ZMP
lrrtm4l1
Ensembl ID:
ZFIN ID:
Description:
cDNA, clone cssl:d0341 [Source:UniProtKB/TrEMBL;Acc:A8BB40]
Human Orthologue:
LRRTM4
Human Description:
leucine rich repeat transmembrane neuronal 4 [Source:HGNC Symbol;Acc:19411]
Mouse Orthologue:
Lrrtm4
Mouse Description:
leucine rich repeat transmembrane neuronal 4 Gene [Source:MGI Symbol;Acc:MGI:2389180]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
hu3329 | Nonsense | Available for shipment | Available now |
sa11361 | Nonsense | Available for shipment | Available now |
sa44722 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21708 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
hu3329
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113737 | Nonsense | 187 | 571 | 2 | 3 |
ENSDART00000141364 | Nonsense | 187 | 456 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 19369203)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 19381549 |
GRCz11 | 10 | 19338983 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCGTGCGTTTTTGGAGTGCCGAAGCTTGGAGTTTCTAGACTTGGGCTA[T/G]AATCGGCTTCGGGTTCTAACTCGCACAGCATTCCTAGGTTTGTCTCGACT
Long Flanking Sequence:
CTCCTGCTGTTCAGTTCTGGGGAACGAATGTGCCCCTATAGCTGTCATTGTGAGGGAAAGATTGTCCACTGTGAGTCGTCTGCCTTCCAGGACGTCCCAGAAAATATTTCAGTTAGTTGCCAAGGTCTGTCTCTGCGCTACAATGACCTGCACACAATGCTCCCTTACCAGTTTGCCCATCTCAACCAGTTGCTTTGGCTTTACCTGGACCACAATCAAATCATGTTCGTTGATAGTCGTGCTTTCCAGGGGGTGCGGCGATTGAAGGAGTTGATCTTGAGCTCGAACAGGATTTCACAGCTCCACAATGTCACATTCCATGGAGTACCTAACCTTCGTAGTCTCGATCTGTCCTATAACAAGTTGCAGGAGTTGCAGCCTGGCCAGTTTTATGGTCTTCGAAAACTGCAAAATCTGCACTTGCGTTCAAATGGGCTTACGGCAATCCCTGTCCGTGCGTTTTTGGAGTGCCGAAGCTTGGAGTTTCTAGACTTGGGCTA[T/G]AATCGGCTTCGGGTTCTAACTCGCACAGCATTCCTAGGTTTGTCTCGACTTATGGAACTCCACCTGGAACACAATCAGTTTTCACGAATCAACTTCTTTCTCTTTCCACGCCTTGCCAACCTTCGAGCCCTTTACCTACAGTGGAACCGTATTCGAGCTGTCAACCAAGGCCTTCCGTGGAGCTGGTATACCCTGCAGAGGCTTGACATCTCTGGCAATGAGATACAGGTACTAGATCCTGTAGTCTTTCAATGCCTTCCCAATCTTCAGGTTCTCAACTTGGAGTCTAACAAACTCGCCAATGTCTCTCAGGAAGTTGTGGCTGCCTGGATCTCACTAACAACTATTAGCCTTGCAGGCAATATGTGGGATTGTGGTCCGGGTATTTGTCCTCTTGTTGTCTGGCTCAAGAATTTCAGAGGCACCAAGGACACTAATATAATCTGCAGCAGTCCCAAACACCTTCAAGGGGAAAAAGTCATTGAGGCTTCAAAGAACTA
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa11361
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113737 | Nonsense | 229 | 571 | 2 | 3 |
