ZMP
sc:d0316
Ensembl ID:
ZFIN ID:
Description:
cDNA, clone cssl:d0316 [Source:UniProtKB/TrEMBL;Acc:A8BAU2]
Human Orthologue:
LRRC4C
Human Description:
leucine rich repeat containing 4C [Source:HGNC Symbol;Acc:29317]
Mouse Orthologue:
Lrrc4c
Mouse Description:
leucine rich repeat containing 4C Gene [Source:MGI Symbol;Acc:MGI:2442636]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41005 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa238 | Nonsense | Confirmed mutation in F2 line | Not yet available |
| sa38639 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34176 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21060 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41005
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 |
|---|---|---|---|---|---|
| ENSDART00000021605 | Nonsense | 23 | 631 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 51566295)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49836531 |
| GRCz11 | 7 | 50109307 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTCCATCAGCGCCAGATGTTGAGAGGTCCTAGATGGAAAGGGGCTTG[G/A]TTTGACCCCTTGTTTCTCCTGCTTTTAGCCCTGCAGTTGCTTGTTGTCGC
Long Flanking Sequence:
ATATACCTGACTAAGCTCTGTTAGATATAGTGCTACAAATATAGTGCTTTCAATCACTTATTCCTATGAATTGTTGTTTGTGCTTCATTGTGCAGACTCATTACACAGCATTAAATAGCAGTAATGAGGCTCAATTCATCAGTCAAATTGTAAAAGTACATTTTGCATGTAAATTGCCTAAACAGCAATACTTGTTTTTGTTCGGCATCATCAGAAATGTACGCACAGCCCCATTTGACGGAAGGATTTGTTCCTTTTTGTTATGATAAACTGCAGAAGATCAGCAGAATTTGATGTTCTGTTTGACTGCCATCATGCTACGCTGACACTTCAACATGACATATTTTGCTAACAGATGTATTTTTCTCTTCTTTTTTTTCAGACTGCCTGTAAATGTTTGGGGAGAGAAAATCAGCAGGCATTAAATTATGAATGTTGAACAAGATGACCTCTTTCCATCAGCGCCAGATGTTGAGAGGTCCTAGATGGAAAGGGGCTTG[G/A]TTTGACCCCTTGTTTCTCCTGCTTTTAGCCCTGCAGTTGCTTGTTGTCGCTGGACTGGTGCGAGCCCAAACCTGTCCATCCGTATGTTCCTGCAGTAATCAGTTTAGCAAGGTCATCTGCACACGCAGAGGGCTAAAAGATGTCCCCGATGGCGTTTCCACTAACACACGGTATCTAAACCTCCAGGACAATCAAATCCAGGTCATCAAAGTGGACAGTTTCAAGCATCTACGGCACCTTGAGATCCTGCAGCTTAGCAGAAACCACATCCGCAACATTGAGATTGGCGCCTTCAATGGGCTGACCAGCCTTAACACACTGGAGCTATTTGACAATCGTCTTACGACCATCCCCAATGGCGCCTTTGAGTACCTATCTAAACTAAAAGAGCTGTGGCTTAGGAATAACCCTATCGAGAGCATACCGTCTGATGCCTTCAGTCGCTTGCCCTCCCTTCGCCGGCTGGACTTGGGGGAGCTAAAGCGTCTCTCCTACATCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa238
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000021605 | Nonsense | 155 | 631 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 51566691)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49836927 |
| GRCz11 | 7 | 50109703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCATCCCCAATGGCGCCTTTGAGTACCTATCTAAACTAAAAGAGCTGTG[G/A]CTTAGGAATAACCCTATCGAGAGCATACCGTCTGATGCCTTCAGTCGCTT
Long Flanking Sequence:
