ZMP
flrt3
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Wu:fb93g11) [Source:UniProtKB/TrEMBL;Acc:B8A507]
Human Orthologue:
FLRT3
Human Description:
fibronectin leucine rich transmembrane protein 3 [Source:HGNC Symbol;Acc:3762]
Mouse Orthologue:
Flrt3
Mouse Description:
fibronectin leucine rich transmembrane protein 3 Gene [Source:MGI Symbol;Acc:MGI:1918686]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa219 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa2686 | Nonsense | F2 line generated | Not yet available |
| sa251 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa219
Status:
Confirmed mutation in F2 line
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 |
|---|---|---|---|---|---|
| ENSDART00000112985 | Nonsense | 107 | 649 | 1 | 1 |
| ENSDART00000143703 | Nonsense | 107 | 649 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 34043781)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 33688681 |
| GRCz11 | 13 | 33814697 |
KASP Assay ID:
554-0157.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATACTGCAACAACCTGGATGAGTTCCCCACCAATTTGCCGCTTAATGTC[A/T]AGGAACTTCATTTACAGGAGAACAATATCCGGACTATCACACACGCCTCA
Long Flanking Sequence:
GCAGTAGAAATATAGTATTCTTTGTCTCAAATTGAATCATTTACAATGAAAGAGGTGCTGCAGGCACTCTACATAAAACAGCAATTAGAGCAGGACATTGCCTTTTCTTCAGACAGCATGATTTTGACTTTTTCTTTTTTTTTCCCCCTCCAAGGGCAACATCTGCAAAGCGGACATTAGCAATGGCAAGCAATTACATGTCCTTCTTCGTCTTCTTCATCAGAGCTGGGCTTTTGCTTGGCCTGGCCAATCCATTGATGACCTCAGCCTCCTGTCCCTCTCAGTGCCGGTGTGATGGGACTTTCATATATTGCAATGACCGGGACTTGACTTCCATCCCTTCAGGTATCCCAGAGGATGCTACGGTACTATTTCTCCAAAACAACCGCATCAAAAGTGCAGGGATTCCTACAGATCTACGAAGGCTAAATGGCGTTGAAAAGATTTACCTATACTGCAACAACCTGGATGAGTTCCCCACCAATTTGCCGCTTAATGTC[A/T]AGGAACTTCATTTACAGGAGAACAATATCCGGACTATCACACACGCCTCACTTGCACAGATTCCCTTCATTGAGGAATTACACCTTGATGACAATTCTGTTTCAGCTGTCAGCATCGAAGAGGGTGCATTCCGGGACAGCAACCATTTGAGGCTGCTTTTTCTGTCCCGCAACCACCTAAGCACCATACCTTCCGGTTTGCCAATGACTATAGAGGAGCTTCGATTTGATGACAACCGCATCTCATCCATCTCAGAGGCATCTCTGCAGGACCTTATAAACCTGAAGCGACTGGTTCTGGATGGCAACCTCCTGAACAACAGGGGCATCGGGGAGATGGCCTTGGTGAATTTAGTAAATCTGACCGAGCTCTCATTGGTACGAAACTCCCTGACGTCCCCACCAGCCAACTTGCCTGGCTCAAGCCTAGAGAAGCTAAATCTTCAAGACAACCACATCAATCACGTACCACCAGGTGCCTTTGCTTTTCTGCGACAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2686
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112985 | Nonsense | 224 | 649 | 1 | 1 |
| ENSDART00000143703 | Nonsense | 224 | 649 | 3 | 3 |
| ENSDART00000112985 | Nonsense | 224 | 649 | 1 | 1 |
| ENSDART00000143703 | Nonsense | 224 | 649 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 34043429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 33688329 |
| GRCz11 | 13 | 33814345 |
KASP Assay ID:
554-2629.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCAACCTCCTGAACAACAGGGGCATCGGGGAGATGGCCTTGGTGAATT[T/A]AGTAAATCTGACCGAGCTCTCATTGGTACGAAACTCCCTGACGTCCCCAC