ENSDART00000141364 | Nonsense | 229 | 456 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 19369327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 19381673 |
GRCz11 | 10 | 19339107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCAGTTTTCACGAATCAACTTCTTTCTCTTTCCACGCCTTGCCAACCTT[C/T]GAGCCCTTTACCTACAGTGGAACCGTATTCGAGCTGTCAACCAAGGCCTT
Long Flanking Sequence:
GTCTGTCTCTGCGCTACAATGACCTGCACACAATGCTCCCTTACCAGTTTGCCCATCTCAACCAGTTGCTTTGGCTTTACCTGGACCACAATCAAATCATGTTCGTTGATAGTCGTGCTTTCCAGGGGGTGCGGCGATTGAAGGAGTTGATCTTGAGCTCGAACAGGATTTCACAGCTCCACAATGTCACATTCCATGGAGTACCTAACCTTCGTAGTCTCGATCTGTCCTATAACAAGTTGCAGGAGTTGCAGCCTGGCCAGTTTTATGGTCTTCGAAAACTGCAAAATCTGCACTTGCGTTCAAATGGGCTTACGGCAATCCCTGTCCGTGCGTTTTTGGAGTGCCGAAGCTTGGAGTTTCTAGACTTGGGCTATAATCGGCTTCGGGTTCTAACTCGCACAGCATTCCTAGGTTTGTCTCGACTTATGGAACTCCACCTGGAACACAATCAGTTTTCACGAATCAACTTCTTTCTCTTTCCACGCCTTGCCAACCTT[C/T]GAGCCCTTTACCTACAGTGGAACCGTATTCGAGCTGTCAACCAAGGCCTTCCGTGGAGCTGGTATACCCTGCAGAGGCTTGACATCTCTGGCAATGAGATACAGGTACTAGATCCTGTAGTCTTTCAATGCCTTCCCAATCTTCAGGTTCTCAACTTGGAGTCTAACAAACTCGCCAATGTCTCTCAGGAAGTTGTGGCTGCCTGGATCTCACTAACAACTATTAGCCTTGCAGGCAATATGTGGGATTGTGGTCCGGGTATTTGTCCTCTTGTTGTCTGGCTCAAGAATTTCAGAGGCACCAAGGACACTAATATAATCTGCAGCAGTCCCAAACACCTTCAAGGGGAAAAAGTCATTGAGGCTTCAAAGAACTACATTGACTGTGATGATTATGAAATTACCGCTCAATCTCCTTTGTATCTGCAGACGTTTGATCCAAATTATGACCTTGCTCTTGAACCAACTGAACCAACAATGGCTCCTACCACACCGCCACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44722
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113737 | Nonsense | 235 | 571 | 2 | 3 |
ENSDART00000141364 | Nonsense | 235 | 456 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 19369346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 19381692 |
GRCz11 | 10 | 19339126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTTTCTCTTTCCACGCCTTGCCAACCTTCGAGCCCTTTACCTACAGT[G/A]GAACCGTATTCGAGCTGTCAACCAAGGCCTTCCGTGGAGCTGGTATACCC
Long Flanking Sequence:
TGACCTGCACACAATGCTCCCTTACCAGTTTGCCCATCTCAACCAGTTGCTTTGGCTTTACCTGGACCACAATCAAATCATGTTCGTTGATAGTCGTGCTTTCCAGGGGGTGCGGCGATTGAAGGAGTTGATCTTGAGCTCGAACAGGATTTCACAGCTCCACAATGTCACATTCCATGGAGTACCTAACCTTCGTAGTCTCGATCTGTCCTATAACAAGTTGCAGGAGTTGCAGCCTGGCCAGTTTTATGGTCTTCGAAAACTGCAAAATCTGCACTTGCGTTCAAATGGGCTTACGGCAATCCCTGTCCGTGCGTTTTTGGAGTGCCGAAGCTTGGAGTTTCTAGACTTGGGCTATAATCGGCTTCGGGTTCTAACTCGCACAGCATTCCTAGGTTTGTCTCGACTTATGGAACTCCACCTGGAACACAATCAGTTTTCACGAATCAACTTCTTTCTCTTTCCACGCCTTGCCAACCTTCGAGCCCTTTACCTACAGT[G/A]GAACCGTATTCGAGCTGTCAACCAAGGCCTTCCGTGGAGCTGGTATACCCTGCAGAGGCTTGACATCTCTGGCAATGAGATACAGGTACTAGATCCTGTAGTCTTTCAATGCCTTCCCAATCTTCAGGTTCTCAACTTGGAGTCTAACAAACTCGCCAATGTCTCTCAGGAAGTTGTGGCTGCCTGGATCTCACTAACAACTATTAGCCTTGCAGGCAATATGTGGGATTGTGGTCCGGGTATTTGTCCTCTTGTTGTCTGGCTCAAGAATTTCAGAGGCACCAAGGACACTAATATAATCTGCAGCAGTCCCAAACACCTTCAAGGGGAAAAAGTCATTGAGGCTTCAAAGAACTACATTGACTGTGATGATTATGAAATTACCGCTCAATCTCCTTTGTATCTGCAGACGTTTGATCCAAATTATGACCTTGCTCTTGAACCAACTGAACCAACAATGGCTCCTACCACACCGCCACCACCCCTGCCATCCCCCGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21708
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 |
---|---|---|---|---|---|
ENSDART00000113737 | Nonsense | 357 | 571 | 2 | 3 |
ENSDART00000141364 | Nonsense | 357 | 456 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 10 (position 19369713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 19382059 |
GRCz11 | 10 | 19339493 |
KASP Assay ID:
2260-3115.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCTTCAAGGGGAAAAAGTCATTGAGGCTTCAAAGAACTACATTGACTG[T/A]GATGATTATGAAATTACCGCTCAATCTCCTTTGTATCTGCAGACGTTTGA
Long Flanking Sequence:
CGGGTTCTAACTCGCACAGCATTCCTAGGTTTGTCTCGACTTATGGAACTCCACCTGGAACACAATCAGTTTTCACGAATCAACTTCTTTCTCTTTCCACGCCTTGCCAACCTTCGAGCCCTTTACCTACAGTGGAACCGTATTCGAGCTGTCAACCAAGGCCTTCCGTGGAGCTGGTATACCCTGCAGAGGCTTGACATCTCTGGCAATGAGATACAGGTACTAGATCCTGTAGTCTTTCAATGCCTTCCCAATCTTCAGGTTCTCAACTTGGAGTCTAACAAACTCGCCAATGTCTCTCAGGAAGTTGTGGCTGCCTGGATCTCACTAACAACTATTAGCCTTGCAGGCAATATGTGGGATTGTGGTCCGGGTATTTGTCCTCTTGTTGTCTGGCTCAAGAATTTCAGAGGCACCAAGGACACTAATATAATCTGCAGCAGTCCCAAACACCTTCAAGGGGAAAAAGTCATTGAGGCTTCAAAGAACTACATTGACTG[T/A]GATGATTATGAAATTACCGCTCAATCTCCTTTGTATCTGCAGACGTTTGATCCAAATTATGACCTTGCTCTTGAACCAACTGAACCAACAATGGCTCCTACCACACCGCCACCACCCCTGCCATCCCCCGCCTCAGAGGCACCTTTTCCTCCTCCCCAGCCTCGCCCACCTCATCGCCCCACCTTTCCCAGTCGTACAAACACAGATCCCAGAGACTCTCATCAACGGACACCTTCATCTTTTGACAGCTCATTAGTGACACCAGTTCCTGAGCAAGACAACGTGTCATTTCACAAAGTGGTTATGGGTGGTGTGGCACTATTCTTCTCAGTGTCCCTTGTTTTGTCAGTAATATATGTCTCCTGCAAACGTTACCCTGGCGCCACTCGGCTGTTGCAGCAGAGTTCAGTGGGCCGAAAGCGAAGGAAAAAAAGTCAGGAGCCAGAGCAGAACCTGAGCTCCCAGCTCCAGGAATATTACATGAGCTACAACCCCGCCGC
Associated Phenotype:
Not determined