ZMP

A8WFV4_DANRE

Ensembl ID:

ENSDARG00000078310

Description:

LOC799918 protein [Source:UniProtKB/TrEMBL;Acc:A8WFV4]

Human Orthologues:

AC090616.1, CECR2

Human Description:

cat eye syndrome chromosome region, candidate 2 [Source:HGNC Symbol;Acc:1840]

Mouse Orthologue:

Cecr2

Mouse Description:

cat eye syndrome chromosome region, candidate 2 homolog (human) Gene [Source:MGI Symbol;Acc:MGI:1923

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38037	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa17892	Essential Splice Site	Available for shipment	Available now
sa39477	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38037

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
ENSDART00000110426	Essential Splice Site	306	1502	9	18

Genomic Location (Zv9):

Chromosome 25 (position 17037016)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16583560
GRCz11	25	16679960

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTGTTTAATGTGATGTAAGCTATAGTTTAATTTCTGCATGTATATGAA[G/A]CAGATGCAAGCCACAACTGAGGAGGAGAGGCAAAGGGATGAGGACCTGGA

Long Flanking Sequence:

TTGACATGGTAGCATCACACAGTTGCTGTTGGCTGCACATCCATTATGCAAATCTCCCATTCCACCACATCCCAATAGTGCTCTCTTGAATTAAGCTCTGGTGGAGGTGGACTCGGAGGCCATTTGAGTACAGTAAACTCGTAATAATGTTCAAAAAACCACCCAGAGATGATTCGAGCTTTATGACATGGTGGTTATTGTCCAATTTTGGTGAGCCTGTGCAAACTGTAGTTTCAGTTTCCTGTTCTTAAATGACGGGAGAGGCACCCAGTGTGGTCTTCTGCTTCTCTTTAAACCCTATGGATGTACGGCGTGAAAATCTCAGTAGATCAGCAGTTTCTGAAATCCTCAGACCTGAGCCATTCTGGCACCAATAATCATGCCACATATCTGTGACTGTGTATATATGTATTTTTTTTTGTGTGTGTGTGTGTGTGTGTGTTAGTGCTTTCTTGTTTAATGTGATGTAAGCTATAGTTTAATTTCTGCATGTATATGAA[G/A]CAGATGCAAGCCACAACTGAGGAGGAGAGGCAAAGGGATGAGGACCTGGAAAGGCAAGTCCTACTTGCTGAACAACGGAAAGAAGATGAGAGACTCCTTCAAGAAGAACGGGAGCGAGAAGAACAGGAGCGAGTCAAAGCTGTTGAGGGTGAGTCACACTCCAGGTAACCGGTGAACAAAGTTTCACCAAAAGCGTGATCAAACACACACTGACGCTTGAGCACATTCTGTGGTCTTCTCCCGACATGGCGTTTTGAAGACTGCATGCTTTTAACCCAAGACTGCTTTAATCATACAAAGAGCTGAGCTAGGGGAAACGATCAACCTCGCTCCTCGTGAGAATTATCCAGCTCTGATATCCTCTGTCAGCGGGTTAATTAACTCTTGATTGTACTGCAGCTGATGGCCCCATCCACATTAATGTATTATGGATGAAGATCGGGCATGCGGTTCTCTCCAGTGGTTCCCTCCTCAAGCTCTTTTAATCCTCCCAGCAGGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa17892

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110426	Essential Splice Site	441	1502	12	18

Genomic Location (Zv9):

Chromosome 25 (position 17038301)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16584845
GRCz11	25	16681245

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGGAACCTGTTGATGAGTCTTACGCACCTAACTATCATGAAATYATACAG[G/A]TGGGCATAAAAGATNNNNNNNNATTAWTCAATTATTATTAAAGAATAATT

Long Flanking Sequence:

