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
sa32208	Essential Splice Site	Available for shipment	Available now
sa13566	Essential Splice Site	Available for shipment	Available now

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