ZMP

zgc:154018

Ensembl ID:

ENSDARG00000068613

ZFIN ID:

ZDB-GENE-060929-172

Description:

hypothetical protein LOC767791 [Source:RefSeq peptide;Acc:NP_001070226]

Human Orthologues:

CNKSR3, IPCEF1

Human Descriptions:

CNKSR family member 3 [Source:HGNC Symbol;Acc:23034]
interaction protein for cytohesin exchange factors 1 [Source:HGNC Symbol;Acc:21204]

Mouse Orthologues:

Cnksr3, Ipcef1

Mouse Descriptions:

Cnksr family member 3 Gene [Source:MGI Symbol;Acc:MGI:2674130]
interaction protein for cytohesin exchange factors 1 Gene [Source:MGI Symbol;Acc:MGI:2444159]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39267	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23629	Nonsense	Available for shipment	Available now
sa43375	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39267

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099298	Essential Splice Site	78	346	3	9

Genomic Location (Zv9):

Chromosome 20 (position 4262360)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	KN149744.1	12675
GRCz11	20	4227344

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCTGAGAGACTTCACTATAGAACAGGCTACCGAATGCAAGAAGAAATTG[T/A]AAGTTTGTCTTCATTATTTATAAAGATTGTTGGATACTTGGTGGGTAAAA

Long Flanking Sequence:

ATCATTAGACGTTGATATTTGATTAATTTTAGGTTGGATGTTGAATATTGACTAGGCCTGACATTGTGAAGTGAAGTAAAAGTACCTGTACTAGAAGGCGGGGCTTCATTCAATGTATTGACCATTACACTTTTTCCCATTCAAAACTATACGAGTGACTCGTCTTGTGTTTTTTTTTTGTCTTTGTACATTCCATTTTTATAAATTACCATTTACAAAGCAAAAAGAATTGCTGATGCTGCTACAAAAGTTGGAGAAAGGAAAATATCTGCCATTAATGGCCATGAGAGCAAATACTGGCATCACCAGTATAACTTTCTGTAAACATGATTTATGAAAAGTCTGGTTTTGAGTTTATACTTGACTGGTTAGCCACTGAAACCAACTTTGTGCAATAGAGGTAAATACTCATTGTTATCTTGCAGGCGGAGAAAGCCGAGGGCTACATCAACCTGAGAGACTTCACTATAGAACAGGCTACCGAATGCAAGAAGAAATTG[T/A]AAGTTTGTCTTCATTATTTATAAAGATTGTTGGATACTTGGTGGGTAAAAAAAGTCACTGATGTAGATGGCAGGTTATGCTTAGCGGGAAATGGCAAAAATGCTAATTGATTTCATGTCAAATCCTTGATATCTATTTGACATCCCCATATTGATGCCCCTTTGACCACCATGTGAAAATGTTAAATCTAATGTTTTTTTAATGTATTTTTAAAAATAATATTTATATATTTCTACTTTATTCTGTATATTCTCTTATTAAAAATAGATTAGTGAAGTTTATTTATGAACTAATTTCTAGAGGCTCACGATTTACGAACTTACGAACTTATGATTGCTTGCAGCTGGTCCTGCATTCAATTTATGATTTACCAATGTGTCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCGCTTGGTCGCTGGTTCAAATCTTGGCTCAGTTGGCGTTTCTGTGTGGAGTTCGCGTGAGTTTCCTCTGGGTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23629

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
ENSDART00000099298	Nonsense	141	346	6	9

Genomic Location (Zv9):

Chromosome 20 (position 4273863)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	KN149744.1	1172
GRCz11	20	4238847

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACAGCGAAGAGAGTGACGATGAGGACGATGAAGAGATGTGTGTGGAGTA[T/A]ATGGATCAGCTGACCCCCGGCTCTCTGCATGTGAGTAACCAGATACACTG

Long Flanking Sequence:

