ZMP
ankrd13c
Ensembl ID:
ZFIN IDs:
Description:
Ankyrin repeat domain-containing protein 13C [Source:UniProtKB/Swiss-Prot;Acc:Q7ZUV0]
Human Orthologue:
ANKRD13C
Human Description:
ankyrin repeat domain 13C [Source:HGNC Symbol;Acc:25374]
Mouse Orthologue:
Ankrd13c
Mouse Description:
ankyrin repeat domain 13c Gene [Source:MGI Symbol;Acc:MGI:2139746]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa6224 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa35170 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21986 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6224
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 |
|---|---|---|---|---|---|
| ENSDART00000062237 | Nonsense | 173 | 488 | 5 | 13 |
| ENSDART00000121622 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 46215738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 45033668 |
| GRCz11 | 11 | 45411234 |
KASP Assay ID:
554-4863.1 (used for ordering genotyping assays)
KASP Sequence:
GCTCTCAGTGATGTTCTGTGTTTCTCTCTTCNNNAGCTTGGAGATTTCTA[T/A]CTRGAGCTGCACTGGGACTTCCAGAGCTGGGGTGAGGCMAGYGTGTGTGT
Long Flanking Sequence:
TAAGATGAGTGTTGCTATGGTGAAGCTGTGCACACTGTGATGTTTCTGTTGGTCCTCCTTTAGCCTGCTCTCAATCAGGTTGTATATACACTGAAGTAGAACCTCTAGATATCGTGACGGTTCACCAGGAACACTCCAGCTGCTCGGAGAAATACAGAGAGTCTCTGAGCGTGACGTGAATCACCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGTCACAGCTCTGCTGCGCAAACTGAAACAGCAGTCCAGAGAGAGTGTGGAGGACAAGAGACCCCGACTGCTGAAAGCACTCAAAGAGGTACACACACACACACACTCACACACACACACACACACACACACACAGGCAGGTTTCTCCTGAGCGCTCTCAGTGATGTTCTGTGTTTCTCTCTTCTTCAGCTTGGAGATTTCTA[T/A]CTAGAGCTGCACTGGGACTTCCAGAGCTGGGGTGAGGCCAGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTGTGTTTGTGTGTGTGTGTTTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGCTTGCCGCTGTGTGTGTGAATCAGCTGTTCTCTCTCCCGCAGTGCCTTTACTCTCCCGGATTCTACCGTCTGACGCCTGCAAGATCTACAAGCAGGGGATCAACATCCGGTACGAGCCGCTTCAGTGGTGTCGTAAACACACTGTTACTGAGCGCTGTGTGTGTTATTCTGACAGTGTGTGTGTGTGTGTGTGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35170
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000062237 | Essential Splice Site | 298 | 488 | 8 | 13 |
| ENSDART00000121622 | None | None | 179 | None | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 46214860)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 45032790 |
| GRCz11 | 11 | 45410356 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCTTCTCGCGCGCTCAGACCGGCTGGCTCTTCAGAGAGGACAAAACG[G/A]TACAGCAGAGCTTCCACACTGTCCAGCAGACGGGTGAAGAGCAACCGTCA
Long Flanking Sequence:
