Busch Lab

ZMP

ankrd13c

Ensembl ID:
ENSDARG00000042444
ZFIN IDs:
ZDB-GENE-030131-3892, ZDB-GENE-030131-3892
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.
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.
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.
Availability:
Order Allele From ZIRC
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