ZMP

gtpbp1l

Ensembl ID:

ENSDARG00000042900

ZFIN ID:

ZDB-GENE-041007-2

Description:

GTP binding protein 1, like [Source:RefSeq peptide;Acc:NP_001019982]

Human Orthologue:

GTPBP1

Human Description:

GTP binding protein 1 [Source:HGNC Symbol;Acc:4669]

Mouse Orthologue:

Gtpbp1

Mouse Description:

GTP binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:109443]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37468	Nonsense	Mutation detected in F1 DNA	Not yet available
sa8398	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa37468

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000062970	Nonsense	69	642	2	11
ENSDART00000122740	Nonsense	74	647	2	11
ENSDART00000125550	Nonsense	79	652	3	12

Genomic Location (Zv9):

Chromosome 22 (position 14982978)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14813526
GRCz11	22	14838101

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGTGTTGTCAGTTTGCGCTGGTCAGCCCCACAGGAGAGCAGTATGACTG[T/A]TTACAAAAACAGTTGCGAGAGCGAATAGAGGAAGGATGTGGAGAAACCAT

Long Flanking Sequence:

TGTAGGAGGCTTTGCAATATTATATTTTGCCAATAATTTAGATTAGTCAGTACTGAAGCCAAATCTGGAGCTTACAATAATGGTTAAAAAATTAGTAGCCCAAATTTATACGTAAGGGAAAAAAATGTTCAAAAATAGCAAAAATCAATAAAAAAATAAATATATATTTATTTTTTGGAATTATCTTTCCATTTCTAAAGATGTTCTGTTTTCTGATGTATCTGTTTTGTTCAAATGCACCAATATATATTACCTATATTCACTGAGAAATAGATAAAAGTATTCATATTCAAAATGGGGTGTACTCGTATATGCTGAGCATTGTAGGTATTAAAAAACAGAATGCATACCAATATTTCTGCGTTACATACAATGTCATATATCAAAATACTCAATATACAATTTTTCTTTGTATTCTTCTAGAAGTTGCTTTACTAATAAACTGCTGTTATGTGTTGTCAGTTTGCGCTGGTCAGCCCCACAGGAGAGCAGTATGACTG[T/A]TTACAAAAACAGTTGCGAGAGCGAATAGAGGAAGGATGTGGAGAAACCATCTATGTGATCGGCATGGGAACAGGTGAGACGTGTGAAGATATTAAGGCAAAACCCTGCAGACGAATAGGGTAAAACCAATGACTAATAACTAGATCATGATCATAACTAATTACACGTTATATGCGGGGTCTTAAAAAGGCCTTAGAAAGTCTGAAATCAACTGAAATGTTGTGTTGTAGGTGGTAAATCTTTTTTAACAGGTCTTAACTTTCCTTCATTCATGTATAGCTACCAAATTTGGCCATTAACACCCATGCAATCACCAACAATCCCAATCTCAATAAAACAAAAAAAAGAGCATTTAATTACTTTAATTACATGAACATTTGCTTTAAAGTTCTTCATTTGTTTACTGCTGAGGATAATGACCTGACCGAGTTTTTATTGTTAAATTATTATTATTGTATACATTGGTATTACATTGACTAAATTATAATTACTGTATATAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8398

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
ENSDART00000062970	Essential Splice Site	270	642	4	11
ENSDART00000122740	Essential Splice Site	275	647	4	11
ENSDART00000125550	Essential Splice Site	280	652	5	12

Genomic Location (Zv9):

Chromosome 22 (position 14987738)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	14818286
GRCz11	22	14842861

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CACAGTATTCGGGATGACAGGCCACTTGCCGGATTTCTGCATGCTAATGG[T/C]GAGAGGCAGTAGGTGTGCCACAAGTGTATGTACCGGGTGGTTTAAAGTTT

Long Flanking Sequence:

AGCTGTTTAAAATTCAGACAATATGGTATTTATGTGACTAAATCTCAGTCTGTATGATTTGATAATTGCACTTAGCCAAATAGCTAAAGCCAATATCGATTTAACCTCCATATTTCATGGTGCCCTAATTTTAATGCACTCTCCCTTCAGAGTGGCGGTTGTAGGGAATGTGGACGCCGGTAAAAGCACACTTCTGGGTGTCCTAACTCATGGTGAACTTGACAACGGTCGTGGATTTGCCCGCCAGAAGCTATTCCGCCACAAACATGAGATGGAGAGTGGCCGGACCAGCAGCGTTGGGAATGACATCCTGGGATTTGACCAGGAAGGGCAGGTGGTCAACAAACCGGACAGTCACGGGGGGAGCCTGGACTGGACCAAAATCTGCGAGAGGTCATCAAAGGTCATTACTTTCATTGACCTTGCAGGGCATGAGAAATATCTGAAGACCACAGTATTCGGGATGACAGGCCACTTGCCGGATTTCTGCATGCTAATGG[T/C]GAGAGGCAGTAGGTGTGCCACAAGTGTATGTACCGGGTGGTTTAAAGTTTTATTAACATTTGTGTTTTTTATTTATTGTAAAGGTGGGAAGTAATGCTGGAATCGTTGGCATGACTAAAGAGCACCTCGGTCTTGCTCTGGCCCTCAACGTTCCTGTTTTTGTAGTCGTAACTAAGATAGACATGTGTCCTGCTAACATCTTACAAGGTAATGCAATTCTTTGTATTAGTCCAGCTATTTTCCAGCTTATAATTTTTGCACATTACACATTTGTGTGTTGCAGAGACACTAAAGTTATTACAGAGGCTACTGAAGTCTCCGGGATGCCGAAAAATTCCAGTTTTAGTGCAAAATAAAGATGATGTCATTGTTACAGCCTCAAACTTCAGCTCAGAGAGGTGACTACCACATTTTCACATGATAGAATGAGCAAAAATTCCACAAACTATATATATTAGCAGCTATATATTTCATGAACATAATTACATATAGAGTAGCAC

Associated Phenotype:

Not determined