ZMP

rnf44

Ensembl ID:

ENSDARG00000068582

ZFIN ID:

ZDB-GENE-060929-604

Description:

RING finger protein 44 [Source:UniProtKB/Swiss-Prot;Acc:Q08CG8]

Human Orthologue:

RNF44

Human Description:

ring finger protein 44 [Source:HGNC Symbol;Acc:19180]

Mouse Orthologue:

Rnf44

Mouse Description:

ring finger protein 44 Gene [Source:MGI Symbol;Acc:MGI:2145310]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa18224	Essential Splice Site	Available for shipment	Available now
sa42444	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa18224

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099235	Essential Splice Site	232	448	5	11
ENSDART00000146134	None	None	83	None	3

The following transcripts of ENSDARG00000068582 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 14 (position 47759135)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	45802335
GRCz11	14	50953567

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GCCGCCGATCAACCAGTTCGTCCCCATTCAGCCGCAGCACCCGCGCATGG[T/C]GAGTAACACTCMGGCAACACAAACTACCATAAATCATACCYGTCAACCCT

Long Flanking Sequence:

AATTAATGTATGTGATAGATTATTTCTAACATATAAATGAATGTTTTTTTTTGCATTGTATAAATTGTGTATACATGCATCACGTTTTCCCAGTACTATGCAGGATTGCTTATCATTAAGCCTGATGCTTTTGAAATAATATATTGGATTGCTACACAGTGCAAAAGTGAGATCTTTTCCAGAGCATTTGACCATGTCTCTTTCTCAGCGTTATTAGAAATATACAAACACGCTTTCAAGTCACAGTCCATTTCAGTGTTCTCTCTCTCTCTGTGTGTGTGTGTGTGTGTGTGTGCAGCTCATTCAGGCCTGCACCATGCAGCATCTGCCGGTGTCCTATCAGGCGTTCCCTCCGCTGATCTCCAGTGAGCATTTCATCCTGCACCCCAGTCCTGCAGTGGCGCCCCACCAGCCTCCACCTCACCCTCCTCATCCTCCTCCTCCTCATCTGCCGCCGATCAACCAGTTCGTCCCCATTCAGCCGCAGCACCCGCGCATGG[T/C]GAGTAACACTCAGGCAACACAAACTACCATAAATCATACCCGTCAACCCTCCAGTTAGTATCAGGATTCTCCGGTATTTTACACTTCTATCCCGCTATCATCCTGTATTTTTAATCTTTCTATGAAGGGTGGCAATAAACATTAAAGCTTCAATCCTCCCTATACACAACCCATACCGCCGAACCACCAGGGGCCGCCCCTCACTCTTAAATGCGAGTCTGTTCTGTGCTTTCGGTTTGTTTAGGCATGAAAACACTTTAAAATAAATGTAAAAACGGCGGGATTCCCTTTTCTTTCCATTCCAGGTGTCATTGCCTCTCCTATGCAATCCTCAAACCAGTCAGTTCATATAGCAGTGCGTGACTGTCAGCTGACGTGCTCCATAGTGATAAATAGACGCTGCTTCCCAAACGGATTCTGCACACGTGATTAAAGCAGAGCGAAAGTGGACACACTGGGTTTTGGGTGCGTGTTTGAACAGACATATGTACATATTATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42444

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099235	Nonsense	299	448	7	11
ENSDART00000146134	None	None	83	None	3

The following transcripts of ENSDARG00000068582 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 14 (position 47748501)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	45812969
GRCz11	14	50964201

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTGTGTTTCCTCAGCCATATCCACACATGCTGCCGAGGCGTATAACGGGA[C/T]AGAGGTATCGGTTACAGCAGCCTCTGCCTCCGCCGCCGCCTCCACCGCCG

Long Flanking Sequence:

AGGAACGAAGCTATTTCTGTAATGCGGAGTCCTGCTAATATCCCTCTGAAAGTGGATAAGCCGTAAGATCTGCCTACTATACATTCAACATGCAACACCGCAATCACTGTAATCAGGTCAACACTCATCGCAATCGGCAGCATTTGCATAAGCAGGTAATCAAATTATGCTAAATAAAAATGTCTAGTCATGTAAAAAAGTGGTTCCTAGATTGGGGTTGGGACCAGGGTGAGAGTTATACATTGACAATCGGGGGTCAACAACTTTAATGATGTTAGTTTGCGTAATACATGTGGTCACTGACAGTTTCTTTGTATACTCGGCACTCGTTGCGTGTATTGCCTCTTCTTGTTGAATCATTGAATGCCTCCTCAATTGTACGTTGCTGTGGACAAAAGCGTTTGCTAAATGTTAATGTAATTGTGCATTGTGCATGTGTTGTGTTTGCGTCTGTGTTTCCTCAGCCATATCCACACATGCTGCCGAGGCGTATAACGGGA[C/T]AGAGGTATCGGTTACAGCAGCCTCTGCCTCCGCCGCCGCCTCCACCGCCGTATTACCCCGGCTTCCTACCATACTTCCTGTGAGAATCCCTAACATGCACATCAGATGTTTCTACACTGTTCAAAGTCGGAGTTTAACTCTAAAGCATTTGTTTGTGCCCTGTTGAACAGCTCGATGCTTCCTGTGCCTCCAACTGCTGTGGGTCCTGCTATCAGTCTGGACCTGGATGTAGACGATGTGGAGATGGAGAACTATGAGGTAAATGGAGGATATAGAAAATGCTGCCAGCCATCATCAGACTATTTTCAGCTGGGAGTACATGAGCATATTAGGGCTGTGCAATTAATCGAAAATCCGATTTCGATTTCGATTTTGGCTTTTAACGATTATGAAAAACCATTAATCGAGATAAACGATTATTCCATCACGTACCGCCTCCTTTCCAGTTGTACACGTGTGAAAACTCTTTGCCTCTGCAAAGCTCAGTTCCACGTGAAAAT

Associated Phenotype:

Not determined