Busch Lab

ZMP

ofd1

Ensembl ID:
ENSDARG00000000529
ZFIN ID:
ZDB-GENE-030131-5427
Description:
Oral-facial-digital syndrome 1 protein homolog [Source:UniProtKB/Swiss-Prot;Acc:Q7SZK7]
Human Orthologue:
OFD1
Human Description:
oral-facial-digital syndrome 1 [Source:HGNC Symbol;Acc:2567]
Mouse Orthologue:
Ofd1
Mouse Description:
oral-facial-digital syndrome 1 gene homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1350328]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa169 Nonsense Confirmed mutation in F2 line Not yet available
sa45382 Nonsense Mutation detected in F1 DNA Not yet available
sa27508 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa34792 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa169
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000552 Nonsense 82 902 2 23
ENSDART00000099672 None None 436 None 11

The following transcripts of ENSDARG00000000529 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 56720914)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 55128730
GRCz11 9 54718243
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTCTGCATGCAACAGTGTGGTGGTCGATCACCTGCGCAGCGCTGGCTA[T/G]GAGTACACACTGTCTGTCTTCCAGCCCGAATGCGGACTGAGCAAAGACAA
Long Flanking Sequence:
ATATTTGTTTGTCTGTCTGTCTGTCTGTCTCTCTATGTGTCTGTGTTATATACCTATACATCCATCTATATCCATCTGTCTATCTATGTGTCTGTCTGTCTGTCTGTTTGTCTGTCTGTCTATCCACCCACCTATCCCTCCATCTATATCCATCTGTCTATCTATGTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTTGTCTGTCTATCTATCCACCCACCTATCTATCCATCTATATCCATCTGTATATCGATGGGTCTGTCTGTCTGTATATCTATCCACCTATCTATCCATCCCACTGTTCTCCAGCAGTTGTTGATAAGCTGTTGTGTTGTTGTTCAGACACAGCTGCGGAATCAGCTGATCCAGGAGCTGCAGGCGCCGGTGCGCAGAGGAGAATCTGCTTCCAGACGCTCTGCAGATCACACTGACTCTGTGTTAGTCTCTGCATGCAACAGTGTGGTGGTCGATCACCTGCGCAGCGCTGGCTA[T/G]GAGTACACACTGTCTGTCTTCCAGCCCGAATGCGGACTGAGCAAAGACAAGGTGAATTCACATCACTGCATCAACATGGTTGCAAAGAGAAGCAATTTTACTTCACGCAGTTTCTGCAACTTGGGGATGTGCAATATAATTATGTATAGTTGAAGTCAGAATTGTTCATGTTAAACTTTAATTCTTTTATCATTTCCAATATCTGTGTAACGGAGAGCAGATTTCTTCAACACACTCCTAATCATATTAGTTTTAATAGCTCATTTTTAATAACTAATTTCTTTTATCTTTGCACATAATATTAGACTAGATATTCTCCAAGACACTAGTATTCAGCTTAAAGTGACGTTTAAAGGTTTAACTAGAGTAATTAGGGTAATGTTAGGGTAATTAGGCAATTCATTGTATAACAGTGGTTTATTCTGTAGACAATCCAAAACTAATATTGCGTAATAATATTGACCTTAAAATGGCTTTAAAATAATTAAAACTGCTTTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45382
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000552 Nonsense 409 902 12 23
ENSDART00000099672 None None 436 None 11

The following transcripts of ENSDARG00000000529 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 56733208)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 55141022
GRCz11 9 54730535
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATGACTGAATGTAAATGTGTTTGCTGCAGATGGAGCTGGAGTCGTCC[C/T]GATCGCAGGCGTCTCTCCTGAAGCAACAGAAGGAGCTGCTGAGAGAACAA
Long Flanking Sequence:
AGAATTGTCCCTCTCCTGTGGTTTGTAATGTAATGGGCAGCACAAATGTCTTGATACCTCAGGCTGTTGATGTTGATCATCCACTCTGCAGATCTCTCACACGCCCCCATACTGAATGAACCACAAACCATGATTTCTCCTTCACCAAACTTGACTGATTTCTGTGAGAATCTTGGTCTATGCTGGTTCCAGTAGTATTGGTGATGATTGGGATACAGATCAGCAAATGATTCAGCAGAGAAATCCACCTTCTGACACTTTTACACATCATCAACTAGAAGTCAAGGTATTATTGGTAGCTTTTACAACTGAGCCTTGCCACAAGACTTTTGTCAGGCAGTGTAGATATAAAGATATAGCACATTTTCACTGAATTCAGCCAATTAGTGGATAGAGTTGAAGGTAAAATAGTTTGACTCTTTGTAAGTTCCTTTGGACAAAAGCATCTGCCAAATGACTGAATGTAAATGTGTTTGCTGCAGATGGAGCTGGAGTCGTCC[C/T]GATCGCAGGCGTCTCTCCTGAAGCAACAGAAGGAGCTGCTGAGAGAACAACTGGAGAACATGAGGGATTATCCAGAGCTGAAGAAACACACGCTGGAGCTGCAGACACGCATCAGCCTGCTGAAACAACAGCTGGAGGAGAAACAACAACACAACCAGAGGCTGACACAAGGTGAACTTCTTATTGTTATTTTCAGAGATGAGTCCCGTGACGTGCTTTGAAATGTGCATTTTTATTAGATGTTTGACGTAATCTGAGCCGAAACATGAAGAGAGCGCGGGGCATAGAGAAGCTCCCCTTTAAACCAAAATACAGCCAATGGTGTATGGTTCTATCACTGCTCTGGCAGGGAGTGGTTGAGCTCAAGCTAAAAGCCAATGAGAAGAAGTGGGCAGGGCATGTCAGATAGTAGGTAGCATTTGATTGGTCAGAGGATTTGATGAGTATGAGGTGACATGTTCTACTATTACACTGTGTTGCCATTTGGCAGCACCATAGAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa27508
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000552 Essential Splice Site 767 902 18 23
ENSDART00000099672 Essential Splice Site 301 436 6 11

