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e.g. ENSDARG00000093395 or slc2a11b or ENSG00000135862 or LAMC1 or sa457
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ENSDARG00000077452
- Ensembl ID:
- ENSDARG00000077452
- Human Orthologues:
- AC009958.4, AC110080.2, AC110080.4, AC110080.7, AC110080.8, AC233264.1, AC233264.4, AC233264.6, AC233264.7, IGKC
- Human Descriptions:
- Ig kappa chain V-II region Cum [Source:UniProtKB/Swiss-Prot;Acc:P01614]
- Ig kappa chain V-II region RPMI 6410 [Source:UniProtKB/Swiss-Prot;Acc:P06310]
- immunoglobulin kappa constant [Source:HGNC Symbol;Acc:5716]
- Mouse Orthologues:
- AC140374.1, Gm10878, Gm16634, Gm16688, Gm16797, Gm16798, Gm16800, Gm16904, Gm16955, Gm4964, Gm4965, Gm5153, Gm5572, Gm6827, Gm6832, Igk-V
- Mouse Descriptions:
- immunoglobulin kappa chain complex variable region Complex/Cluster/Region [Source:MGI Symbol;Acc:MGI
- predicted gene 10878 Gene [Source:MGI Symbol;Acc:MGI:3642626]
- predicted gene 4964 Gene [Source:MGI Symbol;Acc:MGI:3819952]
- predicted gene 4965 Gene [Source:MGI Symbol;Acc:MGI:3648800]
- predicted gene 5153 Gene [Source:MGI Symbol;Acc:MGI:3644894]
- predicted gene 5572 Gene [Source:MGI Symbol;Acc:MGI:3647785]
- predicted gene 6827 Gene [Source:MGI Symbol;Acc:MGI:3648380]
- predicted gene 6832 Gene [Source:MGI Symbol;Acc:MGI:3645551]
- predicted gene, 16634 Gene [Source:MGI Symbol;Acc:MGI:4439558]
- predicted gene, 16688 Gene [Source:MGI Symbol;Acc:MGI:4439612]
- predicted gene, 16797 Gene [Source:MGI Symbol;Acc:MGI:4439721]
- predicted gene, 16798 Gene [Source:MGI Symbol;Acc:MGI:4439722]
- predicted gene, 16800 Gene [Source:MGI Symbol;Acc:MGI:4439724]
- predicted gene, 16904 Gene [Source:MGI Symbol;Acc:MGI:4439828]
- predicted gene, 16955 Gene [Source:MGI Symbol;Acc:MGI:4439879]
Alleles
There is 1 allele of this gene:
| Allele name | Consequence | Status | Availability Estimate |
|---|---|---|---|
| sa30316 | Nonsense | Mutation detected in F1 DNA | During 2018 |
Mutation Details
- Allele Name:
- sa30316
- Current Status:
-
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs. - Availability:
- We currently estimate that this allele will be available during 2018.
- Mutation:
- C > A
- Consequence:
- Nonsense
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111300 | Nonsense | 134 | 148 | 2 | 2 |
- Genomic Location (Zv9):
- Chromosome 25 (position 38288333)
- Other Location(s):
-
Assembly Chromosome Position GRCz10 25 36729356 GRCz11 25 37299915 - KASP Assay ID:
- None (used for ordering genotyping assays from LGC Genomics)
- KASP Sequence:
- None
- Flanking Sequence:
- TTTACTCTGAGCATCAGTGGAGTCCAGACTGAAGATGCTGGAGATTATTA[C/A]TGTCAGAGTTTACACTGTCCTAGTACTAGCTGTGTGTTCACACAGTGATA
- Associated Phenotype:
- Not determined
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