ZMP

pcdh2g29

Ensembl ID:

ENSDARG00000076707

ZFIN ID:

ZDB-GENE-050610-20

Description:

protocadherin 2 gamma 29 [Source:RefSeq peptide;Acc:NP_001019372]

Human Orthologues:

PCDHB1, PCDHG@, PCDHGA1, PCDHGA10, PCDHGA11, PCDHGA12, PCDHGA3, PCDHGA5, PCDHGA6, PCDHGA7, PCDHGA8

Human Descriptions:

protocadherin beta 1 [Source:HGNC Symbol;Acc:8680]
protocadherin gamma cluster [Source:HGNC Symbol;Acc:8695]
protocadherin gamma subfamily A, 1 [Source:HGNC Symbol;Acc:8696]
protocadherin gamma subfamily A, 10 [Source:HGNC Symbol;Acc:8697]
protocadherin gamma subfamily A, 11 [Source:HGNC Symbol;Acc:8698]
protocadherin gamma subfamily A, 12 [Source:HGNC Symbol;Acc:8699]
protocadherin gamma subfamily A, 3 [Source:HGNC Symbol;Acc:8701]
protocadherin gamma subfamily A, 5 [Source:HGNC Symbol;Acc:8703]
protocadherin gamma subfamily A, 6 [Source:HGNC Symbol;Acc:8704]
protocadherin gamma subfamily A, 7 [Source:HGNC Symbol;Acc:8705]
protocadherin gamma subfamily A, 8 [Source:HGNC Symbol;Acc:8706]

Mouse Orthologue:

Pcdhb1

Mouse Description:

protocadherin beta 1 Gene [Source:MGI Symbol;Acc:MGI:2136730]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa24950	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24950

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
ENSDART00000106688	Nonsense	383	812	1	1

Genomic Location (Zv9):

Chromosome 14 (position 2998246)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	2035659
GRCz11	14	1954010

KASP Assay ID:

554-7740.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGAGGACGCAGCGCCAGAAACTGTAATAGCGATGCTGAATGTCAAAGATT[T/A]AGATTCAGGGAAAAATGGGCAGGTTAAATGTTACATTTCTGCAGACATGC

Long Flanking Sequence:

GCACAAGTTAACCCTTACAGCCTTTGATGGCGGCAATCCGCAGAGAACTGGCACTGTTAGGATATGTGTTACGGTCATAGACGCAAACGACAACGCGCCTGTATTTAGTCTGCCTGTTTACCGTGTTTCATTGTTTGAGAATGCACCTAATGGTGCTGTTGTGGTCAGAGTAAGCGCAACTGATAATGACCAAGGCGCAAACGGAGAGATAACATATTCTTTTTCACGCAGTTCTGGAAAAAATCTAGATTTATTCCATATTGGCGCAGATACAGGTGAAATTACTGTAAAAGGACATTTGGATTATGAGAGAGCTAAACAATTTGAGTTAAACATAGATGCTACGGATAAAGGTGGTTTAACTGACTCCAGTAAAGTTATAATCGATATTACAGATGTAAACGACAACCCCCCTGTGATAAGCCTGATTTCATTTTCTAATCCAATACCAGAGGACGCAGCGCCAGAAACTGTAATAGCGATGCTGAATGTCAAAGATT[T/A]AGATTCAGGGAAAAATGGGCAGGTTAAATGTTACATTTCTGCAGACATGCCGTTCAAGGTGAAGTCATCTGCCCAGAATTTTTACAGTTTGATCACTGATCAGCTTTTAGATCGTGAAAAAATATCTGAATACAATATCACAGTAACAGCTACTGATGAGGGCTCTCCATCCTTCTCCACTAATAAAACACTGACTCTGAAAATCTCCGATGTGAATGACAACGCCCCTGTGTTTGAGCGTCAGTCATACACCGCATTTATCATGGAGAATAATTCTCCAGGAGTCTCTGTTTTATCTGTTAAAGCGCACGACAGAGACTCTGGCAATAACGCGCGTATCTCCTATTTTCTAGAGGATGTTGTTGTGAATGGCGTCTCTGCCTCGACCTTTATTTCAGTCAATGCAGAGAGCGGAGAGATTCTTGCTGCTCGCTCTTTTGATTACGAGCAAACAAAAGATTTTAGCATCCGCGTAAAAGCGCAGGACGGAGGCTCTCCTC

Associated Phenotype:

Not determined