The following transcripts of ENSDARG00000000529 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 56744582)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 55152396
GRCz11 9 54741909
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGCAGCCAGAGAAAATCACACTGCACGACCTGACGGAGCCCATACAGAG[T/C]AAGAGCACACACACACACACACACACACACACGTGTCTGTGTTTGTTGTT
Long Flanking Sequence:
GGAACTGAGCTCCTCCATCAGTCCCAGCAGCCCCGTCATGAAGAGCACCACACGACACACACAAAGGTGCACACACACACTCACATGACACACTCACACGACGTAGACACACACACAAATAAAAATTGCATTTTGAAGTGTGTTGTGATCGGAACCGCACAGGTTTGTGTATGAACTCTGCTTGTGTTATTCAGCATGATGTGCTCGAGTAAATCTCTTATTGATATAAGGAATTGTGTATTAGTCTAGTCAATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTTTCTCAGTCCAGCCAAACTGCAGGAAATCCTCTTGTCCAGCTCCTCTCAGGAATCCTCACCGCAGCCAGAGAAAATCACACTGCACGACCTGACGGAGCCCATACAGAG[T/C]AAGAGCACACACACACACACACACACACACACGTGTCTGTGTTTGTTGTTGAATGCGCTTGTGATGTAGATGACTTTTTACTTCTTAGCCTTGTTTTTTTTTTCCAGAAAGTCAAAAAGCTGATTGTTTAGGTTAGGAGAGTATATGCAGGCTCTACAGTACAAAAACAATGGAAACCAATGTAAAGTCCCCACAATTCACTAAAACAAATCTCTCTCTCTCTCACTGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTGTGTACAGTGGTATCTGCAGATCAGCCGTGTCTCCTTCAGGATTGTGAGCCGGAGCTCCAGCAGGATCATCCAGGTGAGATCATCAGGAATCTGTCGCTCAGATCTGTGTGTGTGTGTGTGTGTGTGTTTAGCAGCTTTTCCAACATCAGAGCCAACCCTTCTGTTTGCTTAATCGTTCATCATTTGTGCTGATTTAATCCCGTCTGATGCTCCACGGTGTTGCTGTTGTTTTGATTTTGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34792
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000552 Nonsense 837 902 21 23
ENSDART00000099672 Nonsense 371 436 9 11

The following transcripts of ENSDARG00000000529 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 9 (position 56745532)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 55153346
GRCz11 9 54742859
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGGAACAAACACAAGAGCAGCGTGATGATGCTGGGGGTCATGTGACTT[C/A]AGCGGCCTCACCGACTGGAGGAGCAGAAGAGGCCAATCCGCTGCAGAGAT
Long Flanking Sequence:
ATTTAATCCCGTCTGATGCTCCACGGTGTTGCTGTTGTTTTGATTTTGAGATGTTGTGGGAATGTAATACACATGCGCCAGTCATTGCCGTGGTGTAATGTAAACGTTGATATGGACGACAGTCATGTGTTTCCATGTTGGGACTCTTATTTCTGATGTTTACTTCATTGAATAACAGTAAATAGGCTGTGTTCTTCAGCATTATACTGGACAAGCAGCTTTTTGTGTTTTCCAGATGTACAAATATCATCATCATCATCATCATCATCATCATCACAGCGTGAGGAAGAGCAGCAGAGAGAGACACACACACTCCAGCAGCAGCCGGTGAGATCAGCATATCTTTACTACTGTTGACATTATAGTTTCAGTTACAATCAAATATGAGTTTATTTCCTGTATTTTTCCTTTTATTTGTTCACTGCATGACCCCGGACCGCAAATCCAGCATGAGGAACAAACACAAGAGCAGCGTGATGATGCTGGGGGTCATGTGACTT[C/A]AGCGGCCTCACCGACTGGAGGAGCAGAAGAGGCCAATCCGCTGCAGAGATACATGCAGATGCTGATGCAGGACAAACAGCAGGAACAGGCGAGTGAACAACATCTAGTCTAATATTATTTACTGTCATCATGGCAAAGAGAAAATAAATCAGTTATTAGAGATGAGTTATTTAAACTGTTATGATTAGAAATGTGTTGAGAAAATCGGCTCTGTGTTAAACAGAAATTGGGGGACATTTTCAGGATGGTGAATAATTCTGACGAACTGTGTGTATATATATTTATACAAACCTTTATTTAAATATTTGAACATAATATCATGCAGGGCTGCAGGATCTTGGAAAAAAAACATAGACTGTAAAATATATGGACGTTGTATGCGTGATGTCACTTATAGGTTTCTGAAGAACACAAAAGAAGCCATCAGTAGGCGTGGCCAACCGTCGCCAAACACTTCACACAAAGCCAGAGATGAACATCTGATTCCATCCTGAATGAAT
Associated Phenotype:
Not determined