ZMP

zgc:55733

Ensembl ID:

ENSDARG00000022579

ZFIN IDs:

ZDB-GENE-040426-791, ZDB-GENE-040426-791

Description:

hypothetical protein LOC393968 [Source:RefSeq peptide;Acc:NP_957287]

Human Orthologues:

HNRNPC, HNRNPCL1

Human Descriptions:

heterogeneous nuclear ribonucleoprotein C (C1/C2) [Source:HGNC Symbol;Acc:5035]
heterogeneous nuclear ribonucleoprotein C-like 1 [Source:HGNC Symbol;Acc:29295]

Mouse Orthologue:

Hnrnpc

Mouse Description:

heterogeneous nuclear ribonucleoprotein C Gene [Source:MGI Symbol;Acc:MGI:107795]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa33998	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa33998

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 > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000031255	Nonsense	112	279	4	8
ENSDART00000056538	Nonsense	122	289	5	9

Genomic Location (Zv9):

Chromosome 7 (position 4275619)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	3952541
GRCz11	7	4102045

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTGATTCTTGGGTTTTCCTCCTCCCGCAGTTCTTCGTTTGATCTGGACTA[T/G]GACTTTCAGAGGGATTACTACGACAGGTGAGCGCTCCTAAAACATTCGCT

Long Flanking Sequence:

AAAGTTCAGTGAGTTCATCATGCTCGTCAGTAGTCTGAAGTTACACTGCCGTCTTTGTCATCATCTTCTAGAATTTGCAGCAAAATCGGTCATTTTAGGCTGTGAAAATCAGAAAAAGTCCAGTGAAATTCTGGAGGGATTGACAAATGATATGTCATGTAGAGCTTTTCTTTAGTGTTATGTAAACCTCCTAAATCACTGCGTGCTTAATGTTGTGTGTACACTGATTCATTCAGCTAATGCTTTTATCCAGAGCAATCAGACATGACCTCTATATAGACCGCAGGCCTGTTTCTTTTAATCATGATCATTTCATCTCCTTTTCCAGATATTAATCTGGCTGGCGAGCCCAAACCTCACCGGTCAAAGACCATCAAGCGCTCTGCAGGAGACATGTACAGGTTGGTGTTTTAGATGATTGTGTTCAGTTGTTTGTTTAATTGAGTTCTGTTGATTCTTGGGTTTTCCTCCTCCCGCAGTTCTTCGTTTGATCTGGACTA[T/G]GACTTTCAGAGGGATTACTACGACAGGTGAGCGCTCCTAAAACATTCGCTCGTGTTTAAAGCCATCCAGCGCTGCGCAGAAGAGCTTTTCTATTATTCATTAAAGCCTCACCATGACTGTCTGGACTGGGATTTGAGCTGTTTCCAGGAATGTGTGTTAATCTGTGTGTGCTGGTTTTGGTGGTTCATTTGTGAAACCAAACTAATTTAATTAATTAAATTAATGGTCCCACTTTATAATAAGTGTCCTTAACTACTATGTACTGACATCAAAAAATAAATACAATGTACTTACTGTGTTCATAATGTATTTGAGAACACTTGTGGTGCTCTTGAGTTGGGATAGAGGTTGGGTTATGGACAGGTTTGGTGGTGTGGGTAGGTTTAAGGGTGGGTTAAGGTGTAAGGGATGGTCAACAGTGTATTTACAAATGTAATTACAAAAGTTAATTACAGATATAATTACATACATGCATTTAATCAAGCATAAGTACACAGTAA

Associated Phenotype:

Not determined