ZMP
lrrcc1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate leucine rich repeat and coiled-coil domain containing 1 (LRRCC1)
Human Orthologue:
LRRCC1
Human Description:
leucine rich repeat and coiled-coil domain containing 1 [Source:HGNC Symbol;Acc:29373]
Mouse Orthologue:
Lrrcc1
Mouse Description:
leucine rich repeat and coiled-coil domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1918960]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19792 | Nonsense | Available for shipment | Available now |
sa39854 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19791 | Essential Splice Site | Available for shipment | Available now |
sa32950 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19792
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 |
---|---|---|---|---|---|
ENSDART00000113498 | Nonsense | 109 | 997 | 4 | 19 |
ENSDART00000142366 | None | None | 555 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31425353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31726313 |
GRCz11 | 2 | 31709531 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGAACAAATGTGTATGAAGTCTCTGTTCTGTGGTTTTAGGTCTCTTGTA[T/A]CTTCATGGAGCAAACTACAAACTGAAGTACCTGCAGCTTCACAGCAATCG
Long Flanking Sequence:
AATGCGTTCATTCTTGAATGTTTTAAATTTAGATCTCTGAAAAATCTTACATTTAGGGGAAGAAATTAAAACTACAGTGCAGACGTTTGTAAATTCTCCAGATAAAAATTATTTTATTCTTACCAAGGATGTATTTATTTGATCCAAAGTTTCTACTCTGGTCCTTATTGCCACATGATCATTCCGTAATCATACTGTTATGCTGATTGGGTGCTCTAAAATTGACTTATTAAATAACTTCTATTACCAAGGGTCACAAAAGTTTTTCTGCTTATTTATTTGTTTATTCATTTATGTATGAATAGAAAATTTAAAGAAAACAACATTTATTTGAATTTGAAATGTTACGTAAAAAAAAAAACGTGTTTGCATTTGCACAATTTAATGTATCCCTACTGAATAATAGAATTTGAAAAATGGTACAGTATGGAACCGTAGCAAACATAATTATTGAACAAATGTGTATGAAGTCTCTGTTCTGTGGTTTTAGGTCTCTTGTA[T/A]CTTCATGGAGCAAACTACAAACTGAAGTACCTGCAGCTTCACAGCAATCGTTTGGATAGTATGAACCACTTACTGCAATGCATGGTGGGACTGCAAAATCTGAAATATATCACTCTTAGCAAGGACGGTGCAGAGAATCCAGTCTGCAAAATGATAGGTTTGTTGAAAAAAGTTTGCAAAATGATAGGTTTGTTGAAAAAAGTTATCTTGGAAAACAAGAAAAGATAAAACGTAATATGAACTGGTGTTCGAGCCCCGACTGGGTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCCAGTGTTTGTGTGGGTTTCCTCTGGGTGCTCTGGTTTCCCCCACAAGTACAAAGACATCTGCTGTAGGTGAATTGGGTAAGCTAAATGGTTCGTAGTGTATTTCCTGGTCCTCCAAGATGGGGGTTGAGCGTTGGGCTAATGACCCATACGTCGAACCATCATAAAAATTTGAATGTTACAAACACCAAAATGGTGTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39854
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113498 | Nonsense | 216 | 997 | 5 | 19 |
ENSDART00000142366 | None | None | 555 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31423760)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31724720 |
GRCz11 | 2 | 31707938 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTGAGGACTTCCTAGAGTTTTTGATTTCATCAGACACTAGTGTGAAT[G/T]GAGAACTGGTAAACTAGTTTTACTATGCTTCATAATTTCCTGTATTTGTC
Long Flanking Sequence:
ACTAGGTTAATTAATTTAACTAGGCAGGTTAGGGTAATTCGGAAAGTTATTGTATAACAATGGTTTGTTCTGTAGACTGTCGGAAAAATATATAGCTGAAAGAGGCTAATTTGGCCTTAAAATTAGTTTTAAGAATTGATAACTGCTTTTATTCTTGCTAATATTAAACAAGTAAGACTTTCTCAAACTATAAAAAATCTCTTGCTCTGTTAAACAGTTTTTGCAAAATGTTTTTTTAAAAAAAGAAAAAAATCAAAGGGTTTTCAACTGTTTCTTTATGCACATAAATTCTGTAGGTTGATTTGTTAAACTTATTTATTGTTTTTCTTATTTATTAAGGCTACAGGGAGATGGTTCTTCAATGTCTGCATCAAGTCACTACACTGGATGGAGTAGATCGCATGGGAAACACATGTCCATTAGCAGAGGACAGTCCTATGGACGTTCCTGGTCTTGAGGACTTCCTAGAGTTTTTGATTTCATCAGACACTAGTGTGAAT[G/T]GAGAACTGGTAAACTAGTTTTACTATGCTTCATAATTTCCTGTATTTGTCTGTTTTTAAATGAGAGAATGACGTTTGAATGATTTTGAGTTGGTAGTGAGACACATGCTGATGTTCAGGGTGTTTTGCTGTTATAAAGGCAAAGTCAGATGCTCCTCTAACTACTCCACGGATTGATGAAGTCTTGACCCAGTTTCGACAGCGAGGTGGAAAAGCGTCTACAGAAAATCAAGAGAATGAGCAGCGAATTAAAAAACTTGAGCAGCAGGTTTCCCATTTAATACAGAAGGTACATTTCTGTTCTCAAATATTTCAATATTATCTCTTTCTTTACTTTCTTTTAAAAGCCGTTTTAACGCATTTTAATCTTTTTTAAAATCTTTTTTTCCCTTTATTTTCATTTTCTTGTACTTGTATTTTGTTTCTTTTATTCTTGTTCATGTAAAGCACTTTGAATTTCCACTGTGTACGAAAAGTGCGATATAAATAAACTTGTCTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19791
