ZMP

si:dkey-6e12.6

Ensembl ID:

ENSDARG00000095086

ZFIN ID:

ZDB-GENE-030131-5736

Description:

craniofacial development protein 1 [Source:RefSeq peptide;Acc:NP_001093505]

Human Orthologue:

CFDP1

Human Description:

craniofacial development protein 1 [Source:HGNC Symbol;Acc:1873]

Mouse Orthologue:

Cfdp1

Mouse Description:

craniofacial development protein 1 Gene [Source:MGI Symbol;Acc:MGI:1344403]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa29037	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa32208	Essential Splice Site	Available for shipment	Available now
sa13566	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa29037

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
ENSDART00000079170	Essential Splice Site	181	353	4	8
ENSDART00000115388	Essential Splice Site	140	312	3	7

The following genes are also affected by this mutation:

ENSDARG00000056639

Genomic Location (Zv9):

Chromosome 18 (position 22199084)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	22429307
GRCz11	18	22418373

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTGATATCCCTAGACCCAAAGCAGAAGTTCCAAGTGCAAGCTCTCAGAAG[G/A]TAAAGTATCAGCTCAAGAATACAAACACAAATAAAAGAGGTTTTGTTTAA

Long Flanking Sequence:

CTTACAATTTACTTAACTCAAGTGGTTCCAAACATCTTAAGGGGCTTTTTTTTGTTGTTAAACACACAAAAAAATTTAATAATGCTGAAAACCGCTAGCCATTGACATACAGTGTAGGAAAAAATATTATGGAAGTCAGCGGCTGACGGTTCCAGCATTCTACAAAACGTCTTTTTTTTTTTTTGTTCAAAAGAAGAAGCTCAGCAATTGGAGCAAGTGAACCGTGATTAAATGACAACTGTTTTAATTTGTAGTTGTCACTTTCTCCTTGTTTCCAAAGAAAAAGGAAAAAAGGAGGCCTCAAACTGGTGGAGGATGGCGAGGCAAGTACAGCAGATCAGCAGAAGGACGAAGATGAGCCAAAGGAAGACGATTTTGTAACCAAGTCAGTAGGAGACATTGAAGAGCGGCAGAAGAAGAAAGCAGATGATCTTTGGGCTAGTTTTCTGAGTGATATCCCTAGACCCAAAGCAGAAGTTCCAAGTGCAAGCTCTCAGAAG[G/A]TAAAGTATCAGCTCAAGAATACAAACACAAATAAAAGAGGTTTTGTTTAAAGTCTGTGTGAAATCAAAATTTACTATGTTTATTTTGCTAATGCAGATTGTTATTGTTAAACTTTTTTTTTTTTAGTTAAAGCCCTACCATTTGTTCTGCATTCTTGTGGTCCTTCTCTGTTGATGTATTTACTGCTGAAGGACATTGACCTGGACAGATTGTTGTTCATAGATTTAGTTTATTATAGTTTTAAAATTTTTTAAAACAGTTGTTCAGGTGACGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTGGTTCAAGCCTCAGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCGTTCGCGTGTGTTTCCTCTGGGTGCTCCGGTTTCCCCCCCAGTCCAAAGACATGCGGTTCAGGTGAATTGGGTTGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGTGGATGTTTCCCAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32208

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079170	Essential Splice Site	225	353	None	8
ENSDART00000115388	Essential Splice Site	184	312	None	7

The following genes are also affected by this mutation:

ENSDARG00000056639

Genomic Location (Zv9):

Chromosome 18 (position 22201336)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	22431559
GRCz11	18	22420625

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAAAATCACAATTACTAAGGTGTTCGATTTTGCTGGAGAAGAGGTTCGG[T/C]AAGTACAAGTCGTTTGTGTGGCCACTAGATGGCAGCATCTAATCATGAAA

Long Flanking Sequence:

