ZMP

si:ch211-168n8.1

Ensembl ID:

ENSDARG00000090727

ZFIN ID:

ZDB-GENE-070912-150

Human Orthologue:

CELF5

Human Description:

CUGBP, Elav-like family member 5 [Source:HGNC Symbol;Acc:14058]

Mouse Orthologue:

Celf5

Mouse Description:

CUGBP, Elav-like family member 5 Gene [Source:MGI Symbol;Acc:MGI:2442333]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18527	Nonsense	Available for shipment	Available now
sa33053	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18527

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122509	Nonsense	28	187	1	4
ENSDART00000147581	Nonsense	35	170	1	4

Genomic Location (Zv9):

Chromosome 2 (position 53912167)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	53632955
GRCz11	2	53359336

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTACYGTCTCTTCGAGCCCTACGGAGTCATCGAGGAGTGCACYGTATTA[C/T]GAGGCCCTGATGGAAACAGTAAAGGTGAGATTCAGTTCCTGCTTTTATCT

Long Flanking Sequence:

GTGGGTGGGTCAATCTGTGCTTTTAAAAACACTGTCGGTTGGGTTTAGGTAAGGAGGAGGTTGGGTCAGTTGATCGGTAAGTCAGTCAACAGCGGCCTCTGGTGAATTTGCGCGAGAAGAGCATGTGCGAATGGCACTCTTGAGAGAAATTTGAAATCTAAAAAAAGTGTACACAGCTTGTACAAAGCGTACATCTCTGGTGGATTTACAAAAACATAAACTGCTAAAAACCGTACCTCCTGGGATGTATTTTGGACCCTCCAAAAAAGTATACAGGGGTATGTATCCACAATGAGCCTGGGTTGTAAAAATTCCAATGGCTGTGCCTGCTAATACATCAAGAATTAGGTCAATACAGTACCGTTTATATTGTGGTTGTGTGTTTGTGTATTTCAGAGGACCGGAAGCTGTTTGTGGGCATGCTGAATAAGCAGCAGACTGAAGAGGATGTGTACCGTCTCTTCGAGCCCTACGGAGTCATCGAGGAGTGCACCGTATTA[C/T]GAGGCCCTGATGGAAACAGTAAAGGTGAGATTCAGTTCCTGCTTTTATCTCTCTCGTCTGTGTTCAAGGCAGATTTAATGTGCTCGCTGGTGAATGACAGACATCCACATGTCCTTTTATAGTACAGTCTAAGATGCATTTTAAATTTGAGAAGCGACCTTCAGCTGTAAAAAACACAAAGTCGAAGCAAACAAACAGATCAACCTTGAGTGCTTTCATTTATGCTGTATCTGAAATTGCCCCCTATAGCCTCAATATTCCATTGAAGGAGTAAAAGAAACAAGTGAGTGAGGTACTTTTTTGCTGCTTGGTAAATCTATCAGAGGTATTGATCAGTCAAAGAAAAACAGGCTCAAAGGGAGTGTCCACAGTCATTTTTCATTAAAAAAAGAAGAAATGTTCATTCATTCATTCATTTTCCTTCAGCTTAGTCGCTTATTTATCAAGGGTCGCCACATAATTATTTTTCGTTCAATCCACTTAAATTTGTGAAACTCATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33053

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122509	Nonsense	35	187	1	4
ENSDART00000147581	Nonsense	42	170	1	4

Genomic Location (Zv9):

Chromosome 2 (position 53912146)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	53632976
GRCz11	2	53359357

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGGAGTCATCGAGGAGTGCACCGTATTACGAGGCCCTGATGGAAACAGT[A/T]AAGGTGAGATTCAGTTCCTGCTTTTATCTCTCTCGTCTGTGTTCAAGGCA

Long Flanking Sequence:

TTTAAAAACACTGTCGGTTGGGTTTAGGTAAGGAGGAGGTTGGGTCAGTTGATCGGTAAGTCAGTCAACAGCGGCCTCTGGTGAATTTGCGCGAGAAGAGCATGTGCGAATGGCACTCTTGAGAGAAATTTGAAATCTAAAAAAAGTGTACACAGCTTGTACAAAGCGTACATCTCTGGTGGATTTACAAAAACATAAACTGCTAAAAACCGTACCTCCTGGGATGTATTTTGGACCCTCCAAAAAAGTATACAGGGGTATGTATCCACAATGAGCCTGGGTTGTAAAAATTCCAATGGCTGTGCCTGCTAATACATCAAGAATTAGGTCAATACAGTACCGTTTATATTGTGGTTGTGTGTTTGTGTATTTCAGAGGACCGGAAGCTGTTTGTGGGCATGCTGAATAAGCAGCAGACTGAAGAGGATGTGTACCGTCTCTTCGAGCCCTACGGAGTCATCGAGGAGTGCACCGTATTACGAGGCCCTGATGGAAACAGT[A/T]AAGGTGAGATTCAGTTCCTGCTTTTATCTCTCTCGTCTGTGTTCAAGGCAGATTTAATGTGCTCGCTGGTGAATGACAGACATCCACATGTCCTTTTATAGTACAGTCTAAGATGCATTTTAAATTTGAGAAGCGACCTTCAGCTGTAAAAAACACAAAGTCGAAGCAAACAAACAGATCAACCTTGAGTGCTTTCATTTATGCTGTATCTGAAATTGCCCCCTATAGCCTCAATATTCCATTGAAGGAGTAAAAGAAACAAGTGAGTGAGGTACTTTTTTGCTGCTTGGTAAATCTATCAGAGGTATTGATCAGTCAAAGAAAAACAGGCTCAAAGGGAGTGTCCACAGTCATTTTTCATTAAAAAAAGAAGAAATGTTCATTCATTCATTCATTTTCCTTCAGCTTAGTCGCTTATTTATCAAGGGTCGCCACATAATTATTTTTCGTTCAATCCACTTAAATTTGTGAAACTCATAAACTAACTTAATTCCTTTGTG

Associated Phenotype:

Not determined