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113498 | Essential Splice Site | 443 | 997 | 9 | 19 |
ENSDART00000142366 | None | None | 555 | None | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31419151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31720111 |
GRCz11 | 2 | 31703329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAGCGAGGAAAAAGACCTGCAGAGTTTGGCCTTACACACCACAGACAG[G/A]TCAGGACAAACAGACAAATGCAGTTTCACTTTGTTCCAGTTGTTACCTTT
Long Flanking Sequence:
CACATTACTGTATATATGTAGGCATTATGTTAAACTGCCTCTCTTACTGGGATGAAACTTCTGCTAATATGAATTGTTTTTTATGTATTCATTGCAGTGTGGCAATTACACAGAAGCAGAGGTCCACAAAGCTGACTGTTTGTCCCCGTAGGAGTACATCAATCCAGAGCTCGGAGTCTGCTGACACTTCAGAATCTGTCAAAAGGGGCCCCAAAATAATCAAATCAGGCCTCAAAAGCTCAGGCCAATCGCAAGAGGAAACTTACAAAGTATGCAAACTGCACTGCTTAGGTTTGCCATTAAACTAAACGTGAATATTCAAAGAATAACTGCTTATGTGTTTACATGCAGGCAATAGTGGAAGAAAGAGACCAGGAGCGAGAGCGGCGCTGGAAAGCAGAGCAAGCTGCGAAAAAGCTTACTGAACAGGTCAAGAACTTGCAGACTCGAGCCAGCGAGGAAAAAGACCTGCAGAGTTTGGCCTTACACACCACAGACAG[G/A]TCAGGACAAACAGACAAATGCAGTTTCACTTTGTTCCAGTTGTTACCTTTGTGCTGAAATGAATGTGAATGATATGAATGCAAATTAAGCAGCCTAATTAAGAGTTCCACCGCTGACAGTCAAAGTAATATATATAGTTGCAACTTTTATTTTATCTCTCTCGTTAAAACATTCTCTCCCATCAAGGACACCTTAACATTCTCCAGCCATCCAAGTGTTTGCGGAGAATGTTTGGTTTGACATATTGCACCTAATTGGTGTCAGCTCTAGCTGAAATGTTGGATCGGAATACACTCGAGTATAATTAAATTTTATTAGAAGTTTCCAGAGACCCCACTGTAGGGCCCTGATGTATGAAGCTCCGCCATCCCACCTGCACGGCGCTTTGTGTGGTGTGATGATGGCCCTGATATTTTGCTCTAATATTATAGCCCACGCGCTCCCCCTGGTGATAAATCGTAATTATAATGGAGATTAAAGTCGTGGTGACAGGCACATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32950
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 |
---|---|---|---|---|---|
ENSDART00000113498 | Nonsense | 605 | 997 | 12 | 19 |
ENSDART00000142366 | Nonsense | 163 | 555 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 2 (position 31414206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 31715266 |
GRCz11 | 2 | 31698484 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAACAGACTGATCTTGAAGAAAAAATCAGGGATGCCAGAAGACAGTA[T/A]GCTGCTCTGGAGGAGGAGTTTCGCATGGCTCTCACTATTGAAGCAAAGCG
Long Flanking Sequence:
ACTCAAGCCTAGATAAACTTAAACATAAGTGGAAAATGCTAATTGTTGTAATCTCATTAGAAAATTTTGTGGCCAATAAAATGCAACCTGGAGCACGCATATTATTGATTTTGTGTGGATCGTCAGTGTTTTCTTTGGATTGCCCTGTCCTTCACTGTGAATCTACAATGACAGTATTTAGAGTGAGGAAACAATGGTGTTTGTGTGGCTCATGGTAGGTCTTTTTCCATGTACCGATTGTATTATTCTGCTATGCCTAGGTATACCCAGATTTTCATTCTATGGCACCTATTAGAGTGAAAATGGCTCAAATTACAAAAGAAGAAATGTGTTAATTTGCACCTGTTTAACTGTTACAGGAAAGAGCTTTCTGCACGATTGCTTCCTGGTGGAACTGAGTTTAAAGAGGCTGTAGCCAAAGAGGTTGCTGCAACAGAGCAGAGATTTGCTCAGAAACAGACTGATCTTGAAGAAAAAATCAGGGATGCCAGAAGACAGTA[T/A]GCTGCTCTGGAGGAGGAGTTTCGCATGGCTCTCACTATTGAAGCAAAGCGTTTTACAGAGGTAACATTTAAACTATGAGGAAACATAGTCTGAACATAGTCTTATTTATGATTTTGTGACAGTAAGTTTTAGTTTTCTAATTGAATCCTCAGAGCAGAAAAATAAAAGTAAAAAAATTACAAAATAAAATAGTATTATTGATATAACAATTTAAACTTGCTTTTACCAATTTTTTTCTACATTTTTTCACTTTTTAGATTTTAAGTTTAACTTTTAATTGACTCTCCAAAACAAAAGCAGTTAGAATATTTTGTAATTTTGTTTAGTAACTTTCTTTAAAGTAATTTTTTATGTTTTTCATCTAATATTTGTATTTTGTTTCTTATTTAAAATGTCATTGGGCTCTATTTTGACAATTAATACCCAAAGTGCAGGGCGCAAAAGCATTAAGGTCATGTCAGAATCCACTTTTGCTATTTTAAGGATGGAAAAATACACTT
Associated Phenotype:
Not determined