Long Flanking Sequence:
AGAGGATGCTACGGTACTATTTCTCCAAAACAACCGCATCAAAAGTGCAGGGATTCCTACAGATCTACGAAGGCTAAATGGCGTTGAAAAGATTTACCTATACTGCAACAACCTGGATGAGTTCCCCACCAATTTGCCGCTTAATGTCAAGGAACTTCATTTACAGGAGAACAATATCCGGACTATCACACACGCCTCACTTGCACAGATTCCCTTCATTGAGGAATTACACCTTGATGACAATTCTGTTTCAGCTGTCAGCATCGAAGAGGGTGCATTCCGGGACAGCAACCATTTGAGGCTGCTTTTTCTGTCCCGCAACCACCTAAGCACCATACCTTCCGGTTTGCCAATGACTATAGAGGAGCTTCGATTTGATGACAACCGCATCTCATCCATCTCAGAGGCATCTCTGCAGGACCTTATAAACCTGAAGCGACTGGTTCTGGATGGCAACCTCCTGAACAACAGGGGCATCGGGGAGATGGCCTTGGTGAATT[T/A]AGTAAATCTGACCGAGCTCTCATTGGTACGAAACTCCCTGACGTCCCCACCAGCCAACTTGCCTGGCTCAAGCCTAGAGAAGCTAAATCTTCAAGACAACCACATCAATCACGTACCACCAGGTGCCTTTGCTTTTCTGCGACAGCTGTACCGCTTGGATTTGTCAGGCAACAACTTGAGCAGTCTGCCCATGGGGGTATTTGAGGACCTGGATAACCTTACCCAACTGCTCTTGCGCAACAACCCCTGGCATTGCAACTGCAGGATGAAGTGGGTACGTGATTGGCTGCGCACTCTTCCATCTAAGGTCAATGTGCGTGGCTTCATGTGCCAGGGTCCCGATAAGGTCAAAGGGATGGCCATCAAAGACTTATCCACTGAGCTGTTTGGCTGTTCAGACACAGAGATTCCAACCACATACGAGACCAGCACAGTCTCAAACACTTTGCCTCCCTCTCGACCCCAGTGGCCCTCATATGTAACTAAAAGACCTGTGGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa251
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:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000112985 | Nonsense | 224 | 649 | 1 | 1 |
| ENSDART00000143703 | Nonsense | 224 | 649 | 3 | 3 |
| ENSDART00000112985 | Nonsense | 224 | 649 | 1 | 1 |
| ENSDART00000143703 | Nonsense | 224 | 649 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 13 (position 34043429)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 33688329 |
| GRCz11 | 13 | 33814345 |
KASP Assay ID:
554-2629.1 (used for ordering genotyping assays)
KASP Sequence:
TGGCAACCTCCTGAACAACAGGGGCATCGGGGAGATGGCCTTGGTGAATT[T/A]AGTAAATCTGACCGAGCTCTCATTGGTACGAAACTCCCTGACGTCCCCAC
Long Flanking Sequence:
AGAGGATGCTACGGTACTATTTCTCCAAAACAACCGCATCAAAAGTGCAGGGATTCCTACAGATCTACGAAGGCTAAATGGCGTTGAAAAGATTTACCTATACTGCAACAACCTGGATGAGTTCCCCACCAATTTGCCGCTTAATGTCAAGGAACTTCATTTACAGGAGAACAATATCCGGACTATCACACACGCCTCACTTGCACAGATTCCCTTCATTGAGGAATTACACCTTGATGACAATTCTGTTTCAGCTGTCAGCATCGAAGAGGGTGCATTCCGGGACAGCAACCATTTGAGGCTGCTTTTTCTGTCCCGCAACCACCTAAGCACCATACCTTCCGGTTTGCCAATGACTATAGAGGAGCTTCGATTTGATGACAACCGCATCTCATCCATCTCAGAGGCATCTCTGCAGGACCTTATAAACCTGAAGCGACTGGTTCTGGATGGCAACCTCCTGAACAACAGGGGCATCGGGGAGATGGCCTTGGTGAATT[T/A]AGTAAATCTGACCGAGCTCTCATTGGTACGAAACTCCCTGACGTCCCCACCAGCCAACTTGCCTGGCTCAAGCCTAGAGAAGCTAAATCTTCAAGACAACCACATCAATCACGTACCACCAGGTGCCTTTGCTTTTCTGCGACAGCTGTACCGCTTGGATTTGTCAGGCAACAACTTGAGCAGTCTGCCCATGGGGGTATTTGAGGACCTGGATAACCTTACCCAACTGCTCTTGCGCAACAACCCCTGGCATTGCAACTGCAGGATGAAGTGGGTACGTGATTGGCTGCGCACTCTTCCATCTAAGGTCAATGTGCGTGGCTTCATGTGCCAGGGTCCCGATAAGGTCAAAGGGATGGCCATCAAAGACTTATCCACTGAGCTGTTTGGCTGTTCAGACACAGAGATTCCAACCACATACGAGACCAGCACAGTCTCAAACACTTTGCCTCCCTCTCGACCCCAGTGGCCCTCATATGTAACTAAAAGACCTGTGGTTA
Associated Phenotype:
Not determined