TTTGGGGAGAGAAAATCAGCAGGCATTAAATTATGAATGTTGAACAAGATGACCTCTTTCCATCAGCGCCAGATGTTGAGAGGTCCTAGATGGAAAGGGGCTTGGTTTGACCCCTTGTTTCTCCTGCTTTTAGCCCTGCAGTTGCTTGTTGTCGCTGGACTGGTGCGAGCCCAAACCTGTCCATCCGTATGTTCCTGCAGTAATCAGTTTAGCAAGGTCATCTGCACACGCAGAGGGCTAAAAGATGTCCCCGATGGCGTTTCCACTAACACACGGTATCTAAACCTCCAGGACAATCAAATCCAGGTCATCAAAGTGGACAGTTTCAAGCATCTACGGCACCTTGAGATCCTGCAGCTTAGCAGAAACCACATCCGCAACATTGAGATTGGCGCCTTCAATGGGCTGACCAGCCTTAACACACTGGAGCTATTTGACAATCGTCTTACGACCATCCCCAATGGCGCCTTTGAGTACCTATCTAAACTAAAAGAGCTGTG[G/A]CTTAGGAATAACCCTATCGAGAGCATACCGTCTGATGCCTTCAGTCGCTTGCCCTCCCTTCGCCGGCTGGACTTGGGGGAGCTAAAGCGTCTCTCCTACATCTCGAGTGGAGCATTTCAGGGCTTGAGTAACCTTCGCTACCTAAATCTGGGCATGTGTAACCTCAAAGAGGTCCCAAACATACAGCCCTTGATTCGCCTGGATGAGCTGGAGATGTCCGGGAATCAACTCACTGTCATCCAGCCCAGCTCTTTTAAGGGTCTTGTTCATCTCCAGAAGCTGTGGATGATGCACGCCCAAGTCCAAACCATAGAGCGCAACTCCTTTGACGACCTGCACTCTTTGCGGGAGCTCAACCTGGCTCATAACAACCTTACCTTTTTACCCCATGATCTCTATACGCCTTTGCACCACCTGCAAAGAGTGCACTTGCATCACAATCCCTGGAACTGCAACTGTGATATTCTTTGGCTGAGCTGGTGGCTGAGAGAGACCGTACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38639
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 |
|---|---|---|---|---|---|
| ENSDART00000021605 | Nonsense | 236 | 631 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 51566932)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49837168 |
| GRCz11 | 7 | 50109944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATTCGCCTGGATGAGCTGGAGATGTCCGGGAATCAACTCACTGTCATC[C/T]AGCCCAGCTCTTTTAAGGGTCTTGTTCATCTCCAGAAGCTGTGGATGATG
Long Flanking Sequence:
AAGATGTCCCCGATGGCGTTTCCACTAACACACGGTATCTAAACCTCCAGGACAATCAAATCCAGGTCATCAAAGTGGACAGTTTCAAGCATCTACGGCACCTTGAGATCCTGCAGCTTAGCAGAAACCACATCCGCAACATTGAGATTGGCGCCTTCAATGGGCTGACCAGCCTTAACACACTGGAGCTATTTGACAATCGTCTTACGACCATCCCCAATGGCGCCTTTGAGTACCTATCTAAACTAAAAGAGCTGTGGCTTAGGAATAACCCTATCGAGAGCATACCGTCTGATGCCTTCAGTCGCTTGCCCTCCCTTCGCCGGCTGGACTTGGGGGAGCTAAAGCGTCTCTCCTACATCTCGAGTGGAGCATTTCAGGGCTTGAGTAACCTTCGCTACCTAAATCTGGGCATGTGTAACCTCAAAGAGGTCCCAAACATACAGCCCTTGATTCGCCTGGATGAGCTGGAGATGTCCGGGAATCAACTCACTGTCATC[C/T]AGCCCAGCTCTTTTAAGGGTCTTGTTCATCTCCAGAAGCTGTGGATGATGCACGCCCAAGTCCAAACCATAGAGCGCAACTCCTTTGACGACCTGCACTCTTTGCGGGAGCTCAACCTGGCTCATAACAACCTTACCTTTTTACCCCATGATCTCTATACGCCTTTGCACCACCTGCAAAGAGTGCACTTGCATCACAATCCCTGGAACTGCAACTGTGATATTCTTTGGCTGAGCTGGTGGCTGAGAGAGACCGTACCGACCAACACCAGCTGCTGCGCCCGCTGTAATTCCCCTCCCAGCCTCAAGGGCCGCTACATCGGCGAGCTAGACCAGAGCTACTTTCAGTGCTACGCGCCTGTCATCATCGAGCCACCTGTCGACCTCAATTTGACTGAAGGAATGGCAGCAGAGCTCAAATGCCGGACGAATTCAGTGACTTCAGTCAGCTGGCTAACACCAAATGGCTCCATCATAACACATGGGACACTCAAGATGCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34176
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 |
|---|---|---|---|---|---|
| ENSDART00000021605 | Nonsense | 616 | 631 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 51568073)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49838309 |
