ZMP

hnrnph1l

Ensembl ID:

ENSDARG00000005551

ZFIN ID:

ZDB-GENE-030131-275

Description:

heterogeneous nuclear ribonucleoprotein H1, like [Source:RefSeq peptide;Acc:NP_997754]

Human Orthologues:

HNRNPH1, HNRNPH2

Human Descriptions:

heterogeneous nuclear ribonucleoprotein H1 (H) [Source:HGNC Symbol;Acc:5041]
heterogeneous nuclear ribonucleoprotein H2 (H') [Source:HGNC Symbol;Acc:5042]

Mouse Orthologues:

Hnrnph1, Hnrnph2

Mouse Descriptions:

heterogeneous nuclear ribonucleoprotein H1 Gene [Source:MGI Symbol;Acc:MGI:1891925]
heterogeneous nuclear ribonucleoprotein H2 Gene [Source:MGI Symbol;Acc:MGI:1201779]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa45741	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa45741

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
ENSDART00000015636	Nonsense	318	407	8	11

The following transcripts of ENSDARG00000005551 do not overlap with this mutation:

ENSDART00000065447

Genomic Location (Zv9):

Chromosome 21 (position 28917996)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	30137240
GRCz11	21	30173935

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAACACATGAAGATGCAGTGGCTGCAATGTCAAAGGACAAGGCCAACATG[C/T]GTAAGTTCGGGGTATCCTGACTAGATTGCCTAAATCATGGGTGCCAAGTT

Long Flanking Sequence:

AGCGGAGGAGGACGGGGCTACAATGGCATGAGTCGTGGGGGATCCTTCGACCGGATGCGCCGTGGAGGATATGGTGGAGGTTTGAACTGATTTCTTTTTGATAATCCTCCATTGAGTCTGTGCTTTGCTTGAAATAACAGCTGTGTTTGGTGTAAATAGGAGTGTCAGATGGGCGTTACGGTGATGGTGGTAATTTCCAGAGTACCACAGGCCATTGTGTTCATATGAGGGGACTCCCTTACCGGGCCACAGAACCCGATATCTACAATGTAAGTGGGGGCTGTATGATGGGCTGTACTTTTCTGTGTTTGTTTGAGAATGATGGTAAAATAGAAATTATTTATTGTAAAAAATTTTCTATACAGTTTTTCTCACCTCTAAACCCGGTCCGTGTGCACATTGAGATCGGTCCAGATGGACGGGTGACCGGTGAGGCTGACGTTGAGTTTGCAACACATGAAGATGCAGTGGCTGCAATGTCAAAGGACAAGGCCAACATG[C/T]GTAAGTTCGGGGTATCCTGACTAGATTGCCTAAATCATGGGTGCCAAGTTCAAGTTGTTTTAGTTGTGTTTGATTAGAGGAGCTAAATTCTGCAGGAAGGTAGATCTCCAGGAACAGGGTTGAGCACCCCTGGCCTAAATCTTTAGGCAAGACACTACAGAATATACACTGCGTCTTCATGCACTGGTCATTGTTATTTATAGATTTTTACAGTATTTTTCATTTTTCATTTTACATTTTTCATGTGTTGTTTCAAGTTTGTTTATTTTATTACAAGTAATGGTAACACTTTATTTTGATGGTCCATTTGAGTATTAGTAGACTCTGCTTAATATTTGTTGATACTGCTCCCTTAACACGTGCCTATAATGACCCATTTCCATTGGTATGGTTCGGTATGCTTTTATGGCCATTTCCACTGTCAAAGGGTAACTAATAGTGATCCGTATATTTATCACCCATTGCTAAGGATACCTAGCATGAAAAAACGGTACCAAAAG

Associated Phenotype:

Not determined