TGAAATATAGGTGTCCTAATAGTGTTTTTAGCAGTGTGGGACACATATACGACTGTCAACAGCTCAAAAAAAATGTGTTTTCGTGACCCTTTAAGGCAAAAGGAGGTCCAACCCAGTAGTAGTAAGATGTAGTAAGTGGCTGATGAGTGTATGCGGCATTGAATAGTGTTCCATTTTAGGTTTGATTTCAGTAGTTATATATAAATAAATATGAAAACAAAATAGTAATGTGTTACAAAACCATTAGTAAAATGATCTAAAACTAATCTGATAAAAACAGGAAATTTAGAAACAGTCTCAAAATAAAAACGAACTTAAAAATACAAACCTTGAACTGCACTCACATAAAGCCATAGATGACTTCTATTTGAGTAAACTTCACGTCTTTCAGCAGAGCAGAAGCTGACGCTTTAATATCTGCATTTCTGTGATTGTGTGTACCCAGAGTGCTACAGCGAAGAGAGTGACGATGAGGACGATGAAGAGATGTGTGTGGAGTA[T/A]ATGGATCAGCTGACCCCCGGCTCTCTGCATGTGAGTAACCAGATACACTGAGCGCTAACCGGCGTTGTGGCTTCTGTGCTATTAATGGCTGGCGGTTGAGACGACATAGAAACAGTGACACGAGCAAGTGATAAAAATCTGATGCATCATTGCATGCTGCTCAGTTCAGCAGTTTGGGGTTAGCAAGATAAGTAGGCTAGTTGGTTAAGTAGGATCATAGATATATACTCTAGATATCGCATAGGGACCCTGAGCATGCGTCAATAGCGCCGCCACATTGGTACAGTGCTCCCAGGACAAATGTCATTCAACCGCACTAGTCGAAGACCGTGTTATTACGTGAGTATGCTGGACTTTAGCGCTGTCTACGGGTGTAGTAACGAGCAAACAAAGAAAACAAAGTACAAAGGCAGAACATTTCATAGGTAATATTAAGTTTTTTTCTGTTTTTGTATGTTCTGAACTTTTGTGCTAATCAGGTCACGTTATTGATGATAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43375

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
ENSDART00000099298	Essential Splice Site	270	346	9	9

Genomic Location (Zv9):

Chromosome 20 (position 4283005)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	4512914
GRCz11	20	4247989

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCAGCATGTGATTCTCTCTGTCTCTGTATGTGTGTTCGTGCGGGGTTTCA[G/T]GCTAAGGAGGCTGATCTGCAGGCCATCGAGCAGGTTTTGAGTGAACCATC

Long Flanking Sequence:

GCCTAGAAACAATGCAAAAAAAAATAATAAAAGCATTTTTTTGCATTGTAAAAAGAAATTGACTAAACTTGCTGTACAGCTTCTTTGAAATGATTCAGCTTTTAACCCAAGTACTCCACTTGACTCAATTTAGGTCAACTAAAAAAAAGCTCTGCTGTAAGCTGCCTTATGATTTAAAGTTGAGTTAACTTTTTGGTTTTAAATACATGAACAACTTAGAACCACTTTATTGTATGATAAGGACTTGTAGTTTTTTTGTGAACTATCCCTTTAAATCTGAGTGTGTTTTTTTTCCAAAATGTGTTTGATCACCTTCTGTTGCTTCACAACCATACATTTCAAAATACAAAAAAATATACATGGTGCAAGCTACAATTCTTAATTTCCAGCAAGTCTACAGACACTAGATGGCAGCATTGATGAACCAAAACCATGCCTGGCTTAAACTAACCAGCATGTGATTCTCTCTGTCTCTGTATGTGTGTTCGTGCGGGGTTTCA[G/T]GCTAAGGAGGCTGATCTGCAGGCCATCGAGCAGGTTTTGAGTGAACCATCTCTAAACAGGTCTAAATACAGACAGTGGCGAGACGCGAATGTGCTCCTGCTGCAGGAGATCGGAGAGAAACACAAGAGCGATGTGGAGAAACCGATGGTTCAGACTCGACCTCAGCGCCAGTCGCTGTACGGCCCCAACACTGCTGTCCCTGCTGCACGCGTTTACACAGAGACCAGCCTGTGAAGACCACAAGACCGTTACACACTCAAACAAACACTCCTCAACACTGGAGATACACATCGAGGAACTGAAGTAAAACGATGGTTGGTCAGTTTTCTCTAAATTTCAGAGCCAAACTCCTCTCTTTGATTATTTGGGATCGTTTTAAACTTATTTATTTGCTTGTTCACATCATTTATTGTCTTGATAAGATGTGTTTGTAATGCTTTACCAGTTAAACCGTTGTTTTAAATAGGATTTTGGACTTTTTGGGGGTTGAAAATTGTAAA

Associated Phenotype:

Not determined