ZMP

iqch

Ensembl ID:

ENSDARG00000015476

ZFIN ID:

ZDB-GENE-050419-242

Description:

IQ motif-containing protein H [Source:UniProtKB/Swiss-Prot;Acc:Q1LXZ7]

Human Orthologue:

IQCH

Human Description:

IQ motif containing H [Source:HGNC Symbol;Acc:25721]

Mouse Orthologue:

Iqch

Mouse Description:

IQ motif containing H Gene [Source:MGI Symbol;Acc:MGI:1925500]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36633	Nonsense	Mutation detected in F1 DNA	Not yet available
sa29020	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36633

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079691	Nonsense	97	1079	4	21
ENSDART00000135049	Nonsense	97	1059	4	21
ENSDART00000147470	None	None	180	None	3

Genomic Location (Zv9):

Chromosome 18 (position 19602831)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	19833054
GRCz11	18	19822120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATCAATTGAGATCCAACATATCTAGCCTTTTTTGTAGGCAACCACCATA[C/A]GAAGCATTACCAATTGCACATCCACATAGAAGCCCGATTCCAGGTCCATC

Long Flanking Sequence:

AAACATTTCCGCTGTGGTCTGATATTTGCAGTGCATTTCTGTTTTTGCATGTAATCAAGAAAAAGATACAATTGAAAAAAGTGTTTTACCGTTTCCCGAGTCTAGGAGTATCAAAGTACAGTAACTGAATGTTAAAAATAACTCAGTGAAATAAATCGCTGTTAAAGTTACAAATGGTACAATTTATTATGCCTGGATGCTTTTAAGGTCATTATACAATCACAGGCATCAAAAACACATCCAAATGATGAATTATAATCCCGACTCAACATTGGGTATGCTTGTGTTGTGACTATTGTGAATAATCTCATTGTGATATTGATGCTGAAACAATATATTGTGCAACCCTAATTGCTGTCATGTCATTGAATATTTGCATTAACAAGAAGTTGATCAAGATGTACCTAATACAGTGGCCATGTGTATACAGTATGATTGTAGATTATGTAAAATCAATTGAGATCCAACATATCTAGCCTTTTTTGTAGGCAACCACCATA[C/A]GAAGCATTACCAATTGCACATCCACATAGAAGCCCGATTCCAGGTCCATCTCCAGGGGAAAAGGTTTTTATTTTTATTCATAGTCATAACATTTGTTAATCTCAGATTAGATCTGAATTCACTAAATCTATCTTTGTAACTTGTCCAACAGCACAAGACAGCATTTATCATGCGTCTGCTACATAACCCTTTTCATCCAAGGAACAAGGAGATTTTCCAACAAAATTATGGGATTCAGCTTCCTCACCTGCAAAAGAGAACTAGTGTGAGTTTCTGAAAGATATGCTTTTATTTCTTTGATATTCAAGAAAGTATATTAAAAGATCAGTGCACCTATAATTGCATATTCTGCCATCTTTTACTTACTTTCACGTTGTTCCAAACGTTTATTTCGTCTATAGCACACACAAAAATTATTAGTTATTTTAATTATAATAATTATATTTTAAGGTGTCCTTGTTAATTTAACTAGTCATTTAACAAGTGAATACTATTAAATA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29020

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000079691	Essential Splice Site	578	1079	13	21
ENSDART00000135049	Essential Splice Site	578	1059	13	21
ENSDART00000147470	None	None	180	None	3

Genomic Location (Zv9):

Chromosome 18 (position 19622842)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	19853065
GRCz11	18	19842131

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCCTTTTAGTGTCCCTTTATCTCCTAATGGTGCATTATATTTCTCTTTC[A/T]GACCCGAAACTTATGTCTAGCTTCGCTCCTGAAATACAGTCCACGAACTC

Long Flanking Sequence:

GTCATGAAATTTGCGACAAACACGTGAAGGTGGTGTGATGCTCTCCACGTGTAGCGAAACCATAGAGCAAAACAGATGACAAAATGGGAAAATGTTAGTTTGTGTACTCCTGTTTGGAAAAAGCCGAGTTTAAACAGTGGCTGAAGCCTGTTGCTGAAAACAACCACGTAATTTATTCTTTCAAGCTTTGTTTCTTCCGAGCTTTTCTGAGTTCTGTTGCATGGTTGTGCTCCATTGATTTATTTAACTACAACTGTTTATTAACAAATGTTTATAAAGTTAAAGGTTTGACACTGATTAGAACTTGAAGTGGTGATGAGGTCTCAAAATATTCTCAGAAGGTGTTTAAGAAGTCTTAAAAAGGTATTAAAATTCATTTTAGGGTTCCTGCATTTACCCTGTGTAACCAATTGAGGAAATAGTATTCAATCTTCATTTCTGAATAAACTATCCCTTTTAGTGTCCCTTTATCTCCTAATGGTGCATTATATTTCTCTTTC[A/T]GACCCGAAACTTATGTCTAGCTTCGCTCCTGAAATACAGTCCACGAACTCTAAAGCGCATCAAGAATTTGATCAAGGGAAAACAGGCCTACATGATCAGCGGTGTTACCCACACTGATGACCTGGCTGTGGCAGATGAGCTACAAATTCCTCTTCTGGGCACAGACCCTGTGGTAACCCAGCTCTACTCCACTAAATCTGGAGGGAAAAGAATCTTCAGTAGCGCAGGAGTCGACATGCCTCCAGGAAAGTGGGATATATACACCTTGGAAAAGGTCAGAGTGCCAGCCATCTGAAACTTGCATTTGAGAATATGGAAAACTCACTTTGCAGTAATACATATGTTTTTTTGCTGCAGCTCTATGAAGGTCTAGCTCAGCTGATGGCAAAGCACATGGAAGTCCAGCGATGGCTTTTTAAGATAGACAGTGAAGTGGGTGGACGGGGAACTGCTTATGTTGATGTCTGCCATCTGAAAAGTCGCCCATGGGCACAACAGGA

Associated Phenotype:

Not determined