAGGAGTATCCAAAATTACAGTATCTAAATTGAGAAATATGCCTTTAGTAATAATACAAATAGTAATCTTAATAATAATAATAATAATAATAATAATAATAATAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42629
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099023 | Nonsense | 443 | 584 | 3 | 5 |
ENSDART00000124704 | Nonsense | 443 | 742 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 15 (position 45468416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 45901383 |
GRCz11 | 15 | 46116544 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTCATACACTGGCCCTCAGAGAGACACATTCCTGGCATCCGCATGTA[C/A]CAGATCCAGTACAACAGCACTGTTGATGATACACTCGTCTACAGGTACAA
Long Flanking Sequence:
AAGTTTCCAGTTCTTCAGTTTGAGCATGCATTAAAGCTGATGTTCTCACCACAGGTCACCAAGCCGTATGTGATGGAGGGTCAGGGCGTGACTCTGAAGTGTAAAGCCATGGGTGACCCTGATCCCGCAATCCACTGGCGCTTCCCGGACGGCAAACTGGTGCACAACAACTCCCGCACCATTTTATACGACAACGGCACGCTGGACATCCTGATCACCACACTGAAGGACAGCGGTGCCTTTAACTGCGTGGCGTCTAATGCTGCGGGCATCGCCACCGCTGCCGTACATGTACACATGATCCCGCTACCCCTGCTGGTCAACAACACAGGCCACATGCGGGAGGCTGACCCAGGACTCTCCGACATCAGCACCTCCTCCAGGTCCAGCAGCAACGACAGCAAAACACACAGCAAGAGGGTCCTGGTGGAGAATCTGACCGCTCACTCCGCCGTCATACACTGGCCCTCAGAGAGACACATTCCTGGCATCCGCATGTA[C/A]CAGATCCAGTACAACAGCACTGTTGATGATACACTCGTCTACAGGTACAACACACACACACACACACACACACACACACAGAGGAGTATCCAAAATTACAGTATCTAAATTGAGAAATATGCCTTTAGTAATAATACAAATAGTAATCTTAATAATAATAATAATAATAATAATAATAATAATAATAAAAATAATAATAATATAAATAATAATAATAATGATGATAATGATGATGATGATAATAATAATAATAACAGTAATAATATAATAATAATAATAATTATTATTATTATTATTATAATAATATAAATAATAATAATGATGATGATGATGATGATGATGATGATAATAATAATAATTATTATTATTATTATTATTATTATTATTATTATTATAATGATGATGATGATGATAATAATAACATTAATAATATAATAATAATAAAAATAATACTAATAATACTAATACTAATAATAATAATAAAAATACAAATAATAACA
Associated Phenotype:
Not determined