| GRCz11 | 7 | 50111085 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACCACGTGTCTGCTCTCAGCTCGCTGCATAGTTCAGTGCATGAACCTT[T/A]ACTAATCCAAGCCAGCTCAAAGGATAACGTACAGGAGACGCAAATTTGAC
Long Flanking Sequence:
CGGCTTTAGCTACTTCACAACAGTCACCGTAGAGACAATTGAAACCCCAATCGATGGGGAGAGCAGGACACCCGTCCAGCCTTCTTTTGGCTGGGCATCCTCCTCGACCACAAGGGGAACGCCCATTGCCACCGAGAGAGCGTACACCATCCCCGTGACGGAAATAGACATTGATGGTGCTCTCAACGGTTTGGAGGAGGTGATGAAGACTACCAAGATCATCATCGGCTGCTTTGTGGCCATCACGCTCATGGCGGCCGTCATGCTCATAATATTCTACAAGATGCGCAAGCAGCACCACCAGCAGGATCACGACGGGCCGAGTCGCAGCATGGAGATCATCAGCGTACACGAGGACCTGACCAGGGTTCCTGCCATGGAGAGTCACCTGACTCTTCCACCCCTGGAGCATGACCATTACAACCACTATAACTCCTACAAAACTGCGTATAACCACGTGTCTGCTCTCAGCTCGCTGCATAGTTCAGTGCATGAACCTT[T/A]ACTAATCCAAGCCAGCTCAAAGGATAACGTACAGGAGACGCAAATTTGACCACGTTGGGTGAAACGAACTCTACTAATGCTTTGTCAGTTTTGAAGATGACAGTGTGGATTAAGACATTCAGCAGCGTCATTGAGAGCCAGGGTGTATGTATCATTATTTTAACAAGTGTCTTTACAAATCTTATTTATTTAAAGATATGTGAAGTTATGAAATCATGAGAAAGGTTATCTCTTTTTATTATTTCTAAACTGGGGAATGAATGGTTTATTTCCATCTGCTGGTATAGAATTAAGTTCAACTGCCGTTCTTATCAATGAGATTTTATTTTTAGTCGTGGCATATTACATCCATTTCTCCAGTGTGTTTTCAATTTTGGAGACTGCAAACAAAACCCGGCCCCCGAAAACAGCAGGCGTTAAATCACATGGAGCTCTTAAGATGTGAATGGTGGGCCTGATGGATACGGCAACTCTAGAGAGGTGTATAAATGGTTACATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21060
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 |
|---|---|---|---|---|---|
| ENSDART00000021605 | Nonsense | 622 | 631 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 7 (position 51568091)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49838327 |
| GRCz11 | 7 | 50111103 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCTCGCTGCATAGTTCAGTGCATGAACCTTTACTAATCCAAGCCAGCT[C/A]AAAGGATAACGTACAGGAGACGCAAATTTGACCACGTTGGGTGAAACGAA
Long Flanking Sequence:
AACAGTCACCGTAGAGACAATTGAAACCCCAATCGATGGGGAGAGCAGGACACCCGTCCAGCCTTCTTTTGGCTGGGCATCCTCCTCGACCACAAGGGGAACGCCCATTGCCACCGAGAGAGCGTACACCATCCCCGTGACGGAAATAGACATTGATGGTGCTCTCAACGGTTTGGAGGAGGTGATGAAGACTACCAAGATCATCATCGGCTGCTTTGTGGCCATCACGCTCATGGCGGCCGTCATGCTCATAATATTCTACAAGATGCGCAAGCAGCACCACCAGCAGGATCACGACGGGCCGAGTCGCAGCATGGAGATCATCAGCGTACACGAGGACCTGACCAGGGTTCCTGCCATGGAGAGTCACCTGACTCTTCCACCCCTGGAGCATGACCATTACAACCACTATAACTCCTACAAAACTGCGTATAACCACGTGTCTGCTCTCAGCTCGCTGCATAGTTCAGTGCATGAACCTTTACTAATCCAAGCCAGCT[C/A]AAAGGATAACGTACAGGAGACGCAAATTTGACCACGTTGGGTGAAACGAACTCTACTAATGCTTTGTCAGTTTTGAAGATGACAGTGTGGATTAAGACATTCAGCAGCGTCATTGAGAGCCAGGGTGTATGTATCATTATTTTAACAAGTGTCTTTACAAATCTTATTTATTTAAAGATATGTGAAGTTATGAAATCATGAGAAAGGTTATCTCTTTTTATTATTTCTAAACTGGGGAATGAATGGTTTATTTCCATCTGCTGGTATAGAATTAAGTTCAACTGCCGTTCTTATCAATGAGATTTTATTTTTAGTCGTGGCATATTACATCCATTTCTCCAGTGTGTTTTCAATTTTGGAGACTGCAAACAAAACCCGGCCCCCGAAAACAGCAGGCGTTAAATCACATGGAGCTCTTAAGATGTGAATGGTGGGCCTGATGGATACGGCAACTCTAGAGAGGTGTATAAATGGTTACATTTCCCCATGAAAAATCCTGT
Associated Phenotype:
Not determined