CATCTTTTAGAATAGAAAGTAAATAAATTTAAATTATAGTTCATTATTATCATTATTAAACACTTTATTGGAGAAAAAAATGACAAATTACAACATTTCAACTAAATGTTACATTTTTGTTATTTAGTTGTTATTATATGTTATTTTTAAAAAAAAAATTTAATTGAATAATTCTTTCCAATTTTTTACATTTTAATTTGCGTGTACTTCTTTTGGACTAGACAGATTATATATTATTATTTAAAAAAGAGAGATCTGTGAGCGGTATACACATTTATGGTGAGCACTGTTATATTTAAATAGCATTTTCTGTGATTTTGCTTTTTTAATTTTAAACTAATAAGCATTTTTTTTTCCATCTCATATAGTTCACATCCGCAGCTGCTACAGATGAACCCAGTAAACTCTCTACAGCGTCTTCCCAGAAGGAGGACAAACCCAAAGATTCCTCCAAAATCACAATTACTAAGGTGTTCGATTTTGCTGGAGAAGAGGTTCGG[T/C]AAGTACAAGTCGTTTGTGTGGCCACTAGATGGCAGCATCTAATCATGAAAAAGCTGTGCAAACGATTGCTTTTGAGGTGAAAGCGGCAGTAATATTTTTTATTGCTTATTGCCAAACTCAAACAGCAACAAGGAGATGAGACAAAGTCTCATCACTTGCATGTGAAATATAATACAGGAAAAAACATTGTTATTGTGCCTAAATCAAGCTATGATATCATCAATAGCATAAAAAAAGACTTCAACTCAAAAAGGTTGTCATAATGCATCAGAAATGTAGCACTTTAATTTTTATTTATTCCTCTAAAAGAGTAAGAGAGTTAAGTTCAGTATGAAAGGGGAATGTATAAAGGAGATTTAAGTTCTTTTTGATTATTAATAAAGAATTTAGCATTCTATAGACCATTTTGAGGAATGTAAACAACAGTCCCAACTTATTTTTGGTTTTACATTTTAAATTTCTATAGCTTCTGATAATCCAAAAAGAGACGCATATTTATT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa13566

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079170	Essential Splice Site	324	353	None	8
ENSDART00000115388	Essential Splice Site	283	312	None	7

The following genes are also affected by this mutation:

ENSDARG00000056639

Genomic Location (Zv9):

Chromosome 18 (position 22251713)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	22481936
GRCz11	18	22471002

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

AGGAGGGCATCACAGATGAGCTGGCAATCCATAATMGAGGCAAAGAAGGG[T/A]AWGTTTAAGCCTCATTAGTGACCCAGACAAACACATCATCTCGTATTATC

Long Flanking Sequence:

TCTACACACCTAAATGCATTGAGCTGCTGCCATTTAATTGACTGATTAGACATTTGCGTTAACGAGCAATTGGAAAAGTGTACCCAATAAAGTGGCTGGTGAGTGTATTTACATTTTAATAAAATGTCATTAGTTGTTTACATTAACCAACTGTAATGCAAAGCAACAATTGTTTTGCTAAATATTAATAGCTATATTATACACACATTTTCCTCCTTCCATTTATGCCAATATTTTGATGATGAAAAAAACACACCTCTTTTTGCTTGGAAACTGGCATCTATAATGCATAAAAACAATTATGGTCTAAAATATTTCTGTATGTTTATCCTCTCTCTAGTGCGAAGAGACCAGCAGGCATGGGGAGCATCCTGAATCGCATTGGGGCCAAAAAGCAGAAGATGAGCACTCTGGAGAAGTCGAAGATGGACTGGGATGCCTTTAAATCAGAGGAGGGCATCACAGATGAGCTGGCAATCCATAATCGAGGCAAAGAAGGG[T/A]ATGTTTAAGCCTCATTAGTGACCCAGACAAACACATCATCTCGTATTATCTCCCATTAGAGTCTCACACTAGCCTCTGAGATTTTCATCAGAGCTGAATAAATATCATTAAGTGTCTTAAGTGCTTAAAGCAACAGCACACTGAAATGTTGCATTTCAGGCCGTTTTTGTGATACATTGCGATTTATTAATTATTCACAAGTTAACTGGACAGTGAAATGAATGTATTTGGGAAAAAACCTTATGCTGCGCACGCATTAGATTAATATGTTGACCTTTGTGGTTGCTGTTAGAATTGAGGATGAGCATTTGGAGTACAAAAAATGTACTTGGATTCTGTTCTGGCCACATTATGAGATGATTGTGTACTATTTGTTTTGGGTTTCTGTCTTTAAATTGTTTTCTGCATATGCATGTAAGATCACACTTTACTTTAAAGTAATTCTCACTACTTGATGCTGCTTAATAGTTATTAAAGTAGTAGTTAGTATTAGGTATTGG

Associated Phenotype:

Not determined