Busch Lab

ZMP

dcaf12

Ensembl ID:
ENSDARG00000063155
ZFIN ID:
ZDB-GENE-061013-363
Description:
DDB1- and CUL4-associated factor 12 [Source:UniProtKB/Swiss-Prot;Acc:Q08BB3]
Human Orthologues:
DCAF12, DCAF12L1, DCAF12L2
Human Descriptions:
DDB1 and CUL4 associated factor 12 [Source:HGNC Symbol;Acc:19911]
DDB1 and CUL4 associated factor 12-like 1 [Source:HGNC Symbol;Acc:29395]
DDB1 and CUL4 associated factor 12-like 2 [Source:HGNC Symbol;Acc:32950]
Mouse Orthologues:
Dcaf12, Dcaf12l1, Dcaf12l2
Mouse Descriptions:
DDB1 and CUL4 associated factor 12 Gene [Source:MGI Symbol;Acc:MGI:1916220]
DDB1 and CUL4 associated factor 12-like 1 Gene [Source:MGI Symbol;Acc:MGI:2444462]
DDB1 and CUL4 associated factor 12-like 2 Gene [Source:MGI Symbol;Acc:MGI:2445178]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa14363 Nonsense Available for shipment Available now
sa23871 Nonsense Available for shipment Available now
sa45730 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14363
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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092015 Nonsense 325 482 7 9
ENSDART00000133227 None None 52 None 1
Genomic Location (Zv9):
Chromosome 21 (position 10329815)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 11813178
GRCz11 21 11905806
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AYTTTGTGTTCTGTGANTTTTTCAGGAGCTTTCTACAAAACTCCCTTACTG[T/A]AAGGAGAATGTTTGTCTGGCTTACGGGCYGGACTGGTCTGTTTATGCAGT
Long Flanking Sequence:
AAACACAGCTGATCCAACTAATGAAGGGGTTGTAGACTCCTCAGAACACCTCGATTATTTGGATCAGATGTGTTTGACTAAAGTTGGAGCAAATCTGTGCAGAGCCGCAGCCCTCTAGGACTTGAGTTTGAGACCTATGGTTTAATCCAATACATCTATGTTTACATGTCTATAGAAGCAAGTCTGTGTCTGCTCAGTGTAAAGAAGGTATGCCTTATTAAATGGTCTGCGTAAATGCATGTTTTGTGAATTCATGCCTCTTCATATTTGGTTTCTGTGCCGCTGCATATAGATGATTTAATGAAAACAAAAAAACTTGCTGGGTCTCTTTGTAGATGGTCACATGTTTACGTCAAAAAAGCTAAACCTGACCTGGTCTGCTGTTGGCTGTAATACTACAGGACAAAGTGGGTGGCCACTAATGCACTAATGCACATCTTATCTTATCTTATTTTGTGTTCTGTGATTTTTCAGGAGCTTTCTACAAAACTCCCTTACTG[T/A]AAGGAGAATGTTTGTCTGGCTTACGGGCTGGACTGGTCTGTTTATGCAGTCGGTTCTCAGGCACACGTTTCCTTCCTCGACCCCCGGCAATCTTCTCAGAACATCAAATCCGTGAGCTCCAGAGAGCGTGGCAGCGGTATGACGTTTACTTCATTTCACTTGTCACCCCCTGAAAAGATGATTCACACAAAGTTCTGAAGCCATATTTGATTGTCTTTTTAGGTATTCGCTCTGTGAGCTTCTATGAACACATAGTGACGGTAGGCACTGGTCAGGGTTCCTTGCTCTTCTATGACATCAGGGCCCAGCGTTTTCTGGATGGCCCATCCAGCACACCCGGCGGGTACCGGAATCGCACTGCAGAGGGCATCCTGAAACTCACCACAGGAAGAGGATGGCTGGTAAGATTGTCTAAATTAATAATATATATGTTGATTAGACCTCAAGCAGTTTATGTATATTAGTTTAGACATTATATGCACTTTTGATAAATAATTTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23871
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092015 Nonsense 340 482 7 9
ENSDART00000133227 None None 52 None 1
Genomic Location (Zv9):
Chromosome 21 (position 10329860)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 11813223