AGAGGGAGGAGAAAGCCTGGTTGCTCTCTCAAGGGAAAGAACTTCCACCTGAGCTGCTTAATCTGGAGACTCACTCGCCTATTCGCAGAGCACGTCGCACCAAACAGTTGTAAGGACTTGGTTGCATGTCTCAAATTCAGTAGTTGCTTATAGTTTCAAGCACATTTGATGTTCATTTTACTTTCTAATAACTATGTAAAAGCTTTTATGTGTAGTTTGTTGGTGGCGTTAATGTTAATTACTTTTCTTTTTGATCTGCAGTTATGAGATAGATGACGACTACACTGCTCTCTACAAAGGTATGTTTTGAGAGTGGTGTTTATGTTGTGGTCAAGCCCTAGTGTTCATTTCCTCATTCAGAGCTTGCAACAGTTCCGCTGAAATGATGTCAGATTATTTTCTCTTCAGTTTTGGAGGCCCTGAAAGCTCACAAAGATGCCTGGCCATTTATGGAACCTGTTGATGAGTCTTACGCACCTAACTATCATGAAATTATACAG[G/A]TGGGCATAAAAGATATTAATCAATTAATCAATTATTATTAAAGAATAATTCAATAAAATGATGATAATATTTGGCAGACCCCAATGGACCTGTCAACTATTGAAAGGAAGCTGAATGATGGAGAGTACCTTGCTAAGGATGAGTTTGTGGCCGATGTAAAGCTTATGTTTGGGAACTGTCTGGAATACAATGGAGAAGAGAGTGGTAAATATTACTCAACTCTGTTCTCTTAAAAAGATTTGTTGCTGCTTAACTAAAGAGAAACAAATGTACCCTTGCAAAATGTAGGACTGTGAAGCAGACTTCTAAAAATGATGAGCAAAGCAAGTCATGCTAGAAGTGGAAGTATGTGGATACTGTCTGACTTTGATTAATTGAGAGTGATTGAGCTGTCCTCTAGTGCGCCAGGTCCTGCAGTGCCACAGAGACATTCCAGCCCCGCAGCTCCCCTCCCTGGAGCCATCCATCCATCAGAATGCTCTCTCTTGGGGTGGCGGGGT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39477

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110426	Essential Splice Site	484	1502	14	18

Genomic Location (Zv9):

Chromosome 25 (position 17038905)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16585449
GRCz11	25	16681849

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAAACAGGCTGTGTATGTGTGTGTTGTATTTACCTGTTTTTGTCTCCTCA[G/T]AATACACAATAATGGCTGAGTCCTTGGAACGCTGCTTTACCCGAGCCTTA

Long Flanking Sequence:

AAGGAAGCTGAATGATGGAGAGTACCTTGCTAAGGATGAGTTTGTGGCCGATGTAAAGCTTATGTTTGGGAACTGTCTGGAATACAATGGAGAAGAGAGTGGTAAATATTACTCAACTCTGTTCTCTTAAAAAGATTTGTTGCTGCTTAACTAAAGAGAAACAAATGTACCCTTGCAAAATGTAGGACTGTGAAGCAGACTTCTAAAAATGATGAGCAAAGCAAGTCATGCTAGAAGTGGAAGTATGTGGATACTGTCTGACTTTGATTAATTGAGAGTGATTGAGCTGTCCTCTAGTGCGCCAGGTCCTGCAGTGCCACAGAGACATTCCAGCCCCGCAGCTCCCCTCCCTGGAGCCATCCATCCATCAGAATGCTCTCTCTTGGGGTGGCGGGGTCGGAGGTCAACTGTGGTTCTGTGACCTGGTTGGTGTGCTTGCTCTGGGGAGATGAAACAGGCTGTGTATGTGTGTGTTGTATTTACCTGTTTTTGTCTCCTCA[G/T]AATACACAATAATGGCTGAGTCCTTGGAACGCTGCTTTACCCGAGCCTTACTGAAGCACTTTCCATCTGAAGATGGCGACACTGATGAGGAGTTTCATGTGAGCAGTGAAGACCGCAAGGACAAGAAAAAGAACAAGAATCACAAACAGTCAGGTCCCGAGAGCTTGATCAGAGCCACTGAGCAGGTTCAAAAACGCAAAACGTCTAATAGTGGCAAAGGAAACAATCAACAACAAGAAAAGCCCAAATCCACATTACAACCCCCTCCTCCACATTACAGCAACGGTCCCCCACATCCTCATAACATCCATCCAGGACAGCAGCAGCGTGGCATGCTGCACCCTGCTCAACAGGTTAGACCACACTGTTTCTTAATTTGTTTATTGTTGACAGCTGAAACAGCAGTTCTGGCTAATATCCTTAAGTTCACTCTGCACATGGCAGATATCACTGCAGAAAAGGCACTCAAGCAGAATATTATAGTGTCAAATTCCAGTTGT

Associated Phenotype:

Not determined