ZMP

haus7

Ensembl ID:

ENSDARG00000037432

ZFIN ID:

ZDB-GENE-050506-15

Description:

Im:6894757 protein [Source:UniProtKB/TrEMBL;Acc:Q1RM89]

Human Orthologue:

HAUS7

Human Description:

HAUS augmin-like complex, subunit 7 [Source:HGNC Symbol;Acc:32979]

Mouse Orthologue:

Haus7

Mouse Description:

HAUS augmin-like complex, subunit 7 Gene [Source:MGI Symbol;Acc:MGI:1920988]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43952	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa29904	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43952

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111720	Essential Splice Site	151	384	None	12
ENSDART00000125066	Essential Splice Site	146	379	None	10

The following transcripts of ENSDARG00000037432 do not overlap with this mutation:

ENSDART00000054479

Genomic Location (Zv9):

Chromosome 23 (position 20118697)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	19903804
GRCz11	23	19830147

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAGAGCAGCTTCTAAGGGTTATTCAAGCAGACTCCTCTCTGTGCTCTGGG[T/C]AACTCTTAAAGCATTTTGTAATAGTGATTTAACTAAATATGCTCTGATGT

Long Flanking Sequence:

GACTCATTTTTTGAATTTTTCATGATAATTTGGTTCGTCTTGTTCTTTCTCTCACACAGAGCTCACAAGGTTTGGTTATGAGATGATGTTATGTAAAGCTAACGACAAGGATTTAATCAAGGTATGGAAATAAATAATTATGCAGATTTATACTGAAAAAAAATGTGTTTGCTCTCTTTATTTTTTCTAATGACCAGACTAGACTGTATAAAAAACCGTGCTCTTGGTTTTACTTTGGCTTTCATTATTGAACTTTACAGCAATACCTTTCTTGCACAAAATATTTCTATTAAATCAAGTAGTTTTATACTGGGTACTTGACATTTTAGATAGGAAAGACAATCTTATCTTAAATGTACAAACTAAAATAATTCATTTATTTTGCTATTTCTGACAACCGATTTGTTATTTTTCAGGGTCTTGCACCGCCTTTACGACAGCTGGTGTTTCTAGAGCAGCTTCTAAGGGTTATTCAAGCAGACTCCTCTCTGTGCTCTGGG[T/C]AACTCTTAAAGCATTTTGTAATAGTGATTTAACTAAATATGCTCTGATGTATTTGCTTCATTTTTGATCAATTTCCACTGAAATTTATTTATTTTTTGGTATAATTTTCCTAAACAGATATTACAATTTTCTTAAAACGGTAAAACCACACAGAAACAGTAATATTGTATTAATTAATTAATTTACTCACACTCACATCAGCTACGGTATAGATTATTTTTTTGCAATGCAGAATATTTAAAGAAAATTATTTGGGGATTAATAATATGCTAGTCAATGTCTACTAGCACTATGAAAGTCAAAAAACAAAATGATTCCCTTTAACTCTTGAAGATACAAAGAGCTCGTTGAAGCCAAATGCAAGCAACTGAACATAATTAGCATGTTACCATAATTACATTGTTAATTCACAGCCTCAGCCAAACTGAGCACACTCACGGCAGTCTGGAGCTAAAGCTTCATGATCAAGTTTATATGCATCCCAACTCACTTTTTCACAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29904

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111720	Essential Splice Site	328	384	9	12
ENSDART00000125066	Essential Splice Site	323	379	9	10

The following transcripts of ENSDARG00000037432 do not overlap with this mutation:

ENSDART00000054479

Genomic Location (Zv9):

Chromosome 23 (position 20114499)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	19899606
GRCz11	23	19825949

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTTTGCTTATTCAAATACAAATACTTAGCATTTTCTTTGTGTCCTTTTC[A/G]GGAGCTGGAGGCTGTGAAGCAGCTTTCTGAAACTTCCACGTCTCTTACAC

Long Flanking Sequence:

CTCACAGCTCCACCTCACTGTCGCTCCATTTTAACAACTTGCTGCTTTTCATCAACATATTTTCACCATGTTTTTATAAAGTATATTAAAAAAACTTTAGCACATGAGCATTTTTGGTCCTTTCAGCGTTTATGACCAGTGTTTGGGAAATGACAGAATGGCAGTTCAAAACAGACTTTACAGCTTGATCCAGATTAGTGTAGAAATAGTAAAAGTTTCTCAGGGTACTTGTGCAAAACAATACATTTTGAATGCATTATTTCTGCTTTAGAATATAAAGCTTTTTCAATAGAACGTTTACTTGGAGGAATGCACTGCTGCTTTAGCATAACGCCACAGAGTCTTGCTGAATGCAGTTCTTGTTTGTGGTTGAGAGAACAAAAGTGTTGAGTCAAATTTTTCCACCTTTTTCTTTTTTTCTGTCATCATGTCTCATTAGTGACTACAAATACTTTGCTTATTCAAATACAAATACTTAGCATTTTCTTTGTGTCCTTTTC[A/G]GGAGCTGGAGGCTGTGAAGCAGCTTTCTGAAACTTCCACGTCTCTTACACACACACTTCAACAGCTGCAGACAGACAGACGCTACTGGTCTAAAGGAGAGAAGCACACACTGCGTCAGTGGTTTTTGGTTTGTTTTGTTTTTTAAAGCAAACTTTTTCAAACTTTTTAACATTTTTTTTTTCTTCATTAGCCAAGCAGTTGGAGGAGCTGAAGAACAGATACATGGCTTTTCTCTCCCTGCACCAGTCATAGTCGGAAGGACTCTCTCACAGTCAGCAGAAACCTGCAGTCTAGACCTTCAATTGAAGTTTCAAGTGGCGAAAAGGTGTGAGGTGTAAAACCAAAATAAAACCACTTCTCTATATGGCCAGAACGGTTTTAAAAACATGTTATTTTACATCCCGCAATGTCATGCACTGCTAGACGCAATATGAACTAACAAAAGCATCTACTAATCATGAAATGGCTCCATCTGATAAGAAACTTCATCTTTCTTTATA

Associated Phenotype:

Not determined