GRCz11 21 11905851
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGTAAGGAGAATGTTTGTCTGGCTTACGGGCTGGACTGGTCTGTTTA[T/A]GCAGTCGGTTCTCAGGCACACGTTTCCTTCCTCGACCCCCGGCAATCTTC
Long Flanking Sequence:
ACACCTCGATTATTTGGATCAGATGTGTTTGACTAAAGTTGGAGCAAATCTGTGCAGAGCCGCAGCCCTCTAGGACTTGAGTTTGAGACCTATGGTTTAATCCAATACATCTATGTTTACATGTCTATAGAAGCAAGTCTGTGTCTGCTCAGTGTAAAGAAGGTATGCCTTATTAAATGGTCTGCGTAAATGCATGTTTTGTGAATTCATGCCTCTTCATATTTGGTTTCTGTGCCGCTGCATATAGATGATTTAATGAAAACAAAAAAACTTGCTGGGTCTCTTTGTAGATGGTCACATGTTTACGTCAAAAAAGCTAAACCTGACCTGGTCTGCTGTTGGCTGTAATACTACAGGACAAAGTGGGTGGCCACTAATGCACTAATGCACATCTTATCTTATCTTATTTTGTGTTCTGTGATTTTTCAGGAGCTTTCTACAAAACTCCCTTACTGTAAGGAGAATGTTTGTCTGGCTTACGGGCTGGACTGGTCTGTTTA[T/A]GCAGTCGGTTCTCAGGCACACGTTTCCTTCCTCGACCCCCGGCAATCTTCTCAGAACATCAAATCCGTGAGCTCCAGAGAGCGTGGCAGCGGTATGACGTTTACTTCATTTCACTTGTCACCCCCTGAAAAGATGATTCACACAAAGTTCTGAAGCCATATTTGATTGTCTTTTTAGGTATTCGCTCTGTGAGCTTCTATGAACACATAGTGACGGTAGGCACTGGTCAGGGTTCCTTGCTCTTCTATGACATCAGGGCCCAGCGTTTTCTGGATGGCCCATCCAGCACACCCGGCGGGTACCGGAATCGCACTGCAGAGGGCATCCTGAAACTCACCACAGGAAGAGGATGGCTGGTAAGATTGTCTAAATTAATAATATATATGTTGATTAGACCTCAAGCAGTTTATGTATATTAGTTTAGACATTATATGCACTTTTGATAAATAATTTAAGGGCCATTCTTCAACTACGGGCACTTTTAGCCATGTGAAGTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45730
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
ENSDART00000092015 Nonsense 455 482 9 9
ENSDART00000133227 Nonsense 25 52 1 1
Genomic Location (Zv9):
Chromosome 21 (position 10335597)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 11818960
GRCz11 21 11911588
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTTTTCCGACATCCGCTCGTTCCCGAACGCTGTGTACACGCACTGCTA[T/A]GACGACTCCGGCACCAAGCTCTTCGTAGCCGGCGGCCCGCTGTGTTCGGG
Long Flanking Sequence:
TCATGAACATGTAACACATTCAGACTTACTTGCAGTTTGATACTGACTAGACATTAGTCTATATCATAAATCATAGATGTAAATGCATAGAAATACATTATTTTAGGGGTGGTTCACCCAAAAATGAATATTTACTCACCCTCTAGTGGTTTGAAACTTACTTTCTTCTAATGAACACAAAACAGGATTTTCTGAAGAATGTTGGAAACCAACAGCCATTGACATACACCGAAAATGCAATGGAAATCAAGTGCTGCTTCAACAGTCTTCAGAATATTTTTGAAACAAGTTGATGAGGAATTAATGACAATTCTGTTAAACACTAAATGATTTCTTTTATATGACTGAATTAAATGTTTTTTATACTTCATGTAAATCTCAGAGTCATAAATAAAACATCAGTCTTAATCCACATTTCTCTTTCAGAATCACGACGAAACGTGGAGAAGCTACTTTTCCGACATCCGCTCGTTCCCGAACGCTGTGTACACGCACTGCTA[T/A]GACGACTCCGGCACCAAGCTCTTCGTAGCCGGCGGCCCGCTGTGTTCGGGCCTACACGGAAACTACGCCGGCCTCTGGAGCTAACCTTCCCATCAGCCCTCCTCCATTCACTCTCTCACACACAGGCCATCCTACATCCTTATCTTTAGCTTCTATCCAAGTCAAACCCTCTACAGACTCAGGAGCTCAACCGCTTTTGTGCTCGTCTTTACATTCTCATTTGCCTGTTGTACTTTTTTTCCCACATTTGTTTTTTATTTTTTTTGTGAGAGGGAAAAAAAGTAAAGGAGAGGTGTCGGATTATTTGGAGCTTGTACATCGGCAGCCTGAACCTTTGAGAACTGTGGAACGGTGTAAAAATATACAAAATATATTGAACAGTCTCTCTGGGCATTATGTTGTTGTTTCGTTTGCTGTTAATGCTTCTACTTTTTGCTTTTAAAGGTTGCCGTGTTCAAACCATGGCGTGTTGAGTTTGTTTTGCAGTGTGCGTTTTCAGA
Associated Phenotype:
Not determined