CTGCAAGATCTACAAGCAGGGGATCAACATCCGGTACGAGCCGCTTCAGTGGTGTCGTAAACACACTGTTACTGAGCGCTGTGTGTGTTATTCTGACAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCAGTCTGGACACTACACTGATAGACTTCACTGATATGAAGTGTCAGCGTGGAGATCTGAGCTTCATCTTCTGTGGAGACGCTCCTCCGTCAGAGTCCTTCGTGGTGCTGGACAATGAGCAGAAGGTGTATCAGCGCATACATCACGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTAACCTGCATATAGCATGCTTGAATGTAAAGTGTGTGTATATGACGTGTGTGTGTGTGTTTCAGGAGTCAGAGATGGAGACGGAGGAGGAGGTGGATATCCTGATGAGCAGTGATGTGTACTCCGCCACTCTCTCCACTAAATCCATCACCTTCTCGCGCGCTCAGACCGGCTGGCTCTTCAGAGAGGACAAAACG[G/A]TACAGCAGAGCTTCCACACTGTCCAGCAGACGGGTGAAGAGCAACCGTCACAGCTGATGTGATGTCTGAATGCGTCTGAGAGTGTGCTGTTCCCGCAGGAGCGCGTGGGGAATTTCCTGGCTGATTTCTACATGGTGAACGGGCTGGTTCTGGAGTCGCGGAAGAGACGGGAACACCTGAGCGAGGAGGACATCCTGAGGAACAAGGCCATCATGGAGAGCTTCAGCAAAGGAGGAAGCCTCATCGAGCAGAACTTCGAGGTGAGCGCCGCTTCCCTACATCCAGATATGTGAAGTAGATCAGTACAGCGCTGGGATACGACATCACACATCAGTGAATGAAGCAGCGCGTCCATCCAATGAGAATCAAGAGAACACCTCCTGATGAGCACCTCTAGGCTGTTGATTGGTTGGAGGCTGAAACACCTTTAGTCTGTTCATTGGTTAATGGAAGCGGAGTTTGAAGAACCTGTAGTCTGTTAATAGGCTTTAATATGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21986
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 |
|---|---|---|---|---|---|
| ENSDART00000062237 | Nonsense | 349 | 488 | 9 | 13 |
| ENSDART00000121622 | Nonsense | 40 | 179 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 11 (position 46214611)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 45032541 |
| GRCz11 | 11 | 45410107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAACAAGGCCATCATGGAGAGCTTCAGCAAAGGAGGAAGCCTCATCGAG[C/T]AGAACTTCGAGGTGAGCGCCGCTTCCCTACATCCAGATATGTGAAGTAGA
Long Flanking Sequence:
GAAGGTGTATCAGCGCATACATCACGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTAACCTGCATATAGCATGCTTGAATGTAAAGTGTGTGTATATGACGTGTGTGTGTGTGTTTCAGGAGTCAGAGATGGAGACGGAGGAGGAGGTGGATATCCTGATGAGCAGTGATGTGTACTCCGCCACTCTCTCCACTAAATCCATCACCTTCTCGCGCGCTCAGACCGGCTGGCTCTTCAGAGAGGACAAAACGGTACAGCAGAGCTTCCACACTGTCCAGCAGACGGGTGAAGAGCAACCGTCACAGCTGATGTGATGTCTGAATGCGTCTGAGAGTGTGCTGTTCCCGCAGGAGCGCGTGGGGAATTTCCTGGCTGATTTCTACATGGTGAACGGGCTGGTTCTGGAGTCGCGGAAGAGACGGGAACACCTGAGCGAGGAGGACATCCTGAGGAACAAGGCCATCATGGAGAGCTTCAGCAAAGGAGGAAGCCTCATCGAG[C/T]AGAACTTCGAGGTGAGCGCCGCTTCCCTACATCCAGATATGTGAAGTAGATCAGTACAGCGCTGGGATACGACATCACACATCAGTGAATGAAGCAGCGCGTCCATCCAATGAGAATCAAGAGAACACCTCCTGATGAGCACCTCTAGGCTGTTGATTGGTTGGAGGCTGAAACACCTTTAGTCTGTTCATTGGTTAATGGAAGCGGAGTTTGAAGAACCTGTAGTCTGTTAATAGGCTTTAATATGTTAATTGGAAGTCGGAGGCGGAGTCTGAAGCACCTCTAATTGTTGATTGGATGGAGGCGGAGTCTGAAGTACATTTAATATGTTGATTGGAAGATGGAGGCGGAGTCTGAAGCACCTTTAATATGTTGATTAGTTGGAGGTGGAGTCTGAAGCACTCCTAGTTTGTTGATTGGATGAAGGCGGAGTCGGAAGCACCTTCAATATGTTGATTAATTGATGGAGGCGGACTCTGAAGCACCTCGAGTTTGTTGAT
Associated Phenotype:
Not determined