ZMP

CELF5 (3 of 4)

Ensembl ID:

ENSDARG00000086155

Description:

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

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
sa39950	Nonsense	Mutation detected in F1 DNA	Not yet available
sa39951	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39950

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126442	Nonsense	24	102	1	2

Genomic Location (Zv9):

Chromosome 2 (position 54003110)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	53685953
GRCz11	2	53414176

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAATCTGGCTTCCTCCGCCGTGCCAAGCATCGTGACCCCAATAGTGAAC[G/T]GATTCAGCGGGATCCCGCACCAACCCAATGGTCATCCGGTGGAGGCGGTT

Long Flanking Sequence:

GGTGTGTATGTTAGGTGCCTTATGTAAAATGTAGTGCAGTTCAGTGGTAAAATTGTAGTTCGGGTGATAGTGAGTGTTTTCCGGTTATTTGCAAGAGATAGGACTATTGCAAATGCAGATTATTTACAACTTAGTCAGTCTGTCATAACAGGAGCAAACGGTAGCATGAGGATAATCCAAAACCATAGATCACAGGCAATAAGGTCAATACAGGCGACAAAACAACATCAACACTGCAAGGCTAGACTAGGGTACGCTTTGTAATGTTACAGACATTCTTTCAGACTTTCTTCAGAAAAAAAATAAAAATTTAGGAAAAACTGAAAAAATGTCTGCTCTGTTAAACATCATTTGGAAAAATATTTGAATTACAGACGTAATAATAAAAAGGTTTGAAAAGTTTGAAGAGTTTCTTTATTTTATCGTCCGCAGGTTTGAGCTCTCCTCCGGCTAATCTGGCTTCCTCCGCCGTGCCAAGCATCGTGACCCCAATAGTGAAC[G/T]GATTCAGCGGGATCCCGCACCAACCCAATGGTCATCCGGTGGAGGCGGTTTACACCAATGGGTTGCCGCCGTACTCGACCCAGAGCCCAACCGCAGCCGACACGCTCCAGCAAGCATTCACTGGCGTCCAGCAATACACAGGTGCTCGTTTCTCAAAGATGCTCTTCTCGAAAACTTTGTGTAGTGTTTAAACTGACTATCCTTTCATTATGTTGGTGGCTGTTTTGGGGCCATTGACTTCTATTATAATCACATGTTTTGATTGCAAAGCCACGACACCAAATGCATTGCATGCATTCTTGATTGTTGCTGGTTTTCCCTGTTGGGAAAAGGTAAAAGTCTTAATTTAGTTTTTATTGGGCCACAACTTTCTTTGTGTTTCAGCAAATGGAATGATTTTAGGTGACAAATCTTACTTTGACATAACTTAACTCAACTATACAATCTGGGCAAAACTTTACATATATTTTGGGAAAATGCTGTAAAAAATTTCAGAAACT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39951

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000126442	Nonsense	73	102	2	2

Genomic Location (Zv9):

Chromosome 2 (position 54008353)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	53691196
GRCz11	2	53419419

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCTCATCTGTCCCTCTTTCTCTTCCTCCTGTATGCTTGCGCAGCCATATA[T/A]CCTGCCACAACACTGACCCCTATAGGCCAGACACTGCCACAGCCTGCGCA

Long Flanking Sequence:

ACACACTCACACACACGCTAAAATCTTGGTGTTCAGGAGAAATCATGTAAGCATATCTCTCAACCCGAGCTCAGTTTGAGACGTTTGTTCAAAAAACATTTGCTCTCCATGTAATCTCATTCGGCAGAAATGATCCGATGTTTAAAAAAAATCTAATTTGAGACGTTTCATCCACTGCGGTTGATATTTTTTTCCCCCTCAAATGTCACTTTGACAGAAAAATAACTTTCCTGGCGCAGTGTTATTGCTAGTAGGTGACTTTGCTGTGATTGAAACCTCAGGTTGTATTTGAATTTTCTGGATATTACAGCTATCATACGGACGCCTGGAGATCTGCCGCTTTGAATCAGTTTGATATATGATGAACGTGCCTTCAGAATTCATTGCACTGTGATCCTGTCATATTTCATTAGCATATAAAGGTCAGCCTTCGTCTTGTCCTTATTCTTGCCTCATCTGTCCCTCTTTCTCTTCCTCCTGTATGCTTGCGCAGCCATATA[T/A]CCTGCCACAACACTGACCCCTATAGGCCAGACACTGCCACAGCCTGCGCAGATCATCCAGCAGCAACAGCAGCAGCAGAGAGAAGGTAAAATGCCTCCCTGTAGTAGCTCTCTCCGAATGAAATTCACTTCATGCTGTATATATTCCTGTCTAGGAGTATCAAAGAGTAACTCTTTTTCCTGTGTTGCAACTGAGTTCCGTTTTAGAATCCTCACTTTTGATTACACCACTTTTAGAATGTGATTTTTTGAGGTATTCAGTTTACTATGTGTTTGAGTAAACTACAACTACCTGACAAAAGTCTTGTCGCCTATCCAGGTTTCAGGAAATACAAATAATAACTTGATTTCTAGTTTGTCATTTGGTATCAGAAGTGGCTTATATGAAAGGTAAAGGCCTCTAGATTACGCTTATTTTACCAAAACAAAATATGATCATGCCTTCATTTTTAATTATTTAATTAGGACAGTAAAGTCTGACTTTGCTTAGACAAAAGTCTC

Associated Phenotype:

Not determined